| Position |
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352 |
Skare O, Jugessur A, Lie RT, Wilcox AJ, Murray JC, Lunde A, Nguyen TT, Gjessing HK - Application of a Novel Hybrid Study Design to Explore Gene-Environment Interactions in Orofacial Clefts - Ann Hum Genet 2012 , 221-236 |  | 351 |
Radhakrishna U, Nath SK, McElreavey K, Ratnamala U, Sun C, Maiti AK, Gagnebin M, Béna F, Newkirk HL, Sharp AJ, Everman DB, Murray JC, Schwartz CE, Antonarakis SE, Butler MG - Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele - J Med Genet 2012 , 270-6 | | 350 |
the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Ikram MA, Fornage M, Smith AV, Seshadri S, Schmidt R, Debette S, Vrooman HA et. al - Common variants at 6q22 and 17q21 are associated with intracranial volume - Nat Genet 2012 , in press | | 349 |
Taal HR, St Pourcain B, Thiering E, Das S, Mook-Kanamori DO, Warrington NM, Kaakinen M, Kreiner-Møller E et. al - Common variants at 12q15 and 12q24 are associated with infant head circumference - Nat Genet 2012 , in press | | 348 |
Murray T, Taub MA, Ruczinski I, Scott AF, Hetmanski JB, Schwender H, Patel P, Zhang TX, Munger RG, Wilcox AJ, Ye X, Wang H, Wu T, Wu-Chou YH, Shi B, Jee SH, Chong S, Yeow V, Murray JC, Marazita ML, Beaty TH - Examining Markers in 8q24 to Explain Differences in Evidence for Association With Cleft Lip WithWithout Cleft Palate Between Asians and Europeans - Genet Epidemiol 2012 , in press | | 347 |
Wu T, Fallin MD, Shi M, Ruczinski I, Liang KY, Hetmanski JB, Wang H, Ingersoll RG, Huang S, Ye X, Wu-Chou YH, Chen PK, Jabs EW, Shi B, Redett R, Scott AF, Murray JC, Marazita ML, Munger RG, Beaty TH - Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip withwithout cleft palate - Birth Defects Res A Clin Mol Teratol 2012 , 76-83 | | 346 |
Feenstra B, Geller F, Krogh C, Hollegaard MV, Gortz S, Boyd HA, Murray JC, Hougaard DM, Melbye M - Common Variants near MBNL1 and NKX2-5 are Associated with Infantile Hypertrophic Pyloric Stenosis - Nat Genet 2012 , 334-7 | | 345 |
Wehby G, Murray JC, Wilcox A, Lie RT - Smoking and Body Weight: Evidence Using Genetic Instruments - Econ Hum Biol 2012 , 113-26 | | 344 |
Wehby GL, Castilla EE, Goco N, Rittler M, Cosentino V, Javois L, Kindem M, Chakraborty H, Dutra G, Lopez-Camelo JS, Orioli IM, Murray JC - The Effect of Systematic Pediatric Care on Neonatal Mortality and Hospitalizations of Infants Born with Oral Clefts - BMC Pediatr 2011 , 121 | | 343 |
Boghossian NS, Horbar JD, Murray JC, Carpenter JH for the Vermont Oxford Network - Anthropometric Charts for Infants with Trisomies 21, 18 or 13 Born Between 22 weeks Gestation and Term: The VON Charts - Am J Med Genet A 2012 , 322-332 | | 342 |
Paternoster L, Standl M, Chen C-M, Ramasamy A, Bonnelykke K, Duijts L, Ferreira MA, . . . Murray JC. . . Weidinger S. (112 Authors) - Meta-analysis of genome-wide association studies identified three new risk loci for atopic dermatitis - Nat Genet 2011 , 187-192 | | 341 |
Boghossian NS, Horbar JD, Carpenter JH, Murray JC, Bell EF; Vermont Oxford Network - Major Chromosomal Anomalies among Very Low Birth Weight Infants in the Vermont Oxford Network - J Pediatr 2011 , in press | | 340 |
Dietz A, Pedersen DA, Jacobsen R, Wehby GL, Murray JC, Christensen K - Risk of breast cancer in families with cleft lip and palate - Ann Epidemiol 2012 , 37-42 | | 339 |
Ryckman KK, Dagle JM, Kelsey K, Momany A, Murray JC - Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates - J Perinatol 2011 , in press | | 338 |
Ryckman KK, Feenstra B, Shaffer JR, Bream EN, Geller F, Feingold E, Weeks DE, Gadow E, Cosentino V, Saleme C, Simhan HN, Merrill D, Fong CT, Busch T, Berends SK, Comas B, Camelo JL, Boyd H, Laurie CC, Crosslin D, Zhang Q, Doheny KF, Pugh E, Melbye M, Marazita ML, Dagle JM, Murray JC - Replication of a Genome-Wide Association Study of Birth Weight in Preterm Neonates - J Pediatr 2012 , 19-24 | | 337 |
Wehby GL, Fletcher JM, Lehrer SF, Moreno LM, Murray JC, Wilcox A, Lie RT - A genetic instrumental variables analysis of the effects of prenatal smoking on birth weight: evidence from two samples - Biodemography Soc Biol 2011 , 3-32 | | 336 |
Wehby GL, Prater K, McCarthy AM, Castilla EE, Murray JC - The impact of maternal smoking during pregnancy on early child neurodevelopment - Journal of Human Capital 2011 , 207-254 | | 335 |
Byers HM, Dagle JM, Klein JM, Ryckman KK, McDonald EL, Murray JC, Borowski KS - Variations in CRHR1 are associated with persistent pulmonary hypertension of the newborn - Pediatr Res 2012 , 162-7 | | 334 |
Saadi I, Alkuraya FS, Gisselbrecht SS, Goessling W, Cavallesco R, Turbe-Doan A, Petrin AL, Harris J, Siddiqui U, Grix AW Jr, Hove HD, Leboulch P, Glover TW, Morton CC, Richieri-Costa A, Murray JC, Erickson RP, Maas RL - Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting - Am J Hum Genet 2011 , 44-55 | | 333 |
Geller F, Feenstra B, Zhang H, Shaffer JR, Hansen T, Esserlind A-L, Boyd HA, Nohr EA, Timpson NJ, Fatemifar G, Paternoster L, Evans DM, Weyant RJ, Levy SM, Lathrop M, Davey Smith G, Murray JC, Olesen J, Werge T, Marazita ML, Sorensen TIA, Melbye M - Genome-wide association study identifies four loci associated with eruption of permanent teeth - PLoS Genetics 2011 , e1002275 | | 332 |
Wehby GL, Jugessur A, Murray JC, Moreno LM, Wilcox A, Lie RT - Genes as instruments for studying risk behavior effects: An application to maternal smoking and orofacial clefts - Health Services and Outcomes Research Methodology 2011 , 54-78 | | 331 |
Shaffer JR, Wang X, Feingold E, Myoungkeum L, Begum F, Weeks DE, Cuenco KT, Barmada MM, Wendell SK, Crosslin DR, Laurie CC, Doheny KF, Pugh EW, Zhang Q, Feenstra B, Geller F, Boyd HA, Zhang H, Melbye M, Murray JC, Weyant RJ, Crout R, McNeil DW, Levy SM, Slayton RL, Willing MC, Broffitt B, Vieira AR, Marazita ML - Genome-wide association scan for childhood caries implicates novel genes - Journal of Dental Research 2011 , 1457-62 | | 330 |
Beaty TH, Ruczinski I, Murray JC, Marazita ML, Munger RG, Hetmanski JB, Murray T, Redett RJ, Fallin MD, Liang KY, Wu T, Patel PJ, Jin SC, Zhang TX, Schwender H, Wu-Chou YH, Chen PK, Chong SS, Cheah F, Yeow V, Ye X, Wang H, Huang S, Jabs EW, Shi B, Wilcox AJ, Lie RT, Jee SH, Christensen K, Doheny KF, Pugh EW, Ling H, Scott AF. - Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. - Genet Epidemiol 2011 , 469-78 | | 329 |
Ryckman KK, Dagle JM, Kelsey K, Momany AM, Murray JC. - Replication of genetic associations in the inflammation, complement, and coagulatin pathways with intraventricular hemorrhage in LBW preterm neonates. - Pediatr Res 2011 , 90-5 | | 328 |
Jobling R, Thomas MA, Murray J, Ferrier R, Mcleod R, Lorenco Petrin A. - Monozygotic twins with variable expression of Van der Woude syndrome. - Am J Med Genet 2011 , 2008-10 | | 327 |
Mossey PA, Shaw WC, Munger RG, Murray JC, Murthy J, Little J. - Global oral health inequalities: Challenges in the prevention and management of orofacial clefts and potential solutions. - Adv Dent Res 2011 , 247-258 | | 326 |
Rittler M, Cosentino V, Lopez-Camelo JS, Murray JC, Wehby G, Castilla E. - Associated anomalies among infants with oral clefts at birth and during a 1 year follow-up. - Am J Hum Genet 2011 , 1588-96 | | 325 |
O’Sullivan J, Bitu C, Daley SB, Urquhart JE, Barron MJ, Bhasker SS, Martelli-Junior H, dos Santos Neto, PE, Mansilla MA, Murray JC, Coletta R, Black GCM, Dixon MJ. - Whole-exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta. - Am J Hum Genet 2011 , 616-20 | | 324 |
Grosen D, Bille C, Petersen I, Skytthe A, Hielmborg JB, Pedersen JK, Murray JC, Christensen K. - Risk of oral clefts in twins. - Epidemiology 2011 , 313-19 | | 323 |
Hochheiser H, Aronow BJ, Artinger K, Beaty TH, Brinkley JF, Chai Y, Clouthier D, Cunningham ML, Dixon M, Donahue LR, Fraser SE, Iwata J, Marazita ML, Murray JC, Murray S, Postlethwait J, Potter S, Shapiro L, Spritz R, Visel, Weinberg SM, Trainor PA for the FaceBase Consortium. - The FaceBase Consortium: A Comprehensive Program to Facilitate Craniofacial Research. - Dev Biol 2011 , 175-82 | | 322 |
Dagle JM, Fisher TJ, Haynes SE, Berends SK, Brophy PD, Morriss FH Jr, Murray JC. - Cytochrome P450 (CYP2D6) genotype is associated with elevated systolic blood pressure in preterm infants after discharge from the neonatal intensive care unit. - J Pediatr 2011 , 104-9 | | 321 |
Hansen TG, Pedersen JK, Henneberg SW, Pedersen DA, Murray JC, Morton NS, Christensen K. - Academic performance in adolescence after inguinal hernia repair in infancy. - Anesthesiology 2011 , 1076-85 | | 320 |
Simon CM, L'Heureux J, Murray JC, Winokur P, Weiner G, Newbury E, Shinkunas L, Zimmerman B. - Active choice, but not too active: public perspectives on biobank consent models. - Genet Med 2011 , 821-31 | | 319 |
Bertolacini C, Ribeiro-Bicudo L, Petrin A, Richieri-Costa A, Murray J. - Clinical findings in patients with GLI2 mutations - phenotypic variability. - Clin Genet 2011 , 70-75 | | 318 |
Haataja R, Karjalainen MK, Luukkonen A, Teramo K, Puttonen H, Ojaniemi M, Varilo T, Chaudhari BP, Plunkett J, Murray JC, McCarroll SA, Peltonen L, Muglia LJ, Palotie A, Hallman M - Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis - PLoS Genet 2011 , e1001293 | | 317 |
Butali A, Mossey PA, Adeyemo WL, Jezewski PA,Onwuamah CK , Ogunlewe MO, Ugboko VI, Adejuyigbe O, Adigun AI, Abdur-Rahman LO, Onah II, Audu RA, Idigbe EO, , Mansilla MA, Dragan EA, Petrin AL, Bullard SA, Uduezue AO, , Akpata O, Osaguona AO, Olasoji HO, Ligali TO, Kejeh BM, Iseh KR, Olaitan PB, Adebola AR, Efunkoya E, Adesina OA, Oluwatosin OM, Murray JC, The NigeriaCRAN collaboration. - Genetic studies in the Nigerian population implicate a MSX1 mutation in complex oral facial clefting disorders. - Cleft Palate Craniofac J 2011 , 646-653 | | 316 |
Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Nguyen TT, Christiansen L, Lidral AC, Murray JC - Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: A subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia - Birth Defects Res A 2011 , Feb;91(2):85-92 | | 315 |
Ghassibe-Sabbagh M, Desmyter L, Langenberg T, Claes F, Boute O, Bayet B, Pellerin P, Hermans K, Backx L, Mansilla MA, Imoehl S, Nowak S, Ludwig KU, Baluardo C, Ferrian M, Mossey PA, Noethen M, Dewerchin M, Francois G, Revencu N, Vanwijck R, Hecht J, Mangold E, Murray J, Rubini M, Vermeesch JR, Poirel HA, Carmeliet P, Vikkula M. - FAF1, a gene that is disrupted in cleft palate and has conserved function in Zebrafish. - Am J Hum Genet 2011 , Feb 11;88(2):150-61. | | 314 |
Schutte B, Murray JC. - Genomic strategy identifies a missense mutation in WD-repeat Domain 65 (WDR65) in an individual with Van der Woude Syndrome. - Am J Med Genet A 2011 , 1314-21 | | 313 |
Dixon M, Marazita M, Beaty T, Murray JC - Cleft lip and palate: Understanding genetic and environmental influences - Nat Rev Genet 2011 , Mar;12(3):167-78. | | 312 |
Wehby GL, Murray JC, McCarthy AM, Castilla EE - Racial gaps in child health insurance coverage in four South American countries: The role of wealth, human capital, and other household characteristics - Health Serv Res 2011 , 2119-2138 | | 311 |
Elks CE, Perry JR, Sulem P, Chasman DI, Franceschini N, Murray, JC. Murray A. (175 authors) - Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. - Nat Genet. 2010 , Dec;42(12):1077-85. | | 310 |
Day LJ, Schaa JL, Ryckman KK, Dagle JM, Fong CT, Simhan HN, Merrill DC, Murray JC, England SK. - Single nucleotide polymorphisms in the KCNN3 gene associate with preterm birth. - Reproductive Sciences 2011 , Feb 1. [Epub ahead] | | 309 |
Kao JS, Dawson JD, Murray JC, Dagle JM, Berends SK, Gillen SB, Bell EF. - Possible roles of bilirubin and breast milk in protection against retinopathy of prematurity. - Acta Paediatr. 2011 , Mar;100(3):347-51 | | 308 |
Mumtaz G, Nassar AH, Mahfoud Z, El-Khamra A, Al-Choueiri N, Adra A, Murray JC, Zalloua P, Yunis KA. - Consanguinity: a risk factor for preterm birth at less than 33 weeks' gestation. - Am J Epidemiol. 2010 , Dec 15;172(12):1424- | | 307 |
Mahajan VB, Olney AH, Garrett P, Chary A, Dragan E, Lerner G, Murray J, Bassuk AG. - Collagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemia. - Am J Med Genet A. 2010 , Nov;152A(11):2875-9. | | 306 |
Brémond-Gignac D, Bitoun P, Reis LM, Copin H, Murray JC, Semina EV. - Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia. - Mol Vis 2010 , Aug 22;16:1705-11. | | 305 |
Boghossian NS, Hansen NI, Bell EF, Stoll BJ, Murray JC, Laptook AR, Shankaran S, Walsh MC, Das A, Higgins RD; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. - Survival and morbidity outcomes for very low birth weight infants with Down syndrome. - Pediatrics 2010 , Dec;126(6):1132-40 | | 304 |
Petrin AL, Giacheti CM, Maximino LP, Abramides DV, Zanchetta S, Rossi NF, Richieri-Costa A, Murray JC. - Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. - Am J Med Genet A. 2010 , Dec;152A(12):3164-72 | | 303 |
Félix TM, Petrin AL, Sanseverino MT, Murray JC. - Further characterization of microdeletion syndrome involving 2p15-p16.1. - Am J Med Genet A. 2010 , Oct;152A(10):2604-8. | | 302 |
Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Nguyen TT, Christiansen L, Lidral AC, Murray JC. - Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. - PLoS One. 2010 , Jul 9;5(7):e11493. | | 301 |
Waleh N, Hodnick R, Jhaveri N, McConaghy S, Dagle J, Seidner S, McCurnin D, Murray JC, Ohls R, Clyman RI. - Patterns of gene expression in the ductus arteriosus are related to environmental and genetic risk factors for persistent ductus patency. - Pediatr Res. 2010 , Oct;68(4):292-7. | | 300 |
Boyles AL, DeRoo LA, Lie RT, Taylor JA, Jugessur A, Murray JC, Wilcox AJ. - Maternal alcohol consumption, alcohol metabolism genes, and the risk of oral clefts: a population-based case-control study in Norway, 1996-2001. - Am J Epidemiol. 2010 , Oct 15;172(8):924-31 | | 299 |
Grosen D, Bille C, Pedersen JK, Skytthe A, Murray JC, Christensen K. - Recurrence risk for offspring of twins discordant for oral cleft: a population-based cohort study of the Danish 1936-2004 cleft twin cohort - Am J Med Genet A. 2010 , Oct;152A(10):2468-74 | | 298 |
Abu-Maziad A, Schaa K, Bell EF, Dagle JM, Cooper M, Marazita ML, Murray JC. - Role of polymorphic variants as genetic modulators of infection in neonatal sepsis. - Pediatr Res. 2010 , Oct;68(4):323-9. | | 297 |
Petrin AL, Daack-Hirsch S, L’Heureux J, Murray JC. - A case of 3q29 microdeletion syndrome involving cleft lip and palate inherited from a non-affected mosaic parent: molecular analysis and ethical implications. - Cleft Palate Craniofac J. 2011 , Mar;48(2):222-30 | | 296 |
Schmidt RJ, Romitti PA, Burns TL, Murray JC, Browne ML, Druschel CM, Olney RS; National Birth Defects Prevention Study. - Caffeine, selected metabolic gene variants, and risk for neural tube defects. - Birth Defects Res A Clin Mol Teratol. 2010 , Jul;88(7):560-9. | | 295 |
Beaty TH, Murray JC, Marazita ML, Munger RG, Ruczinsky I, …. Scott AF (53 authors). - A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 - Nat Genet. 2010 , Jun;42(6):525-9. | | 294 |
Jones JL, Canady JW, Brookes JT, Wehby GL, L'Heureux J, Schutte BC, Murray JC, Dunnwald M. - Wound complications after cleft repair in children with Van der Woude syndrome. - J Craniofac Surg. 2010 , Sep;21(5):1350-3. | | 293 |
Tomblin JB, O'Brien M, Shriberg LD, Williams C, Murray J, Patil S, Bjork J, Anderson S, Ballard K. - Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2. - J Speech Lang Hear Res. 2009 , Oct;52(5):1157-74. | | 292 |
Moreno LM, Mansilla MA, Bullard SA, Cooper ME, Busch TD, Machida J, Johnson MK, Brauer D, Krahn K, Daack-Hirsch S, L'heureux J, Valencia-Ramirez C, Rivera D, López AM, Moreno MA, Hing A, Lammer EJ, Jones M, Christensen K, Lie RT, Jugessur A, Wilcox AJ, Chines P, Pugh E, Doheny K, Arcos-Burgos M, Marazita ML, Murray JC, Lidral AC. - FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. - Hum Mol Genet. 2009 , Dec 15;18(24):4879-9 | | 291 |
Boyd HA, Poulsen G, Wohlfahrt J, Murray JC, Feenstra B, Melbye M. - Maternal contributions to preterm delivery. - Am J Epidemiol. 2009 , Dec 1;170(11):1358-6 | | 290 |
Bille C, Pedersen DA, Andersen AM, Mansilla MA, Murray JC, Christensen K, Ballard JL, Gorman EB, Cabrera RM, Finnell RH. - Autoantibodies to folate receptor alpha during early pregnancy and risk of oral clefts in Denmark. - Pediatr Res. 2010 , Mar;67(3):274-9. | | 289 |
Letra A, Menezes R, Cooper ME, Fonseca RF, Tropp S, Govil M, Granjeiro JM, Mansilla MA, Murray JC, Castilla EE, Orioll IM, Czeizel AE, Ma L, Chiquet BT, Hecht JT, Vieira AR, and Marazita ML - CRISPLD2 Variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with our without cleft palate - Cleft Palate Craniofac J 2010 , 363-70 | | 288 |
Mutti DO, Cooper ME, Dragan E, Jones-Jordan LA, Bailey MD, Marazita ML, Murray JC, Zadnik K and CLEERE Study Group - Vitamin D receptor (VDR) polymorphisms in myopia - Ophthalmol Vis Sci 2011 , 3818-3824 | | 287 |
King JL, Yang B, Sparks AE, Mains LM, Murray JC, and Van Voorhis, BJ. - Skewed X inactivation and IVF-conceived infants. - Reprod Biomed Online 2010 , May;20(5):660-3. | | 286 |
Genisca AE, FrÃas JL, Broussard CS, Honein MA, Lammer EJ, Moore CA, Shaw GM, Murray JC, Yang W, Rasmussen SA; National Birth Defects Prevention Study. - Orofacial clefts in the National Birth Defects Prevention Study, 1997-2004. - Am J Med Genet A. 2009 , Jun;149A(6):1149-58. | | 285 |
Grosen D, Chevrier C, Skytthe A, Bille C, Mølsted K, Sivertsen A, Murray JC, Christensen K. - A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance. - J Med Genet. 2010 , Mar;47(3):162-8. Epu | | 284 |
Rahimov F, Murray JC - Genetics of nonsyndromic orofacial clefts - Cleft Palate Craniofac J 2011 , in press | | 283 |
Kimani JW, Yoshiura K, Shi M, Jugessur A, Moretti-Ferreira D, Christensen K, Murray JC. - Search for genomic alterations in monozygotic twins discordant for cleft lip and/or palate. - Twin Res Hum Genet. 2009 , Oct;12(5):462-8. | | 281 |
Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Trung TN, Bille C, Lidral AC, Murray JC. - Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia. - PLoS One. 2009 , 4(4):e5385. Epub 200 | | 280 |
Wehby GL, Murray JC, Castilla EE, Lopez-Camelo JS, Ohsfeldt RL. - Prenatal care effectiveness and utilization in Brazil. - Health Policy Plan. 2009 , May;24(3):175-88. Ep | | 279 |
Wehby GL, Castilla EE, Lopez-Camelo JS, Murray JC. - Predictors of multivitamin use during pregnancy in Brazil. - Int J Public Health. 2009 , 54(2):78-87. | | 278 |
Wehby GL, Murray JC, Castilla EE, Lopez-Camelo JS, Ohsfeldt RL. - Prenatal care demand and its effects on birth outcomes by birth defect status in Argentina. - Econ Hum Biol. 2009 , Mar;7(1):84-95. Epub | | 277 |
Marazita ML, Lidral AC, Murray JC, Field LL, Maher BS, Goldstein McHenry T, Cooper ME, Govil M, Daack-Hirsch S, Riley B, Jugessur A, Felix T, Morene L, Mansilla MA, Vieira AR, Doheny K, Pugh E, Valencia-Ramirez C, Arcos-Burgos M. - Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results. - Hum Hered. 2009 , 68(3):151-70. Epub 2 | | 276 |
Suzuki S, Marazita ML, Cooper ME, Miwa N, Hing A, Jugessur A, Natsume N, Shimozato K, Ohbayashi N, Suzuki Y, Niimi T, Minami K, Yamamoto M, Altannamar TJ, Erkhembaatar T, Furukawa H, Daack-Hirsch S, L'heureux J, Brandon CA, Weinberg SM, Neiswanger K, Deleyiannis FW, de Salamanca JE, Vieira AR, Lidral AC, Martin JF, Murray JC. - Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. - Am J Hum Genet. 2009 , Mar;84(3):406-11. Ep | | 275 |
Wehby GL, Murray JC, Castilla EE, Lopez-Camelo JS, Ohsfeldt RL. - Quantile effects of prenatal care utilization on birth weight in Argentina. - Health Econ. 2009 , Nov;18(11):1307-21. | | 274 |
Ferreira de Lima RL, Hoper SA, Ghassibe M, Cooper ME, Rorick NK, Kondo S., Katz L. Marazita ML, Compton J, Bale S, Hehr U, Dixon MJ, Daack-Hirsch S, Boute O, Bayet B, Revencu N, Verellen-Dumoulin C, Vikkula M, Richieri-Costa A, Moretti-Ferreira D, Murray JC, Schutte B. - Prevalence and non-random distribution of exonic mutations in Interferon Regulatory Factor 6 (IRF6) in 307 cases of Van der Woude syndrome and 37 cases of popliteal pterygium snydrome. - Genet Med. 2009 , Apr;11(4):241-7. | | 273 |
Machida J, Félix TM, Murray JC, Yoshiura K, Tanemura M, Kamamoto M, Shimozato K, Sonta S, Ono T. - Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12). - Cleft Palate Craniofac J. 2009 , Sep;46(5):532-40. Ep | | 272 |
Shi M, Mostowska A, Jugessur A, Johnson MK, Mansilla MA, Christensen K, Lie RT, Wilcox AJ, Murray JC. - Identification of microdeletions in candidate genes for cleft lip and/or palate. - Birth Defects Res A Clin Mol Teratol. 2009 , Jan;85(1):42-51. | | 271 |
Dagle JM, Lepp NT, Cooper ME, Schaa KL, Kelsey KJ, Orr KL, Caprau D, Zimmerman CR, Steffen KM, Johnson KJ, Marazita ML, Murray JC. - Determination of genetic predisposition to patent ductus arteriosus in preterm infants. - Pediatrics. 2009 , Apr;123(4):1116-23. | | 270 |
Rahimov F, Marazita ML, Visel A, Cooper ME, Hitchler MJ, Rubini M, Domann FE, Govil M, Christensen K, Bille C, Melbye M, Jugessur A, Lie RT, Wilcox AJ, Fitzpatrick PA, Green ED, Mossey PA, Little J, Steegers-Theunissen RP, Pennacchio LA, Schutte BC and Murray JC. - Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip. - Nat Genet. 2008 , Nov;40(11):1341-7. | | 269 |
Choi SJ, Marazita ML, Hart PS, Sulima PP, Field LL, McHenry TG, Govil M, Cooper ME, Letra A, Menezes R, Narayanan S, Mansilla MA, Granjeiro JM, Vieira AR, Lidral AC, Murray JC, Hart TC. - The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P. - Eur J Hum Genet. 2009 , Jun;17(6):774-84. Ep | | 268 |
Mohamed S, Schaa K, Cooper ME, Ahrens E, Alvarado A, Colaizy T, Marazita ML, Murray JC, Dagle JM. - Genetic contributions to the development of retinopathy of prematurity. - Pediatr Res. 2009 , Feb;65(2):193-7. | | 267 |
Vieira AR, McHenry TG, Daack-Hirsch S, Murray JC, Marazita ML. - Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts. - Genet Med. 2008 , Sep;10(9):668-74. | | 266 |
Boyles AL, Wilcox AJ, Taylor JA, Shi M, Weinberg CR, Meyer K, Fredriksen A, Ueland PM, Johansen AM, Drevon CA, Jugessur A, Trung TN, Gjessing HK, Vollset SE, Murray JC, Christensen K, Lie RT. - Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study. - Genet Epidemiol. 2009 , Apr;33(3):247-55. | | 265 |
Vieira AR, Howe A, Murray JC. - Studies of gamma-aminobutyric acid type A receptor beta3 (GABRB3) and glutamic acid decarboxylase 67 (GAD67) with oral clefts. - Am J Med Genet A. 2008 , Nov 1;146A(21):2828- | | 264 |
Vieira AR, McHenry TG, Daack-Hirsch S, Murray JC, Marazita ML. - A genome wide linkage scan for cleft lip and palate and dental anomalies. - Am J Med Genet A. 2008 , Jun 1;146A(11):1406- | | 263 |
Shi M, Wehby GL, Murray JC. - Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects. - Birth Defects Res Part C. 2008 , Mar;84(1):16-29. | | 262 |
Wehby GL, Ohsfeldt RL, Murray JC. - 'Mendelian randomization' equals instrumental variable analysis with genetic instruments. - Stat Med. 2008 , Jul 10;27(15):2745-9 | | 261 |
Jugessur A, Rahimov F, Lie RT, Wilcox AJ, Gjessing HK, Nilsen RM, Nguyen TT, Murray JC. - Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway. - Genet Epidemiol. 2008 , Jul;32(5):413-24. | | 260 |
Kimani JW, Shi M, Daack-Hirsch S, Christensen K, Moretti-Ferreira D, Marazita ML, Field LL, Canady JW, Murray JC. - X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate. - Am J Med Genet A. 2007 , Dec 15;143A(24):3267 | | 259 |
Freitas EL, Martinhago CD, Ramos ES, Murray JC, Gil-da-Silva-Lopes VL. - Preliminary molecular studies on blepharocheilodontic syndrome. - Am J Med Genet A. 2007 , Nov 15;143A(22):2757 | | 258 |
Merialdi M, Murray JC. - The changing face of preterm birth. - Pediatrics. 2007 , Nov;120(5):1133-4. | | 257 |
Osoegawa K, Vessere GM, Utami KH, Mansilla MA, Johnson MK, Riley BM, L'Heureux J, Pfundt R, Staaf J, van der Vliet WA, Lidral AC, Schoenmakers EF, Borg A, Schutte BC, Lammer EJ, Murray JC, de Jong PJ. - Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.
- J Med Genet. 2008 , Feb;45(2):81-6. Epub | | 256 |
Riley BM, Murray JC. - Sequence evaluation of FGF and FGFR gene conserved non-coding elements in non-syndromic cleft lip and palate cases. - Am J Med Genet A. 2007 , Dec 15;143A(24):3228 | | 255 |
Steffen KM, Cooper ME, Shi M, Caprau D, Simhan HN, Dagle JM, Marazita ML, Murray JC. - Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery. - J Perinatol. 2007 , Nov;27(11):672-80. E | | 254 |
Ehn NL, Cooper ME, Orr K, Shi M, Johnson MK, Caprau D, Dagle J, Steffen K, Johnson K, Marazita ML, Merrill D, Murray JC. - Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth. - Pediatr Res. 2007 , Nov;62(5):630-5. | | 253 |
Mutti DO, Cooper ME, O'Brien S, Jones LA, Marazita ML, Murray JC, Zadnik K. - Candidate gene and locus analysis of myopia. - Mol Vis. 2007 , Jun 28;13:1012-9. | | 252 |
Wehby GL, Murray JC. - The effects of prenatal use of folic acid and other dietary supplements on early child development. - Matern Child Health J. 2008 , Mar;12(2):180-7. Epu | | 251 |
Nopoulos P, Richman L, Andreasen NC, Murray JC, Schutte B. - Abnormal brain structure in adults with Van der Woude syndrome. - Clin Genet. 2007 , Jun;71(6):511-7. | | 250 |
Félix TM, Tansey MJ, Patil SR, Murray JC, Dagle JM. - Double paternal nondisjunction in an infant with transient neonatal diabetes mellitus and Klinefelter syndrome. - Am J Med Genet A. 2007 , Apr 15;143A(8):895-8 | | 249 |
Abidi FE, Miano MG, Murray JC, Schwartz CE. - A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate. - Clin Genet. 2007 , Jul;72(1):19-22. | | 248 |
Nopoulos P, Richman L, Andreasen N, Murray JC, Schutte B. - Cognitive dysfunction in adults with Van der Woude syndrome. - Genet Med. 2007 , Apr;9(4):213-8. | | 247 |
Christensen K, Murray JC. - What genome-wide association studies can do for medicine. - N Engl J Med. 2007 , Mar 15;356(11):1094- | | 246 |
Bille C, Olsen J, Vach W, Knudsen VK, Olsen SF, Rasmussen K, Murray JC, Andersen AM, Christensen K. - Oral clefts and life style factors--a case-cohort study based on prospective Danish data. - Eur J Epidemiol. 2007 , 22(3):173-81. Epub 2 | | 245 |
Vieira AR, Modesto A, Meira R, Barbosa AR, Lidral AC, Murray JC. - Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis. - Am J Med Genet A. 2007 , Mar 15;143(6):538-45 | | 244 |
Riley BM, Schultz RE, Cooper ME, Goldstein-McHenry T, Daack-Hirsch S, Lee KT, Dragan E, Vieira AR, Lidral AC, Marazita ML, Murray JC. - A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23. - Am J Med Genet A. 2007 , Apr 15;143A(8):846-5 | | 243 |
Damiano PC, Tyler MC, Romitti PA, Momany ET, Jones MP, Canady JW, Karnell MP, Murray JC. - Health-related quality of life among preadolescent children with oral clefts: the mother's perspective. - Pediatrics. 2007 , Aug;120(2):e283-90. | | 242 |
Riley BM, Mansilla MA, Ma J, Daack-Hirsch S, Maher BS, Raffensperger LM, Russo ET, Vieira AR, Dodé C, Mohammadi M, Marazita ML, Murray JC. - Impaired FGF signaling contributes to cleft lip and palate. - Proc Natl Acad Sci U S A. 2007 , Mar 13;104(11):4512- | | 241 |
Shi M, Christensen K, Weinberg CR, Romitti P, Bathum L, Lozada A, Morris RW, Lovett M, Murray JC. - Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants. - Am J Hum Genet. 2007 , Jan;80(1):76-90. Epu | | 240 |
Gurnett CA, Bowcock AM, Dietz FR, Morcuende JA, Murray JC, Dobbs MB. - Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly. - Am J Med Genet A. 2007 , Jan 1;143(1):27-32. | | 239 |
Damiano PC, Tyler MC, Romitti PA, Momany ET, Canady JW, Karnell MP, Murray JC. - Type of oral cleft and mothers' perceptions of care, health status, and outcomes for preadolescent children. - Cleft Palate Craniofac J. 2006 , Nov;43(6):715-21. | | 238 |
Rahimov F, Ribeiro LA, de Miranda E, Richieri-Costa A, Murray JC. - GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum? - Am J Med Genet A. 2006 , Dec 1;140(23):2571-6 | | 237 |
Avila JR, Jezewski PA, Vieira AR, Orioli IM, Castilla EE, Christensen K, Daack-Hirsch S, Romitti PA, Murray JC. - PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations. - Am J Med Genet A. 2006 , Dec 1;140(23):2562-7 | | 236 |
Kleiber C, Schutte DL, McCarthy AM, Floria-Santos M, Murray JC, Hanrahan K. - Predictors of topical anesthetic effectiveness in children.
- J Pain. 2007 , Feb;8(2):168-74. Epu | | 235 |
Ribeiro LA, Murray JC, Richieri-Costa A. - PTCH mutations in four Brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI. - Am J Med Genet A. 2006 , Dec 1;140(23):2584-6 | | 234 |
Ingraham CR, Kinoshita A, Kondo S, Yang B, Sajan S, Trout KJ, Malik MI, Dunnwald M, Goudy SL, Lovett M, Murray JC, Schutte BC. - Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6). - Nat Genet. 2006 , Nov;38(11):1335-40. | | 233 |
Maciolek NL, Alward WL, Murray JC, Semina EV, McNally MT. - Analysis of RNA splicing defects in PITX2 mutants supports a gene dosage model of Axenfeld-Rieger syndrome. - BMC Med Genet. 2006 , Jul 11;7:59. | | 232 |
Félix TM, Hanshaw BC, Mueller R, Bitoun P, Murray JC. - CHD7 gene and non-syndromic cleft lip and palate. - Am J Med Genet A. 2006 , Oct 1;140(19):2110-4 | | 231 |
Schutte DL, McCarthy AM, Floria-Santos M, Hanrahan K, Murray JC, Kleiber C. - Integrating molecular genetics analyses into clinical research. - Biol Res Nurs. 2006 , Jul;8(1):67-77. | | 230 |
Warrington A, Vieira AR, Christensen K, Orioli IM, Castilla EE, Romitti PA, Murray JC. - Genetic evidence for the role of loci at 19q13 in cleft lip and palate. - J Med Genet. 2006 , Jun;43(6):e26. | | 229 |
Neiswanger K, Deleyiannis FW, Avila JR, Cooper ME, Brandon CA, Vieira AR, Noorchashm N, Weinberg SM, Bardi KM, Murray JC, Marazita ML. - Candidate genes for oral-facial clefts in Guatemalan families. - Ann Plast Surg. 2006 , May;56(5):518-21; di | | 228 |
Saadi I, Toro R, Kuburas A, Semina E, Murray JC, Russo AF. - An unusual class of PITX2 mutations in Axenfeld-Rieger syndrome. - Birth Defects Res A Clin Mol Teratol. 2006 , Mar;76(3):175-81. | | 227 |
Espinoza HM, Ganga M, Vadlamudi U, Martin DM, Brooks BP, Semina EV, Murray JC, Amendt BA. - Protein kinase C phosphorylation modulates N- and C-terminal regulatory activities of the PITX2 homeodomain protein. - Biochemistry. 2005 , Mar 15;44(10):3942-5 | | 226 |
Wehby GL, Castilla EE, Goco N, Rittler M, Cosentino V, Javois L, McCarthy AM, Bobashev G, Litavecz S, Mariona A, Dutra G, López-Camelo JS, Orioli IM, Murray JC. - Description of the methodology used in an ongoing pediatric care interventional study of children born with cleft lip and palate in South America [NCT00097149]. - BMC Pediatr. 2006 , Mar 24;6:9. | | 226 |
Scott NM, Weinberg SM, Neiswanger K, Daack-Hirsch S, O'Brien S, Murray JC, Marazita ML. - Dermatoglyphic pattern types in subjects with nonsyndromic cleft lip with or without cleft palate (CL/P) and their unaffected relatives in the Philippines. - Cleft Palate Craniofac J. 2005 , Jul;42(4):362-6. | | 224 |
Wehby GL, Ohsfeldt RL, Murray JC. - Health professionals' assessment of health-related quality of life values for oral clefting by age using a visual analogue scale method. - Cleft Palate Craniofac J. 2006 , Jul;43(4):383-91. | | 223 |
Yoshiura K, Kinoshita A, Ishida T, Ninokata A, Ishikawa T, Kaname T, Bannai M, Tokunaga K, Sonoda S, Komaki R, Ihara M, Saenko VA, Alipov GK, Sekine I, Komatsu K, Takahashi H, Nakashima M, Sosonkina N, Mapendano CK, Ghadami M, Nomura M, Liang DS, Miwa N, Kim DK, Garidkhuu A, Natsume N, Ohta T, Tomita H, Kaneko A, Kikuchi M, Russomando G, Hirayama K, Ishibashi M, Takahashi A, Saitou N, Murray JC, Saito S, Nakamura Y, Niikawa N. - A SNP in the ABCC11 gene is the determinant of human earwax type. - Nat Genet. 2006 , Mar;38(3):324-30. Ep | | 222 |
Vieira AR, Avila JR, Daack-Hirsch S, Dragan E, Félix TM, Rahimov F, Harrington J, Schultz RR, Watanabe Y, Johnson M, Fang J, O'Brien SE, Orioli IM, Castilla EE, Fitzpatrick DR, Jiang R, Marazita ML, Murray JC. - Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. - PLoS Genet. 2005 , Dec;1(6):e64. Epub 2 | | 221 |
Mansilla MA, Cooper ME, Goldstein T, Castilla EE, Lopez Camelo JS, Marazita ML, Murray JC. - Contributions of PTCH gene variants to isolated cleft lip and palate. - Cleft Palate Craniofac J. 2006 , Jan;43(1):21-9. | | 220 |
Bille C, Winther JF, Bautz A, Murray JC, Olsen J, Christensen K. - Cancer risk in persons with oral cleft--a population-based study of 8,093 cases.
- Am J Epidemiol. 2005 , Jun 1;161(11):1047-5 | | 219 |
Etheredge AJ, Christensen K, Del Junco D, Murray JC, Mitchell LE. - Evaluation of two methods for assessing gene-environment interactions using data from the Danish case-control study of facial clefts. - Birth Defects Res A Clin Mol Teratol. 2005 , Aug;73(8):541-6. | | 218 |
Vieira AR, Murray JC, Trembath D, Orioli IM, Castilla EE, Cooper ME, Marazita ML, Lennon-Graham F, Speer M. - Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects. - Am J Med Genet A. 2005 , Jun 1;135(2):220-3. | | 217 |
Dietz FR, Cole WG, Tosi LL, Carroll NC, Werner RD, Comstock D, Murray JC. - A search for the gene(s) predisposing to idiopathic clubfoot. - Clin Genet. 2005 , Apr;67(4):361-2. | | 216 |
Jugessur A, Murray JC. - Orofacial clefting: recent insights into a complex trait. - Curr Opin Genet Dev. 2005 , Jun;15(3):270-8. | | 215 |
Bille C, Skytthe A, Vach W, Knudsen LB, Andersen AMN, Murray JC, Christensen K. - Parent’s Age and the Risk of Oral Clefts. - Epidemiology. 2005 , May;16(3):311-6. | | 214 |
Di Paola J, Jugessur A, Goldman T, Reiland J, Tallman D, Sayago C, Murray JC. - Platelet glycoprotein I(b)alpha and integrin alpha2 beta1 polymorphisms: gene frequencies and linkage disequilibrium in a population diversity panel. - J Thromb Haemost. 2005 , Jul;3(7):1511-21. | | 213 |
Scott NM, Weinberg SM, Neiswanger K, Brandon CA, Daack-Hirsch S, Murray JC, Liu YE, Marazita ML. - Dermatoglyphic fingerprint heterogeneity among individuals with nonsyndromic cleft lip with or without cleft palate and their unaffected relatives in China and the Philippines. - Hum Biol. 2005 , Apr;77(2):257-66. | | 212 |
Mansilla MA, Kimani J, Mitchell LE, Christensen K, Boomsma DI, Daack-Hirsch S, Nepomucena B, Wyszynski DF, Felix TM, Martin NG, Murray JC. - Discordant MZ twins with cleft lip and palate: a model for identifying genes in complex traits. - Twin Res Hum Genet. 2005 , Feb;8(1):39-46. | | 211 |
Vieira AR, Castillo Taucher S, Aravena T, Astete C, Sanz P, Tastets ME, Monasterio L, Murray JC. - [Mutational analysis of the muscle segment homeobox gene 1 (MSX1) in Chilean patients with cleft lip/palate]. [Article in Spanish]. - Rev Med Chil. 2004 , Jul;132(7):816-22. | | 210 |
Lidral AC, Murray JC. - Genetic approaches to identify disease genes for birth defects with cleft lip/palate as a model. - Birth Defects Res A Clin Mol Teratol. 2004 , Dec;70(12):893-901. | | 209 |
Vieira AR, Meira R, Modesto A, Murray JC. - MSX1, PAX9, and TGFA contribute to tooth agenesis in humans. - J Dent Res. 2004 , Sep;83(9):723-7. | | 208 |
Zeng SM, Murray JC, Widness JA, Strauss RG, Yankowitz J. - Association of single nucleotide polymorphisms in the thrombopoietin-receptor gene, but not the thrombopoietin gene, with differences in platelet count. - Am J Hematol. 2004 , Sep;77(1):12-21. | | 207 |
Murray JC, Schutte BC. - Cleft palate: players, pathways, and pursuits. - J Clin Invest. 2004 , Jun;113(12):1676-8. | | 206 |
Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein T, Maher BS, Daack-Hirsch S, Schultz R, Mansilla MA, Field LL, Liu YE, Prescott N, Malcolm S, Winter R, Ray A, Moreno L, Valencia C, Neiswanger K, Wyszynski DF, Bailey-Wilson JE, Albacha-Hejazi H, Beaty TH, McIntosh I, Hetmanski JB, Tunçbilek G, Edwards M, Harkin L, Scott R, Roddick LG. - Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. - Am J Hum Genet. 2004 , Aug;75(2):161-73. Ep | | 205 |
Katz LA, Schultz RE, Semina EV, Torfs CP, Krahn KN, Murray JC. - Mutations in PITX2 may contribute to cases of omphalocele and VATER-like syndromes. - Am J Med Genet A. 2004 , Oct 15;130A(3):277-8 | | 204 |
Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, Moreno L, Arcos-Burgos M, Lidral AC, Field LL, Liu YE, Ray A, Goldstein TH, Schultz RE, Shi M, Johnson MK, Kondo S, Schutte BC, Marazita ML, Murray JC. - Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. - N Engl J Med. 2004 , Aug 19;351(8):769-80 | | 203 |
Christensen K, Juel K, Herskind AM, Murray JC. - Long term follow up study of survival associated with cleft lip and palate at birth. - BMJ. 2004 , Jun 12;328(7453):140 | | 202 |
Suzuki Y, Jezewski PA, Machida J, Watanabe Y, Shi M, Cooper ME, Viet le T, Nguyen TD, Hai H, Natsume N, Shimozato K, Marazita ML, Murray JC. - In a Vietnamese population, MSX1 variants contribute to cleft lip and palate. - Genet Med. 2004 , May-Jun;6(3):117-25. | | 201 |
Shi M, Caprau D, Dagle J, Christiansen L, Christensen K, Murray JC. - Application of kinetic polymerase chain reaction and molecular beacon assays to pooled analyses and high-throughput genotyping for candidate genes. - Birth Defects Res A Clin Mol Teratol. 2004 , Feb;70(2):65-74. | | 200 |
Trembath DG, Semina EV, Jones DH, Patil SR, Qian Q, Amendt BA, Russo AF, Murray JC. - Analysis of two translocation breakpoints and identification of a negative regulatory element in patients with Rieger's syndrome. - Birth Defects Res A Clin Mol Teratol. 2004 , Feb;70(2):82-91. | | 199 |
Marçano AC, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P. - TBX22 mutations are a frequent cause of cleft palate. - J Med Genet. 2004 , Jan;41(1):68-74. | | 198 |
Mintz-Hittner HA, Semina EV, Frishman LJ, Prager TC, Murray JC. - VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells. - Ophthalmology. 2004 , Apr;111(4):828-36. | | 197 |
Schultz RE, Cooper ME, Daack-Hirsch S, Shi M, Nepomucena B, Graf KA, O'Brien EK, O'Brien SE, Marazita ML, Murray JC. - Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families. - Am J Med Genet A. 2004 , Feb 15;125A(1):17-22 | | 196 |
Kayano S, Kure S, Suzuki Y, Kanno K, Aoki Y, Kondo S, Schutte BC, Murray JC, Yamada A, Matsubara Y. - Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion. - J Hum Genet. 2003 , 48(12):622-8. Epub 2 | | 195 |
Jugessur A, Lie RT, Wilcox AJ, Murray JC, Taylor JA, Saugstad OD, Vindenes HA, Abyholm FE. - Cleft palate, transforming growth factor alpha gene variants, and maternal exposures: assessing gene-environment interactions in case-parent triads. - Genet Epidemiol. 2003 , Dec;25(4):367-74. | | 194 |
Slayton RL, Williams L, Murray JC, Wheeler JJ, Lidral AC, Nishimura CJ. - Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region. - Cleft Palate Craniofac J. 2003 , May;40(3):274-9. | | 193 |
Ferreira de Lima RL, Moretti-Ferreira D, Richieri-Costa A, Murray JC. - Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome. - Am J Med Genet A. 2003 , Sep 15;122A(1):56-8. | | 192 |
Shi M, Caprau D, Romitti P, Christensen K, Murray JC. - Genotype frequencies and linkage disequilibrium in the CEPH human diversity panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2. - Birth Defects Res A Clin Mol Teratol. 2003 , Aug;67(8):545-9. | | 191 |
Jezewski PA, Vieira AR, Nishimura C, Ludwig B, Johnson M, O'Brien SE, Daack-Hirsch S, Schultz RE, Weber A, Nepomucena B, Romitti PA, Christensen K, Orioli IM, Castilla EE, Machida J, Natsume N, Murray JC. - Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. - J Med Genet. 2003 , Jun;40(6):399-407. | | 190 |
O'Brien EK, Zhang X, Nishimura C, Tomblin JB, Murray JC. - Association of specific language impairment (SLI) to the region of 7q31. - Am J Hum Genet. 2003 , Jun;72(6):1536-43. E | | 189 |
Jugessur A, Wilcox AJ, Lie RT, Murray JC, Taylor JA, Ulvik A, Drevon CA, Vindenes HA, Abyholm FE. - Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian case-parent triads. - Am J Epidemiol. 2003 , Jun 15;157(12):1083- | | 188 |
Vieira AR, Orioli IM, Castilla EE, Cooper ME, Marazita ML, Murray JC. - MSX1 and TGFB3 contribute to clefting in South America. - J Dent Res. 2003 , Apr;82(4):289-92. | | 187 |
Murray JC. - Genetic Drift. Prenatal diagnosis is for the DR, not just for the OR. - Am J Med Genet A. 2003 , Aug 1;120A(4):594-5. | | 186 |
Zeng SM, Yankowitz J, Murray JC. - Conjoined twins in a monozygotic triplet pregnancy: prenatal diagnosis and X-inactivation. - Teratology. 2002 , Dec;66(6):278-81. | | 185 |
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. - Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. - Am J Hum Genet. 2002 , Dec;71(6):1320-9. Ep | | 184 |
Mitchell LE, Murray JC, O'Brien S, Christensen K. - Retinoic acid receptor alpha gene variants, multivitamin use, and liver intake as risk factors for oral clefts: a population-based case-control study in Denmark, 1991-1994. - Am J Epidemiol. 2003 , Jul 1;158(1):69-76. | | 183 |
Vieira AR, Karras JC, Orioli IM, Castilla EE, Murray JC. - Genetic origins in a South American clefting population. - Clin Genet. 2002 , Dec;62(6):458-63. | | 182 |
Mutti DO, Semina E, Marazita M, Cooper M, Murray JC, Zadnik K. - Genetic loci for pathological myopia are not associated with juvenile myopia. - Am J Med Genet. 2002 , Nov 1;112(4):355-60. | | 181 |
Jugessur A, Lie RT, Wilcox AJ, Murray JC, Taylor JA, Saugstad OD, Vindenes HA, Abyholm F. - Variants of developmental genes (TGFA, TGFB3, and MSX1) and their associations with orofacial clefts: a case-parent triad analysis. - Genet Epidemiol. 2003 , Apr;24(3):230-9. | | 180 |
Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Arcos-Burgos M, Valencia C, Houdayer C, Bahuau M, Moretti-Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC. - Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. - Nat Genet. 2002 , Oct;32(2):285-9. Epu | | 179 |
Barrow LL, van Bokhoven H, Daack-Hirsch S, Andersen T, van Beersum SE, Gorlin R, Murray JC. - Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts. - J Med Genet. 2002 , ug;39(8):559-66. | | 178 |
Vieira AR, Orioli IM, Murray JC. - Maternal age and oral clefts: a reappraisal. - Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002 , Nov;94(5):530-5. | | 177 |
Vieira AR, Trembath D, Vandyke DC, Murray JC, Marker S, Lerner G, Bonner E, Speer M. - Studies with His475Tyr glutamate carboxipeptidase II polymorphism and neural tube defects.
- Am J Med Genet. 2002 , Aug 1;111(2):218-9. | | 176 |
Barrow LL, Wines ME, Romitti PA, Holdener BC, Murray JC. - Aryl hydrocarbon receptor nuclear translocator 2 (ARNT2): structure, gene mapping, polymorphisms, and candidate evaluation for human orofacial clefts. - Teratology. 2002 , Aug;66(2):85-90. | | 175 |
Mitchell LE, Beaty TH, Lidral AC, Munger RG, Murray JC, Saal HM, Wyszynski DF; International Consortium for Oral Clefts Genetics. - Guidelines for the design and analysis of studies on nonsyndromic cleft lip and cleft palate in humans: summary report from a Workshop of the International Consortium for Oral Clefts Genetics. - Cleft Palate Craniofac J. 2002 , an;39(1):93-100. | | 174 |
Watanabe Y, Benson DW, Yano S, Akagi T, Yoshino M, Murray JC. - Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD. - J Med Genet. 2002 , Nov;39(11):807-11. | | 173 |
Karplus TM, Jeronimo SM, Chang H, Helms BK, Burns TL, Murray JC, Mitchell AA, Pugh EW, Braz RF, Bezerra FL, Wilson ME. - Association between the tumor necrosis factor locus and the clinical outcome of Leishmania chagasi infection. - Infect Immun. 2002 , Dec;70(12):6919-25. | | 172 |
Murray JC. - Gene/environment causes of cleft lip and/or palate. - Clin Genet. 2002 , Apr;61(4):248-56. | | 171 |
Colmenares C, Heilstedt HA, Shaffer LG, Schwartz S, Berk M, Murray JC, Stavnezer E. - Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice. - Nat Genet. 2002 , Jan;30(1):106-9. Epu | | 170 |
Rasmussen SA, Lammer EJ, Shaw GM, Finnell RH, McGehee RE Jr, Gallagher M, Romitti PA, Murray JC; National Birth Defects Prevention Study. - Integration of DNA sample collection into a multi-site birth defects case-control study. - Teratology. 2002 , Oct;66(4):177-84. | | 169 |
Murray JC. - Time for T. - Nat Genet. 2001 , Oct;29(2):107-9. | | 168 |
Murray JC. - The unending string. - Arch Pediatr Adolesc Med. 2001 , Nov;155(11):1193-4. | | 167 |
Semina EV, Brownell I, Mintz-Hittner HA, Murray JC, Jamrich M. - Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts. - Hum Mol Genet. 2001 , Feb 1;10(3):231-6. | | 166 |
Kim YJ, Williamson RA, Murray JC, Andrews J, Pietscher JJ, Peraud PJ, Merrill DC. - Genetic susceptibility to preeclampsia: roles of cytosineto-thymine substitution at nucleotide 677 of the gene for methylenetetrahydrofolate reductase, 68-base pair insertion at nucleotide 844 of the gene for cystathionine beta-synthase, and factor V Leiden mutation. - Am J Obstet Gynecol. 2001 , May;184(6):1211-7. | | 165 |
Hjalt TA, Amendt BA, Murray JC. - PITX2 regulates procollagen lysyl hydroxylase (PLOD) gene expression: implications for the pathology of Rieger syndrome. - J Cell Biol. 2001 , Feb 5;152(3):545-52. | | 164 |
Green PD, Hjalt TA, Kirk DE, Sutherland LB, Thomas BL, Sharpe PT, Snead ML, Murray JC, Russo AF, Amendt BA. - Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth development. - Gene Expr. 2001 , 9(6):265-81. | | 163 |
Mitchell LE, Murray JC, O'Brien S, Christensen K. - Evaluation of two putative susceptibility loci for oral clefts in the Danish population. - Am J Epidemiol. 2001 , May 15;153(10):1007- | | 162 |
Kim YJ, Williamson RA, Chen K, Smith JL, Murray JC, Merrill DC. - Lipoprotein lipase gene mutations and the genetic susceptibility of preeclampsia. - Hypertension. 2001 , Nov;38(5):992-6. | | 161 |
Watanabe Y, Murray JC, Bjork BC, Bird CP, Chiang PW, Gregory SG, Kurnit DM, Schutte BC. - Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41. - Hum Mutat. 2001 , Nov;18(5):422-34. | | 160 |
Saadi I, Semina EV, Amendt BA, Harris DJ, Murphy KP, Murray JC, Russo AF. - Identification of a dominant negative homeodomain mutation in Rieger syndrome. - J Biol Chem. 2001 , Jun 22;276(25):23034 | | 159 |
Schutte BC, Bjork BC, Coppage KB, Malik MI, Gregory SG, Scott DJ, Brentzell LM, Watanabe Y, Dixon MJ, Murray JC. - A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41. - Genome Res. 2000 , Jan;10(1):81-94. | | 158 |
Semina EV, Murray JC, Reiter R, Hrstka RF, Graw J. - Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice. - Hum Mol Genet. 2000 , Jul 1;9(11):1575-85. | | 157 |
Lin AE, Semina EV, Daack-Hirsch S, Roeder ER, Curry CJ, Rosenbaum K, Weaver DD, Murray JC. - Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome. - Am J Med Genet. 2000 , Apr 24;91(5):387-90. | | 156 |
Kinoshita A, Saito T, Tomita H, Makita Y, Yoshida K, Ghadami M, Yamada K, Kondo S, Ikegawa S, Nishimura G, Fukushima Y, Nakagomi T, Saito H, Sugimoto T, Kamegaya M, Hisa K, Murray JC, Taniguchi N, Niikawa N, Yoshiura K. - Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease. - Nat Genet. 2000 , Sep;26(1):19-20. | | 155 |
Dobbs MB, Dietz FR, Gurnett CA, Morcuende JA, Steyers CM, Murray JC. - Localization of dominantly inherited isolated triphalangeal thumb to chromosomal region 7q36. - J Orthop Res. 2000 , May;18(3):340-4. | | 154 |
Semina EV, Mintz-Hittner HA, Murray JC. - Isolation and characterization of a novel human paired-like homeodomain-containing transcription factor gene, VSX1, expressed in ocular tissues. - Genomics. 2000 , Jan 15;63(2):289-93. | | 153 |
St Amand TR, Zhang Y, Semina EV, Zhao X, Hu Y, Nguyen L, Murray JC, Chen Y. - Antagonistic signals between BMP4 and FGF8 define the expression of Pitx1 and Pitx2 in mouse tooth-forming anlage. - Dev Biol. 2000 , Jan 15;217(2):323-32 | | 152 |
Hjalt TA, Semina EV, Amendt BA, Murray JC. - The Pitx2 protein in mouse development. - Dev Dyn. 2000 , May;218(1):195-200. | | 151 |
Hjalt TA, Murray JC. - The human BARX2 gene: genomic structure, chromosomal localization, and single nucleotide polymorphisms. - Genomics. 1999 , Dec 15;62(3):456-9. | | 150 |
Fuller BP, Kahn MJ, Barr PA, Biesecker L, Crowley E, Garber J, Mansoura MK, Murphy P, Murray J, Phillips J, Rothenberg K, Rothstein M, Stopfer J, Swergold G, Weber B, Collins FK, Hudson KL. - Privacy in genetics research. - Science. 1999 , Aug 27;285(5432):135 | | 149 |
Schutte BC, Murray JC. - The many faces and factors of orofacial clefts. - Hum Mol Genet. 1999 , 8(10):1853-9. | | 148 |
Hjalt TA, Murray JC. - Genomic structure of the human retinoic acid receptor-alpha1 gene. - Mamm Genome. 1999 , May;10(5):528-9. | | 147 |
Machida J, Yoshiura K, Funkhauser CD, Natsume N, Kawai T, Murray JC. - Transforming growth factor-alpha (TGFA): genomic structure, boundary sequences, and mutation analysis in nonsyndromic cleft lip/palate and cleft palate only. - Genomics. 1999 , Nov 1;61(3):237-42. | | 146 |
Schutte BC, Basart AM, Watanabe Y, Laffin JJ, Coppage K, Bjork BC, Daack-Hirsch S, Patil S, Dixon MJ, Murray JC. - Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome. - Am J Med Genet. 1999 , May 21;84(2):145-50. | | 145 |
Trembath D, Sherbondy AL, Vandyke DC, Shaw GM, Todoroff K, Lammer EJ, Finnell RH, Marker S, Lerner G, Murray JC. - Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population. - Teratology. 1999 , May;59(5):331-41. | | 144 |
Romitti PA, Lidral AC, Munger RG, Daack-Hirsch S, Burns TL, Murray JC. - Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts. - Teratology. 1999 , Jan;59(1):39-50. | | 143 |
Christensen K, Olsen J, Nørgaard-Pedersen B, Basso O, Støvring H, Milhollin-Johnson L, Murray JC. - Oral clefts, transforming growth factor alpha gene variants, and maternal smoking: a population-based case-control study in Denmark, 1991-1994. - Am J Epidemiol. 1999 , Feb 1;149(3):248-55. | | 142 |
Semina EV, Altherr MR, Murray JC. - Cloning and chromosomal localization of two novel human genes encoding LIM-domain binding factors CLIM1 and CLIM2/LDB1/NLI. - Mamm Genome. 1998 , Nov;9(11):921-4. | | 141 |
Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC. - Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. - Am J Hum Genet. 1998 , Aug;63(2):557-68. | | 140 |
Yoshioka H, Meno C, Koshiba K, Sugihara M, Itoh H, Ishimaru Y, Inoue T, Ohuchi H, Semina EV, Murray JC, Hamada H, Noji S. - Pitx2, a bicoid-type homeobox gene, is involved in a lefty-signaling pathway in determination of left-right asymmetry. - Cell. 1998 , Aug 7;94(3):299-305. | | 139 |
el-Shanti H, Murray JC, Semina EV, Beutow KH, Scherpbier T, al-Alami J. - Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene. - Eur J Hum Genet. 1998 , May-Jun;6(3):251-6. | | 138 |
Broman KW, Murray JC, Sheffield VC, White RL and Weber JL. - Comprehensive human genetic maps: Individual and sex-specific variation in recombination. - Am J Hum Genet. 1998 , Sep;63(3):861-9. | | 137 |
Yoshiura K, Machida J, Daack-Hirsch S, Patil SR, Ashworth LK, Hecht JT and Murray JC. - Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate. - Genomics. 1998 , Dec 1;54(2):231-40. | | 136 |
Semina EV, Ferrell RE, Mintz-Hittner HA, Bitoun P, Alward WL, Reiter RS, Funkhauser C, Daack-Hirsch S, Murray JC. - A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. - Nat Genet. 1998 , un;19(2):167-70. | | 135 |
Semina EV, Reiter RS, Murray JC. - A new human homeobox gene OGI2X is a member of the most conserved homeobox gene family and is expressed during heart development in mouse. - Hum Mol Genet. 1998 , Mar;7(3):415-22. | | 134 |
Shaw GM, Wasserman CR, Murray JC, Lammer EJ. - Infant TGF-alpha genotype, orofacial clefts, and maternal periconceptional multivitamin use. - Cleft Palate Craniofac J. 1998 , Jul;35(4):366-70. | | 133 |
Alward WL, Semina EV, Kalenak JW, Héon E, Sheth BP, Stone EM, Murray JC. - Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene. - Am J Ophthalmol. 1998 , Jan;125(1):98-100. | | 132 |
Yoshiura K, Leysens NJ, Reiter RS, Murray JC. - Cloning, characterization, and mapping of the mouse homeobox gene Hmx1. - Genomics. 1998 , May 15;50(1):61-8. | | 131 |
Romitti PA, Munger RG, Murray JC, Daack-Hirsch S, Hanson JW, Burns TL. - The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations. - Eur J Epidemiol. 1998 , Feb;14(2):129-38. | | 130 |
O'Brien S, Even DA, Murray JC. - Complex trinucleotide repeat polymorphism in the HOX B6 gene. - Hum Mutat. 1997 , 9(3):280-1. | | 129 |
Kavanagh GM, Jardine PE, Peachey RD, Murray JC, De Berker D. - The scleroatrophic syndrome of Huriez. - Br J Dermatol. 1997 , Jul;137(1):114-8. | | 128 |
Yandava CN, Gastier JM, Pulido JC, Brody T, Sheffield V, Murray J, Buetow K, Duyk GM. - Characterization of Alu repeats that are associated with trinucleotide and tetranucleotide repeat microsatellites. - Genome Res. 1997 , Jul;7(7):716-24. | | 127 |
Wang W, Yoshiura K, Murray J, Lufkin T. - Assignment of the murine Hmx1 homeobox gene to the proximal region of mouse chromosome 5. - Mamm Genome. 1997 , 8(11):869-70. | | 126 |
Semina EV, Reiter RS, Murray JC. - Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19. - Hum Mol Genet. 1997 , Nov;6(12):2109-16. | | 125 |
Yoshiura KI, Murray JC. - Sequence and chromosomal assignment of human BAPX1, a bagpipe-related gene, to 4p16.1: a candidate gene for skeletal dysplasia. - Genomics. 1997 , Oct 15;45(2):425-8. | | 124 |
Peiffer-Schneider S, Schutte BC, Murray JC, Frees KL, Williamson K, Leysens NJ, Schwartz DA. - Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus. - Mamm Genome. 1997 , Oct;8(10):785-6. | | 123 |
Yoshiura K, Leysens NJ, Chang J, Ward D, Murray JC, Muenke M. - Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes. - Am J Med Genet. 1997 , Oct 31;72(3):354-62. | | 122 |
Romitti PA, Burns TL, Murray JC. - Maternal interview reports of family history of birth defects: evaluation from a population-based case-control study of orofacial clefts. - Am J Med Genet. 1997 , Nov 12;72(4):422-9. | | 121 |
Murray JC, Daack-Hirsch S, Buetow KH, Munger R, Espina L, Paglinawan N, Villanueva E, Rary J, Magee K, Magee W. - Clinical and epidemiologic studies of cleft lip and palate in the Philippines. - Cleft Palate Craniofac J. 1997 , Jan;34(1):7-10. | | 120 |
Lidral AC, Murray JC, Buetow KH, Basart AM, Schearer H, Shiang R, Naval A, Layda E, Magee K, Magee W. - Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines. - Cleft Palate Craniofac J. 1997 , Jan;34(1):1-6. | | 119 |
Wyszynski DF, Maestri N, McIntosh I, Smith EA, Lewanda AF, Garcia-Delgado C, Vinageras-Guarneros E, Wulfsberg E, Beaty TH. - Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families. - Hum Genet. 1997 , Jan;99(1):22-6. | | 118 |
Semina EV, Reiter R, Leysens NJ, Alward WL, Small KW, Datson NA, Siegel-Bartelt J, Bierke-Nelson D, Bitoun P, Zabel BU, Carey JC, Murray JC. - Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. - Nat Genet. 1996 , Dec;14(4):392-9. | | 117 |
Datson NA, Semina E, van Staalduinen AA, Dauwerse HG, Meershoek EJ, Heus JJ, Frants RR, den Dunnen JT, Murray JC, van Ommen GJ. - Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region. - Am J Hum Genet. 1996 , Dec;59(6):1297-305. | | 116 |
Semina EV, Datson NA, Leysens NJ, Zabel BU, Carey JC, Bell GI, Bitoun P, Lindgren C, Stevenson T, Frants RR, van Ommen G, Murray JC. - Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. - Am J Hum Genet. 1996 , Dec;59(6):1288-96. | | 115 |
Schutte BC, Sander A, Malik M, Murray JC. - Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41. - Genomics. 1996 , Sep 15;36(3):507-14. | | 114 |
Munger RG, Romitti PA, Daack-Hirsch S, Burns TL, Murray JC, Hanson J. - Maternal alcohol use and risk of orofacial cleft birth defects. - Teratology. 1996 , Jul;54(1):27-33. | | 113 |
Sertié AL, Quimby M, Moreira ES, Murray J, Zatz M, Antonarakis SE, Passos-Bueno MR. - A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3. - Hum Mol Genet. 1996 , Jun;5(6):843-7. | | 112 |
Gastier JM, Brody T, Pulido JC, Businga T, Sunden S, Hu X, Maitra S, Buetow KH, Murray JC, Sheffield VC, Boguski M, Duyk GM, Hudson TJ. - Development of a screening set for new (CAG/CTG)n dynamic mutations. - Genomics. 1996 , Feb 15;32(1):75-85. | | 111 |
Sunden SL, Businga T, Beck J, McClain A, Gastier JM, Pulido JC, Yandava CN, Brody T, Ghazizadeh J, Weber JL, Duyk GM, Murray JC, Buetow KH, Sheffield VC. - Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2. - Genomics. 1996 , Feb 15;32(1):15-20. | | 110 |
Shaw GM, Wasserman CR, Lammer EJ, O'Malley CD, Murray JC, Basart AM, Tolarova MM. - Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants. - Am J Hum Genet. 1996 , Mar;58(3):551-61. | | 109 |
Murray JC. - Face facts: genes, environment, and clefts. - Am J Hum Genet. 1995 , Aug;57(2):227-32. | | 108 |
Zittergruen MM, Murray JC, Lauer RM, Burns TL, Sheffield VC. - Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defects. - Circulation. 1995 , Nov 15;92(10):2803-1 | | 107 |
Yankowitz J, Li S, Murray JC. - Polymerase chain reaction determination of RhD blood type: an evaluation of accuracy. - Obstet Gynecol. 1995 , Aug;86(2):214-7. | | 106 |
Gastier JM, Pulido JC, Sunden S, Brody T, Buetow KH, Murray JC, Weber JL, Hudson TJ, Sheffield VC, Duyk GM. - Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers. - Hum Mol Genet. 1995 , Oct;4(10):1829-36. | | 105 |
Crosby AH, Scherpbier-Heddema T, Wijmenga C, Altherr MR, Murray JC, Buetow KH, Dixon MJ. - Genetic mapping of the dentinogenesis imperfecta type II locus. - Am J Hum Genet. 1995 , Oct;57(4):832-9. | | 104 |
Mears AJ, el-Shanti H, Murray JC, McDermid HE, Patil SR. - Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. - Am J Hum Genet. 1995 , Sep;57(3):667-73. | | 103 |
Mathews KD, Rapisarda D, Bailey HL, Murray JC, Schelper RL, Smith R. - Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophy. - J Neuropathol Exp Neurol. 1995 , Jul;54(4):601-6. | | 102 |
Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL, et al. - A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. - Hum Mol Genet. 1995 , Oct;4(10):1837-44. | | 101 |
Crosby AH, Edwards SJ, Murray JC, Dixon MJ. - Genomic organization of the human osteopontin gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II. - Genomics. 1995 , May 1;27(1):155-60. | | 100 |
Stadler HS, Murray JC, Leysens NJ, Goodfellow PJ, Solursh M. - Phylogenetic conservation and physical mapping of members of the H6 homeobox gene family. - Mamm Genome. 1995 , Jun;6(6):383-8. | | 99 |
Mills KA, Mathews KD, Scherpbier-Heddema T, Schelper RL, Schmalzel R, Bailey HL, Nadeau JH, Buetow KH, Murray JC. - Genetic mapping near the myd locus on mouse chromosome 8. - Mamm Genome. 1995 , Apr;6(4):278-80. | | 98 |
Mathews KD, Mills KA, Bailey HL, Schelper RL, Murray JC. - Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q. - Muscle Nerve. 1995 , 2:S98-102. | | 97 |
Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR. - Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35. - Muscle Nerve. 1995 , 2:S14-8. | | 96 |
Sander A, Murray JC, Scherpbier-Heddema T, Buetow KH, Weissenbach J, Zingg M, Ludwig K, Schmelzle R. - Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414. - Am J Hum Genet. 1995 , Jan;56(1):310-8. | | 95 |
Cox DW, Billingsley GD, Bale AE, Donis-Keller H, Edwards JH, Litt M, Mcbride W, Persichetti F, Spurr NK, Weber JL, et al. - CEPH consortium map of chromosome 14. - Cytogenet Cell Genet. 1995 , 69(3-4):175-8. | | 94 |
Basart AM, Qian JF, May E, Murray JC. - A PCR method for detecting polymorphism in the TGFA gene. - Hum Mol Genet. 1994 , Apr;3(4):678. | | 93 |
Sander A, Kennedy MA, Rayner JC, Murray JC. - Dinucleotide repeat polymorphism for HLX1 gene. - Hum Mol Genet. 1994 , Jan;3(1):219. | | 92 |
Buetow KH, Ludwigsen S, Scherpbier-Heddema T, Quillen J, Murray JC, Sheffield VC, Duyk GM, Weber JL, Weissenback H, Gyapay G, et al. - Human genetic map. Genome maps V. Wall Chart. - Science. 1994 , Sep 30;265(5181):205 | | 91 |
Murray JC, Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Manion F, Quillen J, Sheffield VC, Sunden S, Duyk GM, et al. - A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC). - Science. 1994 , Sep 30;265(5181):204 | | 90 |
Detera-Wadleigh SD, Hsieh WT, Berrettini WH, Goldin LR, Rollins DY, Muniec D, Grewal R, Guroff JJ, Turner G, Coffman D, et al. - Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter. - Am J Med Genet. 1994 , Sep 15;54(3):206-18. | | 89 |
Francomano CA, Ortiz de Luna RI, Hefferon TW, Bellus GA, Turner CE, Taylor E, Meyers DA, Blanton SH, Murray JC, McIntosh I, et al. - Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4p. - Hum Mol Genet. 1994 , May;3(5):787-92. | | 88 |
Muenke M, Gurrieri F, Bay C, Yi DH, Collins AL, Johnson VP, Hennekam RC, Schaefer GB, Weik L, Lubinsky MS, et al. - Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity. - Proc Natl Acad Sci U S A. 1994 , Aug 16;91(17):8102-6 | | 87 |
Solursh M, Murray J. - Craniofacial morphogenesis workshop report. - Cleft Palate Craniofac J. 1994 , May;31(3):230-1. | | 86 |
Sander A, Schmelzle R, Murray J. - Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome. - Hum Mol Genet. 1994 , Apr;3(4):575-8. | | 85 |
Fan JB, DeYoung J, Lagacé R, Lina RA, Xu Z, Murray JC, Buetow KH, Weissenbach J, Goold RD, Cox DR, et al. - Isolation of yeast artificial chromosome clones from 54 polymorphic loci mapped with high odds on human chromosome 4. - Hum Mol Genet. 1994 , Feb;3(2):243-6. | | 84 |
Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Duyk GM, Sheffield VC, Wang Z, Murray JC. - Integrated human genome-wide maps constructed using the CEPH reference panel. - Nat Genet. 1994 , Apr;6(4):391-3. | | 83 |
Wijmenga C, Winokur ST, Padberg GW, Skraastad MI, Altherr MR, Wasmuth JJ, Murray JC, Hofker MH, Frants RR. - The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus. - Hum Genet. 1993 , Sep;92(2):198-203. | | 82 |
Bascom RA, Liu L, Humphries P, Fishman GA, Murray JC, McInnes RR. - Polymorphisms and rare sequence variants at the ROM1 locus. - Hum Mol Genet. 1993 , Nov;2(11):1975-7. | | 81 |
Winokur ST, Bengtsson U, Feddersen J, Mathews KD, Weiffenbach B, Bailey H, Markovich RP, Murray JC, Wasmuth JJ, Altherr MR, et al. - The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease. - Chromosome Res. 1994 , May;2(3):225-34. | | 80 |
Shiang R, Lidral AC, Ardinger HH, Buetow KH, Romitti PA, Munger RG, Murray JC. - Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO). - Am J Hum Genet. 1993 , Oct;53(4):836-43. | | 79 |
Rebbeck TR, Dietz FR, Murray JC, Buetow KH. - A single-gene explanation for the probability of having idiopathic talipes equinovarus. - Am J Hum Genet. 1993 , Nov;53(5):1051-63. | | 78 |
Nishimura DY, Purchio AF, Murray JC. - Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q. - Genomics. 1993 , Feb;15(2):357-64. | | 77 |
Mills KA, Even D, Murray JC. - Tetranucleotide repeat polymorphism at the human alpha fibrinogen locus (FGA). - Hum Mol Genet. 1992 , Dec;1(9):779. | | 76 |
Nishimura DY, Murray JC. - A tetranucleotide repeat for the F13B locus. - Nucleic Acids Res. 1992 , Mar 11;20(5):1167. | | 75 |
Nishimura DY, Leysens NJ, Murray JC. - A dinucleotide repeat for the D1S53 locus. - Nucleic Acids Res. 1992 , Mar 11;20(5):1167. | | 74 |
Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A, Alward WL, Weber JL, Bell GI, Buetow KH. - Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. - Nat Genet. 1992 , Sep;2(1):46-9. | | 73 |
Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A, Alward WLM, Weber JL, Bell GI, Buetow KH - Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4 - Nat Genet 1992 , 46-49 | | 72 |
A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group. - A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group. - Science. 1992 , Oct 2;258(5079):67-8 | | 71 |
Stadler HS, Padanilam BJ, Buetow K, Murray JC, Solursh M. - Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4. - Proc Natl Acad Sci U S A. 1992 , Dec 1;89(23):11579-8 | | 70 |
Spurr NK, Cox S, Bryant SP, Attwood J, Robson EB, Shields DC, Steinbrueck T, Jenkins T, Murray JC, Kidd KK, et al. - The CEPH consortium linkage map of human chromosome 2. - Genomics. 1992 , Dec;14(4):1055-63. | | 69 |
Padanilam BJ, Stadler HS, Mills KA, McLeod LB, Solursh M, Lee B, Ramirez F, Buetow KH, Murray JC. - Characterization of the human HOX 7 cDNA and identification of polymorphic markers. - Hum Mol Genet. 1992 , Sep;1(6):407-10. | | 68 |
Sleister HM, Mills KA, Blackwell SE, Killary AM, Murray JC, Malone RE. - Construction of a human chromosome 4 YAC pool and analysis of artificial chromosome stability. - Nucleic Acids Res. 1992 , Jul 11;20(13):3419-2 | | 67 |
Spurr NK, Cox S, Bryant SP, Attwood J, Robson EB, Shields DC, Steinbrueck T, Jenkins T, Murray JC, Kidd KK, Summar ML, Tsipouras P, Retief AE, Kruse TA, Bale AE, Vergnaud G, Weber JL, McBride OW, Donis-Keller H, White RL - The CEPH consortium linkage map of human chromosome 2 - Genomics 1992 , 1055-1063 | | 66 |
Mills KA, Buetow KH, Xu Y, Weber JL, Altherr MR, Wasmuth JJ, Murray JC. - Genetic and physical maps of human chromosome 4 based on dinucleotide repeats. - Genomics. 1992 , Oct;14(2):209-19. | | 65 |
Crall MG, Schuler CF, Buetow KH, Murray JC. - Genetic marker study of dentinogenesis imperfecta. - Proc Finn Dent Soc. 1992 , 88 Suppl 1:285-93. | | 64 |
Mathews KD, Mills KA, Bosch EP, Ionasescu VV, Wiles KR, Buetow KH, Murray JC. - Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35. - Am J Hum Genet. 1992 , Aug;51(2):428-31. | | 63 |
Mills KA, Buetow KH, Xu Y, Ritty TM, Mathews KD, Bodrug SE, Wijmenga C, Balazs I, Murray JC. - Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD). - Am J Hum Genet. 1992 , Aug;51(2):432-9. | | 62 |
Sarfarazi M, Wijmenga C, Upadhyaya M, Weiffenbach B, Hyser C, Mathews K, Murray J, Gilbert J, Pericak-Vance M, Lunt P, et al. - Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium. - Am J Hum Genet. 1992 , Aug;51(2):396-403. | | 61 |
Wijmenga C, Sandkuijl LA, Moerer P, van der Boorn N, Bodrug SE, Ray PN, Brouwer OF, Murray JC, van Ommen GJ, Padberg GW, et al. - Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter. - Am J Hum Genet. 1992 , Aug;51(2):411-5. | | 60 |
Byth BC, Love DR, Murray JC, Davies KE. - Localization of two new DNA markers on the linkage map of human chromosome 6q. - Cytogenet Cell Genet. 1992 , 60(3-4):216-8. | | 59 |
MacDougall M, Zeichner-David M, Murray J, Crall M, Davis A, Slavkin H. - Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III. - Am J Hum Genet. 1992 , Jan;50(1):190-4. | | 58 |
Ritty TM, Jaye M, Kaplan R, Murray JC. - EcoRI and PvuII RFLPs in the endonexin II/annexin V (ANX5) gene on chromosome four. - Nucleic Acids Res. 1991 , Apr 11;19(7):1723. | | 57 |
Miller BL, Nishimura DY, Wieben ED, Murray JC. - An EcoO109 RFLP for the SNRPE gene on chromosome 1. - Nucleic Acids Res. 1991 , Apr 11;19(7):1724. | | 56 |
Coleman MP, Murray JC, Willard HF, Nolan KF, Reid KB, Blake DJ, Lindsay S, Bhattacharya SS, Wright A, Davies KE. - Genetic and physical mapping around the properdin P gene. - Genomics. 1991 , Dec;11(4):991-6. | | 55 |
Siniscalco M, Oberlé I, Melis P, Alhadeff B, Murray J, Filippi G, Mattioni T, Chen YT, Furneaux H, Old LJ, et al. - Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site. - Am J Med Genet. 1991 , Feb-Mar;38(2-3):357- | | 54 |
Buetow KH, Shiang R, Yang P, Nakamura Y, Lathrop GM, White R, Wasmuth JJ, Wood S, Berdahl LD, Leysens NJ, et al. - A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates. - Am J Hum Genet. 1991 , May;48(5):911-25. | | 53 |
Tait JF, Frankenberry DA, Shiang R, Murray JC, Adler DA, Disteche CM. - Chromosomal localization of the human gene for annexin V (placental anticoagulant protein I) to 4q26----q28. - Cytogenet Cell Genet. 1991 , 57(4):187-92. | | 52 |
Dracopoli NC, O'Connell P, Elsner TI, Lalouel JM, White RL, Buetow KH, Nishimura DY, Murray JC, Helms C, Mishra SK, et al. - The CEPH consortium linkage map of human chromosome 1. - Genomics. 1991 , Apr;9(4):686-700. | | 51 |
Russo AF, Chamany K, Klemish SW, Hall TM, Murray JC. - Characterization of the calcitonin/CGRP gene in Williams syndrome. - Am J Med Genet. 1991 , Apr 1;39(1):28-33. | | 50 |
Murray JC, van Ommen GB. - Report of the committee on the genetic constitution of chromosome 4. - Cytogenet Cell Genet. 1990 , 55(1-4):97-110. | | 49 |
Buetow KH, Nishimura D, Nakamura Y, Jiang O, Murray JC. - A detailed multipoint gene map of chromosome 1q. - Genomics. 1990 , Sep;8(1):13-21. | | 48 |
Murray JC, Nishimura DY, Buetow KH, Ardinger HH, Spence MA, Sparkes RS, Falk RE, Falk PM, Gardner RJ, Harkness EM, et al. - Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq. - Am J Hum Genet. 1990 , Mar;46(3):486-91. | | 47 |
White RL, Lalouel JM, Nakamura Y, Donis-Keller H, Green P, Bowden DW, Mathew CG, Easton DF, Robson EB, Morton NE, et al. - The CEPH consortium primary linkage map of human chromosome 10. - Genomics. 1990 , Mar;6(3):393-412. | | 46 |
Georgiou C, Shull M, Lane LK, Lingrel JB, Murray JC. - RFLPs for ATP1BL1 (beta subunit Na+/K+ ATPase pseudogene) on chromosome 4. - Nucleic Acids Res. 1989 , Nov 11;17(21):8894. | | 45 |
Beck JS, Sager R, Murray JC. - A ScaI RFLP demonstrated for the GRO gene on chromosome 4. - Nucleic Acids Res. 1989 , Nov 11;17(21):8895. | | 44 |
Nishimura DY, Wieben ED, Stanford DR, Murray JC. - MspI RFLP for SNRNPE gene on 1q. - Nucleic Acids Res. 1989 , Nov 11;17(21):8896. | | 43 |
Ritty TM, Murray JC. - A new HincII RFLP for epidermal growth factor (EGF) on chromosome 4. - Nucleic Acids Res. 1989 , Jul 25;17(14):5870. | | 42 |
Leysens N, Murray JC, Bell GI. - A KpnI polymorphism for the human insulin-responsive glucose transporter gene (GLUT4) on chromosome 17. - Nucleic Acids Res. 1989 , May 11;17(9):3621. | | 41 |
Leysens NJ, Newkirk NG, Murray JC. - SacI and XbaI polymorphisms detected by lipocortin 2A (LPC2A). - Nucleic Acids Res. 1989 , Jul 11;17(13):5417. | | 40 |
Mathews KD, Ardinger HH, Nishimura DY, Buetow KH, Murray JC, Bartley JA. - Linkage localization of Börjeson-Forssman-Lehmann syndrome. - Am J Med Genet. 1989 , Dec;34(4):470-4. | | 39 |
Ardinger HH, Buetow KH, Bell GI, Bardach J, VanDemark DR, Murray JC. - Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate. - Am J Hum Genet. 1989 , Sep;45(3):348-53. | | 38 |
Theilmann J, Kanani S, Shiang R, Robbins C, Quarrell O, Huggins M, Hedrick A, Weber B, Collins C, Wasmuth JJ, et al. - Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene. - J Med Genet. 1989 , Nov;26(11):676-81. | | 37 |
Cox DR, Murray JC, Buetow KH. - Report of the committee on the genetic constitution of chromosome 4. - Cytogenet Cell Genet. 1989 , 51(1-4):121-36. | | 36 |
Buetow KH, Murray JC, Israel JL, London WT, Smith M, Kew M, Blanquet V, Brechot C, Redeker A, Govindarajah S. - Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. - Proc Natl Acad Sci U S A. 1989 , Nov;86(22):8852-6. | | 35 |
Bell GI, Murray JC, Nakamura Y, Kayano T, Eddy RL, Fan YS, Byers MG, Shows TB. - Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13. - Diabetes. 1989 , Aug;38(8):1072-5. | | 34 |
Kittur SD, Bagdon MM, Lubs ML, Phillips JA 3rd, Murray JC, Slaugenhaupt SA, Chakravarti A, Adler WH. - Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers. - Am J Hum Genet. 1989 , Jan;44(1):48-50. | | 33 |
O'Connell P, Lathrop GM, Nakamura Y, Leppert ML, Ardinger RH, Murray JL, Lalouel JM, White R. - Twenty-eight loci form a continuous linkage map of markers for human chromosome 1. - Genomics. 1989 , Jan;4(1):12-20. | | 32 |
Shiang R, Murray JC, Wiggs J, Dryja T. - A TaqI RFLP identified at the retinoblastoma locus on chromosome 13. - Nucleic Acids Res. 1988 , Sep 26;16(18):9069. | | 31 |
Berdahl LD, Murray JC, Besmer P. - A HindIII RFLP demonstrated for the kit oncogene on chromosome 4. - Nucleic Acids Res. 1988 , May 25;16(10):4740. | | 30 |
Berdahl LD, Smith RF, Murray JC, Buetow KH. - A TaqI RFLP demonstrated for pIBS17 [D4S123], a single copy sequence on chromosome 4. - Nucleic Acids Res. 1988 , Mar 25;16(6):2743. | | 29 |
Ardinger HH, Rose KM, Murray JC, Yamada Y. - HincII and KpnI RFLPs for laminin B1 (LAMB1) gene on chromosome 7.
- Nucleic Acids Res. 1988 , Sep 12;16(17):8742. | | 28 |
Ardinger HH, Ardinger RH, Bell GI, Murray JC. - RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19. - Nucleic Acids Res. 1988 , Aug 25;16(16):8202. | | 27 |
Ardinger RH, Murray JC. - A BglI polymorphism for the interleukin-2 receptor gene (IL2R) on chromosome 10. - Nucleic Acids Res. 1988 , Aug 25;16(16):8201. | | 26 |
Nishimura D, Buetow KH, Yamada Y, Murray JC. - RFLPs and linkage relationships of the human laminin B2 gene. - Genomics. 1988 , Nov;3(4):393-5. | | 25 |
Shiang R, Murray JC, Morton CC, Buetow KH, Wasmuth JJ, Olney AH, Sanger WG, Goldberger G. - Mapping of the human complement factor I gene to 4q25. - Genomics. 1989 , Jan;4(1):82-6. | | 24 |
Crowe RR, Tsai LY, Murray JC, Patil SR, Quinn J. - A study of autism using X chromosome DNA probes. - Biol Psychiatry. 1988 , Aug;24(4):473-9. | | 23 |
Smith M, Weiss MJ, Griffin CA, Murray JC, Buetow KH, Emanuel BS, Henthorn PS, Harris H. - Regional assignment of the gene for human liver/bone/kidney alkaline phosphatase to chromosome 1p36.1-p34. - Genomics. 1988 , Feb;2(2):139-43. | | 22 |
Murray JC, Buetow KH, Ferrell RE, Sieberg PD, Fukuda M. - An RFLP for glycoprotein A (MN) is in linkage disequilibrium with MN and Ss. - Cytogenet Cell Genet. 1988 , 47(3):149-51. | | 21 |
Murray JC, Buetow KH, Smith M, Carlock L, Chakravarti A, Ferrell RF, Gedamu L, Gilliam C, Shiang R, DeHaven CR. - Pairwise linkage analysis of 11 loci on human chromosome 4. - Am J Hum Genet. 1988 , Mar;42(3):490-7. | | 20 |
Smith RF, Ardinger HA, Murray JC. - Multiple RFLPs demonstrated for epidermal growth factor receptor (EGFR) on chromosome 7.
- Nucleic Acids Res. 1987 , Aug 25;15(16):6764. | | 19 |
Murray JC, Smith RF, Ardinger HA, Weinberger C. - RFLP for the glucocorticoid receptor (GRL) located at 5q11-5q13. - Nucleic Acids Res. 1987 , Aug 25;15(16):6765. | | 18 |
Carlock LR, Vo TD, DeHaven CR, Murray JC. - An anonymous genomic clone that detects a frequent RFLP adjacent to the D4S10 (G8) marker and Huntington's disease. - Nucleic Acids Res. 1987 , Jan 12;15(1):377. | | 17 |
Ionasescu V, Murray JC, Burns TL, Ionasescu R, Ferrell R, Searby C, Chirgwin J. - Linkage analysis of Charcot-Marie-Tooth neuropathy (HMSN type I). - J Neurol Sci. 1987 , Aug;80(1):73-8. | | 16 |
Ferrell RE, Buetow KH, Darby JK, Eichner JE, Murray JC, Smith R, Waziri M, Huson S, Riccardi VM. - Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes. - J Med Genet. 1987 , Sep;24(9):522-4. | | 15 |
Murray JC, Shiang R, Carlock LR, Smith M, Buetow KH. - Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci. - Hum Genet. 1987 , Jul;76(3):274-7. | | 14 |
Shows TB, Eddy RL, Byers MG, Fukushima Y, Dehaven CR, Murray JC, Bell GI. - Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35. - Diabetes. 1987 , Apr;36(4):546-9. | | 13 |
Murray JC, Buetow KH, Donovan M, Hornung S, Motulsky AG, Disteche C, Dyer K, Swisshelm K, Anderson J, Giblett E, et al. - Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27. - Am J Hum Genet. 1987 , Apr;40(4):338-50. | | 12 |
Chance PF, Murray JC, Bird TD, Kochin RS. - Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markers. - Neurology. 1987 , Feb;37(2):325-9. | | 11 |
Murray JC, Buetow KH, Bell GI. - RFLPs for transforming growth factor alpha (TGFA) gene at 2p13. - Nucleic Acids Res. 1986 , Sep 11;14(17):7136. | | 10 |
Murray JC, DeHaven CR, Bell GI. - RFLPs for epidermal growth factor (EGF), a single copy sequence at 4q25-4q27. - Nucleic Acids Res. 1986 , Jun 25;14(12):5117. | | 9 |
Murph JR, Bale JF Jr, Murray JC, Stinski MF, Perlman S. - Cytomegalovirus transmission in a Midwest day care center: possible relationship to child care practices. - J Pediatr. 1986 , Jul;109(1):35-9. | | 8 |
Murray JC, Watanabe K, Tamaoki T, Hornung S, Motulsky A. - RFLPs for the human alphafetoprotein (AFP), at 4q11-4q13. - Nucleic Acids Res. 1985 , Sep 25;13(18):6794. | | 7 |
Murray JC, Johnson JA, Bird TD. - Dandy-Walker malformation: etiologic heterogeneity and empiric recurrence risks. - Clin Genet. 1985 , Oct;28(4):272-83. | | 6 |
Murray JC, Pagon RA. - Informed consent for research publication of patient-related data. - Clin Res. 1984 , Oct;32(4):404-8. | | 5 |
Murray JC, Mills KA, Demopulos CM, Hornung S, Motulsky AG. - Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus. - Proc Natl Acad Sci U S A. 1984 , Jun;81(11):3486-90. | | 4 |
Murray JC, Karp LE, Williamson RA, Cheng EY, Luthy DA. - Rh isoimmunization related to amniocentesis. - Am J Med Genet. 1983 , Dec;16(4):527-34. | | 3 |
Farquhar M, Gelinas R, Tatsis B, Murray J, Yagi M, Mueller R, Stamatoyannopoulos G. - Restriction endonuclease mapping of gamma-delta-beta-globin region in G gamma (beta)+ HPFH and a Chinese A gamma HPFH variant. - Am J Hum Genet. 1983 , Jul;35(4):611-20. | | 2 |
Mueller RF, Murray JC, Gelinas R, Farquhar M, Papayannopoulou T. - Restriction endonuclease mapping of globin genomic regions of HEL (human erythroleukemia) line. - Hemoglobin. 1983 , 7(3):245-56. | | 1 |
Murray JC, Demopulos CM, Lawn RM, Motulsky AG. - Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia. - Proc Natl Acad Sci U S A. 1983 , Oct;80(19):5951-5. | |
