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. [PubMed - in process]

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, in press, 2010. PMC journal in process.

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, in press, 2010 Oct 22 [Epub ahead of print].

308 - Mumtaz G, Nassar AH, Mahfoud Z, El-Khamra A, Al-Choueiri N, Adra A, Murray JC, Zalloua P, Yunis KA and for the National Collaborative Perinatal Neonatal Network (NCPNN). Consanguinity: A risk factor for preterm birth at less than 33 weeks' gestation. Am J Epidemiol. 2010 Dec 15;172(12):1424-30. Epub 2010 Oct 26. [Available on 2011/12/15]

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. [Available on 2011/11/1]

306 - Bremond-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 16:1705-11, 2010.

305 - Boghossian N, Hansen N, Bell E, Stoll B, Murray J, Laptook A, Shankaran S, Walsh M, Das Abhik, Higgins R. Survival and morbidity outcomes of very low birth weight infants with Down Syndrome. Pediatrics, 126:1132-1140, 2010.

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, (12):3164-3172.

303 - Félix TM, Petrin AL, Sanseverino MT, Murray JC. Further characterization of microdeletion syndrome involving 2p15-p16.1. Am J Med Genet A 152A(10): 2604-2608.

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, Seider S, McCurnin D, Murray JC, Ohls R, Clymann 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, and Wilcox AJ. Maternal alcohol consuption, 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. Epub 2010 Sep 1

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, 2010 Oct;152A(10):2468-74

298 - Abu Maziad AS, Schaa KL, Bell EF, Dagle JM, Cooper ME, Marazita ML, and Murray JC. Role of Polymorphic Variants as Genetic Modulators of Infection in Neonatal Sepsis. Pediatr Res. 2010 Oct;68(4):323-329.

297 - Petrin A, Daack-Hirsch S, L'heureux JA, Murray J. A case of 3q29 microdeletion syndrome involving oral cleft inherited from a non-affected mosaic parent: molecular analysis and ethical implications. Cleft Palate Craniofac J. 2010 May 4. [Epub ahead of print].

296 - Schmidt RJ, Romitti PA, Burns TL, Murray JC, Browne ML, Druschel CM, Olney RS and the National Birth Defects Prevention Study. Caffeine, selected metabolic gene variants, and risk for neural tube defects. Birth Defects Research Part A: Clinical and Molecular Teratology. PMC Journal – In Process. (Accepted for publication, April 2010).

295 - Beaty TH, Murray JC, Marazita ML, Munger RG, Ruczinsky I, Hetmanski JB, Liang KY, Wu T, Murray T, Fallin MD, Redett RA, Raymond G, Schwender H, Jin SC, Cooper ME, Dunnwald M, Mansilla MA, Leslie E, Bullard S, Lidral AC, Moreno LM, Menezes R, Vieira AR, Petrin A, Wilcox AJ, Lie RT, Jabs EW, Wu-Chou YH, Chen PK, Wang H, Ye X, Huang S, Yeow V, Chong SS, Jee SH, Shi B, Christensen K, Melbye M, Doheny KF, Pugh EW, Ling H, Castilla EE, Czeizel AE, MA L, Field L, Brody L, Pangilinan F, Mills JL, Molloy AM, Kirke PN, Scott JM, Arcos-Burgos M, Scott AF. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nature Genetics (in press).

294 - Jones J, Canady JW, Brookes J, Wehby G, Schutte B, 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):4879-96. Epub 2009 Sep 24.

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):1358-64. Epub 2009 Oct 23.

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. 2009 Nov 25. [Epub ahead of print]

286 - Genisca AE, Frías 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 - Bille C, Pedersen DA, Andersen AM, Mansilla MA, Murray JC, Christensen K, Ballard JL, Gorman EB, Cabrera RM, Finnell RH. 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. 2009 Sep 14. [Epub ahead of print]

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 2009 Apr 29.

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. Epub 2009 Mar 12.

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 2008 Oct 30.

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 2009 Jun 11.

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. Epub 2009 Feb 26.

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 - 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 BC. Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. 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. Epub 2009 Feb 2.

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 DR, Green ED, Mossey PA, Little J, Steegers-Theunissen RP, Pennacchio LA, Schutte BC, 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. Epub 2008 Oct 5.

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. Epub 2008 Dec 17.

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 November 1; 146A(21): 2828–2830.

264 - Vieira AR, Goldstein-McHenry T, 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.146A:1406-1413, 2008.

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 C Embryo Today. 2008 Mar;84(1):16-29.

262 - Wehby GL, Ohsfeldt RL, Murray JC.. "Mendelian randomization” equals instrumental variable analysis with genetic instruments.. Stat Med. Jul 10;27(15):2745-2749, 2008.

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 32(5):413-424, 2008.

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. Nov 14;143(24):3267-3272, 2007.

259 - Freitas EL, Martinhago CD, Ramos ES, Murray JC, Gilda-Silva-Lopes VL.. Preliminary molecular studies on blepharocheilodontic syndrome. Am J Med Genet A. 143A:2757-2759, 2007.

258 - Merialdi M and Murray JC.. Commentary. The changing face of preterm birth.. Pediatrics 120(5):1133-1134, 2007.

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 2007 Sep 14.

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):3228-34.

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. Epub 2007 Sep 13.

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. Epub 2007 Jun 7.

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):1094-7.

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 2007 Feb 13.

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):846-52.

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):4512-7. Epub 2007 Mar 6.

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. Epub 2006 Dec 7.

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):2562-70.

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. Epub 2006 Sep 28.

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. Epub 2006 Oct 15.

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; discussion 521.

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):3942-54.

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. BMC Pediatr. 2006 Mar 24;6:9.

225 - 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. Epub 2006 Jan 29.

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 2005 Dec 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):1047-55.

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. Am J Med Genet A. 2005 Jun 1;135(2):220-3.

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 AM, 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. 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. Epub 2004 Jun 4.

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):277-83.

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):1405. Epub 2004 May 14.

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 2003 Nov 15.

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. Genet Epidemiol. 2003 Dec;25(4):367-74.

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. Epub 2003 Apr 29.

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):1083-91.

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. Epub 2002 Nov 1.

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. Epub 2002 Sep 3.

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 Aug;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. 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 Jan;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. Epub 2001 Dec 3.

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):1007-15.

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):23034-41. Epub 2001 Apr 11.

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. GDev 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):1359-61.

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, 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, 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 Jun;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. Assignment of the murine Hmx1 homeobox gene to the proximal region of mouse chromosome 5. Mamm Genome. 1997;8(11):869-70.

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):2803-10.

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, Weissenbach J, Gyapay G, et al. Human genetic map. Genome maps V. Wall chart. Science. 1994 Sep 30;265(5181):2055-70.

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):2049-54.

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 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.

72 - NIH/CEPH Collaborative Mapping Group. A comprehensive genetic linkage map of the human genome. Science. 1992 Oct 2;258(5079):67-86.

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):11579-83.

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):3419-25.

67 - 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.

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):357-62.

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.