Murray H. Brilliant - Publications

Genetics University of Arizona, Tucson, AZ 
Genetics, Medical and Forensic Anthropology

75 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Pasquale LR, Aschard H, Kang JH, Bailey JN, Lindström S, Chasman DI, Christen WG, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert J, et al. Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample. Menopause (New York, N.Y.). PMID 27760082 DOI: 10.1097/Gme.0000000000000741  0.36
2016 Li R, Dudek SM, Kim D, Hall MA, Bradford Y, Peissig PL, Brilliant MH, Linneman JG, McCarty CA, Bao L, Ritchie MD. Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network. Biodata Mining. 9: 18. PMID 27168765 DOI: 10.1186/S13040-016-0094-4  0.36
2016 Mosley JD, Witte JS, Larkin EK, Bastarache L, Shaffer CM, Karnes JH, Stein CM, Phillips E, Hebbring SJ, Brilliant MH, Mayer J, Ye Z, Roden DM, Denny JC. Identifying genetically driven clinical phenotypes using linear mixed models. Nature Communications. 7: 11433. PMID 27109359 DOI: 10.1038/Ncomms11433  0.36
2016 Bush WS, Crosslin DR, Obeng AO, Wallace J, Almoguera B, Basford MA, Bielinski SJ, Carrell DS, Connolly JJ, Crawford D, Doheny KF, Gallego CJ, Gordon AS, Keating B, Kirby J, ... ... Brilliant MH, et al. Genetic Variation among 82 Pharmacogenes: the PGRN-Seq data from the eMERGE Network. Clinical Pharmacology and Therapeutics. PMID 26857349 DOI: 10.1002/Cpt.350  0.36
2016 Bailey JN, Loomis SJ, Kang JH, Allingham RR, Gharahkhani P, Khor CC, Burdon KP, Aschard H, Chasman DI, Igo RP, Hysi PG, Glastonbury CA, Ashley-Koch A, Brilliant M, Brown AA, et al. Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Nature Genetics. PMID 26752265 DOI: 10.1038/Ng.3482  0.36
2016 Van Driest SL, Wells QS, Stallings S, Bush WS, Gordon A, Nickerson DA, Kim JH, Crosslin DR, Jarvik GP, Carrell DS, Ralston JD, Larson EB, Bielinski SJ, Olson JE, Ye Z, ... ... Brilliant MH, et al. Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records. Jama. 315: 47-57. PMID 26746457 DOI: 10.1001/Jama.2015.17701  0.36
2015 Lee S, Schimmenti LA, King RA, Brilliant M, Anderson JL, Schoonveld C, Summers CG. Posterior staphyloma in oculocutaneous albinism: another possible cause of reduced visual acuity. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 19: 562-4. PMID 26691042 DOI: 10.1016/J.Jaapos.2015.06.009  0.36
2015 Mosley JD, Shaffer CM, Van Driest SL, Weeke PE, Wells QS, Karnes JH, Velez Edwards DR, Wei WQ, Teixeira PL, Bastarache L, Crawford DC, Li R, Manolio TA, Bottinger EP, McCarty CA, ... ... Brilliant MH, et al. A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. The Pharmacogenomics Journal. PMID 26169577 DOI: 10.1038/Tpj.2015.51  0.36
2015 McCafferty BK, Wilk MA, McAllister JT, Stepien KE, Dubis AM, Brilliant MH, Anderson JL, Carroll J, Summers CG. Clinical Insights Into Foveal Morphology in Albinism. Journal of Pediatric Ophthalmology and Strabismus. 52: 167-72. PMID 26053207 DOI: 10.3928/01913913-20150427-06  0.36
2015 Schrodi SJ, DeBarber A, He M, Ye Z, Peissig P, Van Wormer JJ, Haws R, Brilliant MH, Steiner RD. Prevalence estimation for monogenic autosomal recessive diseases using population-based genetic data. Human Genetics. 134: 659-69. PMID 25893794 DOI: 10.1007/S00439-015-1551-8  0.36
2015 He M, Person TN, Hebbring SJ, Heinzen E, Ye Z, Schrodi SJ, McPherson EW, Lin SM, Peissig PL, Brilliant MH, O'Rawe J, Robison RJ, Lyon GJ, Wang K. SeqHBase: a big data toolset for family based sequencing data analysis. Journal of Medical Genetics. 52: 282-8. PMID 25587064 DOI: 10.1136/Jmedgenet-2014-102907  0.36
2015 Ye Z, Mayer J, Ivacic L, Zhou Z, He M, Schrodi SJ, Page D, Brilliant MH, Hebbring SJ. Phenome-wide association studies (PheWASs) for functional variants. European Journal of Human Genetics : Ejhg. 23: 523-9. PMID 25074467 DOI: 10.1038/Ejhg.2014.123  0.36
2015 Glurich I, Shukla S, Acharya A, Ginsburg GS, Brilliant MH. The oral microbiome and its relationship to genomics and oral disease Genomics, Personalized Medicine and Oral Disease. 35-65. DOI: 10.1007/978-3-319-17942-1_3  0.36
2014 Liu Y, Garrett ME, Yaspan BL, Bailey JC, Loomis SJ, Brilliant M, Budenz DL, Christen WG, Fingert JH, Gaasterland D, Gaasterland T, Kang JH, Lee RK, Lichter P, Moroi SE, et al. DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma. Investigative Ophthalmology & Visual Science. 55: 8251-8. PMID 25414181 DOI: 10.1167/Iovs.14-15712  0.36
2014 Barrie ES, Weinshenker D, Verma A, Pendergrass SA, Lange LA, Ritchie MD, Wilson JG, Kuivaniemi H, Tromp G, Carey DJ, Gerhard GS, Brilliant MH, Hebbring SJ, Cubells JF, Pinsonneault JK, et al. Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activity. Circulation Research. 115: 1017-25. PMID 25326128 DOI: 10.1161/Circresaha.116.304398  0.36
2014 Springelkamp H, Höhn R, Mishra A, Hysi PG, Khor CC, Loomis SJ, Bailey JN, Gibson J, Thorleifsson G, Janssen SF, Luo X, Ramdas WD, Vithana E, Nongpiur ME, Montgomery GW, et al. Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process. Nature Communications. 5: 4883. PMID 25241763 DOI: 10.1038/ncomms5883  0.36
2014 Wilk MA, Dubra A, Curcio CA, Brilliant MH, Summers CG, Carroll J. Author response: relationship between foveal cone specialization and pit morphology in albinism. Investigative Ophthalmology & Visual Science. 55: 5923. PMID 25237180 DOI: 10.1167/Iovs.14-15470  0.36
2014 Cronin RM, Field JR, Bradford Y, Shaffer CM, Carroll RJ, Mosley JD, Bastarache L, Edwards TL, Hebbring SJ, Lin S, Hindorff LA, Crane PK, Pendergrass SA, Ritchie MD, Crawford DC, ... ... Brilliant MH, et al. Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index. Frontiers in Genetics. 5: 250. PMID 25177340 DOI: 10.3389/Fgene.2014.00250  0.36
2014 Bailey JN, Yaspan BL, Pasquale LR, Hauser MA, Kang JH, Loomis SJ, Brilliant M, Budenz DL, Christen WG, Fingert J, Gaasterland D, Gaasterland T, Kraft P, Lee RK, Lichter PR, et al. Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma. Human Genetics. 133: 1319-30. PMID 25037249 DOI: 10.1007/S00439-014-1468-7  0.36
2014 Rasmussen-Torvik LJ, Stallings SC, Gordon AS, Almoguera B, Basford MA, Bielinski SJ, Brautbar A, Brilliant MH, Carrell DS, Connolly JJ, Crosslin DR, Doheny KF, Gallego CJ, Gottesman O, Kim DS, et al. Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems. Clinical Pharmacology and Therapeutics. 96: 482-9. PMID 24960519 DOI: 10.1038/Clpt.2014.137  0.36
2014 Schrodi SJ, Mukherjee S, Shan Y, Tromp G, Sninsky JJ, Callear AP, Carter TC, Ye Z, Haines JL, Brilliant MH, Crane PK, Smelser DT, Elston RC, Weeks DE. Genetic-based prediction of disease traits: prediction is very difficult, especially about the future. Frontiers in Genetics. 5: 162. PMID 24917882 DOI: 10.3389/Fgene.2014.00162  0.36
2014 Wilk MA, McAllister JT, Cooper RF, Dubis AM, Patitucci TN, Summerfelt P, Anderson JL, Stepien KE, Costakos DM, Connor TB, Wirostko WJ, Chiang PW, Dubra A, Curcio CA, Brilliant MH, et al. Relationship between foveal cone specialization and pit morphology in albinism. Investigative Ophthalmology & Visual Science. 55: 4186-98. PMID 24845642 DOI: 10.1167/Iovs.13-13217  0.36
2014 Summers CG, Connett JE, Holleschau AM, Anderson JL, De Becker I, McKay BS, Brilliant MH. Does levodopa improve vision in albinism? Results of a randomized, controlled clinical trial. Clinical & Experimental Ophthalmology. 42: 713-21. PMID 24641678 DOI: 10.1111/ceo.12325  0.36
2014 Kang JH, Loomis SJ, Yaspan BL, Bailey JC, Weinreb RN, Lee RK, Lichter PR, Budenz DL, Liu Y, Realini T, Gaasterland D, Gaasterland T, Friedman DS, McCarty CA, Moroi SE, ... ... Brilliant M, et al. Vascular tone pathway polymorphisms in relation to primary open-angle glaucoma. Eye (London, England). 28: 662-71. PMID 24603425 DOI: 10.1038/Eye.2014.42  0.36
2014 Loomis SJ, Kang JH, Weinreb RN, Yaspan BL, Cooke Bailey JN, Gaasterland D, Gaasterland T, Lee RK, Lichter PR, Budenz DL, Liu Y, Realini T, Friedman DS, McCarty CA, Moroi SE, ... ... Brilliant M, et al. Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss. Ophthalmology. 121: 508-16. PMID 24572674 DOI: 10.1016/J.Ophtha.2013.09.012  0.36
2014 McCarty CA, Berg R, Rottscheit CM, Waudby CJ, Kitchner T, Brilliant M, Ritchie MD. Validation of PhenX measures in the personalized medicine research project for use in gene/environment studies. Bmc Medical Genomics. 7: 3. PMID 24423110 DOI: 10.1186/1755-8794-7-3  0.36
2014 Ye Z, Vasco DA, Carter TC, Brilliant MH, Schrodi SJ, Shukla SK. Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections Frontiers in Genetics. 5: 1-1. DOI: 10.3389/fgene.2014.00125  0.36
2014 Verma SS, Peissig P, Cross D, Waudby C, Brilliant M, McCarty CA, Ritchie MD. Benefits of accurate imputations in GWAS Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 8602: 877-889. DOI: 10.1007/978-3-662-45523-4_71  0.36
2013 Denny JC, Bastarache L, Ritchie MD, Carroll RJ, Zink R, Mosley JD, Field JR, Pulley JM, Ramirez AH, Bowton E, Basford MA, Carrell DS, Peissig PL, Kho AN, Pacheco JA, ... ... Brilliant MH, et al. Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. Nature Biotechnology. 31: 1102-10. PMID 24270849 DOI: 10.1038/Nbt.2749  0.36
2013 Gottesman O, Kuivaniemi H, Tromp G, Faucett WA, Li R, Manolio TA, Sanderson SC, Kannry J, Zinberg R, Basford MA, Brilliant M, Carey DJ, Chisholm RL, Chute CG, Connolly JJ, et al. The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 761-71. PMID 23743551 DOI: 10.1038/Gim.2013.72  0.36
2013 Maenner MJ, Baker MW, Broman KW, Tian J, Barnes JK, Atkins A, McPherson E, Hong J, Brilliant MH, Mailick MR. FMR1 CGG expansions: prevalence and sex ratios. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 466-73. PMID 23740716 DOI: 10.1002/Ajmg.B.32176  0.36
2013 Hebbring SJ, Schrodi SJ, Ye Z, Zhou Z, Page D, Brilliant MH. A PheWAS approach in studying HLA-DRB1*1501. Genes and Immunity. 14: 187-91. PMID 23392276 DOI: 10.1038/Gene.2013.2  0.36
2013 Manolio TA, Chisholm RL, Ozenberger B, Roden DM, Williams MS, Wilson R, Bick D, Bottinger EP, Brilliant MH, Eng C, Frazer KA, Korf B, Ledbetter DH, Lupski JR, Marsh C, et al. Implementing genomic medicine in the clinic: the future is here. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 258-67. PMID 23306799 DOI: 10.1097/01.Ogx.0000435523.89711.77  0.36
2013 Hebbring SJ, Slager SL, Epperla N, Mazza JJ, Ye Z, Zhou Z, Achenbach SJ, Vasco DA, Call TG, Rabe KG, Kay NE, Caporaso NE, Lanasa MC, Camp NJ, Strom SS, ... ... Brilliant MH, et al. Genetic evidence of PTPN22 effects on chronic lymphocytic leukemia. Blood. 121: 237-8. PMID 23287625 DOI: 10.1182/Blood-2012-08-450221  0.36
2012 Tuli AM, Valenzuela RK, Kamugisha E, Brilliant MH. Albinism and disease causing pathogens in Tanzania: are alleles that are associated with OCA2 being maintained by balancing selection? Medical Hypotheses. 79: 875-8. PMID 23063908 DOI: 10.1016/J.Mehy.2012.09.013  0.36
2011 Onojafe IF, Adams DR, Simeonov DR, Zhang J, Chan CC, Bernardini IM, Sergeev YV, Dolinska MB, Alur RP, Brilliant MH, Gahl WA, Brooks BP. Nitisinone improves eye and skin pigmentation defects in a mouse model of oculocutaneous albinism. The Journal of Clinical Investigation. 121: 3914-23. PMID 21968110 DOI: 10.1172/Jci59372  0.36
2010 Jiang YH, Pan Y, Zhu L, Landa L, Yoo J, Spencer C, Lorenzo I, Brilliant M, Noebels J, Beaudet AL. Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3. Plos One. 5: e12278. PMID 20808828 DOI: 10.1371/Journal.Pone.0012278  0.36
2010 Valenzuela RK, Henderson MS, Walsh MH, Garrison NA, Kelch JT, Cohen-Barak O, Erickson DT, John Meaney F, Bruce Walsh J, Cheng KC, Ito S, Wakamatsu K, Frudakis T, Thomas M, Brilliant MH. Predicting phenotype from genotype: normal pigmentation. Journal of Forensic Sciences. 55: 315-22. PMID 20158590 DOI: 10.1111/J.1556-4029.2009.01317.X  0.36
2010 Odeh H, Hunker KL, Belyantseva IA, Azaiez H, Avenarius MR, Zheng L, Peters LM, Gagnon LH, Hagiwara N, Skynner MJ, Brilliant MH, Allen ND, Riazuddin S, Johnson KR, Raphael Y, et al. Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse. American Journal of Human Genetics. 86: 148-60. PMID 20137774 DOI: 10.1016/J.Ajhg.2010.01.016  0.36
2008 Camenisch TD, Brilliant MH, Segal DJ. Critical parameters for genome editing using zinc finger nucleases. Mini Reviews in Medicinal Chemistry. 8: 669-76. PMID 18537722 DOI: 10.2174/138955708784567458  0.36
2007 Cohen-Barak O, Erickson DT, Badowski MS, Fuchs DA, Klassen CL, Harris DT, Brilliant MH. Stem cell transplantation demonstrates that Sox6 represses epsilon y globin expression in definitive erythropoiesis of adult mice. Experimental Hematology. 35: 358-67. PMID 17309816 DOI: 10.1016/J.Exphem.2006.11.009  0.36
2006 Yi Z, Cohen-Barak O, Hagiwara N, Kingsley PD, Fuchs DA, Erickson DT, Epner EM, Palis J, Brilliant MH. Sox6 directly silences epsilon globin expression in definitive erythropoiesis. Plos Genetics. 2: e14. PMID 16462943 DOI: 10.1371/Journal.Pgen.0020014  0.36
2005 Ikinciogullari A, Tekin M, Dogu F, Reisli I, Tanir G, Yi Z, Garrison N, Brilliant MH, Babacan E. Meningococccal meningitis and complement component 6 deficiency associated with oculocutaneous albinism. European Journal of Pediatrics. 164: 177-9. PMID 15565285 DOI: 10.1007/S00431-004-1582-Y  0.36
2004 Odeh H, Hagiwara N, Skynner M, Mitchem KL, Beyer LA, Allen ND, Brilliant MH, Lebart MC, Dolan DF, Raphael Y, Kohrman DC. Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus. Audiology & Neuro-Otology. 9: 303-14. PMID 15347914 DOI: 10.1159/000080701  0.36
2004 Garrison NA, Yi Z, Cohen-Barak O, Huizing M, Hartnell LM, Gahl WA, Brilliant MH. P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome. Journal of Medical Genetics. 41: e86. PMID 15173252 DOI: 10.1136/Jmg.2003.014902  0.36
2003 Cohen-Barak O, Yi Z, Hagiwara N, Monzen K, Komuro I, Brilliant MH. Sox6 regulation of cardiac myocyte development. Nucleic Acids Research. 31: 5941-8. PMID 14530442 DOI: 10.1093/Nar/Gkg807  0.36
2003 Hagiwara N, Katarova Z, Siracusa LD, Brilliant MH. Nonneuronal expression of the GABA(A) beta3 subunit gene is required for normal palate development in mice. Developmental Biology. 254: 93-101. PMID 12606284 DOI: 10.1016/S0012-1606(02)00030-1  0.36
2003 Yi Z, Garrison N, Cohen-Barak O, Karafet TM, King RA, Erickson RP, Hammer MF, Brilliant MH. A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population. American Journal of Human Genetics. 72: 62-72. PMID 12469324 DOI: 10.1086/345380  0.36
2001 Newton JM, Cohen-Barak O, Hagiwara N, Gardner JM, Davisson MT, King RA, Brilliant MH. Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4. American Journal of Human Genetics. 69: 981-8. PMID 11574907 DOI: 10.1086/324340  0.36
2001 Cohen-Barak O, Hagiwara N, Arlt MF, Horton JP, Brilliant MH. Cloning, characterization and chromosome mapping of the human SOX6 gene. Gene. 265: 157-64. PMID 11255018 DOI: 10.1016/S0378-1119(01)00346-8  0.36
2001 Hagiwara N, Carninci P, Kozak CA, Brilliant MH. Meeting report: 14th international mouse genome conference Mammalian Genome. 12: 401-405. DOI: 10.1007/S003350040004  0.36
2000 Puri N, Gardner JM, Brilliant MH. Aberrant pH of melanosomes in pink-eyed dilution (p) mutant melanocytes. The Journal of Investigative Dermatology. 115: 607-13. PMID 10998131 DOI: 10.1046/J.1523-1747.2000.00108.X  0.36
2000 Hagiwara N, Klewer SE, Samson RA, Erickson DT, Lyon MF, Brilliant MH. Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death. Proceedings of the National Academy of Sciences of the United States of America. 97: 4180-5. PMID 10760285 DOI: 10.1073/Pnas.97.8.4180  0.36
1999 Orlow SJ, Brilliant MH. The pink-eyed dilution locus controls the biogenesis of melanosomes and levels of melanosomal proteins in the eye. Experimental Eye Research. 68: 147-54. PMID 10068480 DOI: 10.1006/Exer.1998.0599  0.36
1998 Oetting WS, Gardner JM, Fryer JP, Ching A, Durham-Pierre D, King RA, Brilliant MH. Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. Online. Human Mutation. 12: 434. PMID 10671067 DOI: 10.1002/(SICI)1098-1004(1998)12:6<434::AID-HUMU16>3.0.CO;2-7  0.36
1998 Sweet HO, Brilliant MH, Cook SA, Johnson KR, Davisson MT. A new allelic series for the underwhite gene on mouse chromosome 15. The Journal of Heredity. 89: 546-51. PMID 9864865 DOI: 10.1093/JHERED/89.6.546  0.36
1998 Lehman AL, Nakatsu Y, Ching A, Bronson RT, Oakey RJ, Keiper-Hrynko N, Finger JN, Durham-Pierre D, Horton DB, Newton JM, Lyon MF, Brilliant MH. A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice. Proceedings of the National Academy of Sciences of the United States of America. 95: 9436-41. PMID 9689098 DOI: 10.1073/Pnas.95.16.9436  0.36
1998 Wildenberg SC, Fryer JP, Gardner JM, Oetting WS, Brilliant MH, King RA. Identification of a novel transcript produced by the gene responsible for the Hermansky-Pudlak syndrome in Puerto Rico. The Journal of Investigative Dermatology. 110: 777-81. PMID 9579545 DOI: 10.1046/J.1523-1747.1998.00183.X  0.36
1997 Gardner JM, Wildenberg SC, Keiper NM, Novak EK, Rusiniak ME, Swank RT, Puri N, Finger JN, Hagiwara N, Lehman AL, Gales TL, Bayer ME, King RA, Brilliant MH. The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome. Proceedings of the National Academy of Sciences of the United States of America. 94: 9238-43. PMID 9256466 DOI: 10.1073/pnas.94.17.9238  0.36
1997 Brilliant MH, Williams RW, Holdener BC, Angel JM, Stern M, Hunter K. Mouse chromosome 7. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: S121-42. PMID 9233390 DOI: 10.1007/s003359900319  0.36
1997 Homanics GE, DeLorey TM, Firestone LL, Quinlan JJ, Handforth A, Harrison NL, Krasowski MD, Rick CE, Korpi ER, Mäkelä R, Brilliant MH, Hagiwara N, Ferguson C, Snyder K, Olsen RW. Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior. Proceedings of the National Academy of Sciences of the United States of America. 94: 4143-8. PMID 9108119 DOI: 10.1073/Pnas.94.8.4143  0.36
1996 Oetting WS, Brilliant MH, King RA. The clinical spectrum of albinism in humans. Molecular Medicine Today. 2: 330-5. PMID 8796918 DOI: 10.1016/1357-4310(96)81798-9  0.36
1995 Gahl WA, Potterf B, Durham-Pierre D, Brilliant MH, Hearing VJ. Melanosomal tyrosine transport in normal and pink-eyed dilution murine melanocytes. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 8: 229-33. PMID 8789196 DOI: 10.1111/J.1600-0749.1995.Tb00668.X  0.36
1995 Greger V, Knoll JH, Woolf E, Glatt K, Tyndale RF, DeLorey TM, Olsen RW, Tobin AJ, Sikela JM, Nakatsu Y. The gamma-aminobutyric acid receptor gamma 3 subunit gene (GABRG3) is tightly linked to the alpha 5 subunit gene (GABRA5) on human chromosome 15q11-q13 and is transcribed in the same orientation. Genomics. 26: 258-64. PMID 7601451 DOI: 10.1016/0888-7543(95)80209-5  0.36
1994 Rosemblat S, Durham-Pierre D, Gardner JM, Nakatsu Y, Brilliant MH, Orlow SJ. Identification of a melanosomal membrane protein encoded by the pink-eyed dilution (type II oculocutaneous albinism) gene. Proceedings of the National Academy of Sciences of the United States of America. 91: 12071-75. PMID 7991586 DOI: 10.1073/Pnas.91.25.12071  0.36
1994 Durham-Pierre D, Gardner JM, Nakatsu Y, King RA, Francke U, Ching A, Aquaron R, del Marmol V, Brilliant MH. African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism. Nature Genetics. 7: 176-9. PMID 7920637 DOI: 10.1038/Ng0694-176  0.36
1994 Brilliant MH, King R, Francke U, Schuffenhauer S, Meitinger T, Gardner JM, Durham-Pierre D, Nakatsu Y. The mouse pink-eyed dilution gene: association with hypopigmentation in Prader-Willi and Angelman syndromes and with human OCA2. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 7: 398-402. PMID 7761348 DOI: 10.1111/J.1600-0749.1994.Tb00068.X  0.36
1993 Nakatsu Y, Tyndale RF, DeLorey TM, Durham-Pierre D, Gardner JM, McDanel HJ, Nguyen Q, Wagstaff J, Lalande M, Sikela JM. A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus. Nature. 364: 448-50. PMID 8392662 DOI: 10.1038/364448a0  0.36
1992 Lyon MF, King TR, Gondo Y, Gardner JM, Nakatsu Y, Elcher EM, Brilliant MH. Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse Proceedings of the National Academy of Sciences of the United States of America. 89: 6968-6972. PMID 1495987 DOI: 10.1073/Pnas.89.15.6968  0.36
1992 Brilliant MH, Gondo Y, Eicher EM. The mouse pink-eyed unstable mutation: a DNA duplication revealed by genome scanning Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 271-274. PMID 1409429  0.36
1991 Brilliant MH, Gondo Y, Eicher EM. Direct molecular identification of the mouse pink-eyed unstable mutation by genome scanning Science. 252: 566-569. PMID 1673574  0.36
1990 Brilliant MH, Szabo G, Katarova Z, Kozak CA, Glaser TM, Greenspan RJ, Housman DE. Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10. Genomics. 6: 115-22. PMID 1968040 DOI: 10.1016/0888-7543(90)90455-4  0.36
1987 Brilliant MH, Niemann MM, Eicher EM. Murine tyrosine hydroxylase maps to the distal end of chromosome 7 within a region conserved in mouse and man Journal of Neurogenetics. 4: 259-266. PMID 2889817 DOI: 10.3109/01677068709102346  0.36
1984 Brilliant MH, Sueoka N, Chikaraishi DM. Cloning of DNA corresponding to rare transcripts of rat brain: evidence of transcriptional and post-transcriptional control and of the existence of nonpolyadenylated transcripts. Molecular and Cellular Biology. 4: 2187-97. PMID 6209557 DOI: 10.1128/MCB.4.10.2187  0.36
1983 Chikaraishi DM, Brilliant MH, Lewis EJ. Cloning and characterization of rat-brain-specific transcripts: rare, brain-specific transcripts and tyrosine hydroxylase. Cold Spring Harbor Symposia On Quantitative Biology. 48: 309-18. PMID 6144414 DOI: 10.1101/SQB.1983.048.01.034  0.36
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