Gregory Barsh - Publications

Genetics Stanford University, Palo Alto, CA 
Color variation

56 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
2015 Dorshorst B, Henegar C, Liao X, Sällman Almén M, Rubin CJ, Ito S, Wakamatsu K, Stothard P, Van Doormaal B, Plastow G, Barsh GS, Andersson L. Dominant Red Coat Color in Holstein Cattle Is Associated with a Missense Mutation in the Coatomer Protein Complex, Subunit Alpha (COPA) Gene. Plos One. 10: e0128969. PMID 26042826 DOI: 10.1371/Journal.Pone.0128969  0.331
2013 Beleza S, Johnson NA, Candille SI, Absher DM, Coram MA, Lopes J, Campos J, Araújo II, Anderson TM, Vilhjálmsson BJ, Nordborg M, Correia E Silva A, Shriver MD, Rocha J, Barsh GS, et al. Genetic architecture of skin and eye color in an African-European admixed population. Plos Genetics. 9: e1003372. PMID 23555287 DOI: 10.1371/Journal.Pgen.1003372  0.757
2013 Silvius D, Pitstick R, Ahn M, Meishery D, Oehler A, Barsh GS, DeArmond SJ, Carlson GA, Gunn TM. Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion disease. Plos One. 8: e55575. PMID 23383230 DOI: 10.1371/Journal.Pone.0055575  0.63
2012 Candille SI, Absher DM, Beleza S, Bauchet M, McEvoy B, Garrison NA, Li JZ, Myers RM, Barsh GS, Tang H, Shriver MD. Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. Plos One. 7: e48294. PMID 23118974 DOI: 10.1371/Journal.Pone.0048294  0.728
2009 Anderson TM, vonHoldt BM, Candille SI, Musiani M, Greco C, Stahler DR, Smith DW, Padhukasahasram B, Randi E, Leonard JA, Bustamante CD, Ostrander EA, Tang H, Wayne RK, Barsh GS. Molecular and evolutionary history of melanism in North American gray wolves. Science (New York, N.Y.). 323: 1339-43. PMID 19197024 DOI: 10.1126/Science.1165448  0.777
2009 Alizadeh A, Hong LZ, Kaelin CB, Raudsepp T, Manuel H, Barsh GS. Genetics of Sex-linked yellow in the Syrian hamster. Genetics. 181: 1427-36. PMID 19189957 DOI: 10.1534/genetics.108.095018  0.31
2009 Barsh GS, Anderson TM, Vonholdt BM, Candille SI, Musiani M, Stahler DR, Leonard JA, Padhukasahasram B, Randi E, Bustamante CD, Ostrander EA, Tang H, Wayne RK. Response Science. 325: 34. DOI: 10.1126/Science.325_34  0.762
2008 Kaelin CB, Candille SI, Yu B, Jackson P, Thompson DA, Nix MA, Binkley J, Millhauser GL, Barsh GS. New ligands for melanocortin receptors. International Journal of Obesity (2005). 32: S19-27. PMID 19136986 DOI: 10.1038/Ijo.2008.234  0.746
2008 McGowan KA, Li JZ, Park CY, Beaudry V, Tabor HK, Sabnis AJ, Zhang W, Fuchs H, de Angelis MH, Myers RM, Attardi LD, Barsh GS. Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. Nature Genetics. 40: 963-70. PMID 18641651 DOI: 10.1038/Ng.188  0.344
2008 Barsh G, Candille S, He L, Aradhya S, Kerns J. The role of accessory proteins in melanocortin receptor signaling Experimental Dermatology. 13: 569-569. DOI: 10.1111/J.0906-6705.2004.00212H.X  0.784
2007 Walker WP, Aradhya S, Hu CL, Shen S, Zhang W, Azarani A, Lu X, Barsh GS, Gunn TM. Genetic analysis of attractin homologs. Genesis (New York, N.Y. : 2000). 45: 744-56. PMID 18064672 DOI: 10.1002/Dvg.20351  0.786
2007 Candille SI, Kaelin CB, Cattanach BM, Yu B, Thompson DA, Nix MA, Kerns JA, Schmutz SM, Millhauser GL, Barsh GS. A -defensin mutation causes black coat color in domestic dogs. Science (New York, N.Y.). 318: 1418-23. PMID 17947548 DOI: 10.1126/Science.1147880  0.775
2007 Kerns JA, Cargill EJ, Clark LA, Candille SI, Berryere TG, Olivier M, Lust G, Todhunter RJ, Schmutz SM, Murphy KE, Barsh GS. Linkage and segregation analysis of black and brindle coat color in domestic dogs. Genetics. 176: 1679-89. PMID 17483404 DOI: 10.1534/Genetics.107.074237  0.749
2007 McGowan KA, Fuchs H, Hrabé de Angelis M, Barsh GS. Identification of a Keratin 4 mutation in a chemically induced mouse mutant that models white sponge nevus. The Journal of Investigative Dermatology. 127: 60-4. PMID 16858417 DOI: 10.1038/Sj.Jid.5700498  0.312
2006 April CS, Barsh GS. Skin layer-specific transcriptional profiles in normal and recessive yellow (Mc1re/Mc1re) mice. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 19: 194-205. PMID 16704453 DOI: 10.1111/j.1600-0749.2006.00305.x  0.325
2005 Kuijper S, Beverdam A, Kroon C, Brouwer A, Candille S, Barsh G, Meijlink F. Genetics of shoulder girdle formation: Roles of Tbx15 and aristaless-like genes Development. 132: 1601-1610. PMID 15728667 DOI: 10.1242/Dev.01735  0.764
2004 Kerns JA, Newton J, Berryere TG, Rubin EM, Cheng JF, Schmutz SM, Barsh GS. Characterization of the dog Agouti gene and a nonagoutimutation in German Shepherd Dogs. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 798-808. PMID 15520882 DOI: 10.1007/S00335-004-2377-1  0.328
2004 Van Raamsdonk CD, Fitch KR, Fuchs H, de Angelis MH, Barsh GS. Effects of G-protein mutations on skin color. Nature Genetics. 36: 961-8. PMID 15322542 DOI: 10.1038/ng1412  0.347
2004 Candille SI, Van Raamsdonk CD, Chen C, Kuijper S, Chen-Tsai Y, Russ A, Meijlink F, Barsh GS. Dorsoventral patterning of the mouse coat by Tbx15. Plos Biology. 2: E3. PMID 14737183 DOI: 10.1371/Journal.Pbio.0020003  0.745
2003 He L, Eldridge AG, Jackson PK, Gunn TM, Barsh GS. Accessory proteins for melanocortin signaling: attractin and mahogunin. Annals of the New York Academy of Sciences. 994: 288-98. PMID 12851328 DOI: 10.1111/J.1749-6632.2003.Tb03192.X  0.696
2003 He L, Lu XY, Jolly AF, Eldridge AG, Watson SJ, Jackson PK, Barsh GS, Gunn TM. Spongiform degeneration in mahoganoid mutant mice. Science (New York, N.Y.). 299: 710-2. PMID 12560552 DOI: 10.1126/Science.1079694  0.695
2002 Barsh GS, He L, Gunn TM. Genetic and biochemical studies of the Agouti-attractin system. Journal of Receptor and Signal Transduction Research. 22: 63-77. PMID 12503608 DOI: 10.1081/Rrs-120014588  0.72
2002 Gunn TM, Azarani A, Kim PH, Hyman RW, Davis RW, Barsh GS. Identification and preliminary characterization of mouse Adam33. Bmc Genetics. 3: 2. PMID 11897009 DOI: 10.1186/1471-2156-3-2  0.654
2001 Gunn TM, Inui T, Kitada K, Ito S, Wakamatsu K, He L, Bouley DM, Serikawa T, Barsh GS. Molecular and phenotypic analysis of Attractin mutant mice. Genetics. 158: 1683-95. PMID 11514456  0.645
2001 Nadeau JH, Balling R, Barsh G, Beier D, Brown SD, Bucan M, Camper S, Carlson G, Copeland N, Eppig J, Fletcher C, Frankel WN, Ganten D, Goldowitz D, Goodnow C, et al. Sequence interpretation. Functional annotation of mouse genome sequences. Science (New York, N.Y.). 291: 1251-5. PMID 11233449 DOI: 10.1126/Science.1058244  0.312
2001 Kawai J, Shinagawa A, Shibata K, Yoshino M, Itoh M, Ishii Y, Arakawa T, Hara A, Fukunishi Y, Konno H, Adachi J, Fukuda S, Aizawa K, Izawa M, Nishi K, ... ... Barsh G, et al. Functional annotation of a full-length mouse cDNA collection. Nature. 409: 685-90. PMID 11217851 DOI: 10.1038/35055500  0.324
2001 He L, Gunn TM, Bouley DM, Lu XY, Watson SJ, Schlossman SF, Duke-Cohan JS, Barsh GS. A biochemical function for attractin in agouti-induced pigmentation and obesity. Nature Genetics. 27: 40-7. PMID 11137996 DOI: 10.1038/83741  0.669
2000 Barsh G, Gunn T, He L, Wilson B, Lu X, Gantz I, Watson S. Neuroendocrine regulation by the Agouti/Agrp-melanocortin system Endocrine Research. 26: 571. PMID 11196430 DOI: 10.3109/07435800009048572  0.678
2000 Gunn TM, Barsh GS. Mahogany/attractin: en route from phenotype to function. Trends in Cardiovascular Medicine. 10: 76-81. PMID 11150734 DOI: 10.1016/S1050-1738(00)00052-9  0.702
2000 Barsh G, Gunn T, He L, Schlossman S, Duke-Cohan J. Biochemical and genetic studies of pigment-type switching. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 13: 48-53. PMID 11041357 DOI: 10.1034/J.1600-0749.13.S8.10.X  0.715
2000 Tang W, Gunn TM, McLaughlin DF, Barsh GS, Schlossman SF, Duke-Cohan JS. Secreted and membrane attractin result from alternative splicing of the human ATRN gene. Proceedings of the National Academy of Sciences of the United States of America. 97: 6025-30. PMID 10811918 DOI: 10.1073/pnas.110139897  0.648
1999 Barsh GS, Ollmann MM, Wilson BD, Miller KA, Gunn TM. Molecular pharmacology of Agouti protein in vitro and in vivo. Annals of the New York Academy of Sciences. 885: 143-52. PMID 10816647 DOI: 10.1111/J.1749-6632.1999.Tb08671.X  0.731
1999 Lu Xy, Gunn TM, Shieh Kr, Barsh GS, Akil H, Watson SJ. Distribution of Mahogany/Attractin mRNA in the rat central nervous system. Febs Letters. 462: 101-7. PMID 10580100 DOI: 10.1016/S0014-5793(99)01494-5  0.612
1999 Barsh G. Of ancient tales and hairless tails Nature Genetics. 22: 315-316. PMID 10431226 DOI: 10.1038/11876  0.351
1999 Wilson BD, Ollmann MM, Barsh GS. The role of agouti-related protein in regulating body weight. Molecular Medicine Today. 5: 250-6. PMID 10366820 DOI: 10.1016/S1357-4310(99)01471-9  0.546
1999 Wilson BD, Bagnol D, Kaelin CB, Ollmann MM, Gantz I, Watson SJ, Barsh GS. Physiological and anatomical circuitry between Agouti-related protein and leptin signaling. Endocrinology. 140: 2387-97. PMID 10218993 DOI: 10.1210/Endo.140.5.6728  0.554
1999 Gunn TM, Miller KA, He L, Hyman RW, Davis RW, Azarani A, Schlossman SF, Duke-Cohan JS, Barsh GS. The mouse mahogany locus encodes a transmembrane form of human attractin. Nature. 398: 152-6. PMID 10086356 DOI: 10.1038/18217  0.701
1998 Furumura M, Sakai C, Potterf SB, Vieira WD, Barsh GS, Hearing VJ. Characterization of genes modulated during pheomelanogenesis using differential display. Proceedings of the National Academy of Sciences of the United States of America. 95: 7374-8. PMID 9636156 DOI: 10.1073/Pnas.95.13.7374  0.322
1998 Ollmann MM, Lamoreux ML, Wilson BD, Barsh GS. Interaction of Agouti protein with the melanocortin 1 receptor in vitro and in vivo. Genes & Development. 12: 316-30. PMID 9450927  0.559
1997 Ollmann MM, Wilson BD, Yang YK, Kerns JA, Chen Y, Gantz I, Barsh GS. Antagonism of central melanocortin receptors in vitro and in vivo by agouti-related protein. Science (New York, N.Y.). 278: 135-8. PMID 9311920 DOI: 10.1126/Science.278.5335.135  0.579
1997 Miller KA, Gunn TM, Carrasquillo MM, Lamoreux ML, Galbraith DB, Barsh GS. Genetic studies of the mouse mutations mahogany and mahoganoid. Genetics. 146: 1407-15. PMID 9258683  0.694
1997 Yang YK, Ollmann MM, Wilson BD, Dickinson C, Yamada T, Barsh GS, Gantz I. Effects of recombinant agouti-signaling protein on melanocortin action. Molecular Endocrinology (Baltimore, Md.). 11: 274-80. PMID 9058374 DOI: 10.1210/Mend.11.3.9898  0.557
1996 Newton JM, Orlow SJ, Barsh GS. Isolation and characterization of a mouse homolog of the X-linked ocular albinism (OA1) gene. Genomics. 37: 219-25. PMID 8921399 DOI: 10.1006/Geno.1996.0545  0.319
1996 Barsh GS. The genetics of pigmentation: from fancy genes to complex traits. Trends in Genetics : Tig. 12: 299-305. PMID 8783939 DOI: 10.1016/0168-9525(96)10031-7  0.349
1995 Wilson BD, Ollmann MM, Kang L, Stoffel M, Bell GI, Barsh GS. Structure and function of ASP, the human homolog of the mouse agouti gene. Human Molecular Genetics. 4: 223-30. PMID 7757071 DOI: 10.1093/Hmg/4.2.223  0.586
1994 Vrieling H, Duhl DM, Millar SE, Miller KA, Barsh GS. Differences in dorsal and ventral pigmentation result from regional expression of the mouse agouti gene. Proceedings of the National Academy of Sciences of the United States of America. 91: 5667-71. PMID 8202545 DOI: 10.1073/Pnas.91.12.5667  0.31
1994 Duhl DM, Stevens ME, Vrieling H, Saxon PJ, Miller MW, Epstein CJ, Barsh GS. Pleiotropic effects of the mouse lethal yellow (Ay) mutation explained by deletion of a maternally expressed gene and the simultaneous production of agouti fusion RNAs. Development (Cambridge, England). 120: 1695-708. PMID 8050375  0.308
1993 Miller MW, Duhl DM, Vrieling H, Cordes SP, Ollmann MM, Winkes BM, Barsh GS. Cloning of the mouse agouti gene predicts a secreted protein ubiquitously expressed in mice carrying the lethal yellow mutation. Genes & Development. 7: 454-67. PMID 8449404  0.352
1985 Barsh GS, Roush CL, Bonadio J, Byers PH, Gelinas RE. Intron-mediated recombination may cause a deletion in an alpha 1 type I collagen chain in a lethal form of osteogenesis imperfecta. Proceedings of the National Academy of Sciences of the United States of America. 82: 2870-4. PMID 3857621 DOI: 10.1073/Pnas.82.9.2870  0.524
1982 Shapiro JE, Phillips JA, Byers PH, Sanders R, Holbrook KA, Levin LS, Dorst J, Barsh GS, Peterson KE, Goldstein P. Prenatal diagnosis of lethal perinatal osteogenesis imperfecta (OI type II). The Journal of Pediatrics. 100: 127-33. PMID 7057300 DOI: 10.1016/S0022-3476(82)80252-7  0.421
1982 Byers PH, Barsh GS, Holbrook KA. Molecular pathology in inherited disorders of collagen metabolism. Human Pathology. 13: 89-95. PMID 7042525 DOI: 10.1016/S0046-8177(82)80112-3  0.491
1982 Barsh GS, David KE, Byers PH. Type I osteogenesis imperfecta: a nonfunctional allele for pro alpha 1 (I) chains of type I procollagen. Proceedings of the National Academy of Sciences of the United States of America. 79: 3838-42. PMID 6954526 DOI: 10.1073/Pnas.79.12.3838  0.448
1981 Barsh GS, Peterson KE, Byers PH. Peptide mapping of collagen chains using CNBr cleavage of proteins within polyacrylamide gels. Collagen and Related Research. 1: 543-8. PMID 7346234 DOI: 10.1016/S0174-173X(81)80035-0  0.453
1981 Barsh GS, Byers PH. Reduced secretion of structurally abnormal type I procollagen in a form of osteogenesis imperfecta. Proceedings of the National Academy of Sciences of the United States of America. 78: 5142-6. PMID 6946461 DOI: 10.1073/Pnas.78.8.5142  0.472
1981 Byers PH, Barsh GS, Holbrook KA. Molecular mechanisms of connective tissue abnormalities in the Ehlers-Danlos syndrome. Collagen and Related Research. 1: 475-89. PMID 6125299 DOI: 10.1016/S0174-173X(81)80030-1  0.503
1981 Byers PH, Barsh GS, Peterson KE, Phillips JH, Shapiro J, Holbrook KA, Levin LS, Rowe DW, Scott CR. 705 BIOCHEMICAL CHARACTERIZATION OF PERINATAL LETHAL OSTEOGENESIS IMPERFECTA (01) AND ITS PRENATAL DETECTION Pediatric Research. 15: 559-559. DOI: 10.1203/00006450-198104001-00728  0.465
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