Jeremy A. Cholfin - Publications

University of California, San Francisco, San Francisco, CA 
developmental neurobiology

8 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
2012 Gennatas ED, Cholfin JA, Zhou J, Crawford RK, Sasaki DA, Karydas A, Boxer AL, Bonasera SJ, Rankin KP, Gorno-Tempini ML, Rosen HJ, Kramer JH, Weiner M, Miller BL, Seeley WW. COMT Val158Met genotype influences neurodegeneration within dopamine-innervated brain structures. Neurology. 78: 1663-9. PMID 22573634 DOI: 10.1212/WNL.0b013e3182574fa1  1
2008 Cholfin JA, Rubenstein JL. Frontal cortex subdivision patterning is coordinately regulated by Fgf8, Fgf17, and Emx2. The Journal of Comparative Neurology. 509: 144-55. PMID 18459137 DOI: 10.1002/cne.21709  1
2008 Scearce-Levie K, Roberson ED, Gerstein H, Cholfin JA, Mandiyan VS, Shah NM, Rubenstein JL, Mucke L. Abnormal social behaviors in mice lacking Fgf17. Genes, Brain, and Behavior. 7: 344-54. PMID 17908176 DOI: 10.1111/j.1601-183X.2007.00357.x  1
2007 Cholfin JA, Rubenstein JL. Genetic regulation of prefrontal cortex development and function. Novartis Foundation Symposium. 288: 165-73; discussion 1. PMID 18494258 DOI: 10.1002/9780470994030.ch12  1
2007 Cholfin JA, Rubenstein JL. Patterning of frontal cortex subdivisions by Fgf17. Proceedings of the National Academy of Sciences of the United States of America. 104: 7652-7. PMID 17442747 DOI: 10.1073/pnas.0702225104  1
2006 Sawamoto K, Wichterle H, Gonzalez-Perez O, Cholfin JA, Yamada M, Spassky N, Murcia NS, Garcia-Verdugo JM, Marin O, Rubenstein JL, Tessier-Lavigne M, Okano H, Alvarez-Buylla A. New neurons follow the flow of cerebrospinal fluid in the adult brain. Science (New York, N.Y.). 311: 629-32. PMID 16410488 DOI: 10.1126/science.1119133  1
2001 Cholfin JA, Sobrido MJ, Perlman S, Pulst SM, Geschwind DH. The SCA12 mutation as a rare cause of spinocerebellar ataxia. Archives of Neurology. 58: 1833-5. PMID 11708992  1
2001 Sobrido MJ, Cholfin JA, Perlman S, Pulst SM, Geschwind DH. SCA8 repeat expansions in ataxia: a controversial association. Neurology. 57: 1310-2. PMID 11591855  1
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