Seth E. Dobrin, Ph.D. - Publications
Affiliations: | 2004 | Arizona State University, Tempe, AZ, United States |
Area:
Genetics, Molecular Biology, Neuroscience Biology, PathologyYear | Citation | Score | |||
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2006 | Strauss KA, Puffenberger EG, Huentelman MJ, Gottlieb S, Dobrin SE, Parod JM, Stephan DA, Morton DH. Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. The New England Journal of Medicine. 354: 1370-7. PMID 16571880 DOI: 10.1056/Nejmoa052773 | 0.359 | |||
2005 | McKeane DP, Meyer J, Dobrin SE, Melmed KM, Ekawardhani S, Tracy NA, Lesch KP, Stephan DA. No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families. Schizophrenia Research. 75: 1-3. PMID 15820317 DOI: 10.1016/j.schres.2004.07.017 | 0.408 | |||
2004 | Puffenberger EG, Hu-Lince D, Parod JM, Craig DW, Dobrin SE, Conway AR, Donarum EA, Strauss KA, Dunckley T, Cardenas JF, Melmed KR, Wright CA, Liang W, Stafford P, Flynn CR, et al. Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function. Proceedings of the National Academy of Sciences of the United States of America. 101: 11689-94. PMID 15273283 DOI: 10.1073/Pnas.0401194101 | 0.455 | |||
2003 | Dobrin SE, Stephan DA. Integrating microarrays into disease-gene identification strategies. Expert Review of Molecular Diagnostics. 3: 375-85. PMID 12779011 DOI: 10.1586/14737159.3.3.375 | 0.428 | |||
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