Michael Seldin
Rowe Chair of Human Genetics
mfseldin@ucdavis.edu
Biological Chemistry -Medicine
Office
4453 Tupper Hall
754-6017
1981
MD
Baylor College of Medicine
1979
PhD
Baylor College of Medicine
Immunology
Genome based approaches towards defining the etiopathogenesis of disease. Approaches towards defining complex genetic disease in humans and mouse. Genetic mechanisms underlying predisposition
Genetics
Molecular, Cellular, and Integrative Physiology
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2002 Collins-Schramm, H.E., C.M. Phillips, D.J. Operario, J.S. Lee, J.LWeber, J.L. Hanson, W.C. Knowler, R. Cooper, H. Li, and M. F. Seldin. Ethnic Difference Markers for Use in Mapping by Admixture Linkage Disequilibrium. American Journal of Human Genetics. 70(3):737-50.
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2004 Seldin MF, Morii T, Collins-Schramm HE, Chima B, Kittles R, Criswell LA, and Li H. Putative Ancestral Origins of Chromosomal Segments in Individual African Americans: Implications for Admixture Mapping. Genome Res, 14: 1076-1084.
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2005 Runstadler JA, H Saila, A Savolainen, M Leirisalo-Repo, K Aho, E Tuomilehto-Wolf, J Tuomilehto, and MF Seldin. SLC11A1 (NRAMP1) is associated with Finnish persistent oligoarticular and polyarticular rheumatoid factor negative juvenile idiopathic arthritis: haplotype analysis in Finnish families. Arth and Rheumatism 52:247-256