UC Davis Genome Center
 
Michael Seldin
Rowe Chair of Human Genetics
Biological Chemistry (School of Medicine)
4453 Tupper Hall
Office 754-6017
Lab
mfseldin@ucdavis.edu
 
Genome based approaches towards defining the etiopathogenesis of disease. Approaches towards defining complex genetic disease in humans and mouse. Genetic mechanisms underlying predisposition

Degrees:
1981 - MD - Baylor College of Medicine -
1979 - PhD - Baylor College of Medicine - Immunology

Grad Group Affiliations and Specialties:
Genetics

Publications:
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.

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.

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

Research Interests:
Genome based approaches towards defining the etiopathogenesis of disease. Approaches towards defining complex genetic disease in humans and mouse. Genetic mechanisms underlying predisposition