Michael Seldin

image of Michael Seldin

Rowe Chair of Human Genetics

Departments

Biochemistry and Molecular Medicine

Offices and Labs

4453 Tupper Hall
754-6017

Profile Introduction

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 Immunology Baylor College of Medicine

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

CBS Grad Group Affiliations

Integrated Genetics and Genomics

Specialties / Focus

Integrated Genetics and Genomics
  • Human Genetics and Genomics

Labs

Seldin Lab website

Publications

5/21/2010 9:26:34 AM
  • 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