K. Walker

发表

Multifactor dimensionality reduction reveals gene–gene interactions associated with multiple sclerosis susceptibility in African Americans

J L Haines, M A Pericak-Vance, S Schmidt, 2006, Genes and Immunity.

Multi-locus interactions predict risk for post-PTCA restenosis: an approach to the genetic analysis of common complex disease

J. Ott, J. Hoh, M. Grow, 2002, The Pharmacogenomics Journal.

Genetic variation in immunoregulatory pathways and atopic phenotypes in infancy.

D. Nicolae, C. Ober, R. Gangnon, 2004, The Journal of allergy and clinical immunology.

Complex gene–gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes

Margaret A. Pericak-Vance, Stephen L. Hauser, Silke Schmidt, 2006, Neurogenetics.

Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis

J. Haines, M. Pericak-Vance, S. Schmidt, 2004, Annals of neurology.

Detection of sequence variation in the HVII region of the human mitochondrial genome in 689 individuals using immobilized sequence-specific oligonucleotide probes.

H. Erlich, M. Allen, R. Reynolds, 2000, Journal of forensic sciences.

Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus.

Mary Sara McPeek, Carole Ober, Raluca Nicolae, 2003, American journal of human genetics.

Are common disease susceptibility alleles the same in outbred and founder populations?

M. McPeek, M. Abney, C. Ober, 2004, European Journal of Human Genetics.

Gene-environment interaction effects on the development of immune responses in the 1st year of life.

D. Nicolae, C. Ober, I. Ostrovnaya, 2005, American journal of human genetics.

Association of endothelial nitric oxide synthase genotypes with bone mineral density, bone loss, hip structure, and risk of fracture in older women: the SOF study.

S. Cummings, K. Ensrud, P. Schreiner, 2006, Bone.