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Faculty List for Program: "Human Genetics"


Faculty Search Results: Results 1 - 20 (List more/fewer results: 10 20 30 40 )
Faculty Member Brief Research Description
Anthony Antonellis Identify and characterize loci involved in axonal and demyelinating peripheral neuropathies.  
Stephanie Bielas Discover new genes for human developmental brain disorders and modeling disease mechanisms with patient induced pluripotent stem cells and mice to understand the associated molecular pathology.  
Dave Burke The genetic basis of the mammalian aging phenotype, using the laboratory mouse as a model system.  
Margit Burmeister Identifying genes involved in behavioral, neurological & psychiatric diseases, novel genetic techniques, gene expression, bioinformatics.  
Sally A. Camper, Ph.D. bioinformatics, cancer, developmental biology, gene expression, genetics of disease, hearing research, hormone action, neuroscience, organogenesis reproductive biology, signaling, skeletal development, stem cell research  
Vivian G Cheung Human Genetics; Regulation of Gene Expression; Gene Transcription and RNA Processing  
Ivo Dinov Dr. Dinov is Director of the Statistics Online Computational Resource (SOCR), the Integrative Biostatistics and Informatics Core, University of Michigan Nutrition Obesity Research Center (MNORC), and the Biostatistics and Data Management Core, University of Michigan Udall Center for Excellence in Parkinson's Disease. He also Co-Directs the Center for Complexity and Self-management of Chronic Disease (CSCD Center), and the multi-institutional Probability Distributome Project.   
Julie Douglas Statistical genetics, genetic epidemiology, cancer genetics  
Eric Fearon Studies of oncogene and tumor suppressor gene defects in cancer pathogenesis, particularly gastrointestinal cancers.  
Renny Franceschi Transcriptional control of mesenchymal cell lineage to bone or fat, role of the Runx2 transcription factor in prostate cancer and cancer stem cells.  
David Ginsburg The components of the blood-clotting system and how disturbances in their function lead to human bleeding and blood-clotting disorders.   
Thomas Glover Genome Instability Copy Number Variants Chromosome Fragile Sites Hutchinson-Gilford Progeria  
Sue Hammoud The Hammoud lab is interested in deciphering intrinsic and extrinsic mechanisms/factors required for spermatogonial stem cell maintenance and differentiation.   
Jeffrey Innis Human molecular genetics; Hox genes; gastrulation defects leading to human and mouse malformation; human syndromes  
Shigeki Iwase Chromatin Dynamics in Brain Development and Function  
Sundeep Kalantry Epigenetic mechanisms of X-chromosome inactivation in early embryos and stem cells.   
Katy Keegan Mouse models of telomere dysfunction, genomic instability, and birth defects. Molecular genetics of caudal and urogenital development.   
Jeffrey Kidd Genomics approaches to explore the structure, content, and evolution of diverse genomes.  
Jacob Kitzman We develop genomic technologies to comprehensively identify sequence and structural variants, and dissect their functional impacts with respect to molecular and cellular phenotypes.  
Dave Kohrman genetics of auditory system development and function; mouse models of inner ear dysfunction  
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