University of Pittsburgh Department of Human Genetics



Primary Faculty



Secondary Faculty

Robert E. Ferrell
 
Recent Publications:

Insulin Resistance is Associated with Higher Intramyocellular Triglycerides in Type I but not Type II Myocytes Concomitant with Higher Ceramide Content.
Paul M Coen, John J Dubé, Francesca Amati, Maja Stefanovic-Racic, Robert E Ferrell, Frederico G S Toledo, Bret H Goodpaster
Diabetes. 2009 Oct

Polymorphisms in the CRP gene moderate an association between depressive symptoms and circulating levels of C-reactive protein.
Indrani Halder, Anna L Marsland, Jeewon Cheong, Matthew F Muldoon, Robert E Ferrell, Stephen B Manuck
Brain Behav. Immun.. 2009 Sep

 


Susanne M. Gollin
 
Recent Publications:

Recurrence in oral and pharyngeal cancer is associated with quantitative MGMT promoter methylation.
Emanuela Taioli, Camille Ragin, Xiao-Hong Wang, Jiangying Chen, Scott M Langevin, Ashley R Brown, Susanne M Gollin, Seymour Garte, Robert W Sobol
BMC Cancer. 2009 ;9:354
PMC2763008

Decreased expression of miR-125b and miR-100 in oral cancer cells contributes to malignancy.
Brian J Henson, Samsiddhi Bhattacharjee, Dawn M O'Dee, Eleanor Feingold, Susanne M Gollin
Genes Chromosomes Cancer. 2009 Jul;48:569-82
PMC2726991

 


M. Ilyas Kamboh
 
About:
Dr. Kamboh is a molecular geneticist/genetic epidemiologist and his research focuses on the genetics of common diseases of public health importance, including coronary heart disease, Alzheimer's disease and lupus. Dr. Kamboh also holds a joint position of Professor of Psychiatry at the School of Medicine and he is a Fellow of the American Heart Association. Dr. Kamboh directs a Human Genetics laboratory and also co-teaches a course in the department entitled "Biochemical and Molecular Genetics of Complex Disease."
 
Research Interests:
The focus of Dr. M. Ilyas Kamboh's research is on the genetics of common diseases of public health importance. Particular attention is being paid to understand the genetic and molecular basis of coronary heart disease (CHD), Alzheimer's disease (AD) and lupus.
 


Daniel E. Weeks
 
About:
Dr. Weeks' research focuses on statistical human genetics in the area of mapping susceptibility loci involved in complex diseases. Dr. Weeks is the Program Director of the International India-US Research Training Program in Genetics. He is also active in external teaching activities, co-leading the annual Wellcome Trust Advanced Course on mapping complex diseases and lecturing in other courses.
 
Research Interests:
Dr. Weeks' research focuses on statistical human genetics in the area of mapping susceptibility loci involved in complex diseases. His primary interest is developing new mapping methods, which involves developing algorithms and statistics, implementing them in computer programs, and testing them on real and simulated data. In addition, he is actively involved in a large number of collaborative disease gene mapping projects, all of which constantly challenge him to develop new and more useful methods for dealing with the complexities of real data. These diseases include age-related macular degeneration, obesity, otitis media, dental caries, pre-term birth, food allergy, autism, and Type II diabetes.
 


M. Michael Barmada
 
About:
My research is primarily concerned with identifying genetic susceptibility loci for common complex disorders. To this end, I apply various methods derived from statistics, genetics, and epidemiology to the analysis of large, typically family-based samples. My current projects include studies of non-insulin dependent diabetes, inflammatory bowel disease, pancreatitis, pancreatic cancer and gastro-esophageal reflux. In addition to studies of diseases, I am also involved in research which describes the quantitative variation associated with non-disease traits, such as thyroid hormone levels. As part of all of these research projects, I am constantly adapting and applying cutting-edge and traditional methods of analysis and also occasionally developing new methods for complex disease analysis. Oh, and I like to ski too...
 
Research Interests:
Genetics of gastro-intestinal disorders; Genetic epidemiology of common diseases; Quantitative genetics; Computational genetics; Genetics informatics
 


Eleanor Feingold
 
Research Interests:
Statistical methods for gene mapping, genetic epidemiology of trisomy and Down syndrome, statistical approaches to bioinformatics.
 


Elizabeth Anne Gettig
 
About:
Research focuses on the process of genetic counseling, genetic education, clinical service delivery, and the role of community service in patient care. Analysis of regional genetic service data from the Middle Atlantic Regional Human Genetic Network (MARHGN) provides information for policy development and establishment of uniform minimum criteria for genetic service delivery nationally.
 
Research Interests:
Genetic counseling, regional genetic services, innovative pedagogy
 


Candace M. Kammerer
 
About:
Dr. Kammerer’s teaching and research interests involve the genetic epidemiology of risk factors of common human diseases such as hypertension, arteriosclerosis, and osteoporosis. Her current research projects involve the statistical analyses of data on large, multigenerational families of Mexican Americans and Afro-Caribbeans, as well as large pedigrees of baboons, which are an animal model used in genetic studies of cardiovascular disease.
 
Research Interests:
The major focus of my research is to use statistical genetic methods to detect, characterize, and locate genes that affect quantitative risk factors of common human diseases. Using both phenotypic and genotypic data on large, multigeneration human families.
 


Lisa S Parker
 
About:
Lisa S. Parker, Associate Professor, Human Genetics and Behavioral and Community Health Sciences, Ph.D., University of Pittsburgh, 1990. Dr. Parker is a philosopher whose research focuses on ethical issues in genetic research and the provision of genetic services, informed consent, and women’s health issues. She serves as Director of Graduate Education for the Center for Bioethics and Health Law, directs the University’s interdisciplinary Master of Arts Program in Bioethics, and teaches courses in bioethics, feminist approaches in bioethics, and ethical and legal issues in genetics.
 


Robin Grubs
 
About:
Dr. Grubs is Co-Director, Genetic Counseling Program. Dr. Grubs' teaching interests are in genetic counseling and clinical genetics. She is responsible for the course work for the graduate program in Genetic Counseling and lectures in genetic courses taught in the Department of Human Genetics and in the University of Pittsburgh Medical School. She also serves as the Genetic Counseling Program coordinator for the clinical rotations sites at several hospitals located in the Pittsburgh area. Dr. Grubs is interested in the development of genetic educational programs for health care professionals and the general public.
 
Research Interests:
Dr. Grubs' research interests include studying the human dilemmas that arise when individuals are confronted with the option of genetic testing and examining the process of genetic counseling. Using grounded theory, Dr. Grubs has studied the experiences of women/couples who were offered prenatal genetic testing. She found that these women/couples did not experience making a decision about prenatal genetic testing as a discrete medical event but rather as an emotionally charged, value-laden dilemma within the fabric of their lives. Dr. Grubs has expanded her research to study other groups of individuals who are offered genetic testing outside of a prenatal setting. Another research interest includes exploring issues related to interpretive approaches to qualitative research and using interpretive inquiry to generate theories of genetic counseling practice and the educational preparation of professionals in genetic counseling.
 


F. Yesim Demirci
 
Recent Publications:

Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.
Jessica A Figgins, Ryan L Minster, F Yesim Demirci, Steven T Dekosky, M Ilyas Kamboh
Am. J. Med. Genet. B Neuropsychiatr. Genet.. 2009 Jun;150B:520-6
PMC2751631

No association between CALHM1 variation and risk of Alzheimer disease.
Ryan L Minster, F Yesim Demirci, Steven T DeKosky, M Ilyas Kamboh
Hum. Mutat.. 2009 Apr;30:E566-9