Renée H. Martin, PhD, FCCMG - Medical Genetics

Dr. Martin is a professor in the Department of Medical Genetics at the University of Calgary in Calgary, Alberta. Dr. Martin supervised postdoctoral fellows, research fellows, and instructed residents in her genetic counseling clinic.

Dr. Martin has reviewed grants for the National Institutes of Health, NATO, the Medical Research Council of Canada, Health and Welfare Canada, March of Dimes, British Columbia Health Care Research Foundation, and other Canadian and United States organizations. She has provided many continuing education courses for nurses and physicians and has been an invited speaker at many national and international medical conferences. Dr. Martin has reviewed articles for a number of American and Canadian professional journals.

Currently, Dr. Martin serves on the editorial board for Human Reproduction, Reproductive Biology and Endocrinology, and the Canada Research Chairs’ College of Reviewers. She is an executive board member of the Prenatal Genetic Diagnosis International Society. She was awarded the Canada Research Chair in Genetics in 2002.

Board Certifications

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Fellow, Canadian College of Medical Geneticists—1981

Healthwise Knowledgebase Topics Reviewed

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Genetic Testing

DNA Fingerprinting

Karyotyping

Galactosemia Testing

Tay-Sach's Disease

Tay-Sach's Screening

Education

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PhD: Medical Genetics, University of British Columbia, Vancouver, BC, 1975

Academic Appointments

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Professor: Medical Genetics, University of Calgary, Calgary, AB, 1988–present

Associate Professor: Pediatrics, University of Calgary, Calgary, AB, 1982–1988

Assistant Professor: Pediatrics, University of Calgary, Calgary, AB, 1978–1982

Hospital Affiliations

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Alberta Children's Hospital, Calgary, AB

Professional Affiliations

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Canadian College of Medical Geneticists

American Society of Human Genetics

European Society of Human Genetics

Canadian Genetics Society

Canadian Fertility and Andrology Society

American Society for Human Reproduction and Embryology

International Society of Prenatal Genetic Diagnosis

Selected Publications

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1. Martin RH, Rademaker AW, Greene C, Ko E, Hoang T, Barclay L, Chernos J (2003). A comparison of the frequency of sperm chromosome abnormalities in men with mild, moderate, and severe oligozoospermia. Biology of Reproduction, 69: 535–539.
2. Sun F, Oliver-Bonet M, Liehr T, Starke H, Ko E, Rademaker A, Navarro J, Benet J, Martin RH (2004). Human male recombination maps for individual chromosomes. American Journal of Human Genetics, 74: 521-531.
3. Martin RH (2005). FISH—Human sperm cells. In J Fuchs et al., eds., Encyclopedia of Medical Genomics and Proteomics, pp. 478–481. New York: Marcel Decker.
4. Martin RH (2005). Mechanisms of nondisjunction in human spermatogenesis. Cytogenetics and Genome Research, 111: 245–249.
5. Oliver-Bonet M, Turek P, Sun F, Ko E, Martin RH (2005). Temporal progression of recombination in human males. Molecular Human Reproduction, 11: 517–522.

Financial Disclosure

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This reviewer reported no financial conflicts.