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Broadview Heights, OH
After earning a Ph.D. from a founding NIH funded Genetics Program at Duke University in 1975, I moved to the University of California San Francisco for 22 years where I advanced to Associate Professor in three departments. When first offered I earned board certification in Clinical Cytogenetics (1978) and Clinical Molecular Genetics (1993) by the American College of Medical Genetics, a member board of the American Medical Associations and signed 5,000 clinical cases in both specialties. Then I directed the Molecular Genetics Laboratory at Boston University where I added 32 disease tests and signed 22,000 patient cases referred from every state in the Union and every country in the Western Hemisphere. As Director of Cytogenetics, Akron Children’s Hospital, I have completed signing 23,000 Clinical Cytogenetics cases and taught Molecular Genetics, Cytogenetics, and Ethics to Northeast Ohio Medical University students as a Pathology Professor. I authored 102 peer reviewed publications and 15 chapters with 278 coauthors in mapping, identification, and diagnosis of genetic disease that were cited 7482 times in 1660 publications by 6236 coauthors [Microsoft Academic Search; 8054 citations in ResearchGate]. I gave 65 invited presentations in 20 states and 5 foreign countries and previously received >$2,000,000 in contracts and grants. I trained 19 fellows from 10 countries who co-authored peer reviewed publications and trained 9 American Board of Medical Genetics certified specialists in Clinical Molecular Genetics or Clinical Cytogenetics. I served on the American College of Medical Genetics Committee for Maternal Screening. I hold 6 patents in genetic disease identification and diagnosis including identifying the Charcot-Marie-Tooth (CMT1B) disease gene (U.S. Patents 5,723,593. 5,876,927) and Optimizing Genome-Wide Mutation Analysis of Chromosomes and Genes.by testing the most Frequent Diseases Worldwide (U.S. Patent 8,548,747; CV.B101, 102). Full Summary
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