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Bryan J. Traynor

Neuroscientist and geneticist (1969-) From Wikipedia, the free encyclopedia

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Bryan J. Traynor is a neurologist and a senior investigator at the National Institute on Aging, and an adjunct professor at Johns Hopkins University.[1] Dr. Traynor studies the genetics of human neurological conditions such as amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). He led the international consortium that identified pathogenic repeat expansions in the C9orf72 gene as a common cause of ALS and FTD.[2] Dr. Traynor also led efforts that identified other Mendelian genes responsible for familial ALS and dementia, including VCP, MATR3, KIF5A, HTT, and SPTLC1.[3][4][5][6][7]

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Dr. Traynor is a co-recipient of the Potamkin Prize for Research in Pick's, Alzheimer's, and Related Diseases for the discovery of the C9orf72 repeat expansions, and the Sheila Essay Award for his contributions to our understanding of ALS. He also received the NIH Director’s Award.

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Education

Dr. Traynor received his medical degree (MB, BCh, BAO, 1993), his Medical Doctorate (MD, 2000), and his Doctor of Philosophy (PhD, 2012) from University College Dublin. He also received his Master of Medical Science (MMSc) in drug development and clinical trial design from Harvard-MIT HST in 2004. He completed his neurology residency and fellowship at Brigham and Women’s Hospital and Massachusetts General Hospital.

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Awards, prizes, and honors

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Notable professional service

References

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