Bryan J. Traynor

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, and KIF5A.[3][4]

Bryan J. Traynor
Born (1969-08-12) August 12, 1969
Dublin, Ireland
CitizenshipIreland, United States
Alma materUniversity College Dublin (MB, MD, PhD)
Harvard–MIT Program in Health Sciences and Technology (MMSc)
Known forDiscovery of the C9orf72 repeat expansion
AwardsNIH Director's award
Sheila Essey Award
Potamkin Prize
Scientific career
FieldsAmyotrophic lateral sclerosis
frontotemporal dementia
genetics
InstitutionsNational Institute on Aging
Johns Hopkins University

Dr. Traynor is co-recipient of the 2016 Potamkin Prize for Research in Pick's, Alzheimer's, and Related Diseases for the discovery of the C9orf72 repeat expansions, and the 2013 Sheila Essay Award for his contributions to our understanding of ALS. He also received the NIH Director’s Award in 2012.

Dr. Traynor has published more than 200 papers in the field of neurology and genetics,[5] and he is an inventor on three patents.

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) from Harvard-MIT HST in 2004. He completed his neurology residency and fellowship at Brigham and Women’s Hospital and Massachusetts General Hospital.

Awards, prizes, and honors

Notable professional service

References
  1. "Neuromuscular Diseases Research Section". National Institute on Aging. Retrieved 2019-03-26.
  2. Renton, Alan E.; Majounie, Elisa; Waite, Adrian; Simón-Sánchez, Javier; Rollinson, Sara; Gibbs, J. Raphael; Schymick, Jennifer C.; Laaksovirta, Hannu; van Swieten, John C.; Myllykangas, Liisa; Kalimo, Hannu; Paetau, Anders; Abramzon, Yevgeniya; Remes, Anne M.; Kaganovich, Alice; Scholz, Sonja W.; Duckworth, Jamie; Ding, Jinhui; Harmer, Daniel W.; Hernandez, Dena G.; Johnson, Janel O.; Mok, Kin; Ryten, Mina; Trabzuni, Danyah; Guerreiro, Rita J.; Orrell, Richard W.; Neal, James; Murray, Alex; Pearson, Justin; Jansen, Iris E.; Sondervan, David; Seelaar, Harro; Blake, Derek; Young, Kate; Halliwell, Nicola; Callister, Janis Bennion; Toulson, Greg; Richardson, Anna; Gerhard, Alex; Snowden, Julie; Mann, David; Neary, David; Nalls, Michael A.; Peuralinna, Terhi; Jansson, Lilja; Isoviita, Veli-Matti; Kaivorinne, Anna-Lotta; Hölttä-Vuori, Maarit; Ikonen, Elina; Sulkava, Raimo; Benatar, Michael; Wuu, Joanne; Chiò, Adriano; Restagno, Gabriella; Borghero, Giuseppe; Sabatelli, Mario; Heckerman, David; Rogaeva, Ekaterina; Zinman, Lorne; Rothstein, Jeffrey D.; Sendtner, Michael; Drepper, Carsten; Eichler, Evan E.; Alkan, Can; Abdullaev, Ziedulla; Pack, Svetlana D.; Dutra, Amalia; Pak, Evgenia; Hardy, John; Singleton, Andrew; Williams, Nigel M.; Heutink, Peter; Pickering-Brown, Stuart; Morris, Huw R.; Tienari, Pentti J.; Traynor, Bryan J. (2011). "A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD". Neuron. 72 (2): 257–268. doi:10.1016/j.neuron.2011.09.010. ISSN 0896-6273. PMC 3200438. PMID 21944779.
  3. Johnson, Janel O.; Mandrioli, Jessica; Benatar, Michael; Abramzon, Yevgeniya; Van Deerlin, Vivianna M.; Trojanowski, John Q.; Gibbs, J. Raphael; Brunetti, Maura; Gronka, Susan; Wuu, Joanne; Ding, Jinhui; McCluskey, Leo; Martinez-Lage, Maria; Falcone, Dana; Hernandez, Dena G.; Arepalli, Sampath; Chong, Sean; Schymick, Jennifer C.; Rothstein, Jeffrey; Landi, Francesco; Wang, Yong-Dong; Calvo, Andrea; Mora, Gabriele; Sabatelli, Mario; Monsurrò, Maria Rosaria; Battistini, Stefania; Salvi, Fabrizio; Spataro, Rossella; Sola, Patrizia; Borghero, Giuseppe; Galassi, Giuliana; Scholz, Sonja W.; Taylor, J. Paul; Restagno, Gabriella; Chiò, Adriano; Traynor, Bryan J. (2010). "Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS". Neuron. 68 (5): 857–864. doi:10.1016/j.neuron.2010.11.036. ISSN 0896-6273. PMC 3032425. PMID 21145000.
  4. Johnson, Janel O; Pioro, Erik P; Boehringer, Ashley; Chia, Ruth; Feit, Howard; Renton, Alan E; Pliner, Hannah A; Abramzon, Yevgeniya; Marangi, Giuseppe; Winborn, Brett J; Gibbs, J Raphael; Nalls, Michael A; Morgan, Sarah; Shoai, Maryam; Hardy, John; Pittman, Alan; Orrell, Richard W; Malaspina, Andrea; Sidle, Katie C; Fratta, Pietro; Harms, Matthew B; Baloh, Robert H; Pestronk, Alan; Weihl, Conrad C; Rogaeva, Ekaterina; Zinman, Lorne; Drory, Vivian E; Borghero, Giuseppe; Mora, Gabriele; Calvo, Andrea; Rothstein, Jeffrey D; Drepper, Carsten; Sendtner, Michael; Singleton, Andrew B; Taylor, J Paul; Cookson, Mark R; Restagno, Gabriella; Sabatelli, Mario; Bowser, Robert; Chiò, Adriano; Traynor, Bryan J (2014). "Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis". Nature Neuroscience. 17 (5): 664–666. doi:10.1038/nn.3688. ISSN 1097-6256. PMC 4000579. PMID 24686783.
  5. "Bryan Traynor - Google Scholar". scholar.google.com. Retrieved 2020-08-11.
  6. "Derek Denny-Brown Neurological Scholar Award | American Neurological Association (ANA)". myana.org. Retrieved 2019-03-26.
  7. "Wings Over Wall Street - Awards". wingsoverwallstreet.org. Retrieved 2019-03-26.
  8. "ALS Association".
  9. "American Academy of Neurology".
  10. "Amyotrophic Lateral Sclerosis Research Program, Programmatic Panels; Congressionally Directed Medical Research Programs". cdmrp.army.mil. Retrieved 2019-03-26.
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