Bryan J. Traynor, M.D., Ph.D.

Senior Investigator

Laboratory of Neurogenetics

NIA

Building 35, Room 1A-213
35 Convent Drive
Bethesda, MD 20814

301-451-7606

traynorb@mail.nih.gov

Research Topics

Dr. Traynor is a neurologist and a Senior Investigator at the National Institute on Aging whose research focuses on the genetic, molecular, and biomarker basis of amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), and related neurodegenerative diseases. His laboratory uses large-scale genomics, proteomics, clinical cohorts, and functional studies to understand disease mechanisms, improve diagnosis, and identify therapeutic targets for ALS and FTD.

Dr. Traynor's laboratory has helped define the modern genetic architecture of ALS and FTD. He received the 2026 Breakthrough Prize in Life Sciences, together with Rosa Rademakers, for discovering the C9orf72 repeat expansion as the most common genetic cause of ALS and frontotemporal dementia. This work helped establish ALS and FTD as overlapping disorders along a shared neurodegenerative spectrum. He is also the co-recipient of the 2013 Sheila Essey Award and the 2016 Potamkin Prize for his contributions to the understanding of neurodegeneration.

Other notable achievements of his laboratory include the identification of mutations in VCP, MATR3, CHCHD10, KIF5A, HTT, and SPTLC1 in familial ALS and related neurodegenerative syndromes. These discoveries have provided new insights into motor neuron degeneration, RNA biology, protein homeostasis, axonal transport, lipid metabolism, and the genetic overlap between ALS, FTD, and other neurodegenerative diseases.

Building on this genetic work, Dr. Traynor's laboratory has expanded into biomarker discovery. In a 2025 Nature Medicine study using the Olink plasma proteomics platform, his team identified a plasma protein signature that distinguishes ALS from controls and other neurological conditions with high accuracy. The study also suggested that ALS-associated molecular changes may begin years before symptom onset, supporting the development of blood-based biomarkers for diagnosis, prognosis, and presymptomatic clinical trials.

Dr. Traynor has authored more than 250 peer-reviewed publications in neurology and neurogenetics and is an inventor on three issued patents. He is co-chair of the NIH Gene Therapy Task Force and an associate editor of Brain.

Biography

Dr. Traynor received his medical degree (MB, BCh, BAO), MD, and PhD from University College Dublin, and a Master of Medical Sciences degree (MMSc) from the Harvard-MIT Division of Health Sciences and Technology. He completed his neurology residency and neuromuscular fellowship training at Massachusetts General Hospital and Brigham and Women's Hospital in Boston.

Selected Publications

  1. Renton AE, Majounie E, Waite A, Simón-Sánchez J, Rollinson S, Gibbs JR, Schymick JC, Laaksovirta H, van Swieten JC, Myllykangas L, Kalimo H, Paetau A, Abramzon Y, Remes AM, Kaganovich A, Scholz SW, Duckworth J, Ding J, Harmer DW, Hernandez DG, Johnson JO, Mok K, Ryten M, Trabzuni D, Guerreiro RJ, Orrell RW, Neal J, Murray A, Pearson J, Jansen IE, Sondervan D, Seelaar H, Blake D, Young K, Halliwell N, Callister JB, Toulson G, Richardson A, Gerhard A, Snowden J, Mann D, Neary D, Nalls MA, Peuralinna T, Jansson L, Isoviita VM, Kaivorinne AL, Hölttä-Vuori M, Ikonen E, Sulkava R, Benatar M, Wuu J, Chiò A, Restagno G, Borghero G, Sabatelli M, ITALSGEN Consortium, Heckerman D, Rogaeva E, Zinman L, Rothstein JD, Sendtner M, Drepper C, Eichler EE, Alkan C, Abdullaev Z, Pack SD, Dutra A, Pak E, Hardy J, Singleton A, Williams NM, Heutink P, Pickering-Brown S, Morris HR, Tienari PJ, Traynor BJ. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron. 2011;72(2):257-68.
  2. Dewan R, Chia R, Ding J, Hickman RA, Stein TD, Abramzon Y, Ahmed S, Sabir MS, Portley MK, Tucci A, Ibáñez K, Shankaracharya FNU, Keagle P, Rossi G, Caroppo P, Tagliavini F, Waldo ML, Johansson PM, Nilsson CF, American Genome Center (TAGC), FALS Sequencing Consortium, Genomics England Research Consortium, International ALS/FTD Genomics Consortium (iAFGC), International FTD Genetics Consortium (IFGC), International LBD Genomics Consortium (iLBDGC), NYGC ALS Consortium, PROSPECT Consortium, Rowe JB, Benussi L, Binetti G, Ghidoni R, Jabbari E, Viollet C, Glass JD, Singleton AB, Silani V, Ross OA, Ryten M, Torkamani A, Tanaka T, Ferrucci L, Resnick SM, Pickering-Brown S, Brady CB, Kowal N, Hardy JA, Van Deerlin V, Vonsattel JP, Harms MB, Morris HR, Ferrari R, Landers JE, Chiò A, Gibbs JR, Dalgard CL, Scholz SW, Traynor BJ. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis. Neuron. 2021;109(3):448-460.e4.
  3. Chia R, Sabir MS, Bandres-Ciga S, Saez-Atienzar S, Reynolds RH, Gustavsson E, Walton RL, Ahmed S, Viollet C, Ding J, Makarious MB, Diez-Fairen M, Portley MK, Shah Z, Abramzon Y, Hernandez DG, Blauwendraat C, Stone DJ, Eicher J, Parkkinen L, Ansorge O, Clark L, Honig LS, Marder K, Lemstra A, St George-Hyslop P, Londos E, Morgan K, Lashley T, Warner TT, Jaunmuktane Z, Galasko D, Santana I, Tienari PJ, Myllykangas L, Oinas M, Cairns NJ, Morris JC, Halliday GM, Van Deerlin VM, Trojanowski JQ, Grassano M, Calvo A, Mora G, Canosa A, Floris G, Bohannan RC, Brett F, Gan-Or Z, Geiger JT, Moore A, May P, Krüger R, Goldstein DS, Lopez G, Tayebi N, Sidransky E, American Genome Center, Norcliffe-Kaufmann L, Palma JA, Kaufmann H, Shakkottai VG, Perkins M, Newell KL, Gasser T, Schulte C, Landi F, Salvi E, Cusi D, Masliah E, Kim RC, Caraway CA, Monuki ES, Brunetti M, Dawson TM, Rosenthal LS, Albert MS, Pletnikova O, Troncoso JC, Flanagan ME, Mao Q, Bigio EH, Rodríguez-Rodríguez E, Infante J, Lage C, González-Aramburu I, Sanchez-Juan P, Ghetti B, Keith J, Black SE, Masellis M, Rogaeva E, Duyckaerts C, Brice A, Lesage S, Xiromerisiou G, Barrett MJ, Tilley BS, Gentleman S, Logroscino G, Serrano GE, Beach TG, McKeith IG, Thomas AJ, Attems J, Morris CM, Palmer L, Love S, Troakes C, Al-Sarraj S, Hodges AK, Aarsland D, Klein G, Kaiser SM, Woltjer R, Pastor P, Bekris LM, Leverenz JB, Besser LM, Kuzma A, Renton AE, Goate A, Bennett DA, Scherzer CR, Morris HR, Ferrari R, Albani D, Pickering-Brown S, Faber K, Kukull WA, Morenas-Rodriguez E, Lleó A, Fortea J, Alcolea D, Clarimon J, Nalls MA, Ferrucci L, Resnick SM, Tanaka T, Foroud TM, Graff-Radford NR, Wszolek ZK, Ferman T, Boeve BF, Hardy JA, Topol EJ, Torkamani A, Singleton AB, Ryten M, Dickson DW, Chiò A, Ross OA, Gibbs JR, Dalgard CL, Traynor BJ, Scholz SW. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Nat Genet. 2021;53(3):294-303.
  4. Saez-Atienzar S, Souza CDS, Chia R, Beal SN, Lorenzini I, Huang R, Levy J, Burciu C, Ding J, Gibbs JR, Jones A, Dewan R, Pensato V, Peverelli S, Corrado L, van Vugt JJFA, van Rheenen W, Tunca C, Bayraktar E, Xia M, International ALS Genomics Consortium, ITALSGEN Consortium, SLAGEN Consortium, Project MinE ALS Sequencing Consortium, Iacoangeli A, Shatunov A, Tiloca C, Ticozzi N, Verde F, Mazzini L, Kenna K, Al Khleifat A, Opie-Martin S, Raggi F, Filosto M, Piccinelli SC, Padovani A, Gagliardi S, Inghilleri M, Ferlini A, Vasta R, Calvo A, Moglia C, Canosa A, Manera U, Grassano M, Mandrioli J, Mora G, Lunetta C, Tanel R, Trojsi F, Cardinali P, Gallone S, Brunetti M, Galimberti D, Serpente M, Fenoglio C, Scarpini E, Comi GP, Corti S, Del Bo R, Ceroni M, Pinter GL, Taroni F, Bella ED, Bersano E, Curtis CJ, Lee SH, Chung R, Patel H, Morrison KE, Cooper-Knock J, Shaw PJ, Breen G, Dobson RJB, Dalgard CL, American Genome Center, Scholz SW, Al-Chalabi A, van den Berg LH, McLaughlin R, Hardiman O, Cereda C, Sorarù G, D'Alfonso S, Chandran S, Pal S, Ratti A, Gellera C, Johnson K, Doucet-O'Hare T, Pasternack N, Wang T, Nath A, Siciliano G, Silani V, Başak AN, Veldink JH, Camu W, Glass JD, Landers JE, Chiò A, Sattler R, Shaw CE, Ferraiuolo L, Fogh I, Traynor BJ. Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data. Cell Genom. 2024;4(11):100679.
  5. Chia R, Moaddel R, Kwan JY, Rasheed M, Ruffo P, Landeck N, Reho P, Vasta R, Calvo A, Moglia C, Canosa A, Manera U, Snyder A, Saez-Atienzar S, Grassano M, Brunetti M, Casale F, Ray A, Arvind K, Comertpay B, Zhu M, Gibbs JR, American Genome Center, Alba C, Dawson TM, Rosenthal LS, Hall AJ, Pantelyat AY, Narendra DP, Ehrlich DJ, Walker KA, Kosa P, Bielekova B, Egan JM, Candia J, Tanaka T, Ferrucci L, Dalgard CL, Scholz SW, Chiò A, Traynor BJ. A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosis. Nat Med. 2025;31(10):3440-3450.

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This page was last updated on Tuesday, August 11, 2026