Harvard Catalyst Profiles

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Vincent Picher-Martel, Ph.D., M.D.


Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Bensaidane MR, Picher-Martel V, Émond F, De Serres G, Dupré N, Beauchemin P. Case Report: Acute Necrotizing Encephalopathy Following COVID-19 Vaccine. Front Neurol. 2022; 13:872734. PMID: 35572945; PMCID: PMC9099242.
    Citations: 2     
  2. Picher-Martel V, Magnussen C, Blais M, Bubela T, Das S, Dionne A, Evans AC, Genge A, Greiner R, Iturria-Medina Y, Johnston W, Jones K, Kaneb H, Karamchandani J, Moradipoor S, Robertson J, Rogaeva E, Taylor DM, Vande Velde C, Yunusova Y, Zinman L, Kalra S, Dupré N. CAPTURE ALS: the comprehensive analysis platform to understand, remedy and eliminate ALS. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Feb 23; 1-7. PMID: 35195049.
    Citations:    Fields:    
  3. Thammisetty SS, Renaud L, Picher-Martel V, Weng YC, Calon F, Saikali S, Julien JP, Kriz J. Targeting TDP-43 Pathology Alleviates Cognitive and Motor Deficits Caused by Chronic Cerebral Hypoperfusion. Neurotherapeutics. 2021 04; 18(2):1095-1112. PMID: 33786804; PMCID: PMC8423945.
    Citations: 4     Fields:    Translation:HumansAnimals
  4. Picher-Martel V, Morin C, Brunet D, Dionne A. SMALED2 with BICD2 gene mutations: Report of two cases and portrayal of a classical phenotype. Neuromuscul Disord. 2020 08; 30(8):669-673. PMID: 32709491.
    Citations:    Fields:    Translation:Humans
  5. Mishra PS, Boutej H, Soucy G, Bareil C, Kumar S, Picher-Martel V, Dupré N, Kriz J, Julien JP. Transmission of ALS pathogenesis by the cerebrospinal fluid. Acta Neuropathol Commun. 2020 05 07; 8(1):65. PMID: 32381112; PMCID: PMC7206749.
    Citations: 13     Fields:    Translation:HumansAnimals
  6. Picher-Martel V, Brunet F, Dupré N, Chrestian N. The Occurrence of FUS Mutations in Pediatric Amyotrophic Lateral Sclerosis: A Case Report and Review of the Literature. J Child Neurol. 2020 07; 35(8):556-562. PMID: 32281455.
    Citations: 7     Fields:    Translation:Humans
  7. Picher-Martel V, Labrie Y, Rivest S, Lace B, Chrestian N. Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report. BMC Neurol. 2020 Feb 15; 20(1):58. PMID: 32061250; PMCID: PMC7023720.
    Citations: 5     Fields:    Translation:Humans
  8. Renaud L, Picher-Martel V, Codron P, Julien JP. Key role of UBQLN2 in pathogenesis of amyotrophic lateral sclerosis and frontotemporal dementia. Acta Neuropathol Commun. 2019 07 18; 7(1):103. PMID: 31319884; PMCID: PMC6889556.
    Citations: 36     Fields:    Translation:HumansAnimalsCells
  9. Picher-Martel V, Renaud L, Bareil C, Julien JP. Neuronal Expression of UBQLN2P497H Exacerbates TDP-43 Pathology in TDP-43G348C Mice through Interaction with Ubiquitin. Mol Neurobiol. 2019 Jul; 56(7):4680-4696. PMID: 30377984; PMCID: PMC6647471.
    Citations: 10     Fields:    Translation:HumansAnimalsCells
  10. Picher-Martel V, Dupre N. Current and Promising Therapies in Autosomal Recessive Ataxias. CNS Neurol Disord Drug Targets. 2018; 17(3):161-171. PMID: 29676235.
    Citations: 3     Fields:    Translation:HumansAnimals
  11. Picher-Martel V, Valdmanis PN, Gould PV, Julien JP, Dupré N. From animal models to human disease: a genetic approach for personalized medicine in ALS. Acta Neuropathol Commun. 2016 07 11; 4(1):70. PMID: 27400686; PMCID: PMC4940869.
    Citations: 53     Fields:    Translation:HumansAnimals
  12. Picher-Martel V, Dutta K, Phaneuf D, Sobue G, Julien JP. Ubiquilin-2 drives NF-?B activity and cytosolic TDP-43 aggregation in neuronal cells. Mol Brain. 2015 Oct 31; 8(1):71. PMID: 26521126; PMCID: PMC4628361.
    Citations: 35     Fields:    Translation:HumansAnimalsCells
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.