Vincent Picher‐Martel

546 total citations
19 papers, 364 citations indexed

About

Vincent Picher‐Martel is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, Vincent Picher‐Martel has authored 19 papers receiving a total of 364 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Neurology, 8 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Vincent Picher‐Martel's work include Amyotrophic Lateral Sclerosis Research (11 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Vincent Picher‐Martel is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (11 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Vincent Picher‐Martel collaborates with scholars based in Canada, United States and Japan. Vincent Picher‐Martel's co-authors include Jean‐Pierre Julien, Nicolas Dupré, Peter V. Gould, Paul N. Valdmanis, Philippe Codron, Gen Sobue, Kallol Dutta, Daniel J. Phaneuf, Christine Bareil and Nicolas Chrestian and has published in prestigious journals such as Neurology, International Journal of Molecular Sciences and Glia.

In The Last Decade

Vincent Picher‐Martel

18 papers receiving 362 citations

Peers

Countries citing papers authored by Vincent Picher‐Martel

Since Specialization

Citations

This map shows the geographic impact of Vincent Picher‐Martel's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Vincent Picher‐Martel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vincent Picher‐Martel more than expected).

Fields of papers citing papers by Vincent Picher‐Martel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vincent Picher‐Martel. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Vincent Picher‐Martel. The network helps show where Vincent Picher‐Martel may publish in the future.

Co-authorship network of co-authors of Vincent Picher‐Martel

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent Picher‐Martel. A scholar is included among the top collaborators of Vincent Picher‐Martel based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Vincent Picher‐Martel. Vincent Picher‐Martel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Chronically activated microglia in ALS gradually lose their immune functions and develop unconventional proteome 2024 ·Glia ·(unknown), Louis‐Charles Béland, (unknown), Vincent Picher‐Martel, Nicolas Dupré, Luis Barbeito, Jasna Križ	4
2	Clinical Characteristics of Charcot-Marie-Tooth Disease Type 4J 2024 ·Neurology ·Reza Sadjadi, Vincent Picher‐Martel, Jasper M. Morrow, Daniel R. Thedens, (unknown), Brett A. McCray, Davide Pareyson, D. Herrmann, Mary M. Reilly, Jun Li, Diana Castro, Michael E. Shy	2
3	Inhibition of NF-κB with an Analog of Withaferin-A Restores TDP-43 Homeostasis and Proteome Profiles in a Model of Sporadic ALS 2024 ·Biomedicines ·(unknown), Daniel J. Phaneuf, (unknown), Vincent Picher‐Martel, Nicolas Dupré, Jasna Križ, Jean‐Pierre Julien	1
4	TARDBP Mutations in Facial-Onset Sensory and Motor Neuronopathy 2024 ·Neurology Genetics ·Vincent Picher‐Martel, Suma Babu, Anthony A. Amato	0
5	Distinct Plasma Immune Profile in ALS Implicates sTNFR-II in pAMPK/Leptin Homeostasis 2023 ·International Journal of Molecular Sciences ·Vincent Picher‐Martel, (unknown), (unknown), Pierre Cordeau, Hannah Kaneb, Jean‐Pierre Julien, Angela Genge, Nicolas Dupré, Jasna Križ	3
6	Parent-of-Origin Effect on the Age at Symptom Onset in Myotonic Dystrophy Type 2 2023 ·Neurology Genetics ·Paloma González-Pérez, (unknown), Vincent Picher‐Martel, (unknown), William S. David, Anthony A. Amato	2
7	Case Report: Acute Necrotizing Encephalopathy Following COVID-19 Vaccine 2022 ·Frontiers in Neurology ·(unknown), Vincent Picher‐Martel, (unknown), Gaston De Serres, Nicolas Dupré, (unknown)	9
8	Targeting TDP-43 Pathology Alleviates Cognitive and Motor Deficits Caused by Chronic Cerebral Hypoperfusion 2021 ·Neurotherapeutics ·Sai Sampath Thammisetty, (unknown), Vincent Picher‐Martel, Yuan Cheng Weng, Frédéric Calon, Stéphan Saïkali, Jean‐Pierre Julien, Jasna Križ	12
9	Changes in Leptin, CCL16 and sTNF-RII as a Distinctive Plasma Immune Profile in Patients with Fast Progressing ALS (1276) 2021 ·Neurology ·Vincent Picher‐Martel, (unknown), Pierre Cordeau, Hannah Kaneb, Jean‐Pierre Julien, Angela Genge, Nicolas Dupré, Jasna Križ	2
10	Transmission of ALS pathogenesis by the cerebrospinal fluid 2020 ·Acta Neuropathologica Communications ·(unknown), (unknown), Geneviève Soucy, Christine Bareil, (unknown), Vincent Picher‐Martel, Nicolas Dupré, Jasna Križ, Jean‐Pierre Julien	30
11	Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report 2020 ·BMC Neurology ·Vincent Picher‐Martel, Yvan Labrie, Serge Rivest, Baiba Lāce, Nicolas Chrestian	6
12	SMALED2 with BICD2 gene mutations: Report of two cases and portrayal of a classical phenotype 2020 ·Neuromuscular Disorders ·Vincent Picher‐Martel, (unknown), Denis Brunet, Annie Dionne	2
13	The Occurrence of FUS Mutations in Pediatric Amyotrophic Lateral Sclerosis: A Case Report and Review of the Literature 2020 ·Journal of Child Neurology ·Vincent Picher‐Martel, (unknown), Nicolas Dupré, Nicolas Chrestian	21
14	Key role of UBQLN2 in pathogenesis of amyotrophic lateral sclerosis and frontotemporal dementia 2019 ·Acta Neuropathologica Communications ·(unknown), Vincent Picher‐Martel, Philippe Codron, Jean‐Pierre Julien	79
15	Neuronal Expression of UBQLN2P497H Exacerbates TDP-43 Pathology in TDP-43G348C Mice through Interaction with Ubiquitin 2018 ·Molecular Neurobiology ·Vincent Picher‐Martel, (unknown), Christine Bareil, Jean‐Pierre Julien	21
16	Current and Promising Therapies in Autosomal Recessive Ataxias 2018 ·CNS & Neurological Disorders - Drug Targets ·Vincent Picher‐Martel, Nicolas Dupré	9
17	Low expression of mutant Ubiquilin-2 exacerbates ALS/FTD features in a TDP-43 mouse model (P4.431) 2018 ·Neurology ·Vincent Picher‐Martel, Jean‐Pierre Julien	1
18	From animal models to human disease: a genetic approach for personalized medicine in ALS 2016 ·Acta Neuropathologica Communications ·Vincent Picher‐Martel, Paul N. Valdmanis, Peter V. Gould, Jean‐Pierre Julien, Nicolas Dupré	105
19	Ubiquilin-2 drives NF-κB activity and cytosolic TDP-43 aggregation in neuronal cells 2015 ·Molecular Brain ·Vincent Picher‐Martel, Kallol Dutta, Daniel J. Phaneuf, Gen Sobue, Jean‐Pierre Julien	55

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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