Vincent Meyer
Overview
Explore the profile of Vincent Meyer including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
46
Citations
1208
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Muret K, Le Goff V, Dandine-Roulland C, Hotz C, Jean-Louis F, Boisson B, et al.
Int J Mol Sci
. 2024 Oct;
25(19).
PMID: 39408704
Hidradenitis suppurativa (HS) is a chronic skin disease characterized by painful, recurrent abscesses, nodules, and scarring, primarily in skin folds. The exact causes of HS are multifactorial, involving genetic, hormonal,...
2.
Alves I, Giemza J, Blum M, Bernhardsson C, Chatel S, Karakachoff M, et al.
Nat Commun
. 2024 Aug;
15(1):6710.
PMID: 39112481
The demographical history of France remains largely understudied despite its central role toward understanding modern population structure across Western Europe. Here, by exploring publicly available Europe-wide genotype datasets together with...
3.
Andre M, Brucato N, Hudjasov G, Pankratov V, Yermakovich D, Montinaro F, et al.
Nat Commun
. 2024 Apr;
15(1):3352.
PMID: 38688933
Highlanders and lowlanders of Papua New Guinea have faced distinct environmental stress, such as hypoxia and environment-specific pathogen exposure, respectively. In this study, we explored the top genomics regions and...
4.
Riquin K, Isidor B, Mercier S, Nizon M, Colin E, Bonneau D, et al.
J Med Genet
. 2023 Jul;
61(1):47-56.
PMID: 37495270
Background: Molecular diagnosis of neurodevelopmental disorders (NDDs) is mainly based on exome sequencing (ES), with a diagnostic yield of 31% for isolated and 53% for syndromic NDD. As sequencing costs...
5.
Lecoquierre F, Quenez O, Fourneaux S, Coutant S, Vezain M, Rolain M, et al.
Hum Genet
. 2023 Apr;
142(6):773-783.
PMID: 37076692
Exome sequencing (ES) has become the method of choice for diagnosing rare diseases, while the availability of short-read genome sequencing (SR-GS) in a medical setting is increasing. In addition, new...
6.
Vallier M, Segurens B, Larsonneur E, Meyer V, Ferreira S, Caloustian C, et al.
RMD Open
. 2023 Mar;
9(1).
PMID: 36963782
Objective: To assess whether gut microbiota composition is associated with patient characteristics and may have predictive value on the response to TNF inhibitor (TNFi) treatment in axial spondyloarthritis (AxSpA). Methods:...
7.
Mangiante L, Alcala N, Sexton-Oates A, Di Genova A, Gonzalez-Perez A, Khandekar A, et al.
Nat Genet
. 2023 Mar;
55(4):607-618.
PMID: 36928603
Malignant pleural mesothelioma (MPM) is an aggressive cancer with rising incidence and challenging clinical management. Through a large series of whole-genome sequencing data, integrated with transcriptomic and epigenomic data using...
8.
Ballinger M, Pattnaik S, Mundra P, Zaheed M, Rath E, Priestley P, et al.
Science
. 2023 Jan;
379(6629):253-260.
PMID: 36656928
Cancer genetics has to date focused on epithelial malignancies, identifying multiple histotype-specific pathways underlying cancer susceptibility. Sarcomas are rare malignancies predominantly derived from embryonic mesoderm. To identify pathways specific to...
9.
Gerber Z, Daviaud C, Delafoy D, Sandron F, Alidjinou E, Mercier J, et al.
Sci Rep
. 2022 Jul;
12(1):12561.
PMID: 35869099
The COVID-19 pandemic caused by the new Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) continues to threaten public health and burden healthcare systems worldwide. Whole SARS-CoV-2 genome sequencing has become...
10.
Gabriel A, Atkins J, Penha R, Smith-Byrne K, Gaborieau V, Voegele C, et al.
J Natl Cancer Inst
. 2022 May;
114(8):1159-1166.
PMID: 35511172
Background: Germline genetic variation contributes to lung cancer (LC) susceptibility. Previous genome-wide association studies (GWAS) have implicated susceptibility loci involved in smoking behaviors and DNA repair genes, but further work...