Vincent Meyer
Overview
Explore the profile of Vincent Meyer including associated specialties, affiliations and a list of published articles.
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46
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1208
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Recent Articles
11.
Nicolas G, Sevigny M, Lecoquierre F, Marguet F, Deschenes A, Del Pelaez M, et al.
Acta Neuropathol Commun
. 2022 Feb;
10(1):20.
PMID: 35151370
Frontotemporal dementia (FTD) is a heterogeneous clinical disorder characterized by progressive abnormalities in behavior, executive functions, personality, language and/or motricity. A neuropathological subtype of FTD, frontotemporal lobar degeneration (FTLD)-FET, is...
12.
Charon C, Allodji R, Meyer V, Deleuze J
Sci Rep
. 2021 Sep;
11(1):19225.
PMID: 34552172
No abstract available.
13.
Brucato N, Andre M, Tsang R, Saag L, Kariwiga J, Sesuki K, et al.
Mol Biol Evol
. 2021 Aug;
38(11):5107-5121.
PMID: 34383935
The settlement of Sahul, the lost continent of Oceania, remains one of the most ancient and debated human migrations. Modern New Guineans inherited a unique genetic diversity tracing back 50,000 ...
14.
Jenstad L, Singh G, Boretzki M, DeLongis A, Fichtl E, Ho R, et al.
Ear Hear
. 2021 May;
42(6):1770-1781.
PMID: 34010249
Purpose: As hearing rehabilitation research evolves to include both retrospective and momentary assessment outcome measures, it is important to understand how in-the-moment contextual factors influence subjective ratings. We aimed to...
15.
Brohard-Julien S, Frouin V, Meyer V, Chalabi S, Deleuze J, Le Floch E, et al.
BMC Ecol Evol
. 2021 Apr;
21(1):59.
PMID: 33882820
Background: The duplication of genes is one of the main genetic mechanisms that led to the gain in complexity of biological tissue. Although the implication of duplicated gene expression in...
16.
Charon C, Allodji R, Meyer V, Deleuze J
Sci Rep
. 2021 Mar;
11(1):6214.
PMID: 33737531
Quality control (QC) methods for genome-wide association studies and fine mapping are commonly used for imputation, however they result in loss of many single nucleotide polymorphisms (SNPs). To investigate the...
17.
Gargaun E, Falcone S, Sole G, Durigneux J, Urtizberea A, Cuisset J, et al.
Biomedicines
. 2021 Mar;
9(2).
PMID: 33672764
In skeletal muscle, long noncoding RNAs (lncRNAs) are involved in dystrophin protein stabilization but also in the regulation of myocytes proliferation and differentiation. Hence, they could represent promising therapeutic targets...
18.
Auzanneau C, Bacq D, Bellera C, Blons H, Boland A, Boucheix M, et al.
ESMO Open
. 2020 Jul;
5(4).
PMID: 32713836
Background: Whole exome sequencing and RNA sequencing (WES/RNASeq) should now be implemented in the clinical practice in order to increase access to optimal care for cancer patients. Providing results to...
19.
Uguen K, Jubin C, Duffourd Y, Bardel C, Malan V, Dupont J, et al.
Mol Genet Genomic Med
. 2020 Jan;
8(3):e1114.
PMID: 31985172
Background: Structural variants (SVs) include copy number variants (CNVs) and apparently balanced chromosomal rearrangements (ABCRs). Genome sequencing (GS) enables SV detection at base-pair resolution, but the use of short-read sequencing...
20.
Florian R, Kraft F, Leitao E, Kaya S, Klebe S, Magnin E, et al.
Nat Commun
. 2019 Oct;
10(1):4919.
PMID: 31664039
Familial Adult Myoclonic Epilepsy (FAME) is a genetically heterogeneous disorder characterized by cortical tremor and seizures. Intronic TTTTA/TTTCA repeat expansions in SAMD12 (FAME1) are the main cause of FAME in...