Quentin Vincent
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Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants
A Belkadi, A Bolze, Y Itan, A Cobat, QB Vincent, A Antipenko, L Shang, ...
Proceedings of the National Academy of Sciences 112 (17), 5473-5478, 2015
Deep dermatophytosis and inherited CARD9 deficiency
F Lanternier, S Pathan, QB Vincent, L Liu, S Cypowyj, C Prando, ...
New England Journal of Medicine 369 (18), 1704-1714, 2013
Clinical epidemiology of laboratory-confirmed Buruli ulcer in Benin: a cohort study
QB Vincent, MF Ardant, A Adeye, A Goundote, JP Saint-André, J Cottin, ...
The Lancet Global Health 2 (7), e422-e430, 2014
Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds
I Sologuren, S Boisson-Dupuis, J Pestano, QB Vincent, ...
Human molecular genetics 20 (8), 1509-1523, 2011
Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients
M Ouederni, QB Vincent, P Frange, F Touzot, S Scerra, M Bejaoui, ...
Blood, The Journal of the American Society of Hematology 118 (19), 5108-5118, 2011
Dual T cell– and B cell–intrinsic deficiency in humans with biallelic RLTPR mutations
Y Wang, CS Ma, Y Ling, A Bousfiha, Y Camcioglu, S Jacquot, K Payne, ...
Journal of Experimental Medicine 213 (11), 2413-2435, 2016
Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage
A Belkadi, V Pedergnana, A Cobat, Y Itan, QB Vincent, A Abhyankar, ...
Proceedings of the National Academy of Sciences 113 (24), 6713-6718, 2016
Assessment of derelict soil quality: Abiotic, biotic and functional approaches
Q Vincent, A Auclerc, T Beguiristain, C Leyval
Science of the Total Environment 613, 990-1002, 2018
Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation
M Moncada-Vélez, R Martinez-Barricarte, D Bogunovic, XF Kong, ...
Blood, The Journal of the American Society of Hematology 122 (14), 2390-2401, 2013
DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis
C Sarnowski, C Laprise, G Malerba, MF Moffatt, MH Dizier, A Morin, ...
Journal of Allergy and Clinical Immunology 138 (3), 748-753, 2016
Effect and localization of phenanthrene in maize roots
J Dupuy, P Leglize, Q Vincent, I Zelko, C Mustin, S Ouvrard, T Sterckeman
Chemosphere 149, 130-136, 2016
Findings in Patients From Benin With Osteomyelitis and Polymerase Chain Reaction–Confirmed Mycobacterium ulcerans Infection
V Pommelet, QB Vincent, MF Ardant, A Adeye, A Tanase, L Tondeur, ...
Clinical Infectious Diseases 59 (9), 1256-1264, 2014
HIV infection and Buruli ulcer in Africa
QB Vincent, MF Ardant, L Marsollier, A Chauty, A Alcaïs
The Lancet infectious diseases 14 (9), 796-797, 2014
Functional structure and composition of Collembola and soil macrofauna communities depend on abiotic parameters in derelict soils
Q Vincent, C Leyval, T Beguiristain, A Auclerc
Applied Soil Ecology 130, 259-270, 2018
Clinical Features of Spontaneous Partial Healing During Mycobacterium ulcerans Infection
E Marion, A Chauty, M Kempf, Y Le Corre, Y Delneste, A Croue, ...
Open forum infectious diseases 3 (1), ofw013, 2016
Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway
J Manry, QB Vincent, C Johnson, M Chrabieh, L Lorenzo, I Theodorou, ...
Communications Biology 3 (1), 177, 2020
Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations
J Quistrebert, M Orlova, G Kerner, LT Ton, NT Luong, NT Danh, ...
PLoS Genetics 17 (3), e1009392, 2021
Clinical epidemiology of laboratory-confirmed Buruli ulcer in Benin: a cohort study. Lancet Glob Health 2: e422–e430
QB Vincent, MF Ardant, A Adeye, A Goundote, JP Saint-Andre, J Cottin, ...
Quantifying genomic imprinting in the presence of linkage
Q Vincent, A Alcaïs, A Alter, E Schurr, L Abel
Biometrics 62 (4), 1071-1080, 2006
Microdeletion on chromosome 8p23. 1 in a familial form of severe Buruli ulcer
QB Vincent, A Belkadi, C Fayard, E Marion, A Adeye, MF Ardant, ...
PLoS neglected tropical diseases 12 (4), e0006429, 2018
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