受强制性开放获取政策约束的文章 - Quentin Vincent了解详情
可在其他位置公开访问的文章：17 篇
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
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, National …
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
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
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
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute
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
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
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
强制性开放获取政策： National Institute of Health and Medical Research, France
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
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
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
强制性开放获取政策： Canadian Institutes of Health Research, Natural Sciences and Engineering …
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
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
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
强制性开放获取政策： National Institute of Health and Medical Research, France
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
强制性开放获取政策： National Institute of Health and Medical Research, France
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
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
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
强制性开放获取政策： Agence Nationale de la Recherche
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
强制性开放获取政策： National Institute of Health and Medical Research, France
Evaluation of approaches to identify associated SNPs that explain the linkage evidence in nuclear families with affected siblings
MH Chen, P Van Eerdewegh, QB Vincent, A Alcais, L Abel, J Dupuis
Human Heredity 69 (2), 104-119, 2010
强制性开放获取政策： US National Institutes of Health
Genome-wide association study of Buruli ulcer in rural Benin
J Manry, QB Vincent, M Chrabieh, L Lorenzo, I Theodorou, MF Ardant, ...
medRxiv, 19012096, 2019
强制性开放获取政策： Agence Nationale de la Recherche
Defining and targeting high-risk populations in Buruli ulcer–Authors' reply
QB Vincent, MF Ardant, L Marsollier, A Chauty, A Alcaïs
The Lancet Global Health 2 (11), e630, 2014
强制性开放获取政策： National Institute of Health and Medical Research, France
Partial IFN-gR2 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 480814, 2013
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
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