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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
1997 2
1998 1
1999 3
2000 3
2001 5
2002 1
2003 4
2004 4
2005 6
2006 6
2007 5
2008 4
2009 6
2010 10
2011 5
2012 6
2013 5
2014 13
2015 4
2016 5
2017 5
2018 1
2019 4
2020 8
2021 5
2023 2
2024 1

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114 results

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Page 1
Leprosy as a genetic disease.
Alter A, Grant A, Abel L, Alcaïs A, Schurr E. Alter A, et al. Among authors: alcais a. Mamm Genome. 2011 Feb;22(1-2):19-31. doi: 10.1007/s00335-010-9287-1. Epub 2010 Oct 9. Mamm Genome. 2011. PMID: 20936290 Review.
Allele-dependent interaction of LRRK2 and NOD2 in leprosy.
Dallmann-Sauer M, Xu YZ, da Costa ALF, Tao S, Gomes TA, Prata RBDS, Correa-Macedo W, Manry J, Alcaïs A, Abel L, Cobat A, Fava VM, Pinheiro RO, Lara FA, Probst CM, Mira MT, Schurr E. Dallmann-Sauer M, et al. Among authors: alcais a. PLoS Pathog. 2023 Mar 27;19(3):e1011260. doi: 10.1371/journal.ppat.1011260. eCollection 2023 Mar. PLoS Pathog. 2023. PMID: 36972292 Free PMC article.
Severe adult hemophagocytic lymphohistiocytosis (HLHa) correlates with HLH-related gene variants.
Bloch C, Jais JP, Gil M, Boubaya M, Lepelletier Y, Bader-Meunier B, Mahlaoui N, Garcelon N, Lambotte O, Launay D, Larroche C, Lazaro E, Liffermann F, Lortholary O, Michel M, Michot JM, Morel P, Cheminant M, Suarez F, Terriou L, Urbanski G, Viallard JF, Alcais A, Fischer A, de Saint Basile G, Hermine O; French HLH Study Group. Bloch C, et al. Among authors: alcais a. J Allergy Clin Immunol. 2024 Jan;153(1):256-264. doi: 10.1016/j.jaci.2023.07.023. Epub 2023 Sep 9. J Allergy Clin Immunol. 2024. PMID: 37678575 Free article.
A Missense LRRK2 Variant Is a Risk Factor for Excessive Inflammatory Responses in Leprosy.
Fava VM, Manry J, Cobat A, Orlova M, Van Thuc N, Ba NN, Thai VH, Abel L, Alcaïs A, Schurr E; Canadian Lrrk2 in Inflammation Team (CLINT). Fava VM, et al. Among authors: alcais a. PLoS Negl Trop Dis. 2016 Feb 4;10(2):e0004412. doi: 10.1371/journal.pntd.0004412. eCollection 2016 Feb. PLoS Negl Trop Dis. 2016. PMID: 26844546 Free PMC article.
A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency.
Coignard-Biehler H, Mahlaoui N, Pilmis B, Barlogis V, Brosselin P, De Vergnes N, Debré M, Malphettes M, Frange P, Catherinot E, Pellier I, Durieu I, Perlat A, Royer B, Le Quellec A, Jeziorski E, Fischer A, Lortholary O; CEREDIH French PID study group; Aaron L, Adoue D, Aguilar C, Aladjidi N, Alcais A, Amoura Z, Arlet P, Armari-Alla C, Bader-Meunier B, Bayart S, Bertrand Y, Bienvenu B, Blanche S, Bodet D, Bonnotte B, Borie R, Boutard P, Briandet C, Brion JP, Brouard J, Cohen-Beaussant S, Costes L, Couderc LJ, Cougoul P, Courteille V, de Saint Basile G, Devoldere C, Deville A, Donadieu J, Dore E, Dulieu F, Edan C, Entz-Werle N, Fieschi C, Forestier A, Fouyssac F, Gajdos V, Galicier L, Gandemer V, Gardembas M, Gaud C, Guillerm G, Hachulla E, Hamidou M, Hermine O, Hoarau C, Humbert S, Jaccard A, Jacquot S, Jais JP, Jaussaud R, Jeandel PY, Kebaili K, Korganow AS, Lambotte O, Lanternier F, Larroche C, Lascaux AS, Le Moigne E, Le Moing V, Lebranchu Y, Lecuit M, Lefevre G, Lemal R, Te VLT, Marie-Cardine A, Silva NM, Masseau A, Massot C, Mazingue F, Merlin E, Michel G, Millot F, Monlibert B, Monpoux F, Moshous D, Mouthon L, Munzer M, Neven B, Nove-Josserand R, Oksenhendler E, Ouaché… See abstract for full author list ➔ Coignard-Biehler H, et al. Among authors: alcais a. J Clin Immunol. 2019 Oct;39(7):702-712. doi: 10.1007/s10875-019-00658-9. Epub 2019 Aug 10. J Clin Immunol. 2019. PMID: 31401750
Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcer.
Vincent QB, Belkadi A, Fayard C, Marion E, Adeye A, Ardant MF, Johnson CR, Agossadou D, Lorenzo L, Guergnon J, Bole-Feysot C, Manry J, Nitschké P, Theodorou I, Casanova JL, Marsollier L, Chauty A, Abel L, Alcaïs A; Franco-Beninese Buruli Research Group. Vincent QB, et al. Among authors: alcais a. PLoS Negl Trop Dis. 2018 Apr 30;12(4):e0006429. doi: 10.1371/journal.pntd.0006429. eCollection 2018 Apr. PLoS Negl Trop Dis. 2018. PMID: 29708969 Free PMC article.
Genetic diagnosis of primary immunodeficiencies: A survey of the French national registry.
Mahlaoui N, Picard C, Bach P, Costes L, Courteille V, Ranohavimparany A, Alcaïs A, Jais JP, Fischer A; CEREDIH French PID study group. Mahlaoui N, et al. Among authors: alcais a. J Allergy Clin Immunol. 2019 Apr;143(4):1646-1649.e10. doi: 10.1016/j.jaci.2018.12.994. Epub 2019 Jan 9. J Allergy Clin Immunol. 2019. PMID: 30639347 No abstract available.
114 results