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Items: 1 to 50 of 116

1.

Cynomolgus macaque IL37 polymorphism and control of SIV infection.

Shiina T, Suzuki S, Congy-Jolivet N, Aarnink A, Garchon HJ, Dereuddre-Bosquet N, Vaslin B, Tchitchek N, Desjardins D, Autran B, Lambotte O, Theodorou I, Le Grand R, Blancher A.

Sci Rep. 2019 May 28;9(1):7981. doi: 10.1038/s41598-019-44235-x.

2.

Genetics and Functional Genomics of Spondyloarthritis.

Costantino F, Breban M, Garchon HJ.

Front Immunol. 2018 Dec 18;9:2933. doi: 10.3389/fimmu.2018.02933. eCollection 2018. Review.

3.

In-Host Adaptation of Salmonella enterica Serotype Dublin during Prosthetic Hip Joint Infection.

El Sayed F, Sapriel G, Fawal N, Gruber A, Bauer T, Heym B, Dupont C, Garchon HJ, Gaillard JL, Rottman M, Le Hello S.

Emerg Infect Dis. 2018 Dec;24(12):2360-2363. doi: 10.3201/eid2412.180214.

4.

Whole genome sequencing in the search for genes associated with the control of SIV infection in the Mauritian macaque model.

de Manuel M, Shiina T, Suzuki S, Dereuddre-Bosquet N, Garchon HJ, Tanaka M, Congy-Jolivet N, Aarnink A, Le Grand R, Marques-Bonet T, Blancher A.

Sci Rep. 2018 May 8;8(1):7131. doi: 10.1038/s41598-018-25071-x.

5.

A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family.

Ben Khelifa M, Ghieh F, Boudjenah R, Hue C, Fauvert D, Dard R, Garchon HJ, Vialard F.

Hum Reprod. 2018 Jun 1;33(6):1034-1037. doi: 10.1093/humrep/dey073.

PMID:
29659827
6.

NKp30 isoforms and NKp46 transcripts in metastatic melanoma patients: Unique NKp30 pattern in rare melanoma patients with favorable evolution.

Messaoudene M, Fregni G, Enot D, Jacquelot N, Neves E, Germaud N, Garchon HJ, Boukouaci W, Tamouza R, Chanal J, Avril MF, Toubert A, Zitvogel L, Rusakiewicz S, Caignard A.

Oncoimmunology. 2016 Mar 10;5(12):e1154251. doi: 10.1080/2162402X.2016.1154251. eCollection 2016.

7.

Rapid dissemination of RET-transgene-driven melanoma in the presence of non-obese diabetic alleles: Critical roles of Dectin-1 and Nitric-oxide synthase type 2.

Dabbeche-Bouricha E, Araujo LM, Kato M, Prévost-Blondel A, Garchon HJ.

Oncoimmunology. 2015 Oct 29;5(5):e1100793. doi: 10.1080/2162402X.2015.1100793. eCollection 2016 May.

8.

A family-based genome-wide association study reveals an association of spondyloarthritis with MAPK14.

Costantino F, Talpin A, Said-Nahal R, Leboime A, Zinovieva E, Zelenika D, Gut I, Charon C, Izac B, Weissman M, Chiocchia G, Reveille J, Breban M, Garchon HJ.

Ann Rheum Dis. 2017 Jan;76(1):310-314. doi: 10.1136/annrheumdis-2016-209449. Epub 2016 Jul 26.

PMID:
27461236
9.

Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.

Seldin MF, Alkhairy OK, Lee AT, Lamb JA, Sussman J, Pirskanen-Matell R, Piehl F, Verschuuren JJGM, Kostera-Pruszczyk A, Szczudlik P, McKee D, Maniaol AH, Harbo HF, Lie BA, Melms A, Garchon HJ, Willcox N, Gregersen PK, Hammarstrom L.

Mol Med. 2016 Mar;21(1):769-781. doi: 10.2119/molmed.2015.00232. Epub 2015 Nov 10.

10.

Whole-genome single nucleotide polymorphism-based linkage analysis in spondyloarthritis multiplex families reveals a new susceptibility locus in 13q13.

Costantino F, Chaplais E, Leturcq T, Said-Nahal R, Leboime A, Zinovieva E, Zelenika D, Gut I, Charon C, Chiocchia G, Breban M, Garchon HJ.

Ann Rheum Dis. 2016 Jul;75(7):1380-5. doi: 10.1136/annrheumdis-2015-207720. Epub 2015 Aug 14.

PMID:
26275432
11.

stringgaussnet: from differentially expressed genes to semantic and Gaussian networks generation.

Chaplais E, Garchon HJ.

Bioinformatics. 2015 Dec 1;31(23):3865-7. doi: 10.1093/bioinformatics/btv450. Epub 2015 Jul 30.

PMID:
26231430
12.

Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1.

Cortes A, Pulit SL, Leo PJ, Pointon JJ, Robinson PC, Weisman MH, Ward M, Gensler LS, Zhou X, Garchon HJ, Chiocchia G, Nossent J, Lie BA, Førre Ø, Tuomilehto J, Laiho K, Bradbury LA, Elewaut D, Burgos-Vargas R, Stebbings S, Appleton L, Farrah C, Lau J, Haroon N, Mulero J, Blanco FJ, Gonzalez-Gay MA, Lopez-Larrea C, Bowness P, Gaffney K, Gaston H, Gladman DD, Rahman P, Maksymowych WP, Crusius JB, van der Horst-Bruinsma IE, Valle-Oñate R, Romero-Sánchez C, Hansen IM, Pimentel-Santos FM, Inman RD, Martin J, Breban M, Wordsworth BP, Reveille JD, Evans DM, de Bakker PI, Brown MA.

Nat Commun. 2015 May 21;6:7146. doi: 10.1038/ncomms8146.

13.

ERAP2 is associated with ankylosing spondylitis in HLA-B27-positive and HLA-B27-negative patients.

Robinson PC, Costello ME, Leo P, Bradbury LA, Hollis K, Cortes A, Lee S, Joo KB, Shim SC, Weisman M, Ward M, Zhou X, Garchon HJ, Chiocchia G, Nossent J, Lie BA, Førre Ø, Tuomilehto J, Laiho K, Jiang L, Liu Y, Wu X, Elewaut D, Burgos-Vargas R, Gensler LS, Stebbings S, Haroon N, Mulero J, Fernandez-Sueiro JL, Gonzalez-Gay MA, Lopez-Larrea C, Bowness P, Gafney K, Gaston JS, Gladman DD, Rahman P, Maksymowych WP, Xu H, van der Horst-Bruinsma IE, Chou CT, Valle-Oñate R, Romero-Sánchez MC, Hansen IM, Pimentel-Santos FM, Inman RD, Martin J, Breban M, Evans D, Reveille JD, Kim TH, Wordsworth BP, Brown MA.

Ann Rheum Dis. 2015 Aug;74(8):1627-9. doi: 10.1136/annrheumdis-2015-207416. Epub 2015 Apr 27. No abstract available.

14.

Revisiting MHC genes in spondyloarthritis.

Breban M, Costantino F, André C, Chiocchia G, Garchon HJ.

Curr Rheumatol Rep. 2015 Jun;17(6):516. doi: 10.1007/s11926-015-0516-1. Review.

PMID:
25903667
15.

ERAP1 Gene Expression Is Influenced by Nonsynonymous Polymorphisms Associated With Predisposition to Spondyloarthritis.

Costantino F, Talpin A, Evnouchidou I, Kadi A, Leboime A, Said-Nahal R, Bonilla N, Letourneur F, Leturcq T, Ka Z, van Endert P, Garchon HJ, Chiocchia G, Breban M.

Arthritis Rheumatol. 2015 Jun;67(6):1525-34. doi: 10.1002/art.39072.

16.

Monocyte-derived dendritic cells from HLA-B27+ axial spondyloarthritis (SpA) patients display altered functional capacity and deregulated gene expression.

Talpin A, Costantino F, Bonilla N, Leboime A, Letourneur F, Jacques S, Dumont F, Amraoui S, Dutertre CA, Garchon HJ, Breban M, Chiocchia G.

Arthritis Res Ther. 2014 Aug 21;16(4):417. doi: 10.1186/s13075-014-0417-0.

17.

Use of whole-blood transcriptomic profiling to highlight several pathophysiologic pathways associated with response to rituximab in patients with rheumatoid arthritis: data from a randomized, controlled, open-label trial.

Sellam J, Marion-Thore S, Dumont F, Jacques S, Garchon HJ, Rouanet S, Taoufik Y, Hendel-Chavez H, Sibilia J, Tebib J, Le Loët X, Combe B, Dougados M, Mariette X, Chiocchia G.

Arthritis Rheumatol. 2014 Aug;66(8):2015-25. doi: 10.1002/art.38671.

18.

Prevalence of spondyloarthritis in reference to HLA-B27 in the French population: results of the GAZEL cohort.

Costantino F, Talpin A, Said-Nahal R, Goldberg M, Henny J, Chiocchia G, Garchon HJ, Zins M, Breban M.

Ann Rheum Dis. 2015 Apr;74(4):689-93. doi: 10.1136/annrheumdis-2013-204436. Epub 2013 Dec 18.

PMID:
24351517
19.

Brief report: the IL23R nonsynonymous polymorphism rs11209026 is associated with radiographic sacroiliitis in spondyloarthritis.

Kadi A, Costantino F, Izac B, Leboime A, Said-Nahal R, Garchon HJ, Chiocchia G, Breban M.

Arthritis Rheum. 2013 Oct;65(10):2655-60. doi: 10.1002/art.38060.

20.

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci.

International Genetics of Ankylosing Spondylitis Consortium (IGAS), Cortes A, Hadler J, Pointon JP, Robinson PC, Karaderi T, Leo P, Cremin K, Pryce K, Harris J, Lee S, Joo KB, Shim SC, Weisman M, Ward M, Zhou X, Garchon HJ, Chiocchia G, Nossent J, Lie BA, Førre Ø, Tuomilehto J, Laiho K, Jiang L, Liu Y, Wu X, Bradbury LA, Elewaut D, Burgos-Vargas R, Stebbings S, Appleton L, Farrah C, Lau J, Kenna TJ, Haroon N, Ferreira MA, Yang J, Mulero J, Fernandez-Sueiro JL, Gonzalez-Gay MA, Lopez-Larrea C, Deloukas P, Donnelly P; Australo-Anglo-American Spondyloarthritis Consortium (TASC); Groupe Française d'Etude Génétique des Spondylarthrites (GFEGS); Nord-Trøndelag Health Study (HUNT); Spondyloarthritis Research Consortium of Canada (SPARCC); Wellcome Trust Case Control Consortium 2 (WTCCC2), Bowness P, Gafney K, Gaston H, Gladman DD, Rahman P, Maksymowych WP, Xu H, Crusius JB, van der Horst-Bruinsma IE, Chou CT, Valle-Oñate R, Romero-Sánchez C, Hansen IM, Pimentel-Santos FM, Inman RD, Videm V, Martin J, Breban M, Reveille JD, Evans DM, Kim TH, Wordsworth BP, Brown MA.

Nat Genet. 2013 Jul;45(7):730-8. doi: 10.1038/ng.2667. Epub 2013 Jun 9.

21.

Increased thymic development of regulatory T cells in NOD mice is functionally dissociated from type I diabetes susceptibility.

Tellier J, Andrianjaka A, Vicente R, Thiault N, Enault G, Garchon HJ, van Meerwijk JP, Romagnoli P.

Eur J Immunol. 2013 May;43(5):1356-62. doi: 10.1002/eji.201243142. Epub 2013 Mar 11.

22.

Comparative analysis in cynomolgus macaque identifies a novel human MHC locus controlling platelet blood counts independently of BAK1.

Aarnink A, Garchon HJ, Okada Y, Takahashi A, Matsuda K, Kubo M, Nakamura Y, Blancher A.

J Thromb Haemost. 2013 Feb;11(2):384-6. doi: 10.1111/jth.12092. No abstract available.

23.

Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.

Gregersen PK, Kosoy R, Lee AT, Lamb J, Sussman J, McKee D, Simpfendorfer KR, Pirskanen-Matell R, Piehl F, Pan-Hammarstrom Q, Verschuuren JJ, Titulaer MJ, Niks EH, Marx A, Ströbel P, Tackenberg B, Pütz M, Maniaol A, Elsais A, Tallaksen C, Harbo HF, Lie BA, Raychaudhuri S, de Bakker PI, Melms A, Garchon HJ, Willcox N, Hammarstrom L, Seldin MF.

Ann Neurol. 2012 Dec;72(6):927-35. doi: 10.1002/ana.23691. Epub 2012 Oct 10.

24.

Impact of MHC class II polymorphism on blood counts of CD4+ T lymphocytes in macaque.

Aarnink A, Garchon HJ, Puissant-Lubrano B, Blancher-Sardou M, Apoil PA, Blancher A.

Immunogenetics. 2011 Feb;63(2):95-102. doi: 10.1007/s00251-010-0492-6. Epub 2010 Nov 18.

PMID:
21086122
25.

European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups.

Tian C, Kosoy R, Nassir R, Lee A, Villoslada P, Klareskog L, Hammarström L, Garchon HJ, Pulver AE, Ransom M, Gregersen PK, Seldin MF.

Mol Med. 2009 Nov-Dec;15(11-12):371-83. doi: 10.2119/molmed.2009.00094. Epub 2009 Aug 27.

26.

Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis.

Zinovieva E, Bourgain C, Kadi A, Letourneur F, Izac B, Said-Nahal R, Lebrun N, Cagnard N, Vigier A, Jacques S, Miceli-Richard C, Garchon HJ, Heath S, Charon C, Bacq D, Boland A, Zelenika D, Chiocchia G, Breban M.

PLoS Genet. 2009 Jun;5(6):e1000528. doi: 10.1371/journal.pgen.1000528. Epub 2009 Jun 19.

27.

Association of HLA-A in autoimmune myasthenia gravis with thymoma.

Vandiedonck C, Raffoux C, Eymard B, Tranchant C, Dulmet E, Krumeich S, Gajdos P, Garchon HJ.

J Neuroimmunol. 2009 May 29;210(1-2):120-3. doi: 10.1016/j.jneuroim.2009.02.004. Epub 2009 Mar 10.

PMID:
19278738
28.

Genetic factors in autoimmune myasthenia gravis.

Giraud M, Vandiedonck C, Garchon HJ.

Ann N Y Acad Sci. 2008;1132:180-92. doi: 10.1196/annals.1405.027.

PMID:
18567868
29.

Polymorphic markers of the fibrillin-1 gene and systemic sclerosis in European Caucasian patients.

Wipff J, Giraud M, Sibilia J, Mouthon L, Meyer O, Tiev K, Airo P, Caramaschi P, Guiducci S, Garchon HJ, Matucci-Cerinic M, Kahan A, Avouac J, Boileau C, Allanore Y.

J Rheumatol. 2008 Apr;35(4):643-9. Epub 2008 Feb 15.

PMID:
18278837
30.

An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymus.

Giraud M, Taubert R, Vandiedonck C, Ke X, Lévi-Strauss M, Pagani F, Baralle FE, Eymard B, Tranchant C, Gajdos P, Vincent A, Willcox N, Beeson D, Kyewski B, Garchon HJ.

Nature. 2007 Aug 23;448(7156):934-7. Epub 2007 Aug 8.

PMID:
17687331
31.

Genetic and functional analysis of the Nkt1 locus using congenic NOD mice: improved Valpha14-NKT cell performance but failure to protect against type 1 diabetes.

Rocha-Campos AC, Melki R, Zhu R, Deruytter N, Damotte D, Dy M, Herbelin A, Garchon HJ.

Diabetes. 2006 Apr;55(4):1163-70.

32.

Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravis.

Vandiedonck C, Capdevielle C, Giraud M, Krumeich S, Jais JP, Eymard B, Tranchant C, Gajdos P, Garchon HJ.

Ann Neurol. 2006 Feb;59(2):404-7.

PMID:
16437561
34.

Genetics of autoimmune myasthenia gravis: the multifaceted contribution of the HLA complex.

Vandiedonck C, Giraud M, Garchon HJ.

J Autoimmun. 2005;25 Suppl:6-11. Epub 2005 Nov 2. Review.

PMID:
16260117
35.

XMR, a dual location protein in the XY pair and in its associated nucleolus in mouse spermatocytes.

Escalier D, Garchon HJ.

Mol Reprod Dev. 2005 Sep;72(1):105-12.

PMID:
15818601
36.

Mapping non-class II H2-linked loci for type 1 diabetes in nonobese diabetic mice.

Deruytter N, Boulard O, Garchon HJ.

Diabetes. 2004 Dec;53(12):3323-7.

37.

Pleiotropic effects of the 8.1 HLA haplotype in patients with autoimmune myasthenia gravis and thymus hyperplasia.

Vandiedonck C, Beaurain G, Giraud M, Hue-Beauvais C, Eymard B, Tranchant C, Gajdos P, Dausset J, Garchon HJ.

Proc Natl Acad Sci U S A. 2004 Oct 26;101(43):15464-9. Epub 2004 Oct 15.

38.

CYP1B1 mutations in French patients with early-onset primary open-angle glaucoma.

Melki R, Colomb E, Lefort N, Brézin AP, Garchon HJ.

J Med Genet. 2004 Sep;41(9):647-51.

39.

A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes.

Guo D, Li M, Zhang Y, Yang P, Eckenrode S, Hopkins D, Zheng W, Purohit S, Podolsky RH, Muir A, Wang J, Dong Z, Brusko T, Atkinson M, Pozzilli P, Zeidler A, Raffel LJ, Jacob CO, Park Y, Serrano-Rios M, Larrad MT, Zhang Z, Garchon HJ, Bach JF, Rotter JI, She JX, Wang CY.

Nat Genet. 2004 Aug;36(8):837-41. Epub 2004 Jul 11. Erratum in: Nat Genet. 2004 Sep;36(9):1024.

PMID:
15247916
40.

Genetic control of autoantibody expression in autoimmune myasthenia gravis: role of the self-antigen and of HLA-linked loci.

Giraud M, Beaurain G, Eymard B, Tranchant C, Gajdos P, Garchon HJ.

Genes Immun. 2004 Aug;5(5):398-404.

PMID:
15201863
41.
42.
43.

The M98K variant of the OPTINEURIN (OPTN) gene modifies initial intraocular pressure in patients with primary open angle glaucoma.

Melki R, Belmouden A, Akhayat O, Brézin A, Garchon HJ.

J Med Genet. 2003 Nov;40(11):842-4. No abstract available.

44.
45.

Myocilin analysis by DHPLC in French POAG patients: increased prevalence of Q368X mutation.

Melki R, Belmouden A, Brézin A, Garchon HJ.

Hum Mutat. 2003 Aug;22(2):179.

PMID:
12872267
46.

Mutational analysis of the Myocilin gene in patients with primary open-angle glaucoma in Morocco.

Melki R, Idhajji A, Driouiche S, Hassani M, Boukabboucha A, Akhayat O, Garchon H, Belmouden A.

Ophthalmic Genet. 2003 Sep;24(3):153-60.

PMID:
12868033
47.

TNFA-TNFB haplotypes modify susceptibility to type I diabetes mellitus independently of HLA class II in a Moroccan population.

Bouqbis L, Akhayat O, Garchon HJ, Calafell F, Izaabel H.

Tissue Antigens. 2003 Jan;61(1):72-9.

PMID:
12622777
48.

A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma.

Nemesure B, Jiao X, He Q, Leske MC, Wu SY, Hennis A, Mendell N, Redman J, Garchon HJ, Agarwala R, Schäffer AA, Hejtmancik F; Barbados Family Study Group.

Hum Genet. 2003 May;112(5-6):600-9. Epub 2003 Mar 4.

PMID:
12616399
50.

A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco.

Belmouden A, Melki R, Hamdani M, Zaghloul K, Amraoui A, Nadifi S, Akhayat O, Garchon HJ.

Clin Genet. 2002 Oct;62(4):334-9.

PMID:
12372064

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