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HLA|November 10, 2023
18th International HLA and Immunogenetics Workshop: Report on the SNP-HLA Reference Consortium (SHLARC) componentNayane S B Silva, Sonia Bourguiba-Hachemi, Venceslas Douillard, et al.JAMIA Open|May 14, 2026
PRIMUS: a precision medicine platform reusing clinical trials and registry data to support treatment selection in multiple sclerosisStanislas Demuth, Igor Faddeenkov, Julien Paris, et al.European Journal of Human Genetics : EJHG|February 3, 2023
KiT-GENIE, the French genetic biobank of kidney transplantationRokhaya Ba, Axelle Durand, Vincent Mauduit, et al.Scientific Reports|April 2, 2024
Investigating the metabolite signature of an altered oral microbiota as a discriminant factor for multiple sclerosis: a pilot studyLéo Boussamet, Emmanuel Montassier, Camille Mathé, et al.HLA|November 11, 2023
Optimal population-specific HLA imputation with dimension reductionVenceslas Douillard, Nayane Dos Santos Brito Silva, Sonia Bourguiba-Hachemi, et al.Frontiers in Immunology|January 31, 2020
Distribution of Bacterial α1,3-Galactosyltransferase Genes in the Human Gut MicrobiomeEmmanuel Montassier, Gabriel A Al-Ghalith, Camille Mathé, et al.HLA|June 5, 2024
A multi-ethnic reference panel to impute HLA classical and non-classical class I alleles in admixed samples: Testing imputation accuracy in an admixed sample from BrazilNayane S B Silva, Sonia Bourguiba-Hachemi, Viviane A O Ciriaco, et al.HLA|April 2, 2023
Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgroundsNayane Dos Santos Brito Silva, Andreia da Silva Souza, Heloisa de Souza Andrade, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|October 8, 2009
Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defectMarion Malphettes, Laurence Gérard, Maryvonnick Carmagnat, et al.Journal of Clinical Immunology|May 4, 2010
B-cell and T-cell phenotypes in CVID patients correlate with the clinical phenotype of the diseaseGaël Mouillot, Maryvonnick Carmagnat, Laurence Gérard, et al.Pageof 6