Laurent-Marcel Abel


Ontology type: schema:Person     


Person Info

NAME

Laurent-Marcel

SURNAME

Abel

Publications in SciGraph latest 50 shown

  • 2021-09-24 Controlling for human population stratification in rare variant association studies in SCIENTIFIC REPORTS
  • 2021-06-28 Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child in NATURE MEDICINE
  • 2021-06-08 Harnessing Type I IFN Immunity Against SARS-CoV-2 with Early Administration of IFN-β in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2021-04-13 Neutralizing Autoantibodies to Type I IFNs in >10% of Patients with Severe COVID-19 Pneumonia Hospitalized in Madrid, Spain in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2021-03-24 Inhibition of HECT E3 ligases as potential therapy for COVID-19 in CELL DEATH & DISEASE
  • 2021-03-03 Rare Pathogenic Variants in Mitochondrial and Inflammation-Associated Genes May Lead to Inflammatory Cardiomyopathy in Chagas Disease in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2021-01-08 Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-06-22 Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-05-27 The human genetic determinism of life-threatening infectious diseases: genetic heterogeneity and physiological homogeneity? in HUMAN GENETICS
  • 2020-04-20 Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway in COMMUNICATIONS BIOLOGY
  • 2019-12-05 Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis in NATURE MEDICINE
  • 2019-11-11 Decreased plasma phospholipid concentrations and increased acid sphingomyelinase activity are accurate biomarkers for community-acquired pneumonia in JOURNAL OF TRANSLATIONAL MEDICINE
  • 2018-08-20 Disruption of an anti-mycobacterial circuit between dendritic and Th cells in human SPPL2a deficiency in NATURE IMMUNOLOGY
  • 2018-07-27 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines in GENOME MEDICINE
  • 2018-07-11 A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2018-05-18 Autosomal Dominant IFN-γR1 Deficiency Presenting with both Atypical Mycobacteriosis and Tuberculosis in a BCG-Vaccinated South African Patient in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2018-03-27 Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2018-03-16 A novel genetic architecture of infectious diseases in NATURE REVIEWS IMMUNOLOGY
  • 2017-10-09 An eQTL variant of ZXDC is associated with IFN-γ production following Mycobacterium tuberculosis antigen-specific stimulation in SCIENTIFIC REPORTS
  • 2017-06-14 Human Genetics of Tuberculosis of the Nervous System in TUBERCULOSIS OF THE CENTRAL NERVOUS SYSTEM
  • 2016-07-18 Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery in NATURE GENETICS
  • 2016-02-18 Erratum to: Severe Mycobacterial Diseases in a Patient with GOF IκBα Mutation Without EDA in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2016-01-28 The mutation significance cutoff: gene-level thresholds for variant predictions in NATURE METHODS
  • 2016-01-14 A genome-wide association study of pulmonary tuberculosis in Morocco in HUMAN GENETICS
  • 2015-12-21 Severe Mycobacterial Diseases in a Patient with GOF IκBα Mutation Without EDA in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2015-05-03 Genotype combinations of two IL4 polymorphisms influencing IL-4 plasma levels are associated with different risks of severe malaria in the Malian population in IMMUNOGENETICS
  • 2014-10-26 A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4 in NATURE IMMUNOLOGY
  • 2014-10-12 Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation in NATURE
  • 2014-08-19 Mycobacterium simiae Infection in Two Unrelated Patients with Different Forms of Inherited IFN-γR2 Deficiency in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2014-04-03 HGCS: an online tool for prioritizing disease-causing gene variants by biological distance in BMC GENOMICS
  • 2014-03-05 Chronic Granulomatous Disease in Morocco: Genetic, Immunological, and Clinical Features of 12 Patients from 10 Kindreds in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2014-02-23 CUBN and NEBL common variants in the chromosome 10p13 linkage region are associated with multibacillary leprosy in Vietnam in HUMAN GENETICS
  • 2012-10-28 Impaired intrinsic immunity to HSV-1 in human iPSC-derived TLR3-deficient CNS cells in NATURE
  • 2012-09-29 Linkage disequilibrium pattern and age-at-diagnosis are critical for replicating genetic associations across ethnic groups in leprosy in HUMAN GENETICS
  • 2012-08-19 EVER2 Deficiency is Associated with Mild T-cell Abnormalities in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2012-07-31 Primary Immunodeficiency Diseases Worldwide: More Common than Generally Thought in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2012-06-07 Integrative study of pandemic A/H1N1 influenza infections: design and methods of the CoPanFlu-France cohort in BMC PUBLIC HEALTH
  • 2012-02-29 Multifocal Tuberculous Osteomyelitis: Possible Inherited Interferon Gamma Axis Defect in THE INDIAN JOURNAL OF PEDIATRICS
  • 2012-01-18 A major locus on chromosome 3p22 conferring predisposition to human herpesvirus 8 infection in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-04-13 Lethal Tuberculosis in a Previously Healthy Adult with IL-12 Receptor Deficiency in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2011-01-30 Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease in NATURE IMMUNOLOGY
  • 2010-10-09 Leprosy as a genetic disease in MAMMALIAN GENOME
  • 2009-12-25 Genetic and functional analysis of common MRC1 exon 7 polymorphisms in leprosy susceptibility in HUMAN GENETICS
  • 2009-07-23 Evidence for a dominant major gene conferring predisposition to hepatitis C virus infection in endemic conditions in HUMAN GENETICS
  • 2008-11-30 Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness in NATURE GENETICS
  • 2008-04-09 A major susceptibility locus for HTLV-1 infection in childhood maps to chromosome 6q27 in RETROVIROLOGY
  • 2008-02-05 Leprosy as a genetic model for susceptibility to common infectious diseases in HUMAN GENETICS
  • 2007-10-19 Immunology in natura: clinical, epidemiological and evolutionary genetics of infectious diseases in NATURE IMMUNOLOGY
  • 2007-03-11 Stepwise replication identifies a low-producing lymphotoxin-α allele as a major risk factor for early-onset leprosy in NATURE GENETICS
  • 2005-12-30 Inclusion of unaffected sibs increases power in model-free linkage analysis of a behavioral trait in BMC GENETICS
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