Author: Laurent Abel

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Preprints

Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants

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A common TMPRSS2 variant protects against severe COVID-19

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Distinct antibody repertoires against endemic human coronaviruses in children and adults

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Superantigenic TCR Vbeta 21.3 signature in Multisystem Inflammatory Syndrome in Children

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Human T-bet governs innate and innate-like adaptive IFN-γ immunity against mycobacteria

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IRF4 haploinsufficiency in a family with Whipple’s disease

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  • In immunology: 1,685
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Genetic factors and age are the strongest predictors of humoral immune responses to common pathogens and vaccines

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  • In genomics: 3,812
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SeqTailor: a user-friendly webserver for the extraction of DNA or protein sequences from next-generation sequencing data

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Controlling for Human Population Stratification in Rare Variant Association Studies

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Heterogeneity of monocyte subsets and susceptibility to influenza virus contribute to inter-population variability of protective immunity

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Negative selection on human genes causing severe inborn errors depends on disease outcome and both the mode and mechanism of inheritance

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Pleiotropic effects for Parkin and LRRK2 in leprosy type-1 reactions and Parkinson's disease

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  • In genetics: 4,119
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Family-based genome-wide association study of leprosy in Vietnam

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  • In infectious diseases: 5,324
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A genome-wide case-only test for the detection of digenic inheritance in human exomes

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Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations

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Early onset leprosy reveals a joint effect of LRRK2 and NOD2 variants

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Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons

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  • In genetics: 4,963
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Genome-wide association study of Buruli ulcer in rural Benin

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Detection of homozygous and hemizygous partial exon deletions by whole-exome sequencing

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  • Site-wide: 150,371
  • In bioinformatics: 11,304
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Genome-wide detection of human variants that disrupt intronic branchpoints

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  • Site-wide: 178,558
  • In genetics: None
• Year to date:
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