about
Pleiotropic effects of the 8.1 HLA haplotype in patients with autoimmune myasthenia gravis and thymus hyperplasiaThe human Major Histocompatibility Complex as a paradigm in genomics researchNetwork-based analysis of omics data: the LEAN methodValidating discovered Cis-acting regulatory genetic variants: application of an allele specific expression approach to HapMap populationsAllele-specific transcription of the asthma-associated PHD finger protein 11 gene (PHF11) modulated by octamer-binding transcription factor 1 (Oct-1).Genetics of autoimmune myasthenia gravis: the multifaceted contribution of the HLA complex.Chromatin profiling across the human tumour necrosis factor gene locus reveals a complex, cell type-specific landscape with novel regulatory elementsFine mapping genetic determinants of the highly variably expressed MHC gene ZFP57.Pervasive haplotypic variation in the spliceo-transcriptome of the human major histocompatibility complex.A functional AT/G polymorphism in the 5'-untranslated region of SETDB2 in the IgE locus on human chromosome 13q14Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravis.Juvenile-Onset Diabetes and Congenital Cataract: "Double-Gene" Mutations Mimicking a Syndromic Diabetes Presentation.Genetic association of molecular traits: a help to identify causative variants in complex diseases.Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Claire Vandiedonck
@ast
Claire Vandiedonck
@en
Claire Vandiedonck
@es
Claire Vandiedonck
@nl
type
label
Claire Vandiedonck
@ast
Claire Vandiedonck
@en
Claire Vandiedonck
@es
Claire Vandiedonck
@nl
prefLabel
Claire Vandiedonck
@ast
Claire Vandiedonck
@en
Claire Vandiedonck
@es
Claire Vandiedonck
@nl
P106
P21
P31
P496
0000-0002-6669-6923