Host-microbe interactions have shaped the genetic architecture of inflammatory bowel diseaseImmunoChip study implicates antigen presentation to T cells in narcolepsyDisruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral refluxThe gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytesA novel role for XIAP in copper homeostasis through regulation of MURR1Characterization of COMMD protein-protein interactions in NF-kappaB signallingFunctional characterization of mutations in the myosin Vb gene associated with microvillus inclusion diseaseMutations in SPINT2 cause a syndromic form of congenital sodium diarrheaMultiple common variants for celiac disease influencing immune gene expressionTwelve type 2 diabetes susceptibility loci identified through large-scale association analysisGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility lociShared and distinct genetic variants in type 1 diabetes and celiac diseaseAbdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1Genome-wide association study of intracranial aneurysm identifies three new risk lociEvolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infectionSusceptibility loci for intracranial aneurysm in European and Japanese populationsHuman dectin-1 deficiency and mucocutaneous fungal infectionsMolecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypesThe DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndromeA genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21Newly identified genetic risk variants for celiac disease related to the immune responseThe SPINK gene family and celiac disease susceptibilityExpressing the differences between Crohn disease and ulcerative colitisGenome-wide association identifies multiple ulcerative colitis susceptibility lociGene expression profiling and phenotype analyses of S. cerevisiae in response to changing copper reveals six genes with new roles in copper and iron metabolism.The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expressionThe canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosisA major non-HLA locus in celiac disease maps to chromosome 19The copper toxicosis gene product Murr1 directly interacts with the Wilson disease proteinThe ubiquitously expressed MURR1 protein is absent in canine copper toxicosisIdentification of a new copper metabolism gene by positional cloning in a purebred dog populationCoeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signallingGenetic susceptibility to respiratory syncytial virus bronchiolitis in preterm children is associated with airway remodeling genes and innate immune genesAssociation analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohortDifferential association of the PTPN22 coding variant with autoimmune diseases in a Dutch populationDefining the contribution of the HLA region to cis DQ2-positive coeliac disease patientsAn association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophreniaA functional candidate screen for coeliac disease genesCoeliac disease and autoimmune disease-genetic overlap and screeningGenetic variation in Toll-like receptors and disease susceptibility
P50
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P50
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Dutch university professor
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Nederlands geneticus
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nederlandsk genetiker
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niederländische Humangenetikerin
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Cisca Wijmenga
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Cisca Wijmenga
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Cisca Wijmenga
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Cisca Wijmenga
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T.N. Wijmenga
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T.N. Wijmenga
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T.N. Wijmenga
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Cisca Wijmenga
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Cisca Wijmenga
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Cisca Wijmenga
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Cisca Wijmenga
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Cisca Wijmenga
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Cisca Wijmenga
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P108
P1006
P1741
P214
P1006
P101
P1153
7005273061
P1477
Tjitske Nienke Wijmenga
@nl