Cisca Wijmenga

Q: What Schools Are Affiliated With Cisca Wijmenga

Cisca Wijmenga is affiliated with the following schools: University of Oslo, University of Amsterdam, University of Hawaiʻi at Mānoa, Utrecht University, University of Basel, University of Groningen

Cisca Wijmenga's AcademicInfluence.com Rankings

Cisca Wijmenga

Biology

#2993

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#4647

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Genetics

#331

World Rank

#389

Historical Rank

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Biology

Cisca Wijmenga's Degrees

PhD Human Genetics University of Groningen
Masters Biology University of Groningen

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Why Is Cisca Wijmenga Influential?

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According to Wikipedia, Tjitske Nienke "Cisca" Wijmenga is a Dutch professor of Human Genetics at the University of Groningen and the University Medical Center Groningen. She has been Rector Magnificus of the University since September 2019.

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Cisca Wijmenga's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease (2012) (4007)
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci (2010) (2516)
Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (2012) (2002)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
Environment dominates over host genetics in shaping human gut microbiota (2018) (1562)
Population-level analysis of gut microbiome variation (2016) (1484)
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 (2011) (1315)
mTOR- and HIF-1α–mediated aerobic glycolysis as metabolic basis for trained immunity (2014) (1314)
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci (2010) (1285)
Population-based metagenomics analysis reveals markers for gut microbiome composition and diversity (2016) (1208)
Epigenetic programming of monocyte-to-macrophage differentiation and trained innate immunity (2014) (1154)
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes (2007) (1066)
Multiple common variants for celiac disease influencing immune gene expression (2010) (958)
The neuroactive potential of the human gut microbiota in quality of life and depression (2019) (936)
Candida albicans infection affords protection against reinfection via functional reprogramming of monocytes. (2012) (828)
Gut microbiome structure and metabolic activity in inflammatory bowel disease (2018) (783)
Proton pump inhibitors affect the gut microbiome (2015) (770)
Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes (2007) (765)
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm (2008) (765)
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC (2006) (764)
BCG Vaccination Protects against Experimental Viral Infection in Humans through the Induction of Cytokines Associated with Trained Immunity. (2018) (742)
The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome. (1999) (731)
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease (2011) (711)
Human dectin-1 deficiency and mucocutaneous fungal infections. (2009) (698)
Newly identified genetic risk variants for celiac disease related to the immune response (2008) (697)
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 (2007) (686)
Whole-genome sequence variation, population structure and demographic history of the Dutch population (2014) (650)
Linking the Human Gut Microbiome to Inflammatory Cytokine Production Capacity (2016) (638)
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2016) (634)
Genome-wide association identifies multiple ulcerative colitis susceptibility loci (2010) (621)
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility (2008) (607)
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy (1992) (602)
High density genetic mapping identifies new susceptibility loci for rheumatoid arthritis (2012) (595)
Shared and distinct genetic variants in type 1 diabetes and celiac disease. (2008) (571)
The effect of host genetics on the gut microbiome (2016) (566)
Cohort Profile: LifeLines, a three-generation cohort study and biobank. (2015) (558)
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity (2012) (555)
Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases (2019) (553)
Pervasive Sharing of Genetic Effects in Autoimmune Disease (2011) (537)
Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes. (2006) (528)
Detecting shared pathogenesis from the shared genetics of immune-related diseases (2009) (517)
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit. (1993) (504)
Interplay of host genetics and gut microbiota underlying the onset and clinical presentation of inflammatory bowel disease (2016) (485)
The Gut Microbiome Contributes to a Substantial Proportion of the Variation in Blood Lipids (2015) (458)
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) (451)
Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy (2011) (411)
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis (2012) (411)
Genome-wide association and large scale follow-up identifies 16 new loci influencing lung function (2011) (401)
Randomized feeding intervention in infants at high risk for celiac disease. (2014) (401)
Identification of fifteen new psoriasis susceptibility loci highlights the role of innate immunity (2012) (397)
Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA (2011) (394)
Identification of a new copper metabolism gene by positional cloning in a purebred dog population. (2002) (362)
Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes (2007) (357)
Identification of PLOD2 as Telopeptide Lysyl Hydroxylase, an Important Enzyme in Fibrosis* (2003) (356)
Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci (2011) (355)
The MHC locus and genetic susceptibility to autoimmune and infectious diseases (2017) (350)
Genome-wide patterns and properties of de novo mutations in humans (2015) (345)
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction (2010) (345)
Host and Environmental Factors Influencing Individual Human Cytokine Responses (2016) (341)
Disease variants alter transcription factor levels and methylation of their binding sites (2015) (341)
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis (2013) (339)
Genetic variation in Toll-like receptors and disease susceptibility (2012) (332)
Identification of context-dependent expression quantitative trait loci in whole blood (2016) (332)
Genome-wide association analysis in primary sclerosing cholangitis. (2010) (323)
Failure of Embryonic Hematopoiesis andLethal Hemorrhages in Mouse Embryos Heterozygousfor a Knocked-In Leukemia Gene CBFB–MYH11 (1996) (311)
Impact of commonly used drugs on the composition and metabolic function of the gut microbiota (2020) (305)
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
Genome-wide association study of intracranial aneurysm identifies three new risk loci (2010) (298)
CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy (2008) (297)
Gene expression analysis identifies global gene dosage sensitivity in cancer (2015) (295)
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. (1994) (295)
Genetic susceptibility to respiratory syncytial virus bronchiolitis is predominantly associated with innate immune genes. (2007) (287)
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation (2015) (285)
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression (2021) (284)
Susceptibility loci for intracranial aneurysm in European and Japanese populations (2008) (283)
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. (2012) (282)
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4 (1990) (270)
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect (2005) (268)
Human Disease-Associated Genetic Variation Impacts Large Intergenic Non-Coding RNA Expression (2013) (266)
Gut microbiota composition and functional changes in inflammatory bowel disease and irritable bowel syndrome (2018) (261)
Genetic and environmental influences interact with age and sex in shaping the human methylome (2016) (260)
The Genome of the Netherlands: design, and project goals (2013) (260)
Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP. (2008) (258)
High density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis (2014) (250)
Genome-wide association study identifies variants associated with autoimmune hepatitis type 1. (2014) (249)
The gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytes (2003) (249)
A Functional Genomics Approach to Understand Variation in Cytokine Production in Humans (2016) (238)
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. (2012) (238)
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis (2008) (232)
Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease (2011) (228)
Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases. (2007) (227)
Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci (2011) (224)
Unraveling the Regulatory Mechanisms Underlying Tissue-Dependent Genetic Variation of Gene Expression (2012) (224)
Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia. (1995) (218)
A novel role for XIAP in copper homeostasis through regulation of MURR1 (2004) (217)
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study (2007) (215)
Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-κB signalling (2009) (211)
ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy (2013) (208)
Large-scale association analyses identify host factors influencing human gut microbiome composition (2020) (206)
A Meta-Analysis of Genome-Wide Association Scans Identifies IL18RAP, PTPN2, TAGAP, and PUS10 As Shared Risk Loci for Crohn's Disease and Celiac Disease (2011) (199)
Using genome‐wide pathway analysis to unravel the etiology of complex diseases (2009) (199)
Genetic evidence of assortative mating in humans (2017) (199)
Structural variation in the gut microbiome associates with host health (2019) (199)
Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci. (2012) (198)
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm (2010) (197)
Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17. (1999) (197)
Molecular prediction of disease risk and severity in a large Dutch Crohn’s disease cohort (2008) (196)
The Itaconate Pathway Is a Central Regulatory Node Linking Innate Immune Tolerance and Trained Immunity. (2019) (195)
Obesity genes identified in genome-wide association studies are associated with adiposity measures and potentially with nutrient-specific food preference. (2009) (192)
Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model (2018) (191)
The Copper Toxicosis Gene Product Murr1 Directly Interacts with the Wilson Disease Protein* (2003) (190)
When is a coeliac a coeliac? Report of a working group of the United European Gastroenterology Week in Amsterdam, 2001. (2001) (190)
Genetic Background of Celiac Disease and Its Clinical Implications (2008) (189)
Host Genetics and Gut Microbiome: Challenges and Perspectives. (2017) (188)
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. (2012) (187)
Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristics (2015) (180)
The influence of a short-term gluten-free diet on the human gut microbiome (2016) (180)
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease (2016) (179)
Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1. (2011) (177)
Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. (2014) (177)
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett’s esophagus (2012) (176)
Wnt signaling and Dupuytren's disease. (2011) (169)
Genome-Wide Joint Meta-Analysis of SNP and SNP-by-Smoking Interaction Identifies Novel Loci for Pulmonary Function (2012) (167)
MeDALL (Mechanisms of the Development of ALLergy): an integrated approach from phenotypes to systems medicine (2011) (166)
Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection. (2010) (166)
Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitisAn unusual case of ascites (2007) (160)
Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans (2013) (160)
Meta‐Analysis of Genome‐wide Linkage Studies in BMI and Obesity (2007) (159)
Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms (2008) (159)
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. (2012) (158)
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases (2015) (156)
Blood lipids influence DNA methylation in circulating cells (2016) (156)
DNA methylation in childhood asthma: an epigenome-wide meta-analysis. (2018) (153)
Genome‐wide association analysis in Primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4 (2013) (153)
Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant. (2000) (153)
A major non-HLA locus in celiac disease maps to chromosome 19. (2003) (152)
Analysis of HLA and non-HLA alleles can identify individuals at high risk for celiac disease. (2009) (150)
Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. (2007) (150)
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. (2014) (150)
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies. (2013) (149)
Autophagy Controls BCG-Induced Trained Immunity and the Response to Intravesical BCG Therapy for Bladder Cancer (2014) (149)
Meta-analyses on suspected chronic obstructive pulmonary disease genes: a summary of 20 years' research. (2009) (149)
Global phylogeography and ancient evolution of the widespread human gut virus crAssphage (2019) (148)
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy (1995) (147)
Loci influencing blood pressure identified using a cardiovascular gene-centric array. (2013) (145)
Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2. (2011) (145)
Innate Immune Activity Is Detected Prior to Seroconversion in Children With HLA-Conferred Type 1 Diabetes Susceptibility (2014) (141)
Genome-wide association analysis identifies six new loci associated with forced vital capacity (2014) (141)
Linking the Human Gut Microbiome to Inflammatory Cytokine Production Capacity (2016) (140)
Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis (2009) (140)
Inter-individual variability and genetic influences on cytokine responses to bacteria and fungi (2016) (139)
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes (2018) (139)
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits (2018) (139)
The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis. (2003) (138)
Common and different genetic background for rheumatoid arthritis and coeliac disease. (2009) (138)
From genome-wide association studies to disease mechanisms: celiac disease as a model for autoimmune diseases (2012) (137)
Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study (2016) (135)
Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism (2009) (135)
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci (2017) (135)
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. (2011) (133)
A large-scale genetic analysis reveals a strong contribution of the HLA class II region to giant cell arteritis susceptibility. (2015) (133)
Differential Effects of Environmental and Genetic Factors on T and B Cell Immune Traits (2016) (133)
Long-term dietary patterns are associated with pro-inflammatory and anti-inflammatory features of the gut microbiome (2021) (132)
Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population (2005) (129)
Card9 mediates intestinal epithelial cell restitution, T-helper 17 responses, and control of bacterial infection in mice. (2013) (129)
Confirmation of Multiple Crohn's Disease Susceptibility Loci in a Large Dutch–Belgian Cohort (2009) (128)
Three ulcerative colitis susceptibility loci are associated with primary sclerosing cholangitis and indicate a role for IL2, REL, and CARD9 (2011) (128)
Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease (2015) (127)
Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease (2013) (126)
Disruption of ROBO2 Is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux (2007) (125)
Complex nature of SNP genotype effects on gene expression in primary human leucocytes (2009) (125)
Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium. (1992) (125)
Relationship between gut microbiota and circulating metabolites in population-based cohorts (2019) (125)
Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants (2013) (124)
Association of variants of transcription factor 7-like 2 (TCF7L2) with susceptibility to type 2 diabetes in the Dutch Breda cohort (2006) (124)
Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization. (1991) (122)
Increased Activity of Hypoxia-Inducible Factor 1 Is Associated with Early Embryonic Lethality in Commd1 Null Mice (2007) (122)
A genetic perspective on coeliac disease. (2010) (122)
Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease. (2010) (120)
Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations (2015) (120)
Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations (2015) (120)
A supersized list of obesity genes (2009) (119)
Mapping of immune-mediated disease genes. (2013) (118)
Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity (2014) (118)
The FSHD‐linked locus D4F104S1 (p13E‐11) ON 4q35 has a homologue on 10qter (1995) (118)
Association of STAT4 with rheumatoid arthritis: a replication study in three European populations. (2008) (118)
Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19 (2012) (116)
Shared gut, but distinct oral microbiota composition in primary Sjögren's syndrome and systemic lupus erythematosus. (2019) (115)
Genetic and epigenetic regulation of gene expression in fetal and adult human livers (2014) (114)
Mutational Characterization of the Bile Acid Receptor TGR5 in Primary Sclerosing Cholangitis (2010) (114)
COMMD1 disrupts HIF-1alpha/beta dimerization and inhibits human tumor cell invasion. (2010) (114)
Clinical implications of shared genetics and pathogenesis in autoimmune diseases (2013) (114)
Characteristics of de novo structural changes in the human genome (2015) (113)
The influence of proton pump inhibitors and other commonly used medication on the gut microbiota (2017) (113)
Gut Microbial Associations to Plasma Metabolites Linked to Cardiovascular Phenotypes and Risk. (2019) (113)
Coeliac disease and autoimmune disease—genetic overlap and screening (2015) (112)
An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia (2008) (111)
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. (2014) (110)
Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23. (2010) (110)
Rewiring cellular metabolism via the AKT/mTOR pathway contributes to host defence against Mycobacterium tuberculosis in human and murine cells (2016) (109)
Defining the genetic contribution of type 2 diabetes mellitus (2001) (108)
Genetic variation in myosin IXB is associated with ulcerative colitis. (2006) (108)
ATG16L1 and IL23R Are Associated With Inflammatory Bowel Diseases but Not With Celiac Disease in The Netherlands (2008) (107)
Farnesoid X Receptor (FXR) Activation and FXR Genetic Variation in Inflammatory Bowel Disease (2011) (107)
Facioscapulohumeral muscular dystrophy in the dutch population (1995) (107)
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families. (1995) (106)
The 15q24/25 susceptibility variant for lung cancer and chronic obstructive pulmonary disease is associated with emphysema. (2010) (106)
Age-related accrual of methylomic variability is linked to fundamental ageing mechanisms (2016) (106)
Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea. (2009) (105)
Cell Specific eQTL Analysis without Sorting Cells (2014) (105)
Genetic studies to identify genes underlying menopausal age. (2005) (104)
Facioscapulohumeral muscular dystrophy in early childhood. (1994) (103)
Chronic Inflammation Permanently Reshapes Tissue-Resident Immunity in Celiac Disease (2019) (103)
Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis (2015) (100)
Pharmacomicrobiomics: a novel route towards personalized medicine? (2018) (99)
Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands' (2014) (98)
52 Genetic Loci Influencing Myocardial Mass. (2016) (98)
Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene. (2009) (98)
A high-quality human reference panel reveals the complexity and distribution of genomic structural variants (2016) (96)
Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux. (2007) (94)
Ubiquitin Ligase TRIM62 Regulates CARD9-Mediated Anti-fungal Immunity and Intestinal Inflammation. (2015) (94)
Polymorphisms Near TBX5 and GDF7 Are Associated With Increased Risk for Barrett’s Esophagus (2015) (93)
Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction. (2013) (93)
Environmental factors shaping the gut microbiome in a Dutch population (2022) (93)
Genetics in coeliac disease. (2005) (92)
Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays. (2005) (92)
MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease (2013) (91)
The long-term genetic stability and individual specificity of the human gut microbiome (2020) (90)
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12 (2014) (90)
Gut microbiota composition associated with stool consistency (2015) (89)
Factors that influence the volatile organic compound content in human breath (2017) (89)
Rapid Targeted Genomics in Critically Ill Newborns (2017) (89)
Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16. (1999) (88)
Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study. (2014) (88)
A microarray screen for novel candidate genes in coeliac disease pathogenesis (2004) (88)
Characterization of COMMD protein–protein interactions in NF-κB signalling (2006) (88)
Metabolomics Profile in Depression: A Pooled Analysis of 230 Metabolic Markers in 5283 Cases With Depression and 10,145 Controls (2020) (88)
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia (2017) (87)
HLA-DRB1*03:01 and HLA-DRB1*04:01 modify the presentation and outcome in autoimmune hepatitis type-1 (2015) (85)
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia (2014) (85)
Genetic variation in ICF syndrome: Evidence for genetic heterogeneity (2000) (84)
Analysis of 1135 gut metagenomes identifies sex-specific resistome profiles (2018) (84)
Profile of volatile organic compounds in exhaled breath changes as a result of gluten-free diet (2013) (84)
Molecular regulation of copper excretion in the liver (2004) (84)
The PreventCD Study design: towards new strategies for the prevention of coeliac disease (2010) (83)
CTLA4 is differentially associated with autoimmune diseases in the Dutch population (2005) (83)
The many faces of the copper metabolism protein MURR1/COMMD1. (2005) (83)
Gene expression profiling and phenotype analyses of S. cerevisiae in response to changing copper reveals six genes with new roles in copper and iron metabolism. (2005) (82)
Gene expression profiling of liver cells after copper overload in vivo and in vitro reveals new copper-regulated genes (2007) (82)
Understanding the complexity of IgE-related phenotypes from childhood to young adulthood: a Mechanisms of the Development of Allergy (MeDALL) seminar. (2012) (82)
MixupMapper: correcting sample mix-ups in genome-wide datasets increases power to detect small genetic effects (2011) (82)
Studying the gut virome in the metagenomic era: challenges and perspectives (2019) (82)
Validation of reported genetic risk factors for periodontitis in a large-scale replication study. (2013) (82)
Immunochip SNP array identifies novel genetic variants conferring susceptibility to candidaemia (2014) (80)
A Variant in LDLR Is Associated With Abdominal Aortic Aneurysm (2013) (79)
Integration of multi-omics data and deep phenotyping enables prediction of cytokine responses (2018) (78)
Heritability of non-HLA genetics in coeliac disease: a population-based study in 107 000 twins (2016) (78)
Population-specific genotype imputations using minimac or IMPUTE2 (2015) (78)
A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides (2013) (77)
Genome-wide Analysis of STAT3-Mediated Transcription during Early Human Th17 Cell Differentiation. (2017) (77)
Shared genetics in coeliac disease and other immune‐mediated diseases (2011) (77)
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways (2019) (77)
Interplay between genetics and the environment in the development of celiac disease: perspectives for a healthy life. (2001) (76)
Lack of association of MYO9B genetic variants with coeliac disease in a British cohort (2006) (76)
Skewed X-inactivation is common in the general female population (2018) (75)
Evidence in favor of the contribution of genes involved in the maintenance of the extracellular matrix of the arterial wall to the development of intracranial aneurysms. (2006) (75)
A liver‐specific long noncoding RNA with a role in cell viability is elevated in human nonalcoholic steatohepatitis (2017) (75)
Skewed X-inactivation is common in the general female population (2018) (75)
Genetic Susceptibility to Respiratory Syncytial Virus Bronchiolitis in Preterm Children Is Associated With Airway Remodeling Genes and Innate Immune Genes (2009) (72)
Genetic and microbial factors modulating the ubiquitin proteasome system in inflammatory bowel disease (2013) (71)
High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays. (2007) (70)
Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases (2018) (70)
Functional Characterization of Mutations in the Myosin Vb Gene Associated With Microvillus Inclusion Disease (2011) (70)
Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genes. (2000) (70)
Genetic Evidence for PLASMINOGEN as a Shared Genetic Risk Factor of Coronary Artery Disease and Periodontitis (2015) (69)
CTLA4+49 A/G and CT60 polymorphisms in Dutch coeliac disease patients (2004) (69)
Associations of autozygosity with a broad range of human phenotypes (2019) (68)
Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients (2004) (68)
Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck (2016) (68)
Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease (2008) (68)
Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome (2018) (68)
Liver-Specific Commd1 Knockout Mice Are Susceptible to Hepatic Copper Accumulation (2011) (67)
Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11. (1993) (65)
Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphrodite. (1998) (65)
Relevance of animal models for understanding mammalian copper homeostasis. (2008) (65)
Understanding Celiac Disease by Genomics. (2016) (65)
Genetic variants of RANTES are associated with serum RANTES level and protection for type 1 diabetes (2006) (65)
Multi-ethnic studies in complex traits (2011) (65)
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (65)
Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels (2014) (65)
Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's disease (1998) (64)
The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression (2011) (63)
Cost-effective HLA typing with tagging SNPs predicts celiac disease risk haplotypes in the Finnish, Hungarian, and Italian populations (2009) (63)
Gut microbial co-abundance networks show specificity in inflammatory bowel disease and obesity (2020) (63)
Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative trait loci influencing variation in human menopausal age. (2004) (63)
Common genes underlying asthma and COPD? Genome-wide analysis on the Dutch hypothesis (2014) (63)
Understanding human immune function using the resources from the Human Functional Genomics Project (2016) (63)
The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility. (2004) (62)
The MYO9B gene is a strong risk factor for developing refractory celiac disease. (2007) (62)
Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs (2016) (62)
The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases (2009) (62)
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations (2018) (62)
Differential association of two PTPN22 coding variants with Crohn’s disease and ulcerative colitis (2010) (61)
A large variety of clinical features and concomitant disorders in celiac disease - A cohort study in the Netherlands. (2016) (61)
A genome-wide scan in type 2 diabetes mellitus provides independent replication of a susceptibility locus on 18p11 and suggests the existence of novel Loci on 2q12 and 19q13. (2003) (61)
The Tip of the “Celiac Iceberg” in China: A Systematic Review and Meta-Analysis (2013) (61)
The importance of cohort studies in the post-GWAS era (2018) (61)
The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis. (2003) (60)
Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events (1993) (60)
An epigenome-wide association study meta-analysis of educational attainment (2017) (60)
Pleiotropic Effects of Lipid Genes on Plasma Glucose, HbA1c, and HOMA-IR Levels (2014) (60)
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter. (1992) (60)
Allele and haplotype frequencies for HLA-DQ in Iranian celiac disease patients. (2014) (60)
Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort. (2006) (60)
Global transcriptional responses of fission and budding yeast to changes in copper and iron levels: a comparative study (2007) (59)
A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis. (2017) (58)
Deleterious Alleles in the Human Genome Are on Average Younger Than Neutral Alleles of the Same Frequency (2013) (58)
Systematic annotation of celiac disease loci refines pathological pathways and suggests a genetic explanation for increased interferon-gamma levels. (2015) (58)
Design and Implementation of the International Genetics and Translational Research in Transplantation Network (2015) (56)
A strategy to search for common obesity and type 2 diabetes genes (2007) (56)
Localization of the ICF syndrome to chromosome 20 by homozygosity mapping. (1998) (56)
The RIG-I-like helicase receptor MDA5 (IFIH1) is involved in the host defense against Candida infections (2015) (56)
Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers. (2005) (56)
The genome revolution and its role in understanding complex diseases. (2014) (56)
Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study (2017) (55)
Identification of the chimeric protein product of the CBFB‐MYH11 fusion gene in inv(16) leukemia cells (1996) (54)
Lack of association between VEGF polymorphisms and ALS in a Dutch population (2005) (54)
Genetic variations in regulatory pathways of fatty acid and glucose metabolism are associated with obesity phenotypes: a population-based cohort study (2009) (54)
Nuclear‐Cytosolic Transport of COMMD1 Regulates NF‐κB and HIF‐1 Activity (2009) (54)
Gluten: a two-edged sword. Immunopathogenesis of celiac disease (2005) (54)
COMMD1 Promotes pVHL and O2-Independent Proteolysis of HIF-1α via HSP90/70 (2009) (53)
Association analysis of functional variants of the FcgRIIa and FcgRIIIa genes with type 1 diabetes, celiac disease and rheumatoid arthritis. (2007) (53)
Association of Polymorphisms and Haplotypes in the Elastin Gene in Dutch Patients With Sporadic Aneurysmal Subarachnoid Hemorrhage (2004) (52)
Co-expressed immune and metabolic genes in visceral and subcutaneous adipose tissue from severely obese individuals are associated with plasma HDL and glucose levels: a microarray study (2010) (52)
GAVIN: Gene-Aware Variant INterpretation for medical sequencing (2017) (52)
Exploring genetic determinants of plasma total cholesterol levels and their predictive value in a longitudinal study. (2010) (51)
Improving prediction of type 1 diabetes by testing non‐HLA genetic variants in addition to HLA markers (2014) (51)
Genetics of intracranial aneurysms (2005) (51)
Early onset facioscapulohumeral muscular dystrophy (1995) (51)
Genetic Analysis in A Dutch Study Sample Identifies More Ulcerative Colitis Susceptibility Loci and Shows Their Additive Role in Disease Risk (2010) (51)
Determining the association between adipokine expression in multiple tissues and phenotypic features of non-alcoholic fatty liver disease in obesity (2015) (50)
“Coelionomics”: towards understanding the molecular pathology of coeliac disease (2005) (50)
DeepSAGE Reveals Genetic Variants Associated with Alternative Polyadenylation and Expression of Coding and Non-coding Transcripts (2013) (49)
Dietary patterns and the risk of type 2 diabetes in overweight and obese individuals (2013) (49)
Novel childhood asthma genes interact with in utero and early-life tobacco smoke exposure☆ (2014) (49)
Differences in Genetic Background Between Active Smokers, Passive Smokers, and Non-Smokers With Crohn's Disease (2010) (49)
The emerging landscape of dynamic DNA methylation in early childhood (2017) (48)
Effects of Non-HLA Gene Polymorphisms on Development of Islet Autoimmunity and Type 1 Diabetes in a Population With High-Risk HLA-DR,DQ Genotypes (2012) (48)
Cu,Zn Superoxide Dismutase Maturation and Activity Are Regulated by COMMD1* (2010) (47)
The SPINK gene family and celiac disease susceptibility (2007) (47)
The region of common allelic losses in sporadic renal cell carcinoma is bordered by the loci D3S2 and THRB. (1991) (47)
Corrections: Linking the Human Gut Microbiome to Inflammatory Cytokine Production Capacity (vol 167, pg 1125, 2016) (2016) (46)
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry (2011) (46)
Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies (2015) (46)
Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pter. (1995) (46)
Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays. (2008) (45)
Transmission of de-novo mutation associated with facioscapulohumeral muscular dystrophy (1992) (45)
Lack of Association Between Genetic Variants at ACE2 and TMPRSS2 Genes Involved in SARS-CoV-2 Infection and Human Quantitative Phenotypes (2020) (45)
Common Variants in the Type 2 Diabetes KCNQ1 Gene Are Associated with Impairments in Insulin Secretion During Hyperglycaemic Glucose Clamp (2012) (45)
Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases. (1996) (45)
Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions. (1994) (45)
Characterization of COMMD protein-protein interactions in NF-kappaB signalling. (2006) (44)
Detection of stable community structures within gut microbiota co-occurrence networks from different human populations (2018) (44)
Genetics of celiac disease. (2015) (44)
Author Correction: Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project (2022) (44)
Association of variants in IL2RA with progression of joint destruction in rheumatoid arthritis. (2013) (44)
The Versican Gene and the Risk of Intracranial Aneurysms (2006) (43)
Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels (2015) (43)
Dysbiosis of the buccal mucosa microbiome in primary Sjögren’s syndrome patients (2018) (43)
A comparison of genetic chromosomal loci for intracranial, thoracic aortic, and abdominal aortic aneurysms in search of common genetic risk factors. (2008) (42)
Volatile organic compounds in breath as markers for irritable bowel syndrome: a metabolomic approach (2016) (42)
Genetics of immune-mediated disorders: from genome-wide association to molecular mechanism. (2014) (42)
Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD). (1992) (41)
WNT2 locus is involved in genetic susceptibility of Peyronie's disease. (2012) (41)
Integrated Genomics of Crohn’s Disease Risk Variant Identifies a Role for CLEC12A in Antibacterial Autophagy (2015) (40)
The Copper Metabolism MURR1 Domain Protein 1 (COMMD1) Modulates the Aggregation of Misfolded Protein Species in a Client-Specific Manner (2014) (40)
Single-Cell RNA Sequencing of Blood and Ileal T Cells From Patients With Crohn's Disease Reveals Tissue-Specific Characteristics and Drug Targets. (2019) (40)
Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements. (1993) (39)
Evaluation of CADD Scores in Curated Mismatch Repair Gene Variants Yields a Model for Clinical Validation and Prioritization (2015) (39)
Maintenance of macrophage transcriptional programs and intestinal homeostasis by epigenetic reader SP140 (2017) (39)
DNA methylation signatures of educational attainment (2018) (39)
HNF4&agr; and CDH1 are associated with ulcerative colitis in a Dutch cohort (2011) (39)
Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes (2011) (39)
A functional candidate screen for coeliac disease genes (2006) (39)
Genes and outcome after aneurysmal subarachnoid haemorrhage (2005) (39)
Neutrophil recruitment and barrier impairment in celiac disease: a genomic study. (2007) (38)
Contrasting the Genetic Background of Type 1 Diabetes and Celiac Disease Autoimmunity (2015) (38)
Genetic and Microbial Associations to Plasma and Fecal Bile Acids in Obesity Relate to Plasma Lipids and Liver Fat Content. (2020) (38)
Heritability estimates for 361 blood metabolites across 40 genome-wide association studies (2020) (38)
Copper metabolism domain-containing 1 represses genes that promote inflammation and protects mice from colitis and colitis-associated cancer. (2014) (37)
Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association (2007) (37)
Understanding the molecular basis of celiac disease: What genetic studies reveal (2006) (37)
MYO9B gene polymorphisms are associated with autoimmune diseases in Spanish population. (2007) (37)
Type 2 Diabetes Mellitus: New Genetic Insights will Lead to New Therapeutics (2009) (37)
Functional and Genomic Architecture of Borrelia burgdorferi-Induced Cytokine Responses in Humans. (2016) (37)
A Genomewide Screen in a Four-Generation Dutch Family with Celiac Disease: Evidence for Linkage to Chromosomes 6 and 9 (2004) (37)
Comprehensive fine mapping of chr12q12-14 and follow-up replication identify activin receptor 1B (ACVR1B) as a muscle strength gene (2011) (36)
Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis (2011) (36)
Genomewide Linkage in a Large Dutch Family With Intracranial Aneurysms: Replication of 2 Loci for Intracranial Aneurysms to Chromosome 1p36.11-p36.13 and Xp22.2-p22.32 (2008) (36)
A systems genomics approach identifies SIGLEC15 as a susceptibility factor in recurrent vulvovaginal candidiasis (2019) (36)
IL12B and IRF1 gene polymorphisms and susceptibility to celiac disease. (2003) (35)
Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant (2013) (35)
The Inter-Relationship of Platelets with Interleukin-1β-Mediated Inflammation in Humans (2018) (35)
Genes in the Ureteric Budding Pathway: Association Study on Vesico-Ureteral Reflux Patients (2012) (34)
A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol (2011) (34)
A novel biomarker panel for irritable bowel syndrome and the application in the general population (2016) (34)
Association study of the IL18RAP locus in three European populations with coeliac disease. (2009) (33)
Core binding factor beta-smooth muscle myosin heavy chain chimeric protein involved in acute myeloid leukemia forms unusual nuclear rod-like structures in transformed NIH 3T3 cells. (1996) (33)
Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered (1999) (33)
Genetic mapping of the dentinogenesis imperfecta type II locus. (1995) (32)
Context-specific effects of genetic variants associated with autoimmune disease (2017) (32)
Epigenome-wide Association Study of Attention-Deficit/Hyperactivity Disorder Symptoms in Adults (2019) (32)
Genes influencing coagulation and the risk of aneurysmal subarachnoid hemorrhage, and subsequent complications of secondary cerebral ischemia and rebleeding (2009) (31)
Celiac disease: moving from genetic associations to causal variants (2011) (31)
TMEM258 Is a Component of the Oligosaccharyltransferase Complex Controlling ER Stress and Intestinal Inflammation. (2016) (31)
Autoimmune Disease in First-Degree Relatives and Spouses of Individuals With Celiac Disease. (2015) (31)
Deconvolution of bulk blood eQTL effects into immune cell subpopulations (2019) (31)
TEAM: a tool for the integration of expression, and linkage and association maps (2004) (30)
Evolutionary and Functional Analysis of Celiac Risk Loci Reveals SH 2 B 3 as a Protective Factor against Bacterial Infection (2010) (30)
GWAS as a Driver of Gene Discovery in Cardiometabolic Diseases (2015) (30)
Systematic review with meta‐analysis: the risks of proton pump inhibitors during pregnancy (2020) (30)
Meta-analysis inmore than 17 , 900 cases of ischemic stroke reveals a novel association at 12 q 24 . 12 (30)
A large candidate-gene association study suggests genetic variants at IRF5 and PRDM1 to be associated with aggressive periodontitis. (2014) (30)
Large-scale plasma metabolome analysis reveals alterations in HDL metabolism in migraine (2019) (30)
Lifelines COVID-19 cohort: investigating COVID-19 infection and its health and societal impacts in a Dutch population-based cohort (2021) (29)
A GWAS meta‐analysis from 5 population‐based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome (2018) (29)
Association of the TGF-β receptor genes with abdominal aortic aneurysm (2010) (29)
The genetics of East African populations: a Nilo-Saharan component in the African genetic landscape (2015) (29)
A system biology perspective on environment-host-microbe interactions. (2018) (29)
Genetic variation in the hypothalamic pathways and its role on obesity (2009) (29)
Refined genetic and comparative physical mapping of the canine copper toxicosis locus (2000) (29)
Is MYO9B the missing link between schizophrenia and celiac disease? (2008) (29)
Apple or pear: size and shape matter. (2015) (29)
Copy number variants on the X chromosome in women with primary ovarian insufficiency. (2011) (29)
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour (2021) (29)
Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis. (2016) (28)
Susceptibility to Chronic Mucus Hypersecretion, a Genome Wide Association Study (2011) (28)
Upstream transcription factor 1 (USF1) in risk of type 2 diabetes: association study in 2000 Dutch Caucasians. (2008) (28)
Identification of TUB as a novel candidate gene influencing body weight in humans. (2006) (28)
Molecular genetics of facioscapulohumeral muscular dystrophy (1993) (27)
Association analysis of MYO9B gene polymorphisms and inflammatory bowel disease in a Norwegian cohort. (2006) (27)
Anti-inflammatory Gut Microbial Pathways Are Decreased During Crohn’s Disease Exacerbations (2019) (27)
Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations. (2014) (27)
Association Analysis of Genes Involved in the Maintenance of the Integrity of the Extracellular Matrix with Intracranial Aneurysms in a Japanese Cohort (2009) (26)
Non-Indian childhood cirrhosis. (1999) (26)
Inflammatory bowel disease and celiac disease: overlaps in the pathology and genetics, and their potential drug targets. (2009) (26)
Eosinophil Count Is a Common Factor for Complex Metabolic and Pulmonary Traits and Diseases: The LifeLines Cohort Study (2016) (26)
Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q (2008) (26)
Apparent primary follicle-stimulating hormone deficiency is a rare cause of treatable male infertility. (2004) (26)
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes (2021) (25)
Polymorphisms of the TUB Gene Are Associated with Body Composition and Eating Behavior in Middle-Aged Women (2008) (25)
THEMIS and PTPRK in celiac intestinal mucosa: coexpression in disease and after in vitro gliadin challenge (2013) (25)
Novel genes for airway wall thickness identified with combined genome-wide association and expression analyses. (2015) (25)
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci (2015) (25)
Haplotype‐based analysis of ulcerative colitis risk loci identifies both IL2 and IL21 as susceptibility genes in Han Chinese (2011) (24)
Linkage study of 14 candidate genes and loci in four large Dutch families with vesico-ureteral reflux (2007) (24)
Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes (2015) (24)
Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24–25 (2005) (24)
HHEX gene polymorphisms are associated with type 2 diabetes in the Dutch Breda cohort (2008) (24)
MICA marks additional risk factors for Type 1 diabetes on extended HLA haplotypes: an association and meta-analysis. (2007) (23)
Correlation of Genetic Risk and Messenger RNA Expression in a Th17/IL23 Pathway Analysis in Inflammatory Bowel Disease (2014) (23)
Celiac Disease Genetics: Past, Present and Future Challenges (2014) (23)
Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2 (2016) (23)
Identification of the chimeric protein product of the CBFB-MYH11 fusion gene in inv(16) leukemia cells. (1996) (22)
Gene expression analysis predicts insect venom anaphylaxis in indolent systemic mastocytosis (2011) (22)
Narrow-sense heritability estimation of complex traits using identity-by-descent information (2017) (22)
A linear mixed-model approach to study multivariate gene–environment interactions (2018) (21)
Dissecting the genetics of chronic mucus hypersecretion in smokers with and without COPD (2014) (21)
Population-wide diversity and stability of serum antibody epitope repertoires against human microbiota (2021) (21)
Characterization of gut microbial structural variations as determinants of human bile acid metabolism (2021) (21)
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease (2019) (21)
Evaluation of European coeliac disease risk variants in a north Indian population (2014) (20)
An integrative genomics approach identifies novel pathways that influence candidaemia susceptibility (2017) (20)
Genome-wide analysis shows no genomic predictors of ovarian response to stimulation by exogenous FSH for IVF. (2011) (20)
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms (2016) (20)
Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region. (1993) (20)
Metabolic Age Based on the BBMRI-NL 1H-NMR Metabolomics Repository as Biomarker of Age-related Disease (2020) (20)
A Genome-Wide Functional Genomics Approach Identifies Susceptibility Pathways to Fungal Bloodstream Infection in Humans. (2019) (20)
COMMD1: A Novel Protein Involved in the Proteolysis of Proteins (2007) (19)
Whole exome sequencing analyses reveal gene–microbiota interactions in the context of IBD (2020) (19)
GAVIN: Gene-Aware Variant INterpretation for medical sequencing (2016) (19)
Hypothesis-free identification of modulators of genetic risk factors (2015) (19)
Gene expression analysis in predicting the effectiveness of insect venom immunotherapy. (2010) (19)
A Meta-Analysis of Genome-Wide Association Scans Identifies IL 18 RAP , PTPN 2 , TAGAP , and PUS 10 As Shared Risk Loci for Crohn ’ s Disease and Celiac Disease (2011) (19)
A locus at 7p14.3 predisposes to refractory celiac disease progression from celiac disease (2018) (19)
Habitual diet and diet quality in Irritable Bowel Syndrome: A case‐control study (2017) (18)
Shared DNA methylation signatures in childhood allergy: the MeDALL study. (2020) (18)
Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability. (2010) (18)
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north–south gradient among Europeans (2016) (18)
Author Correction: Gut microbiome structure and metabolic activity in inflammatory bowel disease (2019) (18)
Association of Crohn's disease-associated NOD2 variants with intestinal failure requiring small bowel transplantation and clinical outcomes (2010) (18)
Exome sequencing in a family segregating for celiac disease (2011) (18)
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS (2022) (18)
Ciliary Genes Are Down-Regulated in Bronchial Tissue of Primary Ciliary Dyskinesia Patients (2014) (18)
The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus (1993) (18)
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markers. (1993) (18)
Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5 (1990) (17)
No genetic association of the human prolyl endopeptidase gene in the Dutch celiac disease population. (2005) (17)
A systematic analysis highlights multiple long non-coding RNAs associated with cardiometabolic disorders (2018) (17)
Influence of the microbiome, diet and genetics on inter-individual variation in the human plasma metabolome (2022) (17)
Variance-component analysis of obesity in type 2 diabetes confirms loci on chromosomes 1q and 11q. (2003) (17)
Integration of metabolomics, genomics, and immune phenotypes reveals the causal roles of metabolites in disease (2021) (17)
Association of FcgR2a, but not FcgR3a, with inflammatory bowel diseases across three Caucasian populations† (2010) (17)
Meta-analysis fine-mapping is often miscalibrated at single-variant resolution (2022) (17)
Anticipation and phenotype in familial intracranial aneurysms (2004) (16)
Habitual dietary intake of IBD patients differs from population controls: a case–control study (2020) (16)
BASIC-ALIMENTARY TRACT Genetic Variation in Myosin IXB Is Associated With Ulcerative Colitis (2006) (16)
Stability of the human gut virome and effect of gluten-free diet. (2021) (16)
Molecular mechanisms of the adaptive, innate and regulatory immune responses in the intestinal mucosa of celiac disease patients (2005) (16)
The Dutch Microbiome Project defines factors that shape the healthy gut microbiome (2020) (15)
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35 (1995) (15)
Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
Expressing the Differences between Crohn Disease and Ulcerative Colitis (2005) (15)
Healthy cotwins share gut microbiome signatures with their inflammatory bowel disease twins and unrelated patients. (2021) (15)
Genome-wide identification of directed gene networks using large-scale population genomics data (2017) (14)
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation (2018) (14)
A characterization of cis- and trans-heritability of RNA-Seq-based gene expression (2019) (14)
Celiac disease-on-chip: Modeling a multifactorial disease in vitro (2019) (14)
Meta-Analysis of Genome-Wide Linkage Studies in Celiac Disease (2009) (14)
Association analysis of myosin IXB and type 1 diabetes. (2010) (14)
Changes in gene expression caused by insect venom immunotherapy responsible for the long-term protection of insect venom-allergic patients. (2011) (14)
Polymorphisms Near TBX 5 and GDF 7 Are Associated With Increased Risk for Barrett ’ s Esophagus (14)
Genetic Association of a Gain‐of‐Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet’s Disease (2021) (14)
Novel celiac disease genetic determinants related to the immune response (2009) (14)
The exon 16–3t variant of the sulphonylurea receptor gene is not a risk factor for Type II diabetes mellitus in the Dutch Breda cohort (2000) (14)
An introduction to LifeLines DEEP: study design and baseline characteristics (2014) (14)
Erratum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 (Nature Genetics (2011) 43 (246-252)) (2011) (13)
Association Analysis of Genetic Variants in the Myosin IXB Gene in Acute Pancreatitis (2013) (13)
How to kickstart a national biobanking infrastructure – experiences and prospects of BBMRI-NL (2012) (13)
A GWAS meta-analysis suggests roles for xenobiotic metabolism and ion channel activity in the biology of stool frequency (2016) (13)
Association Study of Single Nucleotide Polymorphisms on Chromosome 19q13 With Abdominal Aortic Aneurysm (2010) (13)
Variants in Neuropeptide Y Receptor 1 and 5 Are Associated with Nutrient-Specific Food Intake and Are Under Recent Selection in Europeans (2009) (13)
Genome‐wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch population (2003) (13)
Mendelian randomization while jointly modeling cis genetics identifies causal relationships between gene expression and lipids (2020) (13)
The Composition and Metabolic Potential of the Human Small Intestinal Microbiota Within the Context of Inflammatory Bowel Disease (2021) (12)
Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q. (1999) (12)
Systematic Prioritization of Candidate Genes in Disease Loci Identifies TRAFD1 as a Master Regulator of IFNγ Signaling in Celiac Disease (2021) (12)
Indirect molecular diagnosis of copper toxicosis in Bedlington terriers is complicated by haplotype diversity. (2003) (12)
Genetics of human gut microbiome composition (2020) (12)
Impact on parents of HLA-DQ2/DQ8 genotyping in healthy children from coeliac families (2014) (12)
Genes involved in the transforming growth factor beta signalling pathway and the risk of intracranial aneurysms (2007) (12)
An integrative genomics approach identifies KDM4 as a modulator of trained immunity (2021) (11)
Discovery, diversity, and functional associations of crAss-like phages in human gut metagenomes from four Dutch cohorts (2022) (11)
Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies (2020) (11)
Prokaryotic diversity of the Saccharomyces cerevisiae Atx1p-mediated copper pathway (2004) (11)
Anticipation in familial intracranial aneurysms in consecutive generations (2003) (10)
Immunogenetics of Celiac Disease (2014) (10)
Functional Annotation of Genetic Loci Associated With Sepsis Prioritizes Immune and Endothelial Cell Pathways (2019) (10)
Functional polymorphism in IL12B promoter site is associated with ulcerative colitis. (2011) (10)
Genome-wide Analysis of STAT 3-Mediated Transcription during Early Human Th 17 Cell Differentiation (2017) (10)
Role of the gut microbiome in mediating lactose intolerance symptoms (2021) (10)
Long Non-Coding RNAs Involved in Progression of Non-Alcoholic Fatty Liver Disease to Steatohepatitis (2021) (10)
The downstream modulator of interferon-γ, STAT1 is not genetically associated to the Dutch coeliac disease population (2006) (10)
Association of DLG5 variants with gluten-sensitive enteropathy (2008) (9)
Practical Barriers and Facilitators Experienced by Patients, Pharmacists and Physicians to the Implementation of Pharmacogenomic Screening in Dutch Outpatient Hospital Care—An Explorative Pilot Study (2020) (9)
Genome-Wide Association Study Identifies Novel Colony Stimulating Factor 1 Locus Conferring Susceptibility to Cryptococcosis in Human Immunodeficiency Virus-Infected South Africans (2020) (9)
Association of the Jun dimerization protein 2 gene with intracranial aneurysms in Japanese and Korean cohorts as compared to a Dutch cohort (2010) (9)
The Transforming Growth Factor-β Receptor Genes and the Risk of Intracranial Aneurysms (2012) (9)
The tissue transglutaminase gene is not a primary factor predisposing to celiac disease (2001) (9)
The tissue transglutaminase gene is not a primary factor predisposing to celiac disease. (2001) (9)
SLC39A8 missense variant is associated with Crohn's disease but does not have a major impact on gut microbiome composition in healthy subjects (2019) (9)
Impact of Global Fxr Deficiency on Experimental Acute Pancreatitis and Genetic Variation in the FXR Locus in Human Acute Pancreatitis (2014) (9)
Tissue alarmins and adaptive cytokine induce dynamic and distinct transcriptional responses in tissue-resident intraepithelial cytotoxic T lymphocytes (2020) (9)
The Intracranial Aneurysm Susceptibility Genes HSPG2 and CSPG2 Are Not Associated With Abdominal Aortic Aneurysm (2010) (9)
Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations (2011) (9)
Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpura (2016) (9)
University of Groningen Polymorphisms of the TUB Gene Are Associated with Body Composition and Eating Behavior in Middle-Aged Women (2007) (9)
Leukocyte-Released Mediators in Response to Both Bacterial and Fungal Infections Trigger IFN Pathways, Independent of IL-1 and TNF-α, in Endothelial Cells (2019) (9)
Low fertility and the risk of type 2 diabetes in women (2011) (9)
Identification and prioritization of NUAK1 and PPP1CC as positional candidate loci for skeletal muscle strength phenotypes. (2011) (9)
Lifelines NEXT: a prospective birth cohort adding the next generation to the three-generation Lifelines cohort study (2020) (9)
Non-classical clinical presentation at diagnosis by male celiac disease patients of older age. (2020) (8)
Linkage and apparent heterogeneity in proximal spinal muscular atrophies (1993) (8)
Variants in the 15q24/25 Locus Associate with Lung Function Decline in Active Smokers (2013) (8)
Genetic and functional analysis of pyroglutamyl-peptidase I in coeliac disease (2006) (8)
Age at natural menopause is not linked with the follicle-stimulating hormone receptor region: a sib-pair study. (2004) (7)
Characterization and chromosomal localization of five canine ATOX1 pseudogenes (2001) (7)
Comment on: Barker et al. (2008) Two Single Nucleotide Polymorphisms Identify the Highest-Risk Diabetes HLA Genotype: Diabetes 57:3152–3155, 2008 (2009) (7)
Predicting biological age based on the BBMRI-NL 1H-NMR metabolomics repository (2019) (7)
Joint analysis reveals shared autoimmune disease associations and identifies common mechanisms (2021) (7)
Facioscapulohumeral muscular dystrophy: The impact of genetic research (1993) (7)
Gut microbiome dysbiosis is associated with increased mortality after solid organ transplantation (2022) (7)
Early onset facioscapulohumeral muscular dystrophy. (1995) (7)
[Dutch government invests in existing biobanks]. (2010) (7)
Disruption of ROBO2 is associated with congenital anomalies of kidney and urinary tract and confers risk of vesicoureteric reflux. (2007) (7)
3 Population-specific genotype imputations using minimac or IMPUTE 2 (2018) (7)
PTPN1 polymorphisms are associated with total and low-density lipoprotein cholesterol (2010) (7)
Circulating miRNAs as Potential Biomarkers for Celiac Disease Development (2021) (7)
Integrated fecal microbiome–metabolome signatures reflect stress and serotonin metabolism in irritable bowel syndrome (2022) (7)
Systematic genotype–phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autism (2010) (6)
Dutch patients with glycogen storage disease type II show common ancestry for the 525delT and del exon 18 mutations (2001) (6)
Erratum: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (American Journal of Human Genetics (2012) 90 (410-425)) (2012) (6)
Erratum: Genome-wide association identifies multiple ulcerative colitis susceptibility loci (2011) (6)
Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability (2021) (5)
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD) (1994) (5)
Correction: Corrigendum: Inter-individual variability and genetic influences on cytokine responses to bacteria and fungi (2016) (5)
Genome variation in precision medicine (2016) (5)
Relationship of β2-Adrenergic Receptor Polymorphism With Obesity in Type 2 Diabetes (2003) (5)
Gut microbiome structure and metabolic activity in inflammatory bowel disease (2018) (5)
Celiac disease: update from the 14th International Celiac Disease Symposium 2011 (2011) (5)
Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts (2023) (5)
Molecular diagnosis of celiac disease: are we there yet? (2008) (5)
Using genetic information for the identification, classification and treatment of Crohn’s disease: are we there yet? (2008) (5)
Genetic, parental and lifestyle factors influence telomere length (2021) (5)
Corrigendum: Multiple common variants for celiac disease influencing immune gene expression (2010) (5)
204 Genetic and Mucosal Expression Analysis Shows Important Roles for JAK2 and MST1 in the Pathogenesis of Ulcerative Colitis and Identifies More Susceptibility Loci (2009) (4)
No Evidence in a Large UK Collection for Celiac Disease Risk Variants Reported by a Spanish Study (2008) (4)
A Combined mRNA- and miRNA-Sequencing Approach Reveals miRNAs as Potential Regulators of the Small Intestinal Transcriptome in Celiac Disease (2021) (4)
Male-Specific Association between a γ-Secretase Polymorphism and Premature Coronary Atherosclerosis (2008) (4)
Erratum: Meta-analyses on suspected chronic obstructive pulmonary disease genes: a summary of 20 years' research. (2010) (4)
A combined genetics and genomics approach to unravelling molecular pathways in coeliac disease. (2005) (4)
Systematic prioritization of candidate genes in disease loci identifies TRAFD1 as a master regulator of IFNγ signalling in celiac disease (2020) (4)
Potential impact of celiac disease genetic risk factors on T cell receptor signaling in gluten-specific CD4+ T cells (2021) (4)
A high-quality reference panel reveals the complexity and distribution of structural genome changes in a human population (2016) (4)
A novel Mendelian randomization method identifies causal relationships between gene expression and low-density lipoprotein cholesterol levels (2019) (4)
In-depth characterization of the serum antibody epitope repertoire in inflammatory bowel disease using phage-displayed immunoprecipitation sequencing (2021) (4)
Family matters: gene regulation by metal-dependent transcription factors (2005) (4)
No association between gluten sensitivity and amyotrophic lateral sclerosis (2017) (4)
Occupational exposure to gases/fumes and mineral dust affect DNA methylation levels of genes regulating expression (2019) (4)
Non-Indian Childhood Cirrhosis: Using a Founder Population to Identify the Underlying Genetic Defect (2002) (4)
WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene (2019) (4)
Genome-wide analysis of constitutional DNA methylation in familial melanoma (2020) (3)
-to: Shafrir E, Raz I (2003) - For debate. Diabetes: mellitus or lipidus? Diabetologia 46: 433-440 (2003) (3)
Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35 (1995) (3)
Genetic Insights Through Genome Wide Association Studies in Type 2 Diabetes Mellitus will Lead to New Therapeutics (2013) (3)
University of Groningen Mutations in Potassium Channel KCND 3 Cause Spinocerebellar Ataxia Type 19 (2012) (3)
Wnt Signaling and Dupuytren's Disease REPLY (2011) (3)
An epigenome-wide association study of educational attainment (n = 10,767) (2017) (3)
Several COMMD proteins interact with ATP7B; possible candidate genes for hepatic copper overload disorders with unknown etiology (2006) (3)
Patient attitudes towards faecal sampling for gut microbiome studies and clinical care reveal positive engagement and room for improvement (2019) (3)
No Association of PTPN1 Polymorphisms With Macronutrient Intake and Measures of Adiposity (2008) (3)
Dinucleotide repeat polymorphism adjacent to the ANT1 gene on 4q35. (1992) (3)
Genetic, environmental and intrinsic determinants of the human antibody epitope repertoire (2021) (3)
Stability of the Human Gut Virome and Effect of Gluten-Free Diet (2020) (3)
Impact of commonly used drugs on the composition and metabolic function of the gut microbiota (2020) (3)
[Genetic background of diabetes mellitus type 2]. (2009) (3)
Genotype-phenotype analysis across 130 422 genetic variants identifies RSPO3 as the first genome-wide significant modifier gene in primary sclerosing cholangitis (2016) (3)
Comment on: Perry et al. (2009) Interrogating Type 2 Diabetes Genome-Wide Association Data Using a Biological Pathway-Based Approach. Diabetes;58:1463–1467 (2009) (3)
Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity (2014) (2)
DELIMITATION OF THE REGION OF COMMON ALLELIC LOSSES ON 3P IN SPORADIC RENAL-CELL CARCINOMA (1991) (2)
Genomewide high density SNP-CGH reveals several new deletion copy number variants on the x chromosome in POF patients. (2008) (2)
87 Gene-Microbiome Interactions Underlying the Onset and the Clinical Phenotypes of Inflammatory Bowel Disease (2016) (2)
Discovery, diversity and functional associations of crAss-like phages in human gut metagenomes from four Dutch cohorts (2021) (2)
Localization of ICF syndrome by homozygosity mapping (1998) (2)
HLA and non-HLA genes in celiac disease. (2008) (2)
Association of STAT4 gene with rheumatoid arthritis (2008) (2)
Genome-Wide Association Studies Identify CHRNA5/3 and HTR4 in the Development of Airﬂow Obstruction (2012) (2)
A Clinical Genetic Study of Familial Dupuytren’s Disease in the Netherlands (2012) (2)
GWAS defines pathogenic signaling pathways and prioritizes drug targets for IgA nephropathy (2021) (2)
Relationship of beta2-adrenergic receptor polymorphism with obesity in type 2 diabetes. (2003) (2)
Lodewijk A. Sandkuijl, M.D. (July 31, 1953–December 4, 2002). (2003) (2)
17. Regional mapping of the facioscapulohumeral muscular dystrophy gene on 4q35: linkage analysis of the International Consortium (1992) (2)
Erfelijke factoren bij coeliakie (2004) (2)
Correction: Common Variants in the Type 2 Diabetes KCNQ1 Gene Are Associated with Impairments in Insulin Secretion During Hyperglycaemic Glucose Clamp (2012) (2)
Overheid investeert fors in bestaande biobanken (2010) (2)
Transcriptional profiles predict treatment outcome in patients with tuberculosis and diabetes at diagnosis and at two weeks after initiation of anti-tuberculosis treatment (2022) (2)
A combination of fecal calprotectin and human beta-defensin 2 facilitates diagnosis and monitoring of inflammatory bowel disease (2021) (2)
From LD-based mapping to GWAS (2021) (2)
A large, nationwide, case-control study for the association of DLG5, OCTN1/2 and CARD15 with inflammatory bowel diseases in the Netherlands (2008) (2)
Interethnic analyses of blood pressure loci in populations of East Asian and European descent (2018) (2)
snpEnrichR: analyzing co-localization of SNPs and their proxies in genomic regions (2018) (2)
Correction: DeepSAGE Reveals Genetic Variants Associated with Alternative Polyadenylation and Expression of Coding and Non-coding Transcripts (2013) (2)
Identification Of Novel Genes That Contribute To Both Asthma And COPD, With Replication In A Large Population-Based Cohort (2011) (1)
A systematic analysis highlights multiple long non-coding RNAs associated with cardiometabolic disorders (2018) (1)
Author Correction: Gut microbiome structure and metabolic activity in inflammatory bowel disease (2019) (1)
The influence of a short-term gluten-free diet on the human gut microbiome (2016) (1)
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy. (1995) (1)
The Shared Genetics of Immune-related Diseases - What Genome-wide Association Studies Reveal (2009) (1)
University of Groningen A Genome-Wide Screen for Interactions Reveals a New Locus on 4 p 15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol (2011) (1)
An Insertion of Eight Amino Acids in HLA-DQA1 and Three Amino Acid Substitutions in HLA-DQA1 and HLA-DQB1 Confer Risk to Idiopathic Achalasia (2013) (1)
Genetic and epigenetic regulation of gene expression in fetal and adult human livers (2014) (1)
Phenotypic and genetic factors are associated with absence of cardiomyopathy symptoms in PLN c.40_42delAGA carriers (2022) (1)
Changing Views on Living Organisms (2013) (1)
Association of the protein-tyrosine phosphatase nonreceptor type substrate 1 (PTPNS1) gene with inflammatory bowel disease. (2011) (1)
The protease genes CYLD and USP40 are associated with Crohn's disease: results from a European Consortium (2011) (1)
LB-PO-865 ASSOCIATION OF VARIANTS IN UPSTREAM TRANSCRIPTION FACTOR 1 (USF1) WITH TYPE 2 DIABETES IN THE DUTCH POPULATION (2007) (1)
Skewed X-inactivation is common in the general female population (2018) (1)
Skewed X-inactivation is common in the general female population (2018) (1)
Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels (2015) (1)
Linkage and association analysis of the tissue transglutaminase gene: the TTG gene is not involved in celiac disease (2001) (1)
OR7-002 – Pyrin 577 mutations in dominant autoinflammation (2013) (1)
Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations (2022) (1)
iPSC-derived organ-on-a-chip models for personalized human genetics and pharmacogenomics studies. (2023) (1)
Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inference (2020) (1)
Genome-wide association study of coronary and aortic calci fi cation implicates risk loci for coronary artery disease and myocardial infarction (1)
OP19 Genetic and functional evidence for a role for CYLD in Crohn's disease: Results from a European consortium (2012) (1)
University of Groningen Genome-wide association studies identify CHRNA 5 / 3 and HTR 4 in the development of airflow obstruction (2017) (1)
NOVEL SUSCEPTIBILITY LOCI FOR PRIMARY SCLEROSING CHOLANGITIS IDENTIFIED BY GENOME-WIDE ASSOCIATION AND REPLICATION ANALYSIS (2011) (1)
Microbial Impact on Plasma Metabolites is Linked to the Cardiovascular Risk and Phenotypes (2018) (1)
Author Correction: Heritability estimates for 361 blood metabolites across 40 genome-wide association studies (2020) (1)
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (1)
The Versican Gene and the Risk of Intracranial Aneurysms: ISC 130 (2006) (1)
The RIG-I-like helicase receptor MDA5 (IFIH1) is involved in the host defense against Candida infections (2015) (1)
Integration of metabolomics, genomics, and immune phenotypes reveals the causal roles of metabolites in disease (2021) (1)
Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18)) (2012) (1)
CTLA4 is differently associated with autoimmune diseases in the Dutch population (2005) (1)
Sa1677 HLA-DRB1*0301 and HLA-DRB1*0401 Modify the Presentation and Outcome in Autoimmune Hepatitis Type-1 (2015) (1)
Frailty and risk of hospitalization from COVID-19 infection among older adults: evidence from the Dutch Lifelines COVID-19 Cohort study (2022) (1)
Loci influencing blood pressure identified using a cardiovascular gene-centric array (Correction to Ganesh et al. 22 (8): 1663) (2013) (1)
Association of variants in upstream transcription factor I (USF1) with type 2 diabetes in the Dutch population (2007) (1)
Corrigendum: Genetic Analysis in A Dutch Study Sample Identifies More Ulcerative Colitis Susceptibility Loci and Shows Their Additive Role in Disease Risk (2010) (1)
Human Genetics: Questions, Challenges, and the Future (2017) (1)
Genome-wide association and large scale follow-up identifies 16 novel loci for lung function (2011) (1)
Fine-mapping of the coeliac disease linkage region on chromosome 19p13 reveals a new player in the field (2006) (1)
Pharmacomicrobiomics: a novel route towards personalized medicine? (2018) (1)
Discovery and Refinement Supplementary (2015) (1)
Two common variants on 9p21 affect mortality risk in type 2 diabetes patients (ZODIAC-15) (2010) (1)
Genetic mapping of facioscapulohumeral muscular dystrophy. (1993) (1)
ErratumProdynorphin Mutations Cause the Neurodegenerative Disorder Spinocerebellar Ataxia Type 23 (2010) (1)
High proportion of new mutations and possible anticipation following molecular genetic studies in brazilian facioscapulohumeral muscular dystrophy (fshd) families (1994) (1)
New Insights into the Pathogenesis of Giant Cell Arteritis through a Genome-Wide Association Study (2016) (0)
Author Correction: Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome (2018) (0)
University of Groningen Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci Tragante, (2014) (0)
S1814 Genetic Variants of Myosin IXB and Pard3 Predispose to Acute Pancreatitis (2009) (0)
Blood lipids influence DNA methylation in circulating cells (2016) (0)
in IL2RA with progression of joint destruction in Rheumatoid Arthritis (2014) (0)
The MHC locus and genetic susceptibility to autoimmune and infectious diseases (2017) (0)
Single-Cell RNA Sequencing of Peripheral Blood Mononuclear Cells From Pediatric Coeliac Disease Patients Suggests Potential Pre-Seroconversion Markers (2022) (0)
University of Birmingham Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus (0)
University of Groningen TMEM 258 Is a Component of the Oligosaccharyltransferase Complex Controlling ER Stress and Intestinal Inflammation (2018) (0)
Subject Index Vol. 68, 2009 (2009) (0)
The Myo9b gene is a strong risk factor for the development of refractory celiac disease (2007) (0)
INFLAMMATORY BOWEL DISEASE Genetic Analysis in A Dutch Study Sample Identifi es More Ulcerative Colitis Susceptibility Loci and Shows Their Additive Role in Disease Risk (2010) (0)
Wijmenga Genes and outcome after aneurysmal subarachnoid haemorrhage (0)
Resolving Variants of Unknown Significance Through Large-Scale RNA-seq (2013) (0)
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes (2018) (0)
Sa2029 – Habitual Dietary Intake of Dutch IBD Patients Differs from Population Controls: A Case-Control Study (2019) (0)
Genetic susceptibility for Chronic Bronchitis (2010) (0)
O131 GENOME-WIDE ASSOCIATION STUDY IN AUTOIMMUNE HEPATITIS IDENTIFIES RISK VARIANT IN THE SH2B3 REGION (2014) (0)
The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression (2011) (0)
A transcription-based copper sensor enables analysis of copper homeostasis in living cells (2007) (0)
Su510 HEALTHY COTWINS SHARE GUT MICROBIOME SIGNATURES WITH THEIR INFLAMMATORY BOWEL DISEASE TWINS AND UNRELATED PATIENTS (0)
Genome-wide analysis of constitutional DNA methylation in familial melanoma (2020) (0)
University of Groningen Mutational Characterization of the Bile Acid Receptor TGR5 in Primary Sclerosing Cholangitis Hov, (2010) (0)
COMMD1 Is an Inhibitor of Intestinal Inflammation and Colitis in a Myeloid-Specific Knockout Mouse Model (2010) (0)
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation (2018) (0)
Integration of similar to 10,000 metabolite features with genotype data and immune phenotypes reveals genetic determinants and common regulatory modules (2019) (0)
Mechanisms of allergy/immunology Shared DNAmethylation signatures in childhood allergy: The MeDALL study (2021) (0)
FP59-FR-05 Genetic factors in myasthenia gravis and Lambert-Eaton myasthenic syndrome (2009) (0)
PS4 - 19. Expression of lipid genes, but not adipokine genes, in visceral adipose tissue is related to liver damage in obese individuals (2011) (0)
An increase in the number of risk alleles is associated with an increased risk for Crohn's disease and a more severe disease course (2008) (0)
Genes in the ureter budding pathway (2011) (0)
MR-Link : Mendelian Randomization Under Linkage Disequilibrium and Unobserved Pleiotropy (2017) (0)
Association Scans Identifies IL 18 RAP , PTPN 2 , TAGAP , and PUS 10 As Shared Risk Loci for Crohn ' s Disease and Celiac Disease (2018) (0)
Abstract 16003: Rapid Whole Genome Sequencing for Critically Ill Children With Cardiomyopathy (2016) (0)
Activin Receptor 1 B (ACVR1B) as a muscle strength determining gene: genetic fine mapping of chr12q12-14 (2008) (0)
Dupuytrens A-0002 Genome-wide association study finds 9 susceptibility loci for Dupuytren’s disease and suggests a major role for WNT-signaling (2011) (0)
A framework for the detection of de novo mutations in family-based sequencing data (2016) (0)
β2-Adrenergic Receptor Polymorphism and Obesity in Type 2 Diabetes Response to Yoshioka, Yoshida, and Yoshikawa (2003) (0)
Age-related accrual of methylomic variability is linked to fundamental ageing mechanisms (2016) (0)
Genome-wide association study In coeliac disease : identification of novel genetic risk loci (2009) (0)
Correction for both common and rare cell types in blood is important to identify genes that correlate with age (2021) (0)
Impaired resolution of blood transcriptomes through tuberculosis treatment with diabetes comorbidity (2022) (0)
17 Copper Toxicosis in Bedlington Terriers (2006) (0)
Global phylogeography and ancient evolution of the widespread human gut virus crAssphage (2019) (0)
Author Correction: Heritability estimates for 361 blood metabolites across 40 genome-wide association studies (2020) (0)
Genetic factors in myasthenia gravis and Lambert-Eaton myasthenic syndrome (2009) (0)
S1751 Copy Number Variant and Extended SNP Genome Wide Association Study in Celiac Disease (2009) (0)
Genomic Assessment of Inflammatory Bowel Disease (2010) (0)
Genome-wide transcriptome analysis of livers from obese subjects reveals lncRNAs associated with progression of fatty liver to nonalcoholic steatohepatitis (2019) (0)
Identification of novel candidate genes in celiac disease pathogenesis using microarrays (2003) (0)
University of Groningen A Meta-Analysis of Genome-Wide Association Scans Identifies IL18RAP, PTPN2, TAGAP, and PUS10 As Shared Risk Loci for Crohn's Disease and Celiac Disease Festen, (2011) (0)
Polymorphisms of the TUB gene are associated with anthropornetry and eating behaviour in middle-age women (2007) (0)
Expression profiles of coeliac disease biopsies during mucosa recovery (2006) (0)
Correction: Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms (2009) (0)
European Mathematical Genetics Meeting, Rotterdam, the Netherlands, 10th–11th April 2008 (2008) (0)
A CROSS-DISEASE META-GWAS IDENTIFIES IRF1, STAT3 AND ZBTB9-BAK1 AS NEW SHARED SUSCEPTIBILITY LOCI IN SYSTEMIC SCLEROSIS AND CROHN¿S DISEASE (2019) (0)
COMMD proteins as a novel family of regulators of copper homeostasis (2007) (0)
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation (2018) (0)
Additional file 2: of The MHC locus and genetic susceptibility to autoimmune and infectious diseases (2017) (0)
Opposing immunological imprinting of Candida albicans beta-glucan trained immunity and endotoxin tolerance in monocytes. (2015) (0)
Genetic Risk Model for Celiac Disease Helps Identify High-risk Individuals (2009) (0)
Integration of multi-omics data and deep phenotyping enables prediction of cytokine responses (2018) (0)
Overheid investeert tors in bestaande blobanken (2010) (0)
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity Authors (2016) (0)
CHAPTER 86 – Inflammatory Bowel Disease (2009) (0)
A Functional Variant of the Farnesoid X Receptor (FXR) Predisposes to Ileocolonic Localization of Crohn's Disease (2011) (0)
37: A FIRST GENOME-WIDE ASSOCIATION STUDY IN DUPUYTREN'S DISEASE IDENTIFIES 9 SUSCEPTIBILITY LOCI AND SUGGESTS A MAJOR ROLE FOR WNT-SIGNALLING (2011) (0)
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease (2019) (0)
Identifying Causal Variants in Shared Immune-related Diseases Genes by High-throughput Sequencing (2009) (0)
P102 Increased abundance of gut microbial virulence genes and pro-inflammatory pathways during Crohn’s disease exacerbations (2018) (0)
From genome-wide association studies to disease mechanisms: celiac disease as a model for autoimmune diseases (2012) (0)
New Quality Measure for CNV : A Multi-Omics Approach (2017) (0)
Loss or retention of heterozygosity at 3p in renal cell carcinoma (1989) (0)
Intestinal and systemic immune markers in patients with Irritable Bowel Syndrome (2014) (0)
True autosomal dominant inheritance of familial mediterranean fever caused by a mutation in exon 8 of the MEFV gene (2012) (0)
PostersReproductive Genetics (PGD/PGS) (2010) (0)
Dense Genotyping of Immune Related Loci in a Multi-Ethnic Behcet's Disease Cohort Identifies Genetic Associations in a Long Noncoding RNA Near QSOX2, RASIP1/FUT2, and IL12A-AS1 (2016) (0)
Studying the gut virome in the metagenomic era: challenges and perspectives (2019) (0)
CHAPTER 1 Molecular diagnosis of celiac disease : are we there yet ? (2011) (0)
Transmission of gut bacteria and viruses from mothers to infants (2021) (0)
CONGENITAL Na+ - DIARRHEA IS AN AUTOSOMAL RECESSIVE DEFECT OF INTESTINAL Na+ - TRANSPORT (1999) (0)
Transcriptional pro ﬁ les predict treatment outcome in patients with tuberculosis and diabetes at diagnosis and at two weeks after initiation of anti-tuberculosis treatment (2022) (0)
Author Correction: Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome (2018) (0)
Habitual dietary intake of Dutch IBD patients differs from population controls: A case-control study (2018) (0)
Additional file 1: of The MHC locus and genetic susceptibility to autoimmune and infectious diseases (2017) (0)
University of Groningen Farnesoid X Receptor (FXR) Activation and FXR Genetic Variation in Inflammatory Bowel Disease (2011) (0)
The importance of cohort studies in the post-GWAS era (2018) (0)
A SNP panel for identification of DNA and RNA specimens (2018) (0)
Contents Vol. 68, 2009 (2009) (0)
Genome-wide association analysis identifies six new loci associated with forced vital capacity | NOVA. The University of Newcastle's Digital Repository (2014) (0)
Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases (2019) (0)
DOP53 In-depth characterisation of the serum antibody epitope repertoire in Inflammatory Bowel Disease by high-throughput phage-displayed immunoprecipitation sequencing (2022) (0)
FINE-MAPPING OF THE COELIAC DISEASE LINKAGE REGION ON CHROMOSOME 19P13 REVEALS A NEW PLAYER IN THE FIELD: OP1-01 (2005) (0)
[The genetic basis of inflammatory bowel disease unravelled by genetic association studies]. (2009) (0)
BASIC—LIVER, PANCREAS, AND BILIARY TRACT Genome-Wide Association Analysis in Primary Sclerosing Cholangitis (2010) (0)
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter. (1995) (0)
S1807 Genetic Variants of Farnesoid X Receptor (FXR) Predispose to Mortality and Infectious Complications in Acute Pancreatitis (2009) (0)
Cu,Zn Superoxide Dismutase Maturation and Activity Are Regulated by COMMD1 * □ S (2020) (0)
Integration techniques for modern bioinformatics workflows (2018) (0)
University of Groningen The MHC locus and genetic susceptibility to autoimmune and infectious diseases (2017) (0)
DNA methylation signatures of educational attainment (2018) (0)
Physical and genetic mapping of the CT locus on dog 10q26. (1999) (0)
OP014 - Analysis of 1792 gut metagenomes reveals microbial treatment targets for inflammatory bowel disease and irritable bowel syndrome (2018) (0)
OP0283 Cross-disease meta-analysis in four systemic autoimmune diseases to identify shared genetic etiologies (2018) (0)
393 Apical Recycling Endosome-Associated Myosin Vb Is Mutated in Microvillus Inclusion Disease and Is Involved in Intestinal Brush Border Development (2009) (0)
HGV2012: Leveraging Next‐Generation Technology and Large Datasets to Advance Disease Research (2013) (0)
Genome-wide identification of directed gene networks using large-scale population genomics data (2018) (0)
Validation of putative CNVs on the X chromosome in POF patients (2010) (0)
EXPRESSION PROFILES OF COELIAC DISEASE BIOPSIES DURING MUCOSA RECOVERY: SY2-02 (2005) (0)
Nature Genetics | Article (2015) (0)
University of Groningen Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families (2016) (0)
Epigenome-wide association reveals extensive perturbations in DNA methylation associated with adiposity and its adverse metabolic consequences. Authors (2015) (0)
Confirmation of several genetic associations from the WTCCC study and Identification of novel susceptibility loci in a large Dutch-Belgian Crohn's disease cohort (2009) (0)
Candidate Genes for Vesico-Ureteral Reflux (2008) (0)
S1720 The NF-KappaB Inhibitor Commd1 Controls Intestinal Inflammation (2010) (0)
The emerging landscape of dynamic DNA methylation in early childhood (2017) (0)
THE GENETICS OF RCDII (2015) (0)
Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior (2021) (0)
Congenital sodium diarrhea: an autosomal recessive defect of intestinal epithelial sodium absorption (1999) (0)
Structural variation in the gut microbiome associates with host health (2019) (0)
Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35. (1995) (0)
Systematic analysis of relationships between plasma branched-chain amino acid concentrations and cardiometabolic parameters: an association and Mendelian randomization study (2022) (0)
β2-adrenergic receptor polymorphism and obesity in type 2 diabetes. Authors' reply (2003) (0)
M2024 Evaluating the Relation Between Serologic Coeliac Disease Markers and Variants in Intestinal Barrier Genes (2009) (0)
Pooled resequencing of 122 ulcerative colitis genes in a large Dutch population suggests population-specific association of rare variants in MUC2 (2016) (0)
13 Genetische variatie bij het WNT2-locus is geassocieerd met de ziekte van Peyronie (2011) (0)
Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (0)
Facioscapulohumeral muscular dystrophy in the Dutch population. (1995) (0)
THE ROLE OF CELIAC DISEASE LOCI-ASSOCIATED lncRNA GENES: AN EXPLORATIVE STUDY (2015) (0)
United European Gastroenterology Research Prize Awardee 2018 – Cisca Wijmenga (2018) (0)
in a large Dutch Crohn's disease cohort Molecular prediction of disease risk and severity (2009) (0)
MicroRNA profiles by deep- sequencing in plasma and small intestinal biopsies of celiac disease patients (2015) (0)
Polymorphisms near the HHEX gene are associated with type 2 diabetes in the Dutch Breda cohort (2007) (0)
cis-eQTL mapping of TB-T2D comorbidity elucidates the involvement of African ancestry in TB susceptibility (2022) (0)
Correction: Susceptibility to Chronic Mucus Hypersecretion, a Genome Wide Association Study (2015) (0)
Genetic overlap of airway obstruction and emphysema (2011) (0)
Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations Coeliac (2018) (0)
A genome scan for loci linked to quantitative insulin traits in persons without diabetes: the Framingham Offspring Study. (2003) (0)
Genetic Risk Factors For Chronic Mucus Hypersecretion In Chronic Obstructive Pulmonary Disease (2012) (0)
Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (0)
Identification of Novel Genetic Susceptibility Loci in Primary Antiphospholipid Syndrome (2016) (0)
Causal relationships between gut microbiome, short-chain fatty acids and 1 metabolic diseases 2 (2019) (0)
149 – In-Depth Characterization of Host-Genetics and Gut Microbiome Unravels Novel Host-Microbiome Interactions in Inflammatory Bowel Disease (2019) (0)
Chapter 73 – Inflammatory Bowel Disease (2013) (0)
Plasma glucose levels are associated with gene expression levels in subcutaneous and visceral adipose tissue of morbidly obese individuals (2010) (0)
Expression profiling of the recovering mucosa in coeliac disease reveals the molecular basis of the pleiotropic clinical features (2006) (0)
The neuroactive potential of the human gut microbiota in quality of life and depression (2019) (0)
DNA pooling as an efficient screening tool for ADHD candidate gene studies : Correction of PCR-induced artefacts (2001) (0)
MURR1/COMMD1 defines a novel protein family with a possible role in hepatic copper homeostasis and NF-ϕB signaling (2005) (0)
Dominant drivers of the human plasma metabolome (2021) (0)
Association between myelin-related genes and the development of schizophrenia (2005) (0)
OP12 Multiple functional variants at the 3p21 locus contribute to ulcerative colitis: Results from a European consortium (2012) (0)
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35. (1995) (0)
Three Genetic Susceptibility Loci Indicate a Role for IL2, REL and CARD9 in Primary Sclerosing Cholangitis (2011) (0)
Circulating miRNAs as potential biomarkers of early celiac disease Manuscript in preparation (2015) (0)
Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome (2018) (0)
Genetic and environmental effects on the immune phenotypes in type 1 diabetes (2021) (0)
THE REGION 3P21-P24.1, BORDERED BY D3S32 AND THRB, IDENTIFIED AS SMALLEST OVERLAPPING DELETION IN SPORADIC RENAL-CELL CARCINOMA (1991) (0)
34 A Meta-Analysis of Genome Wide Association Scans Identifies TAGAP and Pus10 as Shared Risk Loci for Crohn's Disease and Celiac Disease (2010) (0)
Gut Microbiome Dysbiosis is Associated with Increased Mortality following Solid Organ Transplantation (2021) (0)
ORIGINAL RESEARCH—PEYRONIE'S DISEASE WNT2 Locus Is Involved in Genetic Susceptibility of (2012) (0)
UvA-DARE ( Digital Academic Repository ) Farnesoid X Receptor ( FXR ) Activation and FXR Genetic Variation in Inflammatory Bowel Disease (2012) (0)
COMMD1 is an anti-inflammatory gene that protects against colitis (2011) (0)
Deconvolution of bulk blood eQTL effects into immune cell subpopulations (2020) (0)
A genome-wide functional genomics approach uncovers genetic determinants of immune phenotypes in type 1 diabetes (2022) (0)
Dense Genotyping, Imputation, and Regression Analysis Identifies Multiple Independent Genetic Susceptibility Loci within the HLA Region in Behcet's Disease (2012) (0)
MURR1/COMMD1 defines a novel protein family with a role in hepatic copper homeostasis and NF-KB signaling (2005) (0)
S1172 The Differential Association of the FcgR2a and FcgR3a Genes in Inflammatory Bowel Diseases Across Three Caucasian Populations (2009) (0)
Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies (2015) (0)

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