Lude Franke
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Statistical geneticist
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Mathematics Biology
Lude Franke's Degrees
- PhD Genetics University of Groningen
- Masters Molecular Biology University of Groningen
- Bachelors Biotechnology University of Groningen
Why Is Lude Franke Influential?
(Suggest an Edit or Addition)Lude Franke'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
- Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) (6445)
- Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
- Genetics of rheumatoid arthritis contributes to biology and drug discovery (2013) (1877)
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
- Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations (2015) (1712)
- Systematic identification of trans eQTLs as putative drivers of known disease associations (2013) (1593)
- Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (2013) (1429)
- Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 (2011) (1315)
- New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
- Population-based metagenomics analysis reveals markers for gut microbiome composition and diversity (2016) (1208)
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) (1125)
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) (1114)
- Multiple common variants for celiac disease influencing immune gene expression (2010) (958)
- GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
- Proton pump inhibitors affect the gut microbiome (2015) (770)
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) (736)
- Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease (2011) (711)
- 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)
- Biological interpretation of genome-wide association studies using predicted gene functions (2015) (678)
- Gene co-expression analysis for functional classification and gene–disease predictions (2017) (647)
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2016) (634)
- High density genetic mapping identifies new susceptibility loci for rheumatoid arthritis (2012) (595)
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
- The effect of host genetics on the gut microbiome (2016) (566)
- Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) (563)
- Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases (2019) (553)
- Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci (2016) (549)
- The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
- Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes. (2006) (528)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
- Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche (2014) (511)
- 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)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) (451)
- The transcriptional landscape of age in human peripheral blood (2015) (450)
- Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis (2016) (424)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
- Erratum: Detection and interpretation of shared genetic influences on 42 human traits (2016) (417)
- 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)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk (2017) (359)
- Seventy-five genetic loci influencing the human red blood cell (2012) (357)
- Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci (2011) (355)
- The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
- Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction (2010) (345)
- Disease variants alter transcription factor levels and methylation of their binding sites (2015) (341)
- Identification of context-dependent expression quantitative trait loci in whole blood (2016) (332)
- Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (2015) (308)
- The impact of low-frequency and rare variants on lipid levels (2015) (300)
- Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
- Gene expression analysis identifies global gene dosage sensitivity in cancer (2015) (295)
- 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)
- Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism (2015) (276)
- Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect (2005) (268)
- Correction: Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (2015) (268)
- Human Disease-Associated Genetic Variation Impacts Large Intergenic Non-Coding RNA Expression (2013) (266)
- Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (2014) (262)
- Gut microbiota composition and functional changes in inflammatory bowel disease and irritable bowel syndrome (2018) (261)
- Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization (2014) (260)
- Genetic and environmental influences interact with age and sex in shaping the human methylome (2016) (260)
- Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP. (2008) (258)
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
- Genome-wide association study identifies variants associated with autoimmune hepatitis type 1. (2014) (249)
- Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. (2016) (245)
- New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (2016) (242)
- A Functional Genomics Approach to Understand Variation in Cytokine Production in Humans (2016) (238)
- Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis (2008) (232)
- 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 meta-analysis identifies six novel loci associated with habitual coffee consumption (2014) (224)
- Unraveling the Regulatory Mechanisms Underlying Tissue-Dependent Genetic Variation of Gene Expression (2012) (224)
- Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. (2018) (221)
- 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)
- Endothelial TLR4 and the microbiome drive cerebral cavernous malformations (2017) (210)
- Single-cell RNA sequencing identifies cell type-specific cis-eQTLs and co-expression QTLs (2018) (208)
- Large-scale association analyses identify host factors influencing human gut microbiome composition (2020) (206)
- Using genome‐wide pathway analysis to unravel the etiology of complex diseases (2009) (199)
- Genetic evidence of assortative mating in humans (2017) (199)
- Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing (2009) (199)
- Genetic evidence of assortative mating in humans (2017) (199)
- Detection and replication of epistasis influencing transcription in humans (2014) (193)
- Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations (2012) (181)
- Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristics (2015) (180)
- Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels (2015) (179)
- Blood pressure loci identified with a gene-centric array. (2011) (177)
- Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (2014) (170)
- Wnt signaling and Dupuytren's disease. (2011) (169)
- Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection. (2010) (166)
- Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals (2020) (161)
- Blood lipids influence DNA methylation in circulating cells (2016) (156)
- From genome to function by studying eQTLs. (2014) (146)
- Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances (2018) (144)
- Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits (2018) (139)
- Inter-individual variability and genetic influences on cytokine responses to bacteria and fungi (2016) (139)
- Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism (2009) (135)
- Differential Effects of Environmental and Genetic Factors on T and B Cell Immune Traits (2016) (133)
- Three ulcerative colitis susceptibility loci are associated with primary sclerosing cholangitis and indicate a role for IL2, REL, and CARD9 (2011) (128)
- Complex nature of SNP genotype effects on gene expression in primary human leucocytes (2009) (125)
- GWAS for executive function and processing speed suggests involvement of the CADM2 gene (2016) (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)
- 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)
- High-throughput identification of human SNPs affecting regulatory element activity (2019) (119)
- Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity (2014) (118)
- Genetic and epigenetic regulation of gene expression in fetal and adult human livers (2014) (114)
- A novel common variant in DCST2 is associated with length in early life and height in adulthood (2014) (112)
- Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
- Age-related accrual of methylomic variability is linked to fundamental ageing mechanisms (2016) (106)
- Cell Specific eQTL Analysis without Sorting Cells (2014) (105)
- Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (2021) (104)
- Genotype harmonizer: automatic strand alignment and format conversion for genotype data integration (2014) (101)
- 52 Genetic Loci Influencing Myocardial Mass. (2016) (98)
- Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2015) (98)
- SMIM1 underlies the Vel blood group and influences red blood cell traits (2013) (98)
- Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands' (2014) (98)
- Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene. (2009) (98)
- A large lung gene expression study identifying fibulin-5 as a novel player in tissue repair in COPD (2014) (96)
- Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function (2017) (96)
- The single-cell eQTLGen consortium (2020) (95)
- Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen (2008) (95)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Genome-wide association analyses identify variants in developmental genes associated with hypospadias (2014) (92)
- Identification of co-expression gene networks, regulatory genes and pathways for obesity based on adipose tissue RNA Sequencing in a porcine model (2014) (91)
- A linear mixed-model approach to study multivariate gene–environment interactions (2018) (90)
- A microarray screen for novel candidate genes in coeliac disease pathogenesis (2004) (88)
- Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia (2017) (87)
- Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells (2017) (87)
- Mediation Analysis Demonstrates That Trans-eQTLs Are Often Explained by Cis-Mediation: A Genome-Wide Analysis among 1,800 South Asians (2014) (86)
- 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)
- MixupMapper: correcting sample mix-ups in genome-wide datasets increases power to detect small genetic effects (2011) (82)
- Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals (2022) (80)
- ATR inhibition preferentially targets homologous recombination-deficient tumor cells (2014) (80)
- Immunochip SNP array identifies novel genetic variants conferring susceptibility to candidaemia (2014) (80)
- A Meta-Analysis of Hodgkin Lymphoma Reveals 19p13.3 TCF3 as a Novel Susceptibility Locus (2013) (78)
- Integration of multi-omics data and deep phenotyping enables prediction of cytokine responses (2018) (78)
- Skewed X-inactivation is common in the general female population (2018) (75)
- Discovery and fine mapping of serum protein loci through transethnic meta-analysis. (2012) (75)
- Skewed X-inactivation is common in the general female population (2018) (75)
- Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (2016) (75)
- Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (73)
- Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (73)
- Unintended Side Effects of the Digital Transition: European Scientists’ Messages from a Proposition-Based Expert Round Table (2018) (69)
- eQTL analysis in humans. (2009) (69)
- Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index (2014) (69)
- Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome (2018) (68)
- Associations of autozygosity with a broad range of human phenotypes (2019) (68)
- Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes (2019) (66)
- Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels (2014) (65)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (65)
- 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)
- Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs (2016) (62)
- PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity (2018) (61)
- A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
- An epigenome-wide association study meta-analysis of educational attainment (2017) (60)
- Another Explanation for Apparent Epistasis (2014) (59)
- Systematic annotation of celiac disease loci refines pathological pathways and suggests a genetic explanation for increased interferon-gamma levels. (2015) (58)
- Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development. (2015) (58)
- Human Genetics in Rheumatoid Arthritis Guides a High-Throughput Drug Screen of the CD40 Signaling Pathway (2013) (56)
- Cerebral small vessel disease genomics and its implications across the lifespan (2020) (56)
- Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes. (2016) (56)
- A strategy to search for common obesity and type 2 diabetes genes (2007) (56)
- Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study (2017) (55)
- Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis (2019) (53)
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk (2017) (52)
- CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (52)
- Mapping of Gene Expression Reveals CYP27A1 as a Susceptibility Gene for Sporadic ALS (2012) (52)
- GAVIN: Gene-Aware Variant INterpretation for medical sequencing (2017) (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)
- An integrative approach for building personalized gene regulatory networks for precision medicine (2018) (51)
- Determining the association between adipokine expression in multiple tissues and phenotypic features of non-alcoholic fatty liver disease in obesity (2015) (50)
- DeepSAGE Reveals Genetic Variants Associated with Alternative Polyadenylation and Expression of Coding and Non-coding Transcripts (2013) (49)
- Novel childhood asthma genes interact with in utero and early-life tobacco smoke exposure☆ (2014) (49)
- Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis (2018) (48)
- Shared genetic variants suggest common pathways in allergy and autoimmune diseases (2017) (47)
- Lack of Association Between Genetic Variants at ACE2 and TMPRSS2 Genes Involved in SARS-CoV-2 Infection and Human Quantitative Phenotypes (2020) (45)
- The landscape of chromosomal aberrations in breast cancer mouse models reveals driver-specific routes to tumorigenesis (2016) (45)
- Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays. (2008) (45)
- Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases (2021) (44)
- Genetic variants in the region of the C1q genes are associated with rheumatoid arthritis (2013) (44)
- A Genome-Wide Association Study of Circulating Galectin-3 (2012) (42)
- Extraintestinal Manifestations and Complications in Inflammatory Bowel Disease: From Shared Genetics to Shared Biological Pathways (2014) (40)
- DNA methylation signatures of educational attainment (2018) (39)
- Neutrophil recruitment and barrier impairment in celiac disease: a genomic study. (2007) (38)
- Combination of text-mining algorithms increases the performance (2006) (38)
- Copper metabolism domain-containing 1 represses genes that promote inflammation and protects mice from colitis and colitis-associated cancer. (2014) (37)
- Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
- Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant (2013) (35)
- Genetic variants alter T-bet binding and gene expression in mucosal inflammatory disease (2017) (32)
- Epigenome-wide Association Study of Attention-Deficit/Hyperactivity Disorder Symptoms in Adults (2019) (32)
- Celiac disease: moving from genetic associations to causal variants (2011) (31)
- A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
- Gender differences in the mental health impact of the COVID-19 lockdown: Longitudinal evidence from the Netherlands (2021) (31)
- Deconvolution of bulk blood eQTL effects into immune cell subpopulations (2019) (31)
- An integrative systems genetics approach reveals potential causal genes and pathways related to obesity (2015) (31)
- Large-scale plasma metabolome analysis reveals alterations in HDL metabolism in migraine (2019) (30)
- Evolutionary and Functional Analysis of Celiac Risk Loci Reveals SH 2 B 3 as a Protective Factor against Bacterial Infection (2010) (30)
- TEAM: a tool for the integration of expression, and linkage and association maps (2004) (30)
- Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour (2021) (29)
- Genetic variants in RBFOX3 are associated with sleep latency (2016) (29)
- Lifelines COVID-19 cohort: investigating COVID-19 infection and its health and societal impacts in a Dutch population-based cohort (2021) (29)
- Copy number variants on the X chromosome in women with primary ovarian insufficiency. (2011) (29)
- A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine (2020) (29)
- Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis. (2016) (28)
- A first update on mapping the human genetic architecture of COVID-19 (2022) (27)
- A SNP panel for identification of DNA and RNA specimens (2018) (27)
- Eosinophil Count Is a Common Factor for Complex Metabolic and Pulmonary Traits and Diseases: The LifeLines Cohort Study (2016) (26)
- Single-cell RNA sequencing identifies celltype-specific cis-eQTLs and co-expression QTLs (2018) (26)
- Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (2021) (26)
- Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults (2018) (25)
- Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2016) (25)
- Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies (2017) (25)
- Inter-Tissue Gene Co-Expression Networks between Metabolically Healthy and Unhealthy Obese Individuals (2016) (25)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes (2021) (25)
- HHEX gene polymorphisms are associated with type 2 diabetes in the Dutch Breda cohort (2008) (24)
- A genetic variant in granzyme B is associated with progression of joint destruction in rheumatoid arthritis. (2013) (24)
- Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes (2015) (24)
- A functional brain-derived neurotrophic factor (BDNF) gene variant increases the risk of moderate-to-severe allergic rhinitis. (2015) (24)
- Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure (2020) (23)
- Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache (2020) (23)
- Correlation of Genetic Risk and Messenger RNA Expression in a Th17/IL23 Pathway Analysis in Inflammatory Bowel Disease (2014) (23)
- Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram (2016) (22)
- Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (22)
- A linear mixed-model approach to study multivariate gene–environment interactions (2018) (21)
- A linear mixed-model approach to study multivariate gene–environment interactions (2018) (21)
- Evaluation of commonly used analysis strategies for epigenome- and transcriptome-wide association studies through replication of large-scale population studies (2019) (21)
- 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)
- Evaluation of European coeliac disease risk variants in a north Indian population (2014) (20)
- Identification of the oxidative stress-related gene MSRA as a rheumatoid arthritis susceptibility locus by genome-wide pathway analysis. (2010) (20)
- RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprinting (2018) (20)
- Hypothesis-free identification of modulators of genetic risk factors (2015) (19)
- Author Correction: Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project (2020) (19)
- GAVIN: Gene-Aware Variant INterpretation for medical sequencing (2016) (19)
- Epigenome-wide association meta-analysis of DNA methylation with coffee and tea consumption (2020) (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)
- No genetic association of the human prolyl endopeptidase gene in the Dutch celiac disease population. (2005) (17)
- Meta-analysis fine-mapping is often miscalibrated at single-variant resolution (2022) (17)
- Integration of metabolomics, genomics, and immune phenotypes reveals the causal roles of metabolites in disease (2021) (17)
- Proteomic studies related to genetic determinants of variability in protein concentrations. (2014) (16)
- Habitual dietary intake of IBD patients differs from population controls: a case–control study (2020) (16)
- A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention. (2011) (16)
- Integrating GWAS with bulk and single-cell RNA-sequencing reveals a role for LY86 in the anti-Candida host response (2020) (16)
- Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation (2019) (15)
- DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan (2020) (15)
- Genomic evaluation of circulating proteins for drug target characterisation and precision medicine (2020) (15)
- An introduction to LifeLines DEEP: study design and baseline characteristics (2014) (14)
- 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)
- A characterization of cis- and trans-heritability of RNA-Seq-based gene expression (2019) (14)
- Generalized Ichthyotic Peeling Skin Syndrome due to FLG2 Mutations. (2018) (14)
- Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progression (2022) (14)
- 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)
- Predicted efficacy of a pharmacogenetic passport for inflammatory bowel disease (2020) (13)
- 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)
- Single-cell RNA-sequencing of peripheral blood mononuclear cells reveals widespread, context-specific gene expression regulation upon pathogenic exposure (2022) (12)
- Systematic Prioritization of Candidate Genes in Disease Loci Identifies TRAFD1 as a Master Regulator of IFNγ Signaling in Celiac Disease (2021) (12)
- Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood (2018) (12)
- Genetics of human gut microbiome composition (2020) (12)
- Meta-analyses identify DNA methylation associated with kidney function and damage (2021) (12)
- 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)
- The Lifelines COVID-19 Cohort: a questionnaire-based study to investigate COVID-19 infection and its health and societal impacts in a Dutch population-based cohort (2020) (10)
- Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche DTU Orbit (05/11/2017) (2014) (10)
- Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes (2017) (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)
- Blood Eosinophil Count and Metabolic, Cardiac and Pulmonary Outcomes: A Mendelian Randomization Study (2018) (9)
- The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus (2019) (9)
- Single-cell eQTLGen Consortium: a personalized understanding of disease. (2019) (9)
- An epigenome-wide association study identifies multiple DNA methylation markers of exposure to endocrine disruptors. (2020) (9)
- Hemani et al. reply (2014) (8)
- Phantom epistasis between unlinked loci (2021) (7)
- Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility (2020) (7)
- Discovering patterns of pleiotropy in genome-wide association studies (2018) (7)
- Single-cell RNA-sequencing reveals widespread personalized, context-specific gene expression regulation in immune cells (2021) (6)
- Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation. (2019) (6)
- Systematic genotype–phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autism (2010) (6)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
- Systematic identification of human SNPs affecting regulatory element activity (2018) (6)
- Genome-wide association analysis identi fi es three new susceptibility loci for childhood body mass index (2016) (5)
- Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability (2021) (5)
- Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts (2023) (5)
- Correction: Corrigendum: Inter-individual variability and genetic influences on cytokine responses to bacteria and fungi (2016) (5)
- Genetic, parental and lifestyle factors influence telomere length (2021) (5)
- Corrigendum: Multiple common variants for celiac disease influencing immune gene expression (2010) (5)
- The genetic architecture of molecular traits (2017) (5)
- Correction for both common and rare cell types in blood is important to identify genes that correlate with age (2020) (5)
- Evidence for mitochondrial genetic control of autosomal gene expression. (2016) (5)
- Hypothesis-driven Research On Genomic Data Derived From A Large Scale Lung EQTL Mapping Study (2010) (5)
- Systematic prioritization of candidate genes in disease loci identifies TRAFD1 as a master regulator of IFNγ signalling in celiac disease (2020) (4)
- Demuxafy: Improvement in droplet assignment by integrating multiple single-cell demultiplexing and doublet detection methods (2022) (4)
- No Evidence in a Large UK Collection for Celiac Disease Risk Variants Reported by a Spanish Study (2008) (4)
- Genetic variants of inducible costimulator are associated with allergic asthma susceptibility. (2015) (4)
- Feasibility of predicting allele specific expression from DNA sequencing using machine learning (2021) (4)
- Linking common and rare disease genetics through gene regulatory networks (2021) (4)
- Occupational exposure to gases/fumes and mineral dust affect DNA methylation levels of genes regulating expression (2019) (4)
- Gut mucosa dissociation protocols influence cell type proportions and single-cell gene expression levels (2022) (4)
- Erratum: Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (Proc Natl Acad Sci USA (2014) 111 (13790-13794) DOI: 10.1073/pnas.1404623111) (2015) (4)
- Erratum to: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps : (Nature Genetics, (2016), 48, 11, (1303-1312), 10.1038/ng.3668) (2018) (3)
- Genome-wide analysis of constitutional DNA methylation in familial melanoma (2020) (3)
- The role of gene expression on human sexual dimorphism: too early to call (2020) (3)
- Single-cell RNA sequencing reveals cell-type specific cis-eQTLs in peripheral blood mononuclear cells (2017) (3)
- Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progression (2022) (3)
- An epigenome-wide association study of educational attainment (n = 10,767) (2017) (3)
- Translational insights from single-cell technologies across the cardiovascular disease continuum. (2021) (3)
- Age-dependent sex differences in cardiometabolic risk factors (2022) (2)
- Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility (2016) (2)
- Cardiovascular Genomics. Methods and Protocols (2009) (2)
- Correction: DeepSAGE Reveals Genetic Variants Associated with Alternative Polyadenylation and Expression of Coding and Non-coding Transcripts (2013) (2)
- 87 Gene-Microbiome Interactions Underlying the Onset and the Clinical Phenotypes of Inflammatory Bowel Disease (2016) (2)
- Genomewide high density SNP-CGH reveals several new deletion copy number variants on the x chromosome in POF patients. (2008) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity (2014) (2)
- Increased genetic contribution to wellbeing during the COVID-19 pandemic (2021) (2)
- eQTL Analysis in Humans in Methods in Molecular Biology (2009) (2)
- Interethnic analyses of blood pressure loci in populations of East Asian and European descent (2018) (2)
- Identification of co-expression gene networks, regulatory genes and pathways for obesity based on adipose tissue RNA Sequencing in a porcine model (2014) (2)
- Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (2018) (1)
- Author response: The single-cell eQTLGen consortium (2020) (1)
- Identification of genetic variants that impact gene co-expression relationships using large-scale single-cell data (2022) (1)
- Skewed X-inactivation is common in the general female population (2018) (1)
- The lebercilin-like protein is embedded in a ciliary protein network and is preferentially expressed in motile cilia (2012) (1)
- Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity (2018) (1)
- Phenotypic and genetic factors are associated with absence of cardiomyopathy symptoms in PLN c.40_42delAGA carriers (2022) (1)
- Unbiased identification of unknown cellular and environmental factors that mediate eQTLs using principal interaction component analysis (2022) (1)
- Genetic and epigenetic regulation of gene expression in fetal and adult human livers (2014) (1)
- An integrative systems genetics approach reveals potential causal genes and pathways related to obesity (2015) (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)
- Genotype harmonizer: automatic strand alignment and format conversion for genotype data integration (2014) (1)
- Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inference (2020) (1)
- Fine-mapping of the coeliac disease linkage region on chromosome 19p13 reveals a new player in the field (2006) (1)
- Skewed X-inactivation is common in the general female population (2018) (1)
- Genetic Loci In fl uencing Myocardial Mass (2016) (1)
- Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels (2015) (1)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (1)
- Author Correction: GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk (2018) (1)
- OTTERS: a powerful TWAS framework leveraging summary-level reference data (2022) (1)
- Imbalanced expression for predicted high-impact, autosomal-dominant variants in a cohort of 3,818 healthy samples (2020) (1)
- Systems Genetics Analysis of Obesity using RNA-Seq Data in an F2 Pig Resource Population (2014) (1)
- THU0001 Variation in granzyme-b is associated with progression of joint destruction in rheumatoid arthritis (2013) (1)
- Identification Of Novel Genes That Contribute To Both Asthma And COPD, With Replication In A Large Population-Based Cohort (2011) (1)
- Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations (2022) (1)
- Sa1677 HLA-DRB1*0301 and HLA-DRB1*0401 Modify the Presentation and Outcome in Autoimmune Hepatitis Type-1 (2015) (1)
- Limited evidence for blood eQTLs in human sexual dimorphism (2022) (1)
- Integration of metabolomics, genomics, and immune phenotypes reveals the causal roles of metabolites in disease (2021) (1)
- Identification of heart rate-associated loci and genes (2013) (1)
- PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity (2018) (1)
- Abstract 11627: GWA Meta-Analysis on ST-T Wave Changes Identifies 12 Novel Loci for Human Cardiac Repolarization (2013) (0)
- eQTLGen Consortium (2018). Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. (2018) (0)
- DNA methylation signatures of educational attainment (2018) (0)
- Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (0)
- Integration of public DNA methylation and expression networks via eQTMs improves prediction of functional gene–gene associations (2021) (0)
- University of Groningen Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations Demirkan, (2012) (0)
- Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (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)
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity Authors (2016) (0)
- Resolving Variants of Unknown Significance Through Large-Scale RNA-seq (2013) (0)
- VKučinskas-2001-2016 (2016) (0)
- European Mathematical Genetics Meeting, Rotterdam, the Netherlands, 10th–11th April 2008 (2008) (0)
- Validation of putative CNVs on the X chromosome in POF patients (2010) (0)
- Identification of novel spinocerebellar ataxia disease genes using next generation sequencing approaches (2014) (0)
- Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation (2018) (0)
- Correction: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (0)
- The landscape of chromosomal aberrations in mouse models of breast cancer reveals driver-specific routes to tumor development (2016) (0)
- Plasma glucose levels are associated with gene expression levels in subcutaneous and visceral adipose tissue of morbidly obese individuals (2010) (0)
- Gut mucosa dissociation protocols influence cell type proportions and single-cell gene expression levels (2022) (0)
- Meta-Analysis of Maternal Prenatal Smoking GFI1-Locus and Cardio-Metabolic Phenotypes in Adults (2018) (0)
- S1751 Copy Number Variant and Extended SNP Genome Wide Association Study in Celiac Disease (2009) (0)
- Epigenome-wide association reveals extensive perturbations in DNA methylation associated with adiposity and its adverse metabolic consequences. Authors (2015) (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)
- POS-421 KIDNEYNETWORK: A NEW METHOD TO PREDICT KIDNEY DISEASE GENES USING KIDNEY DERIVED GENE EXPRESSION DATA IDENTIFIES A NEW CANDIDATE GENE FOR MILD ADPKD / PCLD (2021) (0)
- Author Correction: Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome (2018) (0)
- On the Measurement of Genetic Interactions (2007) (0)
- Evaluation of commonly used analysis strategies for epigenome- and transcriptome-wide association studies through replication of large-scale population studies (2019) (0)
- The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus (2019) (0)
- Genome-wide analysis of constitutional DNA methylation in familial melanoma (2020) (0)
- Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (2022) (0)
- Publisher Correction: Age-dependent sex differences in cardiometabolic risk factors (2022) (0)
- University of Groningen Mapping of Gene Expression Reveals CYP 27 A 1 as a Susceptibility Gene for Sporadic (2012) (0)
- Abstract 16003: Rapid Whole Genome Sequencing for Critically Ill Children With Cardiomyopathy (2016) (0)
- A SNP panel for identification of DNA and RNA specimens (2018) (0)
- A SNP panel for identification of DNA and RNA specimens (2018) (0)
- Improving diagnostic yield of exome-sequencing through prioritization of genes with predicted HPO assignments (2019) (0)
- Author Correction: GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk (2018) (0)
- Three Genetic Susceptibility Loci Indicate a Role for IL2, REL and CARD9 in Primary Sclerosing Cholangitis (2011) (0)
- Genome-wide identification of directed gene networks using large-scale population genomics data (2018) (0)
- Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome (2018) (0)
- Sa2029 – Habitual Dietary Intake of Dutch IBD Patients Differs from Population Controls: A Case-Control Study (2019) (0)
- Integration of multi-omics data and deep phenotyping enables prediction of cytokine responses (2018) (0)
- New Quality Measure for CNV : A Multi-Omics Approach (2017) (0)
- Semi-automatic translation of medicine usage data (in Dutch, free-text) from Lifelines COVID-19 questionnaires to ATC codes (2023) (0)
- Beyond genetic associations-transcriptional regulation and colocalisation with complex traits (2019) (0)
- Reply to ‘Misestimation of heritability and prediction accuracy of male-pattern baldness’ (2018) (0)
- Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (2018) (0)
- University of Groningen 52 Genetic Loci Influencing Myocardial Mass (2017) (0)
- Allele specific expression identifies rare variants as cause for extreme allelic imbalance (2019) (0)
- Task 1: Understanding linkage disequilibrium Task 2: permutation p-values Task 3: Mechanism of CD14 association Task 3: Mechanism of CD14 association Colocalisation - using genetics to understand molecular mechanisms (2018) (0)
- Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation (2018) (0)
- Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior (2021) (0)
- Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation. (2019) (0)
- Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (0)
- A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine (2020) (0)
- Limited evidence for blood eQTLs in human sexual dimorphism (2022) (0)
- Age at first birth in women is genetically associated with increased risk of schizophrenia (2018) (0)
- The WISH network method applied to obesity in an F2 pig population (2014) (0)
- Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes (2018) (0)
- Molecular genetic overlap between migraine and major depressive disorder (2018) (0)
- Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation (2022) (0)
- CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (0)
- An integrative approach for building personalized gene regulatory networks for precision medicine (2018) (0)
- KidneyNetwork: Using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease (2021) (0)
- Lipid-induced transcriptomic changes in blood link to lipid metabolism and allergic response (2023) (0)
- University of Groningen Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index Hoggart, (2014) (0)
- Blood lipids influence DNA methylation in circulating cells (2016) (0)
- Genetic regulation of fetal hemoglobin across global populations (2023) (0)
- Systems genetics analysis of obesity in a porcine model using WISH network method (2014) (0)
- Reply to ‘Misestimation of heritability and prediction accuracy of male-pattern baldness’ (2018) (0)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
- Advances in modeling of the bovine estrous cycle: Synchronization with PGF2 (2022) (0)
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk (2017) (0)
- EXPRESSION PROFILES OF COELIAC DISEASE BIOPSIES DURING MUCOSA RECOVERY: SY2-02 (2005) (0)
- Edinburgh Research Explorer Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index (2017) (0)
- Nature Genetics | Article (2015) (0)
- Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations (2018) (0)
- Author Correction: Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome (2018) (0)
- Retraction Note: Detection and replication of epistasis influencing transcription in humans (2021) (0)
- Identification of novel candidate genes in celiac disease pathogenesis using microarrays (2003) (0)
- Expression profiles of coeliac disease biopsies during mucosa recovery (2006) (0)
- Idéfix: identifying accidental sample mix-ups in biobanks using polygenic scores (2021) (0)
- Genome-wide association study In coeliac disease : identification of novel genetic risk loci (2009) (0)
- Integration of similar to 10,000 metabolite features with genotype data and immune phenotypes reveals genetic determinants and common regulatory modules (2019) (0)
- Shared genetic origins of allergy and autoimmune diseases (2015) (0)
- Title: Integration of Candida albicans -induced single-cell gene expression data 1 and circulatory protein concentrations reveal genetic regulators of inflammation 2 (2022) (0)
- University of Groningen Improving the diagnostic yield of exome-sequencing by predicting gene-phenotype associations using large-scale gene expression analysis Deelen, (2019) (0)
- Deconvolution of bulk blood eQTL effects into immune cell subpopulations (2020) (0)
- O131 GENOME-WIDE ASSOCIATION STUDY IN AUTOIMMUNE HEPATITIS IDENTIFIES RISK VARIANT IN THE SH2B3 REGION (2014) (0)
- Correction for both common and rare cell types in blood is important to identify genes that correlate with age (2021) (0)
- PostersReproductive Genetics (PGD/PGS) (2010) (0)
- RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprinting (2019) (0)
- Correction (2019) (0)
- Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases (2019) (0)
- Habitual dietary intake of Dutch IBD patients differs from population controls: A case-control study (2018) (0)
- FINE-MAPPING OF THE COELIAC DISEASE LINKAGE REGION ON CHROMOSOME 19P13 REVEALS A NEW PLAYER IN THE FIELD: OP1-01 (2005) (0)
- Age-related accrual of methylomic variability is linked to fundamental ageing mechanisms (2016) (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)
- Causal relationships between gut microbiome, short-chain fatty acids and 1 metabolic diseases 2 (2019) (0)
- Integration of whole-exome sequencing and RNA sequencing of intestinal biopsies in inflammatory bowel disease identifies inflammation-dependent effects (2018) (0)
- Genome-wide approaches towards identification of susceptibility genes in complex diseases (2008) (0)
- Correction for both common and rare cell types in blood is important to identify genes that correlate with age (2021) (0)
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