Eleftheria Zeggini

Eleftheria Zeggini's AcademicInfluence.com Rankings

Eleftheria Zeggini

Biology

#6171

World Rank

#8828

Historical Rank

Genetics

#795

World Rank

#887

Historical Rank

biology Degrees

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Biology

Eleftheria Zeggini's Degrees

PhD Genetics University of Oxford
Bachelors Genetics University of Thessaly

Why Is Eleftheria Zeggini Influential?

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According to Wikipedia, Eleftheria Zeggini is a director of the institute of translational genomics in Helmholtz Zentrum München and a professor at the Technical University of Munich . Previously she served as a research group leader at the Wellcome Trust Sanger Institute from 2008 to 2018 and an honorary professor in the department of health sciences at the University of Leicester in the UK.

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Eleftheria Zeggini'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

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) (9208)
A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity (2007) (4268)
Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes (2007) (2245)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) (1882)
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2009) (1735)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
Common variants near MC4R are associated with fat mass, weight and risk of obesity (2008) (1307)
Genome-wide association study identifies eight loci associated with blood pressure (2009) (1225)
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (1028)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
The genetic architecture of type 2 diabetes (2016) (927)
The UK10K project identifies rare variants in health and disease (2015) (926)
Variants in MTNR1B influence fasting glucose levels (2009) (742)
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (659)
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge (2010) (648)
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (600)
Meta-analysis in genome-wide association studies. (2009) (559)
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) (547)
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
Rare and low-frequency coding variants alter human adult height (2016) (511)
An Evaluation of Statistical Approaches to Rare Variant Analysis in Genetic Association Studies (2009) (495)
Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) (476)
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
The African Genome Variation Project shapes medical genetics in Africa (2014) (460)
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (428)
Exome-wide association study of plasma lipids in >300,000 individuals (2017) (428)
A common variant of HMGA2 is associated with adult and childhood height in the general population (2007) (419)
Leukemia-Associated Somatic Mutations Drive Distinct Patterns of Age-Related Clonal Hemopoiesis (2015) (418)
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study (2012) (382)
Genome-wide associations for birth weight and correlations with adult disease (2016) (371)
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa. (2017) (357)
Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank (2015) (326)
Common Variation in the FTO Gene Alters Diabetes-Related Metabolic Traits to the Extent Expected Given Its Effect on BMI (2008) (317)
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (314)
Assessing the Combined Impact of 18 Common Genetic Variants of Modest Effect Sizes on Type 2 Diabetes Risk (2008) (299)
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) (296)
Functional annotation of non-coding sequence variants (2014) (295)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
Association Analysis of 6,736 U.K. Subjects Provides Replication and Confirms TCF7L2 as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk (2006) (284)
A genome-wide association study of anorexia nervosa (2014) (284)
Combining Information from Common Type 2 Diabetes Risk Polymorphisms Improves Disease Prediction (2006) (277)
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors (2018) (269)
Rare variant association analysis methods for complex traits. (2010) (262)
Replication in genome-wide association studies. (2009) (258)
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. (2018) (257)
Common Variants of the Novel Type 2 Diabetes Genes CDKAL1 and HHEX/IDE Are Associated With Decreased Pancreatic β-Cell Function (2007) (255)
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (249)
Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites. (2004) (247)
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. (2016) (245)
Genome-wide association studies in type 2 diabetes (2009) (244)
Mutation screening of the macrophage migration inhibitory factor gene: positive association of a functional polymorphism of macrophage migration inhibitory factor with juvenile idiopathic arthritis. (2002) (240)
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension (2016) (234)
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets (2017) (217)
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank (2018) (205)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure underpinning obesity (2017) (193)
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility (2015) (185)
Glucocorticoid sensitivity is determined by a specific glucocorticoid receptor haplotype. (2004) (182)
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis (2018) (176)
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers (2015) (168)
Genomics of disease risk in globally diverse populations (2019) (165)
Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22 (2010) (156)
The Trans-Ancestral Genomic Architecture of Glycemic Traits (2020) (151)
Directional dominance on stature and cognition in diverse human populations (2015) (144)
Type 2 Diabetes Risk Alleles Are Associated With Reduced Size at Birth (2009) (141)
A variant in MCF2L is associated with osteoarthritis. (2011) (137)
Adiposity-Related Heterogeneity in Patterns of Type 2 Diabetes Susceptibility Observed in Genome-Wide Association Data (2009) (135)
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip (2013) (132)
Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study (2010) (131)
Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes (2018) (131)
Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport (2016) (131)
The power of genetic diversity in genome-wide association studies of lipids (2021) (129)
TCF7L2: the biggest story in diabetes genetics since HLA? (2006) (128)
A functional promoter haplotype of macrophage migration inhibitory factor is linked and associated with juvenile idiopathic arthritis. (2004) (126)
HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis (2015) (125)
Synthetic Associations Are Unlikely to Account for Many Common Disease Genome-Wide Association Signals (2011) (123)
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney (2017) (121)
Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications (2016) (118)
Assessment of Osteoarthritis Candidate Genes in a Meta-Analysis of Nine Genome-Wide Association Studies (2014) (117)
An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets (2005) (114)
A novel common variant in DCST2 is associated with length in early life and height in adulthood (2014) (112)
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa (2019) (112)
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation (2015) (110)
Common variants at 6q22 and 17q21 are associated with intracranial volume (2012) (110)
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits (2017) (110)
Interrogating Type 2 Diabetes Genome-Wide Association Data Using a Biological Pathway-Based Approach (2009) (108)
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis (2015) (106)
Is the thrifty genotype hypothesis supported by evidence based on confirmed type 2 diabetes- and obesity-susceptibility variants? (2009) (97)
Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4 (2013) (97)
A Combined Functional Annotation Score for Non-Synonymous Variants (2012) (95)
Translational genomics and precision medicine: Moving from the lab to the clinic (2019) (95)
Height-reducing variants and selection for short stature in Sardinia (2015) (94)
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (93)
Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany (2010) (92)
Whole-genome sequence-based analysis of thyroid function (2015) (89)
An association analysis of the HLA gene region in latent autoimmune diabetes in adults (2006) (89)
Eight blood pressure loci identified by genome-wide association study of 34,433 people of European ancestry (2009) (88)
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation (2020) (88)
In search of low-frequency and rare variants affecting complex traits (2013) (87)
A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates (2013) (84)
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations (2021) (83)
Statistical methods to detect pleiotropy in human complex traits (2017) (83)
Integrative epigenomics, transcriptomics and proteomics of patient chondrocytes reveal genes and pathways involved in osteoarthritis (2016) (83)
Estimating Genome-Wide Significance for Whole-Genome Sequencing Studies (2014) (82)
Dietary Intake, FTO Genetic Variants, and Adiposity: A Combined Analysis of Over 16,000 Children and Adolescents (2015) (81)
Using population isolates in genetic association studies (2014) (79)
Revisiting the thrifty gene hypothesis via 65 loci associated with susceptibility to type 2 diabetes. (2014) (76)
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis (2016) (76)
Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty. (2014) (75)
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (2016) (75)
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci (2019) (72)
Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations (2017) (72)
Linkage and association studies of single-nucleotide polymorphism-tagged tumor necrosis factor haplotypes in juvenile oligoarthritis. (2002) (72)
Analysis of multiple data sets reveals no association between the insulin gene variable number tandem repeat element and polycystic ovary syndrome or related traits. (2005) (70)
Genetic architecture of human thinness compared to severe obesity (2019) (70)
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits (2017) (70)
Synthetic associations in the context of genome-wide association scan signals (2010) (69)
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2014) (69)
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2014) (69)
Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation: Meta-Analysis of Three Genome-Wide Association Studies (2009) (67)
PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION (2018) (67)
Next-generation association studies for complex traits (2011) (66)
A saturated map of common genetic variants associated with human height (2022) (65)
Advances in osteoarthritis genetics (2013) (65)
The DOT1L rs12982744 polymorphism is associated with osteoarthritis of the hip with genome-wide statistical significance in males (2013) (64)
A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis (2017) (63)
Underlying genetic models of inheritance in established type 2 diabetes associations. (2009) (62)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (61)
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
Trans-ethnic study design approaches for fine-mapping (2016) (59)
The effect of next-generation sequencing technology on complex trait research (2011) (58)
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations (2017) (57)
Genome-Wide Association Analysis of Eating Disorder-Related Symptoms, Behaviors, and Personality Traits (2012) (57)
The Variable Number of Tandem Repeats Upstream of the Insulin Gene Is a Susceptibility Locus for Latent Autoimmune Diabetes in Adults (2006) (56)
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures (2019) (56)
The transferability of lipid loci across African, Asian and European cohorts (2019) (55)
Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (55)
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits (2020) (55)
A Powerful Approach to Sub-Phenotype Analysis in Population-Based Genetic Association Studies (2009) (55)
Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants (2014) (54)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (53)
Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia (2018) (53)
Variation Within the Gene Encoding the Upstream Stimulatory Factor 1 Does Not Influence Susceptibility to Type 2 Diabetes in Samples From Populations With Replicated Evidence of Linkage to Chromosome 1q (2006) (52)
A common variant in the FTO gene region is associated with BMI in the general population and predisposes to adult and childhood obesity (2007) (52)
Very low-depth whole-genome sequencing in complex trait association studies (2018) (51)
New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals (2017) (50)
Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts (2012) (50)
ARIEL and AMELIA: Testing for an Accumulation of Rare Variants Using Next-Generation Sequencing Data (2012) (50)
Genetics of type 2 diabetes. (2007) (50)
Large-scale studies of the association between variation at the TNF/LTA locus and susceptibility to type 2 diabetes (2005) (48)
Evaluation of the genetic overlap between osteoarthritis with body mass index and height using genome-wide association scan data (2012) (48)
The effect of FTO variation on increased osteoarthritis risk is mediated through body mass index: a mendelian randomisation study (2013) (48)
Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes (2008) (47)
Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes (2010) (45)
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use (2019) (45)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (45)
Association of HLA-DRB1*13 with susceptibility to uveitis in juvenile idiopathic arthritis in two independent data sets. (2006) (45)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (43)
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
Association studies of insulin receptor substrate 1 gene (IRS1) variants in type 2 diabetes samples enriched for family history and early age of onset. (2004) (43)
Genome‐Wide Association Scan Allowing for Epistasis in Type 2 Diabetes (2011) (42)
Protocol of a population-based prospective COVID-19 cohort study Munich, Germany (KoCo19) (2020) (42)
A new era for Type 2 diabetes genetics (2007) (42)
Genome-wide association study of developmental dysplasia of the hip identifies an association with GDF5 (2018) (40)
Polymorphisms in the tumour necrosis factor gene are not associated with severity of inflammatory polyarthritis (2004) (39)
Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease (2020) (38)
Evidence for large-scale gene-by-smoking interaction effects on pulmonary function (2017) (38)
Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus (2017) (38)
Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches (2019) (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)
Activating Transcription Factor 6 (ATF6) Sequence Polymorphisms in Type 2 Diabetes and Pre-Diabetic Traits (2007) (37)
Evaluation of Association of HNF1B Variants with Diverse Cancers: Collaborative Analysis of Data from 19 Genome-Wide Association Studies (2010) (37)
Disparate genetic influences on polycystic ovary syndrome (PCOS) and type 2 diabetes revealed by a lack of association between common variants within the TCF7L2 gene and PCOS (2007) (36)
Population-Specific Risk of Type 2 Diabetes Conferred by HNF4A P2 Promoter Variants (2008) (36)
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index (2017) (36)
Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts (2020) (35)
Using ancestry-informative markers to identify fine structure across 15 populations of European origin (2014) (34)
Whole Exome Re-Sequencing Implicates CCDC38 and Cilia Structure and Function in Resistance to Smoking Related Airflow Obstruction (2014) (34)
Using ancestry-informative markers to identify fine structure across 15 populations of European origin (2014) (34)
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index (2017) (34)
Using ancestry-informative markers to identify fine structure across 15 populations of European origin (2014) (34)
Common Variation in the LMNA Gene (Encoding Lamin A/C) and Type 2 Diabetes (2007) (34)
Functional genomics in osteoarthritis: Past, present, and future (2016) (34)
Pathways to understanding the genomic aetiology of osteoarthritis (2017) (33)
Chad Genetic Diversity Reveals an African History Marked by Multiple Holocene Eurasian Migrations (2016) (33)
Rare variation at the TNFAIP3 locus and susceptibility to rheumatoid arthritis (2010) (33)
Replication of Associations of Genetic Loci Outside the HLA Region With Susceptibility to Anti–Cyclic Citrullinated Peptide–Negative Rheumatoid Arthritis (2016) (32)
In Search of the SARS-CoV-2 Protection Correlate: Head-to-Head Comparison of Two Quantitative S1 Assays in Pre-characterized Oligo-/Asymptomatic Patients (2021) (32)
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls (2012) (31)
Meta-analysis of exome array data identifies six novel genetic loci for lung function (2017) (31)
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis (2019) (31)
Genome-wide meta-analysis of common variant differences between men and women (2012) (31)
Strengthening Causal Inference for Complex Disease Using Molecular Quantitative Trait Loci. (2019) (31)
Genome-wide association scans for Type 2 diabetes: new insights into biology and therapy. (2007) (31)
Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases (2012) (30)
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa (2017) (30)
Replication of Established Common Genetic Variants for Adult BMI and Childhood Obesity in Greek Adolescents: The TEENAGE Study (2013) (30)
Investigation of Association Between Hip Osteoarthritis Susceptibility Loci and Radiographic Proximal Femur Shape (2015) (30)
Discovery of novel heart rate-associated loci using the Exome Chip (2017) (29)
GLIDERS - A web-based search engine for genome-wide linkage disequilibrium between HapMap SNPs (2009) (29)
Significant Linkage of BMI to Chromosome 10p in the U.K. Population and Evaluation of GAD2 as a Positional Candidate (2006) (29)
Analysis of the contribution to type 2 diabetes susceptibility of sequence variation in the gene encoding stearoyl-CoA desaturase, a key regulator of lipid and carbohydrate metabolism (2004) (28)
The effect of genome-wide association scan quality control on imputation outcome for common variants (2011) (28)
Linkage Disequilibrium Mapping of the Replicated Type 2 Diabetes Linkage Signal on Chromosome 1q (2009) (28)
Maternal and fetal genetic contribution to gestational weight gain (2017) (28)
Evidence for linkage of HLA loci in juvenile idiopathic oligoarthritis: independent effects of HLA-A and HLA-DRB1. (2002) (28)
Radiographic endophenotyping in hip osteoarthritis improves the precision of genetic association analysis (2016) (28)
Finding common susceptibility variants for complex disease: past, present and future (2009) (28)
Epistatic interactions between HLA-DRB1 and interleukin 4, but not interferon-gamma, increase susceptibility to giant cell arteritis. (2004) (28)
Toll-like receptor 4 gene polymorphisms and susceptibility to juvenile idiopathic arthritis (2004) (27)
Examining the relationships between the Pro12Ala variant in PPARG and Type 2 diabetes‐related traits in UK samples (2005) (26)
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits (2018) (26)
Rare and Low Frequency Variant Stratification in the UK Population: Description and Impact on Association Tests (2012) (25)
A novel variant in GLIS3 is associated with osteoarthritis (2018) (25)
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
Polymorphisms in the Glucokinase-Associated, Dual-Specificity Phosphatase 12 (DUSP12) Gene Under Chromosome 1q21 Linkage Peak Are Associated With Type 2 Diabetes (2006) (25)
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations (2021) (25)
A molecular quantitative trait locus map for osteoarthritis (2021) (24)
Population-specific risk of type 2 diabetes ( T 2 D ) conferred by HNF 4 A P 2 promoter variants : a lesson for replication studies (2008) (24)
Familial Hypercholesterolemia and Type 2 Diabetes in the Old Order Amish (2017) (24)
Lack of significant effects of the type 2 diabetes susceptibility loci JAZF1, CDC123/CAMK1D, NOTCH2, ADAMTS9, THADA, and TSPAN8/LGR5 on diabetes and quantitative metabolic traits. (2010) (24)
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms (2016) (23)
High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation (2018) (23)
Using genetically isolated populations to understand the genomic basis of disease (2014) (23)
Family-based analysis of vitamin D receptor gene polymorphisms and type 1 diabetes in the population of South Croatia (2008) (22)
Accelerating functional gene discovery in osteoarthritis (2019) (22)
Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription (2020) (22)
Circulating β-carotene levels and type 2 diabetes—cause or effect? (2009) (22)
Narrow-sense heritability estimation of complex traits using identity-by-descent information (2017) (22)
Whole-genome sequencing analysis of the cardiometabolic proteome (2019) (22)
ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls (2018) (22)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2018) (22)
Defining the power limits of genome‐wide association scan meta‐analyses (2011) (21)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2017) (20)
Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies (2019) (20)
Family-based analysis of tumor necrosis factor and lymphotoxin-alpha tag polymorphisms with type 1 diabetes in the population of South Croatia. (2009) (20)
Sex-specific differences in effect size estimates at established complex trait loci (2012) (20)
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
CCRaVAT and QuTie - enabling analysis of rare variants in large-scale case control and quantitative trait association studies (2010) (20)
Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and Fractures (2018) (20)
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene (2020) (19)
A Variant in MCF 2 L Is Associated with Osteoarthritis (19)
Assessing Rare Variation in Complex Traits (2015) (18)
An evaluation of different meta-analysis approaches in the presence of allelic heterogeneity (2012) (18)
Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation (2016) (18)
An Evaluation of Different Target Enrichment Methods in Pooled Sequencing Designs for Complex Disease Association Studies (2011) (18)
Widespread epigenomic, transcriptomic and proteomic differences between hip osteophytic and articular chondrocytes in osteoarthritis (2018) (18)
Paraoxonase 2 (PON2) polymorphisms and development of renal dysfunction in type 2 diabetes: UKPDS 76 (2006) (17)
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (17)
Analysis with the exome array identifies multiple new independent variants in lipid loci. (2016) (17)
From first to second wave: follow-up of the prospective COVID-19 cohort (KoCo19) in Munich (Germany) (2021) (17)
Evidence for a novel rheumatoid arthritis susceptibility locus on chromosome 6p. (2004) (17)
The mountainous Cretan dietary patterns and their relationship with cardiovascular risk factors: the Hellenic Isolated Cohorts MANOLIS study (2016) (16)
Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels (2007) (16)
The Genetic Epidemiology of Joint Shape and the Development of Osteoarthritis (2020) (15)
Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations (2016) (15)
The type 1 diabetes susceptibility gene SUMO4 at IDDM5 is not associated with susceptibility to rheumatoid arthritis or juvenile idiopathic arthritis. (2005) (15)
Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
Genetic analysis of over one million people identifies 535 novel loci for blood pressure (2017) (14)
Effects of chronic cobalt and chromium exposure after metal‐on‐metal hip resurfacing: An epigenome‐wide association pilot study (2017) (14)
Characterisation of the genomic architecture of human chromosome 17q and evaluation of different methods for haplotype block definition (2005) (13)
Mapping the serum proteome to neurological diseases using whole genome sequencing (2021) (13)
Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa (2017) (13)
MCP-1 gene haplotype association in biopsy proven giant cell arteritis. (2005) (13)
Linking chondrocyte and synovial transcriptional profile to clinical phenotype in osteoarthritis (2021) (12)
Tumour necrosis factor receptor II polymorphism and juvenile idiopathic arthritis. (2002) (12)
Testing for rare variant associations in complex diseases (2011) (12)
New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries (2018) (12)
Imputation of Rare Variants in Next-Generation Association Studies (2013) (12)
Ranking of genome-wide association scan signals by different measures. (2009) (12)
Will the real disease gene please stand up? (2005) (11)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (10)
Identifying susceptibility variants for type 2 diabetes. (2007) (10)
Linkage analysis of cross-sectional and longitudinally derived phenotypic measures to identify loci influencing blood pressure (2003) (10)
Using multivariable Mendelian randomization to estimate the causal effect of bone mineral density on osteoarthritis risk, independently of body mass index (2021) (10)
Whole-exome sequencing in an isolated population from the Dalmatian island of Vis (2016) (10)
Examining the overlap between genome-wide rare variant association signals and linkage peaks in rheumatoid arthritis. (2011) (9)
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data (2019) (9)
Lack of association between juvenile idiopathic arthritis and fas gene polymorphism. (2002) (9)
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation (2019) (9)
Very low depth whole genome sequencing in complex trait association studies (2017) (9)
Do genome-wide association scans have potential for translation? (2011) (9)
Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits : (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x) (2018) (8)
Insights into the molecular landscape of osteoarthritis in human tissues (2021) (8)
Genetic Landscape of the ACE2 Coronavirus Receptor (2022) (8)
The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA? (2019) (8)
Insights from multi-omics integration in complex disease primary tissues. (2022) (7)
Examining the statistical properties of fine‐scale mapping in large‐scale association studies (2008) (7)
Identification of novel putative rheumatoid arthritis susceptibility genes via analysis of rare variants (2009) (7)
Insights into metabolic disease from studying genetics in isolated populations: stories from Greece to Greenland (2016) (7)
Linkage and association studies of discoidin domain receptor 1 (DDR1) single nucleotide polymorphisms (SNPs) in juvenile oligoarthritis. (2004) (6)
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy (2022) (6)
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids (2021) (6)
Decoding the genomic basis of osteoarthritis (2019) (6)
Genetics of type 2 diabetes (2006) (6)
Evaluating the glucose raising effect of established loci via a genetic risk score (2017) (6)
The influence of rare variants in circulating metabolic biomarkers (2018) (5)
Genome Wide Association Meta-Analysis Implicates HLA-DRB1, The BTNL2/HLA-DRA region, and a Novel Susceptibility Locus On Chromosome 1 In Systemic Juvenile Idiopathic Arthritis (2013) (5)
Rare Variant Association Testing for Next-Generation Sequencing Data via Hierarchical Clustering (2013) (5)
Biomedical Research Goes Viral: Dangers and Opportunities (2020) (5)
Index and Predisposes to Childhood and Adult Obesity Gene Is Associated with Body Mass FTO A Common Variant in the (2012) (5)
Erratum: Association analysis of 6,736 U.K. subjects provides replication and confirms TCF7L2 as a type 2 diabetes susceptibility gene with a substantial effect on individual risk. (Diabetes (2006) 55 (2640-2644)) (2006) (5)
A Dietary Pattern with High Sugar Content Is Associated with Cardiometabolic Risk Factors in the Pomak Population (2019) (5)
A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits (2015) (5)
Genome-wide association analysis identi fi es three new susceptibility loci for childhood body mass index (2016) (5)
The use of technology in the subcategorisation of osteoarthritis: a Delphi study approach (2020) (5)
The genetic architecture of osteoarthritis: insights from UK Biobank (2017) (4)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (4)
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
356 COMMON VARIANTS IN SKELETAL DYSPLASIA GENES ARE ASSOCIATED WITH OSTEOARTHRITIS (2011) (4)
Combination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP study (2018) (3)
Genome-wide association and functional analyses identify CASC20 and KIF26B as target loci in heterotopic ossification (2019) (3)
Publisher Correction: Accelerating functional gene discovery in osteoarthritis (2021) (3)
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures (2019) (3)
The interplay of viral loads, clinical presentation, and serological responses in SARS-CoV-2 – Results from a prospective cohort of outpatient COVID-19 cases (2022) (3)
Aberrant expression of agouti signaling protein (ASIP) as a cause of monogenic severe childhood obesity (2022) (3)
An Evaluation of Power to Detect Low-Frequency Variant Associations Using Allele-Matching Tests that Account for Uncertainty (2011) (3)
Powerful detection of osteoarthritis susceptibility loci by comprehensive examination of clinically important endophenotypes (2014) (3)
The Genetic Epidemiology of Developmental Dysplasia of the Hip: A Genome-Wide Association Study Harnessing National Clinical Audit Data (2017) (3)
Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation (2018) (3)
HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis (2015) (3)
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (2019) (3)
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)
83 ANALYSIS OF CANDIDATE OSTEOARTHRITIS GENES IN A META-ANALYSIS OF 8 GENOME-WIDE ASSOCIATION STUDIES (2011) (3)
Genome-Wide Association Meta-Analysis of Eight Independent Systemic Juvenile Idiopathic Arthritis Collections Reveals Regional Association Spanning the Major Histocompatibility Complex Class II and III Gene Cluster (2012) (2)
Erratum to: The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA? (2019) (2)
Systemic juvenile idiopathic arthritis is associated with HLA-DRB1 in Europeans and Americans of European descent (2012) (2)
Large-scale genome-wide meta-analyses provide insights for the development of new disease modifying targets for osteoarthritis (2020) (2)
Polygenic risk score and its potential to improve diagnostic ability in knee and hip osteoarthritis (2020) (2)
Identifi cation of new susceptibility loci for osteoarthritis ( arcOGEN ) : a genome-wide association study (2012) (2)
Susceptibility for latent autoimmune diabetes in adults (LADA) is determined by variation at the 1DDM2 (insulin-gene) locus in white Caucasian patients from UK repositories (2005) (2)
Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes (2018) (2)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (2)
Genome-wide mapping identifies beta-1,4-N-acetyl-galactosaminyl-transferase as a novel determinant of sclerostin levels and bone mineral density (2018) (2)
Large scale case-control and family-based analyses of TCF7L2 variants in > 6000 UK subjects demonstrates an almost two-fold difference in relative risk between homozygote classes (2006) (2)
Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney (2017) (2)
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (2)
Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa (2017) (2)
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions (2023) (2)
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume (2013) (2)
Author Correction: Genomics of disease risk in globally diverse populations (2019) (2)
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk (2023) (2)
Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits (2018) (1)
A molecular map of long non-coding RNA expression, isoform switching and alternative splicing in osteoarthritis (2022) (1)
A GWAS meta-analysis of alpha angle suggests cam-type morphology may be a specific feature of hip osteoarthritis in older adults. (2023) (1)
Genome-wide association study for osteoarthritis – Authors' reply (2013) (1)
Genetics of early-life head circumference and genetic correlations with neurological, psychiatric and cognitive outcomes (2022) (1)
Fas mRNA EXPRESSION IN BLOOD IS REDUCED DURING EPISODES OF HUMAN CORNEAL GRAFT REJECTION1 (2001) (1)
Risk Assessment for Hip and Knee Osteoarthritis Using Polygenic Risk Scores (2022) (1)
Putative association signals identified through high-density LD mapping of the replicated T2D linkage region on chromosome 1q are not confirmed in large-scale follow-up studies (2008) (1)
Major Histocompatibility Complex Class II Gene Cluster Harbors Systemic Juvenile Idiopathic Arthritis Susceptibility Locus (2011) (1)
28GENETIC ASSOCIATION ANALYSES IN DIVERSE ANCESTRY POPULATIONS (2019) (1)
The Uk Bileve Study: The First Genetic Study In Uk Biobank Identifies Novel Regions Associated With Airway Obstruction And Smoking Behaviour (2015) (1)
Common variation in the FTO (fused toes) gene is strongly associated with adiposity measures in the northern finnish birth cohort of 1966 (2007) (1)
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (2018) (1)
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (1)
Candidate gene analysis of genetic susceptibility to aseptic loosening and deep infection of cemented total hip replacement. (2003) (1)
Fine-mapping type 2 diabetes causal variants on chromosome 9p21 in 2000 UK cases and 3000 unselected controls (2008) (1)
Studies of genome-wide association data support a genetic overlap between type 2 diabetes and prostate cancer (2008) (1)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
Meta-Analysis of Rare Variants (2015) (1)
Using multivariable mendelian randomization to estimate the bmi-independent causal effect of bone mineral density on osteoarthritis (2020) (1)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2019) (1)
PW01-038 – Genomewide association study of Still’s disease (2013) (1)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution (2019) (1)
First-generation scan of genome-wide association data allowing for epistasis prioritises multiple interacting candidate loci in T2D (2008) (1)
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy (2022) (1)
Extended analysis of genome-wide scans provides clues about novel common and rare susceptibility loci for type 2 diabetes (2008) (1)
The transcriptome of regenerating zebrafish scales identifies genes involved in human bone disease (2020) (1)
Analyses Conditional on Established Type 2 Diabetes (T2D) Loci Reveal Putative Novel Associations (2009) (1)
Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2015) (1)
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology (2022) (1)
Using genetically isolated populations to understand the genomic basis of disease (2014) (1)
Stratified analysis of the Wellcome Trust Case Control Consortium scan for type 2 diabetes reveals susceptibility loci that may affect age of diagnosis (2008) (1)
Publisher Correction to: Protocol of a population-based prospective COVID-19 cohort study Munich, Germany (KoCo19) (2020) (1)
Improved phenotype definitions of OA in genetic association studies highlight a structural role for a common variant in LRCH1 (2015) (1)
Lowering of circulating sclerostin may increase risk of atherosclerosis and its risk factors: evidence from a genome-wide association meta-analysis followed by Mendelian randomization (2022) (1)
Population‐wide copy number variation calling using variant call format files from 6,898 individuals (2018) (1)
An epigenome-wide view of osteoarthritis in primary tissues (2022) (1)
Reply to "Human genetic studies on osteoarthritis from clinicians' viewpoints". (2012) (1)
Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations (2022) (1)
High-density association mapping and comprehensive tagging of the type 2 diabetes linkage region on chromosome 1q in 4 European populations (2007) (1)
Erratum: Whole-genome sequence-based analysis of thyroid function (2015) (1)
CANDIDATE GENE ANALYSIS OF THE DISTAL EXTENDED MHC REGION IN RHEUMATOID ARTHRITIS (2003) (1)
The Genetic Epidemiology of Joint Shape and the Development of Osteoarthritis (2020) (1)
Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations (2022) (0)
Linkage disequilibrium mapping of the type 2 diabetes susceptibility variants on chromosome Iq in European populations (2005) (0)
University of Southern Denmark Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes Grarup, (2018) (0)
University of Southern Denmark Loss-of-function variants in ADCY 3 increase risk of obesity and type 2 diabetes (2018) (0)
Molecular phenotyping of patient chondrocytes reveals genes and pathways involved in osteoarthritis (2017) (0)
Large-scale follow-up study does not confirm putative association signals in the NOS1AP and PKLR gene regions on chromosome 1q with type 2 diabetes (2008) (0)
Variation in the retinoid X receptor gamma gene is associated with type 2 diabetes in sample sets displaying linkage to chromosome 1q (2006) (0)
Whole-genome sequence-based analysis of thyroid function (vol 6, 5681, 2015) (2015) (0)
University of Groningen Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation (2018) (0)
Mendelian Randomization Studies of the Role of Biomarkers in Type 2 Diabetes (2009) (0)
Identifying causal serum protein–cardiometabolic trait relationships using whole genome sequencing (2022) (0)
Replication of HLA class II locus association with susceptibility to podoconiosis in three Ethiopian ethnic groups (2021) (0)
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
Search for low-frequency variants associated with overall and central adiposity (2009) (0)
Reply to Dlouha et al (2010) (0)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
Genome-wide association analysis of rare variants with type 2 diabetes (2011) (0)
CONFIRMATION OF ASSOCIATION OF HLA-DRB1*13 WITH UVEITIS IN JUVENILE IDIOPATHIC ARTHRITIS (2004) (0)
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2021) (0)
Large-scale association studies of candidate genes and their interactions in Type 2 diabetes (2004) (0)
Genetic mechanisms of 184 neuro-related proteins in human plasma (2023) (0)
Type 2 diabetes genetics: starting to solve the puzzle (2008) (0)
Replicated association between type 2 diabetes and variants in CAPON revealed by high density linkage disequilibrium mapping on chromosome 1q (2006) (0)
The long non-coding RNA CASC20 is a susceptibility locus for heterotopic ossification: results of a genome-wide association study (2018) (0)
National clinical audit data decodes the genetic architecture of developmental dysplasia of the hip (2017) (0)
Universitet Dietary intake , FTO genetic variants and adiposity (2015) (0)
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures (2019) (0)
Genetics of early-life head circumference and genetic correlations with neurological, psychiatric and cognitive outcomes (2022) (0)
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications (2023) (0)
Genetic susceptibility to deep infection and aseptic loosening of cemented total hip replacement. The role of polymorphic variations in the TNF-alpha gene (2003) (0)
THE arcOGEN CONSORTIUM: STAGE 1 OF A GENOME-WIDE ASSOCIATION SCAN FOR OSTEOARTHRITIS (2010) (0)
A comprehensive transcriptional map of knee osteoarthritis (2020) (0)
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders (2023) (0)
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures (2019) (0)
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors (2019) (0)
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations (2017) (0)
Low frequency genetic variation in TP53 is associated with final head circumference (2017) (0)
Translational genomics: from genetic discovery to translational impact (0)
Positional candidate gene selection on chromosome 1q using bioinformatics and large scale association analysis (2005) (0)
Integrative epigenomics, transcriptomics and proteomics of patient chondrocytes reveal genes and pathways involved in osteoarthritis (2017) (0)
Genomics of disease risk in globally diverse populations (2019) (0)
Modelling genetic mechanisms of osteoarthritis using human induced pluripotent stem cells (2018) (0)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (0)
University of Groningen Investigation of common , low-frequency and rare genome-wide variation in anorexia nervosa Kas (2017) (0)
355 GENOME-WIDE ASSOCIATION STUDY TO IDENTIFY NEW GENES AND PATHWAYS CONFERRING RISK TO OA SUSCEPTIBILITY IN MULTIPLE JOINT LOCATIONS AS DEFINED IN THE GARP STUDY (2011) (0)
Fas mRNA expression is reduced in human corneal graft rejection (2001) (0)
Low frequency genetic variation in the TP53 locus has large effects on head circumference and intracranial volume (2018) (0)
arcOGEN Consortium (2019). Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. Nature Genetics , 51 (2), 230-236. (2018) (0)
An epigenome-wide view of osteoarthritis in target tissues (2021) (0)
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (0)
Gene-based whole genome sequencing meta-analysis of 250 circulating proteins in three isolated European populations (2022) (0)
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations (2019) (0)
Relationship between common variants in the Stearoyl CoA desaturase (SCD) gene and intermediate phenotypes associated with type 2 diabetes (2005) (0)
Package ‘GWsignif’ (2016) (0)
Common variation in the LMNA gene increases susceptibility to type 2 diabetes (2006) (0)
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis (2018) (0)
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (2018) (0)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
Exome Sequencing Identifies Multiple Genes and Gene-Sets Contributing to Severe Childhood Obesity (2019) (0)
Review Strengthening Causal Inference for Complex Disease Using Molecular 2 Quantitative Trait Loci 3 (2019) (0)
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (2019) (0)
Identification of five novel osteoarthritis susceptibility loci through the UK biobank resourse of five novel osteoarthritis susceptibility loci through the UK biobank resourse (2017) (0)
Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
Analysis of common and less frequent genetic variation for head circumference: Next-generation genetic association studies within the UK10K COHORTS project (2015) (0)
Using imputation to investigate association of low-frequency variants with adiposity in the 1966 Northern Finnish birth cohort (2010) (0)
Linkage and association analysis of alternative phenotypic measures to identify loci influencing blood pressure (2002) (0)
THE EFFECTS OF CHRONIC COBALT AND CHROMIUM EXPOSURE AFTER METAL-ON-METAL HIP RESURFACING ON DNA METHYLATION: AN EPIGENOME-WIDE ASSOCIATION STUDY (2016) (0)
UK 10 K Consortium (2019) (0)
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (2019) (0)
Candidate gene analysisof susceptibility to aseptic looseningand deep infectionof total hip replacement. (2003) (0)
The effect of sample size on tagging SNP performance and consequences for complex disease gene mapping (2005) (0)
Title : Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (0)
Large-scale association studies to identify diabetes-susceptibility loci on chromosome 1q: The importance of stringent quality control (2006) (0)
Association of FTO variants with BMI, fat mass and waist in the isolated population of Sorbs in Germany (2008) (0)
Causal effects for higher body mass index, but not for triglyceride levels or genetic predisposition to type 2 diabetes, on osteoarthritis (2018) (0)
Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits (2018) (0)
Genome-wide association data highlight an aetiological role for disturbances in cyclin-dependent kinase pathways in type 2 diabetes (2007) (0)
Dissecting the Development of Dupuytren Disease Through Human Genetics (2016) (0)
Integrated molecular phenotyping identifies genes and pathways disrupted in osteoarthritis (2016) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
Contents Vol. 74, 2012 (2013) (0)
GENETIC SUSCEPTIBILITY TO ASEPTIC AND SEPTIC FAILURE OF TOTAL HIP REPLACEMENT (2005) (0)
Genome-wide association study of developmental dysplasia of the hip identifies an association with GDF5 (2018) (0)
Improving the accuracy of clinical risk prediction for hip and knee osteoarthritis by a polygenic risk score (2021) (0)
Front & Back Matter (2012) (0)
Genetic studies of birth weight give biological insights into links with adult disease (2016) (0)
A novel splice-affecting HNF1A variant with large population impact on diabetes in Greenland (2022) (0)
Large-scale transcriptomic analysis reveals new markers of osteoarthritis progression (2021) (0)
Meta-analysis in genome-wide association studies: application to type 2 diabetes (2008) (0)
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (0)
Association analyses based on false discovery rate implicate 243 susceptibility loci for coronary artery disease (2017) (0)
Biological pathway analysis for type 2 diabetes using genome-wide association data (2007) (0)
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits (2018) (0)
Correction (2017) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
365 SNPS ASSOCIATED WITH NORMAL VARIATION IN ADULT HUMAN HEIGHT ARE NOT ASSOCIATED WITH OSTEOARTHRITIS SUSCEPTIBILITY (2008) (0)
Peer Review Status: Peer reviewed Citation for item: (2012) (0)
Genome-wide analyses using UK biobank data povide new therapeutic targets for osteoarthritis (2019) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (0)
Association between polymorphisms within the SUR1/Kir6.2 gene region and polycystic ovary syndrome: a case-control study (2006) (0)
Genome-wide analyses using UK biobank data povide new therapeutic targets for osteoarthritis (2019) (0)
Epigenome-wide association study in knee osteoarthritis generates novel insights into disease mechanisms (2020) (0)
ELECTRONIC HEALTH RECORDS HELP ELUCIDATE THE FIRST GENOME WIDE ASSOCIATION SIGNAL FOR DEVELOPMENTAL DYSPLASIA OF THE HIP (2016) (0)
Front & Back Matter (2012) (0)
THE GENETICS OF OSTEOLYSIS AFTER TOTAL HIP ARTHROPLASTY: RESULTS OF TWO GENOME-WIDE ASSOCIATION STUDIES (2018) (0)
Shared polygenic effects of FEV1 in the first genetic study in UK Biobank (2015) (0)
GENETIC SUSCEPTIBILITY TO DEEP INFECTION AND ASEPTIC LOOSENING OF CEMENTED TOTAL HIP REPLACEMENT. THE ROLE OF ALL KNOWN POLYMORPHIC VARIATIONS IN THE TNF-ALPHA GENE (2004) (0)
Large-scale replication typing of modest signals from genome-wide association studies identifies additional type 2 diabetes susceptibility variants in the IGF2BP2 and VEGFA genes (2007) (0)

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