Panos Deloukas

Q: What Schools Are Affiliated With Panos Deloukas

Panos Deloukas is affiliated with the following schools: Queen Mary University of London, King Abdulaziz University, King's College London, Aristotle University of Thessaloniki, University of Cambridge, University of Leicester, Uppsala University, University of Oxford, Imperial College London

Panos Deloukas's AcademicInfluence.com Rankings

Panos Deloukas

Biology

#9070

World Rank

#12228

Historical Rank

Bioinformatics

#110

World Rank

#112

Historical Rank

Computational Biology

#190

World Rank

#191

Historical Rank

Genetics

#1007

World Rank

#1105

Historical Rank

biology Degrees

Download Badge

Biology

Panos Deloukas's Degrees

Masters Bioinformatics Imperial College London

Why Is Panos Deloukas Influential?

(Suggest an Edit or Addition)

According to Wikipedia, Panagiotis "Panos" Deloukas FMedSci is Professor of Cardiovascular Genomics and Dean for Life Sciences at the William Harvey Research Institute. This institute is a division of Queen Mary University of London 's Barts and the London School of Medicine and Dentistry. He has been an ISI highly cited researcher since 2012 and was elected a fellow of the Academy of Medical Sciences in 2018.

(See a Problem?)

Panos Deloukas'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

Initial sequencing and analysis of the human genome. (2001) (15222)
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) (9208)
A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) (3485)
Integrating common and rare genetic variation in diverse human populations (2010) (2731)
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (2008) (2621)
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) (2511)
Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
Genomewide association analysis of coronary artery disease. (2007) (2067)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
Hundreds of variants clustered in genomic loci and biological pathways affect human height (2010) (1961)
Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2009) (1735)
Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes (2007) (1734)
Common variants in ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease (2011) (1701)
Letter abstract - Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's Disease (2009) (1644)
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) (1567)
Large-scale association analysis identifies new risk loci for coronary artery disease (2012) (1507)
Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) (1455)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease, and shows evidence for additional susceptibility genes (2009) (1441)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2013) (1388)
Convergent adaptation of human lactase persistence in Africa and Europe (2007) (1353)
Common variants near MC4R are associated with fat mass, weight and risk of obesity (2008) (1307)
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility (2007) (1227)
New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
Genome-wide association study identifies eight loci associated with blood pressure (2009) (1225)
Population genomics of human gene expression (2007) (1203)
Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis (2013) (1170)
Genome-wide association study identifies 74 loci associated with educational attainment (2016) (1114)
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants (2009) (1100)
A Gene Map of the Human Genome (1996) (1080)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (1073)
The Fine-Scale Structure of Recombination Rate Variation in the Human Genome (2004) (961)
Multiple common variants for celiac disease influencing immune gene expression (2010) (958)
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 (2010) (947)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
Human metabolic individuality in biomedical and pharmaceutical research (2011) (929)
The genetic architecture of type 2 diabetes (2016) (927)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease (2011) (894)
Genetically distinct subsets within ANCA-associated vasculitis. (2012) (820)
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility (2011) (807)
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
Loss-of-function mutations in APOC3, triglycerides, and coronary disease. (2014) (799)
Common Regulatory Variation Impacts Gene Expression in a Cell Type–Dependent Manner (2009) (790)
Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC (2006) (764)
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (2012) (756)
Mapping cis- and trans-regulatory effects across multiple tissues in twins (2012) (754)
Variants in MTNR1B influence fasting glucose levels (2009) (742)
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)
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci (2013) (689)
Twenty bone mineral density loci identified by large-scale meta-analysis of genome-wide association studies (2009) (687)
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 (2007) (686)
HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans. (2011) (675)
Signatures of mutation and selection in the cancer genome (2010) (671)
A physical map of 30,000 human genes. (1998) (670)
DNA methylation and body-mass index: a genome-wide analysis (2014) (664)
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study (2008) (658)
Highly parallel SNP genotyping. (2003) (658)
Epigenome-Wide Scans Identify Differentially Methylated Regions for Age and Age-Related Phenotypes in a Healthy Ageing Population (2012) (649)
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci (2010) (639)
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease (2011) (638)
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2016) (634)
A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose (2009) (629)
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (600)
High density genetic mapping identifies new susceptibility loci for rheumatoid arthritis (2012) (595)
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility (2019) (589)
Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2010) (587)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
Genome-wide association study identifies five loci associated with lung function (2010) (560)
Obesity accelerates epigenetic aging of human liver (2014) (557)
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity (2012) (555)
Genome-Wide Associations of Gene Expression Variation in Humans (2005) (552)
The largest prospective warfarin-treated cohort supports genetic forecasting. (2009) (551)
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium (2009) (551)
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)
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers (2015) (520)
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci (2011) (518)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region (2009) (513)
Rare and low-frequency coding variants alter human adult height (2016) (511)
New susceptibility locus for coronary artery disease on chromosome 3q22.3 (2009) (510)
The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits (2012) (506)
Common VKORC1 and GGCX polymorphisms associated with warfarin dose (2005) (493)
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) (476)
Patterns of Cis Regulatory Variation in Diverse Human Populations (2012) (470)
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
The Architecture of Gene Regulatory Variation across Multiple Human Tissues: The MuTHER Study (2011) (460)
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals (2012) (459)
Mapping the human genetic architecture of COVID-19 (2021) (455)
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease (2008) (455)
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. (2008) (450)
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease (2016) (434)
Exome-wide association study of plasma lipids in >300,000 individuals (2017) (428)
A first-generation linkage disequilibrium map of human chromosome 22 (2002) (424)
New gene functions in megakaryopoiesis and platelet formation (2011) (423)
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)
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes (2010) (421)
Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease (2010) (417)
Bayesian refinement of association signals for 14 loci in 3 common diseases (2012) (416)
Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease (2008) (410)
Identification of fifteen new psoriasis susceptibility loci highlights the role of innate immunity (2012) (397)
Genome-wide and fine-resolution association analysis of malaria in West Africa (2009) (394)
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke (2012) (392)
Association of warfarin dose with genes involved in its action and metabolism (2006) (390)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study (2012) (382)
A genome-wide association meta-analysis identifies new childhood obesity loci (2012) (375)
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium (2009) (369)
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits (2013) (365)
Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults (2018) (359)
Seventy-five genetic loci influencing the human red blood cell (2012) (357)
LDL-cholesterol concentrations: a genome-wide association study (2008) (355)
Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements. (2013) (341)
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis (2013) (337)
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer (2010) (329)
Genetic variation in LIN28B is associated with the timing of puberty (2009) (327)
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)
META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS (2011) (325)
Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies (2010) (325)
A genome-wide association study of testicular germ cell tumor (2009) (322)
Identification of an imprinted master trans-regulator at the KLF14 locus related to multiple metabolic phenotypes (2011) (316)
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy. (2002) (313)
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (309)
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis (2017) (308)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
Comparison of human genetic and sequence-based physical maps (2001) (292)
Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci. (2015) (291)
Inactivating mutations in NPC1L1 and protection from coronary heart disease. (2014) (289)
Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation (2014) (287)
Association Between Low-Density Lipoprotein Cholesterol-Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis. (2016) (285)
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation (2015) (285)
A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample (2011) (281)
The DNA sequence and comparative analysis of human chromosome 20 (2004) (280)
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease (2017) (278)
A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease (2011) (278)
Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes. (2004) (277)
The Influence of Recombination on Human Genetic Diversity (2006) (270)
Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture (2009) (267)
A genotype calling algorithm for the Illumina BeadArray platform (2007) (263)
Integrated Genetic and Epigenetic Analysis Identifies Haplotype-Specific Methylation in the FTO Type 2 Diabetes and Obesity Susceptibility Locus (2010) (254)
Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight (2010) (250)
A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms. (2005) (248)
Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame Size (2009) (247)
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (2016) (242)
Inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A causes TAR (2012) (239)
Gene expression changes with age in skin, adipose tissue, blood and brain (2013) (237)
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension (2016) (234)
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study (2013) (232)
Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease (2011) (228)
Low copy number of the salivary amylase gene predisposes to obesity (2014) (224)
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms (2017) (224)
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption (2014) (224)
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi (2009) (223)
Integration of Genetic, Clinical, and INR Data to Refine Warfarin Dosing (2010) (223)
Genetically determined height and coronary artery disease. (2015) (220)
Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism. (2015) (216)
Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21 (2010) (215)
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci (2016) (214)
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer (2012) (213)
Metabolomic markers reveal novel pathways of ageing and early development in human populations (2013) (209)
ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy (2013) (208)
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins (2014) (207)
The impact of SNP density on fine-scale patterns of linkage disequilibrium. (2004) (204)
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) (204)
Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes. (2004) (203)
Genetic evidence of assortative mating in humans (2017) (199)
IL23R Variation Determines Susceptibility But Not Disease Phenotype in Inflammatory Bowel Disease (2007) (199)
Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship. (2009) (199)
Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes (2011) (197)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure underpinning obesity (2017) (193)
Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome (2012) (191)
The link between family history and risk of type 2 diabetes is not explained by anthropometric, lifestyle or genetic risk factors: the EPIC-InterAct study (2012) (190)
Gene-Lifestyle Interaction and Type 2 Diabetes: The EPIC InterAct Case-Cohort Study (2014) (187)
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility (2015) (185)
Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1. (2011) (177)
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett’s esophagus (2012) (176)
Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India (2013) (168)
A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels (2009) (164)
Large Scale Association Analysis of Novel Genetic Loci for Coronary Artery Disease (2009) (163)
Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes (2000) (158)
Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22 (2010) (156)
A global network for investigating the genomic epidemiology of malaria (2008) (153)
DNA Methylation of Lipid-Related Genes Affects Blood Lipid Levels (2015) (153)
FTO genetic variants, dietary intake and body mass index: insights from 177,330 individuals. (2014) (151)
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways (2012) (150)
Predicting genome-wide DNA methylation using methylation marks, genomic position, and DNA regulatory elements (2013) (150)
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits (2017) (149)
Meta-analyses identify 13 novel loci associated with age at menopause and highlights DNA repair and immune pathways (2011) (149)
Design and cohort description of the InterAct Project: an examination of the interaction of genetic and lifestyle factors on the incidence of type 2 diabetes in the EPIC Study (2011) (148)
Directional dominance on stature and cognition in diverse human populations (2015) (144)
A functional genomics approach reveals novel quantitative trait loci associated with platelet signaling pathways. (2009) (143)
Loci at chromosomes 13, 19 and 20 influence age at natural menopause (2009) (143)
Phosphodiesterase genes are associated with susceptibility to major depression and antidepressant treatment response (2006) (138)
A variant in MCF2L is associated with osteoarthritis. (2011) (137)
The Molecular Genetic Architecture of Self-Employment (2013) (137)
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci (2017) (135)
Common variants in the region around Osterix are associated with bone mineral density and growth in childhood (2009) (135)
Integrating Genome-Wide Genetic Variations and Monocyte Expression Data Reveals Trans-Regulated Gene Modules in Humans (2011) (134)
Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia (2010) (134)
Differential methylation of the TRPA1 promoter in pain sensitivity (2014) (133)
Differential methylation of the TRPA1 promoter in pain sensitivity (2014) (133)
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)
The power of genetic diversity in genome-wide association studies of lipids (2021) (129)
A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function. (2009) (124)
A genome-wide association study identifies three loci associated with mean platelet volume. (2009) (123)
The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders. (2002) (119)
Cis and Trans Effects of Human Genomic Variants on Gene Expression (2014) (118)
Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake1234 (2013) (118)
Male-pattern baldness susceptibility locus at 20p11 (2008) (117)
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)
The Pakistan Risk of Myocardial Infarction Study: a resource for the study of genetic, lifestyle and other determinants of myocardial infarction in South Asia (2009) (111)
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation (2015) (110)
Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) (2001) (106)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
Association of Genetic Loci With Glucose Levels in Childhood and Adolescence (2011) (103)
The portability of tagSNPs across populations: a worldwide survey. (2006) (101)
An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins (2014) (99)
Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants. (2015) (98)
Common variants in the HLA-DRB1-HLA-DQA1 Class II region are associated with susceptibility to visceral leishmaniasis (2013) (97)
A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. (2010) (97)
The brain-derived neurotrophic factor rs6265 (Val66Met) polymorphism and depression in Mexican-Americans (2007) (92)
A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm. (2013) (92)
Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
A Pharmacometric Model Describing the Relationship Between Warfarin Dose and INR Response With Respect to Variations in CYP2C9, VKORC1, and Age (2010) (92)
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease (2016) (92)
Smoking induces coordinated DNA methylation and gene expression changes in adipose tissue with consequences for metabolic health (2018) (91)
Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases (2012) (90)
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. (2010) (89)
Eight blood pressure loci identified by genome-wide association study of 34,433 people of European ancestry (2009) (88)
Gene × dietary pattern interactions in obesity: analysis of up to 68 317 adults of European ancestry (2015) (87)
Epigenetic Patterns in Blood Associated With Lipid Traits Predict Incident Coronary Heart Disease Events and Are Enriched for Results From Genome-Wide Association Studies (2017) (87)
The correlation between reading and mathematics ability at age twelve has a substantial genetic component (2014) (87)
A Comparison of the Whole Genome Approach of MeDIP-Seq to the Targeted Approach of the Infinium HumanMethylation450 BeadChip® for Methylome Profiling (2012) (86)
The population pharmacokinetics of R- and S-warfarin: effect of genetic and clinical factors. (2012) (85)
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing (2017) (85)
The Presence of Methylation Quantitative Trait Loci Indicates a Direct Genetic Influence on the Level of DNA Methylation in Adipose Tissue (2013) (85)
Facilitating genome navigation: survey sequencing and dense radiation-hybrid gene mapping (2005) (84)
Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation (2015) (84)
Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy (2010) (84)
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations (2021) (83)
Meta-analysis investigating associations between healthy diet and fasting glucose and insulin levels and modification by loci associated with glucose homeostasis in data from 15 cohorts. (2013) (83)
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. (2016) (81)
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals (2022) (80)
A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs. (2009) (79)
A Variant in LDLR Is Associated With Abdominal Aortic Aneurysm (2013) (79)
Fine-mapping, trans-ancestral, and genomic analyses identify causal variants, cells, genes, and drug targets for type 1 diabetes (2020) (79)
High-Throughput Genotyping of Salmonella enterica Serovar Typhi Allowing Geographical Assignment of Haplotypes and Pathotypes within an Urban District of Jakarta, Indonesia (2008) (78)
Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length (2009) (76)
The DNA sequence and analysis of human chromosome 13 (2004) (75)
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process (2014) (75)
Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy (2007) (74)
Human candidate gene polymorphisms and risk of severe malaria in children in Kilifi, Kenya: a case-control association study (2018) (73)
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci (2019) (72)
Genome-Wide Association Meta-Analysis of Cortical Bone Mineral Density Unravels Allelic Heterogeneity at the RANKL Locus and Potential Pleiotropic Effects on Bone (2010) (71)
High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta (2010) (70)
Genetic and environmental factors determining clinical outcomes and cost of warfarin therapy: a prospective study (2009) (69)
Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples. (2004) (68)
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)
Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants (2015) (66)
Association of the 9p21.3 Locus With Risk of First-Ever Myocardial Infarction in Pakistanis: Case-Control Study in South Asia and Updated Meta-Analysis of Europeans (2010) (65)
Genome-wide association study identifies 48 common genetic variants associated with handedness (2019) (65)
A saturated map of common genetic variants associated with human height (2022) (65)
The DNA sequence and comparative analysis of human chromosome 10 (2004) (65)
Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 gene. (2005) (64)
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2009) (64)
Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p. (2003) (63)
The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. (2012) (61)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (61)
Corrigendum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (2011) (60)
A genome-wide association study suggests that a locus within the ataxin 2 binding protein 1 gene is associated with hand osteoarthritis: the Treat-OA consortium (2009) (59)
Overview of the MHC fine mapping data (2009) (59)
Identification of PLCL1 Gene for Hip Bone Size Variation in Females in a Genome-Wide Association Study (2008) (59)
Consumption of meat is associated with higher fasting glucose and insulin concentrations regardless of glucose and insulin genetic risk scores: a meta-analysis of 50,345 Caucasians. (2015) (59)
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
The complete exon-intron structure of the 156-kb human gene NFKB1, which encodes the p105 and p50 proteins of transcription factors NF-kappa B and I kappa B-gamma: implications for NF-kappa B-mediated signal transduction. (1995) (58)
A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site. (2012) (58)
Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project (2012) (58)
The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project (2010) (58)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
Clustered Coding Variants in the Glutamate Receptor Complexes of Individuals with Schizophrenia and Bipolar Disorder (2011) (57)
Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein. (2004) (56)
Genome-Wide Haplotype Analysis of Cis Expression Quantitative Trait Loci in Monocytes (2013) (56)
Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease (2009) (54)
Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium (2018) (54)
The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X (2001) (54)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (53)
Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium maps (2004) (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)
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (52)
Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits (2011) (52)
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases (2018) (52)
New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals (2017) (50)
A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the common deleted region. (1998) (49)
Extent, Causes, and Consequences of Small RNA Expression Variation in Human Adipose Tissue (2012) (49)
Evaluation of the genetic overlap between osteoarthritis with body mass index and height using genome-wide association scan data (2012) (48)
Gamma-glutamyl carboxylase (GGCX) microsatellite and warfarin dosing. (2005) (48)
The HapMap project and its application to genetic studies of drug response (2004) (48)
NME6: a new member of the nm23/nucleoside diphosphate kinase gene family located on human chromosome 3p21.3 (1999) (47)
A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation (2014) (46)
Population Genetic Analysis of Plasmodium falciparum Parasites Using a Customized Illumina GoldenGate Genotyping Assay (2011) (46)
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry (2011) (46)
Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays. (2008) (45)
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness (2017) (45)
Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits (2015) (45)
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants (2021) (45)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (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)
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
Genetic Risk Score for Coronary Disease Identifies Predispositions to Cardiovascular and Noncardiovascular Diseases. (2019) (42)
A multi-factorial analysis of response to warfarin in a UK prospective cohort (2016) (42)
DNA sequence and structural properties as predictors of human and mouse promoters (2008) (42)
Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci (2013) (42)
Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children (2016) (41)
Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions (2017) (41)
Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (39)
Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population (2017) (39)
Expression of Phosphofructokinase in Skeletal Muscle Is Influenced by Genetic Variation and Associated With Insulin Sensitivity (2014) (39)
Modifier Effects between Regulatory and Protein-Coding Variation (2008) (37)
miR-133a Regulates Vitamin K 2,3-Epoxide Reductase Complex Subunit 1 (VKORC1), a Key Protein in the Vitamin K Cycle (2012) (37)
Activating Transcription Factor 6 (ATF6) Sequence Polymorphisms in Type 2 Diabetes and Pre-Diabetic Traits (2007) (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)
Rare coding variants and X-linked loci associated with age at menarche (2015) (36)
Characterization of the imprinted polycomb gene L3MBTL, a candidate 20q tumour suppressor gene, in patients with myeloid malignancies (2004) (36)
A comparison of tagging methods and their tagging space. (2005) (36)
Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression (2012) (36)
SNP allele frequency estimation in DNA pools and variance components analysis. (2004) (36)
Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing (2018) (36)
Population-Specific Risk of Type 2 Diabetes Conferred by HNF4A P2 Promoter Variants (2008) (36)
Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus (2013) (35)
The sex-specific associations of the aromatase gene with Alzheimer’s disease and its interaction with IL10 in the Epistasis Project (2013) (34)
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (34)
Common Variation in the LMNA Gene (Encoding Lamin A/C) and Type 2 Diabetes (2007) (34)
Integrative DNA methylome analysis of pan-cancer biomarkers in cancer discordant monozygotic twin-pairs (2016) (33)
Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants. (2005) (33)
Novel Loci Associated with Increased Risk of Sudden Cardiac Death in the Context of Coronary Artery Disease (2013) (32)
Replication of Associations of Genetic Loci Outside the HLA Region With Susceptibility to Anti–Cyclic Citrullinated Peptide–Negative Rheumatoid Arthritis (2016) (32)
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls (2012) (31)
A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa (2017) (30)
Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake 1 – 4 (2013) (30)
Investigation of Association Between Hip Osteoarthritis Susceptibility Loci and Radiographic Proximal Femur Shape (2015) (30)
The isolation and high-resolution chromosomal mapping of human SOX14 and SOX21; two members of the SOX gene family related to SOX1, SOX2, and SOX3 (1999) (29)
Discovery of novel heart rate-associated loci using the Exome Chip (2017) (29)
Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease (2013) (29)
Using genome-wide complex trait analysis to quantify ‘ missing heritability ’ in Parkinson ’ s disease (2012) (29)
Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease (2016) (29)
Genetic Determinants of Major Blood Lipids in Pakistanis Compared With Europeans (2010) (29)
Association of the GGCX (CAA)16/17 repeat polymorphism with higher warfarin dose requirements in African Americans (2012) (29)
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)
A first update on mapping the human genetic architecture of COVID-19 (2022) (27)
The role of vitamin D receptor gene polymorphisms in the bone mineral density of Greek postmenopausal women with low calcium intake. (2011) (27)
Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function (2022) (27)
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12 (2016) (26)
Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (26)
Genomic risk prediction of coronary artery disease in nearly 500,000 adults: implications for early screening and primary prevention (2018) (26)
Polymorphisms in the Glucokinase-Associated, Dual-Specificity Phosphatase 12 (DUSP12) Gene Under Chromosome 1q21 Linkage Peak Are Associated With Type 2 Diabetes (2006) (25)
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis (2016) (25)
High Prevalence of Posterior Polymorphous Corneal Dystrophy in the Czech Republic; Linkage Disequilibrium Mapping and Dating an Ancestral Mutation (2012) (25)
Allelic expression mapping across cellular lineages to establish impact of non-coding SNPs (2014) (25)
Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
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)
Genetically modulated educational attainment and coronary disease risk. (2019) (24)
MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls (2017) (24)
Interactions between PPAR-α and inflammation-related cytokine genes on the development of Alzheimer's disease, observed by the Epistasis Project. (2012) (23)
Concordance for clonal hematopoiesis is limited in elderly twins. (2019) (23)
Impact of Selection Bias on Estimation of Subsequent Event Risk (2017) (23)
Thyroid function affects the risk of stroke via atrial fibrillation: a Mendelian Randomization study. (2020) (23)
Association of Birth Weight With Type 2 Diabetes and Glycemic Traits (2019) (23)
A systematic evaluation of 151 candidate genes for their association with osteoporosis and osteoporotic fracture in a meta-analysis of genome-wide association data (2009) (22)
Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles (2016) (22)
Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36[S] (2016) (22)
Three human glutamate dehydrogenase genes (GLUD1, GLUDP2, and GLUDP3) are located on chromosome 10q, but are not closely physically linked. (1993) (22)
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events (2019) (21)
Genome Wide Association Studies: Identifying the Genes that Determine the Risk of Abdominal Aortic Aneurysm (2008) (21)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2017) (20)
Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia (2014) (20)
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms (2016) (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)
Higher Nevus Count Exhibits a Distinct DNA Methylation Signature in Healthy Human Skin: Implications for Melanoma (2017) (20)
Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy (2019) (19)
Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion (2009) (19)
Does a short breastfeeding period protect from FTO-induced adiposity in children? (2011) (19)
Emerging applications of genome-editing technology to examine functionality of GWAS-associated variants for complex traits. (2018) (19)
A Variant in MCF 2 L Is Associated with Osteoarthritis (19)
Variation in normal range thyroid function affects serum cholesterol levels, blood pressure and type 2 diabetes risk: A Mendelian randomization study. (2020) (19)
Interaction of insulin and PPAR-α genes in Alzheimer’s disease: the Epistasis Project (2012) (19)
Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits (2016) (18)
Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single‐Patient Data Meta‐Analysis in More Than 15,000 Individuals (2019) (18)
A novel interaction between the FLJ33534 locus and smoking in obesity: a genome-wide study of 14 131 Pakistani adults (2016) (18)
Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids (2014) (18)
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements (2019) (17)
Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem (2014) (17)
Localization of HuC (ELAVL3) to chromosome 19p13.2 by fluorescence in situ hybridization utilizing a novel tyramide labeling technique. (1998) (17)
Analysis with the exome array identifies multiple new independent variants in lipid loci. (2016) (17)
Low-density lipoprotein receptor-related protein 5 polymorphisms are associated with bone mineral density in Greek postmenopausal women: an interaction with calcium intake. (2010) (17)
Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts (2017) (16)
Novel genetic loci associated with long-term deterioration in blood lipid concentrations and coronary artery disease in European adults. (2016) (16)
Genome-wide association study of circulating interleukin 6 levels identifies novel loci (2021) (16)
Genomic organization of the gene encoding the p65 subunit of NF-kappa B: multiple variants of the p65 protein may be generated by alternative splicing. (1993) (16)
Genetic association analyses of non-synonymous single nucleotide polymorphisms in diabetic nephropathy (2008) (15)
Epigenome-Wide Association Study (EWAS) of Blood Lipids in Healthy Population from STANISLAS Family Study (SFS) (2019) (15)
Effect of Genetic Variability in the CYP4F2, CYP4F11, and CYP4F12 Genes on Liver mRNA Levels and Warfarin Response (2017) (15)
Z extensions to the RHMAPPER package (1998) (14)
Novel celiac disease genetic determinants related to the immune response (2009) (14)
Subsequent Event Risk in Individuals With Established Coronary Heart Disease (2019) (14)
Mendelian randomisation analyses find pulmonary factors mediate the effect of height on coronary artery disease (2019) (14)
Thyroid function, sex hormones and sexual function: a Mendelian randomization study (2021) (14)
Whole genome–amplified DNA: insights and imputation (2008) (14)
Dairy Intake and Body Composition and Cardiometabolic Traits among Adults: Mendelian Randomization Analysis of 182041 Individuals from 18 Studies. (2019) (13)
Identification of PLCL 1 Gene for Hip Bone Size Variation in Females in a Genome-Wide Association Study (2008) (12)
Potential Interplay between Dietary Saturated Fats and Genetic Variants of the NLRP3 Inflammasome to Modulate Insulin Resistance and Diabetes Risk: Insights from a Meta‐Analysis of 19 005 Individuals (2019) (12)
A ‘‘Candidate-Interactome’’ Aggregate Analysis of Genome-Wide Association Data in Multiple Sclerosis (2013) (12)
Linkage disequilibrium mapping via cladistic analysis of SNP haplotypes. (2003) (11)
An integrated cytogenetic, radiation-hybrid, and comparative map of dog Chromosome 5 (2001) (11)
Detection of translocations involving the HOX11/TCL3-locus in 10q24 by interphase fluorescence in situ hybridization. (2001) (11)
Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study (2020) (11)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (vol 41, pg 1088, 2009) (2013) (10)
Effect of Mastiha supplementation on NAFLD: The MAST4HEALTH Randomised, Controlled Trial. (2021) (10)
Comprehensive Exploration of the Effects of miRNA SNPs on Monocyte Gene Expression (2012) (10)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (10)
Coordination of human genome sequencing via a consensus framework map. (1998) (10)
A Histone Map of Human Chromosome 20q13.12 (2009) (10)
Construction and integration of radiation-hybrid and cytogenetic maps of dog Chromosome X (2003) (10)
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia. (2002) (9)
Sequencing and association analysis of the type 1 diabetes – linked region on chromosome 10p12-q11 (2007) (9)
DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases (2021) (9)
Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD (2021) (9)
Thrombocytopenia with Absent Radii (TAR) syndrome is cause by compound inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A (2012) (9)
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation (2019) (9)
The human NFKB3 gene encoding the p65 subunit of transcription factor NF-kappa B is located on chromosome 11q12. (1994) (9)
Erratum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (Nature Genetics (2011) 43 (561-564)) (2011) (9)
Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans (2017) (8)
Thyroid function and mood disorders: a Mendelian Randomization study (2021) (8)
From systems biology to systems medicine (2017) (8)
Il-23r is a major determinant of ankylosing spondylitis risk - The tasc study (2007) (8)
Mendelian randomisation analyses find pulmonary factors mediate the effect of height on coronary artery disease (2019) (8)
Association of Factor V Leiden With Subsequent Atherothrombotic Events (2020) (8)
Correction: The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits (2013) (8)
Single Nucleotide Polymorphisms with Cis-Regulatory Effects on Long Non-Coding Transcripts in Human Primary Monocytes (2014) (8)
Twenty loci associated with bone mineral density identified by large-scale meta-analysis of genome-wide association datasets (2009) (8)
COVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases (2021) (8)
Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease (2012) (8)
Single nucleotide polymorphism (SNP) panels for rapid positional cloning in zebrafish. (2011) (7)
Physical mapping of chromosome 6: a strategy for the rapid generation of sequence-ready contigs. (1996) (7)
Report of the third international workshop on human chromosome 10 mapping and sequencing 1999 (2000) (7)
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids (2021) (6)
A linkage disequilibrium map of chromosome 22 (2002) (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)
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy (2006) (6)
The contribution of non-coding regulatory elements to cardiovascular disease (2020) (6)
Evaluating the glucose raising effect of established loci via a genetic risk score (2017) (6)
Haplotype‐based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1–DQA1–DQB1 haplotype (2009) (5)
Erratum: Global analysis of dna methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements ((Journal of Human Genetics (2013) 93 (876-890)) (2013) (5)
First genotype-phenotype study reveals HLA-DQβ1 insertion heterogeneity in high-resolution manometry achalasia subtypes (2019) (5)
A re-examination of proximodistal patterning during vertebrate limb development (5)
Corrigendum: Multiple common variants for celiac disease influencing immune gene expression (2010) (5)
Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization (2022) (5)
1. Peer-reviewed articles (2014) (5)
Single Nucleotide Polymorphism Analysis by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry (2006) (4)
Data analysis issues for allele-specific expression using Illumina's GoldenGate assay (2010) (4)
Genome-wide association study identifies 48 common genetic variants associated with handedness (2020) (4)
Thyroid Function and the Risk of Alzheimer's Disease: A Mendelian Randomization Study. (2021) (4)
Genome-wide association study of age at onset of Alzheimer's disease (2009) (4)
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
Effects of thyroid function on hemostasis, coagulation, and fibrinolysis: a Mendelian Randomization study. (2021) (4)
Correction: Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy (2010) (4)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (4)
No Evidence in a Large UK Collection for Celiac Disease Risk Variants Reported by a Spanish Study (2008) (4)
8th Santorini Conference: Systems medicine and personalized health and therapy, Santorini, Greece, 3–5 October 2016 (2017) (4)
Stranger , Variation on Gene Expression Phenotypes Relative Impact of Nucleotide and Copy Number (2007) (3)
Supplementary Material 3 (2015) (3)
Supplementary Material 7 (2014) (3)
Supplementary Material 6 (2014) (3)
Explorer A GWAS sequence variant for platelet volume marks an alternative DNM 3 promoter in megakaryocytes near a MEIS 1 binding site (2017) (3)
Genome-Wide Association Studies Herald a New Era of Rapid Discoveries in Inflammatory Bowel Disease Research (2007) (3)
Supplementary Material 5 (2014) (3)
Visualizing Chromosome Mosaicism and Detecting Ethnic Outliers by the Method of “Rare” Heterozygotes and Homozygotes (RHH) (2010) (3)
Correction: Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits (2011) (3)
Abstract 19823: Whole-Exome Sequencing in an Extended Family with Myocardial Infarction Identified a Potential Functional Mutation in PDE5A (2012) (3)
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing (2017) (3)
Genetics of educational attainment and coronary risk in Mendelian randomization studies. (2020) (3)
A zebrafish forward genetic screen identifies an indispensable threonine residue in the kinase domain of PRKD2 (2021) (2)
Genome-Wide Association Study Reveals Genetic Variants Associated with Bone Mineral Density, Osteoporosis and Osteoporotic Fractures (2008) (2)
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (2019) (2)
Construction of yeast artificial chromosome (YAC) clone banks covering three genome equivalents and isolation of YACs containing the human gene encoding tumor necrosis factor receptor beta. (1992) (2)
Variation on Gene Expression Phenotypes Relative Impact of Nucleotide and Copy (2007) (2)
Lifestyle may modify the glucose-raising effect of genetic loci. A study in the Greek population. (2016) (2)
CLINICAL-ALIMENTARY TRACT IL23R Variation Determines Susceptibility But Not Disease Phenotype in Inflammatory Bowel Disease (2007) (2)
Gene expression changes with age in skin, adipose tissue, blood and brain (2013) (2)
Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa (2017) (2)
A transnational collaborative network dedicated to the study and applications of the vascular endothelial growth factor-A in medical practice: the VEGF Consortium (2017) (2)
Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2011) (2)
Predicting genome-wide DNA methylation using methylation marks, genomic position, and DNA regulatory elements (2015) (2)
Construction of transcript maps by somatic cell/radiation hybrid mapping. The human gene map. (2001) (2)
A multi-factorial analysis of response to warfarin in a UK prospective cohort (2016) (1)
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus (2020) (1)
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution (2019) (1)
Supplementary Material 4 (2015) (1)
Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids (2014) (1)
Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function (2022) (1)
in MOCS 3 , IFIT 3 and SERPINA 12 (2016) (1)
Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants (2015) (1)
Transcript mapping of the region of chromosome 20q that is deleted in myeloproliferative disorders (1998) (1)
Supplementary Material 15 (2013) (1)
Genome-Wide Association Study of Over One Million Participants Identifies 49 Novel Loci Associated With Coronary Artery Disease (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)
Abstract 19822: Ldlr Splice-Site Mutation (ivs9-1g>A) Identified by Whole-Exome Sequencing in an Extended Family with Myocardial Infarction (2012) (1)
Dinucleotide repeat polymorphism (D10S608) adjacent to the GLUD1 locus. (1993) (1)
Epigenome-wide association study detects a novel loci associated with central obesity in healthy subjects (2021) (1)
High-density association mapping and comprehensive tagging of the type 2 diabetes linkage region on chromosome 1q in 4 European populations (2007) (1)
Single Nucleotide Polymorphism (SNP) Panels for Rapid Positional Cloning in (2011) (1)
A Common Single Nucleotide Polymorphism in the Chromosome 7q22.3 Region, Which Is Frequently Deleted in Myeloid Malignancies, Is Associated with Mean Platelet Volume and Platelet Function in Healthy Individuals (2008) (1)
Fine-mapping type 2 diabetes causal variants on chromosome 9p21 in 2000 UK cases and 3000 unselected controls (2008) (1)
forecasting The largest prospective warfarin-treated cohort supports genetic (2012) (1)
Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration (2021) (1)
The 9th Santorini Conference: Systems Medicine, Personalised Health and Therapy. “The Odyssey from Hope to Practice”, Santorini, Greece, 30 September–3 October 2018 (2018) (1)
Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study (2020) (1)
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
A genome-wide scan of adult human stature and skeletal size. (2008) (1)
Discovery and Refinement Supplementary (2015) (1)
Posterior Polymorphous Corneal Dystrophy in Czech families maps to Chromosome 20p11.2 demonstrating microheterogeneity and exclusion of the candidate gene VSX1 (2005) (1)
Supplementary Material 9 (2013) (1)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
Short communication Detection of translocations involving the HOX11/TCL3 -locus in 10q24 by interphase fluorescence in situ hybridization (2001) (0)
th Meeting of the Irish Society of Human Genetics , Friday 2 nd (0)
Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans (2017) (0)
Vanessa Kellermann Species Distributions Drosophila Fundamental Evolutionary Limits in Ecological Traits Drive (2011) (0)
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (2018) (0)
Edinburgh Research Explorer Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease (2013) (0)
Identification of trait-associated single nucleotide polymorphisms with cis-regulatory effects on long non-coding RNAs (2011) (0)
Epigenome-wide association reveals extensive perturbations in DNA methylation associated with adiposity and its adverse metabolic consequences. Authors (2015) (0)
Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation (2015) (0)
The power of allele-specific gene expression analysis for identification of cis-regulatory SNPs (2011) (0)
The 10th Santorini conference: Systems medicine, personalised health and therapy. “The odyssey from hope to practice: Patient first. Keep Ithaca always in your mind”, Santorini, Greece, 23–26 May 2022 (2023) (0)
Exploratory analysis and error modeling of a sequencing technology (2016) (0)
Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size SORANZO (2019) (0)
Transcript mapping and identification of candidate genes in the 3cM region of chromosome 20p 11.2 spanning the CHED1 locus (2002) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
Peer Review Status: Peer reviewed Citation for item: (2012) (0)
Robust Bioinformatics Approaches Result in the First Polygenic Risk Score for BMI in Greek Adults (2023) (0)
Genome-Wide Association Identi ﬁ es Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes (2011) (0)
Map integration. From a genetic map to a physical gene map and ultimately to the sequence map. (2001) (0)
Correction: Identification of PLCL1 Gene for Hip Bone Size Variation in Females in a Genome-Wide Association Study (2009) (0)
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2021) (0)
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (0)
S1751 Copy Number Variant and Extended SNP Genome Wide Association Study in Celiac Disease (2009) (0)
Functional Genomics of the Platelet ADP and Collagen Signalling Pathways. (2008) (0)
University of Groningen Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation (2018) (0)
COMMON OR RARE GENETIC VARIATION IN THE CHEMOKINE RECEPTORS CCR2, CCR5, AND CX3CR1 DOES NOT RELATE TO CORONARY HEART DISEASE OR MYOCARDIAL INFARCTION IN HUMANS (2016) (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)
LD relationship for FTO Association SNPs and rs7202116. (2010) (0)
Nature Genetics | Article (2015) (0)
Thyroid function and the risk of Alzheimer's disease: A Mendelian Randomisation study (2021) (0)
Positional cloning of the gene for CHED 1: A YAC/PAC and transcript map spanning the locus on 20p11.2. (2000) (0)
Running title: Pfeiffer et al.; genome-wide DNA methylation and blood lipid levels (2015) (0)
Abstract 17979: A Genome-Wide Association Study of Risk of Coronary Artery Disease in European and South Asian Populations (2010) (0)
Genome-wide meta-analysis results for AGA in MAAN. (2012) (0)
Abstract 16492: A Study of 63,253 Cases and 126,820 Controls Identifies Multiple Novel Loci for Coronary Artery Disease and Detects Independent Signals in Many of the Established Ones (2011) (0)
Genetic loci for major lipids in Pakistan (2010) (0)
Correction: Comprehensive Exploration of the Effects of miRNA SNPs on Monocyte Gene Expression (2012) (0)
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial Infarction Genetics Consortium * (2009) (0)
NpgRj_Ng_2142 1..8 (2007) (0)
THE arcOGEN CONSORTIUM: STAGE 1 OF A GENOME-WIDE ASSOCIATION SCAN FOR OSTEOARTHRITIS (2010) (0)
European Mathematical Genetics Meeting, Rotterdam, the Netherlands, 10th–11th April 2008 (2008) (0)
The epigenetic landscape of platelet and red blood cell traits (2013) (0)
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (0)
Errata (2011) (0)
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases (2018) (0)
regulatory sequence variation at hematological trait loci restricted patterns of − Maps of open chromatin highlight cell type Material Supplemental (2013) (0)
Abstract 15963: Toward Development of a Genetic Risk Score for Sudden Cardiac Death (2014) (0)
Epigenome-wide association study detects a novel loci associated with central obesity in healthy subjects (2021) (0)
An examination of previously reported Alzheimer candidate genes within a large genome-wide association dataset (2009) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (0)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
Explorer Epigenetic patterns in blood associated with lipid traits predict incident coronary heart disease events and are enriched for results from genome-wide association studies (2017) (0)
3 WHOLE GENOME-AMPLIFIED DNA: INSIGHTS AND IMPUTATION (2010) (0)
A comprehensive study of candidate genes in two signalling pathways to identify genetic vaiants that regulate platelet responsiveness to collagen and ADP (2007) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
The 36th American Cytogenetics Conference (2000) (0)
Association Between Low-Density Lipoprotein Cholesterol – Lowering Genetic Variants and Risk of Type 2 Diabetes AMeta-analysis (2016) (0)
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements (2019) (0)
articleHigh-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta (2019) (0)
Expression Quantitative Trait Loci Analysis of Stable Warfarin Dose Identifies Novel Associations : Finding Signal within the Noise (2013) (0)
Mendelian Randomization analyses reveal a causal effect of thyroid function on stroke via atrial fibrillation (2019) (0)
Version Other version Link to publication record in King ' s Research Portal (2016) (0)
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (2019) (0)
Genome-Wide Association Study Implicates HLA-C * 01 : 02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia Irish Schizophrenia Genomics (2012) (0)
Continuous and discrete association analyses of body mass index and obesity (2007) (0)
1 Subsequent Event Risk in Individuals with Established Coronary Heart Disease : Design and Rationale of the GENIUS-CHD Consortium Running title : (2019) (0)
Prediction of atrial fibrillation and stroke using machine learning models in UK Biobank. (2022) (0)
Supplementary Material (nature09270-s1) (2012) (0)
A42 A GENOME-WIDE ASSOCIATION STUDY REVEALS A NOVEL LOCUS FOR HAND OSTEOARTHRITIS (2008) (0)
University of Groningen Investigation of common , low-frequency and rare genome-wide variation in anorexia nervosa Kas (2017) (0)
Assessment of candidate imprinted genes in the human term placenta (2009) (0)
TM6SF2-rs58542926 Genetic Variant Modifies the Protective Effect of a “Prudent” Dietary Pattern on Serum Triglyceride Levels (2023) (0)
Replicated association between type 2 diabetes and variants in CAPON revealed by high density linkage disequilibrium mapping on chromosome 1q (2006) (0)
consortiumwith hand osteoarthritis: the Treat-OA locus within the ataxin 2 binding protein 1 gene is A genome-wide association study suggests that a (2009) (0)
Haplotype-specific recombination shapes the genealogy of ancestral European haplotypes (2008) (0)
Edinburgh Research Explorer Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes (2018) (0)
Association analyses based on false discovery rate implicate 243 susceptibility loci for coronary artery disease (2017) (0)
Shared polygenic effects of FEV1 in the first genetic study in UK Biobank (2015) (0)
Linkage disequilibrium mapping of the type 2 diabetes susceptibility variants on chromosome Iq in European populations (2005) (0)
Biomarkers of skin ageing using genome wide transcriptomics (2011) (0)
Association of Dietary Patterns with MRI Markers of Hepatic Inflammation and Fibrosis in the MAST4HEALTH Study (2022) (0)
Thyroid function, pernicious anemia, and erythropoiesis: a two-sample Mendelian randomization study. (2022) (0)
Genotype score associated with the risk of androgenetic alopecia. (2012) (0)
PF196 IDENTICAL TWINS DO NOT DISPLAY INCREASED CONCORDANCE FOR CLONAL HEMATOPOIESIS (2019) (0)
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity Authors (2016) (0)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (0)
PHARMACOGENOMICS & PERSONALIZED THERAPY (2010) (0)
The 100 , 000 Genomes Project-transforming genomics in healthcare (2018) (0)
Radiation Hybrid Mapping (2005) (0)
Positional candidate gene selection on chromosome 1q using bioinformatics and large scale association analysis (2005) (0)
Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36 patient-oriented and epidemiological research (2016) (0)
Genome-wide association study of nevirapine hypersensitivity in a malawian HIV-infected population (2014) (0)
University of Dundee Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children Rautanen, (2017) (0)
Genome-wide association study of Alzheimer's with psychotic symptoms (2009) (0)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (0)
Smoking induces coordinated DNA methylation and gene expression changes in adipose tissue with consequences for metabolic health (2018) (0)
Elucidating the chromatin architecture of loci associated with blood traits and coronary artery disease (2010) (0)
Genome-Wide Association Study of Nevirapine Hypersensitivity in a sub-Saharan 1 African HIV-infected Population 2 3 (2016) (0)
Integrative DNA methylome analysis of pan-cancer biomarkers in cancer discordant monozygotic twin-pairs (2016) (0)
Large-scale association studies to identify diabetes-susceptibility loci on chromosome 1q: The importance of stringent quality control (2006) (0)
Identification of Genetic Variants Associated With Myocardial Infarction in Saudi Arabia. (2020) (0)
haracterization of a Family with Rare Deletions in NTNAP5 and DOCK4 Suggests Novel Risk Loci for utism and Dyslexia (0)
promoter in megakaryocytes near a MEIS1 binding site DNM3 A GWAS sequence variant for platelet volume marks an alternative (2013) (0)
Haplotype effects derived from the rs317657 and rs11177644 at the 12q15 locus in the Gutenberg Health Study (N = 1,467). (2012) (0)
Carbamazepine Hypersensitivity: Progress Toward Predicting the Unpredictable (2011) (0)
Genetic Determinants of Major Blood Lipids in Pakistan Is Compared with Europeans Running title: Saleheen et al.; Genetic loci for major lipids in Pakistan (2010) (0)

This paper list is powered by the following services:

Other Resources About Panos Deloukas

en.wikipedia.org

What Schools Are Affiliated With Panos Deloukas?

Panos Deloukas is affiliated with the following schools:

Panos Deloukas's Academic­Influence.com Rankings

Panos Deloukas's Degrees

Why Is Panos Deloukas Influential?

Panos Deloukas's Published Works

Published Works

Other Resources About Panos Deloukas

What Schools Are Affiliated With Panos Deloukas?

Panos Deloukas's AcademicInfluence.com Rankings