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- 2024
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Mark
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
(
- Contribution to journal › Article
- 2023
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Mark
Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine
(
- Contribution to journal › Article
- 2022
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Mark
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
(
- Contribution to journal › Article
- 2021
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Mark
Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
(
- Contribution to journal › Article
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Mark
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
(
- Contribution to journal › Article
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Mark
The trans-ancestral genomic architecture of glycemic traits
(
- Contribution to journal › Article
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Mark
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
(
- Contribution to journal › Article
- 2020
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Mark
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
(
- Contribution to journal › Article
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Mark
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
(
- Contribution to journal › Letter
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Mark
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
(
- Contribution to journal › Article
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Mark
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
(
- Contribution to journal › Article
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Mark
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
(
- Contribution to journal › Article
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Mark
Comprehensive molecular characterization of mitochondrial genomes in human cancers
(
- Contribution to journal › Article
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Mark
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
(
- Contribution to journal › Article
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Mark
Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
(
- Contribution to journal › Article
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Mark
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
(
- Contribution to journal › Article
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Mark
The landscape of viral associations in human cancers
(
- Contribution to journal › Article
- 2019
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Mark
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
(
- Contribution to journal › Article
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Mark
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
(
- Contribution to journal › Article
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Mark
A catalog of genetic loci associated with kidney function from analyses of a million individuals
(
- Contribution to journal › Article
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Mark
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
(
- Contribution to journal › Article
- 2018
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Mark
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
(
- Contribution to journal › Article
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Mark
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
(
- Contribution to journal › Article
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Mark
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
(
- Contribution to journal › Article
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Mark
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
(
- Contribution to journal › Article
- 2017
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Mark
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
(
- Contribution to journal › Article
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Mark
Exome-wide association study of plasma lipids in >300,000 individuals
(
- Contribution to journal › Article
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Mark
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
(
- Contribution to journal › Article
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Mark
Lgr6 is a stem cell marker in mouse skin squamous cell carcinoma
(
- Contribution to journal › Article
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Mark
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
(
- Contribution to journal › Letter
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Mark
Identification of sequence variants influencing immunoglobulin levels
(
- Contribution to journal › Article
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Mark
Hyperactivation of HUSH complex function by Charcot-Marie-Tooth disease mutation in MORC2
(
- Contribution to journal › Article
- 2016
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Mark
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
2016) In Nature Genetics(
- Contribution to journal › Article
-
Mark
The genomic landscape of core-binding factor acute myeloid leukemias
(
- Contribution to journal › Letter
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Mark
Genetic predisposition for beta cell fragility underlies type 1 and type 2 diabetes
(
- Contribution to journal › Article
- 2015
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Mark
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease
(
- Contribution to journal › Article
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Mark
Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists.
(
- Contribution to journal › Article
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Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
(
- Contribution to journal › Article
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Mark
The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
The impact of low-frequency and rare variants on lipid levels.
(
- Contribution to journal › Article
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Mark
The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias.
(
- Contribution to journal › Article
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Mark
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
(
- Contribution to journal › Article
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Mark
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
(
- Contribution to journal › Article
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Mark
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
(
- Contribution to journal › Article
- 2014
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Mark
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
(
- Contribution to journal › Article
-
Mark
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.
(
- Contribution to journal › Article
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Mark
Defining the role of common variation in the genomic and biological architecture of adult human height.
(
- Contribution to journal › Article
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Mark
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
(
- Contribution to journal › Article
-
Mark
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
(
- Contribution to journal › Article
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Mark
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
(
- Contribution to journal › Article
-
Mark
Meta-analysis of gene-level tests for rare variant association.
(
- Contribution to journal › Article
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Mark
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.
(
- Contribution to journal › Article
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Mark
Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease.
(
- Contribution to journal › Article
- 2013
-
Mark
The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
(
- Contribution to journal › Article
-
Mark
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
(
- Contribution to journal › Article
-
Mark
Discovery and refinement of loci associated with lipid levels
(
- Contribution to journal › Article
-
Mark
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
(
- Contribution to journal › Article
-
Mark
A functional variant in the CFI gene confers a high risk of age-related macular degeneration
(
- Contribution to journal › Article
-
Mark
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
(
- Contribution to journal › Article
-
Mark
A variant in FTO shows association with melanoma risk not due to BMI
(
- Contribution to journal › Article
-
Mark
The genomic landscape of hypodiploid acute lymphoblastic leukemia
(
- Contribution to journal › Article
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Mark
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
(
- Contribution to journal › Article
-
Mark
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
(
- Contribution to journal › Article
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Mark
Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype.
(
- Contribution to journal › Article
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Mark
The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans
(
- Contribution to journal › Article
-
Mark
Common variants associated with plasma triglycerides and risk for coronary artery disease
(
- Contribution to journal › Article
-
Mark
Large-scale association analysis identifies new risk loci for coronary artery disease
(
- Contribution to journal › Article
-
Mark
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
(
- Contribution to journal › Article
- 2012
-
Mark
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
(
- Contribution to journal › Article
-
Mark
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
(
- Contribution to journal › Article
-
Mark
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk
(
- Contribution to journal › Article
-
Mark
Whole-genome analysis of diverse Chlamydia trachomatis strains identifies phylogenetic relationships masked by current clinical typing
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk
(
- Contribution to journal › Article
-
Mark
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
(
- Contribution to journal › Article
-
Mark
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
(
- Contribution to journal › Article
-
Mark
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
(
- Contribution to journal › Article
-
Mark
Natural variation in a homolog of Antirrhinum CENTRORADIALIS contributed to spring growth habit and environmental adaptation in cultivated barley
(
- Contribution to journal › Article
-
Mark
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
(
- Contribution to journal › Article
- 2011
-
Mark
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
(
- Contribution to journal › Article
-
Mark
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Mutations in CEP57 cause mosaic variegated aneuploidy syndrome
(
- Contribution to journal › Article
-
Mark
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies three new melanoma susceptibility loci
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
(
- Contribution to journal › Article
-
Mark
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile
(
- Contribution to journal › Article
-
Mark
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
(
- Contribution to journal › Article
- 2010
-
Mark
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
(
- Contribution to journal › Article
-
Mark
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
(
- Contribution to journal › Article
-
Mark
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
(
- Contribution to journal › Article
-
Mark
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
(
- Contribution to journal › Article
-
Mark
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
(
- Contribution to journal › Article
-
Mark
Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk
(
- Contribution to journal › Article
-
Mark
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
(
- Contribution to journal › Article
-
Mark
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)
(
- Contribution to journal › Letter
-
Mark
Genetic loci influencing kidney function and chronic kidney disease
(
- Contribution to journal › Article
-
Mark
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
(
- Contribution to journal › Article
-
Mark
Open chromatin and diabetes risk.
(
- Contribution to journal › Article
-
Mark
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk
(
- Contribution to journal › Article
-
Mark
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
(
- Contribution to journal › Article
- 2009
-
Mark
Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia
(
- Contribution to journal › Article
-
Mark
Common variants at 30 loci contribute to polygenic dyslipidemia
(
- Contribution to journal › Article
-
Mark
Variants in MTNR1B influence fasting glucose levels
(
- Contribution to journal › Article
-
Mark
Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure
(
- Contribution to journal › Article
-
Mark
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies three loci associated with melanoma risk
(
- Contribution to journal › Article
-
Mark
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
(
- Contribution to journal › Article
-
Mark
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus
(
- Contribution to journal › Article
-
Mark
New susceptibility locus for coronary artery disease on chromosome 3q22.3
(
- Contribution to journal › Article
-
Mark
DNA methylation protects hematopoietic stem cell multipotency from myeloerythroid restriction
(
- Contribution to journal › Article
-
Mark
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion.
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies eight loci associated with blood pressure
(
- Contribution to journal › Article
- 2008
-
Mark
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus
(
- Contribution to journal › Article
-
Mark
Common variants near MC4R are associated with fat mass, weight and risk of obesity
(
- Contribution to journal › Article
-
Mark
Identification of ten loci associated with height highlights new biological pathways in human growth
(
- Contribution to journal › Article
-
Mark
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
(
- Contribution to journal › Article
-
Mark
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
(
- Contribution to journal › Article
-
Mark
Molecular screening for new fusion genes in cancer
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus
(
- Contribution to journal › Article
-
Mark
Common sequence variants on 20q11.22 confer melanoma susceptibility
(
- Contribution to journal › Article
-
Mark
Recurrent gross mutations of the PTEN tumor suppressor gene in breast cancers with deficient DSB repair
(
- Contribution to journal › Article
-
Mark
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
(
- Contribution to journal › Article
- 2007
-
Mark
A common variant of HMGA2 is associated with adult and childhood height in the general population
(
- Contribution to journal › Article
-
Mark
From fused toes in mice to human obesity
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Cystatin C modulates cerebral beta-amyloidosis
(
- Contribution to journal › Article
- 2006
-
Mark
Transferability of tag SNPs in genetic association studies in multiple populations
(
- Contribution to journal › Article
-
Mark
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
(
- Contribution to journal › Article
- 2005
-
Mark
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
(
- Contribution to journal › Article
-
Mark
Demonstrating stratification in a European American population
(
- Contribution to journal › Article
-
Mark
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction
(
- Contribution to journal › Article
- 2004
-
Mark
Statistical concerns about the GSEA procedure - Reply
(
- Contribution to journal › Letter
-
Mark
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer
(
- Contribution to journal › Article
-
Mark
A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling.
(
- Contribution to journal › Article
- 2003
-
Mark
Positional identification of Ncf1 as a gene that regulates arthritis severity in rats.
(
- Contribution to journal › Article
-
Mark
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
(
- Contribution to journal › Article
-
Mark
PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes.
(
- Contribution to journal › Article
-
Mark
Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation
(
- Contribution to journal › Article
- 2002
-
Mark
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
(
- Contribution to journal › Article
-
Mark
The extent of linkage disequilibrium in Arabidopsis thaliana
(
- Contribution to journal › Article
-
Mark
A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans
(
- Contribution to journal › Article
- 2000
-
Mark
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
(
- Contribution to journal › Article
- 1998
-
Mark
Genetic control of arthritis onset, severity and chronicity in a model for rheumatoid arthritis in rats
(
- Contribution to journal › Article