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- 2024
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Mark
Genetic correlations and causal relationships between cardio-metabolic traits and sepsis
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- Contribution to journal › Article
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Mark
A genome-wide association study of social trust in 33,882 Danish blood donors
(
- Contribution to journal › Article
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Mark
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods
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- Contribution to journal › Article
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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
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- Contribution to journal › Article
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Mark
Association of Body Mass Index and Parkinson Disease A Bidirectional Mendelian Randomization Study
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- Contribution to journal › Article
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Mark
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
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- Contribution to journal › Article
- 2023
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Mark
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
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- Contribution to journal › Article
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Mark
Glucagon-like peptide-1 receptor agonists and diabetic retinopathy : nationwide cohort and Mendelian randomization studies
(
- Contribution to journal › Article
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Mark
How Well do Polygenic Risk Scores Identify Men at High Risk for Prostate Cancer? Systematic Review and Meta-Analysis
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- Contribution to journal › Article
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Mark
Genetic insights into resting heart rate and its role in cardiovascular disease
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- Contribution to journal › Article
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Mark
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
(
- Contribution to journal › Article
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Mark
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
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- Contribution to journal › Article
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Mark
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
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- Contribution to journal › Article
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Mark
Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
(
- Contribution to journal › Article
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Mark
Genetic Predisposition to Elevated Levels of Circulating ADAM17 Is Associated with the Risk of Severe COVID-19
(
- Contribution to journal › Article
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Mark
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci
(
- Contribution to journal › Article
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Mark
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
(
- Contribution to journal › Article
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Mark
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
(
- Contribution to journal › Article
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Mark
Sex differences of the shared genetic landscapes between type 2 diabetes and peripheral artery disease in East Asians and Europeans
(
- Contribution to journal › Article
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Mark
Mendelian randomization suggests a potential causal effect of eosinophil count on influenza vaccination responsiveness
(
- Contribution to journal › Article
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Mark
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry
(
- Contribution to journal › Article
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Mark
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
(
- Contribution to journal › Article
- 2022
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Mark
Genome-wide association study identifies Sjögren's risk loci with functional implications in immune and glandular cells
(
- Contribution to journal › Article
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Mark
A saturated map of common genetic variants associated with human height
(
- Contribution to journal › Article
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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
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
(
- Contribution to journal › Article
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Mark
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
(
- Contribution to journal › Article
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Mark
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
(
- Contribution to journal › Article
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Mark
Phenotype Harmonization in the GLIDE2 Oral Health Genomics Consortium
(
- Contribution to journal › Article
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Mark
Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization
(
- Contribution to journal › Article
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Mark
Genetic Landscape of the ACE2 Coronavirus Receptor
(
- Contribution to journal › Article
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Mark
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
(
- Contribution to journal › Article
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Mark
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence from the COURAGE-PD Consortium
(
- Contribution to journal › Article
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Mark
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
(
- Contribution to journal › Article
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Mark
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
(
- Contribution to journal › Article
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Mark
Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk
(
- Contribution to journal › Article
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Mark
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
(
- Contribution to journal › Article
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Mark
Identification of Putative Causal Relationships Between Type 2 Diabetes and Blood-Based Biomarkers in East Asians by Mendelian Randomization
(
- Contribution to journal › Article
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Mark
Genetic evidence for a causal relationship between type 2 diabetes and peripheral artery disease in both Europeans and East Asians
(
- Contribution to journal › Article
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Mark
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors
(
- Contribution to journal › Article
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Mark
Dairy Intake and Parkinson's Disease : A Mendelian Randomization Study
(
- Contribution to journal › Article
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Mark
Rare germline copy number variants (CNVs) and breast cancer risk
(
- Contribution to journal › Article
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Mark
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease
(
- Contribution to journal › Article
- 2021
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Mark
Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma
(
- Contribution to journal › Article
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Mark
Genomic and phenotypic evolution of achromobacter xylosoxidans during chronic airway infections of patients with cystic fibrosis
(
- Contribution to journal › Article
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Mark
Genome-Wide Association Study of Peripheral Artery Disease
(
- 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
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk
(
- Contribution to journal › Article
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Mark
Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium
(
- Contribution to journal › Article
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Mark
Replication of a Novel Parkinson's Locus in a European Ancestry Population
(
- Contribution to journal › Article
- 2020
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Mark
A new efficient method to detect genetic interactions for lung cancer GWAS
(
- Contribution to journal › Article
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Mark
Genome-wide association meta-analysis of single-nucleotide polymorphisms and symptomatic venous thromboembolism during therapy for acute lymphoblastic leukemia and lymphoma in caucasian children
(
- Contribution to journal › Article
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Mark
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
(
- Contribution to journal › Article
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Mark
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus
(
- Contribution to journal › Article
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Mark
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
(
- Contribution to journal › Article
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Mark
Genetic risk factors for venous thromboembolism
(
- Contribution to journal › Scientific review
- 2019
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Mark
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
(
- Contribution to journal › Article
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Mark
PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome
(
- Contribution to journal › Article
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Mark
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
(
- Contribution to journal › Article
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Mark
Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region
(
- Contribution to journal › Article
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Mark
Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration
(
- Contribution to journal › Article
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Mark
Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
(
- Contribution to journal › Article
- 2018
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Mark
A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor
(
- Contribution to journal › Article
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Mark
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
(
- Contribution to journal › Article
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Mark
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes
(
- Contribution to journal › Article
-
Mark
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
(
- Contribution to journal › Article
-
Mark
17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage
(
- Contribution to journal › Article
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Mark
Identification and characterization of DNA sequence variants associated with multiple myeloma
(
- Thesis › Doctoral thesis (compilation)
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Mark
Genome-wide Scan Identifies Role for AOX1 in Prostate Cancer Survival
(
- Contribution to journal › Article
-
Mark
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
(
- Contribution to journal › Article
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Mark
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
(
- Contribution to journal › Article
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Mark
Identification of FAM173B as a protein methyltransferase promoting chronic pain
(
- Contribution to journal › Article
- 2017
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Mark
Genome-wide association study identifies four novel loci associated with Alzheimer’s endophenotypes and disease modifiers
(
- Contribution to journal › Article
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Mark
Genetic determinants of growth hormone and GH-related phenotypes
(
- Contribution to journal › Article
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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
-
Mark
Heritability of Atrial Fibrillation
(
- Contribution to journal › Article
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Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
(
- Contribution to journal › Article
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Mark
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
(
- Contribution to journal › Article
- 2016
-
Mark
Low-frequency and common genetic variation in ischemic stroke : The METASTROKE collaboration
(
- Contribution to journal › Article
-
Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article
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Mark
Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study
(
- Contribution to journal › Article
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Mark
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
(
- Contribution to journal › Article
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Mark
OGS2: genome re-annotation of the jewel wasp Nasonia vitripennis
(
- Contribution to journal › Article
-
Mark
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
(
- Contribution to journal › Article
- 2015
-
Mark
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
(
- Contribution to journal › Article
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Mark
Transcriptome analysis of controlled and therapy-resistant childhood asthma reveals distinct gene expression profiles
(
- Contribution to journal › Article
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Mark
Cell-specific effects in different immune subsets associated with SOCS1 genotypes in multiple sclerosis
(
- Contribution to journal › Article
- 2014
-
Mark
Genome-wide association study for radiographic vertebral fractures: A potential role for the 16q24 BMD locus
(
- Contribution to journal › Article
- 2013
-
Mark
Variation in the interaction between alleles of HvAPETALA2 and microRNA172 determines the density of grains on the barley inflorescence
(
- Contribution to journal › Article
- 2012
-
Mark
Novel Loci Associated With PR Interval in a Genome-Wide Association Study of 10 African American Cohorts
(
- Contribution to journal › Article
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Mark
Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk
(
- Contribution to journal › Letter
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Mark
Large-scale replication and heterogeneity in Parkinson disease genetic loci
(
- Contribution to journal › Article
-
Mark
ANKRD55 and DHCR7 are novel multiple sclerosis risk loci
(
- Contribution to journal › Article
- 2011
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Mark
Pathway-based analysis of a melanoma genome-wide association study : analysis of genes related to tumour-immunosuppression
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma
(
- Contribution to journal › Article
-
Mark
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
(
- Contribution to journal › Article
-
Mark
Molecular alterations associated with liver metastases development in colorectal cancer patients
(
- Contribution to journal › Article
- 2010
-
Mark
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease : large-scale collaborative study
(
- Contribution to journal › Article
-
Mark
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk
(
- Contribution to journal › Article