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- 2020
-
Mark
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus
(
- Contribution to journal › Article
-
Mark
A new efficient method to detect genetic interactions for lung cancer GWAS
(
- Contribution to journal › Article
-
Mark
Genetic risk factors for venous thromboembolism
(
- Contribution to journal › Scientific review
-
Mark
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
(
- Contribution to journal › Article
- 2019
-
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
-
Mark
Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration
(
- Contribution to journal › Article
-
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
-
Mark
PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome
(
- Contribution to journal › Article
-
Mark
Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
(
- Contribution to journal › Article
-
Mark
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
(
- Contribution to journal › Article
- 2018
-
Mark
Identification and characterization of DNA sequence variants associated with multiple myeloma
(
- Thesis › Doctoral thesis (compilation)
-
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
-
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
Genome-wide Scan Identifies Role for AOX1 in Prostate Cancer Survival
(
- Contribution to journal › Article
-
Mark
A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor
(
- Contribution to journal › Article
-
Mark
17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage
(
- 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
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
(
- 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
-
Mark
Identification of FAM173B as a protein methyltransferase promoting chronic pain
(
- Contribution to journal › Article
- 2017
-
Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
(
- Contribution to journal › Article
-
Mark
Heritability of Atrial Fibrillation
(
- Contribution to journal › Article
-
Mark
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
(
- Contribution to journal › Article
-
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
-
Mark
Genome-wide association study identifies four novel loci associated with Alzheimer’s endophenotypes and disease modifiers
(
- Contribution to journal › Article
-
Mark
Genetic determinants of growth hormone and GH-related phenotypes
(
- Contribution to journal › Article
- 2016
-
Mark
Low-frequency and common genetic variation in ischemic stroke : The METASTROKE collaboration
(
- Contribution to journal › Article
-
Mark
OGS2: genome re-annotation of the jewel wasp Nasonia vitripennis
(
- Contribution to journal › Article
-
Mark
Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study
(
- Contribution to journal › Article
-
Mark
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
(
- Contribution to journal › Article
-
Mark
The genetic architecture of type 2 diabetes
(
- 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
-
Mark
Transcriptome analysis of controlled and therapy-resistant childhood asthma reveals distinct gene expression profiles
(
- Contribution to journal › Article
-
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
-
Mark
Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk
(
- Contribution to journal › Letter
-
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
-
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
- 2009
-
Mark
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
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