1 – 50 of 143
- show: 50
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2023
-
Mark
Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine
(
- Contribution to journal › Article
- 2022
-
Mark
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
(
- Contribution to journal › Article
- 2021
-
Mark
Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
(
- Contribution to journal › Article
-
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
-
Mark
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
(
- Contribution to journal › Article
-
Mark
The trans-ancestral genomic architecture of glycemic traits
(
- Contribution to journal › Article
- 2020
-
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
-
Mark
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
(
- Contribution to journal › Letter
-
Mark
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
(
- Contribution to journal › Article
-
Mark
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
(
- Contribution to journal › Article
-
Mark
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
(
- Contribution to journal › Article
-
Mark
Comprehensive molecular characterization of mitochondrial genomes in human cancers
(
- Contribution to journal › Article
-
Mark
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
(
- Contribution to journal › Article
-
Mark
Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
(
- Contribution to journal › Article
-
Mark
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
(
- Contribution to journal › Article
-
Mark
The landscape of viral associations in human cancers
(
- Contribution to journal › Article
- 2019
-
Mark
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
(
- Contribution to journal › Article
-
Mark
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
(
- Contribution to journal › Article
-
Mark
A catalog of genetic loci associated with kidney function from analyses of a million individuals
(
- Contribution to journal › Article
-
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
-
Mark
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
(
- Contribution to journal › Article
-
Mark
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
(
- Contribution to journal › Article
-
Mark
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
(
- Contribution to journal › Article
-
Mark
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
(
- Contribution to journal › Article
- 2017
-
Mark
Lgr6 is a stem cell marker in mouse skin squamous cell carcinoma
(
- 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
Exome-wide association study of plasma lipids in >300,000 individuals
(
- Contribution to journal › Article
-
Mark
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
(
- Contribution to journal › Letter
-
Mark
Identification of sequence variants influencing immunoglobulin levels
(
- Contribution to journal › Article
-
Mark
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Hyperactivation of HUSH complex function by Charcot-Marie-Tooth disease mutation in MORC2
(
- Contribution to journal › Article
- 2016
-
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
-
Mark
Genetic predisposition for beta cell fragility underlies type 1 and type 2 diabetes
(
- Contribution to journal › Article
- 2015
-
Mark
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease
(
- Contribution to journal › Article
-
Mark
Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists.
(
- Contribution to journal › Article
-
Mark
The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
The impact of low-frequency and rare variants on lipid levels.
(
- Contribution to journal › Article
-
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
-
Mark
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
(
- Contribution to journal › Article
-
Mark
The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias.
(
- Contribution to journal › Article
-
Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
(
- Contribution to journal › Article
-
Mark
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
(
- Contribution to journal › Article
- 2014
-
Mark
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
(
- Contribution to journal › Article
-
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
-
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
-
Mark
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
(
- Contribution to journal › Article
-
Mark
Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease.
(
- Contribution to journal › Article