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- 2024
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Mark
The 1+Million Genomes Minimal Dataset for Cancer
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
(
- Contribution to journal › Article
- 2023
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Mark
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
(
- Contribution to journal › Article
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Mark
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
(
- Contribution to journal › Article
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Mark
An atlas of genetic determinants of forearm fracture
(
- Contribution to journal › Article
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Mark
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
(
- 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
- 2022
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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
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 association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
(
- Contribution to journal › Article
- 2020
-
Mark
Establishing the First International Genetic Discrimination Observatory
(
- Contribution to journal › Article
- 2019
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Mark
Roadmap for a precision-medicine initiative in the Nordic region
2019) In Nature Genetics(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Loss of ZnT8 function protects against diabetes by enhanced insulin secretion
(
- Contribution to journal › Article
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Mark
Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes
(
- Contribution to journal › Article
- 2018
-
Mark
Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer
(
- Contribution to journal › Article
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Mark
Multi-ethnic genome-wide association study for atrial fibrillation
(
- Contribution to journal › Article
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Mark
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
(
- Contribution to journal › Article
- 2017
-
Mark
A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers
(
- Contribution to journal › Article
-
Mark
Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance
(
- Contribution to journal › Article
-
Mark
Association analyses based on false discovery rate implicate new loci for coronary artery disease
(
- Contribution to journal › Article
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Mark
Functional screen of MSI2 interactors identifies an essential role for SYNCRIP in myeloid leukemia stem cells
(
- Contribution to journal › Article
-
Mark
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
(
- Contribution to journal › Article
-
Mark
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
(
- Contribution to journal › Article
- 2016
-
Mark
A reference panel of 64,976 haplotypes for genotype imputation
(
- Contribution to journal › Article
-
Mark
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
(
- Contribution to journal › Article
-
Mark
Sequencing of the genus Arabidopsis identifies a complex history of nonbifurcating speciation and abundant trans-specific polymorphism
(
- Contribution to journal › Article
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Mark
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
(
- Contribution to journal › Article
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Mark
Signaling from maize organ primordia via FASCIATED EAR3 regulates stem cell proliferation and yield traits
(
- Contribution to journal › Article
- 2011
-
Mark
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice
(
- Contribution to journal › Article
- 2005
-
Mark
A manually curated functional annotation of the human X chromosome
(
- Contribution to journal › Letter
- 1999
-
Mark
Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome
(
- Contribution to journal › Article
- 1998
-
Mark
Sometimes it's hot, sometimes it's not
(
- Contribution to journal › Debate/Note/Editorial
- 1997
-
Mark
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
(
- Contribution to journal › Article
- 1995
-
Mark
A genetic linkage map of the laboratory rat, Rattus norvegicus
(
- Contribution to journal › Article
- 1992
-
Mark
Genetic dissection of autoimmune type I diabetes in the BB rat
(
- Contribution to journal › Article