|
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
|
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
Association analyses based on false discovery rate implicate new loci for coronary artery disease.
|
28714975 |
2017 |
|
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |
|
Malignant neoplasm of pancreas
|
0.500 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.
|
19648918 |
2009 |
|
Cerebrovascular accident
|
0.430 |
GeneticVariation
|
group |
GWASCAT |
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
|
26908601 |
2016 |
|
Duodenal Ulcer
|
0.430 |
GeneticVariation
|
disease |
GWASCAT |
The T allele of rs2294008 encodes a translation initiation codon upstream of the reported site and changes protein localization from the cytoplasm to the cell surface. rs505922 at ABO was also associated with duodenal ulcer in a recessive model (OR = 1.32; P = 1.15 × 10(-10)).
|
22387998 |
2012 |
|
Duodenal Ulcer
|
0.430 |
GeneticVariation
|
disease |
GWASDB |
The T allele of rs2294008 encodes a translation initiation codon upstream of the reported site and changes protein localization from the cytoplasm to the cell surface. rs505922 at ABO was also associated with duodenal ulcer in a recessive model (OR = 1.32; P = 1.15 × 10(-10)).
|
22387998 |
2012 |
|
Diverticular Diseases
|
0.400 |
GeneticVariation
|
group |
GWASCAT |
Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease.
|
30177863 |
2018 |
|
Venous Thromboembolism
|
0.200 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease.
|
31676865 |
2019 |
|
Venous Thromboembolism
|
0.200 |
GeneticVariation
|
phenotype |
GWASCAT |
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.
|
31420334 |
2019 |
|
Pancreatic carcinoma
|
0.200 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer.
|
29422604 |
2018 |
|
Stomach Carcinoma
|
0.200 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21.
|
30281874 |
2018 |
|
Venous Thromboembolism
|
0.200 |
GeneticVariation
|
phenotype |
GWASCAT |
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor.
|
28373160 |
2017 |
|
Venous Thromboembolism
|
0.200 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
|
26908601 |
2016 |
|
Myocardial Infarction
|
0.200 |
GeneticVariation
|
disease |
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |
|
Pancreatic carcinoma
|
0.200 |
GeneticVariation
|
disease |
GWASCAT |
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer.
|
26098869 |
2015 |
|
Venous Thromboembolism
|
0.200 |
GeneticVariation
|
phenotype |
GWASCAT |
Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism.
|
25772935 |
2015 |
|
Pancreatic carcinoma
|
0.200 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer.
|
25086665 |
2014 |
|
Malaria
|
0.200 |
GeneticVariation
|
disease |
GWASCAT |
Imputation-based meta-analysis of severe malaria in three African populations.
|
23717212 |
2013 |
|
Malaria
|
0.200 |
GeneticVariation
|
disease |
GWASDB |
Imputation-based meta-analysis of severe malaria in three African populations.
|
23717212 |
2013 |
|
Venous Thromboembolism
|
0.200 |
GeneticVariation
|
phenotype |
GWASCAT |
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
|
23650146 |
2013 |
|
Venous Thromboembolism
|
0.200 |
GeneticVariation
|
phenotype |
GWASDB |
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
|
23650146 |
2013 |
|
Malaria
|
0.200 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study indicates two novel resistance loci for severe malaria.
|
22895189 |
2012 |
|
Malaria
|
0.200 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study indicates two novel resistance loci for severe malaria.
|
22895189 |
2012 |
|
Venous Thromboembolism
|
0.200 |
GeneticVariation
|
phenotype |
GWASCAT |
A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
|
22672568 |
2012 |