Breast Carcinoma
|
0.120 |
GeneticVariation
|
disease |
GWASCAT |
Association analysis identifies 65 new breast cancer risk loci.
|
29059683 |
2017 |
Breast Carcinoma
|
0.120 |
GeneticVariation
|
disease |
BEFREE |
In this study, we propose that polymorphisms in the 5'-UTR promoter region of the RAD51 gene are prognostic factors for BC development.
|
26650628 |
2016 |
Breast Carcinoma
|
0.120 |
Biomarker
|
disease |
BEFREE |
Our data suggest that Z2P-UTR can promote breast cancer angiogenesis partly via paracrine pathway of VEGF-A/VEGFR2.
|
25281903 |
2014 |
Tuberculosis
|
0.110 |
GeneticVariation
|
disease |
GWASDB |
Common variants at 11p13 are associated with susceptibility to tuberculosis.
|
22306650 |
2012 |
Tuberculosis
|
0.110 |
GeneticVariation
|
disease |
BEFREE |
The polymorphisms of NRAMP 1 at loci INT4, D543N, 77-385C/T, 3-UTR (CAAA) deletion and 5-(CA)n microsatellite markers were assessed by polymerase chain reaction on tissue DNA isolated from 105 aborigines and 110 Hans with tuberculosis.
|
16638645 |
2006 |
Blood urea nitrogen measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
|
31152163 |
2019 |
Red Blood Cell Count measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Forced expiratory volume function
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
|
30804560 |
2019 |
Vital capacity
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
|
30804560 |
2019 |
Diastolic blood pressure
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
|
30578418 |
2019 |
Systolic Pressure
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Body mass index
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Body mass index
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.
|
30239722 |
2019 |
Blood urea nitrogen measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
|
29403010 |
2018 |
Adolescent idiopathic scoliosis
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
|
30019117 |
2018 |
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
|
30019117 |
2018 |
Alopecia
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genetic prediction of male pattern baldness.
|
28196072 |
2017 |
Other alopecia
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Androgenetic Alopecia
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Systolic Pressure
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.
|
27841878 |
2017 |
Alopecia, Androgenetic, 3
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Alopecia, Androgenetic, 2
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Alopecia, Androgenetic, 1
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Alopecia, Male Pattern
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Other alopecia
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Detection and interpretation of shared genetic influences on 42 human traits.
|
27182965 |
2016 |