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UnknownCommon variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.
Not available
S-EPMC3084173 | biostudies-literature
UnknownPlasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.
Not available
S-EPMC3419820 | biostudies-literature
UnknownThe predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant.
Not available
S-EPMC8460445 | biostudies-literature
UnknownCommon genetic variants and modification of penetrance of BRCA2-associated breast cancer.
Not available
S-EPMC2965747 | biostudies-literature
UnknownFTO genotype is associated with phenotypic variability of body mass index.
Not available
S-EPMC3564953 | biostudies-literature
UnknownCommon variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
Not available
S-EPMC3496151 | biostudies-literature
UnknownLarge-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
Not available
S-EPMC5409098 | biostudies-literature
UnknownMendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers.
Not available
S-EPMC6738050 | biostudies-literature
UnknownWhole-genome sequencing of patients with rare diseases in a national health system.
Not available
S-EPMC7610553 | biostudies-literature
UnknownGenetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Not available
S-EPMC4735748 | biostudies-literature
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