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UnknownGenetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease.
Not available
S-EPMC5800308 | biostudies-literature
UnknownA multicenter assessment of single-cell models aligned to standard measures of cell health for prediction of acute hepatotoxicity.
Not available
S-EPMC5316403 | biostudies-literature
UnknownSex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Not available
S-EPMC8458480 | biostudies-literature
UnknownThe interplay of family history of depression and early trauma: associations with lifetime and current depression in the German national cohort (NAKO).
Not available
S-EPMC10959537 | biostudies-literature
UnknownGenome-wide association analysis of anti-TNF drug response in patients with rheumatoid arthritis.
Not available
S-EPMC4169706 | biostudies-literature
UnknownBiallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.
Not available
S-EPMC12646654 | biostudies-literature
UnknownGWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors.
Not available
S-EPMC10603363 | biostudies-literature
UnknownPartitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.
Not available
S-EPMC4225595 | biostudies-literature
UnknownSystematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.
Not available
S-EPMC5314135 | biostudies-literature
UnknownCoding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
Not available
S-EPMC4850838 | biostudies-literature
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