discovery sample cohort
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Related entities (42)
Mentioned in (42)
Papers in which this entity is mentioned.
- Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
- Punitive legal responses to prenatal drug use in the United States: A survey of state policies and systematic review of their public health impacts. (2024)
- An overview of DNA methylation-derived trait score methods and applications. (2023)
- Pruning and thresholding approach for methylation risk scores in multi-ancestry populations. (2023)
- A saturated map of common genetic variants associated with human height. (2022)
- Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
- Reproducible brain-wide association studies require thousands of individuals. (2022)
- Autosomal sex-associated co-methylated regions predict biological sex from DNA methylation. (2021)
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
- Fetal alcohol spectrum disorder predisposes to metabolic abnormalities in adulthood. (2020)
- Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
- Brain Volume Abnormalities in Youth at High Risk for Depression: Adolescent Brain and Cognitive Development Study. (2020)
- Association of a Schizophrenia-Risk Nonsynonymous Variant With Putamen Volume in Adolescents: A Voxelwise and Genome-Wide Association Study. (2019)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. (2019)
- The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder. (2018)
- Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors. (2018)
- Widespread Selection for Oncogenic Mutant Allele Imbalance in Cancer. (2018)
- Implications of altered maternal cytokine concentrations on infant outcomes in children with prenatal alcohol exposure. (2018)
- Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
- Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior. (2017)
- Imaging Genetics and Genomics in Psychiatry: A Critical Review of Progress and Potential. (2017)
- Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. (2016)
- Novel genetic loci underlying human intracranial volume identified through genome-wide association. (2016)
- KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)
- Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer. (2016)
- Alcohol Dependence Genetics: Lessons Learned From Genome-Wide Association Studies (GWAS) and Post-GWAS Analyses. (2015)
- Genomic influences on alcohol problems in a population-based sample of young adults. (2015)
- Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
- Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. (2014)
- Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. (2014)
- Polygenic risk scores for smoking: predictors for alcohol and cannabis use? (2014)
- Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
- Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. (2012)
- An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia. (2012)
- The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
- Neuronal calcium sensor-1 and cocaine addiction: a genetic association study in African-Americans and European Americans. (2012)
- Novel mutations target distinct subgroups of medulloblastoma. (2012)
- Genome-wide association study of primary open angle glaucoma risk and quantitative traits. (2012)
- Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. (2012)
- The AVPR1A gene and substance use disorders: association, replication, and functional evidence. (2011)
- The neuronal transporter gene SLC6A15 confers risk to major depression. (2011)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. (2010)
Merged raw entities (9)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| discovery cohort | cohort | 21 | 75 |
| discovery sample | cohort | 17 | 29 |
| discovery cohorts | cohort | 3 | 3 |
| nd | cohort | 3 | 3 |
| initial discovery sample | cohort | 2 | 3 |
| 106,336 out of 133,653 individuals | cohort | — | — |
| appropriate discovery cohort | cohort | — | — |
| discovery cases | cohort | — | — |
| enrichment cohort | cohort | — | — |