candidate genes cohort
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Related entities (109)
Mentioned in (43)
Papers in which this entity is mentioned.
- Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
- Estimation of tumor cell total mRNA expression in 15 cancer types predicts disease progression. (2022)
- Shared genetic architecture across psychiatric disorders. (2021)
- Programmed suppression of oxidative phosphorylation and mitochondrial function by gestational alcohol exposure correlate with widespread increases in H3K9me2 that do not suppress transcription. (2021)
- Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
- Transcriptome-Wide Regulation of Key Developmental Pathways in the Mouse Neural Tube by Prenatal Alcohol Exposure. (2020)
- Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors. (2020)
- Highly Efficient CRISPR-Cas9-Based Methods for Generating Deletion Mutations and F0 Embryos that Lack Gene Function in Zebrafish. (2019)
- Genome-wide association study reveals novel loci associated with body size and carcass yields in Pekin ducks. (2019)
- Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
- Candidate gene-environment interaction research: reflections and recommendations. (2015)
- Interparental Relationship Sensitivity Leads to Adolescent Internalizing Problems: Different Genotypes, Different Pathways. (2015)
- Evaluating historical candidate genes for schizophrenia. (2015)
- Reverse genetic screening reveals poor correlation between morpholino-induced and mutant phenotypes in zebrafish. (2015)
- Guidelines for investigating causality of sequence variants in human disease. (2014)
- Heritability and molecular-genetic basis of the P3 event-related brain potential: a genome-wide association study. (2014)
- VariantDB: a flexible annotation and filtering portal for next generation sequencing data. (2014)
- In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. (2014)
- Candidate gene association studies: a comprehensive guide to useful in silico tools. (2013)
- Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
- Preliminary evidence for a gene-environment interaction in predicting alcohol use disorders in adolescents. (2013)
- Genes of experience: explaining the heritability of putative environmental variables through their association with behavioural and emotional traits. (2013)
- Associations between maternal genotypes and metabolites implicated in congenital heart defects. (2012)
- Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. (2012)
- The impact of gene-environment interaction on alcohol use disorders. (2012)
- Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. (2012)
- Large-scale analysis of acute ethanol exposure in zebrafish development: a critical time window and resilience. (2011)
- Liver and adipose expression associated SNPs are enriched for association to type 2 diabetes. (2010)
- Association study of 182 candidate genes in anorexia nervosa. (2010)
- Large copy-number variations are enriched in cases with moderate to extreme obesity. (2010)
- Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction. (2010)
- Conserved role of unc-79 in ethanol responses in lightweight mutant mice. (2010)
- SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies. (2009)
- Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. (2009)
- Ethanol teratogenesis in five inbred strains of mice. (2009)
- Genomewide association studies and human disease. (2009)
- Marker selection for genetic case-control association studies. (2009)
- New insights into the genetics of addiction. (2009)
- Common and rare variants in multifactorial susceptibility to common diseases. (2008)
- Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation. (2008)
- Holoprosencephaly. (2007)
- SNPs3D: candidate gene and SNP selection for association studies. (2006)
- Linkage analysis and association analysis in the presence of linkage using age at onset of COGA alcoholism data. (2005)
Merged raw entities (4)
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 |
|---|---|---|---|
| candidate genes | gene | 32 | 37 |
| candidate gene | gene | 13 | 14 |
| candidate genes | cohort | 1 | 1 |
| genes | cohort | — | — |