African cohort
Evidence from:
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all sources
Related entities (21)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| 1000 Genomes Project | associated_with | African | — | 1 |
| 1000 Genomes Project | interacts_with | African | — | 1 |
| ADMIXMAP | associated_with | African | — | 1 |
| African | associated_with | imputation accuracy | — | 1 |
| African | associated_with | lifetime alcohol use | — | 1 |
| African | associated_with | polygenic risk score | — | 1 |
| African | associated_with | SNP | — | 1 |
| African American | associated_with | African | — | 1 |
| associated SNPs | associated_with | African | — | 1 |
| drug dependence | associated_with | African | — | 1 |
| HapMap | associated_with | African | — | 1 |
| imputation accuracy | associated_with | African | — | 1 |
| lead SNP | associated_with | African | — | 1 |
| MVP | interacts_with | African | — | 1 |
| OPRM1 A118G | associated_with | African | — | 1 |
| polygenic risk score | associated_with | African | — | 1 |
| PRS-CS | associated_with | African | — | 1 |
| rs1426654 | associated_with | African | — | 1 |
| SNP | biomarker_for | African | — | 1 |
| Spit for Science | associated_with | African | — | 1 |
| Structure | associated_with | African | — | 1 |
Mentioned in (90)
Papers in which this entity is mentioned.
- Mapping the genetic landscape across 14 psychiatric disorders. (2026)
- Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes. (2025)
- Efficient and accurate search in petabase-scale sequence repositories. (2025)
- OXSeg: Multidimensional Attention UNet-Based Lip Segmentation Using Semi-Supervised Lip Contours. (2025)
- Nucleotide Transformer: building and evaluating robust foundation models for human genomics. (2025)
- KILDA: identifying KIV-2 repeats from kmers. (2025)
- BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
- MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
- Principles and methods for transferring polygenic risk scores across global populations. (2024)
- The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
- Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
- Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
- A harmonized public resource of deeply sequenced diverse human genomes. (2024)
- Pruning and thresholding approach for methylation risk scores in multi-ancestry populations. (2023)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. (2023)
- Reducing Prenatal Alcohol Exposure and the Incidence of FASD: Is the Past Prologue? (2023)
- Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
- Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. (2022)
- A saturated map of common genetic variants associated with human height. (2022)
- AFA: Ancestry-specific allele frequency estimation in admixed populations: The Hispanic Community Health Study/Study of Latinos. (2022)
- Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
- Early neurodevelopment of HIV-exposed uninfected children in the era of antiretroviral therapy: a systematic review and meta-analysis. (2022)
- Factors associated with phosphatidylethanol (PEth) sensitivity for detecting unhealthy alcohol use: An individual patient data meta-analysis. (2021)
- Epigenome-wide change and variation in DNA methylation in childhood: trajectories from birth to late adolescence. (2021)
- Frequent LPA KIV-2 Variants Lower Lipoprotein(a) Concentrations and Protect Against Coronary Artery Disease. (2021)
- Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
- ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. (2020)
- Neurodevelopmental effects of ante-partum and post-partum antiretroviral exposure in HIV-exposed and uninfected children versus HIV-unexposed and uninfected children in Uganda and Malawi: a prospective cohort study. (2019)
- Rare variant phasing using paired tumor:normal sequence data. (2019)
- The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
- Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
- Polygenic risk for neuropsychiatric disease and vulnerability to abnormal deep grey matter development. (2019)
- Global, regional, and national estimates of levels of preterm birth in 2014: a systematic review and modelling analysis. (2019)
- A SNP panel for identification of DNA and RNA specimens. (2018)
- In-utero exposure to antiretrovirals and neurodevelopment among HIV-exposed-uninfected children in Botswana. (2018)
- Psychiatric Genomics: An Update and an Agenda. (2018)
- Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity. (2018)
- Associations between cortical thickness and neurocognitive skills during childhood vary by family socioeconomic factors. (2017)
- Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (2017)
- Ancient DNA and the rewriting of human history: be sparing with Occam's razor. (2016)
- Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
- KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)
- Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
- The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. (2016)
- Prenatal exposure to cannabis and maternal and child health outcomes: a systematic review and meta-analysis. (2016)
- Epidemiology, Etiology, and Treatment of Isolated Cleft Palate. (2016)
- Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
- Family income, parental education and brain structure in children and adolescents. (2015)
- mHealthApps: A Repository and Database of Mobile Health Apps. (2015)
- Dissecting ancestry genomic background in substance dependence genome-wide association studies. (2015)
- A global reference for human genetic variation. (2015)
- A global reference for human genetic variation. (2015)
- A germline polymorphism of thymine DNA glycosylase induces genomic instability and cellular transformation. (2014)
- Intended and unintended pregnancies worldwide in 2012 and recent trends. (2014)
- Is vitamin D deficiency a major global public health problem? (2014)
- 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. (2014)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
- Face shape differs in phylogenetically related populations. (2014)
- EWS-FLI1 utilizes divergent chromatin remodeling mechanisms to directly activate or repress enhancer elements in Ewing sarcoma. (2014)
- Reliability and validity of instruments for assessing perinatal depression in African settings: systematic review and meta-analysis. (2013)
- DNA methylation contributes to natural human variation. (2013)
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
- The Genomic Revolution and Beliefs about Essential Racial Differences: A Backdoor to Eugenics? (2013)
- The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
- Phosphatidylethanol (PEth) as a biomarker of alcohol consumption in HIV-positive patients in sub-Saharan Africa. (2012)
- An integrated map of genetic variation from 1,092 human genomes. (2012)
- Microsatellites with macro-influence in ewing sarcoma. (2012)
- The genetic basis of addictive disorders. (2012)
- The genetics of the opioid system and specific drug addictions. (2012)
- A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (2011)
- Haplotype block structure of the genomic region of the mu opioid receptor gene. (2011)
- The prevalence and clinical presentation of antenatal depression in rural South Africa. (2011)
- Genome-wide scan for self-rating of the effects of alcohol in American Indians. (2010)
- Discovering genetic ancestry using spectral graph theory. (2010)
- A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. (2010)
- Genome-wide association studies in diverse populations. (2010)
- A new statistic to evaluate imputation reliability. (2010)
- Race and psychological distress: the South african stress and health study. (2010)
- Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
- Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
- Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation. (2008)
- Toward a global view of alcohol, tobacco, cannabis, and cocaine use: findings from the WHO World Mental Health Surveys. (2008)
- Geographic patterns of genome admixture in Latin American Mestizos. (2008)
- Heterogeneity in meta-analyses of genome-wide association investigations. (2007)
- The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
- The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
- Population structure and eigenanalysis. (2006)
- The nutrient intakes of mothers of low birth weight babies - a comparison of ethnic groups in East London, UK. (2005)
- Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN
Merged raw entities (7)
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 |
|---|---|---|---|
| african | cohort | 37 | 65 |
| africa | cohort | 28 | 44 |
| african population | cohort | 27 | 43 |
| african populations | cohort | 15 | 23 |
| africans | cohort | 14 | 54 |
| african | phenotype | 7 | 9 |
| african (afr) | cohort | 3 | 3 |