# Genetic Associations and Epidemiology
**Type:** Topics
**Canonical URL:** https://scholariq.org/topics/genetic-associations-and-epidemiology/
## Facts
| Field | Value |
| --- | --- |
| Description | This cluster of papers encompasses a wide range of topics in genomic studies, including genome-wide association analyses, genetic variation, haplotype mapping, population genetics, Mendelian randomization, polygenic risk scores, gene expression, and the study of complex diseases. It explores methods for analyzing genetic data and understanding the genetic basis of various traits and diseases. |
| Domain | Life Sciences |
| Field | Biochemistry, Genetics and Molecular Biology |
| OpenAlex ID | t10261 |
| Works | 489 |
## Topic papers all
Showing 15 of 489.
- [A global reference for human genetic variation](https://scholariq.org/papers/a-global-reference-for-human-genetic-variation/)
- [UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age](https://scholariq.org/papers/uk-biobank-an-open-access-resource-for-identifying-the-causes-of-a-wide-range-of/)
- [Statistical significance for genomewide studies](https://scholariq.org/papers/statistical-significance-for-genomewide-studies/)
- [Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls](https://scholariq.org/papers/genome-wide-association-study-of-14-000-cases-of-seven-common-diseases-and-3-000/)
- [An integrated map of genetic variation from 1,092 human genomes](https://scholariq.org/papers/an-integrated-map-of-genetic-variation-from-1-092-human-genomes/)
- [Biological insights from 108 schizophrenia-associated genetic loci](https://scholariq.org/papers/biological-insights-from-108-schizophrenia-associated-genetic-loci/)
- [A map of human genome variation from population-scale sequencing](https://scholariq.org/papers/a-map-of-human-genome-variation-from-population-scale-sequencing-2/)
- [Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data](https://scholariq.org/papers/mendelian-randomization-analysis-with-multiple-genetic-variants-using-summarized/)
- [The International HapMap Project](https://scholariq.org/papers/the-international-hapmap-project/)
- [The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans](https://scholariq.org/papers/the-genotype-tissue-expression-gtex-pilot-analysis-multitissue-gene-regulation/)
- [Mendelian randomization: Using genes as instruments for making causal inferences in epidemiology](https://scholariq.org/papers/mendelian-randomization-using-genes-as-instruments-for-making-causal-inferences/)
- [Genetic studies of body mass index yield new insights for obesity biology](https://scholariq.org/papers/genetic-studies-of-body-mass-index-yield-new-insights-for-obesity-biology/)
- [Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease](https://scholariq.org/papers/meta-analysis-of-74-046-individuals-identifies-11-new-susceptibility-loci-for/)
- [A second generation human haplotype map of over 3.1 million SNPs](https://scholariq.org/papers/a-second-generation-human-haplotype-map-of-over-3-1-million-snps/)
- [A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity](https://scholariq.org/papers/a-common-variant-in-the-i-fto-i-gene-is-associated-with-body-mass-index-and/)
## Topic primary papers
Showing 15 of 272.
- [A global reference for human genetic variation](https://scholariq.org/papers/a-global-reference-for-human-genetic-variation/)
- [UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age](https://scholariq.org/papers/uk-biobank-an-open-access-resource-for-identifying-the-causes-of-a-wide-range-of/)
- [Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls](https://scholariq.org/papers/genome-wide-association-study-of-14-000-cases-of-seven-common-diseases-and-3-000/)
- [An integrated map of genetic variation from 1,092 human genomes](https://scholariq.org/papers/an-integrated-map-of-genetic-variation-from-1-092-human-genomes/)
- [Biological insights from 108 schizophrenia-associated genetic loci](https://scholariq.org/papers/biological-insights-from-108-schizophrenia-associated-genetic-loci/)
- [Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data](https://scholariq.org/papers/mendelian-randomization-analysis-with-multiple-genetic-variants-using-summarized/)
- [The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans](https://scholariq.org/papers/the-genotype-tissue-expression-gtex-pilot-analysis-multitissue-gene-regulation/)
- [Mendelian randomization: Using genes as instruments for making causal inferences in epidemiology](https://scholariq.org/papers/mendelian-randomization-using-genes-as-instruments-for-making-causal-inferences/)
- [Genetic studies of body mass index yield new insights for obesity biology](https://scholariq.org/papers/genetic-studies-of-body-mass-index-yield-new-insights-for-obesity-biology/)
- [A second generation human haplotype map of over 3.1 million SNPs](https://scholariq.org/papers/a-second-generation-human-haplotype-map-of-over-3-1-million-snps/)
- [A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity](https://scholariq.org/papers/a-common-variant-in-the-i-fto-i-gene-is-associated-with-body-mass-index-and/)
- [FinnGen provides genetic insights from a well-phenotyped isolated population](https://scholariq.org/papers/finngen-provides-genetic-insights-from-a-well-phenotyped-isolated-population/)
- [Biological, clinical and population relevance of 95 loci for blood lipids](https://scholariq.org/papers/biological-clinical-and-population-relevance-of-95-loci-for-blood-lipids/)
- [Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease](https://scholariq.org/papers/genome-wide-association-study-identifies-variants-at-clu-and-picalm-associated/)
- [Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression](https://scholariq.org/papers/genome-wide-association-analyses-identify-44-risk-variants-and-refine-the/)
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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.