Pages that link to "Q22337263"
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The following pages link to How many diseases does it take to map a gene with SNPs? (Q22337263):
Displaying 50 items.
- ‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?* (Q22066036) (← links)
- The use of racial, ethnic, and ancestral categories in human genetics research (Q22066114) (← links)
- MULTIFACTORIAL GENETICSUNDERSTANDING QUANTITATIVE GENETIC VARIATION (Q22121996) (← links)
- Genetic predisposition to cancer — insights from population genetics (Q22122022) (← links)
- Complex Diseases, Complex Genes (Q24289171) (← links)
- The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes (Q24290189) (← links)
- A genomewide screen of 345 families for autism-susceptibility loci (Q24532783) (← links)
- Variation in GRM3 affects cognition, prefrontal glutamate, and risk for schizophrenia (Q24562939) (← links)
- Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia (Q24612644) (← links)
- Single nucleotide polymorphisms (SNPs) are inherited from parents and they measure heritable events (Q24795928) (← links)
- The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia (Q24798030) (← links)
- The genetics of rheumatoid arthritis and the need for animal models to find and understand the underlying genes (Q24805318) (← links)
- Genetic epidemiology. Approaches to the genetic analysis of rheumatoid arthritis (Q24805566) (← links)
- Complex genetic diseases: controversy over the Croesus code (Q24805821) (← links)
- Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case-control study of African Americans and whites (Q24805844) (← links)
- Genome-wide association mapping in Arabidopsis identifies previously known flowering time and pathogen resistance genes (Q24816825) (← links)
- Using haplotype blocks to map human complex trait loci (Q28180092) (← links)
- Chromosome 21: from sequence to applications (Q28191044) (← links)
- Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancers (Q28207853) (← links)
- Accessing genetic variation: genotyping single nucleotide polymorphisms (Q28208864) (← links)
- Population stratification and spurious allelic association (Q28211105) (← links)
- Beyond race: towards a whole-genome perspective on human populations and genetic variation (Q28290268) (← links)
- Tilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causation (Q28385221) (← links)
- The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics (Q28482577) (← links)
- Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology (Q28755468) (← links)
- Mendelian Randomization for Strengthening Causal Inference in Observational Studies (Q29037397) (← links)
- Human non-synonymous SNPs: server and survey (Q29547603) (← links)
- Genetic mapping in human disease (Q29614943) (← links)
- Genome-wide association studies for common diseases and complex traits (Q29615822) (← links)
- Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence (Q29618819) (← links)
- Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease (Q29619085) (← links)
- Genetics of Type 2 Diabetes: the Power of Isolated Populations (Q30250281) (← links)
- Genetic dissection of a model complex trait using the Drosophila Synthetic Population Resource. (Q30464636) (← links)
- Rethinking genetic strategies to study complex diseases (Q30482242) (← links)
- Prefrontal neurons and the genetics of schizophrenia (Q30666934) (← links)
- Full-exon resequencing reveals toll-like receptor variants contribute to human susceptibility to tuberculosis disease (Q30839566) (← links)
- Molecular haplotyping at high throughput. (Q30859785) (← links)
- Reducing INDEL calling errors in whole genome and exome sequencing data (Q30872081) (← links)
- Large-scale genotyping by mass spectrometry: experience, advances and obstacles (Q31037370) (← links)
- Single nucleotide polymorphism identification in candidate gene systems of obesity. (Q31044189) (← links)
- Heritability of cardiovascular and personality traits in 6,148 Sardinians (Q33255344) (← links)
- Detecting rare variants for complex traits using family and unrelated data (Q33511799) (← links)
- Toward the use of genomics to study microevolutionary change in bacteria (Q33512516) (← links)
- Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia (Q33842912) (← links)
- Interpretation of association signals and identification of causal variants from genome-wide association studies (Q33847237) (← links)
- Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q (Q33905086) (← links)
- Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome (Q33905170) (← links)
- Generating large-scale longitudinal data resources for aging research (Q33956715) (← links)
- Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups (Q34020356) (← links)
- The power to detect linkage disequilibrium with quantitative traits in selected samples (Q34020848) (← links)