Pages that link to "Q43213939"
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The following pages link to Discovering genetic ancestry using spectral graph theory (Q43213939):
Displaying 50 items.
- Functional impact of global rare copy number variation in autism spectrum disorders (Q24596191) (← links)
- Genome-wide association study of intracranial aneurysm identifies three new risk loci (Q24630663) (← links)
- Softwares and methods for estimating genetic ancestry in human populations (Q26859706) (← links)
- Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies (Q27330547) (← links)
- Recent genomic heritage in Scotland (Q28645673) (← links)
- Enhanced localization of genetic samples through linkage-disequilibrium correction (Q28681804) (← links)
- Genome-wide association study heterogeneous cohort homogenization via subject weight knock-down (Q28714390) (← links)
- Individual common variants exert weak effects on the risk for autism spectrum disorders (Q28943296) (← links)
- A genome-wide scan for common alleles affecting risk for autism (Q28943508) (← links)
- Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy (Q29417026) (← links)
- Genome-wide association study of Alzheimer's disease with psychotic symptoms (Q29417042) (← links)
- Association of CLU and PICALM variants with Alzheimer's disease. (Q30422270) (← links)
- Common genetic variants, acting additively, are a major source of risk for autism (Q30536405) (← links)
- Adjusting for population stratification in a fine scale with principal components and sequencing data (Q30677104) (← links)
- Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project (Q31034686) (← links)
- Inference and Analysis of Population Structure Using Genetic Data and Network Theory (Q31047279) (← links)
- ROADTRIPS: case-control association testing with partially or completely unknown population and pedigree structure (Q33645960) (← links)
- The potential for enhancing the power of genetic association studies in African Americans through the reuse of existing genotype data (Q33686851) (← links)
- Using principal components of genetic variation for robust and powerful detection of gene-gene interactions in case-control and case-only studies (Q33708556) (← links)
- Clustering by genetic ancestry using genome-wide SNP data (Q33767014) (← links)
- Testing for an unusual distribution of rare variants (Q33847792) (← links)
- Screen and clean: a tool for identifying interactions in genome-wide association studies (Q34042021) (← links)
- Pharmacogenomics of suicidal events (Q34066818) (← links)
- Manifold learning for human population structure studies (Q34137404) (← links)
- Correction for hidden confounders in the genetic analysis of gene expression (Q34151779) (← links)
- Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls (Q34672061) (← links)
- No association of psychosis in Alzheimer disease with neurodegenerative pathway genes (Q34728992) (← links)
- Control for confounding in case-control studies using the stratification score, a retrospective balancing score (Q34760347) (← links)
- GAGA: a new algorithm for genomic inference of geographic ancestry reveals fine level population substructure in Europeans (Q35105578) (← links)
- Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders (Q35304267) (← links)
- Novel genetic matching methods for handling population stratification in genome-wide association studies (Q35603770) (← links)
- Correcting for Population Stratification in Genomewide Association Studies (Q35857407) (← links)
- Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis (Q35927065) (← links)
- A permutation procedure to correct for confounders in case-control studies, including tests of rare variation (Q36152921) (← links)
- GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway (Q36276884) (← links)
- Retrospective Binary-Trait Association Test Elucidates Genetic Architecture of Crohn Disease (Q36559281) (← links)
- Sparse principal component analysis for identifying ancestry-informative markers in genome-wide association studies (Q36680666) (← links)
- Genome-wide association analysis of circulating vitamin D levels in children with asthma (Q36828929) (← links)
- A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies (Q36893391) (← links)
- Stratification-score matching improves correction for confounding by population stratification in case-control association studies (Q36899672) (← links)
- SNPs in CAST are associated with Parkinson disease: a confirmation study (Q36936945) (← links)
- Statistical distributions of test statistics used for quantitative trait association mapping in structured populations (Q37279970) (← links)
- Gene expression elucidates functional impact of polygenic risk for schizophrenia (Q37372402) (← links)
- Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants (Q37432581) (← links)
- Genetics in psychiatry: common variant association studies (Q37777200) (← links)
- Detecting individual ancestry in the human genome (Q38456928) (← links)
- Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome (Q38713712) (← links)
- Prediction of biogeographical ancestry from genotype: a comparison of classifiers. (Q38725359) (← links)
- A comparison of association methods correcting for population stratification in case-control studies (Q39080489) (← links)
- Adjustment for population stratification via principal components in association analysis of rare variants (Q41004097) (← links)