Linkage disequilibrium and the search for complex disease genes

Predicting smallpox epidemics: A statistical analysis of two Finnish populations.

American journal of human biology : the official journal of the Human Biology Council·2017

Pharmacogenomics of 17-alpha hydroxyprogesterone caproate for recurrent preterm birth: a case-control study.

BJOG : an international journal of obstetrics and gynaecology·2017

Combined variants in factor VIII and prostaglandin synthase-1 amplify hemorrhage severity across three generations of descendants.

Journal of thrombosis and haemostasis : JTH·2016

Adaptive genetic changes related to haemoglobin concentration in native high-altitude Tibetans.

Experimental physiology·2015

Lack of association between beta 2-adrenergic receptor polymorphisms and juvenile idiopathic arthritis.

Scandinavian journal of rheumatology·2009

Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms.

BMC genetics·2008

Nuclear mitochondrial sequences in great ape Telomere-to-Telomere genomes.

Genome research·2026

A biobank-scale method for learning modulators of gene-environment interaction underlying human complex traits from multiple environmental exposures.

Genome research·2026

Characterizing intra- and intertumor heterogeneity in ovarian high-grade serous carcinoma subtypes using single-cell and spatial transcriptomics.

Genome research·2026

Private information leakage from polygenic risk scores.

Genome research·2026

Massively parallel characterization of adolescent idiopathic scoliosis risk variants.

Genome research·2026

Detecting somatic mutations in rare clones using single-cell multiomics.

Genome research·2026

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

Proteome-wide QTL mapping enables gene-protein-phenotype metabolic network construction in a genetically diverse MASLD mouse model.

bioRxiv : the preprint server for biology·2026

Sequence determinants of pathogenicity in glucose-6-phosphatase linked to glycogen storage disease type 1a.

bioRxiv : the preprint server for biology·2026

Estimating the Penetrance of PRNP Mutations in Chinese Prion Disease Patients based on the Genome Databases.

Genomics, proteomics & bioinformatics·2026

Genome-wide linkage and association mapping identified a novel candidate gene, TaGLK-A1, underlying fructan content in wheat grain.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026

Deletion of ARPKD-associated Pkhd1 gene in mice results in decreased Tfap2b expression and eye abnormalities.

Nature communications·2026

Related Experiment Videos

Linkage disequilibrium and the search for complex disease genes

Related Concept Videos

Predicting smallpox epidemics: A statistical analysis of two Finnish populations.

Pharmacogenomics of 17-alpha hydroxyprogesterone caproate for recurrent preterm birth: a case-control study.

Combined variants in factor VIII and prostaglandin synthase-1 amplify hemorrhage severity across three generations of descendants.

Adaptive genetic changes related to haemoglobin concentration in native high-altitude Tibetans.

Lack of association between beta 2-adrenergic receptor polymorphisms and juvenile idiopathic arthritis.

Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms.

Nuclear mitochondrial sequences in great ape Telomere-to-Telomere genomes.

A biobank-scale method for learning modulators of gene-environment interaction underlying human complex traits from multiple environmental exposures.

Characterizing intra- and intertumor heterogeneity in ovarian high-grade serous carcinoma subtypes using single-cell and spatial transcriptomics.

Private information leakage from polygenic risk scores.

Massively parallel characterization of adolescent idiopathic scoliosis risk variants.

Detecting somatic mutations in rare clones using single-cell multiomics.

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Proteome-wide QTL mapping enables gene-protein-phenotype metabolic network construction in a genetically diverse MASLD mouse model.

Sequence determinants of pathogenicity in glucose-6-phosphatase linked to glycogen storage disease type 1a.

Estimating the Penetrance of PRNP Mutations in Chinese Prion Disease Patients based on the Genome Databases.

Genome-wide linkage and association mapping identified a novel candidate gene, TaGLK-A1, underlying fructan content in wheat grain.

Deletion of ARPKD-associated Pkhd1 gene in mice results in decreased Tfap2b expression and eye abnormalities.

Related Experiment Videos

Linkage disequilibrium and the search for complex disease genes

Related Concept Videos

Related Articles