"Mixture models for linkage analysis of affected sibling pairs with covariates"

The fibromyalgia family study: a genome-wide linkage scan study.

Arthritis and rheumatism·2013

Candidate-gene association study of mothers with pre-eclampsia, and their infants, analyzing 775 SNPs in 190 genes.

Human heredity·2006

Prediction of empirical p values from asymptotic p values for conditional logistic affected relative pair linkage analysis.

Human heredity·2006

Genetic linkage of systemic lupus erythematosus to 13q32 in African American families with affected male members.

Human genetics·2005

Tapasin gene polymorphism in systemic onset juvenile rheumatoid arthritis: a family-based case-control study.

Arthritis research & therapy·2005

The Family Investigation of Nephropathy and Diabetes (FIND): design and methods.

Journal of diabetes and its complications·2005

Mendelianization: Concentrating Polygenic Signal Into a Single Causal Locus.

Genetic epidemiology·2026

Robust Inference With Ghostknockoffs in Genome-Wide Association Studies With Sample Relatedness.

Genetic epidemiology·2026

The Omnicausal Model Reveals the Highly Polyfactorial Nature of Complex Diseases.

Genetic epidemiology·2026

Applying Bayesian Multivariable Mendelian Randomisation to Prioritise Candidate Causal Traits From High-Dimensional Data: Illustration From Estimation of the Effect of Maternal Metabolites on Offspring Birthweight.

Genetic epidemiology·2026

Individualized Bayesian Inference Identifies Novel Genetic Variants for Parkinson's Disease.

Genetic epidemiology·2026

DRIVE v3: Command Line Application for Identity-by-Descent Haplotype Clustering in Large Biobank Scale Data.

Genetic epidemiology·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·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

Related Experiment Videos

"Mixture models for linkage analysis of affected sibling pairs with covariates"

Related Concept Videos

The fibromyalgia family study: a genome-wide linkage scan study.

Candidate-gene association study of mothers with pre-eclampsia, and their infants, analyzing 775 SNPs in 190 genes.

Prediction of empirical p values from asymptotic p values for conditional logistic affected relative pair linkage analysis.

Genetic linkage of systemic lupus erythematosus to 13q32 in African American families with affected male members.

Tapasin gene polymorphism in systemic onset juvenile rheumatoid arthritis: a family-based case-control study.

The Family Investigation of Nephropathy and Diabetes (FIND): design and methods.

Mendelianization: Concentrating Polygenic Signal Into a Single Causal Locus.

Robust Inference With Ghostknockoffs in Genome-Wide Association Studies With Sample Relatedness.

The Omnicausal Model Reveals the Highly Polyfactorial Nature of Complex Diseases.

Applying Bayesian Multivariable Mendelian Randomisation to Prioritise Candidate Causal Traits From High-Dimensional Data: Illustration From Estimation of the Effect of Maternal Metabolites on Offspring Birthweight.

Individualized Bayesian Inference Identifies Novel Genetic Variants for Parkinson's Disease.

DRIVE v3: Command Line Application for Identity-by-Descent Haplotype Clustering in Large Biobank Scale Data.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

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Related Experiment Videos

"Mixture models for linkage analysis of affected sibling pairs with covariates"

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