Introduction: linkage analyses in the Hutterites

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Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.

Human genetics·2018

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Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease.

Genes, brain, and behavior·2017

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Association of rare missense variants in the second intracellular loop of Na<sub>V</sub>1.7 sodium channels with familial autism.

Molecular psychiatry·2016

Same author

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.

Human genetics·2016

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Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data.

Genes, brain, and behavior·2015

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Identification of rare variants from exome sequence in a large pedigree with autism.

Human heredity·2013

Same journal

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

Same journal

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

Genetic epidemiology·2026

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

Genetic epidemiology·2026

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Deep Unsupervised Domain Adaptation for Translating Cancer Dependency Maps From Cell Lines to Breast Cancer Tumor Genomics.

Genetic epidemiology·2026

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Polygenic Risk Scores for Incident Dementia in the Multi-Ethnic Study of Atherosclerosis.

Genetic epidemiology·2026

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Outcome and Exposure Polygenic Risk Scores Can Help Reduce Information Bias and Selection Bias in Regression Estimates From Biobank Data.

Genetic epidemiology·2026

Related Experiment Videos

Introduction: linkage analyses in the Hutterites

Related Concept Videos

Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.

Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease.

Association of rare missense variants in the second intracellular loop of Na<sub>V</sub>1.7 sodium channels with familial autism.

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.

Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data.

Identification of rare variants from exome sequence in a large pedigree with autism.

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.

Deep Unsupervised Domain Adaptation for Translating Cancer Dependency Maps From Cell Lines to Breast Cancer Tumor Genomics.

Polygenic Risk Scores for Incident Dementia in the Multi-Ethnic Study of Atherosclerosis.

Outcome and Exposure Polygenic Risk Scores Can Help Reduce Information Bias and Selection Bias in Regression Estimates From Biobank Data.

Related Experiment Videos

Introduction: linkage analyses in the Hutterites

Related Concept Videos

Related Articles

Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.

Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease.

Association of rare missense variants in the second intracellular loop of Na<sub>V</sub>1.7 sodium channels with familial autism.

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.

Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data.

Identification of rare variants from exome sequence in a large pedigree with autism.

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.

Deep Unsupervised Domain Adaptation for Translating Cancer Dependency Maps From Cell Lines to Breast Cancer Tumor Genomics.

Polygenic Risk Scores for Incident Dementia in the Multi-Ethnic Study of Atherosclerosis.

Outcome and Exposure Polygenic Risk Scores Can Help Reduce Information Bias and Selection Bias in Regression Estimates From Biobank Data.