Genetic analysis workshop IV: Huntington disease linkage analysis summary

Complex association patterns for inflammatory mediators in induced sputum from subjects with asthma.

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology·2018

Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function.

Journal of Alzheimer's disease & Parkinsonism·2017

Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease.

Neuroscience letters·2017

GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis.

Genes and immunity·2016

Utility of blood pressure genetic risk score in admixed Hispanic samples.

Journal of human hypertension·2016

eQTL of bronchial epithelial cells and bronchial alveolar lavage deciphers GWAS-identified asthma genes.

Allergy·2015

HLA haplotype sharing and proband genotype in IDDM.

Genetic epidemiology. Supplement·1986

A log-linear model for binary pedigree data.

Genetic epidemiology. Supplement·1986

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

The first 25 years of the NICHD Structural Birth Defects Initiative.

Developmental biology·2026

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Genetic analysis workshop IV: Huntington disease linkage analysis summary

Related Concept Videos

Complex association patterns for inflammatory mediators in induced sputum from subjects with asthma.

Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function.

Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease.

GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis.

Utility of blood pressure genetic risk score in admixed Hispanic samples.

eQTL of bronchial epithelial cells and bronchial alveolar lavage deciphers GWAS-identified asthma genes.

HLA haplotype sharing and proband genotype in IDDM.

A log-linear model for binary pedigree data.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

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Genetic analysis workshop IV: Huntington disease linkage analysis summary

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