Path analysis of family resemblance in the presence of gene-environment interaction

Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.

Nature communications·2016

A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction.

Scientific reports·2016

The effects of exercise on the lipoprotein subclass profile: A meta-analysis of 10 interventions.

Atherosclerosis·2015

Genomic and transcriptomic predictors of triglyceride response to regular exercise.

British journal of sports medicine·2015

Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.

International journal of obesity (2005)·2015

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.

PLoS genetics·2015

The genetic architecture of pentanucleotide repeat variation and disease association.

American journal of human genetics·2026

Accurate detection of sub-1% frequency somatic mutations by whole-genome sequencing.

American journal of human genetics·2026

De novo MAP2K4 variants cause a neurodevelopmental syndrome and impaired JNK signaling in iPSC-derived neurons.

American journal of human genetics·2026

Large-scale integration of functional assay data for the resolution of germline BRCA1 and BRCA2 variants of uncertain significance.

American journal of human genetics·2026

Loss of the human BRIP1 C terminus does not cause Fanconi anemia.

American journal of human genetics·2026

A massively parallel reporter assay of MECP2cis-regulatory elements reveals genetic candidates for male-biased autism.

American journal of human genetics·2026

Combined Karyotyping, Copy Number Variation Sequencing, and Whole Exome Sequencing in the Prenatal Diagnosis of Congenital Heart Disease: Detection Rates and Phenotypic Associations.

Journal of clinical laboratory analysis·2026

Advancing genetic pathogenicity prediction with three-dimensional proteoform-phenotype analysis.

medRxiv : the preprint server for health sciences·2026

Genetic Spectrum and Family-Based Cascade Screening in Vietnamese Families With Autosomal Dominant Polycystic Kidney Disease.

Nephrology (Carlton, Vic.)·2026

Construction of an AI-Assisted Pedigree Mapping System for Hereditary Gynecological Tumors: Algorithm Development and Pilot Validation Study.

JMIR medical informatics·2026

Characteristics of predicated pathogenic missense variants in human genes for Mendelian disorders.

Frontiers in bioinformatics·2026

Identification and splicing assessment of a novel homozygous CFAP65 splice-site variant associated with oligozoospermia and complete asthenozoospermia.

BMC medical genomics·2026

Related Experiment Videos

Path analysis of family resemblance in the presence of gene-environment interaction

Related Concept Videos

Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.

A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction.

The effects of exercise on the lipoprotein subclass profile: A meta-analysis of 10 interventions.

Genomic and transcriptomic predictors of triglyceride response to regular exercise.

Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.

The genetic architecture of pentanucleotide repeat variation and disease association.

Accurate detection of sub-1% frequency somatic mutations by whole-genome sequencing.

De novo MAP2K4 variants cause a neurodevelopmental syndrome and impaired JNK signaling in iPSC-derived neurons.

Large-scale integration of functional assay data for the resolution of germline BRCA1 and BRCA2 variants of uncertain significance.

Loss of the human BRIP1 C terminus does not cause Fanconi anemia.

A massively parallel reporter assay of MECP2cis-regulatory elements reveals genetic candidates for male-biased autism.

Combined Karyotyping, Copy Number Variation Sequencing, and Whole Exome Sequencing in the Prenatal Diagnosis of Congenital Heart Disease: Detection Rates and Phenotypic Associations.

Advancing genetic pathogenicity prediction with three-dimensional proteoform-phenotype analysis.

Genetic Spectrum and Family-Based Cascade Screening in Vietnamese Families With Autosomal Dominant Polycystic Kidney Disease.

Construction of an AI-Assisted Pedigree Mapping System for Hereditary Gynecological Tumors: Algorithm Development and Pilot Validation Study.

Characteristics of predicated pathogenic missense variants in human genes for Mendelian disorders.

Identification and splicing assessment of a novel homozygous CFAP65 splice-site variant associated with oligozoospermia and complete asthenozoospermia.

Related Experiment Videos

Path analysis of family resemblance in the presence of gene-environment interaction

Related Concept Videos

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