HLA haplotype sharing in IDDM affected sib pairs as a function of HLA DR genotype

Locus ordering based on crossover information in family haplotypes: application of a "minimum break" algorithm.

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Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1.

American journal of human genetics·2000

Systematic search for disease loci for complex genetic traits: a study based on simulated population data.

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Design of artificial neural network and its applications to the analysis of alcoholism data.

Genetic epidemiology·1999

Simulated data for a complex genetic trait (problem 2 for GAW11): how the model was developed, and why.

Genetic epidemiology·1999

Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophy.

American journal of human genetics·1998

HLA haplotype sharing and proband genotype in IDDM.

Genetic epidemiology. Supplement·1986

A log-linear model for binary pedigree data.

Genetic epidemiology. Supplement·1986

CRISPR/Cas9-Driven Fndc5 Knockout Reveals Augmented Mitochondrial Structural and Dynamic Alterations in Diabetic Nephropathy.

International journal of medical sciences·2026

Chromatin Remodeling Subunit ARID1A Negatively Regulates the Malignant Progression of Gastrointestinal Stromal Tumors by Targeting the MEMO1 Promoter.

International journal of medical sciences·2026

Excitation/Inhibition Balance as a Mechanistic Link Between Sleep Disturbance and Autism Spectrum Disorder: A Bidirectional Framework.

Alpha psychiatry·2026

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Alpha psychiatry·2026

A regulatory network underlying idiopathic pulmonary fibrosis.

Frontiers in immunology·2026

Peripheral γδ T-cell remodeling in psoriasis is associated with effector-biased transcriptional organization and reduced representation of a circulating CSMD1-marked state.

Frontiers in immunology·2026

Related Experiment Videos

HLA haplotype sharing in IDDM affected sib pairs as a function of HLA DR genotype

Related Concept Videos

Locus ordering based on crossover information in family haplotypes: application of a "minimum break" algorithm.

Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1.

Systematic search for disease loci for complex genetic traits: a study based on simulated population data.

Design of artificial neural network and its applications to the analysis of alcoholism data.

Simulated data for a complex genetic trait (problem 2 for GAW11): how the model was developed, and why.

Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophy.

HLA haplotype sharing and proband genotype in IDDM.

A log-linear model for binary pedigree data.

CRISPR/Cas9-Driven Fndc5 Knockout Reveals Augmented Mitochondrial Structural and Dynamic Alterations in Diabetic Nephropathy.

Chromatin Remodeling Subunit ARID1A Negatively Regulates the Malignant Progression of Gastrointestinal Stromal Tumors by Targeting the MEMO1 Promoter.

Excitation/Inhibition Balance as a Mechanistic Link Between Sleep Disturbance and Autism Spectrum Disorder: A Bidirectional Framework.

Metabolic-Brain Functional Coupling Mechanism Underlying iTBS Treatment for Adolescent Depression.

A regulatory network underlying idiopathic pulmonary fibrosis.

Peripheral γδ T-cell remodeling in psoriasis is associated with effector-biased transcriptional organization and reduced representation of a circulating CSMD1-marked state.

Related Experiment Videos

HLA haplotype sharing in IDDM affected sib pairs as a function of HLA DR genotype

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