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Publications by Cheol Woo Ko

Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing

Hormone Research in Paediatrics

English

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Identification of CDH23 Mutations in Korean Families With Hearing Loss by Whole-Exome Sequencing

BMC Medical Genetics

English

Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

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Whole Exome Sequencing in Extended Families With Autism Spectrum Disorder Implicates Four Candidate Genes

English

A Semi-Automated Whole Exome Sequencing Workflow Leads to Increased Diagnostic Yield and Identification of Novel Candidate Variants

Cold Spring Harbor molecular case studies

Molecular Medicine

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TCOF1 Pathogenic Variants Identified by Whole-Exome Sequencing in Chinese Treacher Collins Syndrome Families and Hearing Rehabilitation Effect

Orphanet Journal of Rare Diseases

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Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease

Arthritis and Rheumatology

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Whole Exome Sequencing for the Identification of CYP3A7 Variants Associated With Tacrolimus Concentrations in Kidney Transplant Patients

Scientific Reports

Multidisciplinary

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A Stroke Gene Panel for Whole-Exome Sequencing

European Journal of Human Genetics

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Whole-Exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer's Disease

Annals of Clinical and Translational Neurology

English