Hae-mi Woo

Cheongju-si, Republic of Korea

Last Updated: 09/26/2026

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Found 8 publications

Genetic analysis of parathyroid and pancreatic tumors in a patient with multiple endocrine neoplasia type 1 using whole-exome sequencing.

Genetic analysis of parathyroid and pancreatic tumors in a patient with multiple endocrine neoplasia type 1 using whole-exome sequencing.

Journal: BMC medical genetics

Published: December 28, 2016

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.

Journal: BMC medical genetics

Published: December 23, 2013

Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy.

Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy.

Journal: Neurogenetics

Published: December 19, 2013

Patterns of gene expression associated with Pten deficiency in the developing inner ear.

Patterns of gene expression associated with Pten deficiency in the developing inner ear.

Journal: PloS one

Published: September 27, 2013

Comprehensive analysis to improve the validation rate for single nucleotide variants detected by next-generation sequencing.

Comprehensive analysis to improve the validation rate for single nucleotide variants detected by next-generation sequencing.

Journal: PloS one

Published: September 06, 2013

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.

Journal: BMC medical genetics

Published: January 08, 2013

Conditional deletion of pten leads to defects in nerve innervation and neuronal survival in inner ear development.

Conditional deletion of pten leads to defects in nerve innervation and neuronal survival in inner ear development.

Journal: PloS one

Published: April 23, 2012

Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth disease.

Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth disease.

Journal: Human mutation

Published: December 07, 2011

Showing 1-8 of 8

Last Updated: 09/26/2026