Hae-Mi Woo - Concepedia

Author

Hae-Mi Woo

Korea National Institute of Health

Also Known As

H.-M. Woo, H.‐M. Woo, Hae-Mi Woo

Publications

178

Citations

H-Index

Concepts

All Affiliations

Korea National Institute of Health Kongju National University Sungkyunkwan University Samsung Medical Center Ewha Womans University

About

Hae-Mi Woo is an author at Korea National Institute of Health specializing in medicine, genetics, and cell signaling.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	72
2	Cell Biology	2	2	30
3	Neurology	2	2	42
4	Arts	1	1	15
5	Social Sciences	1	1	15

Hae-Mi Woo

Publications

178

Citations

H-Index

Page 1

	Year	Citations
Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families Hae-Mi Woo, Hong-Joon Park, Jeong‐In Baek, BMC Medical Genetics	2013	39
Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing Hae-Mi Woo, Hong-Joon Park, Mi‐Hyun Park, BMC Medical Genetics	2014	32
Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2 B. O. Choi, M.‐H. Park, Ki Wha Chung, Neurogenetics Novel S90w MutationMendelian DisorderGenetic DisorderGeneticsPathology	2012	28
Comprehensive Analysis to Improve the Validation Rate for Single Nucleotide Variants Detected by Next-Generation Sequencing Mi‐Hyun Park, Hwanseok Rhee, Jung Hoon Park, PLoS ONE	2014	22
Conditional Deletion of Pten Leads to Defects in Nerve Innervation and Neuronal Survival in Inner Ear Development Hyung Jin Kim, Hae-Mi Woo, Jihee Ryu, PLoS ONE Organ DevelopmentPten DeficiencySynaptic SignalingPten LeadsSocial Sciences	2013	15
Patterns of Gene Expression Associated with Pten Deficiency in the Developing Inner Ear Hyung Jin Kim, Jihee Ryu, Hae-Mi Woo, PLoS ONE GeneticsGene Expression AssociatedPten DeficiencyCellular NeurobiologyDeveloping Inner Ear	2014	15
Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy Mihyun Park, Hae-Mi Woo, Young Bin Hong, Neurogenetics GeneticsMotor DevelopmentDisease Gene IdentificationSensorimotor PolyneuropathyMitochondrial Myopathy	2014	14
Application of whole‐exome sequencing for detecting copy number variants in CMT1A/HNPP Hyun Youn Jo, M.‐H. Park, Hae-Mi Woo, Clinical Genetics	2015	13

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