Cha Gon Lee

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 8

Top Topics

Intellectual Disability

Dna Methylation

Middle Cerebral Artery

Top Venues

Neurology. Genetics

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Cha Gon Lee, Hyun Jung Kim, Chang Ahn Seol, Chang-Seok Ki
Novel In-Frame Deletion CNOT3 Variant in a Family With Intellectual Developmental Disorder With Speech Delay and Dysmorphic Facies. Neurology. Genetics 10 (1) (2024)
Cha Gon Lee, Hyun Jung Kim, Chang Ahn Seol, Chang-Seok Ki
Novel In-Frame Deletion CNOT3 Variant in a Family With Intellectual Developmental Disorder With Speech Delay and Dysmorphic Facies. Neurology. Genetics 10 (1) (2024)
Woong-Woo Lee, Cha Gon Lee, Chang-Seok Ki
KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (2024)
Kyusik Kang, Cha Gon Lee, Byung-Kun Kim
Intracranial Vessel Wall Magnetic Resonance Imaging of Middle Cerebral Artery Dissection in Neurofibromatosis Type 1. Stroke (2023)
Cha Gon Lee, Change Seok Ki
A Novel De Novo Heterozygous ARID1A Missense Variant Cluster in cis c.[5954C>G;6314C>T;6334C>T;6843G>C] causes a Coffin-Siris Syndrome. Annals of laboratory medicine 41 (3) (2021)
Cha Gon Lee, Chang Ahn Seol, Chang-Seok Ki
The first familial case of inherited intellectual developmental disorder with dysmorphic facies and behavioral abnormalities (IDDFBA) with a novel FBXO11 variant. American journal of medical genetics. Part A 182 (11) (2020)
Cha Gon Lee, Jeehun Lee, Munhyang Lee
Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes. PloS one 13 (6) (2018)
Hyun-Seok Jin, Jeonhyun Kim, Woori Kwak, Hyeonsoo Jeong, Gyu-Bin Lim, Cha Gon Lee
Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies. PloS one 12 (1) (2017)