Byung Chan Lim

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 12

Top Topics

Intellectual Disability

Autism Spectrum Disorder

Patient Reported Outcomes

Top Venues

American journal of medical genetics. Part A

Yonsei medical journal

Annals of laboratory medicine

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

Publications

Hye Jin Kim, Minhye Kim, Seoyun Jang, Jae So Cho, Soo Yeon Kim, Anna Cho, Hunmin Kim, Byung Chan Lim, Jong-Hee Chae, Jieun Choi, Ki Joong Kim, WooJoong Kim
SYNGAP1-related developmental and epileptic encephalopathy: Genotypic and phenotypic characteristics and longitudinal insights. American journal of medical genetics. Part A 194 (8) (2024)
Hye Jin Kim, Minhye Kim, Seoyun Jang, Jae So Cho, Soo Yeon Kim, Anna Cho, Hunmin Kim, Byung Chan Lim, Jong-Hee Chae, Jieun Choi, Ki Joong Kim, WooJoong Kim
SYNGAP1-related developmental and epileptic encephalopathy: Genotypic and phenotypic characteristics and longitudinal insights. American journal of medical genetics. Part A 194 (8) (2024)
Seungbok Lee, Mi-Kyoung Kang, Ki Hurn So, Riyul Jang, Yong Woo Shin, Se Song Jang, Jihoon G Yoon, Sheehyun Kim, Manjin Kim, Kon Chu, Sang Kun Lee, Ki Joong Kim, Seung Tae Baek, Byung Chan Lim, Jangsup Moon
Broadening the scope of multigene panel analysis for adult epilepsy patients. Epilepsia open 9 (4) (2024)
Seungbok Lee, Mi-Kyoung Kang, Ki Hurn So, Riyul Jang, Yong Woo Shin, Se Song Jang, Jihoon G Yoon, Sheehyun Kim, Manjin Kim, Kon Chu, Sang Kun Lee, Ki Joong Kim, Seung Tae Baek, Byung Chan Lim, Jangsup Moon
Broadening the scope of multigene panel analysis for adult epilepsy patients. Epilepsia open 9 (4) (2024)
Hye Jin Kim, Minhye Kim, Seoyun Jang, Jae So Cho, Soo Yeon Kim, Anna Cho, Hunmin Kim, Byung Chan Lim, Jong-Hee Chae, Jieun Choi, Ki Joong Kim, WooJoong Kim
SYNGAP1-related developmental and epileptic encephalopathy: Genotypic and phenotypic characteristics and longitudinal insights. American journal of medical genetics. Part A (2024)
Seungbok Lee, Mi-Kyoung Kang, Ki Hurn So, Riyul Jang, Yong Woo Shin, Se Song Jang, Jihoon G Yoon, Sheehyun Kim, Manjin Kim, Kon Chu, Sang Kun Lee, Ki Joong Kim, Seung Tae Baek, Byung Chan Lim, Jangsup Moon
Broadening the scope of multigene panel analysis for adult epilepsy patients. Epilepsia open 9 (4) (2024)
Hye Jin Kim, Minhye Kim, Seoyun Jang, Jae So Cho, Soo Yeon Kim, Anna Cho, Hunmin Kim, Byung Chan Lim, Jong-Hee Chae, Jieun Choi, Ki Joong Kim, WooJoong Kim
SYNGAP1-related developmental and epileptic encephalopathy: Genotypic and phenotypic characteristics and longitudinal insights. American journal of medical genetics. Part A 194 (8) (2024)
Seungbok Lee, Mi-Kyoung Kang, Ki Hurn So, Riyul Jang, Yong Woo Shin, Se Song Jang, Jihoon G Yoon, Sheehyun Kim, Manjin Kim, Kon Chu, Sang Kun Lee, Ki Joong Kim, Seung Tae Baek, Byung Chan Lim, Jangsup Moon
Broadening the scope of multigene panel analysis for adult epilepsy patients. Epilepsia open (2024)
Yeji Moon, Kyung-Ah Park, Jinu Han, Jeong-Min Hwang, Seong Joon Kim, Sueng-Han Han, Byung Joo Lee, Min Chae Kang, Yong Hyu Goh, Byung Chan Lim, Hee Kyung Yang, Jae Ho Jung
Risk of central nervous system demyelinating attack or optic neuritis recurrence after pediatric optic neuritis in Korea. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)
Dayun Kang, Soo Yeon Kim, Jong Hee Chae, Ki Joong Kim, Sung-Hye Park, Byung Chan Lim
Angiography-negative childhood primary angiitis of the central nervous system diagnosed by open brain biopsy: a case report. Encephalitis (Seoul, Korea) 2 (1) (2021)
Hyuna Kim, Jin Sook Lee, Youngha Lee, Soo Yeon Kim, Byung Chan Lim, Ki Joong Kim, Murim Choi, Jong-Hee Chae
Diagnostic Challenges Associated with GLUT1 Deficiency: Phenotypic Variabilities and Evolving Clinical Features. Yonsei medical journal 60 (12) (2020)
Jin Sook Lee, Hee Hwang, Soo Yeon Kim, Ki Joong Kim, Jin Sun Choi, Mi Jung Woo, Young Min Choi, Jong Kwan Jun, Byung Chan Lim, Jong Hee Chae
Chromosomal Microarray With Clinical Diagnostic Utility in Children With Developmental Delay or Intellectual Disability. Annals of laboratory medicine 38 (5) (2018)