People / Lim

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BYUNG CHAN LIM

Visiting Associate Professor
Pediatric Neurology

139 Irvine Hall
Lab Phone: 949-824-3463
SNU profile | ResearchGate


EDUCATION

MD, Seoul National University

RESEARCH

I am joining the Hunt lab as a visiting Associate Professor from Seoul National University. While I am at UCI, I will use patient-derived stem cells to study brain development in epilepsy.

PUBLICATIONS

ARS2 mutation and epilepsy: Possible link with early-onset epileptic encephalopathy
Cho JS, Kim SH, Kim HY, Chung T, Kim D, Jang S, Lee SB, Yoo SK, Shin J, Kim JI, Kim H, Hwang H, Chae JH, Choi J, Kim KJ, Lim BC
Epilepsy Research (2017)

Noninvasive prenatal diagnosis of duchenne muscular dystrophy: comprehensive genetic diagnosis in carrier, proband, and fetus
Yoo SK, Lim BC, Byeun J, Hwang H, Kim KJ, Hwang YS, Lee J, Park JS, Lee YS, Namkung J, Park J, Lee S, Shin JY, Seo JS, Kim JI, Chae JH
Clinical Chemistry (2015)

Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
Lim BC, Hwang H, Kim H, Chae JH, Choi J, Kim KJ, Hwang YS, Yum MS, Ko TS
Epilepsy Research (2015)

Aquaporin-4 autoimmunity masquerading as a brainstem tumor
Lim BC, Chae JH, Kim SK, Park SH, Wang KC, Lee JY, Phi JH
Journal of Neurosurgery: Pediatrics (2014)

Hoyeraal-Hreidarsson syndrome with a DKC1 mutation identified by whole-exome sequencing
Lim BC, Yoo SK, Lee S, Shin JY, Hwang H, Chae JH, Hwang YS, Seo JS, Kim JI, Kim KJ
Gene (2014)

Clinical and biochemical features guiding the diagnostics in neurometabolic cutis laxa
Gardeitchik T, Mohamed M, Fischer B, Lammens M, Lefeber D, Lace B, Parker M, Kim KJ, Lim BC, Häberle J, Garavelli L, Jagadeesh S, Kariminejad A, Guerra D, Leão M, Keski-Filppula R, Brunner H, Nijtmans L, van den Heuvel B, Wevers R, Kornak U, Morava E.
European Journal of Human Genetics (2014)

A unique phenotype of 2q24.3-2q32.1 duplication: early infantile epileptic encephalopathy without mesomelic dysplasia
Lim BC, Min BJ, Park WY, Oh SK, Woo MJ, Choi JS, Kim KJ, Hwang YS, Chae JH.
Journal of Child Neurology (2014)

Molecular diagnosis of congenital muscular dystrophies with defective glycosylation of alpha-dystroglycan using next-generation sequencing technology
Lim BC, Lee S, Shin JY, Hwang H, Kim KJ, Hwang YS, Seo JS, Kim JI, Chae JH
Neuromuscular Disorders (2013)

Pantothenate kinase-associated neurodegeneration in Korea: recurrent R440P mutation in PANK2 and outcome of deep brain stimulation
Lim BC, Ki CS, Cho A, Hwang H, Kim KJ, Hwang YS, Kim YE, Yun JY, Jeon BS, Lim YH, Paek SH, Chae JH
European Journal of Neurology (2012)

Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform
Lim BC, Lee S, Shin JY, Kim JI, Hwang H, Kim KJ, Hwang YS, Seo JS, Chae JH
Journal of Medical Genetics (2011)

SCN1A mutational analysis in Korean patients with Dravet syndrome
Lim BC, Hwang H, Chae JH, Choi JE, Hwang YS, Kang SH, Ki CS, Kim KJ
Seizure (2011)

Relapsing demyelinating CNS disease in a Korean pediatric population: multiple sclerosis versus neuromyelitis optica
Lim BC, Hwang H, Kim KJ, Hwang YS, Cheon JE, Kim IO, Kim HJ, Chae JH
Multiple Sclerosis (2011)

De novo interstitial deletion of 3q22.3-q25.2 encompassing FOXL2, ATR, ZIC1, and ZIC4 in a patient with blepharophimosis/ptosis/epicanthus inversus syndrome, Dandy-Walker malformation, and global developmental delay
Lim BC, Park WY, Seo EJ, Kim KJ, Hwang YS, Chae JH
Journal of Child Neurology (2011)

De novo interstitial deletion of 3q22.3-q25.2 encompassing FOXL2, ATR, ZIC1, and ZIC4 in a patient with blepharophimosis/ptosis/epicanthus inversus syndrome, Dandy-Walker malformation, and global developmental delay
Lim BC, Park WY, Seo EJ, Kim KJ, Hwang YS, Chae JH
Journal of Child Neurology (2011)

Andersen cardiodysrhythmic periodic paralysis with KCNJ2 mutations: a novel mutation in the pore selectivity filter residue
Lim BC, Kim GB, Bae EJ, Noh CI, Hwang H, Kim KJ, Hwang YS, Ko TS, Chae JH
Journal of Child Neurology (2010)

Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism
Kim SH, Hwang H, Chae JH, Kim KJ, Hwang YS, Lim BC
Journal of Child Neurology (2010)

Mutations in ND subunits of complex I are an important genetic cause of childhood mitochondrial encephalopathies
Lim BC, Park JD, Hwang H, Kim KJ, Hwang YS, Chae JH, Cheon JE, Kim IO, Lee R, Moon HK
Journal of Child Neurology (2009)