Hyunglok Chung

基本信息

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职业迁徙

个人简介

Neuroscience and Human genetics Research focus: Functional genomics using Drosophila

研究兴趣

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Exploiting Fly Models to Investigate Rare Human Neurological Disorders

Tomomi Tanaka,Hyung-Lok Chung

Neural Regeneration Researchno. 1 (2025)

引用0浏览0WOS引用

Genetic Analysis of the X-linked Adrenoleukodystrophy ABCD1 Gene in Drosophila Uncovers a Role in Peroxisomal Dynamics

Joshua Manor,Sharayu V Jangam,Hyung-Lok Chung,Pranjali Bhagwat,Jonathan Andrews, Hillary Chester,Shu Kondo, Saurabh Srivastav,Juan Botas,Ann B Moser, Suzette M Huguenin,Michael F Wangler

bioRxiv the preprint server for biology (2024)

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Cdk8/CDK19 Promotes Mitochondrial Fission Through Drp1 Phosphorylation and Can Phenotypically Suppress Pink1 Deficiency in Drosophila

Jenny Zhe Liao,Hyung-lok Chung,Claire Shih,Kenneth Kin Lam Wong,Debdeep Dutta,Zelha Nil,Catherine Grace Burns,Oguz Kanca,Ye-Jin Park,Zhongyuan Zuo,Paul C. Marcogliese, Katherine Sew,Hugo J. Bellen,Esther M. Verheyen

NATURE COMMUNICATIONSno. 1 (2024)

引用0浏览0WOSNATURE引用

De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in Drosophila

Hyung-Lok Chung,Patrick Rump,Di Lu,Megan R Glassford,Jung-Wan Mok,Jawid Fatih,Adily Basal,Paul C Marcogliese,Oguz Kanca,Michele Rapp,Johanna M Fock,Erik-Jan Kamsteeg,James R Lupski,Austin Larson, Mark C Haninbal,Hugo Bellen,Tamar Harel

HUMAN MOLECULAR GENETICS（2022）

引用4浏览0WOS引用

Drosophila Functional Screening of De Novo Variants in Autism Uncovers Damaging Variants and Facilitates Discovery of Rare Neurodevelopmental Diseases

Paul C. Marcogliese,Samantha L. Deal,Jonathan Andrews,J. Michael Harnish,V. Hemanjani Bhavana,Hillary K. Graves,Sharayu Jangam,Xi Luo,Ning Liu,Danqing Bei,Yu-Hsin Chao,Brooke Hull,Pei-Tseng Lee,Hongling Pan,Pradnya Bhadane,Mei-Chu Huang,Colleen M. Longley,Hsiao-Tuan Chao,Hyung-lok Chung,Nele A. Haelterman,Oguz Kanca,Sathiya N. Manivannan,Linda Z. Rossetti,Ryan J. German,Amanda Gerard,Eva Maria Christina Schwaibold,Sarah Fehr,Renzo Guerrini,Annalisa Vetro,Eleina England,Chaya N. Murali,Tahsin Stefan Barakat,Marieke F. van Dooren,Martina Wilke,Marjon van Slegtenhorst,Gaetan Lesca,Isabelle Sabatier,Nicolas Chatron,Catherine A. Brownstein,Jill A. Madden,Pankaj B. Agrawal,Boris Keren,Thomas Courtin,Laurence Perrin,Melanie Brugger,Timo Roser,Steffen Leiz,Frederic Tran Mau-Them,Julian Delanne,Elena Sukarova-Angelovska,Slavica Trajkova,Erik Rosenhahn,Vincent Strehlow,Konrad Platzer,Roberto Keller,Lisa Pavinato,Alfredo Brusco,Jill A. Rosenfeld,Ronit Marom,Michael F. Wangler,Shinya Yamamoto

Cell Reportsno. 11 (2022): 110517-110517

引用12浏览0WOS引用

The Fly Homolog of SUPT16H, a Gene Associated with Neurodevelopmental Disorders, is Required in a Cell-Autonomous Fashion for Cell Survival

Mengqi Ma,Xi Zhang,Yiming Zheng,Shenzhao Lu,Xueyang Pan,Xiao Mao,Hongling Pan,Hyung-lok Chung,Hua Wang,Hong Guo,Hugo J. Bellen

Human Molecular Genetics（2022）

引用4浏览0WOS引用

Loss-of-function Variants in TIAM1 Are Associated with Developmental Delay, Intellectual Disability, and Seizures

Shenzhao Lu,Rebecca Hernan,Paul C. Marcogliese, Yan Huang,Tracy S. Gertler,Meltem Akcaboy,Shiyong Liu,Hyung-lok Chung,Xueyang Pan,Xiaoqin Sun,Melahat Melek Oguz,Ulkuhan Oztoprak,Jeroen H. F. de Baaij, Jelena Ivanisevic,Erin McGinnis,Maria J. Guillen Sacoto,Wendy K. Chung,Hugo J. Bellen

The American Journal of Human Geneticsno. 4 (2022): 571-586

引用15浏览0WOS引用

Very-long-chain Fatty Acids Induce Glial-Derived Sphingosine-1-phosphate Synthesis, Secretion, and Neuroinflammation

Hyunglok Chung

SSRN Electronic Journal（2022）

引用6浏览0WOS引用

ABCD1 and X-linked adrenoleukodystrophy: A disease with a markedly variable phenotype showing conserved neurobiology in animal models

Joshua Manor,Hyunglok Chung,Pranjali K Bhagwat,Michael F Wangler

JOURNAL OF NEUROSCIENCE RESEARCH（2021）

引用6浏览0WOS引用

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论文共 25 篇作者统计合作学者相似作者