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Hon-Chung Fung

Research Profile

Disorders

Genes & Molecular Sequences

Physiology

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Chemicals & Drugs

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Taiwan

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Hsiao-Lung Chan; Pei-Kuang Chao; Ju-His Chu; Hon-Chung Fung; Wen-Chun Hsu; Chin-Chang Huang; Jiann-Der Lee; Ling-Fu Meng; Yu-Tai Tsai; Yau-Yau Wai; Jiun-Jie Wang; Meng-Tsan Tsai
Brain connectivity of patients with Alzheimer's disease by coherence and cross mutual information of electroencephalograms during photic stimulation.
Hsiang-Yao Hsieh; Chao-Jan Wang; Shy-Chyi Chin; Hon-Chung Fung; Tony Wu
Epileptic seizures in neurofibromatosis type 1 are related to intracranial tumors but not to neurofibromatosis bright objects.
Yih-Ru Wu; Chiung-Mei Chen; Yi-Chun Chen; Chih-Ying Chao; Long-Sun Ro; Hon-Chung Fung; Ya-Chin Hsiao; Fen-Ju Hu; Guey-Jen Lee-Chen
Ubiquitin specific proteases USP24 and USP40 and ubiquitin thiolesterase UCHL1 polymorphisms have synergic effect on the risk of Parkinson's disease among Taiwanese.

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All Publications

2013: Hsiao-Lung Chan; Pei-Kuang Chao; Ju-His Chu; Hon-Chung Fung; Wen-Chun Hsu; Chin-Chang Huang; Jiann-Der Lee; Ling-Fu Meng; Yu-Tai Tsai; Yau-Yau Wai; Jiun-Jie Wang; Meng-Tsan Tsai
Brain connectivity of patients with Alzheimer's disease by coherence and cross mutual information of electroencephalograms during photic stimulation.
Medical engineering & physics 2013;35(2):241-52.
2011: Hsiang-Yao Hsieh; Chao-Jan Wang; Shy-Chyi Chin; Hon-Chung Fung; Tony Wu
Epileptic seizures in neurofibromatosis type 1 are related to intracranial tumors but not to neurofibromatosis bright objects.
Seizure : the journal of the British Epilepsy Association 2011;20(8):606-11.
2010: Yih-Ru Wu; Chiung-Mei Chen; Yi-Chun Chen; Chih-Ying Chao; Long-Sun Ro; Hon-Chung Fung; Ya-Chin Hsiao; Fen-Ju Hu; Guey-Jen Lee-Chen
Ubiquitin specific proteases USP24 and USP40 and ubiquitin thiolesterase UCHL1 polymorphisms have synergic effect on the risk of Parkinson's disease among Taiwanese.
Clinica chimica acta; international journal of clinical chemistry 2010;411(13-14):955-8.
2010: Chiung-Mei Chen; Li-Ching Lee; Bing-Wen Soong; Hon-Chung Fung; Wen-Chuin Hsu; Pei-Ying Lin; Hui-Ju Huang; Fen-Lin Chen; Cheng-Yueh Lin; Guey-Jen Lee-Chen; Yih-Ru Wu
SCA17 repeat expansion: mildly expanded CAG/CAA repeat alleles in neurological disorders and the functional implications.
Clinica chimica acta; international journal of clinical chemistry 2010;411(5-6):375-80.
2009: Yih-Ru Wu; I-Cheng Chen; Bing-Wen Soong; Shih-Huan Kao; Ghin-Chueh Lee; Shu-Yi Huang; Hon-Chung Fung; Guey-Jen Lee-Chen; Chiung-Mei Chen
SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications.
Human genetics 2009;125(4):437-44.
2009: Chiung-Mei Chen; Yi-Ting Hou; Ju-Yun Liu; Yih-Ru Wu; Chih-Hsin Lin; Hon-Chung Fung; Wen-Chuin Hsu; Yuying Hsu; Shen-Hung Lee; Hsiu Mei Hsieh-Li; Ming-Tsan Su; Shui-Tein Chen; Hsien-Yuan Lane; Guey-Jen Lee-Chen
PPP2R2B CAG repeat length in the Han Chinese in Taiwan: Association analyses in neurological and psychiatric disorders and potential functional implications.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(1):124-9.
2008: Wen-Chuin Hsu; Hsiu-Kuan Wang; Li-Ching Lee; Hon-Chung Fung; Jun-Cheng Lin; H-P Hsu; Yih-Ru Wu; Long-Sun Ro; Fen-Ju Hu; Y-T Chang; Guey-Jen Lee-Chen; Chiung-Mei Chen
Promoter polymorphisms modulating HSPA5 expression may increase susceptibility to Taiwanese Alzheimer's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2008;115(11):1537-43.
2008: Michael C Zody; Zhaoshi Jiang; Hon-Chung Fung; Francesca Antonacci; LaDeana W Hillier; Maria Francesca Cardone; Tina A Graves; Jeffrey M Kidd; Ze Cheng; Amr Abouelleil; Lin Chen; John Wallis; Jarret Glasscock; Richard K Wilson; Amy Denise Reily; Jaime Duckworth; ventura Mario; John Hardy; Wesley C Warren; Evan E Eichler
Evolutionary toggling of the MAPT 17q21.31 inversion region.
Nature genetics 2008;40(9):1076-83.
2008: Usha Gutti; Hon-Chung Fung; Kathleen S Hruska; Mary E Lamarca; Chiung-Mei Chen; Yih-Ru Wu; Ellen Sidransky
The need for appropriate genotyping strategies for glucocerebrosidase mutations in cohorts with Parkinson disease.
Archives of neurology 2008;65(6):850-1; author reply 851.
2008: Mar Matarin; Javier Simon-Sanchez; Hon-Chung Fung; Sonja Scholz; J Raphael Gibbs; Dena G Hernandez; Cynthia Crews; Angela Britton; Fabienne Wavrant De Vrieze; Thomas G Brott; Robert D Brown; Bradford Worrall; Scott Silliman; L Douglas Case; John Hardy; Stephen S Rich; James F Meschia; Andrew Singleton
Structural genomic variation in ischemic stroke.
Neurogenetics 2008;9(2):101-8.
2008: Mattias Jakobsson; Sonja W Scholz; Paul Scheet; J Raphael Gibbs; Jenna M VanLiere; Hon-Chung Fung; Zachary A Szpiech; James H Degnan; Kai Wang; Rita Guerreiro; Jose M Bras; Jennifer C Schymick; Dena G Hernandez; Bryan Joseph Traynor; Javier Simon-Sanchez; Mar Matarin; Angela Britton; Joyce van de Leemput; Ian Rafferty; Maja Bucan; Howard M Cann; John Hardy; Noah A Rosenberg; Andrew Singleton
Genotype, haplotype and copy-number variation in worldwide human populations.
Nature 2008;451(7181):998-1003.
2008: Javier Simon-Sanchez; Sonja Scholz; Maria del Mar Matarin; Hon-Chung Fung; Dena Hernandez; J Raphael Gibbs; Angela Britton; John Hardy; Andrew Singleton
Genomewide SNP assay reveals mutations underlying Parkinson disease.
Human mutation 2008;29(2):315-22.
2007: Joyce van de Leemput; Jayanth Chandran; Melanie A Knight; Lynne A Holtzclaw; Sonja Scholz; Mark Cookson; Henry Houlden; Katrina Gwinn-Hardy; Hon-Chung Fung; Xian Lin; Dena Hernandez; Javier Simon-Sanchez; Nicholas W Wood; Paola Giunti; Ian Rafferty; John Hardy; Elsdon Storey; R J McKinlay Gardner; Susan M Forrest; Elizabeth M C Fisher; James T Russell; Huaibin Cai; Andrew Singleton
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.
PLoS genetics 2007;3(6):e108.
2007: Mar Matarín; W Mark Brown; Sonja Scholz; Javier Simón-Sánchez; Hon-Chung Fung; Dena Hernandez; J Raphael Gibbs; Fabienne Wavrant De Vrieze; Cynthia Crews; Angela Britton; Carl D Langefeld; Thomas G Brott; Robert D Brown; Bradford Worrall; Michael R Frankel; Scott L Silliman; L Douglas Case; Andrew Singleton; John Hardy; Stephen S Rich; James F Meschia
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.
Lancet neurology 2007;6(5):414-20.
2007: Jennifer C Schymick; Sonja Scholz; Hon-Chung Fung; Angela Britton; Sampath Arepalli; J Raphael Gibbs; Federica Lombardo; Mar Matarin; Dalia Kasperaviciute; Dena G Hernandez; Cynthia Crews; Lucie Bruijn; Jeffrey rothstein; Gabriele Mora; Gabriella Restagno; Adriano Chio; Andrew Singleton; John Hardy; Bryan Joseph Traynor
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.
Lancet neurology 2007;6(4):322-8.
2007: Jun-Cheng Lin; Wen-Chuin Hsu; Hai-Pei Hsu; Hon-Chung Fung; Sien-Tsong Chen
Risk factors for vascular dementia: a hospital-based study in Taiwan.
Acta neurologica Taiwanica 2007;16(1):22-6.
2007: Hsiu-Kuan Wang; Wen-Chuin Hsu; Hon-Chung Fung; Jun-Cheng Lin; Hai-Pei Hsu; Yih-Ru Wu; Yuying Hsu; Fen-Ju Hu; Guey-Jen Lee-Chen; Chiung-Mei Chen
Interleukin-1alpha and -1beta promoter polymorphisms in Taiwanese patients with dementia.
Dementia and geriatric cognitive disorders 2007;24(2):104-10.
2007: Javier Simon-Sanchez; Sonja Scholz; Hon-Chung Fung; Mar Matarin; Dena Hernandez; J Raphael Gibbs; Angela Britton; Fabienne Wavrant De Vrieze; Elizabeth Peckham; Katrina Gwinn-Hardy; Anthony Crawley; Judith C Keen; Josefina Nash; Digamber Borgaonkar; John Hardy; Andrew Singleton
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals.
Human molecular genetics 2007;16(1):1-14.
2006: Hon-Chung Fung; Sonja Scholz; Mar Matarin; Javier Simón-Sánchez; Dena Hernandez; Angela Britton; J Raphael Gibbs; Carl Langefeld; Matt L Stiegert; Jennifer C Schymick; Michael S Okun; Ronald J Mandel; Hubert H Fernandez; Kelly D Foote; Ramón L Rodríguez; Elizabeth Peckham; Fabienne Wavrant De Vrieze; Katrina Gwinn-Hardy; John Hardy; Andrew Singleton
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
Lancet neurology 2006;5(11):911-6.
2006: Alan Pittman; Hon-Chung Fung; Rohan de Silva
Untangling the tau gene association with neurodegenerative disorders.
Human molecular genetics 2006;15 Spec No 2():R188-95.
2006: Hsiu-Kuan Wang; Hon-Chung Fung; Wen-Chuin Hsu; Yih-Ru Wu; Jun-Cheng Lin; Long-Sun Ro; Kuo-Hsuan Chang; F J Hwu; Yuying Hsu; S Y Huang; Guey-Jen Lee-Chen; Chiung-Mei Chen
Apolipoprotein E, angiotensin-converting enzyme and kallikrein gene polymorphisms and the risk of Alzheimer's disease and vascular dementia.
Journal of neural transmission (Vienna, Austria : 1996) 2006;113(10):1499-509.
2006: Jordi Clarimon; Sonja Scholz; Hon-Chung Fung; John Hardy; Johanna Eerola; Olli Hellstrom; Chiung-Mei Chen; Yih-Ru Wu; Pentti J Tienari; Andrew Singleton
Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease.
American journal of human genetics 2006;78(6):1082-4; author reply 1092-4.
2006: Hon-Chung Fung; Chiung-Mei Chen; John Hardy; Dena Hernandez; Andrew Singleton; Yih-Ru Wu
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2006;21(6):880-1.
2006: Sonja Scholz; Georgia Xiromerisiou; Hon-Chung Fung; Johanna Eerola; Olli Hellström; Alexandros Papadimitriou; Georgios M Hadjigeorgiou; Pentti J Tienari; Hubert H Fernandez; Ronald Mandel; Michael S Okun; Katrina Gwinn-Hardy; Andrew Singleton
The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations.
Neuroscience letters 2006;395(3):227-9.
2006: Hon-Chung Fung; Chiung-Mei Chen; John Hardy; Andrew Singleton; Guey-Jen Lee-Chen; Yih-Ru Wu
Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan.
Neuroscience letters 2006;394(1):33-6.
2006: Hon-Chung Fung; Georgia Xiromerisiou; J Raphael Gibbs; Y R Wu; Johanna Eerola; Vanessa Gourbali; Olli Hellström; C M Chen; Jaime Duckworth; Alexandros Papadimitriou; Pentti J Tienari; Georgios M Hadjigeorgiou; John Hardy; Andrew Singleton
Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohorts.
Neuro-degenerative diseases 2006;3(6):327-33.
2006: Hon-Chung Fung; Chiung-Mei Chen; John Hardy; Andrew Singleton; Yih-Ru Wu
A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan.
BMC neurology 2006;6():47.
2006: Parastoo Momeni; Jennifer C Schymick; Shushant Jain; Mark Cookson; Nigel J Cairns; Elisa Greggio; Matthew J Greenway; Stephen Berger; Stuart Pickering-Brown; Adriano Chio; Hon-Chung Fung; David M Holtzman; Edward D Huey; Eric M Wassermann; Jennifer Adamson; Michael Hutton; Ekaterina Rogaeva; Peter St George-Hyslop; Jeffrey rothstein; Orla Hardiman; Jordan Grafman; Andrew Singleton; John Hardy; Bryan Joseph Traynor
Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD.
BMC neurology 2006;6():44.
2006: John Hardy; Alan Pittman; Amanda Myers; Hon-Chung Fung; Rohan de Silva; Jaime Duckworth
Tangle diseases and the tau haplotypes.
Alzheimer disease and associated disorders 2006;20(1):60-2.
2005: Alan Pittman; Amanda Myers; Patrick M Abou-Sleiman; Hon-Chung Fung; Mona Kaleem; Lauren Marlowe; Jaime Duckworth; Doris Leung; D Williams; Linda Kilford; N Thomas; Christopher M Morris; dennis dickson; Nicholas W Wood; John Hardy; Andrew J Lees; Rohan de Silva
Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration.
Journal of medical genetics 2005;42(11):837-46.
2005: Amanda Myers; Mona Kaleem; Lauren Marlowe; Alan Pittman; Andrew J Lees; Hon-Chung Fung; Jaime Duckworth; Doris Leung; A Gibson; Christopher M Morris; Rohan de Silva; John Hardy
The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.
Human molecular genetics 2005;14(16):2399-404.
2005: John Hardy; Alan Pittman; Amanda Myers; Katrina Gwinn-Hardy; Hon-Chung Fung; Rohan de Silva; Michael Hutton; Jaime Duckworth
Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens.
Biochemical Society transactions 2005;33(Pt 4):582-5.
2005: Yih-Ru Wu; Hon-Chung Fung; Guey-Jen Lee-Chen; Katrina Gwinn-Hardy; Long-Sun Ro; Sien-Tsong Chen; Hsiu Mei Hsieh-Li; Hsuan-Yuan Lin; Cheng-Yueh Lin; S N Li; Chiung-Mei Chen
Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseases.
Journal of neural transmission (Vienna, Austria : 1996) 2005;112(4):539-46.
2005: Hon-Chung Fung; Jessica Evans; Whitney Evans; Jaime Duckworth; Alan Pittman; Rohan de Silva; Amanda Myers; John Hardy
The architecture of the tau haplotype block in different ethnicities.
Neuroscience letters 2005;377(2):81-4.
2005: Hon-Chung Fung; Chiung-Mei Chen; Yih-Ru Wu; Wen-Chuin Hsu; Long-Sun Ro; Jun-Cheng Lin; Kuo-Hsuan Chang; Hsiu-Kuan Wang; S J Lin; H Chan; Y Y Lin; S L Wei; Yuying Hsu; Ji-Chuu Hwang; Li-Chu Tung; Guey-Jen Lee-Chen
Heat shock protein 70 and tumor necrosis factor alpha in Taiwanese patients with dementia.
Dementia and geriatric cognitive disorders 2005;20(1):1-7.
2004: Whitney Evans; Hon-Chung Fung; John Steele; Johanna Eerola; Pentti J Tienari; Alan Pittman; Rohan de Silva; Amanda Myers; Fabienne Wavrant-De Vrieze; Andrew Singleton; John Hardy
The tau H2 haplotype is almost exclusively Caucasian in origin.
Neuroscience letters 2004;369(3):183-5.
2004: Yih-Ru Wu; Cheng-Kuang Wang; Chiung-Mei Chen; Yuying Hsu; Sih-Jing Lin; Yi-Ying Lin; Hon-Chung Fung; Kuo-Hsuan Chang; Guey-Jen Lee-Chen
Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson's disease.
Human genetics 2004;114(3):236-41.
2002: Hon-Chung Fung; Sien-Tsong Chen; Lok-Ming Tang; Long-Sun Ro
Triparesis: MRI documentation of bipyramidal medullary infarction.
Neurology 2002;58(7):1130-1.