Marcus C.Y. Chan - Department of Paediatrics and Adolescent Medicine, University of Hong Kong

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论文共 12 篇作者统计合作学者相似作者

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Socio-economic Costs of Rare Diseases and the Risk of Financial Hardship: a Cross-Sectional Study

Claudia C. Y. Chung,Nicole Y. T. Ng,Yvette N. C. Ng,Adrian C. Y. Lui,Jasmine L. F. Fung,Marcus C. Y. Chan,Wilfred H. S. Wong,So Lun Lee,Martin Knapp,Brian H. Y. Chung

LANCET REGIONAL HEALTH-WESTERN PACIFIC (2023)

引用9浏览0WOS引用

Standardised tool for measurement of rare genetic disease costs: development, contextualisation, translation, and validation of the Client Service Receipt Inventory

Claudia C. Y. Chung,Jasmine L. F. Fung,Adrian C. Y. Lui,Marcus C. Y. Chan,Yvette N. C. Ng,Wilfred H. S. Wong,So Lun Lee,Martin Knapp,Brian H. Y. Chung

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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Rare Coding Variation Provides Insight into the Genetic Architecture and Phenotypic Context of Autism

Jack M. Fu,F. Kyle Satterstrom,Minshi Peng,Harrison Brand,Ryan L. Collins,Shan Dong,Brie Wamsley,Lambertus Klei,Lily Wang,Stephanie P. Hao,Christine R. Stevens,Caroline Cusick,Mehrtash Babadi,Eric Banks,Brett Collins,Sheila Dodge,Stacey B. Gabriel,Laura Gauthier,Samuel K. Lee,Lindsay Liang,Alicia Ljungdahl,Behrang Mahjani,Laura Sloofman,Andrey N. Smirnov,Mafalda Barbosa,Catalina Betancur,Alfredo Brusco,Brian H. Y. Chung,Edwin H. Cook,Michael L. Cuccaro,Enrico Domenici,Giovanni Battista Ferrero,J. Jay Gargus,Gail E. Herman,Irva Hertz-Picciotto,Patricia Maciel,Dara S. Manoach,Maria Rita Passos-Bueno,Antonio M. Persico,Alessandra Renieri,James S. Sutcliffe,Flora Tassone,Elisabetta Trabetti,Gabriele Campos,Simona Cardaropoli,Diana Carli,Marcus C. Y. Chan,Chiara Fallerini,Elisa Giorgio,Ana Cristina Girardi,Emily Hansen-Kiss,So Lun Lee,Carla Lintas,Yunin Ludena,Rachel Nguyen,Lisa Pavinato,Margaret Pericak-Vance,Isaac N. Pessah,Rebecca J. Schmidt,Moyra Smith, Claudia I. S. Costa,Slavica Trajkova,Jaqueline Y. T. Wang,Mullin H. C. Yu,Branko Aleksic,David J. Cutler,Silvia De Rubeis,Joseph D. Buxbaum,Mark J. Daly,Bernie Devlin,Kathryn Roeder,Stephan J. Sanders,Michael E. Talkowski

Nature geneticsno. 9 (2022): 1320-1331

引用207浏览0WOSNATURE引用

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O'Donnell-Luria-Rodan Syndrome: Description of a Second Multinational Cohort and Refinement of the Phenotypic Spectrum

Journal of Medical Geneticsno. 7 (2021): 697-705

引用10浏览0WOS引用

108 Actionable Pharmacogenetic Variants in Hong Kong Chinese Exome Data and Projected Prescription Impact in the Hong Kong Population Leading to Precision Medicine

Kit San Yeung,Brian Chung,Mullin Yu,Marcus Chan, Clara Tang,Claudia Chung

BMJ Paediatrics Open（2021）

引用1浏览0引用

Rare Coding Variation Illuminates the Allelic Architecture, Risk Genes, Cellular Expression Patterns, and Phenotypic Context of Autism

Jack M. Fu,F. Kyle Satterstrom,Minshi Peng,Harrison Brand,Ryan L. Collins,Shan Dong,Lambertus Klei,Christine R. Stevens,Caroline Cusick,Mehrtash Babadi,Eric Banks,Brett Collins,Sheila Dodge,Stacey B. Gabriel,Laura Gauthier,Samuel K. Lee,Lindsay Liang,Alicia Ljungdahl,Behrang Mahjani,Laura Sloofman,Andrey Smirnov,Mafalda Barbosa,Alfredo Brusco,Brian H.Y. Chung,Michael L. Cuccaro,Enrico Domenici,Giovanni Battista Ferrero,Jay J. Gargus,Gail E. Herman,Irva Hertz-Picciotto,Patricia Maciel,Dara S. Manoach,Maria Rita Passos-Bueno,Antonio M. Persico,Alessandra Renieri,Flora Tassone,Elisabetta Trabetti,Gabriele Campos,Marcus C.Y. Chan,Chiara Fallerini,Elisa Giorgio, Ana Cristina Girard,Emily Hansen-Kiss,So Lun Lee,Carla Lintas,Yunin Ludena,Rachel Nguyen,Lisa Pavinato,Margaret Pericak-Vance,Isaac Pessah,Evelise Riberi,Rebecca Schmidt,Moyra Smith, Claudia I.C. Souza,Slavica Trajkova,Jaqueline Y.T. Wang,Mullin H.C. Yu,David J. Cutler,Silvia De Rubeis,Joseph D. Buxbaum,Mark J. Daly,Bernie Devlin,Kathryn Roeder,Stephan J. Sanders,Michael E. Talkowski

medRxiv（2021）

引用27浏览0引用

Client Service Receipt Inventory As a Standardised Tool for Measurement of Socio-Economic Costs in the Rare Genetic Disease Population (Csri-Ra)

Claudia C. Y. Chung,Jasmine L. F. Fung,Adrian C. Y. Lui,Marcus C. Y. Chan,Yvette N. C. Ng,Wilfred H. S. Wong,So Lun Lee,Martin Knapp,Brian H. Y. Chung

Scientific Reports（2021）

引用9浏览0WOSNATURE引用

A Three-Year Follow-Up Study Evaluating Clinical Utility of Exome Sequencing and Diagnostic Potential of Reanalysis

Jasmine L. F. Fung,Mullin H. C. Yu,Shushu Huang,Claudia C. Y. Chung,Marcus C. Y. Chan,Sander Pajusalu,Christopher C. Y. Mak,Vivian C. C. Hui,Mandy H. Y. Tsang,Kit San Yeung,Monkol Lek,Brian H. Y. Chung

npj Genomic Medicine（2020）

引用56浏览0WOSNATURE引用

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