Brian H. Y. Chung - Department of Paediatrics and Adolescent Medicine,The University of Hong Kong

基本信息

Career Trajectory

Bio

Awards 2013 - Outstanding Oral Presentation Award - Identifying genetic mutations in patients with RASopathies using a new generation sequencing diagnostic pipeline in Hong Kong; Annual Scientific Meeting 2013, Hong Kong College of Paediatricians 2013 - Outstanding Poster Presentation Award - Integration of chromosomal microarray into paediatric clinical care in Hong Kong; Annual Scientific Meeting 2013, Hong Kong College of Paediatricians 2013 - Certificate of Excellence - Master of Science in Genomics & Bioinformatics; Division of Genomics & Bioinformatics, CUHK-BGI Innovation Institute of Trans-omics 2012 - Outstanding Team award - The Hong Kong West Cluster 2010 - 10-year Loyalty Award - Queen Mary Hospital 2010 - First Runner-up Best Poster Presentation - 7th Asia Pacific Medical Education Conference (APMEC) 2010 - One of the Top 4 submissions - 34th Annual Scientific Meeting, Canadian College of Medical Genetics 2010 - Best Basic Research - Annual Research Day, Paediatrics, Hospital for Sick Children, Toronto 2009 & 2010 - Fellow Award - 30th Annual David W. Smith Workshop on Malformations and Morphogenesis 2005 - Silver Medal in Best Original Research Contest - Clinical Markers Useful in Enhancing Diagnostic Yield for Children with Global Developmental Delay (GDD); HK Academy of Medicine 2005 - Most Outstanding Free Paper - (SMARD1) Spinal muscular atrophy with respiratory distress type 1 mutation in a Chinese boy; The 3rd Hong Kong Genetic Symposium 2005

Research Interests

Papers共 362 篇Author StatisticsCo-AuthorSimilar Experts

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The Incremental Yield of Prenatal Exome Sequencing over Chromosome Microarray for Congenital Heart Abnormalities: A Systematic Review and Meta-Analysis

K. Reilly, S. Sonner, N. McCay,D. L. Rolnik,F. Casey,A. N. Seale, C. J. Watson, A. Kan,T. H. T. Lai,B. H. Y. Chung,K. E. M. Diderich,M. I. Srebniak,E. Dempsey,S. Drury, J. Giordano,R. Wapner,M. D. Kilby,L. S. Chitty,F. Mone

PRENATAL DIAGNOSISno. 6-7 (2024): 821-831

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Client Service Receipt Inventory for Rare Genetic Diseases in Hong Kong: Abridged Secondary Publication

C,W H S Wong, S L Lee,B H Y Chung

Hong Kong medical journal = Xianggang yi xue za zhino. 1 (2024): 23-26

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Personalised Genomic Medicine is Shaping the Future of Healthcare

Annie Tsz Wai Chu,Brian Hon Yin Chung

Journal of translational genetics and genomicsno. 1 (2024): 49-54

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Genome-wide DNA Methylation Profiling for Central Nervous System Embryonal Tumours in Children: Abridged Secondary Publication

A P Y Liu,G C F Chan,B H Y Chung, W Yang,H K Ng

Hong Kong medical journal = Xianggang yi xue za zhino. 1 (2024): 29-33

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Simpson-Golabi-Behmel Syndrome Type 1 with Normal Birth Parameters

Brian Hon Yin Chung, Shu-ling Sophie Yeow,Joshua Chun Ki Chan,Mianne Lee

BMJ CASE REPORTSno. 3 (2024): 1-5

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Whole Genome Sequencing in Paediatric Channelopathy and Cardiomyopathy

Sit Yee Kwok,Anna Ka Yee Kwong, Julia Zhuo Shi, Connie Fong Ying Shih,Mianne Lee,Christopher C. Y. Mak,Martin Chui,Sabrina Tsao,Brian Hon Yin Chung

FRONTIERS IN CARDIOVASCULAR MEDICINE（2024）

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GestaltMatcher Database - A Global Reference for Facial Phenotypic Variability in Rare Human Diseases

Hellen Lesmann,Alexander Hustinx,Shahida Moosa,Hannah Klinkhammer,Elaine Marchi,Pilar Caro, Ibrahim M Abdelrazek,Jean Tori Pantel, Merle Ten Hagen, Meow-Keong Thong, Rifhan Azwani Binti Mazlan, Sok Kun Tae,Tom Kamphans,Wolfgang Meiswinkel,Jing-Mei Li,Behnam Javanmardi,Alexej Knaus,Annette Uwineza,Cordula Knopp,Tinatin Tkemaladze,Miriam Elbracht, Larissa Mattern,Rami Abou Jamra,Clara Velmans,Vincent Strehlow, Maureen Jacob, Angela Peron, Cristina Dias,Beatriz Carvalho Nunes, Thainá Vilella, Isabel Furquim Pinheiro,Chong Ae Kim,Maria Isabel Melaragno, Hannah Weiland, Sophia Kaptain, Karolina Chwiałkowska, Miroslaw Kwasniewski, Ramy Saad, Sarah Wiethoff,Himanshu Goel, Clara Tang, Anna Hau,Tahsin Stefan Barakat, Przemysław Panek,Amira Nabil, Julia Suh, Frederik Braun, Israel Gomy,Luisa Averdunk,Ekanem Ekure, Gaber Bergant, Borut Peterlin,Claudio Graziano, Nagwa Gaboon, Moisés Fiesco-Roa, Alessandro Mauro Spinelli, Nina-Maria Wilpert,Prasit Phowthongkum,Nergis Güzel,Tobias B Haack, Rana Bitar, Andreas Tzschach, Agusti Rodriguez-Palmero,Theresa Brunet,Sabine Rudnik-Schöneborn, Silvina Noemi Contreras-Capetillo, Ava Oberlack, Carole Samango-Sprouse, Teresa Sadeghin, Margaret Olaya,Konrad Platzer,Artem Borovikov,Franziska Schnabel,Lara Heuft, Vera Herrmann, Renske Oegema, Nour Elkhateeb, Sheetal Kumar, Katalin Komlosi, Khoushoua Mohamed, Silvia Kalantari, Fabio Sirchia, Antonio F Martinez-Monseny, Matthias Höller, Louiza Toutouna, Amal Mohamed,Amaia Lasa-Aranzasti, John A Sayer, Nadja Ehmke, Magdalena Danyel, Henrike Sczakiel, Sarina Schwartzmann, Felix Boschann, Max Zhao, Ronja Adam, Lara Einicke, Denise Horn, Kee Seang Chew, Choy Chen Kam, Miray Karakoyun, Ben Pode-Shakked, Aviva Eliyahu, Rachel Rock, Teresa Carrion, Odelia Chorin, Yuri A Zarate, Marcelo Martinez Conti, Mert Karakaya, Moon Ley Tung, Bharatendu Chandra, Arjan Bouman, Aime Lumaka, Naveed Wasif, Marwan Shinawi, Patrick R Blackburn, Tianyun Wang, Tim Niehues, Axel Schmidt, Regina Rita Roth, Dagmar Wieczorek, Ping Hu,Rebekah L Waikel,Suzanna E Ledgister Hanchard,Gehad Elmakkawy,Sylvia Safwat,Frédéric Ebstein,Elke Krüger,Sébastien Küry, Stéphane Bézieau,Annabelle Arlt, Eric Olinger,Felix Marbach, Dong Li,Lucie Dupuis,Roberto Mendoza-Londono,Sofia Douzgou Houge,Denisa Weis,Brian Hon-Yin Chung,Christopher C Y Mak, Hülya Kayserili, Nursel Elcioglu, Ayca Aykut, Peli Özlem Şimşek-Kiper, Nina Bögershausen, Bernd Wollnik, Heidi Beate Bentzen, Ingo Kurth,Christian Netzer,Aleksandra Jezela-Stanek,Koen Devriendt,Karen W Gripp,Martin Mücke,Alain Verloes,Christian P Schaaf,Christoffer Nellåker,Benjamin D Solomon,Markus M Nöthen,Ebtesam Abdalla,Gholson J Lyon,Peter M Krawitz,Tzung-Chien Hsieh

medRxiv the preprint server for health sciences (2024)

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Long-surviving Neu-Laxova syndrome confirmed by whole exome sequencing: a case report

C. W. Kong, Y. Y. Li, Sandy L. K. Au,Anita S. Y. Kan, Martin MC Chui,Brian H. Y. Chung, Y. C. Ho,William W. K. To

HONG KONG MEDICAL JOURNAL（2024）

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PSMF1variants Cause a Phenotypic Spectrum from Early-Onset Parkinson's Disease to Perinatal Lethality by Disrupting Mitochondrial Pathways

Francesca Magrinelli,Christelle Tesson,Plamena R Angelova, Ainara Salazar-Villacorta,Jose A Rodriguez,Annarita Scardamaglia,Brian Hon-Yin Chung, Matthew Jaconelli,Barbara Vona,Noemi Esteras,Anna Ka-Yee Kwong,Thomas Courtin,Reza Maroofian,Shahryar Alavi,Raja Nirujogi,Mariasavina Severino,Patrick A Lewis,Stephanie Efthymiou,Benjamin O'Callaghan,Rebecca Buchert,Linda Sofan,Pawel Lis, Chloé Pinon,Guido J Breedveld, Martin Man-Chun Chui,David Murphy,Vanessa Pitz,Mary B Makarious,Marlene Cassar,Bassem A Hassan,Sana Iftikhar,Clarissa Rocca,Peter Bauer,Michele Tinazzi,Marina Svetel,Bedia Samanci,Haşmet A Hanağası,Basar Bilgiç,José A Obeso,Monica M Kurtis, Guillaume Cogan,Ayşe Nazlı Başak,Güneş Kiziltan,Tuğçe Gül, Gül Yalçın,Bülent Elibol,Nina Barišić, Earny Wei-Sen Ng, Sze-Shing Fan,Tova Hershkovitz,Karin Weiss,Javeria Raza Alvi,Tipu Sultan,Issam Azmi Alkhawaja,Tawfiq Froukh, Hadeel Abdollah E Alrukban,Christine Fauth,Ulrich A Schatz,Thomas Zöggeler,Michael Zech,Karen Stals,Vinod Varghese,Sonia Gandhi,Cornelis Blauwendraat,John A Hardy,Suzanne Lesage,Vincenzo Bonifati,Tobias B Haack,Aida M Bertoli-Avella,Robert Steinfeld,Dario R Alessi,Hermann Steller,Alexis Brice,Andrey Y Abramov, Kailash P Bhatia,Henry Houlden

medRxiv the preprint server for health sciences (2024)

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Brian H. Y. Chung(鍾侃言)

Clinical Associate Professor

Papers共 362 篇Author StatisticsCo-AuthorSimilar Experts