Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Brian Hon Yin, Chung"'
Autor:
Michelle Bishop, Aditi Vedi, Sarah Bowdin, Ruth Armstrong, Jack Bartram, David Bentley, Mark Ross, C. Elizabeth Hook, Brian Hon Yin Chung, Parker Moss, David H. Rowitch, Patrick Tarpey, Sam Behjati, Matthew J. Murray
Publikováno v:
BMC Medical Education, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background The clinical utility of whole genome sequencing (WGS) in paediatric cancer has been demonstrated in recent years. WGS has been routinely available in the National Health Service (NHS) England for all children with cancer in Englan
Externí odkaz:
https://doaj.org/article/b596a2e9f4594a5cbc378334e4100a46
Autor:
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
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroundPrecision medicine in paediatric cardiac channelopathy and cardiomyopathy has a rapid advancement over the past years. Compared to conventional gene panel and exome-based testing, whole genome sequencing (WGS) offers additional coverage at
Externí odkaz:
https://doaj.org/article/0ea45a1e97ed4009b1e09e81530f9309
Autor:
Brian Hon-Yin Chung, Anna Ka Yee Kwong, Martin Man Chun Chui, Christopher CY Mak, Ines Scheller, Sheila Suet-Na Wong, Cheuk-Wing Fung, Vicente Yépez
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101019- (2024)
Externí odkaz:
https://doaj.org/article/2358715853e7449d81ca1ac3b61a24f1
Autor:
Kevin Booth, Sharayu Jangam, Martin Man Chun Chui, Kayla Treat, Lorenzo Graziani, Alessia Soldano, Kerry White, Celanie Christensen, Ty Lynnes, Shinya Yamamoto, Oguz Kanca, Mandy Tsang, Sally Lynch, Sureni Mullegama, Julia Baptista, Daniela Iancu, Shelag Joss, Christopher CY Mak, Anna Kwong, Hugo Bellen, Erin Conboy, Remo Sanges, Michael F. Wangler, Brian Hon-Yin Chung, Francesco Vetrini
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101494- (2024)
Externí odkaz:
https://doaj.org/article/f55f71aa0f3040a5a34c8dbdffa4fbb9
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
The need for the expansion of genomic services has been at a record time high in the past decade. As technological advancement continues to strengthen the entire genetic and genomic pipeline and clinical operational workflow, the major challenge rema
Externí odkaz:
https://doaj.org/article/f9a543d3a6734fa89d6537970cf0a443
Autor:
Joshua Chun Ki Chan, Evelyn Eugenie Kuong, Joyce Pui Kwan Chan, Ho Ming Luk, Jasmine Lee Fong Fung, Joanna Yuet-ling Tung, Brian Hon Yin Chung
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare condition. The diagnosis could be challenging due to its rarity and non-specific presenting symptoms. However, early diagnosis and appropriate management help in preserving patients' functi
Externí odkaz:
https://doaj.org/article/0b16706a00c94464bd574f859eb4fbe5
Autor:
Jeffrey Fong Ting Chau, Mullin Ho Chung Yu, Martin Man Chun Chui, Cyrus Chun Wing Yeung, Aaron Wing Cheung Kwok, Xuehan Zhuang, Ryan Lee, Jasmine Lee Fong Fung, Mianne Lee, Christopher Chun Yu Mak, Nicole Ying Ting Ng, Claudia Ching Yan Chung, Marcus Chun Yin Chan, Mandy Ho Yin Tsang, Joshua Chun Ki Chan, Kelvin Yuen Kwong Chan, Anita Sik Yau Kan, Patrick Ho Yu Chung, Wanling Yang, So Lun Lee, Godfrey Chi Fung Chan, Paul Kwong Hang Tam, Yu Lung Lau, Kit San Yeung, Brian Hon Yin Chung, Clara Sze Man Tang
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-9 (2022)
Abstract Traditional carrier screening has been utilized for the detection of carriers of genetic disorders. Since a comprehensive assessment of the carrier frequencies of recessive conditions in the Southern Chinese population is not yet available,
Externí odkaz:
https://doaj.org/article/a4439854ca474791ac85c6eeb89fbddb
Autor:
Hannah Klinkhammer, Hellen Lesmann, Shahida Moosa, Alexander Hustinx, Behnam Javanmardi, Jing-Mei Li, Martin M.C. Chui, Christopher C.Y. Mak, Luisa Averdunk, Felix Distelmaier, Brian Hon-Yin Chung, Peter Krawitz, Tzung-Chien Hsieh
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100113- (2023)
Externí odkaz:
https://doaj.org/article/ac937ab2e8ff436880dd772dbcb45d4b
Publikováno v:
Frontiers in Public Health, Vol 10 (2022)
The genomics revolution over the past three decades has led to great strides in rare disease (RD) research, which presents a major shift in global policy landscape. While RDs are individually rare, there are common challenges and unmet medical and so
Externí odkaz:
https://doaj.org/article/ef98804a829141cf8884f865b3cd96c1
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/2056fec2a6fa4682a569f6454df68132