Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mullin Ho Chung, Yu"'
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:
Jeffrey Fong Ting Chau, Mianne Lee, Martin Man Chun Chui, Mullin Ho Chung Yu, Jasmine Lee Fong Fung, Christopher Chun Yu Mak, Christy Shuk-Kuen Chau, Ka Ka Siu, Jacqueline Hung, Kit San Yeung, Anna Ka Yee Kwong, Christopher O'Callaghan, Yu Lung Lau, Chun-Wai Davy Lee, Brian Hon-Yin Chung, So-Lun Lee
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Bronchiectasis is the abnormal dilation of the airway which may be caused by various etiologies in children. Beyond the more recognized cause of bacterial and viral infections and primary immunodeficiencies, other genetic conditions such as cystic fi
Externí odkaz:
https://doaj.org/article/1354567d67c147fb8a3fb1d9e75939ea
Autor:
Mullin Ho Chung Yu, Marcus Chun Yin Chan, Claudia Ching Yan Chung, Andrew Wang Tat Li, Chara Yin Wa Yip, Christopher Chun Yu Mak, Jeffrey Fong Ting Chau, Mianne Lee, Jasmine Lee Fong Fung, Mandy Ho Yin Tsang, Joshua Chun Ki Chan, Wilfred Hing Sang Wong, Jing Yang, William Chun Ming Chui, Patrick Ho Yu Chung, Wanling Yang, So Lun Lee, Godfrey Chi Fung Chan, Paul Kwong Hang Tam, Yu Lung Lau, Clara Sze Man Tang, Kit San Yeung, Brian Hon Yin Chung
Publikováno v:
PLoS Genetics, Vol 17, Iss 2, p e1009323 (2021)
Preemptive pharmacogenetic testing has the potential to improve drug dosing by providing point-of-care patient genotype information. Nonetheless, its implementation in the Chinese population is limited by the lack of population-wide data. In this stu
Externí odkaz:
https://doaj.org/article/17bc0de37ec248a2bc84c547426580ef
Autor:
Mullin Ho Chung Yu, Jeffrey Fong Ting Chau, Sandy Leung Kuen Au, Hei Man Lo, Kit San Yeung, Jasmine Lee Fong Fung, Christopher Chun Yu Mak, Claudia Ching Yan Chung, Kelvin Yuen Kwong Chan, Brian Hon Yin Chung, Anita Sik Yau Kan
Publikováno v:
Frontiers in Genetics, Vol 11 (2021)
Balanced chromosomal abnormalities (BCAs) are changes in the localization or orientation of a chromosomal segment without visible gain or loss of genetic material. BCAs occur at a frequency of 1 in 500 newborns and are associated with an increased ri
Externí odkaz:
https://doaj.org/article/cb6b8e42a9e64cac834d66ea5759d89c
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. 7(1)
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, we perfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d237aecededd7fce66cf66494f604fb
https://pubmed.ncbi.nlm.nih.gov/35314707
https://pubmed.ncbi.nlm.nih.gov/35314707
Autor:
Fong Ting Chau, Jeffrey, Mianne Lee, Man Chun Chui, Martin, Mullin Ho Chung Yu, Lee Fong Fung, Jasmine, Chun Yu Mak, Christopher, Shuk-Kuen Chau, Christy, Ka Ka Siu, Hung, Jacqueline, Kit San Yeung, Ka Yee Kwong, Anna, O'Callaghan, Christopher, Yu Lung Lau, Chun-Wai Davy Lee, Hon-Yin Chung, Brian, So-Lun Lee
Publikováno v:
Frontiers in Genetics; 8/8/2022, Vol. 13, p01-14, 14p
Autor:
Mandy Ho-Yin Tsang, Anna Ka-Yee Kwong, Kate Lok-San Chan, Jasmine Lee-Fong Fung, Mullin Ho-Chung Yu, Christopher Chun-Yu Mak, Kit-San Yeung, Richard J.T. Rodenburg, Jam A.M. Smeitink, Rachel Chan, Thomas Tsoi, Joannie Hui, Sheila Suet-Na Wong, Shuk-Mui Tai, Victor Chi-Man Chan, Che-Kwan Ma, Tsiu-Hang Sharon Fung, Shun-Ping Wu, WK Chan, Brian Hon-Yin Chung, Cheuk-wing Fung
Background Mitochondrial diseases (MDs) are a group of clinically and genetically heterogeneous disorders characterized by defects in oxidative phosphorylation. Since clinical phenotypes of MDs may be non-specific, genetic diagnosis is crucial for gu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8abf1db67e9dcdc1316872c588d761f5
https://doi.org/10.21203/rs.3.rs-23585/v2
https://doi.org/10.21203/rs.3.rs-23585/v2
Autor:
Mullin Ho Chung, Yu, Christopher Chun Yu, Mak, Jasmine Lee Fong, Fung, Mianne, Lee, Mandy Ho Yin, Tsang, Jeffrey Fong Ting, Chau, Patrick Ho-Yu, Chung, Wanling, Yang, Godfrey Chi Fung, Chan, So Lun, Lee, Yu Lung, Lau, Paul Kwong Hang, Tam, Clara Sze Man, Tang, Kit San, Yeung, Brian Hon Yin, Chung
Publikováno v:
Journal of human genetics. 66(6)
The use of exome and genome sequencing has increased rapidly nowadays. After primary analysis, further analysis can be performed to identify secondary findings that offer medical benefit for patient care. Multiple studies have been performed to evalu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c3e3bfbed105ad8231560b7d5e196818
https://pubmed.ncbi.nlm.nih.gov/33223521
https://pubmed.ncbi.nlm.nih.gov/33223521