Jasmine Lee Fong Fung
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Explore the profile of Jasmine Lee Fong Fung including associated specialties, affiliations and a list of published articles.
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70
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Recent Articles
1.
Chan J, Kuong E, Chan J, Luk H, Fung J, Tung J, et al.
Front Pediatr
. 2023 May;
11:1152731.
PMID: 37181433
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...
2.
Chau J, Lee M, Chui M, Yu M, Fung J, Mak C, et al.
Front Genet
. 2022 Aug;
13:933381.
PMID: 36003331
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,...
3.
Chau J, Yu M, Chui M, Yeung C, Kwok A, Zhuang X, et al.
NPJ Genom Med
. 2022 Mar;
7(1):23.
PMID: 35314707
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...
4.
Cheung N, Fung J, Ng Y, Wong W, Chung C, Mak C, et al.
Hum Genomics
. 2021 Aug;
15(1):54.
PMID: 34407885
Background: The global development and advancement of genomic medicine in the recent decade has accelerated the implementation of personalized medicine (PM) and pharmacogenomics (PGx) into clinical practice, while catalyzing the...
5.
Yu M, Fung J, Ng A, Li Z, Lan W, Chung C, et al.
Mol Genet Genomic Med
. 2021 May;
9(7):e1702.
PMID: 34002545
Purpose: The aim was to evaluate knowledge, attitudes, and clinical practice concerning medical genetics, genetic testing, and counseling among primary care physicians (PCPs) in Hong Kong and Shenzhen, China. Methods:...
6.
Sheppard S, Campbell I, Harr M, Gold N, Li D, Bjornsson H, et al.
Am J Med Genet A
. 2021 Mar;
185(6):1649-1665.
PMID: 33783954
Wiedemann-Steiner syndrome (WSS) is an autosomal dominant disorder caused by monoallelic variants in KMT2A and characterized by intellectual disability and hypertrichosis. We performed a retrospective, multicenter, observational study of 104...
7.
Yu M, Chan M, Chung C, Li A, Yip C, Mak C, et al.
PLoS Genet
. 2021 Feb;
17(2):e1009323.
PMID: 33600428
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...
8.
Yu M, Chau J, Au S, Lo H, Yeung K, Fung J, et al.
Front Genet
. 2021 Feb;
11:620162.
PMID: 33584815
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...
9.
Yu M, Mak C, Fung J, Lee M, Tsang M, Chau J, et al.
J Hum Genet
. 2020 Nov;
66(6):637-641.
PMID: 33223521
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....
10.
Chung C, Chan K, Hui P, Au P, Tam W, Li S, et al.
BMC Pregnancy Childbirth
. 2020 Feb;
20(1):109.
PMID: 32059709
Background: Chromosomal microarray (CMA) has been shown to be cost-effective over karyotyping in invasive prenatal diagnosis for pregnancies with fetal ultrasound anomalies. Yet, information regarding preceding and subsequent tests must...