Detalhe da pesquisa
1.
Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population.
PLoS Genet
; 17(2): e1009323, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33600428
2.
Perception of personalized medicine, pharmacogenomics, and genetic testing among undergraduates in Hong Kong.
Hum Genomics
; 15(1): 54, 2021 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34407885
3.
Prevalence and healthcare utilization of rare neurological diseases in Hong Kong: 2014-2018.
Eur J Neurol
; 28(7): 2305-2312, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33793024
4.
Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong.
BMC Pregnancy Childbirth
; 20(1): 109, 2020 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32059709
5.
The growing needs of genetic counselling-Feasibility in utilization of tele-genetic counselling in Asia and Hong Kong.
Front Genet
; 14: 1239817, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37600657
6.
Rare disease emerging as a global public health priority.
Front Public Health
; 10: 1028545, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36339196
7.
Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese.
NPJ Genom Med
; 7(1): 23, 2022 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35314707
8.
A thematic study: impact of COVID-19 pandemic on rare disease organisations and patients across ten jurisdictions in the Asia Pacific region.
Orphanet J Rare Dis
; 16(1): 119, 2021 03 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33673852
9.
Hospital mortality in patients with rare diseases during pandemics: lessons learnt from the COVID-19 and SARS pandemics.
Orphanet J Rare Dis
; 16(1): 361, 2021 08 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34384469
10.
Preparing genomic revolution: Attitudes, clinical practice, and training needs in delivering genetic counseling in primary care in Hong Kong and Shenzhen, China.
Mol Genet Genomic Med
; 9(7): e1702, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34002545
11.
Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis.
Front Genet
; 11: 620162, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33584815
12.
Healthcare burden of rare diseases in Hong Kong - adopting ORPHAcodes in ICD-10 based healthcare administrative datasets.
Orphanet J Rare Dis
; 13(1): 147, 2018 08 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-30153866