Detalhe da pesquisa
1.
Impact of BRCA1/2 cascade testing on anxiety, depression, and cancer worry levels among unaffected relatives in a multiethnic Asian cohort.
J Genet Couns
; 32(1): 43-56, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35913122
2.
The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review.
Hum Genet
; 141(11): 1697-1704, 2022 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-35488921
3.
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low-to-middle income Asian country.
J Genet Couns
; 31(5): 1080-1089, 2022 10.
Artigo
Inglês
| MEDLINE | ID: mdl-35481858
4.
Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting.
J Genet Couns
; 30(3): 720-729, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33245177
5.
Rubinstein-Taybi syndrome in diverse populations.
Am J Med Genet A
; 182(12): 2939-2950, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32985117
6.
Turner syndrome in diverse populations.
Am J Med Genet A
; 182(2): 303-313, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31854143
7.
International perspectives on the implementation of reproductive carrier screening.
Prenat Diagn
; 40(3): 301-310, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31774570
8.
Growth hormone therapy for people with thalassaemia.
Cochrane Database Syst Rev
; 5: CD012284, 2020 05 28.
Artigo
Inglês
| MEDLINE | ID: mdl-32463488
9.
Achieving the targets of sustainable development goals (2030 agenda) for congenital disorders in Asia: Bottlenecks and interventions.
Am J Med Genet C Semin Med Genet
; 181(2): 254-261, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30801969
10.
Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia.
Am J Med Genet C Semin Med Genet
; 181(2): 155-165, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-31050142
11.
Training in clinical genetics and genetic counseling in Asia.
Am J Med Genet C Semin Med Genet
; 181(2): 177-186, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-31037827
12.
ß-Thalassemias.
N Engl J Med
; 384(22): 2165, 2021 Jun 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34077655
13.
Cornelia de Lange syndrome in diverse populations.
Am J Med Genet A
; 179(2): 150-158, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30614194
14.
Ten-year trend in prevalence and outcome of Down syndrome with congenital heart disease in a middle-income country.
Eur J Pediatr
; 178(8): 1267-1274, 2019 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-31222391
15.
Medical genetics in developing countries in the Asia-Pacific region: challenges and opportunities.
Genet Med
; 20(10): 1114-1121, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-30093710
16.
GWAS signals revisited using human knockouts.
Genet Med
; 20(1): 64-68, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28640246
17.
Williams-Beuren syndrome in diverse populations.
Am J Med Genet A
; 176(5): 1128-1136, 2018 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29681090
18.
A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia.
J Genet Couns
; 27(1): 21-32, 2018 02.
Artigo
Inglês
| MEDLINE | ID: mdl-28699126
19.
22q11.2 deletion syndrome in diverse populations.
Am J Med Genet A
; 173(4): 879-888, 2017 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-28328118
20.
Down syndrome in diverse populations.
Am J Med Genet A
; 173(1): 42-53, 2017 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-27991738