Detalhe da pesquisa
1.
Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore.
Cell
; 179(3): 736-749.e15, 2019 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31626772
2.
Clinical implementation of plasma EGFR T790M testing using droplet digital PCR in TKI-resistant NSCLC patients.
Exp Mol Pathol
; 116: 104515, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32738312
3.
Validation of a next generation sequencing assay for BRCA1, BRCA2, CHEK2 and PALB2 genetic testing.
Exp Mol Pathol
; 116: 104483, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32531196
4.
CYP2C19 phenotype in South-East Asian Acute Coronary Syndrome patients and impact on major adverse cardiovascular events.
J Clin Pharm Ther
; 45(1): 52-58, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31670842
5.
NLRP1, PTPN22 and PADI4 gene polymorphisms and rheumatoid arthritis in ACPA-positive Singaporean Chinese.
Rheumatol Int
; 37(8): 1295-1302, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28653215
6.
A case of VEXAS syndrome manifesting as Kikuchi-Fujimoto disease, relapsing polychondritis, venous thromboembolism and macrocytic anaemia.
Rheumatology (Oxford)
; 60(9): e304-e306, 2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33630036
7.
Inflammatory risk contributes to post-COVID endothelial dysfunction through anti-ACKR1 autoantibody.
Life Sci Alliance
; 7(7)2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38740432
8.
The GTPase-deficient Rnd proteins are stabilized by their effectors.
J Biol Chem
; 287(37): 31311-20, 2012 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22807448
9.
The Singapore National Precision Medicine Strategy.
Nat Genet
; 55(2): 178-186, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36658435
10.
A five-safes approach to a secure and scalable genomics data repository.
iScience
; 26(4): 106546, 2023 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37123247
11.
TPMT and NUDT15 testing for thiopurine therapy: A major tertiary hospital experience and lessons learned.
Front Pharmacol
; 13: 837164, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36210828
12.
Compound Heterozygous Factor VII Deficiency c.1025G>A p.(Arg342Gln) With Novel Missense Variant c.194C>G p.(Ala65Gly).
J Hematol
; 11(1): 29-33, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35356632
13.
Self-Reported Frailty Screening Tools: Comparing Construct Validity of the Frailty Phenotype Questionnaire and FRAIL.
J Am Med Dir Assoc
; 23(11): 1870.e1-1870.e7, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35660384
14.
Analysis of clinically relevant variants from ancestrally diverse Asian genomes.
Nat Commun
; 13(1): 6694, 2022 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36335097
15.
Sex Modifies the Association of Fibroblast Growth Factor 21 With Subclinical Carotid Atherosclerosis.
Front Cardiovasc Med
; 8: 627691, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33996935
16.
Impact of Vitamin E supplementation on vascular function in haptoglobin genotype stratified diabetes patients (EVAS Trial): a randomised controlled trial.
Nutr Diabetes
; 10(1): 13, 2020 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32341356
17.
Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report.
BMC Med Genomics
; 11(1): 37, 2018 04 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29615056
18.
Non-invasive detection of actionable mutations in advanced non-small-cell lung cancer using targeted sequencing of circulating tumor DNA.
Lung Cancer
; 124: 154-159, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30268455
19.
Endothelial cell apoptosis correlates with low haptoglobin concentrations in diabetes.
Diab Vasc Dis Res
; 14(6): 534-539, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28830235
20.
Analysis of Genetic Variation in CYP450 Genes for Clinical Implementation.
PLoS One
; 12(1): e0169233, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28046094