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1.
The DNA Structure-Specific Endonuclease MUS81 Mediates DNA Sensor STING-Dependent Host Rejection of Prostate Cancer Cells.
Immunity
; 44(5): 1177-89, 2016 05 17.
Article
in English
| MEDLINE | ID: mdl-27178469
2.
RETINITIS PIGMENTOSA ASSOCIATED WITH THE EYS C2139Y VARIANT : An Important Cause of Blindness in East Asian Populations.
Retina
; 43(10): 1788-1796, 2023 10 01.
Article
in English
| MEDLINE | ID: mdl-37418643
3.
High-Resolution Digital Phenotypes From Consumer Wearables and Their Applications in Machine Learning of Cardiometabolic Risk Markers: Cohort Study.
J Med Internet Res
; 24(7): e34669, 2022 07 29.
Article
in English
| MEDLINE | ID: mdl-35904853
4.
Investigation into the origins of an ancient BRCA1 founder mutation identified among Chinese families in Singapore.
Int J Cancer
; 148(3): 637-645, 2021 02 01.
Article
in English
| MEDLINE | ID: mdl-32745242
5.
NOTCH2NLC GGC Repeat Expansions Are Associated with Sporadic Essential Tremor: Variable Disease Expressivity on Long-Term Follow-up.
Ann Neurol
; 88(3): 614-618, 2020 09.
Article
in English
| MEDLINE | ID: mdl-32495371
6.
Beyond fitness tracking: The use of consumer-grade wearable data from normal volunteers in cardiovascular and lipidomics research.
PLoS Biol
; 16(2): e2004285, 2018 02.
Article
in English
| MEDLINE | ID: mdl-29485983
7.
Variation in predicted COVID-19 risk among lemurs and lorises.
Am J Primatol
; 83(6): e23255, 2021 06.
Article
in English
| MEDLINE | ID: mdl-33792947
8.
Integrated paired-end enhancer profiling and whole-genome sequencing reveals recurrent CCNE1 and IGF2 enhancer hijacking in primary gastric adenocarcinoma.
Gut
; 69(6): 1039-1052, 2020 06.
Article
in English
| MEDLINE | ID: mdl-31542774
9.
Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohort.
Clin Genet
; 98(3): 274-281, 2020 09.
Article
in English
| MEDLINE | ID: mdl-32602554
10.
Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.
Genet Med
; 21(1): 207-212, 2019 01.
Article
in English
| MEDLINE | ID: mdl-29961769
11.
Harnessing technology and molecular analysis to understand the development of cardiovascular diseases in Asia: a prospective cohort study (SingHEART).
BMC Cardiovasc Disord
; 19(1): 259, 2019 11 21.
Article
in English
| MEDLINE | ID: mdl-31752689
12.
Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.
Genet Med
; 20(12): 1692, 2018 12.
Article
in English
| MEDLINE | ID: mdl-30089799
13.
NOTCH2NLC-linked neuronal intranuclear inclusion body disease and fragile X-associated tremor/ataxia syndrome.
Brain
; 143(8): e69, 2020 08 01.
Article
in English
| MEDLINE | ID: mdl-32789443
14.
Activity of a heptad of transcription factors is associated with stem cell programs and clinical outcome in acute myeloid leukemia.
Blood
; 121(12): 2289-300, 2013 Mar 21.
Article
in English
| MEDLINE | ID: mdl-23327922
15.
Cluster analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.
Sci Rep
; 14(1): 5056, 2024 03 01.
Article
in English
| MEDLINE | ID: mdl-38424111
16.
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry.
J Mov Disord
; 17(2): 213-217, 2024 Apr.
Article
in English
| MEDLINE | ID: mdl-38291878
17.
Characterizing the genotypic spectrum of retinitis pigmentosa in East Asian populations: a systematic review.
Ophthalmic Genet
; 44(2): 109-118, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36856324
18.
DEGS1 -related leukodystrophy: a clinical report and review of literature.
Clin Dysmorphol
; 32(3): 106-111, 2023 Jul 01.
Article
in English
| MEDLINE | ID: mdl-37195341
19.
C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort.
Ann Clin Transl Neurol
; 10(4): 568-578, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36799407
20.
A novel intronic variant in ROBO3 associated with horizontal gaze palsy with progressive scoliosis: case report and literature review.
J AAPOS
; 27(6): 359-363, 2023 12.
Article
in English
| MEDLINE | ID: mdl-37931836