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1.
Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore.
Cell
; 179(3): 736-749.e15, 2019 10 17.
Article
in English
| MEDLINE | ID: mdl-31626772
2.
Destabilization of ß Cell FIT2 by saturated fatty acids alter lipid droplet numbers and contribute to ER stress and diabetes.
Proc Natl Acad Sci U S A
; 119(11): e2113074119, 2022 03 15.
Article
in English
| MEDLINE | ID: mdl-35254894
3.
Genome-Wide Association Analysis of Protein-Coding Variants in IgA Nephropathy.
J Am Soc Nephrol
; 34(11): 1900-1913, 2023 11 01.
Article
in English
| MEDLINE | ID: mdl-37787447
4.
Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain.
Mol Psychiatry
; 26(10): 5766-5788, 2021 10.
Article
in English
| MEDLINE | ID: mdl-32647257
5.
Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds.
BMC Musculoskelet Disord
; 23(1): 818, 2022 Aug 30.
Article
in English
| MEDLINE | ID: mdl-36042462
6.
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
7.
Trans-Ethnic Fine-Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease.
Mov Disord
; 36(8): 1805-1814, 2021 08.
Article
in English
| MEDLINE | ID: mdl-33973677
8.
Polygenic Risk Scores in a Prospective Parkinson's Disease Cohort.
Mov Disord
; 36(12): 2936-2940, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34402545
9.
Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy.
J Am Soc Nephrol
; 31(12): 2949-2963, 2020 12.
Article
in English
| MEDLINE | ID: mdl-32912934
10.
Identification of a recurrent nonsense mutation in HR gene responsible for atrichia with papular lesions in two Kashmiri families.
J Gene Med
; 22(5): e3167, 2020 05.
Article
in English
| MEDLINE | ID: mdl-32020700
11.
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
12.
The Parkinson's Disease Genome-Wide Association Study Locus Browser.
Mov Disord
; 35(11): 2056-2067, 2020 11.
Article
in English
| MEDLINE | ID: mdl-32864809
13.
Parkinson's disease GWAS-linked Park16 carriers show greater motor progression.
J Med Genet
; 56(11): 765-768, 2019 11.
Article
in English
| MEDLINE | ID: mdl-30814270
14.
Genome-wide association study of Parkinson's disease in East Asians.
Hum Mol Genet
; 26(1): 226-232, 2017 01 01.
Article
in English
| MEDLINE | ID: mdl-28011712
15.
A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families.
J Gene Med
; 21(9): e3113, 2019 09.
Article
in English
| MEDLINE | ID: mdl-31310406
16.
Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta.
J Biomed Sci
; 26(1): 31, 2019 04 28.
Article
in English
| MEDLINE | ID: mdl-31030663
17.
An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma.
Hum Mol Genet
; 25(16): 3626-3634, 2016 08 15.
Article
in English
| MEDLINE | ID: mdl-27436580
18.
Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta.
J Biomed Sci
; 25(1): 82, 2018 Nov 17.
Article
in English
| MEDLINE | ID: mdl-30447692
19.
Possible Interaction Between Cigarette Smoking and HLA-DRB1 Variation in the Risk of Follicular Lymphoma.
Am J Epidemiol
; 185(8): 681-687, 2017 04 15.
Article
in English
| MEDLINE | ID: mdl-28369180
20.
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region.
Am J Hum Genet
; 95(4): 462-71, 2014 Oct 02.
Article
in English
| MEDLINE | ID: mdl-25279986