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Irfahan Kassam
Irfahan Kassam
Verified email at illumina.com
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Cited by
Cited by
Year
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
15812019
Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci
M Lemire, SHE Zaidi, M Ban, B Ge, D Aïssi, M Germain, I Kassam, ...
Nature communications 6 (1), 6326, 2015
1472015
Analysis of DNA methylation associates the cystine–glutamate antiporter SLC7A11 with risk of Parkinson’s disease
CL Vallerga, F Zhang, J Fowdar, AF McRae, T Qi, MF Nabais, Q Zhang, ...
Nature communications 11 (1), 1238, 2020
1082020
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability
RH Reynolds, J Botía, MA Nalls, J Hardy, SA Gagliano Taliun, M Ryten
npj Parkinson's Disease 5 (1), 6, 2019
912019
The effect of X-linked dosage compensation on complex trait variation
J Sidorenko, I Kassam, KE Kemper, J Zeng, LR Lloyd-Jones, ...
Nature communications 10 (1), 3009, 2019
552019
Tissue-specific sex differences in human gene expression
I Kassam, Y Wu, J Yang, PM Visscher, AF McRae
Human molecular genetics 28 (17), 2976-2986, 2019
502019
Association of the APOE-ε4 allele with outcome of traumatic brain injury in children and youth: a meta-analysis and meta-regression
I Kassam, F Gagnon, MD Cusimano
Journal of Neurology, Neurosurgery & Psychiatry 87 (4), 433-440, 2016
502016
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease
H Leonard, C Blauwendraat, L Krohn, F Faghri, H Iwaki, G Ferguson, ...
Journal of medical genetics 57 (5), 331-338, 2020
442020
Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH
V Truong, S Huang, J Dennis, M Lemire, N Zwingerman, D Aïssi, ...
Scientific reports 7 (1), 11207, 2017
362017
Integrative profiling of T790M-negative EGFR-mutated NSCLC reveals pervasive lineage transition and therapeutic opportunities
KP Chua, YHF Teng, AC Tan, A Takano, JJS Alvarez, R Nahar, N Rohatgi, ...
Clin Cancer Res 27 (21), 5939-5950, 2021
232021
Impact of BMI and waist circumference on epigenome-wide DNA methylation and identification of epigenetic biomarkers in blood: an EWAS in multi-ethnic Asian individuals
Y Chen, I Kassam, SH Lau, JS Kooner, R Wilson, A Peters, J Winkelmann, ...
Clinical Epigenetics 13, 1-13, 2021
212021
Autosomal genetic control of human gene expression does not differ across the sexes
I Kassam, L Lloyd-Jones, A Holloway, KS Small, B Zeng, A Bakshi, ...
Genome biology 17 (1), 1-10, 2016
162016
New Polygenic Risk Score to Predict High Myopia in Singapore Chinese Children
C Lanca, I Kassam, K Patasova, LL Foo, J Li, M Ang, QV Hoang, YY Teo, ...
Translational vision science & technology 10 (8), 26-26, 2021
152021
Genetic determinants of tissue factor pathway inhibitor plasma levels
J Dennis, I Kassam, PE Morange, DA Tregouet, F Gagnon
Thrombosis and haemostasis 114 (08), 245-257, 2015
152015
Sex-specific effect of CPB2 Ala147Thr but not Thr325Ile variants on the risk of venous thrombosis: A comprehensive meta-analysis
N Zwingerman, A Medina-Rivera, I Kassam, MD Wilson, PE Morange, ...
PloS one 12 (5), e0177768, 2017
92017
Evidence for mitochondrial genetic control of autosomal gene expression
I Kassam, T Qi, L Lloyd-Jones, A Holloway, M Jan Bonder, AK Henders, ...
Human molecular genetics 25 (24), 5332-5338, 2016
82016
The Potential of Current Polygenic Risk Scores to Predict High Myopia and Myopic Macular Degeneration in Multiethnic Singapore Adults
I Kassam, LL Foo, C Lanca, LQ Xu, QV Hoang, CY Cheng, P Hysi, ...
Ophthalmology 129 (8), 890-902, 2022
72022
Genome-wide identification of cis DNA methylation quantitative trait loci in three Southeast Asian Populations
I Kassam, S Tan, FF Gan, WY Saw, LWL Tan, DKN Moong, R Soong, ...
Human Molecular Genetics 30 (7), 603-618, 2021
72021
The autosomal genetic control of sexually dimorphic traits in humans is largely the same across the sexes
I Kassam, AF McRae
Genome biology 17 (1), 1-3, 2016
62016
Main existing datasets for open data research on humans
B Couvy-Duchesne, S Bottani, E Camenen, F Fang, M Fikere, ...
22022
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