Naisha Shah
Naisha Shah
Associate Professor
Verified email at
Cited by
Cited by
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
InnateDB: facilitating systems‐level analyses of the mammalian innate immune response
DJ Lynn, GL Winsor, C Chan, N Richard, MR Laird, A Barsky, JL Gardy, ...
Molecular systems biology 4 (1), 218, 2008
Individual common variants exert weak effects on the risk for autism spectrum disorders
R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ...
Human molecular genetics 21 (21), 4781-4792, 2012
Deep sequencing of 10,000 human genomes
A Telenti, LCT Pierce, WH Biggs, J Di Iulio, EHM Wong, MM Fabani, ...
Proceedings of the National Academy of Sciences 113 (42), 11901-11906, 2016
Incidence of acquired demyelination of the CNS in Canadian children
B Banwell, J Kennedy, D Sadovnick, DL Arnold, S Magalhaes, ...
Neurology 72 (3), 232-239, 2009
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ...
Human genetics 131 (4), 565-579, 2012
Colchicine in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
RC Group
The Lancet Respiratory Medicine 9 (12), 1419-1426, 2021
Profound perturbation of the metabolome in obesity is associated with health risk
ET Cirulli, L Guo, CL Swisher, N Shah, L Huang, LA Napier, EF Kirkness, ...
Cell metabolism 29 (2), 488-500. e2, 2019
Abnormal B cell memory subsets dominate HIV-specific responses in infected individuals
L Kardava, S Moir, N Shah, W Wang, R Wilson, CM Buckner, BH Santich, ...
The Journal of clinical investigation 124 (7), 3252-3262, 2014
The human noncoding genome defined by genetic diversity
J Di Iulio, I Bartha, EHM Wong, HC Yu, V Lavrenko, D Yang, I Jung, ...
Nature genetics 50 (3), 333-337, 2018
Identification of misclassified ClinVar variants via disease population prevalence
N Shah, YCC Hou, HC Yu, R Sainger, CT Caskey, JC Venter, A Telenti
The American Journal of Human Genetics 102 (4), 609-619, 2018
Precision medicine screening using whole-genome sequencing and advanced imaging to identify disease risk in adults
BA Perkins, CT Caskey, P Brar, E Dec, DS Karow, AM Kahn, YCC Hou, ...
Proceedings of the National Academy of Sciences 115 (14), 3686-3691, 2018
Towards the identification of a genetic basis for L andau‐K leffner s yndrome
J Conroy, PA McGettigan, D McCreary, N Shah, K Collins, B Parry‐Fielder, ...
Epilepsia 55 (6), 858-865, 2014
Systematic analysis of cell-to-cell expression variation of T lymphocytes in a human cohort identifies aging and genetic associations
Y Lu, A Biancotto, F Cheung, E Remmers, N Shah, JP McCoy, JS Tsang
Immunity 45 (5), 1162-1175, 2016
Acetaminophen (paracetamol) use modifies the sulfation of sex hormones
IV Cohen, ET Cirulli, MW Mitchell, TJ Jonsson, J Yu, N Shah, TD Spector, ...
EBioMedicine 28, 316-323, 2018
A crowdsourcing approach for reusing and meta-analyzing gene expression data
N Shah, Y Guo, KV Wendelsdorf, Y Lu, R Sparks, JS Tsang
Nature biotechnology 34 (8), 803-806, 2016
Enrichment, isolation and identification of hydrocarbon degrading bacteria
M Udgire, N Shah, M Jadhav
J Int of Curr Microbiol Appl Sci 4, 708-713, 2015
High-resolution genome-wide copy-number analyses identify localized copy-number alterations in Ewing sarcoma
M Lynn, Y Wang, J Slater, N Shah, J Conroy, S Ennis, T Morris, DR Betts, ...
Diagnostic molecular pathology 22 (2), 76-84, 2013
An unsupervised learning approach to identify novel signatures of health and disease from multimodal data
I Shomorony, ET Cirulli, L Huang, LA Napier, RR Heister, M Hicks, ...
Genome medicine 12 (1), 1-14, 2020
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