Naisha Shah
Naisha Shah
Associate Professor
Verified email at jcvi.org
Title
Cited by
Cited by
Year
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
18742010
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
5802010
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
JS Kooner, D Saleheen, X Sim, J Sehmi, W Zhang, P Frossard, LF Been, ...
Nature genetics 43 (10), 984-989, 2011
4682011
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
3552008
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
3512012
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
HR Warren, E Evangelou, CP Cabrera, H Gao, M Ren, B Mifsud, I Ntalla, ...
Nature genetics 49 (3), 403, 2017
3092017
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
2492016
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
1722012
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
912014
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
742019
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
652018
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
612018
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
462014
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
452018
No increased risk of symptomatic intracerebral hemorrhage after thrombolysis in patients with European Cooperative Acute Stroke Study (ECASS) exclusion criteria
CA Cronin, N Shah, T Morovati, LD Hermann, KN Sheth
Stroke 43 (6), 1684-1686, 2012
392012
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
362016
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders
RJL Anney, EM Kenny, C O'dushlaine, BL Yaspan, E Parkhomenka, ...
European journal of human genetics 19 (10), 1082-1089, 2011
362011
How I use clinical decision support to improve red blood cell utilization
L Tim Goodnough, S Andrew Baker, N Shah
Transfusion 56 (10), 2406-2411, 2016
222016
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
202013
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
172016
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