Neville Sanjana
Neville Sanjana
Core Faculty, New York Genome Center. Associate Professor, NYU.
Verified email at - Homepage
Cited by
Cited by
Genome-scale CRISPR-Cas9 knockout screening in human cells
O Shalem, NE Sanjana, E Hartenian, X Shi, DA Scott, TS Mikkelsen, ...
Science 343 (6166), 84-87, 2014
Improved vectors and genome-wide libraries for CRISPR screening
NE Sanjana, O Shalem, F Zhang
Nature methods 11 (8), 783-784, 2014
High-throughput functional genomics using CRISPR–Cas9
O Shalem, NE Sanjana, F Zhang
Nature Reviews Genetics 16 (5), 299-311, 2015
Perturbation of m6A writers reveals two distinct classes of mRNA methylation at internal and 5′ sites
S Schwartz, MR Mumbach, M Jovanovic, T Wang, K Maciag, GG Bushkin, ...
Cell reports 8 (1), 284-296, 2014
Genome-scale CRISPR-Cas9 knockout and transcriptional activation screening
J Joung, S Konermann, JS Gootenberg, OO Abudayyeh, RJ Platt, ...
Nature protocols 12 (4), 828-863, 2017
Genome-wide CRISPR screen in a mouse model of tumor growth and metastasis
S Chen, NE Sanjana, K Zheng, O Shalem, K Lee, X Shi, DA Scott, J Song, ...
Cell 160 (6), 1246-1260, 2015
A transcription activator-like effector toolbox for genome engineering
NE Sanjana, L Cong, Y Zhou, MM Cunniff, G Feng, F Zhang
Nature protocols 7 (1), 171-192, 2012
BCL11A enhancer dissection by Cas9-mediated in situ saturating mutagenesis
MC Canver, EC Smith, F Sher, L Pinello, NE Sanjana, O Shalem, ...
Nature 527 (7577), 192-197, 2015
Identification of essential genes for cancer immunotherapy
SJ Patel, NE Sanjana, RJ Kishton, A Eidizadeh, SK Vodnala, M Cam, ...
Nature 548 (7669), 537-542, 2017
CRISPR-Cas component systems, methods and compositions for sequence manipulation
F Zhang
US Patent 8,795,965, 2014
Engineering and optimization of systems, methods and compositions for sequence manipulation with functional domains
F Zhang, L Cong, RJ Platt, NE Sanjana, RAN Fei
US Patent 8,993,233, 2015
Identification of required host factors for SARS-CoV-2 infection in human cells
Z Daniloski, TX Jordan, HH Wessels, DA Hoagland, S Kasela, M Legut, ...
Cell 184 (1), 92-105. e16, 2021
A genome-wide CRISPR screen in primary immune cells to dissect regulatory networks
O Parnas, M Jovanovic, TM Eisenhaure, RH Herbst, A Dixit, CJ Ye, ...
Cell 162 (3), 675-686, 2015
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), e1000841, 2010
Hypoxia as a therapy for mitochondrial disease
IH Jain, L Zazzeron, R Goli, K Alexa, S Schatzman-Bone, H Dhillon, ...
Science 352 (6281), 54-61, 2016
Multiplexed detection of proteins, transcriptomes, clonotypes and CRISPR perturbations in single cells
EP Mimitou, A Cheng, A Montalbano, S Hao, M Stoeckius, M Legut, ...
Nature methods 16 (5), 409-412, 2019
Genome-scale activation screen identifies a lncRNA locus regulating a gene neighbourhood
J Joung, JM Engreitz, S Konermann, OO Abudayyeh, VK Verdine, F Aguet, ...
Nature 548 (7667), 343-346, 2017
High-resolution interrogation of functional elements in the noncoding genome
NE Sanjana, J Wright, K Zheng, O Shalem, P Fontanillas, J Joung, ...
Science 353 (6307), 1545-1549, 2016
A fast flexible ink-jet printing method for patterning dissociated neurons in culture
NE Sanjana, SB Fuller
Journal of neuroscience methods 136 (2), 151-163, 2004
Mice with Shank3 mutations associated with ASD and schizophrenia display both shared and distinct defects
Y Zhou, T Kaiser, P Monteiro, X Zhang, MS Van der Goes, D Wang, ...
Neuron 89 (1), 147-162, 2016
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