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Gilad D. Evrony
Gilad D. Evrony
Assistant Professor, New York University
Verified email at nyulangone.org - Homepage
Title
Cited by
Cited by
Year
Somatic mutation, genomic variation, and neurological disease
A Poduri, GD Evrony, X Cai, CA Walsh
Science 341 (6141), 2013
6092013
Single-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain
GD Evrony, X Cai, E Lee, LB Hills, PC Elhosary, HS Lehmann, JJ Parker, ...
Cell 151 (3), 483-496, 2012
5882012
Somatic mutation in single human neurons tracks developmental and transcriptional history
MA Lodato, MB Woodworth, S Lee, GD Evrony, BK Mehta, A Karger, ...
Science 350 (6256), 94-98, 2015
5712015
Somatic activation of AKT3 causes hemispheric developmental brain malformations
A Poduri, GD Evrony, X Cai, PC Elhosary, R Beroukhim, MK Lehtinen, ...
Neuron 74 (1), 41-48, 2012
4832012
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain
X Cai, GD Evrony, HS Lehmann, PC Elhosary, BK Mehta, A Poduri, ...
Cell reports 8 (5), 1280-1289, 2014
3192014
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain
X Cai, GD Evrony, HS Lehmann, PC Elhosary, BK Mehta, A Poduri, ...
Cell reports 8 (5), 1280-1289, 2014
3192014
Cell lineage analysis in human brain using endogenous retroelements
GD Evrony, E Lee, BK Mehta, Y Benjamini, RM Johnson, X Cai, L Yang, ...
Neuron 85 (1), 49-59, 2015
2462015
Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning
BI Bae, I Tietjen, KD Atabay, GD Evrony, MB Johnson, E Asare, PP Wang, ...
Science 343 (6172), 764-768, 2014
2022014
Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation
YJ Yang, AE Baltus, RS Mathew, EA Murphy, GD Evrony, DM Gonzalez, ...
Cell 151 (5), 1097-1112, 2012
2022012
Resolving rates of mutation in the brain using single-neuron genomics
GD Evrony, E Lee, PJ Park, CA Walsh
Elife 5, e12966, 2016
1632016
Tetanus toxin C fragment-conjugated nanoparticles for targeted drug delivery to neurons
SA Townsend, GD Evrony, FX Gu, MP Schulz, RH Brown Jr, R Langer
Biomaterials 28 (34), 5176-5184, 2007
1342007
Complex autoinflammatory syndrome unveils fundamental principles of JAK1 kinase transcriptional and biochemical function
CN Gruber, JJA Calis, S Buta, G Evrony, JC Martin, SA Uhl, R Caron, ...
Immunity 53 (3), 672-684. e11, 2020
722020
Loss of PCLO function underlies pontocerebellar hypoplasia type III
MY Ahmed, BA Chioza, A Rajab, K Schmitz-Abe, A Al-Khayat, S Al-Turki, ...
Neurology 84 (17), 1745-1750, 2015
592015
Applications of Single-Cell DNA Sequencing
GD Evrony, AG Hinch, C Luo
Annual Review of Genomics and Human Genetics 22, 2021
562021
METTL23, a transcriptional partner of GABPA, is essential for human cognition
RE Reiff, BR Ali, B Baron, TW Yu, S Ben-Salem, ME Coulter, CR Schubert, ...
Human molecular genetics 23 (13), 3456-3466, 2014
472014
Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome
GD Evrony, DR Cordero, J Shen, JN Partlow, WY Timothy, RE Rodin, ...
Genome research 27 (8), 1323-1335, 2017
432017
DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients
R Urreizti, K Mayer, GD Evrony, E Said, L Castilla-Vallmanya, NAL Cody, ...
European Journal of Human Genetics 28 (1), 64-75, 2020
202020
One brain, many genomes
GD Evrony
Science 354 (6312), 557-558, 2016
152016
Single duplex DNA sequencing with CODEC detects mutations with high sensitivity
JH Bae, R Liu, E Roberts, E Nguyen, S Tabrizi, J Rhoades, T Blewett, ...
Nature Genetics 55 (5), 871-879, 2023
142023
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome
S Choufani, V McNiven, C Cytrynbaum, M Jangjoo, MP Adam, ...
The American Journal of Human Genetics 109 (10), 1867-1884, 2022
142022
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