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Sahar Gelfman
Sahar Gelfman
Regeneron Genetics Center
Verified email at regeneron.com
Title
Cited by
Cited by
Year
Differential GC content between exons and introns establishes distinct strategies of splice-site recognition
M Amit, M Donyo, D Hollander, A Goren, E Kim, S Gelfman, G Lev-Maor, ...
Cell reports 1 (5), 543-556, 2012
3182012
DNA-methylation effect on cotranscriptional splicing is dependent on GC architecture of the exon–intron structure
S Gelfman, N Cohen, A Yearim, G Ast
Genome research 23 (5), 789-799, 2013
2492013
HP1 is involved in regulating the global impact of DNA methylation on alternative splicing
A Yearim, S Gelfman, R Shayevitch, S Melcer, O Glaich, JP Mallm, ...
Cell reports 10 (7), 1122-1134, 2015
2212015
Annotating pathogenic non-coding variants in genic regions
S Gelfman, Q Wang, KM McSweeney, Z Ren, F La Carpia, M Halvorsen, ...
Nature communications 8 (1), 236, 2017
1382017
Changes in exon–intron structure during vertebrate evolution affect the splicing pattern of exons
S Gelfman, D Burstein, O Penn, A Savchenko, M Amit, S Schwartz, ...
Genome research 22 (1), 35-50, 2012
1212012
Enhancer methylation dynamics contribute to cancer plasticity and patient mortality
RE Bell, T Golan, D Sheinboim, H Malcov, D Amar, A Salamon, T Liron, ...
Genome research 26 (5), 601-611, 2016
1132016
Exome-based rare-variant analyses in CKD
S Cameron-Christie, CJ Wolock, E Groopman, S Petrovski, ...
Journal of the American Society of Nephrology 30 (6), 1109-1122, 2019
492019
Inhibition of microRNA 128 promotes excitability of cultured cortical neuronal networks
KM McSweeney, AB Gussow, SS Bradrick, SA Dugger, S Gelfman, ...
Genome research 26 (10), 1411-1416, 2016
462016
When epigenetics meets alternative splicing: the roles of DNA methylation and GC architecture
S Gelfman, G Ast
Epigenomics 5 (4), 351-353, 2013
442013
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays
S Gelfman, Q Wang, YF Lu, D Hall, CD Bostick, R Dhindsa, M Halvorsen, ...
PLoS computational biology 14 (10), e1006506, 2018
282018
A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS
S Gelfman, S Dugger, CAM Moreno, Z Ren, CJ Wolock, NA Shneider, ...
Genome research 29 (5), 809-818, 2019
262019
Differential GC content between exons and introns establishes distinct strategies of splice-site recognition. Cell Rep 1: 543–556
M Amit, M Donyo, D Hollander, A Goren, E Kim, S Gelfman, G Lev-Maor, ...
202012
The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders
A Alkelai, L Greenbaum, AR Docherty, AA Shabalin, G Povysil, A Malakar, ...
Molecular Psychiatry 27 (3), 1435-1447, 2022
162022
G protein-coupled potassium channels implicated in mouse and cellular models of GNB1 Encephalopathy
S Colombo, S Petri, B Shalomov, HP Reddy, G Tabak, RS Dhindsa, ...
BioRxiv, 697235, 2019
162019
Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
SO Erjavec, S Gelfman, AR Abdelaziz, EY Lee, I Monga, A Alkelai, ...
Nature communications 13 (1), 800, 2022
152022
ERAP1, ERAP2, and two copies of HLA-aw19 alleles increase the risk for birdshot chorioretinopathy in HLA-A29 carriers
S Gelfman, D Monnet, AJ Ligocki, T Tabary, A Moscati, X Bai, ...
Investigative Ophthalmology & Visual Science 62 (14), 3-3, 2021
142021
Incorporating external information to improve sparse signal detection in rare‐variant gene‐set‐based analyses
M Zhang, S Gelfman, J McCarthy, MB Harms, CAM Moreno, DB Goldstein, ...
Genetic Epidemiology 44 (4), 330-338, 2020
82020
Rare coding variants in CHRNB2 reduce the likelihood of smoking
VM Rajagopal, K Watanabe, J Mbatchou, A Ayer, P Quon, D Sharma, ...
Nature Genetics 55 (7), 1138-1148, 2023
72023
Regional collapsing of rare variation implicates specific genic regions in ALS
S Gelfman, S Dugger, CA Martins Moreno, Z Ren, CJ Wolock, ...
BioRxiv, 375774, 2018
42018
A deep catalog of protein-coding variation in 985,830 individuals
KY Sun, X Bai, S Chen, S Bao, M Kapoor, C Zhang, J Backman, T Joseph, ...
bioRxiv, 2023
32023
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