S. Gelfman

发表

HP1 is involved in regulating the global impact of DNA methylation on alternative splicing.

Karsten Rippe, Gil Ast, Eran Meshorer, 2015, Cell reports.

DNA-methylation effect on cotranscriptional splicing is dependent on GC architecture of the exon–intron structure

G. Ast, Ahuvi Yearim, S. Gelfman, 2013, Genome research.

intron structure − on GC architecture of the exon DNA-methylation effect on cotranscriptional splicing is dependent Material Supplemental

G. Ast, Ahuvi Yearim, S. Gelfman, 2013 .

Changes in exon-intron structure during vertebrate evolution affect the splicing pattern of exons.

D. Burstein, Osnat Penn, G. Ast, 2012, Genome research.

Differential GC content between exons and introns establishes distinct strategies of splice-site recognition.

Schraga Schwartz, Tal Pupko, Gil Ast, 2012, Cell reports.

Annotating pathogenic non-coding variants in genic regions

Zhong Ren, Kelly Schoch, Slavé Petrovski, 2017, Nature Communications.

the splicing pattern of exons intron structure during vertebrate evolution affect − Changes in exon Material

D. Burstein, Osnat Penn, G. Ast, 2011 .

Enhancer methylation dynamics contribute to cancer plasticity and patient mortality

R. Shamir, Carmit Levy, R. E. Bell, 2016, Genome research.

The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders

V. Jobanputra, A. Shabalin, Anthony W. Zoghbi, 2021, Molecular Psychiatry.

Rare coding variants in CHRNB2 reduce the likelihood of smoking

J. Marchini, S. Balasubramanian, A. Shuldiner, 2022, Nature Genetics.

Testing for Natural Selection in Human Exonic Splicing Regulators Associated with Evolutionary Rate Shifts

G. Ast, S. Gelfman, D. Meyer, 2013, Journal of Molecular Evolution.

G protein-coupled potassium channels implicated in mouse and cellular models of GNB1 Encephalopathy

D. Goldstein, Yueqing Peng, R. Dhindsa, 2019, bioRxiv.

Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82

I. Ionita-Laza, S. Gelfman, A. Alkelai, 2022, Nature Communications.

Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82

I. Ionita-Laza, A. Christiano, S. Gelfman, 2022, Nature communications.

ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers

E. Stahl, G. Coppola, J. Kosmicki, 2021, medRxiv.

HP 1 Is Involved in Regulat ing the Global Impact of DNA Methylation on Alternative Splicing Graphical

G. Ast, K. Rippe, E. Meshorer, 2015 .

Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

Alexander E. Lopez, Eurie L. Hong, G. D. Gatta, 2022, Nature Genetics.

meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays

Quanli Wang, Ellese Cotterill, Stephen J Eglen, 2018, bioRxiv.

Annotating pathogenic non-coding variants in genic regions

K. M. McSweeney, D. Goldstein, S. Petrovski, 2017, Nature Communications.

A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS

Brittany N. Lasseigne, D. Goldstein, R. Myers, 2019, Genome research.

Regional Collapsing of Rare Variation Implicates Specific Genic Regions in ALS

Brittany N. Lasseigne, D. Goldstein, R. Myers, 2018, bioRxiv.

When epigenetics meets alternative splicing: the roles of DNA methylation and GC architecture.

G. Ast, S. Gelfman, 2013, Epigenomics.

Exome-Based Rare-Variant Analyses in CKD.

D. Goldstein, A. Allen, S. Petrovski, 2019, Journal of the American Society of Nephrology : JASN.

Inhibition of microRNA 128 promotes excitability of cultured cortical neuronal networks

Ayal B. Gussow, Wayne N Frankel, Slavé Petrovski, 2016, Genome research.

Incorporating external information to improve sparse signal detection in rare‐variant gene‐set‐based analyses

D. Goldstein, A. Allen, S. Gelfman, 2020, Genetic epidemiology.

Incorporating prior information into signal-detection analyses across biologically informed gene-sets

D. Goldstein, A. Allen, S. Gelfman, 2019, bioRxiv.

A deep catalog of protein-coding variation in 985,830 individuals

Alexander E. Lopez, R. Collins, G. Abecasis, 2023, bioRxiv.

Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor

Yueqing Peng, R. Dhindsa, W. Frankel, 2023, Frontiers in Cellular Neuroscience.

A deep catalog of protein-coding variation in 985,830 individuals

Alexander E. Lopez, R. Collins, G. Abecasis, 2023, bioRxiv.