| Year |
Citation |
Score |
| 2022 |
Eitan C, Siany A, Barkan E, Olender T, van Eijk KR, Moisse M, Farhan SMK, Danino YM, Yanowski E, Marmor-Kollet H, Rivkin N, Yacovzada NS, Hung ST, Cooper-Knock J, Yu CH, et al. Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3'UTR protect against ALS. Nature Neuroscience. PMID 35361972 DOI: 10.1038/s41593-022-01040-6 |
0.61 |
|
| 2022 |
Zhang S, Cooper-Knock J, Weimer AK, Shi M, Moll T, Marshall JNG, Harvey C, Nezhad HG, Franklin J, Souza CDS, Ning K, Wang C, Li J, Dilliott AA, Farhan S, ... ... Eitan C, et al. Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis. Neuron. PMID 35045337 DOI: 10.1016/j.neuron.2021.12.019 |
0.707 |
|
| 2021 |
Cooper-Knock J, Zhang S, Kenna KP, Moll T, Franklin JP, Allen S, Nezhad HG, Iacoangeli A, Yacovzada NY, Eitan C, Hornstein E, Elhaik E, Celadova P, Bose D, Farhan S, et al. Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene. Cell Reports. 34: 108730. PMID 33535055 DOI: 10.1016/j.celrep.2021.108730 |
0.635 |
|
| 2020 |
Cooper-Knock J, Zhang S, Kenna KP, Moll T, Franklin JP, Allen S, Nezhad HG, Iacoangeli A, Yacovzada NY, Eitan C, Hornstein E, Ehilak E, Celadova P, Bose D, Farhan S, et al. Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene. Cell Reports. 33: 108456. PMID 33264630 DOI: 10.1016/j.celrep.2020.108456 |
0.707 |
|
| 2020 |
Marmor-Kollet H, Siany A, Kedersha N, Knafo N, Rivkin N, Danino YM, Moens TG, Olender T, Sheban D, Cohen N, Dadosh T, Addadi Y, Ravid R, Eitan C, Toth Cohen B, et al. Spatiotemporal Proteomic Analysis of Stress Granule Disassembly Using APEX Reveals Regulation by SUMOylation and Links to ALS Pathogenesis. Molecular Cell. PMID 33217318 DOI: 10.1016/j.molcel.2020.10.032 |
0.692 |
|
| 2019 |
Reichenstein I, Eitan C, Diaz-Garcia S, Haim G, Magen I, Siany A, Hoye ML, Rivkin N, Olender T, Toth B, Ravid R, Mandelbaum AD, Yanowski E, Liang J, Rymer JK, et al. Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology. Science Translational Medicine. 11. PMID 31852800 DOI: 10.1126/Scitranslmed.Aav5264 |
0.567 |
|
| 2016 |
Eitan C, Hornstein E. Vulnerability of microRNA biogenesis in FTD-ALS. Brain Research. PMID 26778173 DOI: 10.1016/J.Brainres.2015.12.063 |
0.684 |
|
| 2016 |
Eitan C, Hornstein E. Vulnerability of microRNA biogenesis in FTD-ALS Brain Research. DOI: 10.1016/j.brainres.2015.12.063 |
0.712 |
|
| 2015 |
Emde A, Eitan C, Liou LL, Libby RT, Rivkin N, Magen I, Reichenstein I, Oppenheim H, Eilam R, Silvestroni A, Alajajian B, Ben-Dov IZ, Aebischer J, Savidor A, Levin Y, et al. Dysregulated miRNA biogenesis downstream of cellular stress and ALS-causing mutations: a new mechanism for ALS. The Embo Journal. 34: 2633-51. PMID 26330466 DOI: 10.15252/Embj.201490493 |
0.72 |
|
| 2015 |
Eitan C, Hornstein E. Astro-logics with microRNAs. The Embo Journal. 34: 1143-4. PMID 25736376 DOI: 10.15252/Embj.201591241 |
0.703 |
|
| 2014 |
Volk N, Paul ED, Haramati S, Eitan C, Fields BK, Zwang R, Gil S, Lowry CA, Chen A. MicroRNA-19b associates with Ago2 in the amygdala following chronic stress and regulates the adrenergic receptor beta 1. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 15070-82. PMID 25378171 DOI: 10.1523/Jneurosci.0855-14.2014 |
0.426 |
|
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