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International Journal of Molecular Sciences|September 13, 2025
Nuclear Roles of Spliceosome-Associated microRNAs in Neuronal Cancer CellsShelly Mahlab-Aviv, Keren Or Swissa, Maram Arafat, et al.
Genetics|October 14, 2017
RL-SKAT: An Exact and Efficient Score Test for Heritability and Set TestsRegev Schweiger, Omer Weissbrod, Elior Rahmani, et al.
Blood|August 3, 2006
Apoptotic cell thrombospondin-1 and heparin-binding domain lead to dendritic-cell phagocytic and tolerizing statesAlon Krispin, Yaniv Bledi, Mizhir Atallah, et al.
Nucleic Acids Research|December 21, 2004
ProtoNet 4.0: a hierarchical classification of one million protein sequencesNoam Kaplan, Ori Sasson, Uri Inbar, et al.
Viruses|November 27, 2021
Identification of Hepatitis E Virus Genotypes 3 and 7 in Israel: A Public Health Concern?Rachel Shirazi, Paolo Pozzi, Yael Gozlan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2020
De novo STXBP1 mutation in a child with developmental delay and spasticity reveals a major structural alteration in the interface with syntaxin 1AEhud Banne, Tzipora Falik-Zaccai, Esther Brielle, et al.
Nature Communications|August 2, 2019
Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biologyElior Rahmani, Regev Schweiger, Brooke Rhead, et al.
Genome Biology|February 20, 2009
Protein function annotation by homology-based inferenceYaniv Loewenstein, Domenico Raimondo, Oliver C Redfern, et al.
Nature Communications|November 23, 2018
Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-testsRegev Schweiger, Eyal Fisher, Omer Weissbrod, et al.
The Journal of Biological Chemistry|June 17, 2003
Direct interaction of target SNAREs with the Kv2.1 channel. Modal regulation of channel activation and inactivation gatingIzhak Michaelevski, Dodo Chikvashvili, Sharon Tsuk, et al.
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