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Autophagy|February 27, 2013
TECPR2: a new autophagy link for neurodegenerationDanit Oz-Levi, Amir Gelman, Zvulun Elazar, et al.
Biomedical Engineering Online|August 24, 2017
Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElectNoa Rappaport, Simon Fishilevich, Ron Nudel, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|February 19, 2022
Effective bubble-based testing for SARS-CoV-2 using swab-poolingYuval Cohen, Nadav Bamberger, Orna Mor, et al.
Human Genomics|December 14, 2011
In-silico human genomics with GeneCardsGil Stelzer, Irina Dalah, Tsippi Iny Stein, et al.
JCI Insight|December 20, 2024
Talin1 dysfunction is genetically linked to systemic capillary leak syndromeNaama Elefant, Georgia Rouni, Christina Arapatzi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 7, 2015
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disabilityGali Heimer, Danit Oz-Levi, Eran Eyal, et al.
BMC Genomics|July 1, 2016
VarElect: the phenotype-based variation prioritizer of the GeneCards SuiteGil Stelzer, Inbar Plaschkes, Danit Oz-Levi, et al.
American Journal of Human Genetics|November 27, 2012
Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesisDanit Oz-Levi, Bruria Ben-Zeev, Elizabeth K Ruzzo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 16, 2015
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 triosXiaolin Zhu, Slavé Petrovski, Pingxing Xie, et al.
Nature|June 21, 2019
Noncoding deletions reveal a gene that is critical for intestinal functionDanit Oz-Levi, Tsviya Olender, Ifat Bar-Joseph, et al.
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