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American Journal of Human Genetics|October 1, 2013
Cole Disease Results from Mutations in ENPP1Ori Eytan, Fanny Morice-Picard, Ofer Sarig, et al.
Harefuah|February 20, 2019
[THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES]Dror Sharon, Tamar Ben-Yosef, Eran Pras, et al.
Journal of Medical Internet Research|July 14, 2025
Performance of Large Language Models in Numerical Versus Semantic Medical Knowledge: Cross-Sectional Benchmarking Study on Evidence-Based Questions and AnswersEden Avnat, Michal Levy, Daniel Herstain, et al.
Clinical & Experimental Ophthalmology|February 16, 2025
Characterisation of SLC38A8 and Its Role in Retinal Pathways and DiseaseChen Weiner, Idan Hecht, Jiri Lindovsky, et al.
Gene|January 17, 2017
X-linked elliptocytosis with impaired growth is related to mutated AMMECR1Lina Basel-Vanagaite, Nir Pillar, Ofer Isakov, et al.
Plos Neglected Tropical Diseases|January 26, 2016
Whole-Genome Sequencing Analysis from the Chikungunya Virus Caribbean Outbreak Reveals Novel Evolutionary Genomic ElementsKenneth A Stapleford, Gonzalo Moratorio, Rasmus Henningsson, et al.
JAMA Neurology|March 16, 2026
Safety and Efficacy of PrimeC in Amyotrophic Lateral Sclerosis: The PARADIGM Randomized Clinical TrialMerit Cudkowicz, Vivian E Drory, Adriano Chio, et al.
ACS Nano|January 28, 2016
Identification of Dormancy-Associated MicroRNAs for the Design of Osteosarcoma-Targeted Dendritic Polyglycerol NanopolyplexesGalia Tiram, Ehud Segal, Adva Krivitsky, et al.
Human Mutation|February 18, 2021
Re-evaluating the pathogenicity of the c.783+2T>C BAP1 germline variantYael Goldberg, Yael Laitman, Merav Ben David, et al.
The Journal of Investigative Dermatology|June 29, 2021
Slow Transcription of the 99a/let-7c/125b-2 Cluster Results in Differential MiRNA Expression and Promotes Melanoma Phenotypic PlasticityDanna Sheinboim, Shivang Parikh, Roma Parikh, et al.
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