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Nature Genetics|September 6, 2000
Identification of the gene causing mucolipidosis type IVR Bargal, N Avidan, E Ben-Asher, et al.
Ciba Foundation Symposium|January 1, 1993
Olfactory receptors: transduction, diversity, human psychophysics and genome analysisD Lancet, N Ben-Arie, S Cohen, et al.
The Israel Medical Association Journal : IMAJ|November 4, 2000
Harvesting the human genome: the Israeli perspectiveE Ben-Asher, V Chalifa-Caspi, S Horn-Saban, et al.
Gene|December 6, 2001
The RUNX3 gene--sequence, structure and regulated expressionC Bangsow, N Rubins, G Glusman, et al.
Genomics|February 16, 2000
Sequence, structure, and evolution of a complete human olfactory receptor gene clusterG Glusman, A Sosinsky, E Ben-Asher, et al.
Human Mutation|April 24, 2001
Mucolipidosis type IV: novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish populationR Bargal, N Avidan, T Olender, et al.
American Journal of Human Genetics|November 13, 2001
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelH Lahat, E Pras, T Olender, et al.
DNA and Cell Biology|September 1, 1991
The UDP glucuronosyltransferase gene superfamily: suggested nomenclature based on evolutionary divergenceB Burchell, D W Nebert, D R Nelson, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 3, 2017
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavinG Heimer, E Eyal, X Zhu, et al.
Clinical Genetics|April 5, 2016
A role for TENM1 mutations in congenital general anosmiaA Alkelai, T Olender, R Haffner-Krausz, et al.
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