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Clinical and Experimental Rheumatology|October 5, 2011
MEFV, TNFRSF1A and CARD15 mutation analysis in Behçet's diseaseYoav Baruch, Efrat Dagan, Itzhak Rosner, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|January 29, 2019
The association between patients' perceived continuity of care and beliefs about oral anticancer treatmentOrit Cohen Castel, Efrat Shadmi, Lital Keinan-Boker, et al.
Pediatric Pulmonology|January 30, 2013
Duplication in CHIT1 gene and the risk for Aspergillus lung disease in CF patientsGalit Livnat, Ronen Bar-Yoseph, Adi Mory, et al.
Dementia and Geriatric Cognitive Disorders|July 25, 2016
LRRK2, GBA and SMPD1 Founder Mutations and Parkinson's Disease in Ashkenazi JewsEfrat Dagan, Ilana Schlesinger, Alina Kurolap, et al.
Familial Cancer|May 8, 2004
The 1100delAT BRCA1 and the 8765delAG BRCA2 mutations: occurrence in high-risk non-Ashkenazi Jews and haplotype comparison of Jewish and non-Jewish carriersInbar Gal, Ruth Gershoni Baruch, Daniel Haber, et al.
European Journal of Cancer (Oxford, England : 1990)|April 21, 2006
A specific RAD51 haplotype increases breast cancer risk in Jewish non-Ashkenazi high-risk womenInabr Gal, Gad Kimmel, Ruth Gershoni-Baruch, et al.
European Journal of Human Genetics : EJHG|July 25, 2013
A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindredAdi Mory, Francesc X Ruiz, Efrat Dagan, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
BRCA1/2 mutations and FMR1 alleles are randomly distributed: a case control studyEfrat Dagan, Yoram Cohen, Adi Mory, et al.
Familial Cancer|September 1, 2006
The 471delAAAG mutation and C353T polymorphism in the RNASEL gene in sporadic and inherited cancer in IsraelEfrat Dagan, Yael Laitman, Nurit Levanon, et al.
Pediatric Neurology|March 18, 2014
Kohlschutter-Tonz syndrome: clinical and genetic insights gained from 16 cases deriving from a close-knit village in Northern IsraelAdi Mory, Efrat Dagan, Ishai Shahor, et al.
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