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Rheumatology International|July 7, 2009
MEFV, TNF1rA, CARD15 and NLRP3 mutation analysis in PFAPAEfrat Dagan, Ruth Gershoni-Baruch, Ihab Khatib, et al.
Genetic Testing and Molecular Biomarkers|June 11, 2014
"I do not want my baby to suffer as I did"; prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: a case report and genetic counseling considerationsEfrat Dagan, Ruth Gershoni-Baruch, Alina Kurolap, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Androgen receptor CAG repeat length in Jewish Israeli women who are BRCA1/2 mutation carriers: association with breast/ovarian cancer phenotypeEfrat Dagan, Eitan Friedman, Tamar Paperna, et al.
Pediatric Diabetes|December 31, 2019
Glycemic control in adolescents with type 1 diabetes: Are computerized simulations effective learning tools?Ilana Dubovi, Sharona T Levy, Milana Levy, et al.
Journal of Advanced Nursing|June 15, 2019
Adherence to diabetes care: Knowledge of biochemical processes has a high impact on glycaemic control among adolescents with type 1 diabetesEfrat Dagan, Ilana Dubovi, Milana Levy, et al.
Nurse Education Today|December 8, 2017
Nursing students learning the pharmacology of diabetes mellitus with complexity-based computerized models: A quasi-experimental studyIlana Dubovi, Efrat Dagan, Ola Sader Mazbar, et al.
Lymphatic Research and Biology|June 20, 2015
A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary LymphedemaSvetlana Melikhan-Revzin, Alina Kurolap, Efrat Dagan, et al.
Frontiers in Genetics|May 25, 2023
Privacy and utility of genetic testing in families with hereditary cancer syndromes living in three countries: the international cascade genetic screening experienceSivia Barnoy, Efrat Dagan, Sue Kim, et al.
Journal of General Internal Medicine|March 26, 2021
Patients' Perceived Continuity of Care and Adherence to Oral Anticancer Therapy: a Prospective Cohort Mediation StudyOrit Cohen Castel, Efrat Dagan, Lital Keinan-Boker, et al.
Genetic Testing and Molecular Biomarkers|August 25, 2011
Vascular behcet and mutations in thrombogenic genes: methylene tetrahydrofolate reductase, factor V, and prothrombinEfrat Dagan, Yoav Baruch, Massimo Fiorilli, et al.
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