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Efrat Dagan

university of haifa

22H指数
78论文数
1.7K被引数
收录论文 34
发表时间
Staying in the Unknown: Avoidance of Genetic Testing in Families With Hereditary Cancer Syndromes—A Qualitative Study滞留于未知:遗传性癌症综合征家庭的基因检测回避——一项定性研究
err2026-09-07
err0
errOAAI
errRonit G. Tsemach; Elizabeth E. Half; Hagit Baris-Feldman; Anastasia Weis; Sharon Simchoni; Sue Kim; Maria C. Katapodi; Sivia Barnoy; Efrat Dagan
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Glycemic control in adolescents with type 1 diabetes: Are computerized simulations effective learning tools?
err2020-01-09
err9
errOAAI
errDubovi, Ilana; Levy, Sharona T.; Levy, Milana; Levin, Nehama Zuckerman; Dagan, Efrat
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EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy
errBRAIN
IF11.7
err2016-02-25
err94
errOAAI
errByrne, Susan; Jansen, Lara; U-King-Im, Jean-Marie; Siddiqui, Ata; Lidov, Hart G. W.; Bodi, Istvan; Smith, Luke; Mein, Rachael; Cullup, Thomas; Dionisi-Vici, Carlo; Al-Gazali, Lihadh; Al-Owain, Mohammed; Bruwer, Zandre; Al Thihli, Khalid; El-Garhy, Rana; Flanigan, Kevin M.; Manickam, Kandamurugu; Zmuda, Erik; Banks, Wesley; Gershoni-Baruch, Ruth; Mandel, Hanna; Dagan, Efrat; Raas-Rothschild, Annick; Barash, Hila; Filloux, Francis; Creel, Donnell; Harris, Michael; Hamosh, Ada; Koelker, Stefan; Ebrahimi-Fakhari, Darius; Hoffmann, Georg F.; Manchester, David; Boyer, Philip J.; Manzur, Adnan Y.; Lourenco, Charles Marques; Pilz, Daniela T.; Kamath, Arveen; Prabhakar, Prab; Rao, Vamshi K.; Rogers, R. Curtis; Ryan, Monique M.; Brown, Natasha J.; McLean, Catriona A.; Said, Edith; Schara, Ulrike; Stein, Anja; Sewry, Caroline; Travan, Laura; Wijburg, Frits A.; Zenker, Martin; Mohammed, Shehla; Fanto, Manolis; Gautel, Mathias; Jungbluth, Heinz
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SMPD1 mutations and Parkinson disease Response
err2015-10-01
err9
PREAI
errDagan, E.; Adir, V.; Schlesinger, I.; Borochowitz, Z.; Ayoub, M.; Mory, A.; Nassar, M.; Kurolap, A.; Aharon-Peretz, J.; Gershoni-Baruch, R.
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The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews
err2015-09-01
err53
PREAI
errDagan, E.; Schlesinger, I.; Ayoub, M.; Mory, A.; Nassar, M.; Kurolap, A.; Peretz-Aharon, J.; Gershoni-Baruch, R.
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What do women want? Fertility preservation preferences of young Israeli breast cancer patients
errBREAST
IF7.9
err2014-11-01
err0
PREAI
errDagan, E.; Gatengo-Modiano, S.; Birenbaum-Carmel, D. I.
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Kohlschutter-Tonz Syndrome: Clinical and Genetic Insights Gained From 16 Cases Deriving From a Close-Knit Village in Northern Israel
err2014-04-01
err17
PREAI
errMory, Adi; Dagan, Efrat; Shahor, Ishai; Mandel, Hanna; Illi, Barbara; Zolotushko, Jenny; Kurolap, Alina; Chechik, Emilia; Valente, Enza M.; Amselem, Serge; Gershoni-Baruch, Ruth
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BRCA1/2 mutations and FMR1 alleles are randomly distributed: a case control
err2013-11-27
err8
errOAAI
errDagan, Efrat; Cohen, Yoram; Mory, Adi; Adir, Vardit; Borochowitz, Zvi; Raanani, Hila; Kurolap, Alina; Melikhan-Revzin, Svetlana; Meirow, Dror; Gershoni-Baruch, Ruth
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A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred
err2013-07-24
err22
errOAAI
errMory, Adi; Ruiz, Francesc X.; Dagan, Efrat; Yakovtseva, Evgenia A.; Kurolap, Alina; Pares, Xavier; Farres, Jaume; Gershoni-Baruch, Ruth
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A Nonsense Mutation in the Human Homolog of Drosophila rogdi Causes Kohlschutter-Tonz Syndrome
err2012-04-01
err26
errOAAI
errMory, Adi; Dagan, Efrat; Illi, Barbara; Duquesnoy, Philippe; Mordechai, Shikma; Shahor, Ishai; Romani, Sveva; Hawash-Moustafa, Nivin; Mandel, Hanna; Valente, Enza M.; Amselem, Serge; Gershoni-Baruch, Ruth
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The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers
err2012-03-13
err60
PREAI
errInzelberg, R.; Cohen, O. S.; Aharon-Peretz, J.; Schlesinger, I.; Gershoni-Baruch, R.; Djaldetti, R.; Nitsan, Z.; Ephraty, L.; Tunkel, O.; Kozlova, E.; Inzelberg, L.; Kaplan, N.; Mehr, T. Fixler; Mory, A.; Dagan, E.; Schechtman, E.; Friedman, E.; Hassin-Baer, S.
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A follow-up study on men tested for BRCA1/BRCA2 mutations: impacts and coping processes
err2011-12-02
err20
PREAI
errShiloh, Shoshana; Dagan, Efrat; Friedman, Irit; Blank, Natalie; Friedman, Eitan
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Germline mutations in BRCA1 and BRCA2 genes in ethnically diverse high risk families in Israel
err2010-10-20
err25
PREAI
errLaitman, Yael; Borsthein, Roni Tsipora; Stoppa-Lyonnet, Dominique; Dagan, Efrat; Castera, Laurent; Goislard, Maud; Gershoni-Baruch, Ruth; Goldberg, Hadassah; Kaufman, Bella; Ben-Baruch, Noa; Zidan, Jamal; Maray, Taiseer; Soussan-Gutman, Lior; Friedman, Eitan
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