Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel
Abu Freha, Naim, Leibovici Weissman, Yaara, Fich, Alexander, Barnes Kedar, Inbal, Halpern, Marisa, Sztarkier, Ignacio, Behar, Doron M., Arbib Sneh, Orly, Vilkin, Alex, Baris, Hagit N., Gingold, Rachel, Lejbkowicz, Flavio, Niv, Yaron, Goldberg, Yael, Levi, Zohar
Published in Familial cancer (2018)
Published in Familial cancer (2018)
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Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity
Baris, Hagit N., Barnes-Kedar, Inbal, Toledano, Helen, Halpern, Marisa, Hershkovitz, Dov, Lossos, Alexander, Lerer, Israela, Peretz, Tamar, Kariv, Revital, Cohen, Shlomi, Half, Elizabeth E., Magal, Nurit, Drasinover, Valerie, Wimmer, Katharina, Goldberg, Yael, Bercovich, Dani, Levi, Zohar
Published in Pediatric blood & cancer (01.03.2016)
Published in Pediatric blood & cancer (01.03.2016)
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Familial Clustering of Site-Specific Cancer Risks Associated with BRCA1 and BRCA2 Mutations in the Ashkenazi Jewish Population
Simchoni, Sharon, Friedman, Eitan, Kaufman, Bella, Gershoni-Baruch, Ruth, Orr-Urtreger, Avi, Kedar-Barnes, Inbal, Shiri-Sverdlov, Ronit, Dagan, Efrat, Tsabari, Sigal, Shohat, Mordechai, Catane, Raphael, King, Mary-Claire, Lahad, Amnon, Levy-Lahad, Ephrat
Published in Proceedings of the National Academy of Sciences - PNAS (07.03.2006)
Published in Proceedings of the National Academy of Sciences - PNAS (07.03.2006)
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Counseling the at risk patient in the BRCA1 and BRCA2 Era
Barnes-Kedar, Inbal M, Plon, Sharon E
Published in Obstetrics and gynecology clinics of North America (01.06.2002)
Published in Obstetrics and gynecology clinics of North America (01.06.2002)
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The yield of full BRCA1/2 genotyping in Israeli high-risk breast/ovarian cancer patients who do not carry the predominant mutations
Barnes-Kedar, Inbal, Bernstein-Molho, Rinat, Ginzach, Nava, Hartmajer, Shulamit, Shapira, Tamar, Magal, Nurit, Kalis, Marina Lifshitc, Peretz, Tamar, Shohat, Mordechai, Basel-Salmon, Lina, Friedman, Eitan, Bazak, Lily, Goldberg, Yael
Published in Breast cancer research and treatment (01.11.2018)
Published in Breast cancer research and treatment (01.11.2018)
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The yield of full BRCA1/2 genotyping in Israeli Arab high-risk breast/ovarian cancer patients
Bernstein-Molho, Rinat, Barnes-Kedar, Inbal, Ludman, Mark D., Reznik, Gili, Feldman, Hagit Baris, Samra, Nadra Nasser, Eilat, Avital, Peretz, Tamar, Peretz, Lilach Peled, Shapira, Tamar, Magal, Nurit, Kalis, Marina Lifshitc, Yerushalmi, Rinat, Vinkler, Chana, Liberman, Sari, Basel-Salmon, Lina, Shohat, Mordechai, Levy-Lahad, Ephrat, Friedman, Eitan, Bazak, Lily, Goldberg, Yael
Published in Breast cancer research and treatment (01.11.2019)
Published in Breast cancer research and treatment (01.11.2019)
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Correspondence on "Neurocutaneous Syndromes and Brain Tumors"
Toledano, Helen, Barnes-Kedar, Inbal, Baris, Hagit N
Published in Journal of child neurology (01.06.2016)
Published in Journal of child neurology (01.06.2016)
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Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel
Yablonski-Peretz, Tamar, Paluch-Shimon, Shani, Gutman, Lior Soussan, Kaplan, Yulia, Dvir, Addie, Barnes-Kedar, Inbal, Kadouri, Luna, Semenisty, Valeriya, Efrat, Noa, Neiman, Victoria, Glasser, Yafit, Michaelson-Cohen, Rachel, Katz, Lior, Kaufman, Bella, Golan, Talia, Reish, Orit, Hubert, Ayala, Safra, Tamar, Yaron, Yuval, Friedman, Eitan
Published in Breast cancer research and treatment (01.01.2016)
Published in Breast cancer research and treatment (01.01.2016)
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Clinical Characteristics and Prognosis of Gastric Cancer Patients with BRCA 1/2 Germline Mutations: Report of Ten Cases and a Literature Review
Halpern, Naama, Grinshpun, Albert, Boursi, Ben, Golan, Talia, Margalit, Ofer, Aderka, Dan, Friedman, Eitan, Laitman, Yael, Hubert, Ayala, Kadouri, Luna, Hamburger, Tamar, Barnes-Kedar, Inbal, Levi, Zohar, Ben-Aharon, Irit, Brenner, Baruch, Goldberg, Yael, Peretz, Tamar, Shacham-Shmueli, Einat
Published in OncoTargets and therapy (01.01.2020)
Published in OncoTargets and therapy (01.01.2020)
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Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity: CMMRD, Founder Mutations, and Consanguinity in Israel
Baris, Hagit N., Barnes-Kedar, Inbal, Toledano, Helen, Halpern, Marisa, Hershkovitz, Dov, Lossos, Alexander, Lerer, Israela, Peretz, Tamar, Kariv, Revital, Cohen, Shlomi, Half, Elizabeth E., Magal, Nurit, Drasinover, Valerie, Wimmer, Katharina, Goldberg, Yael, Bercovich, Dani, Levi, Zohar
Published in Pediatric blood & cancer (01.03.2016)
Published in Pediatric blood & cancer (01.03.2016)
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Homozygosity of MSH2 c.1906G→C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I
Toledano, Helen, Goldberg, Yael, Kedar-Barnes, Inbal, Baris, Hagit, Porat, Rinnat M., Shochat, Chen, Bercovich, Dani, Pikarsky, Eli, Lerer, Israela, Yaniv, Isaac, Abeliovich, Dvorah, Peretz, Tamar
Published in Familial cancer (01.09.2009)
Published in Familial cancer (01.09.2009)
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Homozygosity of MSH2 c.1906G1C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I
Toledano, Helen, Goldberg, Yael, Kedar-Barnes, Inbal, Baris, Hagit, Porat, Rinnat M, Shochat, Chen, Bercovich, Dani, Pikarsky, Eli, Lerer, Israela, Yaniv, Isaac, Abeliovich, Dvorah, Peretz, Tamar
Published in Familial cancer (01.09.2009)
Published in Familial cancer (01.09.2009)
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