Traumatic Brain Injury, Boredom and Depression

por Goldberg, Yael, Danckert, James
Publicado 2013

Nonmalignant Features Associated with Inherited Colorectal Cancer Syndromes-Clues for Diagnosis

por Haimov, Diana, Lieberman, Sari, Castellvi-Bel, Sergi, Nielsen, Maartje, Goldberg, Yael
Publicado 2022

In-silico phenotype prediction by normal mode variant analysis in TUBB4A-related disease

por Fellner, Avi, Goldberg, Yael, Lev, Dorit, Basel-Salmon, Lina, Shor, Oded, Benninger, Felix
Publicado 2022

Clinical course and outcome of patients with high-level microsatellite instability cancers in a real-life setting: a retrospective analysis

por Halpern, Naama, Goldberg, Yael, Kadouri, Luna, Duvdevani, Morasha, Hamburger, Tamar, Peretz, Tamar, Hubert, Ayala
Publicado 2017

MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence

por Goldberg, Yael, Aleme, Ola, Peled-Perets, Lilach, Castellvi-Bel, Sergi, Nielsen, Maartje, Shalev, Stavit A.
Publicado 2021

Low Doses of Ionizing Radiation as a Treatment for Alzheimer’s Disease: A Pilot Study

por Cuttler, Jerry M., Abdellah, Eslam, Goldberg, Yael, Al-Shamaa, Sarmad, Symons, Sean P., Black, Sandra E., Freedman, Morris
Publicado 2021

OMIC-08. COMPOUND HETEROZYGOSITY OF POLE AND PMS2 LEADS TO CMMRD-LIKE PHENOTYPE- “POLYNCH” SYNDROME

por Michaeli, Orli, Ladany, Hagay, Maruvka, Yosef E, Erez, Ayelet, Shachar, Shay Ben, Izraeli, Shai, Goldberg, Yael, Toledano, Helen
Publicado 2021

Microdeletion of 16q24.1–q24.2—A unique etiology of Lymphedema–Distichiasis syndrome and neurodevelopmental disorder

por Michelson, Marina, Lidzbarsky, Gabriel, Nishri, Daniella, Israel‐Elgali, Ifat, Berger, Rachel, Gafner, Michal, Shomron, Noam, Lev, Dorit, Goldberg, Yael
Publicado 2022

BRCA mutations detected by tumour next-generation sequencing in non-small cell lung cancer: impact on response to therapy and disease course

por Tschernichovsky, Roi, Averbuch, Itamar, Goldstein, Daniel Alex, Mutai, Raz, Dudnik, Elizabeth, Rotem, Ofer, Laufer-Geva, Smadar, Peled, Nir, Goldberg, Yael, Zer, Alona
Publicado 2023

Molecular functions of MCM8 and MCM9 and their associated pathologies

por Helderman, Noah Cornelis, Terlouw, Diantha, Bonjoch, Laia, Golubicki, Mariano, Antelo, Marina, Morreau, Hans, van Wezel, Tom, Castellví-Bel, Sergi, Goldberg, Yael, Nielsen, Maartje
Publicado 2023

Correlations between pathogenic variants in DNA repair genes and anticancer treatment efficacy in stage IV non‐small cell lung cancer: A large real‐world cohort and review of the l...

por Averbuch, Itamar, Tschernichovsky, Roi, Icht, Oded, Goldstein, Daniel A., Mutai, Raz, Dudnik, Elizabeth, Rotem, Ofer, Peled, Nir, Allen, Aaron M., Laufer‐Geva, Smadar, Goldberg, Yael, Zer, Alona
Publicado 2023

Phenotypic diversity among juvenile polyposis syndrome patients from different ethnic background

por Katz, Lior Haim, Gingold-Belfer, Rachel, Vainer, Elez, Hegger, Shani, Laish, Ido, Derazne, Estela, Weintraub, Ilana, Reznick-Levi, Gili, Goldberg, Yael, Levi, Zohar, Cohen, Shlomi, Half, Elizabeth E.
Publicado 2022

Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of Wolframin

por Wilf-Yarkoni, Adi, Shor, Oded, Fellner, Avi, Hellmann, Mark Andrew, Pras, Elon, Yonath, Hagit, Shkedi-Rafid, Shiri, Basel-Salmon, Lina, Bazak, Lili, Eliahou, Ruth, Greenbaum, Lior, Stiebel-Kalish, Hadas, Benninger, Felix, Goldberg, Yael
Publicado 2021

Clinical Characteristics and Prognosis of Gastric Cancer Patients with BRCA 1/2 Germline Mutations: Report of Ten Cases and a Literature Review

por 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
Publicado 2020

Treatment inferred from mutations identified using massive parallel sequencing leads to clinical benefit in some heavily pretreated cancer patients

por Zick, Aviad, Peretz, Tamar, Lotem, Michal, Hubert, Ayala, Katz, Daniela, Temper, Mark, Rottenberg, Yakir, Uziely, Beatrice, Nechushtan, Hovav, Meirovitz, Amichai, Sonnenblick, Amir, Sapir, Eli, Edelman, David, Goldberg, Yael, Lossos, Alexander, Rosenberg, Shai, Fried, Iris, Finklstein, Ruth, Pikarsky, Eli, Goldshmidt, Hanoch
Publicado 2017

Constitutional mismatch repair deficiency–associated brain tumors: report from the European C4CMMRD consortium

por Guerrini-Rousseau, Léa, Varlet, Pascale, Colas, Chrystelle, Andreiuolo, Felipe, Bourdeaut, Franck, Dahan, Karin, Devalck, Christine, Faure-Conter, Cécile, Genuardi, Maurizio, Goldberg, Yael, Kuhlen, Michaela, Moalla, Salma, Opocher, Enrico, Perez-Alonso, Vanessa, Sehested, Astrid, Slavc, Irene, Unger, Sheila, Wimmer, Katharina, Grill, Jacques, Brugières, Laurence
Publicado 2019

Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay

por Eliyahu, Aviva, Barel, Ortal, Greenbaum, Lior, Zaks Hoffer, Gal, Goldberg, Yael, Raas-Rothschild, Annick, Singer, Amihood, Bar-Joseph, Ifat, Kunik, Vered, Javasky, Elisheva, Staretz-Chacham, Orna, Pode-Shakked, Naomi, Bazak, Lily, Ruhrman-Shahar, Noa, Pras, Elon, Frydman, Moshe, Shohat, Mordechai, Pode-Shakked, Ben
Publicado 2022

Vici syndrome in Israel: Clinical and molecular insights

por Chorin, Odelia, Hirsch, Yoel, Rock, Rachel, Salzer Sheelo, Liat, Goldberg, Yael, Mandel, Hanna, Hershkovitz, Tova, Fleischer, Nicole, Greenbaum, Lior, Katz, Uriel, Barel, Ortal, Hamed, Nasrin, Ben-Zeev, Bruria, Greenberger, Shoshana, Nasser Samra, Nadra, Stern Zimmer, Michal, Raas-Rothschild, Annick, Pode-Shakked, Ben
Publicado 2022

Variable Features of Juvenile Polyposis Syndrome With Gastric Involvement Among Patients With a Large Genomic Deletion of BMPR1A

por Lieberman, Sari, Beeri, Rachel, Walsh, Tom, Schechter, Menachem, Keret, Dan, Half, Elizabet, Gulsuner, Suleyman, Tomer, Ariela, Jacob, Harold, Cohen, Shlomi, Basel-Salmon, Lina, Mansur, Mahmud, Berger, Rachel, Katz, Lior H., Golomb, Eliahu, Peretz, Tamar, Levy, Zohar, Kedar, Inbal, King, Mary-Claire, Levy-Lahad, Ephrat, Goldberg, Yael
Publicado 2019

Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome

por Golubicki, Mariano, Bonjoch, Laia, Acuña-Ochoa, José G., Díaz-Gay, Marcos, Muñoz, Jenifer, Cuatrecasas, Miriam, Ocaña, Teresa, Iseas, Soledad, Mendez, Guillermo, Cisterna, Daniel, Schubert, Stephanie A., Nielsen, Maartje, van Wezel, Tom, Goldberg, Yael, Pikarsky, Eli, Robbio, Juan, Roca, Enrique, Castells, Antoni, Balaguer, Francesc, Antelo, Marina, Castellví-Bel, Sergi
Publicado 2020