| Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘care for CMMRD’(C4CMMRD) K Wimmer, CP Kratz, HFA Vasen, O Caron, C Colas, N Entz-Werle, ... Journal of medical genetics 51 (6), 355-365, 2014 | 432 | 2014 |
| The anti-proliferative effect of sulindac and sulindac sulfide on HT-29 colon cancer cells: alterations in tumor suppressor and cell cycle-regulatory proteins. Y Goldberg, II Nassif, A Pittas, LL Tsai, BD Dynlacht, B Rigas, SJ Shiff Oncogene 12 (4), 893-901, 1996 | 217 | 1996 |
| Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D”(C4CMMR-D) HFA Vasen, Z Ghorbanoghli, F Bourdeaut, O Cabaret, O Caron, A Duval, ... Journal of medical genetics 51 (5), 283-293, 2014 | 199 | 2014 |
| Update on genetic predisposition to colorectal cancer and polyposis L Valle, RM de Voer, Y Goldberg, W Sjursen, A Försti, C Ruiz-Ponte, ... Molecular aspects of medicine 69, 10-26, 2019 | 150 | 2019 |
| Resistance to activated protein C and the Leiden mutation: high prevalence in patients with abruptio placentae Z Wiener-Megnagi, I Ben-Shlomo, Y Goldberg, E Shalev American journal of obstetrics and gynecology 179 (6), 1565-1567, 1998 | 147 | 1998 |
| Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in … M Koczkowska, T Callens, Y Chen, A Gomes, AD Hicks, A Sharp, E Johns, ... Human mutation 41 (1), 299-315, 2020 | 110 | 2020 |
| Clinical and ultrasonographic weight estimation in large for gestational age fetus Z Weiner, I Ben-Shlomo, R Beck-Fruchter, Y Goldberg, E Shalev European Journal of Obstetrics & Gynecology and Reproductive Biology 105 (1 …, 2002 | 110 | 2002 |
| Diagnosis of constitutional mismatch repair-deficiency syndrome based on microsatellite instability and lymphocyte tolerance to methylating agents S Bodo, C Colas, O Buhard, A Collura, J Tinat, N Lavoine, A Guilloux, ... Gastroenterology 149 (4), 1017-1029. e3, 2015 | 92 | 2015 |
| Laparoscopic resection of ovarian benign cystic teratomas: experience with 84 cases. E Shalev, M Bustan, S Romano, Y Goldberg, I Ben-Shlomo Human reproduction (Oxford, England) 13 (7), 1810-1812, 1998 | 80 | 1998 |
| Complete remission, in BRCA2 mutation carrier with metastatic pancreatic adenocarcinoma, treated with cisplatin based therapy A Sonnenblick, L Kadouri, L Appelbaum, T Peretz, M Sagi, Y Goldberg, ... Cancer biology & therapy 12 (3), 165-168, 2011 | 78 | 2011 |
| EU-Consortium Care for CMMRD (C4CMMRD). Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘care for CMMRD’(C4CMMRD) K Wimmer, CP Kratz, HF Vasen, O Caron, C Colas, N Entz-Werle, ... J Med Genet 51 (6), 355-365, 2014 | 75 | 2014 |
| Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group M Aronson, C Colas, A Shuen, H Hampel, WD Foulkes, HB Feldman, ... Journal of Medical Genetics 59 (4), 318-327, 2022 | 71 | 2022 |
| First trimester diagnosis of conjoined twins in a triplet pregnancy after IVF and ICSI: case report Y Goldberg, I Ben-Shlomo, E Weiner, E Shalev Human reproduction 15 (6), 1413-1415, 2000 | 65 | 2000 |
| Secondary cytomegalovirus infection can cause severe fetal sequelae despite maternal preconceptional immunity Y Zalel, Y Gilboa, M Berkenshtat, R Yoeli, R Auslander, R Achiron, ... Ultrasound in Obstetrics and Gynecology: The Official Journal of the …, 2008 | 64 | 2008 |
| Mutated MCM9 is associated with predisposition to hereditary mixed polyposis and colorectal cancer in addition to primary ovarian failure Y Goldberg, N Halpern, A Hubert, SN Adler, S Cohen, ... Cancer genetics 208 (12), 621-624, 2015 | 63 | 2015 |
| Double heterozygosity in the BRCA1 and BRCA2 genes in the Jewish population O Lavie, S Narod, F Lejbkowicz, S Dishon, Y Goldberg, O Gemer, ... Annals of oncology 22 (4), 964-966, 2011 | 60 | 2011 |
| Genetic predisposition to radiation induced sarcoma: possible role for BRCA and p53 mutations L Kadouri, M Sagi, Y Goldberg, I Lerer, T Hamburger, T Peretz Breast cancer research and treatment 140, 207-211, 2013 | 58 | 2013 |
| Neurofibromatosis type 1—an update and review for the primary pediatrician Y Goldberg, K Dibbern, J Klein, VM Riccardi, JM Graham Jr Clinical pediatrics 35 (11), 545-561, 1996 | 58 | 1996 |
| Antiphospholipid syndrome manifested by ischemic stroke in a patient with Crohn's disease D Mevorach, Y Goldberg, JM Gomori, D Rachmilewitz Journal of clinical gastroenterology 22 (2), 141-143, 1996 | 55 | 1996 |
| Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy M Suerink, T Ripperger, L Messiaen, FH Menko, F Bourdeaut, C Colas, ... Journal of medical genetics 56 (2), 53-62, 2019 | 52 | 2019 |
