| Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy P Navon Elkan, SB Pierce, R Segel, T Walsh, J Barash, S Padeh, ... New England Journal of Medicine 370 (10), 921-931, 2014 | 649 | 2014 |
| A dual role for interleukin-1 in hippocampal-dependent memory processes I Goshen, T Kreisel, H Ounallah-Saad, P Renbaum, Y Zalzstein, ... Psychoneuroendocrinology 32 (8-10), 1106-1115, 2007 | 578 | 2007 |
| Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia M Kaplan, P Renbaum, E Levy-Lahad, C Hammerman, A Lahad, ... Proceedings of the National Academy of Sciences 94 (22), 12128-12132, 1997 | 391 | 1997 |
| Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2 E Gabai-Kapara, A Lahad, B Kaufman, E Friedman, S Segev, P Renbaum, ... Proceedings of the National Academy of Sciences 111 (39), 14205-14210, 2014 | 371 | 2014 |
| A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers E Levy-Lahad, A Lahad, S Eisenberg, E Dagan, T Paperna, L Kasinetz, ... Proceedings of the National Academy of Sciences 98 (6), 3232-3236, 2001 | 263 | 2001 |
| Cloning, characterization, and expression in Escherichia coli of the gene coding for the CpG DNA methylase from Spiroplasma sp. strain MQ1 (M Sssl) P Renbaum, D Abrahamove, A Fainsod, GG Wilson, S Rottem, A Razin Nucleic acids research 18 (5), 1145-1152, 1990 | 255 | 1990 |
| Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene P Renbaum, E Kellerman, R Jaron, D Geiger, R Segel, M Lee, MC King, ... The American Journal of Human Genetics 85 (2), 281-289, 2009 | 181 | 2009 |
| Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes M Kaplan, E Beutler, HJ Vreman, C Hammerman, E Levy-Lahad, ... Pediatrics 104 (1), 68-74, 1999 | 162 | 1999 |
| Suppression of growth of renal carcinoma cells by the von Hippel-Lindau tumor suppressor gene F Chen, T Kishida, FM Duh, P Renbaum, ML Orcutt, L Schmidt, B Zbar Cancer research 55 (21), 4804-4807, 1995 | 161 | 1995 |
| Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population A Shaag, T Walsh, P Renbaum, T Kirchhoff, K Nafa, S Shiovitz, ... Human molecular genetics 14 (4), 555-563, 2005 | 148 | 2005 |
| XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription D Zangen, Y Kaufman, S Zeligson, S Perlberg, H Fridman, M Kanaan, ... The American Journal of Human Genetics 89 (4), 572-579, 2011 | 118 | 2011 |
| Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish population M Horowitz, M Pasmanik‐Chor, Z Borochowitz, T Falik‐Zaccai, ... Human mutation 12 (4), 240-244, 1998 | 116 | 1998 |
| Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure Y Tenenbaum-Rakover, A Weinberg-Shukron, P Renbaum, O Lobel, ... Journal of medical genetics 52 (6), 391-399, 2015 | 110 | 2015 |
| Is uterine serous papillary carcinoma a BRCA1-related disease? Case report and review of the literature G Hornreich, U Beller, O Lavie, P Renbaum, Y Cohen, E Levy-Lahad Gynecologic oncology 75 (2), 300-304, 1999 | 99 | 1999 |
| Single nucleotide polymorphisms that increase expression of the guanosine triphosphatase RAC1 are associated with ulcerative colitis AM Muise, T Walters, W Xu, G Shen–Tu, CH Guo, R Fattouh, GY Lam, ... Gastroenterology 141 (2), 633-641, 2011 | 92 | 2011 |
| A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis A Weinberg-Shukron, P Renbaum, R Kalifa, S Zeligson, Z Ben-Neriah, ... The Journal of Clinical Investigation 125 (11), 4295-4304, 2015 | 90 | 2015 |
| Essential Role of BRCA2 in Ovarian Development and Function A Weinberg-Shukron, M Rachmiel, P Renbaum, S Gulsuner, T Walsh, ... New England Journal of Medicine 379 (11), 1042-1049, 2018 | 85 | 2018 |
| FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cells M Avitzour, H Mor-Shaked, S Yanovsky-Dagan, S Aharoni, G Altarescu, ... Stem Cell Reports 3 (5), 699-706, 2014 | 78 | 2014 |
| Non-invasive prenatal diagnosis using cell-free fetal DNA in maternal plasma from PGD pregnancies Y Li, G Altarescu, P Renbaum, T Eldar-Geva, E Levy-Lahad, ... Reproductive BioMedicine Online 19 (5), 714-720, 2009 | 77 | 2009 |
| Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates M Kaplan, C Hammerman, P Renbaum, G Klein, E Levy-Lahad The Lancet 356 (9230), 652-653, 2000 | 76 | 2000 |
