| Candidate gene for the chromosome 1 familial Alzheimer's disease locus E Levy-Lahad, W Wasco, P Poorkaj, DM Romano, J Oshima, ... Science 269 (5226), 973-977, 1995 | 3577 | 1995 |
| Secreted amyloid β–protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to … D Scheuner, C Eckman, M Jensen, X Song, M Citron, N Suzuki, TD Bird, ... Nature medicine 2 (8), 864-870, 1996 | 3559 | 1996 |
| X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy RS Wildin, F Ramsdell, J Peake, F Faravelli, JL Casanova, N Buist, ... Nature genetics 27 (1), 18-20, 2001 | 2309 | 2001 |
| A familial Alzheimer's disease locus on chromosome 1 E Levy-Lahad, EM Wijsman, E Nemens, L Anderson, KAB Goddard, ... Science 269 (5226), 970-973, 1995 | 1110 | 1995 |
| 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 | 650 | 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 | 579 | 2007 |
| Cancer risks among BRCA1 and BRCA2 mutation carriers E Levy-Lahad, E Friedman British journal of cancer 96 (1), 11-15, 2007 | 466 | 2007 |
| Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families. E Levy-Lahad, R Catane, S Eisenberg, B Kaufman, G Hornreich, ... American journal of human genetics 60 (5), 1059, 1997 | 403 | 1997 |
| 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 | 392 | 1997 |
| Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood G Toperoff, D Aran, JD Kark, M Rosenberg, T Dubnikov, B Nissan, ... Human molecular genetics 21 (2), 371-383, 2012 | 381 | 2012 |
| 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 | 374 | 2014 |
| Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome SB Pierce, T Walsh, KM Chisholm, MK Lee, AM Thornton, A Fiumara, ... The American Journal of Human Genetics 87 (2), 282-288, 2010 | 297 | 2010 |
| Population-based screening for BRCA1 and BRCA2: 2014 Lasker Award MC King, E Levy-Lahad, A Lahad Jama 312 (11), 1091-1092, 2014 | 291 | 2014 |
| New ISSCR guidelines underscore major principles for responsible translational stem cell research I Hyun, O Lindvall, L Ährlund-Richter, E Cattaneo, M Cavazzana-Calvo, ... Cell stem cell 3 (6), 607-609, 2008 | 272 | 2008 |
| 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 | 262 | 2001 |
| Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families Z Brownstein, LM Friedman, H Shahin, V Oron-Karni, N Kol, AA Rayyan, ... Genome biology 12, 1-11, 2011 | 231 | 2011 |
| Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome SB Pierce, K Gersak, R Michaelson-Cohen, T Walsh, MK Lee, D Malach, ... The American Journal of Human Genetics 92 (4), 614-620, 2013 | 228 | 2013 |
| 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 |
| Replacement therapy with imiglucerase for type 1 Gaucher's disease. A Zimran, D Elstein, E Levy-Lahad, S Zevin, I Hadas-Halpern, Y Bar-Ziv, ... Lancet (London, England) 345 (8963), 1479-1480, 1995 | 164 | 1995 |
| 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 |
