| Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA JR Riordan, JM Rommens, B Kerem, NOA Alon, R Rozmahel, Z Grzelczak, ... Science 245 (4922), 1066-1073, 1989 | 9563 | 1989 |
| Identification of the cystic fibrosis gene: genetic analysis B Kerem, JM Rommens, JA Buchanan, D Markiewicz, TK Cox, ... Science 245 (4922), 1073-1080, 1989 | 5738 | 1989 |
| Identification of the cystic fibrosis gene: chromosome walking and jumping JM Rommens, MC Iannuzzi, B Kerem, ML Drumm, G Melmer, M Dean, ... Science 245 (4922), 1059-1065, 1989 | 4479 | 1989 |
| Nucleotide deficiency promotes genomic instability in early stages of cancer development AC Bester, M Roniger, YS Oren, MM Im, D Sarni, M Chaoat, A Bensimon, ... Cell 145 (3), 435-446, 2011 | 974 | 2011 |
| The Relation between Genotype and Phenotype in Cystic Fibrosis — Analysis of the Most Common Mutation (ΔF508) E Kerem, M Corey, B Kerem, J Rommens, D Markiewicz, H Levison, ... New England Journal of Medicine 323 (22), 1517-1522, 1990 | 970 | 1990 |
| Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice C Castellani, H Cuppens, M Macek Jr, JJ Cassiman, E Kerem, P Durie, ... Journal of cystic fibrosis 7 (3), 179-196, 2008 | 899 | 2008 |
| Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene J Zielenski, R Rozmahel, D Bozon, B Kerem, Z Grzelczak, JR Riordan, ... Genomics 10 (1), 214-228, 1991 | 687 | 1991 |
| Gentamicin-Induced Correction of CFTR Function in Patients with Cystic Fibrosis and CFTR Stop Mutations M Wilschanski, Y Yahav, Y Yaacov, H Blau, L Bentur, J Rivlin, M Aviram, ... New England Journal of Medicine 349 (15), 1433-1441, 2003 | 646 | 2003 |
| Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene. B Kerem, J Zielenski, D Markiewicz, D Bozon, E Gazit, J Yahav, ... Proceedings of the National Academy of Sciences 87 (21), 8447-8451, 1990 | 577 | 1990 |
| Recommendations for the classification of diseases as CFTR-related disorders C Bombieri, M Claustres, K De Boeck, N Derichs, J Dodge, E Girodon, ... Journal of Cystic Fibrosis 10, S86-S102, 2011 | 509 | 2011 |
| Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial E Kerem, S Hirawat, S Armoni, Y Yaakov, D Shoseyov, M Cohen, ... The Lancet 372 (9640), 719-727, 2008 | 489 | 2008 |
| Developmental dyscalculia is a familial learning disability RS Shalev, O Manor, B Kerem, M Ayali, N Badichi, Y Friedlander, ... Journal of learning disabilities 34 (1), 59-65, 2001 | 439 | 2001 |
| A role for common fragile site induction in amplification of human oncogenes A Hellman, E Zlotorynski, SW Scherer, J Cheung, JB Vincent, DI Smith, ... Cancer cell 1 (1), 89-97, 2002 | 350 | 2002 |
| Nonsense-mediated mRNA decay affects nonsense transcript levels and governs response of cystic fibrosis patients to gentamicin L Linde, S Boelz, M Nissim-Rafinia, YS Oren, M Wilschanski, Y Yaacov, ... The Journal of clinical investigation 117 (3), 683-692, 2007 | 337 | 2007 |
| lannuzzi, MC, Collins, FS and Tsui, L.-C.(1989). Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA' JR Riordan, JM Rommens, BS Kerem, NOA Alon, R Rozmahel, ... Science 245, 1066-1073, 0 | 313 | |
| Molecular basis for expression of common and rare fragile sites E Zlotorynski, A Rahat, J Skaug, N Ben-Porat, E Ozeri, R Hershberg, ... Molecular and cellular biology 23 (20), 7143-7151, 2003 | 312 | 2003 |
| The presence of extra chromosomes leads to genomic instability V Passerini, E Ozeri-Galai, MS De Pagter, N Donnelly, S Schmalbrock, ... Nature communications 7 (1), 10754, 2016 | 310 | 2016 |
| Splicing regulation as a potential genetic modifier M Nissim-Rafinia, B Kerem TRENDS in Genetics 18 (3), 123-127, 2002 | 302 | 2002 |
| Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosis WK Lemna, GL Feldman, B Kerem, SD Fernbach, EP Zevkovich, ... New England Journal of Medicine 322 (5), 291-296, 1990 | 290 | 1990 |
| Human chromosome 7: DNA sequence and biology SW Scherer, J Cheung, JR MacDonald, LR Osborne, K Nakabayashi, ... Science 300 (5620), 767-772, 2003 | 278 | 2003 |