| Potential adverse effects of resveratrol: A literature review A Shaito, AM Posadino, N Younes, H Hasan, S Halabi, D Alhababi, ... International journal of molecular sciences 21 (6), 2084, 2020 | 562 | 2020 |
| Spectral karyotyping suggests additional subsets of colorectal cancers characterized by pattern of chromosome rearrangement WM Abdel-Rahman, K Katsura, W Rens, PA Gorman, D Sheer, D Bicknell, ... Proceedings of the National Academy of Sciences 98 (5), 2538-2543, 2001 | 211 | 2001 |
| Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency TT Nieminen, MF O’Donohue, Y Wu, H Lohi, SW Scherer, AD Paterson, ... Gastroenterology 147 (3), 595-598. e5, 2014 | 178 | 2014 |
| Molecular analysis of familial endometrial carcinoma: a manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome? M Ollikainen, WM Abdel-Rahman, AL Moisio, A Lindroos, R Kariola, ... Journal of clinical oncology 23 (21), 4609-4616, 2005 | 167 | 2005 |
| Is gastric cancer part of the tumour spectrum of hereditary non-polyposis colorectal cancer? A molecular genetic study A Gylling, WM Abdel-Rahman, M Juhola, K Nuorva, E Hautala, ... Gut 56 (7), 926-933, 2007 | 148 | 2007 |
| The genetics of HNPCC: application to diagnosis and screening WM Abdel-Rahman, JP Mecklin, P Peltomäki Critical reviews in oncology/hematology 58 (3), 208-220, 2006 | 142 | 2006 |
| The endocrine disruptor bisphenol A (BPA) exerts a wide range of effects in carcinogenesis and response to therapy SA Hafezi, WM Abdel-Rahman Current molecular pharmacology 12 (3), 230-238, 2019 | 127 | 2019 |
| Molecular analysis of endometrial tumorigenesis: importance of complex hyperplasia regardless of atypia TT Nieminen, A Gylling, WM Abdel-Rahman, K Nuorva, M Aarnio, ... Clinical Cancer Research 15 (18), 5772-5783, 2009 | 124 | 2009 |
| Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer E Renkonen, Y Zhang, H Lohi, R Salovaara, WM Abdel-Rahman, ... Journal of clinical oncology 21 (19), 3629-3637, 2003 | 121 | 2003 |
| Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations WM Abdel-Rahman, M Ollikainen, R Kariola, HJ Järvinen, JP Mecklin, ... Oncogene 24 (9), 1542-1551, 2005 | 114 | 2005 |
| Epigenetic signatures of familial cancer are characteristic of tumor type and family category EI Joensuu, WM Abdel-Rahman, M Ollikainen, S Ruosaari, S Knuutila, ... Cancer research 68 (12), 4597-4605, 2008 | 111 | 2008 |
| Differential cancer predisposition in Lynch syndrome: insights from molecular analysis of brain and urinary tract tumors AHS Gylling, TT Nieminen, WM Abdel-Rahman, K Nuorva, M Juhola, ... Carcinogenesis 29 (7), 1351-1359, 2008 | 106 | 2008 |
| Adenomatous Polyposis Families That Screen APC Mutation–Negative by Conventional Methods Are Genetically Heterogeneous ET Renkonen, P Nieminen, WM Abdel-Rahman, AL Moisio, I Järvelä, ... Journal of Clinical Oncology 23 (24), 5651-5659, 2005 | 105 | 2005 |
| Patterns of PIK3CA alterations in familial colorectal and endometrial carcinoma M Ollikainen, A Gylling, M Puputti, NN Nupponen, WM Abdel‐Rahman, ... International Journal of Cancer 121 (4), 915-920, 2007 | 84 | 2007 |
| Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach M Ollikainen, U Hannelius, CM Lindgren, WM Abdel-Rahman, J Kere, ... Oncogene 26 (31), 4541-4549, 2007 | 73 | 2007 |
| Genomic instability and carcinogenesis: an update WM Abdel-Rahman Current genomics 9 (8), 535-541, 2008 | 68 | 2008 |
| BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency TT Nieminen, WM Abdel–Rahman, A Ristimäki, M Lappalainen, ... Gastroenterology 141 (1), e23-e26, 2011 | 67 | 2011 |
| Molecular basis and diagnostics of hereditary colorectal cancers W Abdel‐Rahman, P Peltomäki Annals of medicine 36 (5), 379-388, 2004 | 65 | 2004 |
| Clinicopathological characterization and genomic aberrations in subcutaneous panniculitis-like T-cell lymphoma S Hahtola, E Burghart, L Jeskanen, L Karenko, WM Abdel-Rahman, ... Journal of investigative dermatology 128 (9), 2304-2309, 2008 | 64 | 2008 |
| HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1 TE Raevaara, AM Gerdes, KE Lönnqvist, A Tybjærg‐Hansen, ... Genes, Chromosomes and Cancer 40 (3), 261-265, 2004 | 63 | 2004 |
