| Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1 TE Raevaara, MK Korhonen, H Lohi, H Hampel, E Lynch, KE Lönnqvist, ... Gastroenterology 129 (2), 537-549, 2005 | 224 | 2005 |
| Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR) PA Chan, S Duraisamy, PJ Miller, JA Newell, C McBride, JP Bond, ... Human mutation 28 (7), 683-693, 2007 | 157 | 2007 |
| Functional analysis of MSH6 mutations linked to kindreds with putative hereditary non-polyposis colorectal cancer syndrome R Kariola, TE Raevaara, KE Lönnqvist, M Nyström-Lahti Human molecular genetics 11 (11), 1303-1310, 2002 | 101 | 2002 |
| 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 |
| MSH6 missense mutations are often associated with no or low cancer susceptibility R Kariola, H Hampel, WL Frankel, TE Raevaara, A de la Chapelle, ... British journal of cancer 91 (7), 1287-1292, 2004 | 56 | 2004 |
| Two mismatch repair gene mutations found in a colon cancer patient–which one is pathogenic? R Kariola, R Otway, KE Lönnqvist, TE Raevaara, F Macrae, YJ Vos, ... Human genetics 112, 105-109, 2003 | 53 | 2003 |
| Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein TE Raevaara, C Vaccaro, WM Abdel-Rahman, E Mocetti, S Bala, ... Gastroenterology 125 (2), 501-509, 2003 | 51 | 2003 |
| Conditional nuclear localization of hMLH3 suggests a minor activity in mismatch repair and supports its role as a low-risk gene in HNPCC MK Korhonen, TE Raevaara, H Lohi, M Nyström Oncology reports 17 (2), 351-354, 2007 | 29 | 2007 |
| The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC S Ollila, R Fitzpatrick, L Sarantaus, R Kariola, I Ambus, L Velsher, E Hsieh, ... International journal of oncology 28 (1), 149-153, 2006 | 26 | 2006 |
| Description and functional analysis of a novel in frame mutation linked to hereditary non-polyposis colorectal cancer TE Raevaara, T Timoharju, KE Lönnqvist, R Kariola, M Steinhoff, ... Journal of medical genetics 39 (10), 747-750, 2002 | 18 | 2002 |
| Yliopistojen kolmas tehtävä jää vaille toteutusta ja tukea A Heinonen, T Raevaara Tieteessä tapahtuu 30 (5), 2012 | 9 | 2012 |
| Functional significance of minor MLH1 germline alterations found in colon cancer patients T Raevaara Helsingin yliopisto, 2005 | 1 | 2005 |
| Tiedon perässä hullun tai ainakin hölmön lailla T Raevaara Tieteessä tapahtuu 36 (6), 2018 | | 2018 |
| Aina kannattaa yleistajuistaa tiedettä T Raevaara Suomen eläinlääkärilehti 123 (2017): 1, 2017 | | 2017 |
| Pakko lisääntyä, tavalla tai toisella T Raevaara Tieteessä tapahtuu 30 (1), 2012 | | 2012 |
| Ahne ihminen eläimineen T Raevaara Tieteessä tapahtuu 29 (7), 2011 | | 2011 |
| Calista, D.; Goldstein, AM. & Landi, MT.(2000). Familial melanoma aggregation in north-eastern Italy. Journal of Investigative Dermatology, 115, 764-765 Campisi, J.(1997). The … M Capasso, F Ayala, RA Avvisati, R Russo, A Gambale, N Mozzillo, ... Human Genetics 55, 518-524, 2007 | | 2007 |
| Functional analysis of MMR gene mutations linked to hereditary non-polyposis colorectal cancer M Nystrom-Lahti, R Kariola, T Raevaara, K Lonnqvist EUROPEAN JOURNAL OF HUMAN GENETICS 10, 69-69, 2002 | | 2002 |
Anne-Marie GerdesProfessor of Clinical Genetics, University of CopenhagenVerified email at regionh.dk
