Tiina Raevaara

Interpreting missense variants: comparing computational methods in human disease genes<i>CDKN2A</i>,<i>MLH1</i>,<i>MSH2</i>,<i>MECP2</i>, and tyrosinase (<i>TYR</i>)

Philip A. Chan, Sekhar Duraisamy, Peter J. Miller et al. · Human Mutation · 2007 · 130 citations

Life Sciences, Bioinformatics, Genetics +17

HNPCC mutation <i>MLH1</i> P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1

Tiina Raevaara, Anne‐Marie Gerdes, Karin E. Lönnqvist et al. · Genes Chromosomes and Cancer · 2004 · 54 citations

Life Sciences, Genetics, Oncology +17

MSH6 missense mutations are often associated with no or low cancer susceptibility

Reetta Kariola, Heather Hampel, Wendy L. Frankel et al. · British Journal of Cancer · 2004 · 51 citations · Full text

Life Sciences, Genetics, Oncology +17

Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein

Tiina Raevaara, Carlos Vaccaro, Wael M. Abdel‐Rahman et al. · Gastroenterology · 2003 · 40 citations

Medicine, Genetics, Molecular Genetics +12

Two mismatch repair gene mutations found in a colon cancer patient – which one is pathogenic?

Reetta Kariola, Robyn Otway, Karin E. Lönnqvist et al. · Human Genetics · 2003 · 36 citations

Medicine, Genetics, Oncology +14