Publications by authors named "Reetta Kariola"

Claim this Profile
M
Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patients.
Jukka Kantelinen, Minttu Kansikas, Satu Candelin, Heather Hampel, Betsy Smith, Reetta Kariola

Hum Mutat· August 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one.
Jukka Kantelinen, Thomas V O Hansen, Minttu Kansikas, Lotte Nylandsted Krogh, Mari K Korhonen, Reetta Kariola

Fam Cancer· September 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variants.
Minttu Kansikas, Reetta Kariola, Minna Nyström

Hum Mutat· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients.
Lise Lotte Christensen, Reetta Kariola, Mari K Korhonen, Friedrik P Wikman, Lone Sunde

Fam Cancer· January 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein.
Saara Ollila, Laura Sarantaus, Reetta Kariola, Philip Chan, Heather Hampel

Gastroenterology· November 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC.
Saara Ollila, Roslyn Fitzpatrick, Laura Sarantaus, Reetta Kariola, Ingrid Ambus

Int J Oncol· January 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
APC and beta-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers.
Reetta Kariola, Wael M Abdel-Rahman, Miina Ollikainen, Ralf Butzow, Päivi Peltomäki

Fam Cancer· September 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular analysis of familial endometrial carcinoma: a manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome?
Miina Ollikainen, Wael M Abdel-Rahman, Anu-Liisa Moisio, Annette Lindroos, Reetta Kariola

J Clin Oncol· July 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations.
Wael M Abdel-Rahman, Miina Ollikainen, Reetta Kariola, Heikki J Järvinen, Jukka-Pekka Mecklin

Oncogene· February 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1.
Tiina E Raevaara, Anne-Marie Gerdes, Karin E Lönnqvist, Anne Tybjaerg-Hansen, Wael M Abdel-Rahman, Reetta Kariola

Genes Chromosomes Cancer· July 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein.
Tiina E Raevaara, Carlos Vaccaro, Wael M Abdel-Rahman, Esteban Mocetti, Shashi Bala, Reetta Kariola

Gastroenterology· August 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Two mismatch repair gene mutations found in a colon cancer patient--which one is pathogenic?
Reetta Kariola, Robyn Otway, Karin E Lönnqvist, Tiina E Raevaara, Finlay Macrae

Hum Genet· February 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional analysis of MSH6 mutations linked to kindreds with putative hereditary non-polyposis colorectal cancer syndrome.
Reetta Kariola, Tiina E Raevaara, Karin E Lönnqvist, Minna Nyström-Lahti

Hum Mol Genet· May 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis