Publications by authors named "Friedrik Wikman"

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Deleterious mis-splicing of STK11 caused by a novel single-nucleotide substitution in the 3' polypyrimidine tract of intron five.
Thorkild Terkelsen, Ole H Larsen, Søren Vang, Uffe B Jensen, Friedrik Wikman

Mol Genet Genomic Med· September 2020

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New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients.
Malene Djursby, Majbritt B Madsen, Jane H Frederiksen, Lukas A Berchtold, Christina Therkildsen, Friedrik Wikman

Front Genet· September 2020

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Detection of Mutations by Screening Hereditary Nonpolyposis Colon Cancer Families from Denmark and Sweden.
Henrik Okkels, Kristina Lagerstedt-Robinsson, Friedrik P Wikman, Thomas V O Hansen, Ihab Lolas

Genet Test Mol Biomarkers· September 2019

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A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.
Mette Nyegaard, Nanna D Rendtorff, Morten S Nielsen, Thomas J Corydon, Ditte Demontis, Friedrik P Wikman

PLoS Genet· July 2015

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[Juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia syndrome in a patient a with SMAD4 mutation].
Anne Marie Jelsig, Pernille Mathiesen Tørring, Friedrik Wikman, Michael Bau Mortensen, Niels Qvist

Ugeskr Laeger· October 2014

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Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients.
Sanne M Petersen, Mette Dandanell, Lene J Rasmussen, Anne-Marie Gerdes, Lotte N Krogh, Friedrik Wikman

BMC Med Genet· October 2013

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Frequent genomic loss at chr16p13.2 is associated with poor prognosis in colorectal cancer.
Claus Lindbjerg Andersen, Philippe Lamy, Kasper Thorsen, Eigil Kjeldsen, Friedrik Wikman

Int J Cancer· October 2011

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Leiden Open Variation Database of the MUTYH gene.
Astrid A Out, Carli M J Tops, Maartje Nielsen, Marjan M Weiss, Ivonne J H M van Minderhout, Friedrik P Wikman

Hum Mutat· November 2010

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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

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Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population.
Mef Nilbert, Friedrik P Wikman, Thomas V O Hansen, Henrik B Krarup, Torben F Orntoft

Fam Cancer· April 2009

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BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer.
Mads Thomassen, Thomas V O Hansen, Ake Borg, Henriette Theilmann Lianee, Friedrik Wikman

Acta Oncol· June 2008

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The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population.
Lise Lotte Christensen, Bo E Madsen, Friedrik P Wikman, Carsten Wiuf, Karen Koed

BMC Med Genet· June 2008

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Genotyping and annotation of Affymetrix SNP arrays.
Philippe Lamy, Claus L Andersen, Friedrik P Wikman, Carsten Wiuf

Nucleic Acids Res· September 2006

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Presymptomatic diagnosis using a deletion of a single codon in families with hereditary non-polyposis colorectal cancer.
Rasmus S Ripa, Niels Katballe, Friedrik P Wikman, Anne Charlotte Jäger, Inge Bernstein

Mutat Res· February 2005

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High-density single nucleotide polymorphism array defines novel stage and location-dependent allelic imbalances in human bladder tumors.
Karen Koed, Carsten Wiuf, Lise-Lotte Christensen, Friedrik P Wikman, Karsten Zieger

Cancer Res· January 2005

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EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer.
Shantie Jagmohan-Changur, Taija Poikonen, Susa Vilkki, Virpi Launonen, Friedrik Wikman

Cancer Res· January 2003

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Antibody-based screening for hereditary nonpolyposis colorectal carcinoma compared with microsatellite analysis and sequencing.
Mariann Christensen, Niels Katballe, Friedrik Wikman, Hanne Primdahl, Flemming B Sørensen

Cancer· December 2002

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Neural network predicts sequence of TP53 gene based on DNA chip.
Jeppe S Spicker, Friedrik Wikman, Ming-Lan Lu, Carlos Cordon-Cardo, Christopher Workman

Bioinformatics· August 2002

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Allelic imbalances in human bladder cancer: genome-wide detection with high-density single-nucleotide polymorphism arrays.
Hanne Primdahl, Friedrik P Wikman, Hans von der Maase, Xiao-ge Zhou, Hans Wolf

J Natl Cancer Inst· February 2002

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Impact of alterations affecting the p53 pathway in bladder cancer on clinical outcome, assessed by conventional and array-based methods.
Ming-Lan Lu, Friedrik Wikman, Torben F Orntoft, Elizabeth Charytonowicz, Farhang Rabbani

Clin Cancer Res· January 2002

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