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Human Mutation|April 27, 2011
Biomedical informatics as support to individual healthcare in hereditary colon cancer: the Danish HNPCC systemInge T Bernstein, Karen Lindorff-Larsen, Susanne Timshel, et al.Frontiers in Genetics|November 16, 2020
New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer PatientsMalene Djursby, Majbritt B Madsen, Jane H Frederiksen, et al.Familial Cancer|August 22, 2009
Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patientsLise Lotte Christensen, Reetta Kariola, Mari K Korhonen, et al.Neuro-Oncology|July 28, 2022
Genetic predisposition and evolutionary traces of pediatric cancer risk: a prospective 5-year population-based genome sequencing study of children with CNS tumorsUlrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, et al.Journal of Assisted Reproduction and Genetics|March 7, 2021
Cell-based non-invasive prenatal testing for monogenic disorders: confirmation of unaffected fetuses following preimplantation genetic testingChristian Liebst Frisk Toft, Hans Jakob Ingerslev, Ulrik Schiøler Kesmodel, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2020
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportMev Dominguez-Valentin, Emma J Crosbie, Christoph Engel, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2020
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 25, 2019
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.Hereditary Cancer in Clinical Practice|October 1, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortiumPål Møller, Toni Seppälä, James G Dowty, et al.Pageof 3