Hans K. Schackert - Publications

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 22, 2020

Value of upper gastrointestinal endoscopy for gastric cancer surveillance in patients with Lynch syndrome.

Journal: International journal of cancer

Published: May 10, 2020

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: February 05, 2019

Cancer Risks for PMS2-Associated Lynch Syndrome.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology

Published: August 31, 2018

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.

Journal: Cancer cell

Published: June 01, 2018

The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect.

Journal: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology

Published: May 24, 2018

No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies.

Journal: Gastroenterology

Published: January 21, 2018

Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.

Journal: International journal of cancer

Published: November 15, 2017

Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility.

Journal: Journal of medical genetics

Published: August 07, 2017

Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6.

Journal: Familial cancer

Published: May 22, 2017

Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing.

Journal: European journal of human genetics : EJHG

Published: November 21, 2016

An unusual case of Cowden syndrome associated with ganglioneuromatous polyposis.

Journal: Hereditary cancer in clinical practice

Published: March 21, 2016