Germ-line variants identified by next generation sequencing in a panel of estrogen and cancer associated genes correlate with poor clinical outcome in Lynch syndrome patients-Reference-Cited by-同舟云学术

Germ-line variants identified by next generation sequencing in a panel of estrogen and cancer associated genes correlate with poor clinical outcome in Lynch syndrome patients

Published:2015-10-22 Issue:38 Volume:6 Page:41108-41122
ISSN:1949-2553
Container-title:Oncotarget
language:en
Short-container-title:Oncotarget

Author:

Jóri Balazs¹²,Kamps Rick³,Xanthoulea Sofia¹,Delvoux Bert¹,Blok Marinus J.²,Van de Vijver Koen K.⁴⁵,de Koning Bart²,Oei Felicia Trups²,Tops Carli M.⁶,Speel Ernst J. M.⁴,Kruitwagen Roy F.¹,Gomez-Garcia Encarna B.²,Romano Andrea¹

Affiliation:

1. Department of Gynecology and Obstetrics, GROW - School for Oncology & Developmental Biology, Maastricht University Medical Centre, The Netherlands

2. Department of Clinical Genetics, GROW - School for Oncology & Developmental Biology, Maastricht University Medical Centre, The Netherlands

3. Department of Clinical Genetics, Genomics & Bioinformatics, CARIM - School for Cardiovascular Diseases, Maastricht University Medical Centre, The Netherlands

4. Department of Pathology, GROW - School for Oncology & Developmental Biology, Maastricht University Medical Centre, The Netherlands

5. Current address: Divisions of Diagnostic Oncology & Molecular Pathology, Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, The Netherlands

6. Department of Clinical Genetics, Leiden University Medical Centre, The Netherlands

Publisher

Impact Journals, LLC

Subject

Oncology

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3. Investigation of APC, MLH1 and MSH2 Mutations in Patients with Hereditary Colorectal Carcinoma: A Single Center Experience;Medical Bulletin of Haseki;2021-01-01

4. SNP association study in PMS2-associated Lynch syndrome;Familial Cancer;2017-11-17

5. Increasing awareness and knowledge of lifestyle recommendations for cancer prevention in Lynch syndrome carriers: Randomized controlled trial;Clinical Genetics;2017-09-29