Does breast carcinoma belong to the Lynch syndrome tumor spectrum? – Somatic mutational profiles vs. ovarian and colorectal carcinomas-Reference-Cited by-同舟云学术

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Does breast carcinoma belong to the Lynch syndrome tumor spectrum? – Somatic mutational profiles vs. ovarian and colorectal carcinomas

Published:2020-04-07 Issue:14 Volume:11 Page:1244-1256
ISSN:1949-2553
Container-title:Oncotarget
language:en
Short-container-title:Oncotarget

Author:

Porkka Noora K.¹,Olkinuora Alisa¹,Kuopio Teijo²³,Ahtiainen Maarit⁴,Eldfors Samuli⁵,Almusa Henrikki⁵,Mecklin Jukka-Pekka⁶⁷⁸,Peltomäki Päivi¹

Affiliation:

1. Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland

2. Department of Pathology, Jyväskylä Central Hospital, Jyväskylä, Finland

3. Department of Biological and Environmental Science, University of Jyväskylä, Jyväskylä, Finland

4. Department of Education and Research, Jyväskylä Central Hospital and University of Eastern Finland, Jyväskylä, Finland

5. Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland

6. Faculty of Sport and Health Sciences, University of Jyväskylä, Jyväskylä, Finland

7. Department of Surgery, Jyväskylä Central Hospital, Jyväskylä, Finland

8. Department of Education & Science, Jyväskylä Central Hospital, Jyväskylä, Finland

Publisher

Impact Journals, LLC

Subject

Oncology

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. An Unusual Presentation of Synchronous Breast Cancer and Skin Malignancy in a Patient with Lynch Syndrome: A Case Report and Review of the Literature;Biomedicines;2024-06-03

2. Hormone Receptor–Positive Breast Cancer Sensitive to Pembrolizumab: Evidence of the Pathogenicity of the MLH1 Variant 1835del3;Journal of the National Comprehensive Cancer Network;2023-11

3. New stochastic devices for simultaneous analysis of mismatch repair proteins and KRAS in biological samples;Journal of Pharmaceutical and Biomedical Analysis;2023-10

4. Lynch Syndrome Genetics and Clinical Implications;Gastroenterology;2023-04

5. An MSH6 germline pathogenic variant p.Gly162Ter associated with Lynch syndrome;Human Genome Variation;2022-10-26

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