Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer-Reference-Cited by-同舟云学术

Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer

Published:2018-01-31 Issue:11 Volume:142 Page:2286-2292
ISSN:0020-7136
Container-title:International Journal of Cancer
language:en
Short-container-title:Int. J. Cancer

Author:

Tervasmäki Anna¹,Mantere Tuomo¹,Hartikainen Jaana M.²³,Kauppila Saila⁴,Lee Hang-Mao⁵,Koivuluoma Susanna¹,Grip Mervi⁶,Karihtala Peeter⁷,Jukkola-Vuorinen Arja⁷,Mannermaa Arto²³,Winqvist Robert¹,Pylkäs Katri¹^ORCID

Affiliation:

1. Laboratory of Cancer Genetics and Tumor Biology; Cancer and Translational Medicine Research Unit and Biocenter Oulu, Northern Finland Laboratory Centre Nordlab Oulu, University of Oulu; Oulu Finland

2. School of Medicine; Institute of Clinical Medicine, Pathology and Forensic Medicine, and Translational Cancer Research Area, University of Eastern Finland; Kuopio Finland

3. Department of Clinical Pathology, Imaging Center; Kuopio University Hospital; Kuopio Finland

4. Department of Pathology; Oulu University Hospital and University of Oulu; Oulu Finland

5. Biocenter Oulu and Faculty of Biochemistry and Molecular Medicine; University of Oulu; Oulu Finland

6. Department of Surgery; Oulu University Hospital and University of Oulu; Oulu Finland

7. Department of Oncology and Radiotherapy; Medical Research Center Oulu, Oulu University Hospital and University of Oulu; Oulu Finland

Funder

Academy of Finland

Center of Excellence

The Cancer Foundation of Finland

The Sigrid Juselius Foundation

University of Oulu

The special Governmental EVO

K. Albin Johansson's Foundation

University of Eastern Finland

Publisher

Wiley

Subject

Cancer Research,Oncology

Reference50 articles.

1. Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning?;Ghoussaini;Am J Pathol,2013

2. Breast-cancer risk in families with mutations in PALB2;Antoniou;N Engl J Med,2014

3. Growing recognition of the role for rare missense substitutions in breast cancer susceptibility;Tavtigian;Biomarkers Med,2014

4. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles;Seal;Nat Genet,2006

5. Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer;Ruark;Nature,2012

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