Evaluation of rare variants in the new fanconi anemia gene ERCC4 (FANCQ) as familial breast/ovarian cancer susceptibility alleles. (Q52643351)

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21 February 2020

title

Evaluation of rare variants in the new fanconi anemia gene ERCC4 (FANCQ) as familial breast/ovarian cancer susceptibility alleles (English)

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21 February 2020

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21 February 2020

Massimo Bogliolo

2

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21 February 2020

Miguel de la Hoya

5

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21 February 2020

Adriana Lasa

7

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21 February 2020

Orland Diez

13

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21 February 2020

Mercedes Durán

16

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21 February 2020

Jordi Surrallés

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21 February 2020

8

Teresa Ramón y Cajal

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21 February 2020

author name string

Victoria Fernández

3

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21 February 2020

Alicia Barroso

4

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21 February 2020

Trinidad Caldés

6

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21 February 2020

Marta Santamariña

9

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21 February 2020

Ana Vega

10

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21 February 2020

Francisco Quiles

11

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21 February 2020

Conxi Lázaro

12

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21 February 2020

Daniel Fernández

14

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21 February 2020

Rogelio González-Sarmiento

15

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21 February 2020

José Fernández Piqueras

17

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21 February 2020

Maria Marín

18

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21 February 2020

Roser Pujol

19

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21 February 2020

Javier Benítez

21

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21 February 2020

publication date

7 October 2013

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21 February 2020

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21 February 2020

volume

34

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21 February 2020

issue

12

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21 February 2020

page(s)

1615-1618

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Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia

21 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22438

Mutation analysis of the SHFM1 gene in breast/ovarian cancer families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22438

Mapping of interaction domains between human repair proteins ERCC1 and XPF

21 January 2018

1 reference

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Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families.

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22438

Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22438

Biallelic inactivation of BRCA2 in Fanconi anemia

21 January 2018

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Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

21 January 2018

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A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis

21 January 2018

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Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNA

21 January 2018

1 reference

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PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

21 January 2018

1 reference

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Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

21 January 2018

1 reference

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Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease

21 January 2018

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On the role of FAN1 in Fanconi anemia

21 January 2018

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Fanconi anemia and breast cancer susceptibility meet again

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22438

Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families

21 January 2018

1 reference

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inferred from DOI database lookup

7 January 2021

based on heuristic

A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22438