(Q39053021)

3 March 2018

title

Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer (English)

1 reference

3 March 2018

Stefanie Heilmann-Heimbach

author

11

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3 March 2018

Alfredo Ramirez

21

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3 March 2018

Christoph Engel

Christoph Engel

23

0 references

Peter Nürnberg

16

Peter Nürnberg

1 reference

PMC publication ID

5824291

3 March 2018

Barbara Wappenschmidt

22

Barbara Wappenschmidt

1 reference

3 March 2018

25

Alfons Meindl

1 reference

3 March 2018

26

Rita K Schmutzler

1 reference

3 March 2018

15

Janine Altmüller

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3 March 2018

Holger Thiele

14

Holger Thiele

1 reference

3 March 2018

Juliane Ramser

3

Juliane Ramser

1 reference

3 March 2018

Kerstin Rhiem

24

Kerstin Rhiem

1 reference

3 March 2018

Frank Jessen

20

Frank Jessen

1 reference

3 March 2018

author name string

Guido Neidhardt

1

1 reference

3 March 2018

Jan Hauke

2

1 reference

3 March 2018

Eva Groß

4

1 reference

3 March 2018

Andrea Gehrig

5

1 reference

3 March 2018

Clemens R Müller

6

1 reference

3 March 2018

Anne-Karin Kahlert

7

1 reference

3 March 2018

Karl Hackmann

8

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3 March 2018

Ellen Honisch

9

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3 March 2018

Dieter Niederacher

10

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3 March 2018

André Franke

12

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3 March 2018

Wolfgang Lieb

13

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3 March 2018

Kristina Klaschik

17

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3 March 2018

Corinna Ernst

18

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3 March 2018

Nina Ditsch

19

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3 March 2018

Eric Hahnen

27

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3 March 2018

publication date

29 December 2016

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3 March 2018

published in

JAMA Oncology

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3 March 2018

volume

3

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3 March 2018

issue

9

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3 March 2018

page(s)

1245-1248

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3 March 2018

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5824291

Gene-panel sequencing and the prediction of breast-cancer risk

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5824291

Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5824291

Breast-cancer risk in families with mutations in PALB2

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5824291

Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5824291

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5824291

Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5824291

Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5824291

10.1001/JAMAONCOL.2016.5592

21 August 2018

Identifiers

DOI

1 reference

3 March 2018

PMC publication ID

5824291

1 reference

3 March 2018

PubMed publication ID

28033443

1 reference

3 March 2018