(Q60315437)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24556926%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

title

PALB2 sequencing in Italian familial breast cancer cases reveals a high-risk mutation recurrent in the province of Bergamo (English)

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8 March 2020

2

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8 March 2020

Sara Ciceri

3

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8 March 2020

Mara Colombo

4

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8 March 2020

Paolo Verderio

8

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8 March 2020

Sara Pizzamiglio

9

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8 March 2020

Anna Falanga

11

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8 March 2020

Marina Marchetti

12

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8 March 2020

Stefano Fortuzzi

18

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8 March 2020

Bernard Peissel

21

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8 March 2020

Siranoush Manoukian

22

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8 March 2020

7

Bernardo Bonanni

1 reference

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8 March 2020

1

Irene Catucci

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8 March 2020

23

Carlo Tondini

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8 March 2020

15

Chiara Corna

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8 March 2020

20

Giulietta Scuvera

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8 March 2020

10

Claudia Foglia

1 reference

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8 March 2020

24

Paolo Radice

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8 March 2020

16

Fernando Ravagnani

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8 March 2020

13

Laura Galastri

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8 March 2020

5

Graziella Pasquini

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8 March 2020

19

Domenico Sardella

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8 March 2020

author name string

Monica Barile

6

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8 March 2020

Tiziana Bianchi

14

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8 March 2020

Loris Bernard

17

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8 March 2020

language of work or name

English

0 references

publication date

20 February 2014

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8 March 2020

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8 March 2020

volume

16

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8 March 2020

issue

9

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8 March 2020

page(s)

688-694

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https://scigraph.springernature.com/pub.10.1038/gim.2014.13

8 March 2020

exact match

0 references

cites work

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

Genetic susceptibility to breast cancer

1 reference

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7 January 2021

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

Biallelic inactivation of BRCA2 in Fanconi anemia

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

Germline RAD51C mutations confer susceptibility to ovarian cancer

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7 January 2021

Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families

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https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases

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7 January 2021

Assessment of SLX4 Mutations in Hereditary Breast Cancers

1 reference

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7 January 2021

Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Rare mutations in XRCC2 increase the risk of breast cancer

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7 January 2021

Rare variants in XRCC2 as breast cancer susceptibility alleles

1 reference

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7 January 2021

PALB2 and breast cancer: ready for clinical translation!

1 reference

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7 January 2021

Detection of a large rearrangement in PALB2 in Spanish breast cancer families with male breast cancer

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7 January 2021

Mutation analysis of BRCA1, BRCA2, PALB2 and BRD7 in a hospital-based series of German patients with triple-negative breast cancer

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7 January 2021

Prevalence of PALB2 mutations in breast cancer patients in multi-ethnic Asian population in Malaysia and Singapore.

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7 January 2021

Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer.

1 reference

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7 January 2021

A PALB2 mutation associated with high risk of breast cancer

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7 January 2021

Rare germline mutations in PALB2 and breast cancer risk: a population-based study

1 reference

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7 January 2021

Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer

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7 January 2021

Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families.

1 reference

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7 January 2021

A recurrent mutation in PALB2 in Finnish cancer families.

1 reference

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7 January 2021

The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

The contribution of founder mutations to early-onset breast cancer in French-Canadian women

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

A novel germline PALB2 deletion in Polish breast and ovarian cancer patients

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.13

7 January 2021

Comparative in vitro and in silico analyses of variants in splicing regions of BRCA1 and BRCA2 genes and characterization of novel pathogenic mutations

1 reference

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7 January 2021

PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer

1 reference

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7 January 2021

Identifiers

DOI

10.1038/GIM.2014.13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24556926%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

1 reference