(Q36909238)

17 August 2017

Germline BAP1 mutations predispose to renal cell carcinomas (English)

1 reference

17 August 2017

Dominique Stoppa-Lyonnet

33

Dominique Stoppa-Lyonnet

0 references

Virginie Caux-Moncoutier

5

Virginie Caux-Moncoutier

0 references

Xavier Sastre-Garau

11

Brigitte Bressac-de Paillerets

Xavier Sastre-Garau

0 references

32

Brigitte Bressac-de Paillerets

0 references

Marc-Henri Stern

Marc-Henri Stern

34

0 references

Emmanuel Barillot

Emmanuel Barillot

24

0 references

Olivier Delattre

Olivier Delattre

26

0 references

Xavier Renaudin

Xavier Renaudin

8

0 references

Virginie Jacquemin

3

Virginie Jacquemin

1 reference

17 August 2017

Marie-Françoise Avril

23

Marie-Françoise Avril

1 reference

17 August 2017

20

Valérie Bonadona

1 reference

17 August 2017

25

Odile Cabaret

1 reference

17 August 2017

19

Paul Gesta

1 reference

17 August 2017

Catherine Dubois-d'Enghien

6

Catherine Dubois-d'Enghien

1 reference

17 August 2017

16

Nadine Andrieu

1 reference

17 August 2017

15

Olga M Sinilnikova

1 reference

17 August 2017

22

Clotilde Penet

1 reference

17 August 2017

Tatiana Popova

1

1 reference

17 August 2017

Lucie Hebert

2

1 reference

17 August 2017

Sophie Gad

4

1 reference

17 August 2017

Bénédicte Richaudeau

7

1 reference

17 August 2017

Jason Sellers

9

1 reference

17 August 2017

André Nicolas

10

1 reference

17 August 2017

Laurence Desjardins

12

1 reference

17 August 2017

Gabor Gyapay

13

1 reference

17 August 2017

Virginie Raynal

14

1 reference

17 August 2017

Elodie Manié

17

1 reference

17 August 2017

Antoine de Pauw

18

1 reference

17 August 2017

Christine M Maugard

21

1 reference

17 August 2017

Stéphane Richard

27

1 reference

17 August 2017

Olivier Caron

28

1 reference

17 August 2017

Meriem Benfodda

29

1 reference

17 August 2017

Hui-Han Hu

30

1 reference

17 August 2017

Nadem Soufir

31

1 reference

17 August 2017

language of work or name

English

0 references

publication date

16 May 2013

1 reference

American Journal of Human Genetics

17 August 2017

1 reference

17 August 2017

92

1 reference

17 August 2017

6

1 reference

17 August 2017

974-980

1 reference

The landscape of cancer genes and mutational processes in breast cancer

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

BAP1 loss defines a new class of renal cell carcinoma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Germline mutations in BAP1 predispose to melanocytic tumors

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Germline BAP1 mutations predispose to malignant mesothelioma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Frequent mutation of BAP1 in metastasizing uveal melanomas

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Hereditary causes of kidney tumours

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

A method and server for predicting damaging missense mutations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Estimates of cancer incidence and mortality in Europe in 2008.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

The Sequence Alignment/Map format and SAMtools

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Association of C-terminal ubiquitin hydrolase BRCA1-associated protein 1 with cell cycle regulator host cell factor 1

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Somatic mutations affect key pathways in lung adenocarcinoma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

BRCA1-associated protein-1 is a tumor suppressor that requires deubiquitinating activity and nuclear localization

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

The genomic landscapes of human breast and colorectal cancers

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Searching for the hereditary causes of renal-cell carcinoma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

BAP1: a novel ubiquitin hydrolase which binds to the BRCA1 RING finger and enhances BRCA1-mediated cell growth suppression

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Germline BAP1 mutations and tumor susceptibility

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

A cryptic BAP1 splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Frequent mutations of genes encoding ubiquitin-mediated proteolysis pathway components in clear cell renal cell carcinoma

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

Cancer incidence and mortality in France over the period 1980–2005

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3675229

BAP1 and breast cancer risk

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23684012

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCN

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23684012

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

EMMA, a cost- and time-effective diagnostic method for simultaneous detection of point mutations and large-scale genomic rearrangements: application to BRCA1 and BRCA2 in 1,525 patients

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23684012

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2013.04.012

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

23684012

1 reference