Monogenic and polygenic determinants of sarcoma risk: an international genetic study (Q32491318)

7 September 2017

Monogenic and polygenic determinants of sarcoma risk: an international genetic study (English)

1 reference

7 September 2017

1

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12 June 2020

David L Goode

2

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12 June 2020

Robert G. Maki

11

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12 June 2020

Andrew S Brohl

12

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12 June 2020

Eva Wessel Stratford

14

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12 June 2020

Ian G. Campbell

24

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12 June 2020

Sean O'Donoghue

28

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12 June 2020

David M Thomas

29

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12 June 2020

13

Ola Myklebost

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12 June 2020

3

Isabelle Ray-Coquard

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12 June 2020

22

Ian Judson

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12 June 2020

author name string

Paul A James

4

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12 June 2020

Gillian Mitchell

5

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12 June 2020

Eveline Niedermayr

6

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12 June 2020

Ajay Puri

7

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12 June 2020

Joshua D Schiffman

8

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12 June 2020

Arcadi Cipponi

10

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12 June 2020

Susanne Lorenz

15

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12 June 2020

Sung-Min Ahn

16

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12 June 2020

Jin-Hee Ahn

17

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12 June 2020

Jeong Eun Kim

18

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12 June 2020

Sue Shanley

19

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12 June 2020

Victoria Beshay

20

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12 June 2020

Robert Lor Randall

21

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12 June 2020

Beatrice Seddon

23

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12 June 2020

Mary-Anne Young

25

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12 June 2020

Rajiv Sarin

26

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12 June 2020

International Sarcoma Kindred Study

30

1 reference

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12 June 2020

Gillian S Dite

9

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12 June 2020

Jean-Yves Blay

27

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12 June 2020

publication date

4 August 2016

1 reference

Lancet Oncology Commission

7 September 2017

1 reference

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12 June 2020

volume

17

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12 June 2020

page(s)

1261-1271

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12 June 2020

issue

9

1 reference

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Familial Risk and Heritability of Cancer Among Twins in Nordic Countries

12 June 2020

cites work

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7 January 2021

Most common 'sporadic' cancers have a significant germline genetic component

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7 January 2021

The mystery of missing heritability: Genetic interactions create phantom heritability

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7 January 2021

Searching for missing heritability: designing rare variant association studies

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7 January 2021

Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

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7 January 2021

Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment

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7 January 2021

Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.

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7 January 2021

Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel

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7 January 2021

Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients

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7 January 2021

Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA.

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7 January 2021

Germline Mutations in Predisposition Genes in Pediatric Cancer

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7 January 2021

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7 January 2021

Increased risk of malignancies in a population-based study of 818 soft-tissue sarcoma patients

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7 January 2021

Incidence of second sarcomas: a cancer registry-based study

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7 January 2021

An increased incidence of Hodgkin's lymphoma in patients with adult-onset sarcoma.

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7 January 2021

Increased cancer risks for relatives of very early-onset breast cancer cases with and without BRCA1 and BRCA2 mutations

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7 January 2021

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

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7 January 2021

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

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7 January 2021

Molecular cloning and characterization of a mammalian excision repair gene that partially restores UV resistance to xeroderma pigmentosum complementation group D cells

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7 January 2021

Somatic ERCC2 mutations correlate with cisplatin sensitivity in muscle-invasive urothelial carcinoma

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7 January 2021

Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers

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7 January 2021

RecQ helicases and PARP1 team up in maintaining genome integrity

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7 January 2021

Olaparib monotherapy in patients with advanced cancer and a germline BRCA1/2 mutation

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7 January 2021

Inhibition of the hedgehog pathway in advanced basal-cell carcinoma

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7 January 2021

Sirolimus for angiomyolipoma in tuberous sclerosis complex or lymphangioleiomyomatosis

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7 January 2021

PD-1 Blockade in Tumors with Mismatch-Repair Deficiency

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7 January 2021

BRCA2: a cause of Li-Fraumeni-like syndrome

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7 January 2021

Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene

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7 January 2021

XPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutations

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7 January 2021

Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer.

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7 January 2021

Cell cycle deregulation and mosaic loss of Ext1 drive peripheral chondrosarcomagenesis in the mouse and reveal an intrinsic cilia deficiency

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7 January 2021

A role for common genomic variants in the assessment of familial breast cancer

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7 January 2021

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study

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7 January 2021

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Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27498913%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

1 reference