Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

scientific article

Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1200/JCO.2016.66.5844
P932PMC publication ID5019754
P698PubMed publication ID27269948

P50authorElza KhusnutdinovaQ4502509
Julian PetoQ6307461
Jan LubińskiQ11718282
Manjeet K BollaQ114270702
Ans M W van den OuwelandQ114292607
Muriel A AdankQ114292627
Sten CornelissenQ114292659
Lizet E van der KolkQ114337508
Richard R van HienQ114337683
Georgia Chenevix-TrenchQ17517031
Kenneth OffitQ20732365
Jenny Chang-ClaudeQ21263057
Rita SchmutzlerQ21264574
Alison DunningQ30506457
Graham GilesQ30524411
Hoda Anton-CulverQ28052887
Montserrat García-ClosasQ28356305
Kamila CzeneQ28484009
Angela CoxQ28484012
Hiltrud BrauchQ28484013
Barbara BurwinkelQ28484015
Hermann BrennerQ28958315
Heli NevanlinnaQ29840669
Simon S. CrossQ30505778
Marjanka K SchmidtQ37372106
Tjoung-Won Park-SimonQ42170981
Alice S. WhittemoreQ42423380
Amanda SpurdleQ45904058
Mark RobsonQ51026477
Melissa C. SoutheyQ55446228
Anja RudolphQ56722646
John HopperQ56726496
Roger L. MilneQ56855807
Volker ArndtQ57305816
Harald SurowyQ58144748
Anna JakubowskaQ58323317
Esther M. JohnQ59752419
Douglas F. EastonQ59812154
Olivia FletcherQ60472843
Anthony SwerdlowQ60492223
Argyrios ZiogasQ30831638
Veli-Matti KosmaQ37068464
Arto MannermaaQ37070123
Antoinette HollestelleQ37074515
Caroline SeynaeveQ37342673
Thilo DörkQ37342847
Vessela KristensenQ37344701
Quinten WaisfiszQ37357772
Marina BermishevaQ37360473
Taru A. MuranenQ37371838
Paul D P PharoahQ61822938
Per HallQ62593354
Alfons MeindlQ63015490
Fergus J. CouchQ63018779
Ian TomlinsonQ63213090
Peter A. FaschingQ64005064
Annika LindblomQ64516098
Irene L AndrulisQ64516140
Jonine FigueroaQ71778357
Sara MargolinQ72940025
Stig Egil BojesenQ72992763
Annegien BroeksQ73632596
Henrik FlygerQ74012148
Maartje J. HooningQ74014444
Natalia V. BogdanovaQ74171899
Elinor J. SawyerQ74173254
Celine M. VachonQ74173260
Rob TollenaarQ77085802
Julia A. KnightQ78316584
Thomas BrüningQ84487350
Lothar HaeberleQ87976657
Polly A NewcombQ89454622
Eva GalleQ89720784
Antonis C AntoniouQ89766295
Peter HillemannsQ91084009
Michael E JonesQ92480941
Frans HogervorstQ95989542
P2093author name stringAndrew Lee
Qin Wang
Amy Trentham-Dietz
Mieke Schutte
Julie Soens
Natalia N Antonenkova
Hanne Meijers
P2860cites workThe human homologs of checkpoint kinases Chk1 and Cds1 (Chk2) phosphorylate p53 at multiple DNA damage-inducible sitesQ24610054
Risk determination and prevention of breast cancerQ26991921
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutationsQ28215462
Large-scale genotyping identifies 41 new loci associated with breast cancer riskQ29416989
Chk1 and Chk2 kinases in checkpoint control and cancerQ29617706
BOADICEA breast cancer risk prediction model: updates to cancer incidences, tumour pathology and web interfaceQ37507410
Breast cancer in patients carrying a germ-line CHEK2 mutation: Outcome after breast conserving surgery and adjuvant radiotherapyQ40249058
One-time general consent for research on biological samples: opt out system for patients is optimal and endorsed in many countriesQ43242370
Excess breast cancer risk in first degree relatives of CHEK2∗1100delC positive familial breast cancer casesQ46247419
[CHEK2-mutation in Dutch breast cancer families: expanding genetic testing for breast cancer].Q51287680
CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women.Q51392341
Frequency of the CHEK2 1100delC mutation among women with breast cancer: an international study.Q53217889
Gene expression profiling assigns CHEK2 1100delC breast cancers to the luminal intrinsic subtypes.Q54587377
Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibilityQ33904964
CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studiesQ33910280
Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK2*1100delC variantQ35443960
Gene-panel sequencing and the prediction of breast-cancer riskQ36175072
CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancerQ36449203
Prediction of breast cancer risk based on profiling with common genetic variantsQ36583004
CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controlsQ37048943
Family history, genetic testing, and clinical risk prediction: pooled analysis of CHEK2 1100delC in 1,828 bilateral breast cancers and 7,030 controlsQ37307305
Breast Cancer Survival and Tumor Characteristics in Premenopausal Women Carrying theCHEK2*1100delCGermline MutationQ61970254
Empirical Bayes estimates of age-standardized relative risks for use in disease mappingQ69417787
Presymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutationQ73966464
CHEK2-positive breast cancers in young Polish womenQ80128998
The regulation of CHK2 in human cancerQ80551940
CHEK2*1100delC screening of Asian women with a family history of breast cancer is unwarrantedQ81244092
P433issue23
P407language of work or nameEnglishQ1860
P304page(s)2750-2760
P577publication date2016-06-06
P1433published inJournal of Clinical OncologyQ400292
P1476titleAge- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers
P478volume34

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cites work (P2860)
Q56888162A Clinical Decision Support Tool to Predict Cancer Risk for Commonly Tested Cancer-Related Germline Mutations
Q57111436Association Between CHEK2*1100delC and Breast Cancer: A Systematic Review and Meta-Analysis
Q91045517BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors
Q30238753Breast Cancer Screening in the Precision Medicine Era: Risk-Based Screening in a Population-Based Trial.
Q91211233Cancer genetics, precision prevention and a call to action
Q99243158Comprehensive analysis and ACMG-based classification of CHEK2 variants in hereditary cancer patients
Q92524053Computational analysis of high-risk SNPs in human CHK2 gene responsible for hereditary breast cancer: A functional and structural impact
Q92161965Consensus Guidelines on Genetic` Testing for Hereditary Breast Cancer from the American Society of Breast Surgeons
Q92630618Contralateral Prophylactic Mastectomy in Women with Unilateral Breast Cancer Who Are Genetic Carriers, Have a Strong Family History or Are just Young at Presentation
Q33712610Current perspectives on CHEK2 mutations in breast cancer.
Q90292766Editorial: Accomplishments, Collaborative Projects and Future Initiatives in Breast Cancer Genetic Predisposition
Q89253231Efficient computation of the joint probability of multiple inherited risk alleles from pedigree data
Q30234614Endometrial cancer gene panels: clinical diagnostic vs research germline DNA testing
Q92480972Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Q64065191Frequency of pathogenic germline variants in BRCA1, BRCA2, PALB2, CHEK2 and TP53 in ductal carcinoma in situ diagnosed in women under the age of 50 years
Q38627916Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication
Q64251583Genetic Epidemiology of Breast Cancer in Latin America
Q37739048Genetic modifiers of CHEK2*1100delC-associated breast cancer risk
Q91362827Genetic predisposition to mosaic Y chromosome loss in blood
Q39370774Germline Mutations in Triple-Negative Breast Cancer
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Q99408631Pathogenic Variants in CHEK2 Are Associated With an Adverse Prognosis in Symptomatic Early-Onset Breast Cancer
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Q41011976Predicting Triple-Negative Breast Cancer Subtype Using Multiple Single Nucleotide Polymorphisms for Breast Cancer Risk and Several Variable Selection Methods
Q40094101Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks
Q92710828Recurrent moderate-risk mutations in Finnish breast and ovarian cancer patients
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Q91178389The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Q92282131The Landscape of Somatic Genetic Alterations in Breast Cancers from CHEK2 Germline Mutation Carriers
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Q92036319Whole-genome sequencing reveals clinically relevant insights into the aetiology of familial breast cancers

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