The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Age- and Tumor Subtype–Specific Breast Cancer Risk Estimates for CH EK 2 *1100delC Carriers
Open accessAbstract
Purpose: CHEK2*1100delC is a well-established breast cancer risk variant that is most prevalent in European populations; however, there are limited data on risk of breast cancer by age and tumor subtype, which limits its usefulness in breast cancer risk prediction. We aimed to generate tumor subtype- and age-specific risk estimates by using data from the Breast Cancer Association Consortium, including 44,777 patients with breast cancer and 42,997 controls from 33 studies genotyped for CHEK2*1100delC. Patients and Methods: CHEK2*1100delC genotyping was mostly done by a custom Taqman assay. Breast cancer odds ratios (ORs) for CHEK2*1100delC carriers versus noncarriers were estimated by using logistic regression and adjusted for study (categorical) and age. Main analyses included patients with invasive breast cancer from population- and hospital-based studies. Results: Proportions of heterozygous CHEK2*1100delC carriers in controls, in patients with breast cancer from population- and hospital-based studies, and in patients with breast cancer from familial- and clinical genetics center–based studies were 0.5%, 1.3%, and 3.0%, respectively. The estimated OR for invasive breast cancer was 2.26 (95%CI, 1.90 to 2.69; P = 2.3 × 10 −20 ). The OR was higher for estrogen receptor (ER)–positive disease (2.55 [95%CI, 2.10 to 3.10; P = 4.9 × 10 −21 ]) than it was for ER-negative disease (1.32 [95%CI, 0.93 to 1.88; P = .12]; P interaction = 9.9 × 10 −4 ). The OR significantly declined with attained age for breast cancer overall (P = .001) and for ER-positive tumors (P = .001). Estimated cumulative risks for development of ER-positive and ER-negative tumors by age 80 in CHEK2*1100delC carriers were 20% and 3%, respectively, compared with 9% and 2%, respectively, in the general population of the United Kingdom. Conclusion: These CHEK2*1100delC breast cancer risk estimates provide a basis for incorporating CHEK2*1100delC into breast cancer risk prediction models and into guidelines for intensified screening and follow-up.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Four cases within this group harboured germline pathogenic variants in ATM [23], CHEK2 [24] or TP53 [25], all with somatic LOH.”
From Whole-genome sequencing reveals clinically relevant insights into the aetiology of familial breast cancers (2019) · cites this paper as [24]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Chk1 and Chk2 kinases in checkpoint control and cancer
Bartek, J., & Lukas, J. (2003) · Cancer Cell · doi:10.1016/s1535-6108(03)00110-7 · Cited by 1,513
Empirical Bayes Estimates of Age-Standardized Relative Risks for Use in Disease Mapping
Clayton, D. G., & Kaldor, J. M. (1987) · Biometrics · doi:10.2307/2532003 · Cited by 1,277
The CHEK2-Breast Cancer Consortium (2002) · Nature Genetics · doi:10.1038/ng879 · Cited by 1,104
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Michailidou, K., kConFab Investigators, Australian Ovarian Cancer Study Group, The GENICA (Gene Environment Interaction and Breast Cancer in Germany) Network, Hall, P. N., González‐Neira, A., Ghoussaini, M., Dennis, J., Milne, R. L., Schmidt, M. K., et al. (2013) · Nature Genetics · doi:10.1038/ng.2563 · Cited by 1,080
Self-citationShieh, S.-Y., Ahn, J., Tamai, K., Taya, Y., & Prives, C. (2000) · Genes & Development · doi:10.1101/gad.14.3.289 · Cited by 972
Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk
Easton, D. F., Pharoah, P. D. P., Antoniou, A. C., Tischkowitz, M. D., Tavtigian, S. V., Nathanson, K. L., Devilee, P., Meindl, A., Couch, F. J., Southey, M. C., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmsr1501341 · Cited by 947
Self-citationPrediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
Mavaddat, N., Pharoah, P. D. P., Michailidou, K., Tyrer, J. P., Brook, M. N., Bolla, M. K., Wang, Q., Dennis, J., Dunning, A. M., Shah, M., et al. (2015) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djv036 · Cited by 562
Self-citation* (2004) · The American Journal of Human Genetics · doi:10.1086/421251 · Cited by 476
Self-citationRisk determination and prevention of breast cancer
Howell, A., Anderson, A. S., Clarke, R. B., Duffy, S. W., Evans, D. G., García‐Closas, M., Gescher, A. J., Key, T. J., Saxton, J., & Harvie, M. (2014) · Breast Cancer Research · doi:10.1186/s13058-014-0446-2 · Cited by 349
Self-citationPresymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutation.
Meijers-Heijboer, E. J., Verhoog, L., Brekelmans, C., Seynaeve, C., Tilanus-Linthorst, M., Wagner, A., Dukel, L., Devilee, P., van den Ouweland, A. V. D., van Geel, A. V., et al. (2000) · The Lancet · doi:10.1016/s0140-6736(00)02347-3 · Cited by 328
Self-citation
Flagged first, then by citations
Research works printed but not linked: 1
- Adank M, 2015, Ned Tijdschr Geneeskd, 159, A8910
Cited by
Sorted by citations
Items 101–178 of 178
Louro, J., Román, M., Moshina, N., Olstad, C. F., Larsen, M., Sagstad, S., Castells, X., & Hofvind, S. S. H. (2023) · Cancers · doi:10.3390/cancers15184517 · Cited by 6
“We did not include height, as a breast cancer risk factor, in addition to BMI as our model was attributed to the population of screened women, and not to women with genetic mutations, for whom the significance of height was indicated [45,64,65].”
BackgroundWaha, A., Versmold, B., Kast, K., Kiechle, M. B., Ditsch, N. C., Meindl, A., Niederacher, D., Hahnen, E., Arnold, N., Mundhenke, C., et al. (2018) · TumorDiagnostik & Therapie · doi:10.1055/a-0574-4879 · Cited by 6
“[23] Schmidt MK, Hogervorst F, van Hien R et al.”
BackgroundInfluentialSelf-citationWallander, K., Thonberg, H., Nilsson, D., & Tham, E. (2021) · Hereditary Cancer in Clinical Practice · doi:10.1186/s13053-021-00203-z · Cited by 6
Dumont, M., Weber‐Lassalle, N., Joly-Beauparlant, C., Ernst, C., Droit, A., Feng, B., Dubois, S., Collin-Deschesnes, A. C., Soucy, P., Vallée, M., et al. (2022) · Cancers · doi:10.3390/cancers14143363 · Cited by 6
“A scoring system was established for the selection of families based on the assumption that rare, moderate-risk variants might be expected to confer a higher relative risk at young ages, as is the case for most known susceptibility genes [10].”
BackgroundMethodSelf-citationIs prophylactic mastectomy justified in women without BRCA mutation?
Rutgers, E. J. T. (2019) · The Breast · doi:10.1016/s0960-9776(19)31126-9 · Cited by 6
Thompson, D. J., Genovese, G., Halvardson, J., Ulirsch, J. C., Wright, D. J., Terao, C., Davidsson, O. B., Day, F. R., Sulem, P., Jiang, Y., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/514026 · Cited by 7
Self-citationGenetic predisposition to mosaic Y chromosome loss in blood.
Thompson, D. J., Genovese, G., Halvardson, J., Ulirsch, J. C., Wright, D. J., Terao, C. C., Davidsson, O. B., Day, F. R., Sulem, P., Jiang, Y., et al. (2019) · Apollo (University of Cambridge) · doi:10.17863/cam.42407 · Cited by 5
Self-citationAndersen, L. V. B., Larsen, M. J., Davies, H. R., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A., Lænkholm, A., Kruse, T. A., et al. (2023) · Breast Cancer Research · doi:10.1186/s13058-023-01655-y · Cited by 5
Germline Susceptibility to Renal Cell Carcinoma and Implications for Genetic Screening
Glennon, K. I., Endo, M., Usui, Y., Iwasaki, Y., Breau, R. H., Kapoor, A., Lathrop, M. G., Tanguay, S., Momozawa, Y., & Riazalhosseini, Y. (2024) · JCO Precision Oncology · doi:10.1200/po.24.00094 · Cited by 5
Breast Cancer Susceptibility—Towards Individualised Risk Prediction
Lakeman, I. M. M., Schmidt, M. K., van Asperen, C. J., & Devilee, P. (2019) · Current Genetic Medicine Reports · doi:10.1007/s40142-019-00168-5 · Cited by 5
Self-citationKleiblová, P., Stolařová, L., Křížová, K., Lhota, F., Hojný, J., Zemánková, P., Havránek, O., Vočka, M., Černá, M., Lhotová, K., et al. (2019) · Klinicka onkologie · doi:10.14735/amko2019s36 · Cited by 5
CHEK2-related breast cancer: real-world challenges
Weis, L. N., Bychkovsky, B., Hernandez, A. R., Barroso‐Sousa, R., & Sandoval, R. L. (2025) · Familial Cancer · doi:10.1007/s10689-025-00448-w · Cited by 4
Statistical methods for Mendelian models with multiple genes and cancers
Liang, J. W., Idos, G., Hong, C., Gruber, S. B., Parmigiani, G., & Braun, D. (2022) · Genetic Epidemiology · doi:10.1002/gepi.22460 · Cited by 4
Germline mutations in the PALB2 and CHEK2 genes and hereditary cancer
Golotyuk, M. A., Berezhnoy, A. A., Kazantseva, N. V., Dorofeev, A., & Borzunova, T. I. (2023) · Ural Medical Journal · doi:10.52420/2071-5943-2023-22-3-126-136 · Cited by 4
Ding, K., Zhou, Z., Ma, Y., Li, X., Xiao, H., Wu, Y., Wu, T., & Chen, D. (2022) · Biomedicines · doi:10.3390/biomedicines10123093 · Cited by 3
“Recent examples of proposed subtypes span diverse disease domains, including type 2 diabetes [3,27], breast cancer [28,29], asthma [30,31], autism [32,33], bipolar disorder, and schizophrenia [34,35].”
BackgroundBreast cancer: genetic personal risk factors: A review
Zolotykh, M. A., Bilyalov, A. I., Nesterova, A. I., Гимранов, А. М., Filina, Y. V., Rizvanov, A. A., & Рифкатовна, М. Р. (2023) · Journal of Modern Oncology · doi:10.26442/18151434.2023.2.202110 · Cited by 3
Thiruchelvam, P. T. R., Fisher, C. S., Leff, D. R., & Domchek, S. M. (2018) · The Lancet · doi:10.1016/s0140-6736(18)30997-8 · Cited by 3
Ethnic Features of Genetic Susceptibility to Breast Cancer
Bermisheva, M., Bogdanova, N. V., Gilyazova, I. R., Zinnatullina, G., Бисултанова, З. И., & Хуснутдинова, Э. К. (2018) · Russian Journal of Genetics · doi:10.1134/s1022795418020047 · Cited by 4
Self-citationUpdate Breast Cancer 2022 Part 1 – Early Stage Breast Cancer
Welslau, M., Müller, V., Lüftner, D., Schütz, F., Stickeler, E., Fasching, P. A., Janni, W., Thomssen, C., Witzel, I., Fehm, T. N., et al. (2022) · Geburtshilfe und Frauenheilkunde · doi:10.1055/a-1811-6106 · Cited by 3
Self-citationManaging Patient with Mutations in PALB2, CHEK2, or ATM
Francisco Acevedo, C., Deng, Z., Armengol, V. D., & Hughes, K. S. (2018) · Current Breast Cancer Reports · doi:10.1007/s12609-018-0269-8 · Cited by 2
Multi-gene panel testing and association analysis in Cypriot breast cancer cases and controls
Zanti, M., Loizidou, M. A., O'Mahony, D. G., Dorling, L., Dennis, J., Devilee, P., Easton, D. F., Panayiotidis, M. I., Hadjisavvas, A., & Michailidou, K. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1248492 · Cited by 2
“Cumulative risks of breast cancer in the absence of other events were calculated by combining age-specific odds ratios with population incidence rates for Cyprus (2020) as a baseline, as previously described (Schmidt et al., 2016).”
MethodSelf-citationClinical Impact of Constitutional Genomic Testing on Current Breast Cancer Care
Cheah, W., Cutress, R., Eccles, D., & Copson, E. (2024) · Clinical Oncology · doi:10.1016/j.clon.2024.08.006 · Cited by 2
Schreurs, M. A. C., Adank, M. A., Hollestelle, A., de Groot, R., Stommel-Jenner, D. J., van Asperen, C. J., Ausems, M. G. E. M., Berger, L. P. V., Blok, M. J., van Engelen, K., et al. (2024) · BMJ Open · doi:10.1136/bmjopen-2024-086688 · Cited by 2
Self-citationBeyond BRCA: A Case Series Examining the Advent of Multigene Panel Testing
Reap, L. E., Ahsan, S., & Saleh, M. (2018) · Clinical Breast Cancer · doi:10.1016/j.clbc.2018.03.015 · Cited by 2
“One large caseecontrol study demonstrated increased risk for thyroid, prostate, colon, and renal cancer among individuals found to be CHEK2 positive.(19) Whether the presence of a CHEK2 mutation increases the risk of the development of early (younger than 35 years old) versus late onset breast cancer seems to be uncle…”
BackgroundMethodDiagnostic yield of a custom-designed multi-gene cancer panel in Irish patients with breast cancer
McVeigh, U. M., McVeigh, T. P., Curran, C. E., Miller, N., Morris, D. W., & Kerin, M. J. (2020) · Irish Journal of Medical Science (1971 -) · doi:10.1007/s11845-020-02174-x · Cited by 2
Schütz, F., Fasching, P. A., Welslau, M., Hartkopf, A. D., Wöckel, A., Lux, M. P., Janni, W., Ettl, J., Lüftner, D., Belleville, E., et al. (2019) · Senologie - Zeitschrift für Mammadiagnostik und -therapie · doi:10.1055/a-1036-0961 · Cited by 2
“[20] Schmidt MK, Hogervorst F, van Hien R et al.”
BackgroundSelf-citationDNA methylation and breast cancer risk: value of twin and family studies
Li, S., Ye, Z., kConFab Investigators, Hopper, J. L., & Southey, M. C. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820951-6.00004-1 · Cited by 2
Self-citationPanel Testing for Hereditary Breast Cancer: More or Less?
Landry, K. K., & Wood, M. E. (2020) · Current Breast Cancer Reports · doi:10.1007/s12609-020-00361-4 · Cited by 1
Malignant fibroadenoma with CHEK2 mutation: a novel case
Ching, D., Pirasteh, S., Vora, B., Martin, R., & Gill, J. (2020) · Pathology · doi:10.1016/j.pathol.2020.04.009 · Cited by 1
Çine, N., Ugurtas, C., Gökbayrak, M. E., Aydın, D., Demir, G., Kuru, S., Akkoyunlu, D. S., KESKİN, S. E., Şimşek, T., Çabuk, D., et al. (2022) · Annals of Human Genetics · doi:10.1111/ahg.12488 · Cited by 1
Moderate-Penetrance Predisposition to Breast Cancer
Robson, M. E. (2018) · Current Breast Cancer Reports · doi:10.1007/s12609-018-0289-4 · Cited by 1
Self-citationBreast Cancer with Hereditary Cancer Predisposition Syndromes
Rao, R., Mauer, C. B., Chen-Seetoo, M., & Peng, Y. S. (2019) · Springer eBooks · doi:10.1007/978-3-030-16518-5_8 · Cited by 1
Genetic Predictors of Malignancy: a Literature Review
Пушкарев, А. В., Галеев, М. Г., Пушкарев, В. А., & Султанбаев, А. В. (2021) · Creative Surgery and Oncology · doi:10.24060/2076-3093-2021-11-2-157-165 · Cited by 1
Hereditary Cancer Counseling and Germline Genetic Testing
Menendez, C. S., Marcom, P. K., & Sutton, L. (2021) · Springer eBooks · doi:10.1007/978-3-030-75377-1_20 · Cited by 1
Statistical approaches for meta‐analysis of genetic mutation prevalence
Hujoel, M. L. A., Parmigiani, G., & Braun, D. (2020) · Genetic Epidemiology · doi:10.1002/gepi.22364 · Cited by 1
“Beyond the challenge of rare mutations, the second challenge is that large population‐based studies are not feasible in every ethnic group and the prevalence of genetic mutations can differ greatly depending on the population (Schmidt et al., 2016).”
BackgroundNGS zur Selektion innovativer Therapien – Was bringt das?
Schulmeyer, C. E., Bader, S., Hübner, H., Rübner, M., & Fasching, P. A. (2021) · Der Gynäkologe · doi:10.1007/s00129-021-04774-9 · Cited by 1
Self-citation2. Wissenschaftspreis: Verbesserung der Risikokalkulation für Brustkrebs durch polygenen Risikoscore
Borde, J., Ernst, C., Hahnen, E., & Schmutzler, R. K. (2021) · Senologie - Zeitschrift für Mammadiagnostik und -therapie · doi:10.1055/a-1376-3533 · Cited by 1
“Cancer Med 2018; 7: 1349–1358 [3] Schmidt MK, Hogervorst F, van Hien R et al.”
BackgroundSelf-citationWilcox, N., Dumont, M., González‐Neira, A., Carvalho, S., Beauparlant, C. J., Crotti, M., Luccarini, C., Soucy, P., Dubois, S., Núñez‐Torres, R., et al. (2022) · medRxiv · doi:10.1101/2022.06.17.22276537 · Cited by 1
Self-citationManagement of the Patient with a Genetic Predisposition for Breast Cancer
Colonna, S. V., & Gammon, A. (2016) · Springer eBooks · doi:10.1007/978-3-319-46356-8_31
Hereditäre Tumordiagnostik – Mammakarzinom: BRCA1, BRCA2 und derzeitiger Stand der Multigenanalysen
Hahnen, E., Wappenschmidt, B., Rhiem, K., & Schmutzler, R. K. (2017) · Geburtshilfe und Frauenheilkunde · doi:10.1055/s-0042-122159
“[40] Schmidt MK, Hogervorst F, van Hien R et al.”
Self-citationMammakarzinom: BRCA1, BRCA2 und derzeitiger Stand der Multigenanalysen
Hahnen, E., Waha, A., Wappenschmidt, B., Rhiem, K., & Schmutzler, R. K. (2017) · Senologie - Zeitschrift für Mammadiagnostik und -therapie · doi:10.1055/s-0043-105663
“JAMA oncology 2015; 1 (1): 23–32 [40] Schmidt MK, Hogervorst F, van Hien R et al.”
Self-citationMutations in CHEK2 and risk of gastric cancer: a case-control study
Lv, Z.-C., Liu, R., Mu, L., Ma, J., & Yang, L. (2017) · Biomedical Research-tokyo
Witzel, I., & Speiser, D. (2018) · Der Gynäkologe · doi:10.1007/s00129-018-4203-y
Früherkennung von Mammakarzinomen
Witzel, I., & Speiser, D. (2018) · Im Focus Onkologie · doi:10.1007/s15015-018-4024-9
Update Mammakarzinom 2018 (Teil 2) – Fortgeschrittenes Mammakarzinom, Lebensqualität und Prävention
Schneeweiß, A., Lux, M. P., Janni, W., Hartkopf, A. D., Nabieva, N., Taran, F., Overkamp, F., Kolberg, H., Hadji, P., Tesch, H., et al. (2018) · Senologie - Zeitschrift für Mammadiagnostik und -therapie · doi:10.1055/s-0043-124850
Self-citationProphylactic Mastectomy in Patients with Atypical Breast Lesions
Boughey, J. C., & Degnim, A. C. (2018) · Springer eBooks · doi:10.1007/978-3-319-92657-5_11
Peterlongo, P., & Carvajal‐Carmona, L. G. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.00841
“The moderate-penetrance genes ATM and CHEK2 are also associated with breast cancer, conferring a 20% average lifetime risk (3, 4).”
BackgroundVargas‐Parra, G., Valle, J. D., Rofes, P., Gausachs, M., Stradella, A., Moreno-Cabrera, J. M., Velasco, À., Tornero, E., Menéndez, M., Muñoz, X., et al. (2020) · doi:10.22541/au.159050458.86704879
Genetische Grundlagen des erblichen Mamma- und Ovarialkarzinoms
Hahnen, E., & Meindl, A. (2020) · Der Gynäkologe · doi:10.1007/s00129-020-04696-y
Self-citationPanelPRO: a general framework for multi-gene, multi-cancer Mendelian risk prediction modelsPreprint
Liang, J. W., Idos, G., Hong, C., Gruber, S. B., Parmigiani, G., & Braun, D. (2021) · arXiv (Cornell University)
Escudero, L. S., Garcés, M. Y. R., & Ruiz, F. J. J. (2022) · Cirugía Española · doi:10.1016/j.ciresp.2022.03.014
Update Mammakarzinom 2021 Teil 4 – Prävention und frühe Krankheitsstadien
Thomssen, C., Fehm, T. N., Stickeler, E., Fasching, P. A., Janni, W., Kolberg‐Liedtke, C., Kolberg, H., Lüftner, D., Müller, V., Schütz, F., et al. (2022) · Senologie - Zeitschrift für Mammadiagnostik und -therapie · doi:10.1055/a-1816-1625
Self-citationLiang, J. W., Christensen, K. D., Green, R. C., & Kraft, P. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.10.503415
Escudero, L. S., Garcés, M. Y. R., & Ruiz, F. J. J. (2022) · Cirugía Española (English Edition) · doi:10.1016/j.cireng.2022.03.021
Update Mammakarzinom 2022 Teil 1 – Brustkrebs in frühen Krankheitsstadien
Welslau, M., Müller, V., Lüftner, D., Schütz, F., Stickeler, E., Fasching, P. A., Janni, W., Thomssen, C., Witzel, I., Fehm, T. N., et al. (2022) · Senologie - Zeitschrift für Mammadiagnostik und -therapie · doi:10.1055/a-1898-4367
“[18] Schmidt MK, Hogervorst F, van Hien R et al.”
BackgroundSelf-citationPrävention des Mamma- und Ovarialkarzinoms bei Frauen mit Genmutationen
Tüchler, A., Hahnen, E., Schmutzler, R., & Rhiem, K. (2023) · Die Gynäkologie · doi:10.1007/s00129-023-05163-0
Self-citationFamiliärer Brust- und Eierstockkrebs – Prävention und Therapie
Rhiem, K., Tüchler, A., Schmutzler, R. K., & Hahnen, E. (2024) · Die Gynäkologie · doi:10.1007/s00129-024-05222-0
Self-citationLiang, J. W., Christensen, K. D., Green, R. C., & Kraft, P. (2024) · npj Genomic Medicine · doi:10.1038/s41525-024-00414-y
Mukhtar, T. K., Wilcox, N., Dennis, J., Yang, X., Naven, M., Mavaddat, N., Perry, J. R. B., Gardner, E. J., & Easton, D. F. (2024) · medRxiv · doi:10.1101/2024.07.01.24309756
Self-citationSarin, R. (2024) · Springer eBooks · doi:10.1007/978-981-99-3378-5_74
Petelin, L., Cunich, M. M., Procopio, P., SCHOFIELD, D. J., Devereux, L., Nickson, C., James, P. A., Campbell, I., & Trainer, A. H. (2024) · Cancers · doi:10.3390/cancers16244165
Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597108
Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597120
Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597114
Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597105
Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597126
Smid, M., Schmidt, M. K., der Smissen, W. J. C. P., Ruigrok-Ritstier, K., Schreurs, M. A. C., Cornelissen, S., Garcia, A. M., Broeks, A., Timmermans, A. M., Trapman-Jansen, A., et al. (2023) · Figshare · doi:10.6084/m9.figshare.22792719
Self-citationAndersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597111
Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597102
Wallander, K., Thonberg, H., Nilsson, D., & Tham, E. (2021) · Figshare · doi:10.6084/m9.figshare.16900764
Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597123
Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597117
Andersen, L. V. B., Larsen, M. J., Davies, H., Degasperi, A., Nielsen, H. R., Jensen, L. A., Kroeldrup, L., Gerdes, A.-M., Lænkholm, A.-V., Kruse, T. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26597129
Lee, J. H., Ryu, J. M., Park, J. S., Kim, J. H., Cha, C., Eoh, K. J., Yang, Y., Lee, B.-Y., Han, S.-A., & Kim, S.-W. (2026) · Journal of Breast Cancer · doi:10.4048/jbc.2025.0279
“For moderate-penetrance genes, including CHEK2 [28-30], ATM [5,6,31,32], MRI-based surveillance is usually preferred over prophylactic surgery, with RRM reserved for additional modifiers (e.g., a strong family history and prior chest irradiation).”
Schreurs, M. A. C., Hollestelle, A., Adank, M. A., Louwers, Y. V., van Asperen, C. J., Ausems, M. G. E. M., van de Beek, I., Collee, M. J., Dommering, C. J., Gómez-García, E. B., et al. (2026) · Journal of Medical Genetics · doi:10.1136/jmg-2025-111339
“17 21 29–31 Therefore, it is unclear whether the longer oestrogen exposure should be considered as an important breast cancer risk factor in CHEK2 c.1100delC heterozygotes.”
Self-citationThe contribution of rare germline variants to the immune landscape of breast cancer
Rojas-Rodríguez, F., Canisius, S., Keeman, R., Bernstein, A. J., Hurson, A. N., Ahearn, T. U., Andrulis, I. L., Antoniou, A. C., Behrens, S., Białkowska, K., et al. (2026) · Genome Medicine · doi:10.1186/s13073-026-01662-6
Self-citationHjelm, T. E., Gebremariam, T. Y., Weldearegay, M. F., Ayele, B. G., Assefa, M., Anberber, E., Kvist, A., Törngren, T., Borg, Å., Margolin, S., et al. (2026) · JCO Global Oncology · doi:10.1200/go-25-00699
Self-citationMultidisciplinary Management Considerations in Invasive Lobular Breast Cancer: It Isn’t Just Ductal
Beck, A. C., Carroll, E. F., Mukhtar, R. A., Cassidy, M. R., Flanagan, M. R., Gamble, L. A., & Erdahl, L. M. (2026) · Annals of Surgical Oncology · doi:10.1245/s10434-026-20368-y
Metadata
- Authors
- Schmidt, M. K., Hogervorst, F., van Hien, R., Cornelissen, S., Broeks, A., Adank, M. A., Meijers, H., Waisfisz, Q., Hollestelle, A., Schutte, M., van den Ouweland, A., Hooning, M., Andrulis, I. L., Anton-Culver, H., Antonenkova, N. N., Antoniou, A. C., Arndt, V., Bermisheva, M., Bogdanova, N. V., Bolla, M. K., Brauch, H., Brenner, H., Brüning, T., Burwinkel, B., Chang-Claude, J., Chenevix-Trench, G., Couch, F. J., Cox, A., Cross, S. S., Czene, K., Dunning, A. M., Fasching, P. A., Figueroa, J., Fletcher, O., Flyger, H., Galle, E., García-Closas, M., Giles, G. G., Haeberle, L., Hall, P., Hillemanns, P., Hopper, J. L., Jakubowska, A., John, E. M., Jones, M., Khusnutdinova, E., Knight, J. A., Kosma, V.-M., Kristensen, V., Lee, A., Lindblom, A., Lubinski, J., Mannermaa, A., Margolin, S., Meindl, A., Milne, R. L., Muranen, T. A., Newcomb, P. A., Offit, K., Park-Simon, T.-W., Peto, J., Pharoah, P. D. P., Robson, M., Rudolph, A., Sawyer, E. J., Schmutzler, R. K., Seynaeve, C., Soens, J., Southey, M. C., Spurdle, A. B., Surowy, H., Swerdlow, A., Tollenaar, R. A. E. M., Tomlinson, I., Trentham-Dietz, A., Vachon, C., Wang, Q., Whittemore, A. S., Ziogas, A., van der Kolk, L., Nevanlinna, H., Dörk, T., Bojesen, S., & Easton, D. F.
- Affiliations
- F. Hoffmann-La Roche AG (CH)
- Marjanka K. Schmidt, Frans Hogervorst, Richard van Hien, Sten Cornelissen, Annegien Broeks, and Lizet van der Kolk, Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital; Muriel A. Adank, Hanne Meijers, and Quinten Waisfisz, VU University Medical Center, Amsterdam; Antoinette Hollestelle, Mieke Schutte, Maartje Hooning, and Caroline Seynaeve, Erasmus MC Cancer Institute; Ans van den Ouweland, Erasmus University Medical Center, Rotterdam; Rob A.E.M. Tollenaar, Leiden University Medical Center,...
- Corresponding author
- Schmidt, Marjanka K.
- ORCID
- Schmidt, Marjanka K.
- Cornelissen, Sten
- Broeks, Annegien
- Adank, Muriel A.
- Waisfisz, Quinten
- Hollestelle, Antoinette
- Hooning, Maartje
- Andrulis, Irene L.
- Antoniou, Antonis C.
- Arndt, Volker
- Bermisheva, Marina
- Bogdanova, Natalia V.
- Bolla, Manjeet K.
- Brauch, Hiltrud
- Brenner, Hermann
- Brüning, Thomas
- Burwinkel, Barbara
- Chang-Claude, Jenny
- Couch, Fergus J.
- Cox, Angela
- Cross, Simon S.
- Czene, Kamila
- Dunning, Alison M.
- Fasching, Peter A.
- Figueroa, Jonine
- Fletcher, Olivia
- Galle, Eva
- Giles, Graham G.
- Hall, Per
- Hillemanns, Peter
- Hopper, John L.
- Jakubowska, Anna
- John, Esther M.
- Knight, Julia A.
- Kosma, Veli-Matti
- Kristensen, Vessela
- Lindblom, Annika
- Margolin, Sara
- Milne, Roger L.
- Muranen, Taru A.
- Newcomb, Polly A.
- Pharoah, Paul D.P.
- Robson, Mark
- Rudolph, Anja
- Sawyer, Elinor J.
- Southey, Melissa C.
- Spurdle, Amanda B.
- Surowy, Harald
- Swerdlow, Anthony
- Tollenaar, Rob A.E.M.
- Tomlinson, Ian
- Vachon, Celine
- Wang, Qin
- Whittemore, Alice S.
- Ziogas, Argyrios
- Nevanlinna, Heli
- Dörk, Thilo
- Bojesen, Stig
- Easton, Douglas F.
- Venue
- Journal of Clinical Oncology
- Published
- 2016-08-10
- Volume
- 34
- Issue
- 23
- Pages
- 2750-2760
- ISSN
- 0732-183X (ISSN-L)
- 1527-7755
- PMC
- PMC5019754
- OpenAlex
- W2400927555
- Cited by
- 173
- References
- 27
- Citations by year
- 2026: 5 · 2025: 1 · 2024: 16 · 2023: 17 · 2022: 30 · 2021: 19 · 2020: 19 · 2019: 27 · 2018: 22 · 2017: 14 · 2016: 3
- FWCI
- 17.59
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Clinical Oncology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Kölner Universitäts PublikationsServer (Universität zu Köln) (publishedVersion)
- Pure Amsterdam UMC (publishedVersion, other-oa)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (acceptedVersion)
- LSHTM Research Online (London School of Hygiene and Tropical Medicine) (acceptedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Leiden Repository (Leiden University) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Research Portal (King's College London) (submittedVersion)
- mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) (submittedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
- Apollo (University of Cambridge) (submittedVersion)
- Apollo
- Funders
- U.S. Department of Health and Human Services
- Susan G. Komen for the Cure (CA116201, 39346, DDHK 2009-4318, 70492, 193387/V50, C1287/A10118, 01KW9976/8, DDHK 2004-3124, HEALTH-F2-2009-223175, CA92044, LVS39420, 01KW9975/5, 2007-3839, CA58860, 01KW9977/0, 2009 4363, 193387/H10, BBMRI-NL CP16, RUS08/017, 209057, 110837, 01KW0114, RUL 1997-1505, PBZ_KBN_122/P05/2004, UM1 CA164920, C490/A10124)
- Mayo Clinic (CA116201)
- Breast Cancer Research Foundation (UM1 CA164920, C490/A10124, 2007-3839, 39346, 01KW0114, 70492, 01KW9977/0, DDHK 2009-4318, C1287/A10118, CA116201, 01KW9976/8, RUL 1997-1505, CA92044, 209057, 110837, RUS08/017, BBMRI-NL CP16, CA58860, 2009 4363, LVS39420, 01KW9975/5, 193387/V50, 193387/H10, PBZ_KBN_122/P05/2004, HEALTH-F2-2009-223175, DDHK 2004-3124)
- Memorial Sloan-Kettering Cancer Center
- Itä-Suomen Yliopisto (RUL 1997-1505, 110837, DDHK 2009-4318, CA92044, LVS39420, 70492, 2007-3839, 193387/V50, C1287/A10118, PBZ_KBN_122/P05/2004, RUS08/017, C490/A10124, 193387/H10, 01KW9977/0, CA116201, 39346, 209057, 2009 4363, UM1 CA164920, HEALTH-F2-2009-223175, BBMRI-NL CP16, 01KW9976/8, 01KW9975/5, CA58860, DDHK 2004-3124, 01KW0114)
- Helsingin Yliopisto
- Helsingin ja Uudenmaan Sairaanhoitopiiri
- Sundhed og Sygdom, Det Frie Forskningsråd (C1287/A10118, DDHK 2009-4318, 39346, PBZ_KBN_122/P05/2004, CA116201, HEALTH-F2-2009-223175, 01KW9977/0, CA92044, UM1 CA164920, 01KW9975/5, LVS39420, CA58860, RUS08/017, 70492, C490/A10124, 01KW0114, 2007-3839, 193387/H10, 01KW9976/8, 209057, 2009 4363, BBMRI-NL CP16, 193387/V50, DDHK 2004-3124, 110837, RUL 1997-1505)
- Deutsches Krebsforschungszentrum (PBZ_KBN_122/P05/2004, 110837, 01KW9976/8, DDHK 2004-3124, UM1 CA164920, 01KW9977/0, 01KW0114, RUS08/017, 193387/H10, C490/A10124, 2009 4363, 70492, 193387/V50, C1287/A10118, CA116201, 2007-3839, CA92044, HEALTH-F2-2009-223175, LVS39420, BBMRI-NL CP16, CA58860, 209057, DDHK 2009-4318, 01KW9975/5, RUL 1997-1505, 39346)
- Kreftforeningen (BBMRI-NL CP16, PBZ_KBN_122/P05/2004, UM1 CA164920, RUL 1997-1505, 70492, DDHK 2009-4318, HEALTH-F2-2009-223175, 2009 4363, 2007-3839, C1287/A10118, 193387/V50, DDHK 2004-3124, 39346, CA58860, 01KW9975/5, 209057, RUS08/017, 193387/H10, C490/A10124, 01KW0114, 110837, 01KW9976/8, LVS39420, CA116201, CA92044, 01KW9977/0)
- London School of Hygiene and Tropical Medicine
- David F. and Margaret T. Grohne Family Foundation (01KW9977/0, CA92044, 01KW9975/5, 2009 4363, PBZ_KBN_122/P05/2004, UM1 CA164920, BBMRI-NL CP16, CA58860, C1287/A10118, 70492, CA116201, DDHK 2009-4318, C490/A10124, 110837, DDHK 2004-3124, 209057, HEALTH-F2-2009-223175, 2007-3839, 193387/V50, RUL 1997-1505, 193387/H10, 01KW0114, 39346, 01KW9976/8, RUS08/017, LVS39420)
- Wellcome Trust (090532, 090532/Z/09/Z)
- Francis Crick Institute (10124, 10119)
- QIMR Berghofer Medical Research Institute
- Lon V. Smith Foundation (01KW0114, LVS39420, 70492, RUS08/017, 01KW9975/5, DDHK 2009-4318, C490/A10124, 209057, CA116201, PBZ_KBN_122/P05/2004, UM1 CA164920, 2007-3839, 01KW9976/8, 01KW9977/0, C1287/A10118, BBMRI-NL CP16, 110837, CA92044, HEALTH-F2-2009-223175, CA58860, RUL 1997-1505, DDHK 2004-3124, 2009 4363, 39346, 193387/H10, 193387/V50)
- Cancer Research UK (LVS39420, 223175, 11174, 70492, 10119, 01KW9977/0, C1287/A10118, C1287/A12014, RUS08/017, C1287‐A10118, 12014, HEALTHF2-2009-223175, 16561, 01KW9975/5, 16565, RUL 1997-1505, 209057, C1287/ A12014, 110837, C1287, CA92044, PBZ_KBN_122/P05/2004, 20861, 2007-3839, 01KW9976/8, 193387/V50, 10118, CA116201, 10124, 2009 4363, DDHK 2004-3124, C490/A10124, UM1 CA164920, 39346, 01KW0114, CA58860, 193387/H10, BBMRI-NL CP16, DDHK 2009-4318)
- National Institute for Health and Care Research (110837, 39346, RUS08/017, 193387/V50, 01KW9976/8, HEALTH-F2-2009-223175, 03/DHCS/03/G121/51, DDHK 2009-4318, PBZ_KBN_122/P05/2004, 209057, CA116201, CA92044, C1287/A10118, 01KW9975/5, BBMRI-NL CP16, 01KW9977/0, RUL 1997-1505, 70492, UM1 CA164920, LVS39420, DDHK 2004-3124, 2009 4363, 01KW0114, CA58860, 2007-3839, C490/A10124, 193387/H10)
- King's College London
- University of Oxford
- National Breast Cancer Foundation (01KW9975/5, LVS39420, 2009 4363, HEALTH-F2-2009-223175, BBMRI-NL CP16, 39346, CA116201, RUS08/017, 193387/H10, 110837, CA58860, DDHK 2009-4318, DDHK 2004-3124, 2007-3839, 01KW9977/0, 193387/V50, 01KW9976/8, C490/A10124, RUL 1997-1505, 70492, CA92044, 01KW0114, 209057, UM1 CA164920, C1287/A10118, PBZ_KBN_122/P05/2004)
- Agency for Science, Technology and Research
- Robert Bosch Stiftung (01KW9976/8, 193387/H10, 01KW0114, DDHK 2009-4318, DDHK 2004-3124, C1287/A10118, UM1 CA164920, 70492, BBMRI-NL CP16, RUS08/017, CA116201, CA92044, HEALTH-F2-2009-223175, 01KW9977/0, 01KW9975/5, 193387/V50, 2009 4363, C490/A10124, 39346, PBZ_KBN_122/P05/2004, 110837, RUL 1997-1505, CA58860, 2007-3839, 209057, LVS39420)
- Universität Heidelberg
- Universiteit Leiden
- University of Melbourne
- Universiteit van Amsterdam
- Vrije Universiteit Amsterdam
- Eberhard Karls Universität Tübingen
- Bundesministerium für Bildung und Forschung (193387/V50, 2007-3839, 70492, BBMRI-NL CP16, 01KW9977/0, 39346, 01KW9975/5, 01KW9976/8, 2009 4363, C1287/A10118, C490/A10124, HEALTH-F2-2009-223175, 01KW0114, PBZ_KBN_122/P05/2004, RUS08/017, 110837, CA92044, CA58860, DDHK 2009-4318, CA116201, UM1 CA164920, 193387/H10, RUL 1997-1505, 209057, LVS39420, DDHK 2004-3124)
- Cancerfonden
- Gentofte Hospital
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (184021007, NWO 184.021.007)
- Deutsche Gesetzliche Unfallversicherung
- Herlev Hospital
- University of Toronto
- Karolinska Institutet (DDHK 2004-3124, 01KW9977/0, 39346, C1287/A10118, CA58860, HEALTH-F2-2009-223175, DDHK 2009-4318, LVS39420, CA116201, PBZ_KBN_122/P05/2004, RUL 1997-1505, RUS08/017, 2009 4363, C490/A10124, CA92044, 01KW9975/5, 01KW0114, 193387/H10, UM1 CA164920, BBMRI-NL CP16, 193387/V50, 110837, 70492, 01KW9976/8, 2007-3839, 209057)
- Kuopion Yliopistollinen Sairaala
- Stockholms Läns Landsting
- KWF Kankerbestrijding (193387/V50, NKI 2007–3839; 2009 4363, PBZ_KBN_122/P05/2004, DDHK 2004‐3124, 2007-3839, 2004-3124, LVS39420, RUS08/017, 01KW9976/8, UM1 CA164920, 70492, 1997-1505, HEALTH-F2-2009-223175, C490/A10124, 2009 4363, 01KW9977/0, CA116201, 193387/H10, NKI 2007–3839, DDHK 2009‐4318, CA58860, RUL1997-1505, CA92044, 01KW0114, 39346, 209057, 110837, C1287/A10118, 01KW9975/5, BBMRI-NL CP16)
- Leids Universitair Medisch Centrum
- Universitetet i Oslo (209057)
- Norges Forskningsråd (01KW0114, 209057, BBMRI-NL CP16, 193387/H10, 2007-3839, C1287/A10118, 01KW9975/5, 110837, 2009 4363, RUL 1997-1505, 01KW9976/8, CA58860, PBZ_KBN_122/P05/2004, DDHK 2004-3124, CA116201, UM1 CA164920, C490/A10124, LVS39420, 39346, 193387/V50, 01KW9977/0, RUS08/017, HEALTH-F2-2009-223175, CA92044, DDHK 2009-4318, 70492)
- Medizinischen Hochschule Hannover (01KW0114, 2007-3839, 39346, 2009 4363, DDHK 2004-3124, 209057, 193387/H10, C1287/A10118, 01KW9976/8, 01KW9975/5, 193387/V50, 110837, RUL 1997-1505, RUS08/017, C490/A10124, BBMRI-NL CP16, CA92044, CA58860, DDHK 2009-4318, CA116201, LVS39420, 70492, HEALTH-F2-2009-223175, PBZ_KBN_122/P05/2004, 01KW9977/0, UM1 CA164920)
- Technische Universität München
- Deutsche Krebshilfe (HEALTH-F2-2009-223175, 193387/H10, (#110837, 2007-3839, 01KW0114, DDHK 2004-3124, CA58860, RUL 1997-1505, UM1 CA164920, 01KW9976/8, C490/A10124, DDHK 2009-4318, CA92044, 209057, PBZ_KBN_122/P05/2004, 01KW9977/0, BBMRI-NL CP16, 01KW9975/5, 39346, CA116201, 2009 4363, C1287/A10118, 70492, 193387/V50, LVS39420, RUS08/017)
- Universität zu Köln
- Pomorski Uniwersytet Medyczny W Szczecinie
- Universitätsklinikum Köln
- National Institutes of Health (LVS39420, CA11620 1, DDHK 2009-4318, 01KW0114, 01KW9977/0, 01KW9975/5, 223175, 39346, 184.021.007, 193387/V50, 2007-3839, RUL 1997-1505, 193387/H10, 110837, 70492, C490/A10124, PBZ_KBN_122/P05/2004, RUS08/017, 01KW9976/8, C1287/A10118, BBMRI-NL CP16, 209057, HEALTH-F2-2009-223175, 3u01ca164920-07s1, DDHK 2004-3124, 2009 4363, CA116167, CA164920, CA58860)
- School of Medicine, Stanford University
- U.S. Army (DAMD17-01-1-0729)
- University of California, Los Angeles
- University of California, Irvine
- Medical Research Council (110837, CA58860, 70492, CA116201, PBZ_KBN_122/P05/2004, RUL 1997-1505, DDHK 2004-3124, RUS08/017, MC_PC_14105, BBMRI-NL CP16, HEALTH-F2-2009-223175, UM1 CA164920, 01KW9975/5, 01KW9976/8, 193387/V50, 01KW0114, 193387/H10, 2009 4363, 2007-3839, C490/A10124, C1287/A10118, CA92044, 39346, 209057, LVS39420, 01KW9977/0, DDHK 2009-4318)
- National Health and Medical Research Council (251553, 199600, 400281, 209057, 400413, 400281, 400413, 504711)
- Cancer Council South Australia
- Cancer Council Victoria (DDHK 2004-3124, UM1 CA164920, 110837, C1287/A10118, CA92044, 39346, 209057, HEALTH-F2-2009-223175, 2007-3839, CA116201, 193387/V50, 01KW9976/8, 01KW0114, DDHK 2009-4318, C490/A10124, PBZ_KBN_122/P05/2004, CA58860, 2009 4363, RUS08/017, RUL 1997-1505, BBMRI-NL CP16, 01KW9977/0, 01KW9975/5, 70492, LVS39420, 193387/H10)
- Cancer Council NSW
- Cancer Council Tasmania
- Russian Academy of Sciences
- Erasmus Universitair Medisch Centrum Rotterdam
- Universitätsklinikum Hamburg-Eppendorf
- National Cancer Institute (01KW9976/8, RUS08/017, PBZ_KBN_122/P05/2004, U01CA058860, HEALTH-F2-2009-223175, CA116167, DDHK 2009-4318, R01CA058860, 01KW9975/5, R01CA116167, UM1CA164920, 193387/H10, R01CA069664, R01CA047305, RUL 1997-1505, CA-116201, 2009 4363, R01CA192393, 209057, CA164920, CA58860, 01KW9977/0, 2007-3839, 193387/V50, 39346, CA176785, 01KW0114, K07CA092044, CA192393, C1287/A10118, 110837, DAMD17-01-1-0729, U01CA116167, DDHK 2004-3124, BBMRI-NL-CP16, R01CA176785, C490/A10124, CA92044, R01CA047147, 70492, P30CA008748, P50CA116201, LVS39420)
- David Geffen School of Medicine, University of California, Los Angeles
- Medical Research and Materiel Command (DAMD17-01–1-0729)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › BRCA gene mutations in cancer
- Health Sciences › Medicine › Pathology and Forensic Medicine › Breast Lesions and Carcinomas
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- CHEK2 1100delC, germline mutation carriers, breast cancer risk, tumor subtypes, estrogen receptor-positive breast cancer, age-specific risk, cumulative risk, breast cancer risk prediction, Breast Cancer Association Consortium, hereditary breast cancer, odds ratio, heterozygous carriers
- MeSH terms
- Adult, Age Factors, Aged, Aged, 80 and over, Breast Neoplasms, Female, Heterozygote, Homozygote, Humans, Middle Aged, Receptors, Estrogen, Receptors, Progesterone, Odds Ratio, Case-Control Studies, Sequence Deletion, Risk Assessment, Genetic Predisposition to Disease, Checkpoint Kinase 2
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review