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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk
Douglas F. Easton, Paul D.P. Pharoah, Antonis C. Antoniou, et al.
New England Journal of Medicine (2015) Vol. 372, Iss. 23, pp. 2243-2257
Open Access | Times Cited: 855

Showing 1-25 of 855 citing articles:

The personal and clinical utility of polygenic risk scores
Ali Torkamani, Nathan E. Wineinger, Eric J. Topol
Nature Reviews Genetics (2018) Vol. 19, Iss. 9, pp. 581-590
Closed Access | Times Cited: 1366
ClinGen — The Clinical Genome Resource
Heidi L. Rehm, Jonathan S. Berg, Lisa Brooks, et al.
New England Journal of Medicine (2015) Vol. 372, Iss. 23, pp. 2235-2242
Open Access | Times Cited: 1247
Precision Medicine — Personalized, Problematic, and Promising
J. Larry Jameson, Dan L. Longo
New England Journal of Medicine (2015) Vol. 372, Iss. 23, pp. 2229-2234
Closed Access | Times Cited: 971
Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women
Leila Dorling, Sara Carvalho, Jamie Allen, et al.
New England Journal of Medicine (2021) Vol. 384, Iss. 5, pp. 428-439
Open Access | Times Cited: 824
Key steps for effective breast cancer prevention
Kara L. Britt, Jack Cuzick, Kelly‐Anne Phillips
Nature reviews. Cancer (2020) Vol. 20, Iss. 8, pp. 417-436
Closed Access | Times Cited: 777
Accurate classification of BRCA1 variants with saturation genome editing
Gregory M. Findlay, Riza M. Daza, Beth Martin, et al.
Nature (2018) Vol. 562, Iss. 7726, pp. 217-222
Open Access | Times Cited: 706
Developing and evaluating polygenic risk prediction models for stratified disease prevention
Nilanjan Chatterjee, Jianxin Shi, Montserrat García‐Closas
Nature Reviews Genetics (2016) Vol. 17, Iss. 7, pp. 392-406
Open Access | Times Cited: 657
NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017
Mary B. Daly, Robert Pilarski, Michael P. Berry, et al.
Journal of the National Comprehensive Cancer Network (2016) Vol. 15, Iss. 1, pp. 9-20
Open Access | Times Cited: 623
A Population-Based Study of Genes Previously Implicated in Breast Cancer
Chunling Hu, Steven N. Hart, Rohan Gnanaolivu, et al.
New England Journal of Medicine (2021) Vol. 384, Iss. 5, pp. 440-451
Open Access | Times Cited: 612
BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors
Andrew Lee, Nasim Mavaddat, Amber N. Wilcox, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 8, pp. 1708-1718
Open Access | Times Cited: 586
Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer
Fergus J. Couch, Hermela Shimelis, Chunling Hu, et al.
JAMA Oncology (2017) Vol. 3, Iss. 9, pp. 1190-1190
Open Access | Times Cited: 546
A mutational signature reveals alterations underlying deficient homologous recombination repair in breast cancer
Paz Polak, Jaegil Kim, Lior Z. Braunstein, et al.
Nature Genetics (2017) Vol. 49, Iss. 10, pp. 1476-1486
Open Access | Times Cited: 470
Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer
Nadine Tung, Nancy U. Lin, John Kidd, et al.
Journal of Clinical Oncology (2016) Vol. 34, Iss. 13, pp. 1460-1468
Open Access | Times Cited: 469
Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer
Matthew B. Yurgelun, Matthew H. Kulke, Charles S. Fuchs, et al.
Journal of Clinical Oncology (2017) Vol. 35, Iss. 10, pp. 1086-1095
Open Access | Times Cited: 438
Epidemiology and Mechanisms of the Increasing Incidence of Colon and Rectal Cancers in Young Adults
Elena M. Stoffel, Caitlin C. Murphy
Gastroenterology (2019) Vol. 158, Iss. 2, pp. 341-353
Open Access | Times Cited: 434
Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification
Rick Kamps, Rita D. Brandão, B.J.C. van den Bosch, et al.
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 2, pp. 308-308
Open Access | Times Cited: 414
Global Increase in Breast Cancer Incidence: Risk Factors and Preventive Measures
Dharambir Kashyap, Deeksha Pal, Riya Sharma, et al.
BioMed Research International (2022) Vol. 2022, pp. 1-16
Open Access | Times Cited: 399
Pathogenesis of Triple-Negative Breast Cancer
Fatemeh Derakhshan, Jorge S. Reis‐Filho
Annual Review of Pathology Mechanisms of Disease (2022) Vol. 17, Iss. 1, pp. 181-204
Open Access | Times Cited: 362
Prevention and screening in BRCA mutation carriers and other breast/ovarian hereditary cancer syndromes: ESMO Clinical Practice Guidelines for cancer prevention and screening
Shani Paluch‐Shimon, Fátima Cardoso, Cristiana Sessa, et al.
Annals of Oncology (2016) Vol. 27, pp. v103-v110
Open Access | Times Cited: 361
A study of over 35,000 women with breast cancer tested with a 25‐gene panel of hereditary cancer genes
Saundra S. Buys, John F. Sandbach, Amanda Gammon, et al.
Cancer (2017) Vol. 123, Iss. 10, pp. 1721-1730
Open Access | Times Cited: 360
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Roger L. Milne, Karoline Kuchenbaecker, Kyriaki Michailidou, et al.
Nature Genetics (2017) Vol. 49, Iss. 12, pp. 1767-1778
Open Access | Times Cited: 358
Improving reporting standards for polygenic scores in risk prediction studies
Hannah Wand, Samuel A. Lambert, Cecelia P. Tamburro, et al.
Nature (2021) Vol. 591, Iss. 7849, pp. 211-219
Open Access | Times Cited: 358
Germline Mutation Status, Pathological Complete Response, and Disease-Free Survival in Triple-Negative Breast Cancer
Eric Hahnen, Bianca Lederer, Jan Hauke, et al.
JAMA Oncology (2017) Vol. 3, Iss. 10, pp. 1378-1378
Open Access | Times Cited: 327
Hereditary breast and ovarian cancer: new genes in confined pathways
Finn Cilius Nielsen, Thomas van Overeem Hansen, Claus Storgaard Sørensen
Nature reviews. Cancer (2016) Vol. 16, Iss. 9, pp. 599-612
Closed Access | Times Cited: 326
Personalized early detection and prevention of breast cancer: ENVISION consensus statement
Nora Pashayan, Antonis C. Antoniou, Urška Ivanuš, et al.
Nature Reviews Clinical Oncology (2020) Vol. 17, Iss. 11, pp. 687-705
Open Access | Times Cited: 306
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