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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:

Genetics, genomics, and cancer risk assessment
Jeffrey N. Weitzel, Kathleen R. Blazer, Deborah J. MacDonald, et al.
CA A Cancer Journal for Clinicians (2011) Vol. 61, Iss. 5, pp. 327-359
Open Access | Times Cited: 240

Showing 1-25 of 240 citing articles:

Genetic/Familial High-Risk Assessment: Breast and Ovarian
Mary B. Daly, Jennifer E. Axilbund, Saundra S. Buys, et al.
Journal of the National Comprehensive Cancer Network (2010) Vol. 8, Iss. 5, pp. 562-594
Open Access | Times Cited: 617
Radiomics strategies for risk assessment of tumour failure in head-and-neck cancer
Martin Vallières, Emily Kay‐Rivest, Léo Jean Perrin, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 485
Multiplex Genetic Testing for Cancer Susceptibility: Out on the High Wire Without a Net?
Susan M. Domchek, Angela R. Bradbury, Judy E. Garber, et al.
Journal of Clinical Oncology (2013) Vol. 31, Iss. 10, pp. 1267-1270
Closed Access | Times Cited: 227
Etiologic field effect: reappraisal of the field effect concept in cancer predisposition and progression
Paul Lochhead, Andrew T. Chan, Reiko Nishihara, et al.
Modern Pathology (2014) Vol. 28, Iss. 1, pp. 14-29
Open Access | Times Cited: 184
Epigenetics and the Transition from Acute to Chronic Pain
Thomas Edward Buchheit, Thomas Van de Ven, Andrew Shaw
Pain Medicine (2012) Vol. 13, Iss. 11, pp. 1474-1490
Open Access | Times Cited: 166
Prevalence and Type ofBRCAMutations in Hispanics Undergoing Genetic Cancer Risk Assessment in the Southwestern United States: A Report From the Clinical Cancer Genetics Community Research Network
Jeffrey N. Weitzel, Jessica Clague, Arelis Martir-Negron, et al.
Journal of Clinical Oncology (2012) Vol. 31, Iss. 2, pp. 210-216
Open Access | Times Cited: 146
Personalized Medicine: Review and Perspectives of Promising Baseline EEG Biomarkers in Major Depressive Disorder and Attention Deficit Hyperactivity Disorder
Sebastian Olbrich, Rik van Dinteren, Martijn Arns
Neuropsychobiology (2015) Vol. 72, Iss. 3-4, pp. 229-240
Open Access | Times Cited: 137
Cancer Genomics and Inherited Risk
Zsofia K. Stadler, Kasmintan A. Schrader, Joseph Vijai, et al.
Journal of Clinical Oncology (2014) Vol. 32, Iss. 7, pp. 687-698
Open Access | Times Cited: 134
The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk
Thomas P. Slavin, Kara N. Maxwell, Jenna Lilyquist, et al.
npj Breast Cancer (2017) Vol. 3, Iss. 1
Open Access | Times Cited: 121
Awareness of Cancer Susceptibility Genetic Testing
L. Phuong, Susan T. Vadaparampil, Nancy Breen, et al.
American Journal of Preventive Medicine (2014) Vol. 46, Iss. 5, pp. 440-448
Open Access | Times Cited: 114
Translating cancer ‘omics’ to improved outcomes: Figure 1.
Emily A. Vucic, Kelsie L. Thu, Keith Robison, et al.
Genome Research (2012) Vol. 22, Iss. 2, pp. 188-195
Open Access | Times Cited: 113
Somatic TP53 variants frequently confound germ-line testing results
Jeffrey N. Weitzel, Elizabeth Chao, Bita Nehoray, et al.
Genetics in Medicine (2017) Vol. 20, Iss. 8, pp. 809-816
Open Access | Times Cited: 109
Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management
Thomas P. Slavin, Mariana Niell‐Swiller, Ilana Solomon, et al.
Frontiers in Oncology (2015) Vol. 5
Open Access | Times Cited: 107
Primary care providers’ cancer genetic testing-related knowledge, attitudes, and communication behaviors: A systematic review and research agenda
Jada G. Hamilton, Ekland Abdiwahab, Heather M. Edwards, et al.
Journal of General Internal Medicine (2016) Vol. 32, Iss. 3, pp. 315-324
Open Access | Times Cited: 106
Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer
Jeanna McCuaig, Susan Randall Armel, Melanie Care, et al.
Cancers (2018) Vol. 10, Iss. 11, pp. 435-435
Open Access | Times Cited: 88
The new genomic medicine service and implications for patients
Katie Snape, Sarah Wedderburn, Julian Barwell
Clinical Medicine (2019) Vol. 19, Iss. 4, pp. 273-277
Open Access | Times Cited: 81
Highly multiplexed rapid DNA detection with single-nucleotide specificity via convective PCR in a portable device
Dmitriy A. Khodakov, Jiaming Li, Jinny Xuemeng Zhang, et al.
Nature Biomedical Engineering (2021) Vol. 5, Iss. 7, pp. 702-712
Open Access | Times Cited: 72
Exploring the antimicrobial, antioxidant and cytotoxic activities of organyltellurium (IV) complexes incorporating 2‐hydroxy‐1‐naphthaldehyde schiff base ligand: Synthesis, spectroscopic investigations and theoretical studies
Mahak Dalal, Jai Devi, Nidhi Antil, et al.
Applied Organometallic Chemistry (2023) Vol. 38, Iss. 2
Closed Access | Times Cited: 22
Variants of uncertain significance in BRCA testing: evaluation of surgical decisions, risk perception, and cancer distress
JO Culver, CD Brinkerhoff, Jessica Clague, et al.
Clinical Genetics (2013) Vol. 84, Iss. 5, pp. 464-472
Open Access | Times Cited: 100
An Index of Barriers for the Implementation of Personalised Medicine and Pharmacogenomics in Europe
Denis Horgan, Marleen E. Jansen, Lada Leyens, et al.
Public Health Genomics (2014) Vol. 17, Iss. 5-6, pp. 287-298
Closed Access | Times Cited: 93
Risk Prediction Models for Colorectal Cancer: A Review
Aung Ko Win, Robert J. MacInnis, John L. Hopper, et al.
Cancer Epidemiology Biomarkers & Prevention (2012) Vol. 21, Iss. 3, pp. 398-410
Closed Access | Times Cited: 92
Significant clinical impact of recurrent BRCA1 and BRCA2 mutations in Mexico
Cynthia Villarreal‐Garza, Rosa María Álvarez-Gómez, Carlos Pérez‐Plasencia, et al.
Cancer (2014) Vol. 121, Iss. 3, pp. 372-378
Open Access | Times Cited: 86
A systematic comparison and evaluation of high density exon arrays and RNA-seq technology used to unravel the peripheral blood transcriptome of sickle cell disease
Nalini Raghavachari, Jennifer J. Barb, Yanqin Yang, et al.
BMC Medical Genomics (2012) Vol. 5, Iss. 1
Open Access | Times Cited: 86
Translating Genomics in Cancer Care
Yvonne Bombard, Peter B. Bach, Kenneth Offit
Journal of the National Comprehensive Cancer Network (2013) Vol. 11, Iss. 11, pp. 1343-1353
Closed Access | Times Cited: 75
Use of BRCA Mutation Test in the U.S., 2004–2014
Fangjian Guo, Jacqueline M. Hirth, Yu‐Li Lin, et al.
American Journal of Preventive Medicine (2017) Vol. 52, Iss. 6, pp. 702-709
Open Access | Times Cited: 70
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