The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index.
Primary-care providers’ perceived barriers to integration of genetics services: a systematic review of the literature
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Cites
Saam, J., Arnell, C., Theisen, A., Moyes, K., Marino, I., Roundy, K. M., & Wenstrup, R. J. (2015) · Oncology · doi:10.1159/000437307 · Cited by 1,526
Health Supervision for Children With Down Syndrome
Bull, M. J., & the Committee on Genetics (2011) · Pediatrics · doi:10.1542/peds.2011-1605 · Cited by 1,231
Robson, M. E., Bradbury, A. R., Arun, B., Domchek, S. M., Ford, J. M., Hampel, H. L., Lipkin, S. M., Syngal, S., Wollins, D. S., & Lindor, N. M. (2015) · Journal of Clinical Oncology · doi:10.1200/jco.2015.63.0996 · Cited by 934
Implications of the Human Genome Project for Medical Science
Collins, F. S. (2001) · JAMA · doi:10.1001/jama.285.5.540 · Cited by 838
Primary care: America's health in a new era
(1997) · Choice Reviews Online · doi:10.5860/choice.34-6304 · Cited by 816
Robson, M. E., Storm, C. D., Weitzel, J., Wollins, D. S., & Offit, K. (2010) · Journal of Clinical Oncology · doi:10.1200/jco.2009.27.0660 · Cited by 421
South, S. T., Lee, C., Lamb, A. N., Higgins, A. W., & Kearney, H. M. (2013) · Genetics in Medicine · doi:10.1038/gim.2013.129 · Cited by 371
Primary Care: America's Health in a New Era
Hunt, V. R. (1997) · The Journal of the American Board of Family Practice/The journal of the American Board of Family Practice · doi:10.3122/jabfm.10.5.383 · Cited by 294
Suther, S., & Goodson, P. (2003) · Genetics in Medicine · doi:10.1097/01.gim.0000055201.16487.61 · Cited by 263
Development and use of active clinical decision support for preemptive pharmacogenomics
Bell, G. C., Crews, K. R., Wilkinson, M. R., Haidar, C. E., Hicks, J. K., Baker, D. K., Kornegay, N. M., Yang, W., Cross, S. J., Howard, S. C., et al. (2014) · Journal of the American Medical Informatics Association · doi:10.1136/amiajnl-2013-001993 · Cited by 208
Cited by
Owusu Obeng, A., Fei, K., Levy, K. D., Elsey, A. R., Pollin, T. I., Ramirez, A. H., Weitzel, K. W., & Horowitz, C. R. (2018) · Journal of Personalized Medicine · doi:10.3390/jpm8030024 · Cited by 131
Primary care providers' experiences with and perceptions of personalized genomic medicine.
(2016) · PubMed Central · Cited by 118
Family health history: underused for actionable risk assessment
Ginsburg, G. S., Wu, R. R., & Orlando, L. A. (2019) · The Lancet · doi:10.1016/s0140-6736(19)31275-9 · Cited by 105
Pearce, C., Goettke, E., Hallowell, N., McCormack, P., Flinter, F., & McKevitt, C. (2019) · Genetics in Medicine · doi:10.1038/s41436-019-0579-x · Cited by 33
Cohen, A. S. A., Berrios, C. D., Zion, T. N., Barrett, C. M., Moore, R., Boillat, E., Belden, B., Farrow, E. G., Thiffault, I., Zuccarelli, B. D., et al. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2024.03.016 · Cited by 21
Metadata
- Authors
- Mikat-Stevens, N. A., Larson, I. A., & Tarini, B. A.
- Venue
- Genetics in Medicine
- Publisher
- Elsevier BV
- Published
- 2015-03
- Volume
- 17
- Issue
- 3
- Pages
- 169-176
- ISSN
- 1098-3600 (ISSN-L)
- OpenAlex
- W2030982209
- Cited by
- 261
- References
- 44
- FWCI
- 4.06
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: Primary-care providers’ perceived barriers to integration of genetics services: a systematic review of the literature. https://app.cochat.ai/papers/10.1038/gim.2014.101
- The paper
- Mikat-Stevens, N. A., Larson, I. A., & Tarini, B. A. (2015). Primary-care providers’ perceived barriers to integration of genetics services: a systematic review of the literature. Genetics in Medicine. https://doi.org/10.1038/gim.2014.101
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
