| Year |
Citation |
Score |
| 2024 |
Feigelson HS, Mittendorf KF, Okuyama S, Porter KM, Bulkley J, Shuster E, Anderson KP, Gilmore MJ, Zepp JM, Kauffman TL, Lindberg NM, Muessig KR, Bellcross C, Ukaegbu C, Syngal S, et al. Feasibility of an electronic patient-facing cancer family history tool in medically underserved populations. Genetics in Medicine Open. 2: 101860. PMID 39669603 DOI: 10.1016/j.gimo.2024.101860 |
0.341 |
|
| 2023 |
Zhao J, McBride CM, Campbell GP, Pentz RD, Escoffery C, Konomos M, Bellcross C, Ward K, Shepperd JR, Guan Y. Your Family Connects: A Theory-Based Intervention to Encourage Communication About Possible Inherited Cancer Risk among Ovarian Cancer Survivors and Close Relatives. Public Health Genomics. PMID 37487468 DOI: 10.1159/000531772 |
0.335 |
|
| 2022 |
Veitinger JK, Kerber AS, Gabram-Mendola SGA, Liu Y, Durham LM, Durrence D, Berzen AK, Shin JY, Snyder C, Bellcross CA, Guan Y. Screening for Individuals at Risk for Hereditary Breast and Ovarian Cancer: A Statewide Initiative, Georgia, 2012-2020. American Journal of Public Health. e1-e4. PMID 35862880 DOI: 10.2105/AJPH.2022.306932 |
0.541 |
|
| 2022 |
Bellcross CA. Hereditary Breast and Ovarian Cancer: An Updated Primer for OB/GYNs. Obstetrics and Gynecology Clinics of North America. 49: 117-147. PMID 35168766 DOI: 10.1016/j.ogc.2021.11.005 |
0.477 |
|
| 2022 |
Ritchie JB, Frey LJ, Lamy JB, Bellcross C, Morrison H, Schiffman JD, Welch BM. Automated Clinical Practice Guideline Recommendations for Hereditary Cancer Risk Using Chatbots and Ontologies: System Description. Jmir Cancer. 8: e29289. PMID 35099392 DOI: 10.2196/29289 |
0.421 |
|
| 2021 |
Ritchie JB, Welch BM, Allen CG, Frey LJ, Morrison H, Schiffman JD, Alekseyenko AV, Dean B, Hughes Halbert C, Bellcross C. Comparison of a Cancer Family History Collection and Risk Assessment Tool - ItRunsInMyFamily - with Risk Assessment by Health-Care Professionals. Public Health Genomics. 1-9. PMID 34872100 DOI: 10.1159/000520001 |
0.372 |
|
| 2021 |
Ritchie JB, Bellcross C, Allen CG, Frey L, Morrison H, Schiffman JD, Welch BM. Evaluation and comparison of hereditary Cancer guidelines in the population. Hereditary Cancer in Clinical Practice. 19: 31. PMID 34274008 DOI: 10.1186/s13053-021-00188-9 |
0.453 |
|
| 2020 |
Juarez OA, Pencheva BB, Bellcross C, Schneider KW, Turner J, Porter CC. Cancer genetic counseling for childhood cancer predisposition is associated with improved levels of knowledge and high satisfaction in parents. Journal of Genetic Counseling. PMID 33179831 DOI: 10.1002/jgc4.1357 |
0.308 |
|
| 2019 |
Rahm AK, Bellcross C, Cragun D, Duquette D, Hampel H, Heald B. Implementing universal cancer screening programs can help sustain genomic medicine programs. Personalized Medicine. PMID 31797715 DOI: 10.2217/Pme-2019-0126 |
0.362 |
|
| 2019 |
Guan Y, Condit CM, Escoffery C, Bellcross CA, McBride CM. Do Women who Receive a Negative BRCA1/2 Risk Result Understand the Implications for Breast Cancer Risk? Public Health Genomics. 1-8. PMID 31597139 DOI: 10.1159/000503129 |
0.471 |
|
| 2019 |
Guan Y, Nehl E, Pencea I, Condit CM, Escoffery C, Bellcross CA, McBride CM. Willingness to decrease mammogram frequency among women at low risk for hereditary breast cancer. Scientific Reports. 9: 9599. PMID 31270367 DOI: 10.1038/S41598-019-45967-6 |
0.431 |
|
| 2019 |
Wernke K, Bellcross C, Gabram S, Ali N, Stanislaw C. Impact of Implementing B-RST to Screen for Hereditary Breast and Ovarian Cancer on Risk Perception and Genetic Counseling Uptake Among Women in an Academic Safety Net Hospital. Clinical Breast Cancer. PMID 31005475 DOI: 10.1016/j.clbc.2019.02.014 |
0.479 |
|
| 2018 |
Bellcross C, Hermstad A, Tallo C, Stanislaw C. Validation of Version 3.0 of the Breast Cancer Genetics Referral Screening Tool (B-RST™). Genetics in Medicine : Official Journal of the American College of Medical Genetics. 21: 181-184. PMID 29740170 DOI: 10.1038/s41436-018-0020-x |
0.496 |
|
| 2015 |
Nair N, Bellcross C, Haddad L, Martin M, Matthews R, Gabram-Mendola S, Crane B, Meaney-Delman D. Georgia Primary Care Providers' Knowledge of Hereditary Breast and Ovarian Cancer Syndrome. Journal of Cancer Education : the Official Journal of the American Association For Cancer Education. PMID 26637472 DOI: 10.1007/s13187-015-0950-9 |
0.467 |
|
| 2015 |
Mange S, Bellcross C, Cragun D, Duquette D, Gorman L, Hampel H, Jasperson K. Creation of a network to promote universal screening for Lynch syndrome: the LynchSyndrome Screening Network. Journal of Genetic Counseling. 24: 421-7. PMID 25220566 DOI: 10.1007/S10897-014-9770-Z |
0.397 |
|
| 2015 |
Bellcross CA, Peipins LA, McCarty FA, Rodriguez JL, Hawkins NA, Hensley Alford S, Leadbetter S. Characteristics associated with genetic counseling referral and BRCA1/2 testing among women in a large integrated health system. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 43-50. PMID 24946155 DOI: 10.1038/Gim.2014.68 |
0.375 |
|
| 2014 |
Bellcross CA. The changing landscape of genetic testing for hereditary breast and ovarian cancer. Current Problems in Cancer. 38: 209-15. PMID 25497408 DOI: 10.1016/j.currproblcancer.2014.10.001 |
0.366 |
|
| 2014 |
Brannon Traxler L, Martin ML, Kerber AS, Bellcross CA, Crane BE, Green V, Matthews R, Paris NM, Gabram SG. Implementing a screening tool for identifying patients at risk for hereditary breast and ovarian cancer: a statewide initiative. Annals of Surgical Oncology. 21: 3342-7. PMID 25047474 DOI: 10.1245/s10434-014-3921-1 |
0.469 |
|
| 2013 |
Meaney-Delman D, Bellcross CA. Hereditary breast/ovarian cancer syndrome: a primer for obstetricians/gynecologists. Obstetrics and Gynecology Clinics of North America. 40: 475-512. PMID 24021253 DOI: 10.1016/j.ogc.2013.05.009 |
0.523 |
|
| 2013 |
Bellcross CA, Leadbetter S, Alford SH, Peipins LA. Prevalence and healthcare actions of women in a large health system with a family history meeting the 2005 USPSTF recommendation for BRCA genetic counseling referral. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 22: 728-35. PMID 23371291 DOI: 10.1158/1055-9965.EPI-12-1280 |
0.382 |
|
| 2012 |
Bellcross CA, Page PZ, Meaney-Delman D. Direct-to-consumer personal genome testing and cancer risk prediction. Cancer Journal (Sudbury, Mass.). 18: 293-302. PMID 22846729 DOI: 10.1097/PPO.0b013e3182610e38 |
0.353 |
|
| 2012 |
Bellcross CA, Bedrosian SR, Daniels E, Duquette D, Hampel H, Jasperson K, Joseph DA, Kaye C, Lubin I, Meyer LJ, Reyes M, Scheuner MT, Schully SD, Senter L, Stewart SL, et al. Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 152-62. PMID 22237445 DOI: 10.1038/Gim.0B013E31823375Ea |
0.39 |
|
| 2011 |
Bellcross CA, Kolor K, Goddard KA, Coates RJ, Reyes M, Khoury MJ. Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians. American Journal of Preventive Medicine. 40: 61-6. PMID 21146769 DOI: 10.1016/J.Amepre.2010.09.027 |
0.343 |
|
| 2011 |
Weissman SM, Bellcross C, Bittner CC, Freivogel ME, Haidle JL, Kaurah P, Leininger A, Palaniappan S, Steenblock K, Vu TM, Daniels MS. Genetic counseling considerations in the evaluation of families for Lynch syndrome--a review. Journal of Genetic Counseling. 20: 5-19. PMID 20931355 DOI: 10.1007/s10897-010-9325-x |
0.321 |
|
| 2010 |
Bellcross C, Dotson WD. Tumor gene expression profiling in women with breast cancer. Test category: prognostic. Plos Currents. 2. PMID 20877449 DOI: 10.1371/currents.RRN1178 |
0.325 |
|
| 2010 |
Bellcross C. Further development and evaluation of a breast/ovarian cancer genetics referral screening tool. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 12: 240. PMID 20395744 DOI: 10.1097/GIM.0b013e3181d4bc3a |
0.488 |
|
| 2009 |
Bellcross CA, Lemke AA, Pape LS, Tess AL, Meisner LT. Evaluation of a breast/ovarian cancer genetics referral screening tool in a mammography population. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 783-9. PMID 19752737 DOI: 10.1097/Gim.0B013E3181B9B04A |
0.331 |
|
| 2006 |
Ormond KE, Bellcross C, Weissman S. Genetic risk assessment and BRCA mutation testing. Annals of Internal Medicine. 144: 303-4; discussion 30. PMID 16490919 |
0.331 |
|
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