
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:
Randomized Trial of Telegenetics vs. In‐Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance
Adam H. Buchanan, Santanu Datta, Celette Sugg Skinner, et al.
Journal of Genetic Counseling (2015) Vol. 24, Iss. 6, pp. 961-970
Open Access | Times Cited: 174
Adam H. Buchanan, Santanu Datta, Celette Sugg Skinner, et al.
Journal of Genetic Counseling (2015) Vol. 24, Iss. 6, pp. 961-970
Open Access | Times Cited: 174
Showing 26-50 of 174 citing articles:
The role of Internet resources in clinical oncology: promises and challenges
Bradford W. Hesse, Alexandra J. Greenberg, Lila J. Finney Rutten
Nature Reviews Clinical Oncology (2016) Vol. 13, Iss. 12, pp. 767-776
Closed Access | Times Cited: 57
Bradford W. Hesse, Alexandra J. Greenberg, Lila J. Finney Rutten
Nature Reviews Clinical Oncology (2016) Vol. 13, Iss. 12, pp. 767-776
Closed Access | Times Cited: 57
The Use of Cancer-Specific Patient-Centered Technologies Among Underserved Populations in the United States: Systematic Review
Will L. Tarver, David A. Haggstrom
Journal of Medical Internet Research (2018) Vol. 21, Iss. 4, pp. e10256-e10256
Open Access | Times Cited: 56
Will L. Tarver, David A. Haggstrom
Journal of Medical Internet Research (2018) Vol. 21, Iss. 4, pp. e10256-e10256
Open Access | Times Cited: 56
Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service
Irena Vrečar, Dimitar Hristovski, Borut Peterlin
Journal of Medical Systems (2016) Vol. 41, Iss. 2
Closed Access | Times Cited: 55
Irena Vrečar, Dimitar Hristovski, Borut Peterlin
Journal of Medical Systems (2016) Vol. 41, Iss. 2
Closed Access | Times Cited: 55
Comparison of Telephone and Televideo Modes for Delivery of Genetic Counseling: a Randomized Trial
Corrine I. Voils, Vickie L. Venne, Hollis J. Weidenbacher, et al.
Journal of Genetic Counseling (2017) Vol. 27, Iss. 2, pp. 339-348
Closed Access | Times Cited: 54
Corrine I. Voils, Vickie L. Venne, Hollis J. Weidenbacher, et al.
Journal of Genetic Counseling (2017) Vol. 27, Iss. 2, pp. 339-348
Closed Access | Times Cited: 54
Online genetic counseling from the providers’ perspective: counselors’ evaluations and a time and cost analysis
Ellen Otten, Erwin Birnie, Adelita V. Ranchor, et al.
European Journal of Human Genetics (2016) Vol. 24, Iss. 9, pp. 1255-1261
Open Access | Times Cited: 53
Ellen Otten, Erwin Birnie, Adelita V. Ranchor, et al.
European Journal of Human Genetics (2016) Vol. 24, Iss. 9, pp. 1255-1261
Open Access | Times Cited: 53
Genetic Counseling and the Central Tenets of Practice
Barbara B. Biesecker
Cold Spring Harbor Perspectives in Medicine (2019) Vol. 10, Iss. 3, pp. a038968-a038968
Open Access | Times Cited: 53
Barbara B. Biesecker
Cold Spring Harbor Perspectives in Medicine (2019) Vol. 10, Iss. 3, pp. a038968-a038968
Open Access | Times Cited: 53
Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations
Ranjit Manchanda, Matthew Burnell, K Loggenberg, et al.
Journal of Medical Genetics (2016) Vol. 53, Iss. 7, pp. 472-480
Open Access | Times Cited: 51
Ranjit Manchanda, Matthew Burnell, K Loggenberg, et al.
Journal of Medical Genetics (2016) Vol. 53, Iss. 7, pp. 472-480
Open Access | Times Cited: 51
Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network
Georgia L. Wiesner, Alanna Kulchak Rahm, Paul S. Appelbaum, et al.
Journal of Personalized Medicine (2020) Vol. 10, Iss. 2, pp. 30-30
Open Access | Times Cited: 47
Georgia L. Wiesner, Alanna Kulchak Rahm, Paul S. Appelbaum, et al.
Journal of Personalized Medicine (2020) Vol. 10, Iss. 2, pp. 30-30
Open Access | Times Cited: 47
Videoconferencing to deliver genetics services: a systematic review of telegenetics in light of the COVID-19 pandemic
Elizabeth Gaspar Brown, Isabella Watts, Emily Beales, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 8, pp. 1438-1449
Open Access | Times Cited: 34
Elizabeth Gaspar Brown, Isabella Watts, Emily Beales, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 8, pp. 1438-1449
Open Access | Times Cited: 34
Challenges to genetic testing for germline mutations associated with breast cancer among African Americans
Sailaja Kamaraju, Meghan Conroy, Alexandra Harris, et al.
Cancer Treatment Reviews (2024) Vol. 124, pp. 102695-102695
Closed Access | Times Cited: 5
Sailaja Kamaraju, Meghan Conroy, Alexandra Harris, et al.
Cancer Treatment Reviews (2024) Vol. 124, pp. 102695-102695
Closed Access | Times Cited: 5
A Randomized Trial of Two Remote Health Care Delivery Models on the Uptake of Genetic Testing and Impact on Patient-Reported Psychological Outcomes in Families With Pancreatic Cancer: The Genetic Education, Risk Assessment, and Testing (GENERATE) Study
Nicolette J. Rodriguez, C. Sloane Furniss, Matthew B. Yurgelun, et al.
Gastroenterology (2024) Vol. 166, Iss. 5, pp. 872-885.e2
Closed Access | Times Cited: 5
Nicolette J. Rodriguez, C. Sloane Furniss, Matthew B. Yurgelun, et al.
Gastroenterology (2024) Vol. 166, Iss. 5, pp. 872-885.e2
Closed Access | Times Cited: 5
Access to Genetic Counselors in the Southern United States
Catalina Villegas, Susanne B. Haga
Journal of Personalized Medicine (2019) Vol. 9, Iss. 3, pp. 33-33
Open Access | Times Cited: 39
Catalina Villegas, Susanne B. Haga
Journal of Personalized Medicine (2019) Vol. 9, Iss. 3, pp. 33-33
Open Access | Times Cited: 39
The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing
Monisha Sebastin, Jacqueline A. Odgis, Sabrina A. Suckiel, et al.
Pilot and Feasibility Studies (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 11
Monisha Sebastin, Jacqueline A. Odgis, Sabrina A. Suckiel, et al.
Pilot and Feasibility Studies (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 11
The breast cancer genetic testing experience: probing the potential utility of an online decision aid in risk perception and decision making
Anna Vaynrub, Brian Salazar, Yilin Eileen Feng, et al.
BMC Cancer (2025) Vol. 25, Iss. 1
Open Access
Anna Vaynrub, Brian Salazar, Yilin Eileen Feng, et al.
BMC Cancer (2025) Vol. 25, Iss. 1
Open Access
Breaking barriers: fostering equitable access to pediatric genomics through innovative care models and technologies
Sabrina Malone Jenkins, Rachel Palmquist, Brian J. Shayota, et al.
Pediatric Research (2025)
Closed Access
Sabrina Malone Jenkins, Rachel Palmquist, Brian J. Shayota, et al.
Pediatric Research (2025)
Closed Access
Investigating the impact of screen-sharing visual aids during genomic results disclosure via telehealth in diverse families in the TeleKidSeq pilot study
Jacqueline A. Odgis, Nicole Kelly, Monisha Sebastin, et al.
Public Health Genomics (2025), pp. 1-24
Open Access
Jacqueline A. Odgis, Nicole Kelly, Monisha Sebastin, et al.
Public Health Genomics (2025), pp. 1-24
Open Access
Acceptability and Future Considerations for Telegenetic Counseling After the COVID Pandemic: Interviews with Genetic Counselors, Clinicians, and Patients
Meghan C. Martinez, Nina Szwerinski, Su‐Ying Liang, et al.
INQUIRY The Journal of Health Care Organization Provision and Financing (2025) Vol. 62
Open Access
Meghan C. Martinez, Nina Szwerinski, Su‐Ying Liang, et al.
INQUIRY The Journal of Health Care Organization Provision and Financing (2025) Vol. 62
Open Access
Genetic Services in Appalachia Conference Series
Kimberly M. Kelly, Trupti Dhumal, Virginia Scott, et al.
American Journal of Medical Genetics Part A (2025)
Open Access
Kimberly M. Kelly, Trupti Dhumal, Virginia Scott, et al.
American Journal of Medical Genetics Part A (2025)
Open Access
Digital Psychiatry for the Treatment of Comorbid Disorders
Laura Orsolini, Michele Fiorani, Giulio Longo, et al.
(2025), pp. 447-476
Closed Access
Laura Orsolini, Michele Fiorani, Giulio Longo, et al.
(2025), pp. 447-476
Closed Access
Online Genetic Counseling as a Solution for Unmet Needs in Genetic Medicine: The First Survey in Japan
Kazuki Yamazawa, Haruka Murakami, Satomi Inoue, et al.
Research Square (Research Square) (2025)
Closed Access
Kazuki Yamazawa, Haruka Murakami, Satomi Inoue, et al.
Research Square (Research Square) (2025)
Closed Access
Educational Video as an Alternative to Pretest In-Person Genetic Counseling in Candidates for Cancer Genetic Testing: A Randomized Controlled Noninferiority Trial
Yanin Chávarri-Guerra, Mayte Cruz-Zermeño, Cesar Alcacio-Vazquez, et al.
JCO Oncology Practice (2025)
Closed Access
Yanin Chávarri-Guerra, Mayte Cruz-Zermeño, Cesar Alcacio-Vazquez, et al.
JCO Oncology Practice (2025)
Closed Access
Physician Experiences and Understanding of Genomic Sequencing in Oncology
Caroline Weipert, Kerry A. Ryan, Jessica N. Everett, et al.
Journal of Genetic Counseling (2017) Vol. 27, Iss. 1, pp. 187-196
Open Access | Times Cited: 36
Caroline Weipert, Kerry A. Ryan, Jessica N. Everett, et al.
Journal of Genetic Counseling (2017) Vol. 27, Iss. 1, pp. 187-196
Open Access | Times Cited: 36
Implementing a Virtual Health Telemedicine Program in a Community Setting
Scott M. Weissman, Kate Zellmer, Nicole Gill, et al.
Journal of Genetic Counseling (2017) Vol. 27, Iss. 2, pp. 323-325
Closed Access | Times Cited: 36
Scott M. Weissman, Kate Zellmer, Nicole Gill, et al.
Journal of Genetic Counseling (2017) Vol. 27, Iss. 2, pp. 323-325
Closed Access | Times Cited: 36
How Can We Reach At-Risk Relatives? Efforts to Enhance Communication and Cascade Testing Uptake: a Mini-Review
Rachel Schwiter, Alanna Kulchak Rahm, Janet L. Williams, et al.
Current Genetic Medicine Reports (2018) Vol. 6, Iss. 2, pp. 21-27
Closed Access | Times Cited: 36
Rachel Schwiter, Alanna Kulchak Rahm, Janet L. Williams, et al.
Current Genetic Medicine Reports (2018) Vol. 6, Iss. 2, pp. 21-27
Closed Access | Times Cited: 36
Group genetic counseling: An alternate service delivery model in a high risk prenatal screening population
M. Cloutier, Lauren Gallagher, Claire Goldsmith, et al.
Prenatal Diagnosis (2017) Vol. 37, Iss. 11, pp. 1112-1119
Closed Access | Times Cited: 34
M. Cloutier, Lauren Gallagher, Claire Goldsmith, et al.
Prenatal Diagnosis (2017) Vol. 37, Iss. 11, pp. 1112-1119
Closed Access | Times Cited: 34