A citation-based method for searching scientific literature

Nan M Solomons, Amanda E Lamb, Frances L Lucas, Eileen F McDonald, Susan Miesfeldt. Telemed J E Health 2018
Times Cited: 18







List of co-cited articles
87 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Inherited Mutations in Women With Ovarian Carcinoma.
Barbara M Norquist, Maria I Harrell, Mark F Brady, Tom Walsh, Ming K Lee, Suleyman Gulsuner, Sarah S Bernards, Silvia Casadei, Qian Yi, Robert A Burger,[...]. JAMA Oncol 2016
331
11

New paradigms for BRCA1/BRCA2 testing in women with ovarian cancer: results of the Genetic Testing in Epithelial Ovarian Cancer (GTEOC) study.
Inga Plaskocinska, Hannah Shipman, James Drummond, Edward Thompson, Vanessa Buchanan, Barbara Newcombe, Charlotte Hodgkin, Elisa Barter, Paul Ridley, Rita Ng,[...]. J Med Genet 2016
33
11

Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling.
Beth N Peshkin, Scott Kelly, Rachel H Nusbaum, Morgan Similuk, Tiffani A DeMarco, Gillian W Hooker, Heiddis B Valdimarsdottir, Andrea D Forman, Jessica Rispoli Joines, Claire Davis,[...]. J Genet Couns 2016
27
11

Genetic consultation embedded in a gynecologic oncology clinic improves compliance with guideline-based care.
Leigha Senter, David M O'Malley, Floor J Backes, Larry J Copeland, Jeffery M Fowler, Ritu Salani, David E Cohn. Gynecol Oncol 2017
20
11

Scoping studies: advancing the methodology.
Danielle Levac, Heather Colquhoun, Kelly K O'Brien. Implement Sci 2010
11

Real world experience with cancer genetic counseling via telephone.
Rebecca Sutphen, Barbara Davila, Heather Shappell, Tricia Holtje, Susan Vadaparampil, Sue Friedman, Michele Toscano, Joanne Armstrong. Fam Cancer 2010
29
11

Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach.
Goli Samimi, Marcus Q Bernardini, Lawrence C Brody, Charlisse F Caga-Anan, Ian G Campbell, Georgia Chenevix-Trench, Fergus J Couch, Michael Dean, Joanne A de Hullu, Susan M Domchek,[...]. J Clin Oncol 2017
32
11

Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations.
Ranjit Manchanda, Matthew Burnell, Kelly Loggenberg, Rakshit Desai, Jane Wardle, Saskia C Sanderson, Sue Gessler, Lucy Side, Nyala Balogun, Ajith Kumar,[...]. J Med Genet 2016
25
11

Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients.
Angela George, Daniel Riddell, Sheila Seal, Sabrina Talukdar, Shazia Mahamdallie, Elise Ruark, Victoria Cloke, Ingrid Slade, Zoe Kemp, Martin Gore,[...]. Sci Rep 2016
94
11

Genetic counselor opinions of, and experiences with telephone communication of BRCA1/2 test results.
A R Bradbury, L Patrick-Miller, D Fetzer, B Egleston, S A Cummings, A Forman, L Bealin, C Peterson, M Corbman, J O'Connell,[...]. Clin Genet 2011
30
11

A pilot study of telegenetics.
J Gray, K Brain, R Iredale, J Alderman, E France, H Hughes. J Telemed Telecare 2000
44
11

Effectiveness of telemedicine: a systematic review of reviews.
Anne G Ekeland, Alison Bowes, Signe Flottorp. Int J Med Inform 2010
384
11

Telemedicine for genetic and neurologic evaluation in the neonatal intensive care unit.
T L Wenger, J Gerdes, K Taub, D T Swarr, M A Deardorff, N S Abend. J Perinatol 2014
27
11


Barriers and facilitators for utilization of genetic counseling and risk assessment services in young female breast cancer survivors.
Beth Anderson, Jennifer McLosky, Elizabeth Wasilevich, Sarah Lyon-Callo, Debra Duquette, Glenn Copeland. J Cancer Epidemiol 2012
60
11

Randomized Noninferiority Trial of Telephone vs In-Person Disclosure of Germline Cancer Genetic Test Results.
Angela R Bradbury, Linda J Patrick-Miller, Brian L Egleston, Michael J Hall, Susan M Domchek, Mary B Daly, Pamela Ganschow, Generosa Grana, Olufunmilayo I Olopade, Dominique Fetzer,[...]. J Natl Cancer Inst 2018
17
11

Analysis of Reimbursement of Genetic Counseling Services at a Single Institution in a State Requiring Licensure.
Jennifer R Leonhard, Paul J Munson, Jason D Flanagan, Kristen L De Berg, Paul A Thompson, Lori W Dean, Quinn P Stein. J Genet Couns 2017
10
20

Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.
Colin C Pritchard, Joaquin Mateo, Michael F Walsh, Navonil De Sarkar, Wassim Abida, Himisha Beltran, Andrea Garofalo, Roman Gulati, Suzanne Carreira, Rosalind Eeles,[...]. N Engl J Med 2016
639
11


Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing.
Courtney Doughty Rice, Jennifer Gamm Ruschman, Lisa J Martin, Jennifer B Manders, Erin Miller. Fam Cancer 2010
18
11

Recent Enhancements to the Genetic Risk Prediction Model BRCAPRO.
Emanuele Mazzola, Amanda Blackford, Giovanni Parmigiani, Swati Biswas. Cancer Inform 2015
18
11

Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.
Nadine Tung, Chiara Battelli, Brian Allen, Rajesh Kaldate, Satish Bhatnagar, Karla Bowles, Kirsten Timms, Judy E Garber, Christina Herold, Leif Ellisen,[...]. Cancer 2015
249
11

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
Karoline B Kuchenbaecker, John L Hopper, Daniel R Barnes, Kelly-Anne Phillips, Thea M Mooij, Marie-José Roos-Blom, Sarah Jervis, Flora E van Leeuwen, Roger L Milne, Nadine Andrieu,[...]. JAMA 2017
760
11

Gene-panel sequencing and the prediction of breast-cancer risk.
Douglas F Easton, Paul D P Pharoah, Antonis C Antoniou, Marc Tischkowitz, Sean V Tavtigian, Katherine L Nathanson, Peter Devilee, Alfons Meindl, Fergus J Couch, Melissa Southey,[...]. N Engl J Med 2015
480
11

Underdiagnosis of Hereditary Breast Cancer: Are Genetic Testing Guidelines a Tool or an Obstacle?
Peter D Beitsch, Pat W Whitworth, Kevin Hughes, Rakesh Patel, Barry Rosen, Gia Compagnoni, Paul Baron, Rache Simmons, Linda Ann Smith, Ian Grady,[...]. J Clin Oncol 2019
106
11

Risk assessment, genetic counseling, and genetic testing for BRCA-related cancer in women: a systematic review to update the U.S. Preventive Services Task Force recommendation.
Heidi D Nelson, Miranda Pappas, Bernadette Zakher, Jennifer Priest Mitchell, Leila Okinaka-Hu, Rongwei Fu. Ann Intern Med 2014
151
11

Telehealth to provide prenatal genetics services: Feasibility and importance revealed during global pandemic.
Neeta L Vora, Emily Hardisty, Elizabeth Coviello, Alison Stuebe. Prenat Diagn 2020
5
40


Utilization of health information technology among cancer genetic counselors.
Jordon B Ritchie, Caitlin G Allen, Heath Morrison, Michelle Nichols, Steven D Lauzon, Joshua D Schiffman, Chanita Hughes Halbert, Brandon M Welch. Mol Genet Genomic Med 2020
5
40

Genetic Counseling Service Delivery Models in the United States: Assessment of changes in use from 2010 to 2017.
Samantha E Greenberg, Emily Boothe, Christine L Delaney, Ryan Noss, Stephanie A Cohen. J Genet Couns 2020
5
40


The Medical Virtualist: Is Pediatric Patient Care Using Telemedicine, a New Specialty?
Morgan Waller, Luisa Taylor, Jay Portnoy. Pediatr Ann 2019
6
33

Telegenetics: a systematic review of telemedicine in genetics services.
Jennifer S Hilgart, Julie A Hayward, Bernadette Coles, Rachel Iredale. Genet Med 2012
7
28

Rapid deployment of a telemedicine care model for genetics and metabolism during COVID-19.
Natasha Shur, Shireen M Atabaki, Monisha S Kisling, Abir Tabarani, Clarence Williams, Jamie L Fraser, Debra S Regier, Marshall Summar. Am J Med Genet A 2021
7
28


Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility.
Angela R Bradbury, Linda Patrick-Miller, Jessica Long, Jacquelyn Powers, Jill Stopfer, Andrea Forman, Christina Rybak, Kristin Mattie, Amanda Brandt, Rachelle Chambers,[...]. Genet Med 2015
51
11


Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
121
5

Interventions to improve risk communication in clinical genetics: systematic review.
A Edwards, J Gray, A Clarke, J Dundon, G Elwyn, C Gaff, K Hood, R Iredale, S Sivell, C Shaw,[...]. Patient Educ Couns 2008
73
5


Randomized trial of a decision aid for BRCA1/BRCA2 mutation carriers: impact on measures of decision making and satisfaction.
Marc D Schwartz, Heiddis B Valdimarsdottir, Tiffani A DeMarco, Beth N Peshkin, William Lawrence, Jessica Rispoli, Karen Brown, Claudine Isaacs, Suzanne O'Neill, Rebecca Shelby,[...]. Health Psychol 2009
72
5


BRCA1/2 testing in hereditary breast and ovarian cancer families: effectiveness of problem-solving training as a counseling intervention.
Aideen McInerney-Leo, Barbara Bowles Biesecker, Donald W Hadley, Ronald G Kase, Therese R Giambarresi, Elizabeth Johnson, Caryn Lerman, Jeffery P Struewing. Am J Med Genet A 2004
29
5

Validation of a decisional conflict scale.
A M O'Connor. Med Decis Making 1995
5

Patient satisfaction with cancer genetic counseling: a psychometric analysis of the Genetic Counseling Satisfaction Scale.
Tiffani A DeMarco, Beth N Peshkin, Bryn D Mars, Kenneth P Tercyak. J Genet Couns 2004
61
5


A randomized trial comparing alternative approaches to prenatal diagnosis counseling in advanced maternal age patients.
A G W Hunter, M Cappelli, L Humphreys, J E Allanson, T T Chiu, C Peeters, D Moher, A Zimak. Clin Genet 2005
69
5

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.
Leslie G Biesecker, James C Mullikin, Flavia M Facio, Clesson Turner, Praveen F Cherukuri, Robert W Blakesley, Gerard G Bouffard, Peter S Chines, Pedro Cruz, Nancy F Hansen,[...]. Genome Res 2009
201
5

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
339
5

Communication in genetic counseling: cognitive and emotional processing.
Lee Ellington, Kimberly M Kelly, Maija Reblin, Seth Latimer, Debra Roter. Health Commun 2011
26
5


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.