A citation-based method for searching scientific literature

Amanda S Freed, Inga Gruß, Carmit K McMullen, Michael C Leo, Tia L Kauffman, Kathryn M Porter, Kristin R Muessig, Donna Eubanks, Katrina A B Goddard, Benjamin S Wilfond, Elizabeth G Liles. Patient Educ Couns 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model.
Leslie Riddle, Laura M Amendola, Marian J Gilmore, Claudia Guerra, Barbara Biesecker, Tia L Kauffman, Katherine Anderson, Alan F Rope, Michael C Leo, Mikaella Caruncho,[...]. Patient Educ Couns 2021
5
66

Information Mismatch: Cancer Risk Counseling with Diverse Underserved Patients.
Galen Joseph, Rena J Pasick, Dean Schillinger, Judith Luce, Claudia Guerra, Janice Ka Yan Cheng. J Genet Couns 2017
58
66

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
66

Family communication about genomic sequencing: A qualitative study with cancer patients and relatives.
Amelia K Smit, Nicci Bartley, Megan C Best, Christine E Napier, Phyllis Butow, Ainsley J Newson, Kathy Tucker, Mandy L Ballinger, David M Thomas, Chris Jacobs,[...]. Patient Educ Couns 2021
4
33

The Genetic Counseling Video Project (GCVP): models of practice.
D Roter, L Ellington, L Hamby Erby, S Larson, W Dudley. Am J Med Genet C Semin Med Genet 2006
78
33

Testing a best practices risk result format to communicate genetic risks.
Kyle W Davis, Debra L Roter, Tara Schmidlen, Laura B Scheinfeldt, William M P Klein. Patient Educ Couns 2021
4
33

Analyzing communication in genetic consultations--a systematic review.
Jean Paul, Sylvia Metcalfe, Lesley Stirling, Brenda Wilson, Jan Hodgson. Patient Educ Couns 2015
27
33

Utility of a virtual counselor (VICKY) to collect family health histories among vulnerable patient populations: A randomized controlled trial.
Catharine Wang, Michael K Paasche-Orlow, Deborah J Bowen, Howard Cabral, Michael R Winter, Tricia Norkunas Cunningham, Michelle Trevino-Talbot, Diana M Toledo, Dharma E Cortes, MaryAnn Campion,[...]. Patient Educ Couns 2021
2
50

Communication in genetic counseling: cognitive and emotional processing.
Lee Ellington, Kimberly M Kelly, Maija Reblin, Seth Latimer, Debra Roter. Health Commun 2011
28
33

How patients deal with an ambiguous medical test: Decision-making after genetic testing.
Courtney L Scherr, Sanjana Ramesh, Hannah Getachew-Smith, Kerstin Kalke, Kyra Ramsey, Baruch Fischhoff, Susan T Vadaparampil. Patient Educ Couns 2021
2
50

Consumers' use of web-based information and their decisions about multiplex genetic susceptibility testing.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Lawrence C Brody, Andreas D Baxevanis. J Med Internet Res 2010
47
33

Ask, understand, remember: a brief measure of patient communication self-efficacy within clinical encounters.
Marla L Clayman, Anjali U Pandit, Ashley R Bergeron, Kenzie A Cameron, Emily Ross, Michael S Wolf. J Health Commun 2010
37
33

Validation of Version 3.0 of the Breast Cancer Genetics Referral Screening Tool (B-RST™).
Cecelia Bellcross, April Hermstad, Christine Tallo, Christine Stanislaw. Genet Med 2019
13
33

Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.
Stephanie A Kraft, Kathryn M Porter, Devan M Duenas, Claudia Guerra, Galen Joseph, Sandra Soo-Jin Lee, Kelly J Shipman, Jake Allen, Donna Eubanks, Tia L Kauffman,[...]. AJOB Empir Bioeth 2021
4
33

Assessment of clinical practices among cancer genetic counselors.
Deborah Wham, Thuy Vu, Gayun Chan-Smutko, Christine Kobelka, Diana Urbauer, Brandie Heald. Fam Cancer 2010
43
33

Hereditary cancer predisposition syndromes.
Judy E Garber, Kenneth Offit. J Clin Oncol 2005
325
33

Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.
Kimberly A Kaphingst, Melvin Blanchard, Laurel Milam, Manusheela Pokharel, Ashley Elrick, Melody S Goodman. J Health Commun 2016
37
33

The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine.
Katie Stoll, Shobana Kubendran, Stephanie A Cohen. Am J Med Genet C Semin Med Genet 2018
64
33

Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
57
33

Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome.
Fay Kastrinos, Hajime Uno, Chinedu Ukaegbu, Carmelita Alvero, Ashley McFarland, Matthew B Yurgelun, Matthew H Kulke, Deborah Schrag, Jeffrey A Meyerhardt, Charles S Fuchs,[...]. J Clin Oncol 2017
71
33

The association between knowledge and attitudes about genetic testing for cancer risk in the United States.
Abigail Rose, Nikki Peters, Judy A Shea, Katrina Armstrong. J Health Commun 2005
50
33

Automatic Genetic Risk Assessment Calculation Using Breast Cancer Family History Data from the EHR compared to Self-Report.
Margaret Sin, Julia E McGuinness, Meghna S Trivedi, Alejandro Vanegas, Thomas B Silverman, Katherine D Crew, Rita Kukafka. AMIA Annu Symp Proc 2018
4
33

Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
Douglas K Owens, Karina W Davidson, Alex H Krist, Michael J Barry, Michael Cabana, Aaron B Caughey, Chyke A Doubeni, John W Epling, Martha Kubik, C Seth Landefeld,[...]. JAMA 2019
121
33

The REDCap consortium: Building an international community of software platform partners.
Paul A Harris, Robert Taylor, Brenda L Minor, Veida Elliott, Michelle Fernandez, Lindsay O'Neal, Laura McLeod, Giovanni Delacqua, Francesco Delacqua, Jacqueline Kirby,[...]. J Biomed Inform 2019
33

Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer.
Jeanna M McCuaig, Susan Randall Armel, Melanie Care, Alexandra Volenik, Raymond H Kim, Kelly A Metcalfe. Cancers (Basel) 2018
37
33

Educating underserved Latino communities about family health history using lay health advisors.
K A Kaphingst, C R Lachance, A Gepp, L Hoyt D'Anna, B Rios-Ellis. Public Health Genomics 2011
31
33

Lessons learned about harmonizing survey measures for the CSER consortium.
Katrina A B Goddard, Frank A N Angelo, Sara L Ackerman, Jonathan S Berg, Barbara B Biesecker, Maria I Danila, Kelly M East, Lucia A Hindorff, Carol R Horowitz, Jessica Ezzell Hunter,[...]. J Clin Transl Sci 2020
3
33


Development of a revised Health Care System Distrust scale.
Judy A Shea, Ellyn Micco, Lorraine T Dean, Suzanne McMurphy, J Sanford Schwartz, Katrina Armstrong. J Gen Intern Med 2008
96
33



Differences in Family Health History Knowledge Among Bisexual and Lesbian Women.
Megan C Roberts, Melinda Krakow, Christopher W Wheldon, Michelle I Silver. LGBT Health 2019
3
33

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.
Glenn E Palomaki, Monica R McClain, Stephanie Melillo, Heather L Hampel, Stephen N Thibodeau. Genet Med 2009
327
33

Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
Francis M Giardiello, John I Allen, Jennifer E Axilbund, C Richard Boland, Carol A Burke, Randall W Burt, James M Church, Jason A Dominitz, David A Johnson, Tonya Kaltenbach,[...]. Am J Gastroenterol 2014
269
33

A systematic review of factors that act as barriers to patient referral to genetic services.
Türem Delikurt, Graham R Williamson, Violetta Anastasiadou, Heather Skirton. Eur J Hum Genet 2015
85
33

Validation of a Short, 3-Item Version of the Subjective Numeracy Scale.
Candace D McNaughton, Kerri L Cavanaugh, Sunil Kripalani, Russell L Rothman, Kenneth A Wallston. Med Decis Making 2015
65
33

Increasing access to individualized medicine: a matched-cohort study examining Latino participant experiences of genomic screening.
Joel E Pacyna, Gabriel Q Shaibi, Alex Lee, Jamie O Byrne, Idali Cuellar, Erica J Sutton, Valentina Hernandez, Noralane M Lindor, Davinder Singh, Iftikhar J Kullo,[...]. Genet Med 2021
2
50

Genetic Counselor and Healthcare Interpreter Perspectives on the Role of Interpreters in Cancer Genetic Counseling.
Karlena Lara-Otero, Jon Weil, Claudia Guerra, Janice Ka Yan Cheng, Janey Youngblom, Galen Joseph. Health Commun 2019
9
33

Variants of unknown significance in BRCA testing: impact on risk perception, worry, prevention and counseling.
S Richter, I Haroun, T C Graham, A Eisen, A Kiss, E Warner. Ann Oncol 2013
60
33

Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?
Roberta Zuntini, Simona Ferrari, Elena Bonora, Francesco Buscherini, Benedetta Bertonazzi, Mina Grippa, Lea Godino, Sara Miccoli, Daniela Turchetti. Front Genet 2018
8
33

Barriers and facilitators to dissemination and adoption of precision medicine among Hispanics/Latinos.
Juan R Canedo, Consuelo H Wilkins, Nicole Senft, Araceli Romero, Kemberlee Bonnet, David Schlundt. BMC Public Health 2020
4
33

Development of the Multidimensional Health Locus of Control (MHLC) Scales.
K A Wallston, B S Wallston, R DeVellis. Health Educ Monogr 1978
33


Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
Mary B Daly, Robert Pilarski, Jennifer E Axilbund, Michael Berry, Saundra S Buys, Beth Crawford, Meagan Farmer, Susan Friedman, Judy E Garber, Seema Khan,[...]. J Natl Compr Canc Netw 2016
112
33

Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
53
33

Assessing patients' experiences with communication across the cancer care continuum.
Kathleen M Mazor, Richard L Street, Valerie M Sue, Andrew E Williams, Borsika A Rabin, Neeraj K Arora. Patient Educ Couns 2016
20
33

Translation and validation of a Spanish-language genetic health literacy screening tool.
Sally Ann Rodríguez, Debra L Roter, Carlos Castillo-Salgado, Gillian W Hooker, Lori H Erby. Health Psychol 2015
11
33

Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.
Deborah Cragun, Anne Weidner, Courtney Lewis, Devon Bonner, Jongphil Kim, Susan T Vadaparampil, Tuya Pal. Cancer 2017
89
33


Family health history and health behaviors in Alaska native and American Indian people.
Martha L Slattery, Maureen A Murtaugh, Anne P Lanier, Khe-Ni Ma, Elizabeth D Ferucci, Ruth A Etzel, Sandra Edwards. J Health Care Poor Underserved 2009
6
33


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.