A citation-based method for searching scientific literature

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, Gail P Jarvik, Benjamin Wilfond, Katrina A B Goddard, Galen Joseph. Patient Educ Couns 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Laura M Amendola, Jonathan S Berg, Carol R Horowitz, Frank Angelo, Jeannette T Bensen, Barbara B Biesecker, Leslie G Biesecker, Gregory M Cooper, Kelly East, Kelly Filipski,[...]. Am J Hum Genet 2018
40
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
46
66

A decision aid for additional findings in genomic sequencing: Development and pilot testing.
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,[...]. Patient Educ Couns 2021
2
100

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.
Jonathan S Berg, Laura M Amendola, Christine Eng, Eliezer Van Allen, Stacy W Gray, Nikhil Wagle, Heidi L Rehm, Elizabeth T DeChene, Matthew C Dulik, Fuki M Hisama,[...]. Genet Med 2013
88
33

A dynamic approach to communication in health literacy education.
Herman Veenker, Wolter Paans. BMC Med Educ 2016
9
33

GUÍA: a digital platform to facilitate result disclosure in genetic counseling.
Sabrina A Suckiel, Jaqueline A Odgis, Katie M Gallagher, Jessica E Rodriguez, Dana Watnick, Gabrielle Bertier, Monisha Sebastin, Nicole Yelton, Estefany Maria, Jessenia Lopez,[...]. Genet Med 2021
4
33



The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics.
Alice B Popejoy, Deborah I Ritter, Kristy Crooks, Erin Currey, Stephanie M Fullerton, Lucia A Hindorff, Barbara Koenig, Erin M Ramos, Elena P Sorokin, Hannah Wand,[...]. Hum Mutat 2018
30
33

The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
163
33

Interpreters' perceptions of culture bumps in genetic counseling.
Marc Rosenbaum, Richard Dineen, Karen Schmitz, Jessica Stoll, Melissa Hsu, Priscila D Hodges. J Genet Couns 2020
2
50

Recommendations for the integration of genomics into clinical practice.
Sarah Bowdin, Adel Gilbert, Emma Bedoukian, Christopher Carew, Margaret P Adam, John Belmont, Barbara Bernhardt, Leslie Biesecker, Hans T Bjornsson, Miriam Blitzer,[...]. Genet Med 2016
79
33


Return of results in the genomic medicine projects of the eMERGE network.
Iftikhar J Kullo, Ra'ad Haddad, Cynthia A Prows, Ingrid Holm, Saskia C Sanderson, Nanibaa' A Garrison, Richard R Sharp, Maureen E Smith, Helena Kuivaniemi, Erwin P Bottinger,[...]. Front Genet 2014
32
33

A Culture of Understanding: Reflections and Suggestions from a Genomics Research Community Board.
Benjamin Kaplan, Carolyn Caddle-Steele, Gregory Chisholm, Warria A Esmond, Kadija Ferryman, Melvin Gertner, Crispin Goytia, Diane Hauser, Lynne D Richardson, Mimsie Robinson,[...]. Prog Community Health Partnersh 2017
16
33

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, D'Andra M Lindbuchler, Miranda L G Hallquist, Kandamurugu Manickam, Adam H Buchanan, Alanna Kulchak Rahm, Monica A Giovanni, Lauren Frisbie,[...]. Am J Hum Genet 2018
57
33

Illustrative case studies in the return of exome and genome sequencing results.
Laura M Amendola, Denise Lautenbach, Sarah Scollon, Barbara Bernhardt, Sawona Biswas, Kelly East, Jessica Everett, Marian J Gilmore, Patricia Himes, Victoria M Raymond,[...]. Per Med 2015
31
33

Experiences with obtaining informed consent for genomic sequencing.
Barbara A Bernhardt, Myra I Roche, Denise L Perry, Sarah R Scollon, Ashley N Tomlinson, Debra Skinner. Am J Med Genet A 2015
63
33

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
32
33

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
518
33

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
3
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
76
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
3
33

Analyzing communication in genetic consultations--a systematic review.
Jean Paul, Sylvia Metcalfe, Lesley Stirling, Brenda Wilson, Jan Hodgson. Patient Educ Couns 2015
26
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
26
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
36
33

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
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
12
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
41
33

Hereditary cancer predisposition syndromes.
Judy E Garber, Kenneth Offit. J Clin Oncol 2005
320
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
35
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
54
33

Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
55
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
67
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
107
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
29
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
1
100


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
91
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


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.