A citation-based method for searching scientific literature

Stephanie A Kraft, Carmit McMullen, Nangel M Lindberg, David Bui, Kelly Shipman, Katherine Anderson, Galen Joseph, Devan M Duenas, Kathryn M Porter, Tia L Kauffman, Alyssa Koomas, Chelese L Ransom, Paige Jackson, Katrina A B Goddard, Benjamin S Wilfond, Sandra Soo-Jin Lee. Genet Med 2020
Times Cited: 8







List of co-cited articles
29 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
64
87

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
18
75

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
84
75

Prioritizing diversity in human genomics research.
Lucia A Hindorff, Vence L Bonham, Lawrence C Brody, Margaret E C Ginoza, Carolyn M Hutter, Teri A Manolio, Eric D Green. Nat Rev Genet 2018
164
62

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
683
50

Using Genetic Technologies To Reduce, Rather Than Widen, Health Disparities.
Caren E Smith, Stephanie M Fullerton, Keith A Dookeran, Heather Hampel, Adrienne Tin, Nisa M Maruthur, Jonathan C Schisler, Jeffrey A Henderson, Katherine L Tucker, José M Ordovás. Health Aff (Millwood) 2016
46
37

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
25

Online Education and e-Consent for GeneScreen, a Preventive Genomic Screening Study.
R Jean Cadigan, Rita Butterfield, Christine Rini, Margaret Waltz, Kristine J Kuczynski, Kristin Muessig, Katrina A B Goddard, Gail E Henderson. Public Health Genomics 2017
12
25

Reframing Consent for Clinical Research: A Function-Based Approach.
Neal W Dickert, Nir Eyal, Sara F Goldkind, Christine Grady, Steven Joffe, Bernard Lo, Franklin G Miller, Rebecca D Pentz, Robert Silbergleit, Kevin P Weinfurt,[...]. Am J Bioeth 2017
61
25

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
25


Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium.
Susan M Wolf, Laura M Amendola, Jonathan S Berg, Wendy K Chung, Ellen Wright Clayton, Robert C Green, Julie Harris-Wai, Gail E Henderson, Gail P Jarvik, Barbara A Koenig,[...]. Genet Med 2018
22
25

Online BRCA1/2 screening in the Australian Jewish community: a qualitative study.
Jeanette Yuen, Nicole Cousens, Kristine Barlow-Stewart, Rosie O'Shea, Lesley Andrews. J Community Genet 2020
8
25


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
8
25

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
67
25


A review and definition of 'usual care' in genetic counseling trials to standardize use in research.
Barbara B Biesecker, Sarah E Lillie, Laura M Amendola, Katherine E Donohue, Kelly M East, Ann Katherine M Foreman, Marian J Gilmore, Veronica Greve, Billie Liangolou, Julianne M O'Daniel,[...]. J Genet Couns 2021
4
50

Closing the loop: physician communication with diabetic patients who have low health literacy.
Dean Schillinger, John Piette, Kevin Grumbach, Frances Wang, Clifford Wilson, Carolyn Daher, Krishelle Leong-Grotz, Cesar Castro, Andrew B Bindman. Arch Intern Med 2003
745
25

Cancer genetic counseling communication with low-income Chinese immigrants.
Janice Ka Yan Cheng, Claudia Guerra, Rena J Pasick, Dean Schillinger, Judith Luce, Galen Joseph. J Community Genet 2018
16
25

Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: missed opportunities.
Larissa A Meyer, Meaghan E Anderson, Robin A Lacour, Anuj Suri, Molly S Daniels, Diana L Urbauer, Graciela M Nogueras-Gonzalez, Kathleen M Schmeler, David M Gershenson, Karen H Lu. Obstet Gynecol 2010
90
25

Health Care Segregation, Physician Recommendation, and Racial Disparities in BRCA1/2 Testing Among Women With Breast Cancer.
Anne Marie McCarthy, Mirar Bristol, Susan M Domchek, Peter W Groeneveld, Younji Kim, U Nkiru Motanya, Judy A Shea, Katrina Armstrong. J Clin Oncol 2016
96
25

Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature.
Megan C Roberts, W David Dotson, Christopher S DeVore, Erica M Bednar, Deborah J Bowen, Theodore G Ganiats, Ridgely Fisk Green, Georgia M Hurst, Alisdair R Philp, Charité N Ricker,[...]. Health Aff (Millwood) 2018
72
25

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
5
40

Lack Of Diversity In Genomic Databases Is A Barrier To Translating Precision Medicine Research Into Practice.
Latrice G Landry, Nadya Ali, David R Williams, Heidi L Rehm, Vence L Bonham. Health Aff (Millwood) 2018
100
25

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children.
Jacqueline A Odgis, Katie M Gallagher, Sabrina A Suckiel, Katherine E Donohue, Michelle A Ramos, Nicole R Kelly, Gabrielle Bertier, Christina Blackburn, Kaitlyn Brown, Lena Fielding,[...]. Trials 2021
5
40

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
6
33

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
8
25


The Use of Web-Based Technologies in Health Research Participation: Qualitative Study of Consumer and Researcher Experiences.
Patrick Cheong-Iao Pang, Shanton Chang, Karin Verspoor, Ornella Clavisi. J Med Internet Res 2018
5
20

A review of approaches to improve participation of culturally and linguistically diverse populations in clinical trials.
Jo-Anne Hughson, Robyn Woodward-Kron, Anna Parker, John Hajek, Agnese Bresin, Ute Knoch, Tuong Phan, David Story. Trials 2016
47
12



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
331
12

Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.
Joon-Ho Yu, Paul S Appelbaum, Kyle B Brothers, Steven Joffe, Tia L Kauffman, Barbara A Koenig, Anya Er Prince, Sarah Scollon, Susan M Wolf, Barbara A Bernhardt,[...]. Per Med 2019
6
16

"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
Ashley N Tomlinson, Debra Skinner, Denise L Perry, Sarah R Scollon, Myra I Roche, Barbara A Bernhardt. J Genet Couns 2016
39
12


Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials.
Adam Nishimura, Jantey Carey, Patricia J Erwin, Jon C Tilburt, M Hassan Murad, Jennifer B McCormick. BMC Med Ethics 2013
258
12

Research participants' experiences with return of genetic research results and preferences for web-based alternatives.
Jill B Gaieski, Linda Patrick-Miller, Brian L Egleston, Kara N Maxwell, Sarah Walser, Laura DiGiovanni, Jamie Brower, Dominique Fetzer, Amanda Ganzak, Danielle McKenna,[...]. Mol Genet Genomic Med 2019
11
12

Is informed consent broken?
Gail E Henderson. Am J Med Sci 2011
43
12

Ethical issues in human genomics research in developing countries.
Jantina de Vries, Susan J Bull, Ogobara Doumbo, Muntaser Ibrahim, Odile Mercereau-Puijalon, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2011
82
12

Can research and care be ethically integrated?
Emily A Largent, Steven Joffe, Franklin G Miller. Hastings Cent Rep 2011
69
12

MAGENTA (Making Genetic testing accessible): a prospective randomized controlled trial comparing online genetic education and telephone genetic counseling for hereditary cancer genetic testing.
Nadine Rayes, Deborah J Bowen, Tara Coffin, Denise Nebgen, Christine Peterson, Mark F Munsell, Kathleen Gavin, Rebecca Lechner, Jamie Crase, Deborah Polinsky,[...]. BMC Cancer 2019
16
12

Bench to bedside: mapping the moral terrain of clinical research.
Steven Joffe, Franklin G Miller. Hastings Cent Rep 2008
73
12

Understanding respect: learning from patients.
N W Dickert, N E Kass. J Med Ethics 2009
47
12


Patient perspectives on the use of categories of conditions for decision making about genomic carrier screening results.
Stephanie A Kraft, Carmit K McMullen, Kathryn M Porter, Tia L Kauffman, James V Davis, Jennifer L Schneider, Katrina A B Goddard, Benjamin S Wilfond. Am J Med Genet A 2018
15
12

Patient-Consent Disconnects in Clinical Research.
Neal W Dickert, JoAnne Brabson, Rodney J Hunter, Michele Riedford. Patient 2018
3
33

Conceptualizing trust in community-academic research partnerships using concept mapping approach: A multi-CTSA study.
Gaurav Dave, Leah Frerichs, Jennifer Jones, Mimi Kim, Jennifer Schaal, Stefanie Vassar, Deepthi Varma, Catherine Striley, Corrine Ruktanonchai, Adina Black,[...]. Eval Program Plann 2018
11
12

Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.
Isabelle Budin-Ljøsne, Harriet J A Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D'Abramo, Heike Felzmann, Teresa Finlay,[...]. BMC Med Ethics 2017
109
12


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.