A citation-based method for searching scientific literature

Anita Y Kinney, Laurie E Steffen, Barbara H Brumbach, Wendy Kohlmann, Ruofei Du, Ji-Hyun Lee, Amanda Gammon, Karin Butler, Saundra S Buys, Antoinette M Stroup, Rebecca A Campo, Kristina G Flores, Jeanne S Mandelblatt, Marc D Schwartz. J Clin Oncol 2016
Times Cited: 60







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



Times Cited
  Times     Co-cited
Similarity


Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq® cohort.
Katie L Lewis, Alexis R Heidlebaugh, Sandra Epps, Paul K J Han, Kristen P Fishler, William M P Klein, Ilana M Miller, David Ng, Charlotte Hepler, Barbara B Biesecker,[...]. Genet Med 2019
9
11

Genetic Test Availability And Spending: Where Are We Now? Where Are We Going?
Kathryn A Phillips, Patricia A Deverka, Gillian W Hooker, Michael P Douglas. Health Aff (Millwood) 2018
66
1

A Pilot study of the Sharing Risk Information Tool (ShaRIT) for Families with Hereditary Breast and Ovarian Cancer Syndrome.
Ani Kardashian, Julia Fehniger, Jennifer Creasman, Eleanor Cheung, Mary Stanley Beattie. Hered Cancer Clin Pract 2012
21
4

Family letters are an effective way to inform relatives about inherited cardiac disease.
Wilma P van der Roest, José M Pennings, Marian Bakker, Maarten P van den Berg, J Peter van Tintelen. Am J Med Genet A 2009
52
1

Enhancing genomic laboratory reports: A qualitative analysis of provider review.
Janet L Williams, Alanna Kulchak Rahm, Heather Stuckey, Jamie Green, Lynn Feldman, Doris T Zallen, Michele Bonhag, Michael M Segal, Audrey L Fan, Marc S Williams. Am J Med Genet A 2016
21
4

Public preferences for communicating personal genomic risk information: a focus group study.
Amelia K Smit, Louise A Keogh, Jolyn Hersch, Ainsley J Newson, Phyllis Butow, Gabrielle Williams, Anne E Cust. Health Expect 2016
22
4

Projected Prevalence of Actionable Pharmacogenetic Variants and Level A Drugs Prescribed Among US Veterans Health Administration Pharmacy Users.
Catherine Chanfreau-Coffinier, Leland E Hull, Julie A Lynch, Scott L DuVall, Scott M Damrauer, Francesca E Cunningham, Benjamin F Voight, Michael E Matheny, David W Oslin, Michael S Icardi,[...]. JAMA Netw Open 2019
29
3


Focus group interviews part 3: analysis.
Owen Doody, Eamonn Slevin, Laurence Taggart. Br J Nurs 2013
24
4

Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions.
Sulev Reisberg, Kristi Krebs, Maarja Lepamets, Mart Kals, Reedik Mägi, Kristjan Metsalu, Volker M Lauschke, Jaak Vilo, Lili Milani. Genet Med 2019
28
3

Impact of a Patient-Facing Enhanced Genomic Results Report to Improve Understanding, Engagement, and Communication.
Janet L Williams, Alanna Kulchak Rahm, Doris T Zallen, Heather Stuckey, Kara Fultz, Audrey L Fan, Michele Bonhag, Lynn Feldman, Michael M Segal, Marc S Williams. J Genet Couns 2018
15
6

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
31
3

Electronic health record adoption in US hospitals: the emergence of a digital "advanced use" divide.
Julia Adler-Milstein, A Jay Holmgren, Peter Kralovec, Chantal Worzala, Talisha Searcy, Vaishali Patel. J Am Med Inform Assoc 2017
102
1

Generation and Implementation of a Patient-Centered and Patient-Facing Genomic Test Report in the EHR.
Jessica M Goehringer, Michele A Bonhag, Laney K Jones, Tara Schmidlen, Marci Schwartz, Alanna Kulchak Rahm, Janet L Williams, Marc S Williams. EGEMS (Wash DC) 2018
6
16

Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes.
Ilana M Miller, Katie L Lewis, Tokunbor A Lawal, David Ng, Jennifer J Johnston, Barbara B Biesecker, Leslie G Biesecker. Genet Med 2019
2
50

SLCO1B1 variants and statin-induced myopathy--a genomewide study.
E Link, S Parish, J Armitage, L Bowman, S Heath, F Matsuda, I Gut, M Lathrop, R Collins. N Engl J Med 2008
1

Making the Case for Investment in Rural Cancer Control: An Analysis of Rural Cancer Incidence, Mortality, and Funding Trends.
Kelly D Blake, Jennifer L Moss, Anna Gaysynsky, Shobha Srinivasan, Robert T Croyle. Cancer Epidemiol Biomarkers Prev 2017
99
1

Cancer risk and risk communication in urban, lower-income neighborhoods.
Kimberly M Kelly, Amy K Ferketich, Amy C Sturm, Kyle Porter, Kevin Sweet, Kathleen Kemp, Patricia Schwirian, Judith A Westman. Prev Med 2009
13
7

Using Health Chatbots for Behavior Change: A Mapping Study.
Juanan Pereira, Óscar Díaz. J Med Syst 2019
20
5

Determining Onset for Familial Breast and Colorectal Cancer from Family History Comments in the Electronic Health Record.
Danielle L Mowery, Kensaku Kawamoto, Rick Bradshaw, Wendy Kohlmann, Joshua D Schiffman, Charlene Weir, Damian Borbolla, Wendy W Chapman, Guilherme Del Fiol. AMIA Jt Summits Transl Sci Proc 2019
9
11

Primary care providers' responses to patient-generated family history.
Melissa Fuller, Melanie Myers, Thomas Webb, Meredith Tabangin, Cynthia Prows. J Genet Couns 2010
21
4

Genetic counselor workflow study: The times are they a-changin'?
Courtney A Attard, Erin P Carmany, Angela M Trepanier. J Genet Couns 2019
13
7

Testing for germline mutations in sporadic pheochromocytoma/paraganglioma: a systematic review.
Juan P Brito, Noor Asi, Irina Bancos, Michael R Gionfriddo, Claudia L Zeballos-Palacios, Aaron L Leppin, Chaitanya Undavalli, Zhen Wang, Juan P Domecq, Gabriela Prustsky,[...]. Clin Endocrinol (Oxf) 2015
46
2

Genetic counseling among minority populations in the era of precision medicine.
Chanita H Halbert, Barbara W Harrison. Am J Med Genet C Semin Med Genet 2018
10
10

Family history-taking in community family practice: implications for genetic screening.
L S Acheson, G L Wiesner, S J Zyzanski, M A Goodwin, K C Stange. Genet Med 2000
174
1

Acceptability of artificial intelligence (AI)-led chatbot services in healthcare: A mixed-methods study.
Tom Nadarzynski, Oliver Miles, Aimee Cowie, Damien Ridge. Digit Health 2019
32
3

Behavioral health outcomes associated with religious faith and media exposure about human genetics.
Roxanne Parrott, Kami Silk, Janice Raup Krieger, Tina Harris, Celeste Condit. Health Commun 2004
19
5

Rural-Urban Differences in Cancer Incidence and Trends in the United States.
Whitney E Zahnd, Aimee S James, Wiley D Jenkins, Sonya R Izadi, Amanda J Fogleman, David E Steward, Graham A Colditz, Laurent Brard. Cancer Epidemiol Biomarkers Prev 2018
99
1

Trust and sources of health information: the impact of the Internet and its implications for health care providers: findings from the first Health Information National Trends Survey.
Bradford W Hesse, David E Nelson, Gary L Kreps, Robert T Croyle, Neeraj K Arora, Barbara K Rimer, Kasisomayajula Viswanath. Arch Intern Med 2005
774
1




Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management.
Thomas Paul Slavin, Mariana Niell-Swiller, Ilana Solomon, Bita Nehoray, Christina Rybak, Kathleen R Blazer, Jeffrey N Weitzel. Front Oncol 2015
64
1

Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population.
Tuan A Dinh, Benjamin I Rosner, James C Atwood, C Richard Boland, Sapna Syngal, Hans F A Vasen, Stephen B Gruber, Randall W Burt. Cancer Prev Res (Phila) 2011
120
1

Cancer Predisposition Cascade Screening for Hereditary Breast/Ovarian Cancer and Lynch Syndromes in Switzerland: Study Protocol.
Maria C Katapodi, Valeria Viassolo, Maria Caiata-Zufferey, Christos Nikolaidis, Rosmarie Bührer-Landolt, Nicole Buerki, Rossella Graffeo, Henrik Csaba Horváth, Christian Kurzeder, Manuela Rabaglio,[...]. JMIR Res Protoc 2017
12
8


Primary care providers' cancer genetic testing-related knowledge, attitudes, and communication behaviors: A systematic review and research agenda.
Jada G Hamilton, Ekland Abdiwahab, Heather M Edwards, Min-Lin Fang, Andrew Jdayani, Erica S Breslau. J Gen Intern Med 2017
45
2

The future is now: Technology's impact on the practice of genetic counseling.
Erynn S Gordon, Deepti Babu, Dawn A Laney. Am J Med Genet C Semin Med Genet 2018
18
5

Evaluating the NCCN Clinical Criteria for Recommending BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer.
Caiqian Cropper, Ashley Woodson, Banu Arun, Carlos Barcenas, Jennifer Litton, Sarah Noblin, Diane Liu, Minjeong Park, Molly Daniels. J Natl Compr Canc Netw 2017
5
20

Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.
Maria Currás-Freixes, Lucía Inglada-Pérez, Veronika Mancikova, Cristina Montero-Conde, Rocío Letón, Iñaki Comino-Méndez, María Apellániz-Ruiz, Lara Sánchez-Barroso, Miguel Aguirre Sánchez-Covisa, Victoria Alcázar,[...]. J Med Genet 2015
65
1

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 2.2019.
Samir Gupta, Dawn Provenzale, Xavier Llor, Amy L Halverson, William Grady, Daniel C Chung, Sigurdis Haraldsdottir, Arnold J Markowitz, Thomas P Slavin, Heather Hampel,[...]. J Natl Compr Canc Netw 2019
67
1

Reconsidering the family history in primary care.
Eugene C Rich, Wylie Burke, Caryl J Heaton, Susanne Haga, Linda Pinsky, M Priscilla Short, Louise Acheson. J Gen Intern Med 2004
224
1

Validity of models for predicting BRCA1 and BRCA2 mutations.
Giovanni Parmigiani, Sining Chen, Edwin S Iversen, Tara M Friebel, Dianne M Finkelstein, Hoda Anton-Culver, Argyrios Ziogas, Barbara L Weber, Andrea Eisen, Kathleen E Malone,[...]. Ann Intern Med 2007
73
1


Participation in genetic testing research varies by social group.
Sharon Hensley Alford, Colleen M McBride, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Public Health Genomics 2011
76
1

eHEALS: The eHealth Literacy Scale.
Cameron D Norman, Harvey A Skinner. J Med Internet Res 2006
491
1

Rural-urban disparities in health status among US cancer survivors.
Kathryn E Weaver, Ann M Geiger, Lingyi Lu, L Douglas Case. Cancer 2013
111
1

Genetic counseling, 2030: An on-demand service tailored to the needs of a price conscious, genetically literate, and busy world.
Misha D Rashkin, Johnathan Bowes, Keith Dunaway, Jasmine Dhaliwal, Erick Loomis, Stephen Riffle, Nicole L Washington, Chris Ziegler, James Lu, Elissa Levin. J Genet Couns 2019
5
20

Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
Lisa R Susswein, Megan L Marshall, Rachel Nusbaum, Kristen J Vogel Postula, Scott M Weissman, Lauren Yackowski, Erica M Vaccari, Jeffrey Bissonnette, Jessica K Booker, M Laura Cremona,[...]. Genet Med 2016
150
1

Rural-urban differences in acute myocardial infarction mortality: Evidence from Nebraska.
Soumitra Sudip Bhuyan, Yang Wang, Samuel Opoku, Ge Lin. J Cardiovasc Dis Res 2013
22
4


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.