A citation-based method for searching scientific literature

Lauren Puryear, Natalie Downs, Andrea Nevedal, Eleanor T Lewis, Kelly E Ormond, Maria Bregendahl, Carlos J Suarez, Sean P David, Steven Charlap, Isabella Chu, Steven M Asch, Neda Pakdaman, Sang-Ick Chang, Mark R Cullen, Latha Palaniappan. J Community Genet 2018
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Genomic medicine: a decade of successes, challenges, and opportunities.
Jeanette J McCarthy, Howard L McLeod, Geoffrey S Ginsburg. Sci Transl Med 2013
137
11

The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementation.
A R Shuldiner, M V Relling, J F Peterson, J K Hicks, R R Freimuth, W Sadee, N L Pereira, D M Roden, J A Johnson, T E Klein,[...]. Clin Pharmacol Ther 2013
115
11

Survey of family history taking and genetic testing in pediatric practice.
Robert A Saul, Tracy Trotter, Kerry Sease, Beth Tarini. J Community Genet 2017
12
11

Nurses' Use of Race in Clinical Decision Making.
Sherrill L Sellers, Melissa E Moss, Kathleen Calzone, Khadijah E Abdallah, Jean F Jenkins, Vence L Bonham. J Nurs Scholarsh 2016
3
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
17
11


Family physicians' awareness and knowledge of the Genetic Information Non-Discrimination Act (GINA).
Amanda L Laedtke, Suzanne M O'Neill, Wendy S Rubinstein, Kristen J Vogel. J Genet Couns 2012
39
11

Can Communicating Personalised Disease Risk Promote Healthy Behaviour Change? A Systematic Review of Systematic Reviews.
David P French, Elaine Cameron, Jack S Benton, Christi Deaton, Michelle Harvie. Ann Behav Med 2017
60
11

Reducing Racial/Ethnic Disparities in Cardiovascular Genetic Testing.
Lisa M Dellefave-Castillo, Megan J Puckelwartz, Elizabeth M McNally. JAMA Cardiol 2018
2
50

What hinders minority ethnic access to cancer genetics services and what may help?
Anna Allford, Nadeem Qureshi, Julian Barwell, Celine Lewis, Joe Kai. Eur J Hum Genet 2014
39
11

Physicians' anxiety due to uncertainty and use of race in medical decision making.
Brooke A Cunningham, Vence L Bonham, Sherrill L Sellers, Hsin-Chieh Yeh, Lisa A Cooper. Med Care 2014
16
11

Stakeholder engagement: a key component of integrating genomic information into electronic health records.
Andrea Hartzler, Catherine A McCarty, Luke V Rasmussen, Marc S Williams, Murray Brilliant, Erica A Bowton, Ellen Wright Clayton, William A Faucett, Kadija Ferryman, Julie R Field,[...]. Genet Med 2013
40
11

Physicians' attitudes toward race, genetics, and clinical medicine.
Vence L Bonham, Sherrill L Sellers, Thomas H Gallagher, Danielle Frank, Adebola O Odunlami, Eboni G Price, Lisa A Cooper. Genet Med 2009
25
11

Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestry.
C R Horowitz, N S Abul-Husn, S Ellis, M A Ramos, R Negron, M Suprun, R E Zinberg, T Sabin, D Hauser, N Calman,[...]. Contemp Clin Trials 2016
26
11


Inclusion of diverse populations in genomic research and health services: Genomix workshop report.
Savio S Mathew, Julian Barwell, Nasaim Khan, Ella Lynch, Michael Parker, Nadeem Qureshi. J Community Genet 2017
16
11

Public health genomics and personalized prevention: lessons from the COGS project.
N Pashayan, A Hall, S Chowdhury, T Dent, P D P Pharoah, H Burton. J Intern Med 2013
19
11

Association of Attending Surgeon With Variation in the Receipt of Genetic Testing After Diagnosis of Breast Cancer.
Steven J Katz, Irina Bondarenko, Kevin C Ward, Ann S Hamilton, Monica Morrow, Allison W Kurian, Timothy P Hofer. JAMA Surg 2018
15
11

Impact of BRCA1/BRCA2 counseling and testing on newly diagnosed breast cancer patients.
Marc D Schwartz, Caryn Lerman, Barbara Brogan, Beth N Peshkin, Chanita Hughes Halbert, Tiffani DeMarco, William Lawrence, David Main, Clinton Finch, Colette Magnant,[...]. J Clin Oncol 2004
189
11


Effects of communicating DNA-based disease risk estimates on risk-reducing behaviours.
Theresa M Marteau, David P French, Simon J Griffin, A T Prevost, Stephen Sutton, Clare Watkinson, Sophie Attwood, Gareth J Hollands. Cochrane Database Syst Rev 2010
195
11

Genomics in general practice: Generation Genome.
Sarah C Hillman, Jeremy Dale. Br J Gen Pract 2017
4
25

Standards for reporting qualitative research: a synthesis of recommendations.
Bridget C O'Brien, Ilene B Harris, Thomas J Beckman, Darcy A Reed, David A Cook. Acad Med 2014
11


Social and behavioral science priorities for genomic translation.
Laura M Koehly, Susan Persky, Erica Spotts, Gillian Acca. Transl Behav Med 2018
2
50

Does personalized melanoma genomic risk information trigger conversations about skin cancer prevention and skin examination with family, friends and health professionals?
A K Smit, L A Keogh, A J Newson, P N Butow, K Dunlop, R L Morton, J Kirk, D Espinoza, A E Cust. Br J Dermatol 2017
13
11

A Pilot Randomized Controlled Trial of the Feasibility, Acceptability, and Impact of Giving Information on Personalized Genomic Risk of Melanoma to the Public.
Amelia K Smit, David Espinoza, Ainsley J Newson, Rachael L Morton, Georgina Fenton, Lucinda Freeman, Kate Dunlop, Phyllis N Butow, Matthew H Law, Michael G Kimlin,[...]. Cancer Epidemiol Biomarkers Prev 2017
28
11

Consumer use and response to online third-party raw DNA interpretation services.
Catharine Wang, Tiernan J Cahill, Andrew Parlato, Blake Wertz, Qiankun Zhong, Tricia Norkunas Cunningham, James J Cummings. Mol Genet Genomic Med 2018
22
11

Do Health Professionals Need Additional Competencies for Stratified Cancer Prevention Based on Genetic Risk Profiling?
Susmita Chowdhury, Lidewij Henneman, Tom Dent, Alison Hall, Alice Burton, Paul Pharoah, Nora Pashayan, Hilary Burton. J Pers Med 2015
8
12

A Clinical Decision Support Tool to Predict Cancer Risk for Commonly Tested Cancer-Related Germline Mutations.
Danielle Braun, Jiabei Yang, Molly Griffin, Giovanni Parmigiani, Kevin S Hughes. J Genet Couns 2018
18
11

A systematic review of interventions to provide genetics education for primary care.
Milena Paneque, Daniela Turchetti, Leigh Jackson, Peter Lunt, Elisa Houwink, Heather Skirton. BMC Fam Pract 2016
40
11

Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.
Barbara B Biesecker, Katie L Lewis, Kendall L Umstead, Jennifer J Johnston, Erin Turbitt, Kristen P Fishler, John H Patton, Ilana M Miller, Alexis R Heidlebaugh, Leslie G Biesecker. JAMA Intern Med 2018
46
11

Shared decision making and decision aids - a literature review.
Jill Thistlethwaite, Rebecca Evans, Rod Nan Tie, Clare Heal. Aust Fam Physician 2006
22
11

Public health implications from COGS and potential for risk stratification and screening.
Hilary Burton, Susmita Chowdhury, Tom Dent, Alison Hall, Nora Pashayan, Paul Pharoah. Nat Genet 2013
85
11

Distress, uncertainty, and positive experiences associated with receiving information on personal genomic risk of melanoma.
Amelia K Smit, Ainsley J Newson, Megan Best, Caro-Anne Badcock, Phyllis N Butow, Judy Kirk, Kate Dunlop, Georgina Fenton, Anne E Cust. Eur J Hum Genet 2018
13
11

Genetics and primary care: where are we headed?
Vasiliki Rahimzadeh, Gillian Bartlett. J Transl Med 2014
15
11


Genetic education, knowledge and experiences between nurses and physicians in primary care in Brazil: A cross-sectional study.
Luís Carlos Lopes-Júnior, Paulo Marcondes Carvalho Júnior, Victor Evangelista de Faria Ferraz, Lucila Castanheira Nascimento, Marcia Van Riper, Milena Flória-Santos. Nurs Health Sci 2017
12
11


A 1000 Arab genome project to study the Emirati population.
Mariam Al-Ali, Wael Osman, Guan K Tay, Habiba S AlSafar. J Hum Genet 2018
20
11

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
36
11

The Human Genome Project, and recent advances in personalized genomics.
Brenda J Wilson, Stuart G Nicholls. Risk Manag Healthc Policy 2015
26
11

The genetic heterogeneity of Arab populations as inferred from HLA genes.
Abdelhafidh Hajjej, Wassim Y Almawi, Antonio Arnaiz-Villena, Lasmar Hattab, Slama Hmida. PLoS One 2018
21
11


Towards establishing a multiple sclerosis biobank in Jordan.
Mamoun Ahram, Rand Zaza, Leena Ibayyan, Said Dahbour, Yacoub Bahou, Ammar El-Omar, Bilal Samhouri, Mohammad El-Khateeb. Int J Neurosci 2014
5
20

Differences in attitudes toward genetic testing among the public, patients, and health-care professionals in Korea.
Heesang Eum, Mangyeong Lee, Junghee Yoon, Juhee Cho, Eun Sook Lee, Kui Son Choi, Sangwon Lee, So-Youn Jung, Myong Cheol Lim, Sun-Young Kong,[...]. Eur J Hum Genet 2018
7
14

New literacy challenge for the twenty-first century: genetic knowledge is poor even among well educated.
Robert Chapman, Maxim Likhanov, Fatos Selita, Ilya Zakharov, Emily Smith-Woolley, Yulia Kovas. J Community Genet 2019
30
11

Introducing the first whole genomes of nationals from the United Arab Emirates.
Habiba S AlSafar, Mariam Al-Ali, Gihan Daw Elbait, Mustafa H Al-Maini, Dymitr Ruta, Braulio Peramo, Andreas Henschel, Guan K Tay. Sci Rep 2019
6
16

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.
Eric M Scott, Anason Halees, Yuval Itan, Emily G Spencer, Yupeng He, Mostafa Abdellateef Azab, Stacey B Gabriel, Aziz Belkadi, Bertrand Boisson, Laurent Abel,[...]. Nat Genet 2016
155
11


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.