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



Attitudes and practices among internists concerning genetic testing.
Robert Klitzman, Wendy Chung, Karen Marder, Anita Shanmugham, Lisa J Chin, Meredith Stark, Cheng-Shiun Leu, Paul S Appelbaum. J Genet Couns 2013
105
33

Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018
117
33

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
47
33

Primary Care Physicians' Knowledge, Attitudes, and Experience with Personal Genetic Testing.
Susanne B Haga, Esther Kim, Rachel A Myers, Geoffrey S Ginsburg. J Pers Med 2019
14
33

Physician-Reported Benefits and Barriers to Clinical Implementation of Genomic Medicine: A Multi-Site IGNITE-Network Survey.
Aniwaa Owusu Obeng, Kezhen Fei, Kenneth D Levy, Amanda R Elsey, Toni I Pollin, Andrea H Ramirez, Kristin W Weitzel, Carol R Horowitz. J Pers Med 2018
56
33

Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics.
Bruce R Korf, Anna B Berry, Melvin Limson, Ali J Marian, Michael F Murray, P Pearl O'Rourke, Eugene R Passamani, Mary V Relling, John Tooker, Gregory J Tsongalis,[...]. Genet Med 2014
79
22

Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives.
Elisa Jf Houwink, Scheltus J van Luijk, Lidewij Henneman, Cees van der Vleuten, Geert Jan Dinant, Martina C Cornel. BMC Fam Pract 2011
80
22

Race, Genomics and Chronic Disease: What Patients with African Ancestry Have to Say.
Carol R Horowitz, Kadija Ferryman, Rennie Negron, Tatiana Sabin, Mayra Rodriguez, Randi F Zinberg, Erwin Böttinger, Mimsie Robinson. J Health Care Poor Underserved 2017
17
22

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
31
22

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
534
22

Consumer Perceptions of Interactions With Primary Care Providers After Direct-to-Consumer Personal Genomic Testing.
Cathelijne H van der Wouden, Deanna Alexis Carere, Anke H Maitland-van der Zee, Mack T Ruffin, J Scott Roberts, Robert C Green. Ann Intern Med 2016
66
22

The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
231
22

Adopting clinical genomics: a systematic review of genomic literacy among physicians in cancer care.
Vu T Dung Ha, Julie Frizzo-Barker, Peter Chow-White. BMC Med Genomics 2018
17
22

What does my doctor think? Preferences for knowing the doctor's opinion among women considering clinical testing for BRCA1/2 mutations.
Katrina Armstrong, Jill Stopfer, Kathleen Calzone, Genevieve Fitzgerald, James Coyne, Barbara Weber. Genet Test 2002
24
22

Family history in primary care: understanding GPs' resistance to clinical genetics--qualitative study.
Jonathan Mathers, Sheila Greenfield, Alison Metcalfe, Trevor Cole, Sarah Flanagan, Sue Wilson. Br J Gen Pract 2010
23
22

Physicians' perspectives on receiving unsolicited genomic results.
Douglas B Pet, Ingrid A Holm, Janet L Williams, Melanie F Myers, Laurie L Novak, Kyle B Brothers, Georgia L Wiesner, Ellen W Clayton. Genet Med 2019
26
22

Genomics in routine clinical care: what does this mean for primary care?
Judith Hayward, Michelle Bishop, Imran Rafi, Val Davison. Br J Gen Pract 2017
10
22

Physician preparedness for big genomic data: a review of genomic medicine education initiatives in the United States.
Caryn Kseniya Rubanovich, Cynthia Cheung, Jess Mandel, Cinnamon S Bloss. Hum Mol Genet 2018
39
22

Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background.
Kelly E Ormond, Miranda L G Hallquist, Adam H Buchanan, Danielle Dondanville, Mildred K Cho, Maureen Smith, Myra Roche, Kyle B Brothers, Curtis R Coughlin, Laura Hercher,[...]. Genet Med 2019
24
22

Views Of Primary Care Providers On Testing Patients For Genetic Risks For Common Chronic Diseases.
Diane Hauser, Aniwaa Owusu Obeng, Kezhen Fei, Michelle A Ramos, Carol R Horowitz. Health Aff (Millwood) 2018
26
22

Primary care providers' experiences with and perceptions of personalized genomic medicine.
June C Carroll, Tutsirai Makuwaza, Donna P Manca, Nicolette Sopcak, Joanne A Permaul, Mary Ann O'Brien, Ruth Heisey, Elizabeth A Eisenhauer, Julie Easley, Monika K Krzyzanowska,[...]. Can Fam Physician 2016
51
22


The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
100
22

Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning.
Belinda J McClaren, Erin Crellin, Monika Janinski, Amy E Nisselle, Larissa Ng, Sylvia A Metcalfe, Clara L Gaff. Front Genet 2020
17
22

Informing Integration of Genomic Medicine Into Primary Care: An Assessment of Current Practice, Attitudes, and Desired Resources.
June C Carroll, Judith Allanson, Shawna Morrison, Fiona A Miller, Brenda J Wilson, Joanne A Permaul, Deanna Telner. Front Genet 2019
14
22

Primary care providers' lived experiences of genetics in practice.
Brittany Harding, Colleen Webber, Lucia Ruhland, Nancy Dalgarno, Christine M Armour, Richard Birtwhistle, Glenn Brown, June C Carroll, Michael Flavin, Susan Phillips,[...]. J Community Genet 2019
13
22


Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine.
Katherine Bonter, Clarissa Desjardins, Nathan Currier, Jason Pun, Fredrick D Ashbury. BMJ Open 2011
58
22

Racial disparities in health among nonpoor African Americans and Hispanics: The role of acute and chronic discrimination.
Cynthia G Colen, David M Ramey, Elizabeth C Cooksey, David R Williams. Soc Sci Med 2018
81
11

APOL1 risk variants, race, and progression of chronic kidney disease.
Afshin Parsa, W H Linda Kao, Dawei Xie, Brad C Astor, Man Li, Chi-yuan Hsu, Harold I Feldman, Rulan S Parekh, John W Kusek, Tom H Greene,[...]. N Engl J Med 2013
446
11


Adoption of pharmacogenomic testing by US physicians: results of a nationwide survey.
E J Stanek, C L Sanders, K A Johansen Taber, M Khalid, A Patel, R R Verbrugge, B C Agatep, R E Aubert, R S Epstein, F W Frueh. Clin Pharmacol Ther 2012
266
11

Association between DNA methylation and coronary heart disease or other atherosclerotic events: A systematic review.
Alba Fernández-Sanlés, Sergi Sayols-Baixeras, Isaac Subirana, Irene R Degano, Roberto Elosua. Atherosclerosis 2017
52
11


How to know when physicians are ready for genomic medicine.
Jason L Vassy, Bruce R Korf, Robert C Green. Sci Transl Med 2015
41
11

Disparities in Diabetes Deaths Among Children and Adolescents - United States, 2000-2014.
Sharon Saydah, Giuseppina Imperatore, Yiling Cheng, Linda S Geiss, Ann Albright. MMWR Morb Mortal Wkly Rep 2017
19
11

Attitudes of African American premedical students toward genetic testing and screening.
Sara L Laskey, Joseph Williams, Jacqui Pierre-Louis, MaryAnn O'Riordan, Anne Matthews, Nathaniel H Robin. Genet Med 2003
40
11

GINA, genetic discrimination, and genomic medicine.
Robert C Green, Denise Lautenbach, Amy L McGuire. N Engl J Med 2015
97
11

Attitudes of clinicians following large-scale pharmacogenomics implementation.
J F Peterson, J R Field, Y Shi, J S Schildcrout, J C Denny, T L McGregor, S L Van Driest, J M Pulley, I M Lubin, M Laposata,[...]. Pharmacogenomics J 2016
47
11

Is race medically relevant? A qualitative study of physicians' attitudes about the role of race in treatment decision-making.
Shedra Amy Snipes, Sherrill L Sellers, Adebola Odunlami Tafawa, Lisa A Cooper, Julie C Fields, Vence L Bonham. BMC Health Serv Res 2011
30
11

Practical considerations in genomic decision support: The eMERGE experience.
Timothy M Herr, Suzette J Bielinski, Erwin Bottinger, Ariel Brautbar, Murray Brilliant, Christopher G Chute, Beth L Cobb, Joshua C Denny, Hakon Hakonarson, Andrea L Hartzler,[...]. J Pathol Inform 2015
31
11

The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.
Loukas Moutsianas, Vineeta Agarwala, Christian Fuchsberger, Jason Flannick, Manuel A Rivas, Kyle J Gaulton, Patrick K Albers, Gil McVean, Michael Boehnke, David Altshuler,[...]. PLoS Genet 2015
78
11

Behavioural changes, sharing behaviour and psychological responses after receiving direct-to-consumer genetic test results: a systematic review and meta-analysis.
Kelly F J Stewart, Anke Wesselius, Maartje A C Schreurs, Annemie M W J Schols, Maurice P Zeegers. J Community Genet 2018
32
11

Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience.
Carolyn R Rohrer Vitek, Noura S Abul-Husn, John J Connolly, Andrea L Hartzler, Terrie Kitchner, Josh F Peterson, Luke V Rasmussen, Maureen E Smith, Sarah Stallings, Marc S Williams,[...]. Pharmacogenomics 2017
20
11

Primary care and genetics and genomics.
Joan Scott, Tracy Trotter. Pediatrics 2013
15
11

APOL1 Risk Variants and Cardiovascular Disease: Results From the AASK (African American Study of Kidney Disease and Hypertension).
Teresa K Chen, Lawrence J Appel, Morgan E Grams, Adrienne Tin, Michael J Choi, Michael S Lipkowitz, Cheryl A Winkler, Michelle M Estrella. Arterioscler Thromb Vasc Biol 2017
27
11

The genetic architecture of type 2 diabetes.
Christian Fuchsberger, Jason Flannick, Tanya M Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J Gaulton, Clement Ma, Pierre Fontanillas, Loukas Moutsianas, Davis J McCarthy,[...]. Nature 2016
550
11

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
Robert A Scott, Laura J Scott, Reedik Mägi, Letizia Marullo, Kyle J Gaulton, Marika Kaakinen, Natalia Pervjakova, Tune H Pers, Andrew D Johnson, John D Eicher,[...]. Diabetes 2017
298
11

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
335
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.