A citation-based method for searching scientific literature

Kevin Sweet, Amy C Sturm, Tara Schmidlen, Joseph McElroy, Laura Scheinfeldt, Kandamurugu Manickam, Erynn S Gordon, Shelly Hovick, J Scott Roberts, Amanda Ewart Toland, Michael Christman. J Genet Couns 2017
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Design and implementation of a randomized controlled trial of genomic counseling for patients with chronic disease.
Kevin Sweet, Erynn S Gordon, Amy C Sturm, Tara J Schmidlen, Kandamurugu Manickam, Amanda Ewart Toland, Margaret A Keller, Catharine B Stack, J Felipe García-España, Mark Bellafante,[...]. J Pers Med 2014
16
63

Coriell Personalized Medicine Collaborative®: a prospective study of the utility of personalized medicine.
Margaret A Keller, Erynn S Gordon, Catharine B Stack, Neda Gharani, Courtney J Sill, Tara J Schmidlen, Mintzer Joseph, John Pallies, Norman P Gerry, Michael F Christman. Per Med 2010
41
45

Identification of genetic counseling service delivery models in practice: a report from the NSGC Service Delivery Model Task Force.
Stephanie A Cohen, Monica L Marvin, Bronson D Riley, Hetal S Vig, Julie A Rousseau, Shanna L Gustafson. J Genet Couns 2013
71
36

Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing.
David J Kaufman, Juli M Bollinger, Rachel L Dvoskin, Joan A Scott. J Genet Couns 2012
101
27


Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
48
27

Personalized genomic results: analysis of informational needs.
Tara J Schmidlen, Lisa Wawak, Rachel Kasper, J Felipe García-España, Michael F Christman, Erynn S Gordon. J Genet Couns 2014
24
27

Analysis of Advantages, Limitations, and Barriers of Genetic Counseling Service Delivery Models.
Stephanie A Cohen, Rachelle C Huziak, Shanna Gustafson, Robin E Grubs. J Genet Couns 2016
24
27

"It's not like judgment day": public understanding of and reactions to personalized genomic risk information.
Erynn S Gordon, Georgia Griffin, Lisa Wawak, Hauchie Pang, Sarah E Gollust, Barbara A Bernhardt. J Genet Couns 2012
41
27

Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
41
27

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
27

Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative.
Tara J Schmidlen, Laura Scheinfeldt, Ruixue Zhaoyang, Rachel Kasper, Kevin Sweet, Erynn S Gordon, Margaret Keller, Cathy Stack, Neda Gharani, Mary B Daly,[...]. J Genet Couns 2016
19
27

Global implementation of genomic medicine: We are not alone.
Teri A Manolio, Marc Abramowicz, Fahd Al-Mulla, Warwick Anderson, Rudi Balling, Adam C Berger, Steven Bleyl, Aravinda Chakravarti, Wasun Chantratita, Rex L Chisholm,[...]. Sci Transl Med 2015
85
27

A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephone.
Kurt D Christensen, Wendy R Uhlmann, J Scott Roberts, Erin Linnenbringer, Peter J Whitehouse, Charmaine D M Royal, Thomas O Obisesan, L Adrienne Cupples, Melissa B Butson, Grace-Ann Fasaye,[...]. Genet Med 2018
18
27

Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.
Marc D Schwartz, Heiddis B Valdimarsdottir, Beth N Peshkin, Jeanne Mandelblatt, Rachel Nusbaum, An-Tsun Huang, Yaojen Chang, Kristi Graves, Claudine Isaacs, Marie Wood,[...]. J Clin Oncol 2014
138
27

Delivery of Internet-based cancer genetic counselling services to patients' homes: a feasibility study.
Neal J Meropol, Mary B Daly, Hetal S Vig, Frank J Manion, Sharon L Manne, Carla Mazar, Camara Murphy, Nicholas Solarino, Vadim Zubarev. J Telemed Telecare 2011
31
27

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
39
27

How to know when physicians are ready for genomic medicine.
Jason L Vassy, Bruce R Korf, Robert C Green. Sci Transl Med 2015
37
18

Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
267
18

Translational research is a key to nongeneticist physicians' genomics education.
W Gregory Feero, Teri A Manolio, Muin J Khoury. Genet Med 2014
25
18

Evaluating the utility of personal genomic information.
Morris W Foster, John J Mulvihill, Richard R Sharp. Genet Med 2009
121
18

High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic Counseling.
Aisha S Sie, Liesbeth Spruijt, Wendy A G van Zelst-Stams, Arjen R Mensenkamp, Marjolijn J L Ligtenberg, Han G Brunner, Judith B Prins, Nicoline Hoogerbrugge. J Genet Couns 2016
18
18

Impact of direct-to-consumer genomic testing at long term follow-up.
Cinnamon S Bloss, Nathan E Wineinger, Burcu F Darst, Nicholas J Schork, Eric J Topol. J Med Genet 2013
89
18

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
209
18

A systematic review of the impact of genetic counseling on risk perception accuracy.
Chris M R Smerecnik, Ilse Mesters, Eline Verweij, Nanne K de Vries, Hein de Vries. J Genet Couns 2009
76
18


Genomic counseling: next generation counseling.
Rachel Mills, Susanne B Haga. J Genet Couns 2014
18
18

Coming full circle: a reciprocal-engagement model of genetic counseling practice.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S Leroy. J Genet Couns 2007
121
18

Evolving Roles for Physicians and Genetic Counselors in Managing Complex Genetic Disorders.
Celeste A Shelton, David C Whitcomb. Clin Transl Gastroenterol 2015
13
18

mHealth plus community health worker interventions: the future research agenda.
Shiva Raj Mishra, Dinesh Neupane, Tom G Briffa, Per Kallestrup. Lancet Diabetes Endocrinol 2016
6
33

Impact of delivery models on understanding genomic risk for type 2 diabetes.
S B Haga, W T Barry, R Mills, L Svetkey, S Suchindran, H F Willard, G S Ginsburg. Public Health Genomics 2014
15
18

Communicating genetic risk information for common disorders in the era of genomic medicine.
Denise M Lautenbach, Kurt D Christensen, Jeffrey A Sparks, Robert C Green. Annu Rev Genomics Hum Genet 2013
78
18

Patient engagement as a risk factor in personalized health care: a systematic review of the literature on chronic disease.
Leigh Ann Simmons, Ruth Q Wolever, Elizabeth M Bechard, Ralph Snyderman. Genome Med 2014
75
18

Upending the social ecological model to guide health promotion efforts toward policy and environmental change.
Shelley D Golden, Kenneth R McLeroy, Lawrence W Green, Jo Anne L Earp, Lisa D Lieberman. Health Educ Behav 2015
51
18

Information-seeking and sharing behavior following genomic testing for diabetes risk.
Rachel Mills, Jill Powell, William Barry, Susanne B Haga. J Genet Couns 2015
10
20

From genetic counseling to "genomic counseling".
Kelly E Ormond. Mol Genet Genomic Med 2013
42
18

Effect of Lifestyle-Focused Text Messaging on Risk Factor Modification in Patients With Coronary Heart Disease: A Randomized Clinical Trial.
Clara K Chow, Julie Redfern, Graham S Hillis, Jay Thakkar, Karla Santo, Maree L Hackett, Stephen Jan, Nicholas Graves, Laura de Keizer, Tony Barry,[...]. JAMA 2015
290
18

EMR documentation of physician-patient communication following genomic counseling for actionable complex disease and pharmacogenomic results.
K Sweet, A C Sturm, T Schmidlen, S Hovick, J Peng, K Manickam, A Salikhova, J McElroy, L Scheinfeldt, A E Toland,[...]. Clin Genet 2017
6
33

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Jason L Vassy, Denise M Lautenbach, Heather M McLaughlin, Sek Won Kong, Kurt D Christensen, Joel Krier, Isaac S Kohane, Lindsay Z Feuerman, Jennifer Blumenthal-Barby, J Scott Roberts,[...]. Trials 2014
94
18

Clinical Pharmacogenetics Implementation Consortium guidelines for CYP2C19 genotype and clopidogrel therapy: 2013 update.
S A Scott, K Sangkuhl, C M Stein, J-S Hulot, J L Mega, D M Roden, T E Klein, M S Sabatine, J A Johnson, A R Shuldiner. Clin Pharmacol Ther 2013
484
18


The clinical pharmacogenetics implementation consortium guideline for SLCO1B1 and simvastatin-induced myopathy: 2014 update.
L B Ramsey, S G Johnson, K E Caudle, C E Haidar, D Voora, R A Wilke, W D Maxwell, H L McLeod, R M Krauss, D M Roden,[...]. Clin Pharmacol Ther 2014
194
18

Patient experiences with pharmacogenetic testing in a primary care setting.
Susanne B Haga, Rachel Mills, Jivan Moaddeb, Nancy Allen Lapointe, Alex Cho, Geoffrey S Ginsburg. Pharmacogenomics 2016
20
18

Are patients willing to incur out-of-pocket costs for pharmacogenomic testing?
S J Bielinski, J L St Sauver, J E Olson, M L Wieland, C R Vitek, E J Bell, M E Mc Gree, D J Jacobson, J B McCormick, P Y Takahashi,[...]. Pharmacogenomics J 2017
15
18

The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.
David J Carey, Samantha N Fetterolf, F Daniel Davis, William A Faucett, H Lester Kirchner, Uyenlinh Mirshahi, Michael F Murray, Diane T Smelser, Glenn S Gerhard, David H Ledbetter. Genet Med 2016
136
18

My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings.
Holly K Tabor, Seema M Jamal, Joon-Ho Yu, Julia M Crouch, Aditi G Shankar, Karin M Dent, Nick Anderson, Damon A Miller, Brett T Futral, Michael J Bamshad. Genet Med 2017
17
18

Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling.
Beth N Peshkin, Scott Kelly, Rachel H Nusbaum, Morgan Similuk, Tiffani A DeMarco, Gillian W Hooker, Heiddis B Valdimarsdottir, Andrea D Forman, Jessica Rispoli Joines, Claire Davis,[...]. J Genet Couns 2016
24
18

Preferences for genetic and behavioral health information: the impact of risk factors and disease attributions.
Suzanne C O'Neill, Colleen M McBride, Sharon Hensley Alford, Kimberly A Kaphingst. Ann Behav Med 2010
26
18

Genetics/genomics education for nongenetic health professionals: a systematic literature review.
Divya Talwar, Tung-Sung Tseng, Margaret Foster, Lei Xu, Lei-Shih Chen. Genet Med 2017
31
18

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
60
18


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.