A citation-based method for searching scientific literature

K Sweet, A C Sturm, T Schmidlen, S Hovick, J Peng, K Manickam, A Salikhova, J McElroy, L Scheinfeldt, A E Toland, J S Roberts, M Christman. Clin Genet 2017
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Genomic counseling: next generation counseling.
Rachel Mills, Susanne B Haga. J Genet Couns 2014
18
66

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
112
50


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
50

Coming full circle: a reciprocal-engagement model of genetic counseling practice.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S Leroy. J Genet Couns 2007
132
50

Evolving Roles for Physicians and Genetic Counselors in Managing Complex Genetic Disorders.
Celeste A Shelton, David C Whitcomb. Clin Transl Gastroenterol 2015
14
50

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
50

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
83
50


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
50

"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
47
50

Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
48
50

From genetic counseling to "genomic counseling".
Kelly E Ormond. Mol Genet Genomic Med 2013
43
50

Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports.
Kevin Sweet, Amy C Sturm, Tara Schmidlen, Joseph McElroy, Laura Scheinfeldt, Kandamurugu Manickam, Erynn S Gordon, Shelly Hovick, J Scott Roberts, Amanda Ewart Toland,[...]. J Genet Couns 2017
11
33

Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
55
33

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
33
33

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
74
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
33

Patients' understanding of and responses to multiplex genetic susceptibility test results.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Robert Reid, Eric Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2012
84
33

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
100
33

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
79
33

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
58
33

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
33

Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.
S E Gollust, E S Gordon, C Zayac, G Griffin, M F Christman, R E Pyeritz, L Wawak, B A Bernhardt. Public Health Genomics 2012
110
33

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
20
33

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
94
33


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
82
33

Genetic counselors and Genomic Counseling in the United Kingdom.
Anna Middleton, Georgina Hall, Christine Patch. Mol Genet Genomic Med 2015
18
33

A systematic review of perceived risks, psychological and behavioral impacts of genetic testing.
Jodi T Heshka, Crystal Palleschi, Heather Howley, Brenda Wilson, Philip S Wells. Genet Med 2008
219
33

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
27
33

Participant use and communication of findings from exome sequencing: a mixed-methods study.
Katie L Lewis, Gillian W Hooker, Philip D Connors, Travis C Hyams, Martha F Wright, Samantha Caldwell, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2016
45
33

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
354
33

Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.
Kevin Sweet, Shelly Hovick, Amy C Sturm, Tara Schmidlen, Erynn Gordon, Barbara Bernhardt, Lisa Wawak, Karen Wernke, Joseph McElroy, Laura Scheinfeldt,[...]. J Genet Couns 2017
10
33

Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.
Joon-Ho Yu, Tanya M Harrell, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Hum Genet 2014
86
33

The potential impact of pharmacogenetic testing on medication adherence.
S B Haga, N M A LaPointe. Pharmacogenomics J 2013
37
33

Primary care physicians' knowledge of and experience with pharmacogenetic testing.
S B Haga, W Burke, G S Ginsburg, R Mills, R Agans. Clin Genet 2012
155
33

Adoption of a clinical pharmacogenomics implementation program during outpatient care--initial results of the University of Chicago "1,200 Patients Project".
Peter H O'Donnell, Keith Danahey, Michael Jacobs, Nisha R Wadhwa, Shennin Yuen, Angela Bush, Yasmin Sacro, Matthew J Sorrentino, Mark Siegler, William Harper,[...]. Am J Med Genet C Semin Med Genet 2014
79
33



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
16


Preferences for results delivery from exome sequencing/genome sequencing.
Martha F Wright, Katie L Lewis, Tyler C Fisher, Gillian W Hooker, Toby E Emanuel, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2014
43
16

Moving toward NextGenetic counseling.
Myra I Roche. Genet Med 2012
9
16

Health coaching for patients with chronic illness.
Heather D Bennett, Eric A Coleman, Carla Parry, Thomas Bodenheimer, Ellen H Chen. Fam Pract Manag 2010
63
16

Information-seeking and sharing behavior following genomic testing for diabetes risk.
Rachel Mills, Jill Powell, William Barry, Susanne B Haga. J Genet Couns 2015
11
16


How can polygenic inheritance be used in population screening for common diseases?
Muin J Khoury, A Cecile J W Janssens, David F Ransohoff. Genet Med 2013
32
16

A one-page summary report of genome sequencing for the healthy adult.
Jason L Vassy, Heather M McLaughlin, Calum A MacRae, Christine E Seidman, Denise Lautenbach, Joel B Krier, William J Lane, Isaac S Kohane, Michael F Murray, Amy L McGuire,[...]. Public Health Genomics 2015
29
16



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.