A citation-based method for searching scientific literature

Tara J Schmidlen, Lisa Wawak, Rachel Kasper, J Felipe García-España, Michael F Christman, Erynn S Gordon. J Genet Couns 2014
Times Cited: 24







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



Times Cited
  Times     Co-cited
Similarity


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
37

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
35

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
81
25

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
37

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
20

From genetic counseling to "genomic counseling".
Kelly E Ormond. Mol Genet Genomic Med 2013
42
20

Genetic risk estimation in the Coriell Personalized Medicine Collaborative.
Catharine B Stack, Neda Gharani, Erynn S Gordon, Tara Schmidlen, Michael F Christman, Margaret A Keller. Genet Med 2011
33
20

Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration.
Laura B Scheinfeldt, Neda Gharani, Rachel S Kasper, Tara J Schmidlen, Erynn S Gordon, Joseph P Jarvis, Susan Delaney, Courtney J Kronenthal, Norman P Gerry, Michael F Christman. Am J Med Genet B Neuropsychiatr Genet 2015
22
22

The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation system.
Neda Gharani, Margaret A Keller, Catharine B Stack, Laura M Hodges, Tara J Schmidlen, Daniel E Lynch, Erynn S Gordon, Michael F Christman. Genome Med 2013
21
23

Common genetic risk for melanoma encourages preventive behavior change.
Lori Diseati, Laura B Scheinfeldt, Rachel S Kasper, Ruixue Zhaoyang, Neda Gharani, Tara J Schmidlen, Erynn S Gordon, Cecili K Sessions, Susan K Delaney, Joseph P Jarvis,[...]. J Pers Med 2015
19
26

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
111
16

Genomic counseling: next generation counseling.
Rachel Mills, Susanne B Haga. J Genet Couns 2014
18
22

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
26
16

Coming full circle: a reciprocal-engagement model of genetic counseling practice.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S Leroy. J Genet Couns 2007
123
16

Evolving Roles for Physicians and Genetic Counselors in Managing Complex Genetic Disorders.
Celeste A Shelton, David C Whitcomb. Clin Transl Gastroenterol 2015
14
28

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
72
16

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
98
16

Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
46
16

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
19
21

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research.
Flavia M Facio, Stephanie Brooks, Johanna Loewenstein, Susannah Green, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2011
96
12

Teaching genomic counseling: preparing the genetic counseling workforce for the genomic era.
Gillian W Hooker, Kelly E Ormond, Kevin Sweet, Barbara B Biesecker. J Genet Couns 2014
42
12

Recommendations for returning genomic incidental findings? We need to talk!
Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers,[...]. Genet Med 2013
211
12



Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
118
12

Preemptive clinical pharmacogenetics implementation: current programs in five US medical centers.
Henry M Dunnenberger, Kristine R Crews, James M Hoffman, Kelly E Caudle, Ulrich Broeckel, Scott C Howard, Robert J Hunkler, Teri E Klein, William E Evans, Mary V Relling. Annu Rev Pharmacol Toxicol 2015
244
12

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
41
12


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
27

Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
52
12

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
20

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
80
12


"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
46
12

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
12

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
50

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
90
12


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
12

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
12

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
40
12

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
26
12

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
17

The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial Results.
Iftikhar J Kullo, Janet Olson, Xiao Fan, Merin Jose, Maya Safarova, Carmen Radecki Breitkopf, Erin Winkler, David C Kochan, Sara Snipes, Joel E Pacyna,[...]. Mayo Clin Proc 2018
19
15

Evaluation of the validity and utility of genetic testing for rare diseases.
Scott D Grosse, Lisa Kalman, Muin J Khoury. Adv Exp Med Biol 2010
37
8


Communicating genetic and genomic information: health literacy and numeracy considerations.
D H Lea, K A Kaphingst, D Bowen, I Lipkus, D W Hadley. Public Health Genomics 2011
132
8

Bridging the Communication Divide: A Role for Health Psychology in the Genomic Era.
Kenneth P Tercyak, Suzanne C O'Neill, Debra L Roter, Colleen M McBride. Prof Psychol Res Pr 2012
6
33

Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care.
Fiona A Miller, Robin Z Hayeems, Jessica P Bytautas, Philippe L Bedard, Scott Ernst, Hal Hirte, Sebastien Hotte, Amit Oza, Albiruni Razak, Stephen Welch,[...]. Eur J Hum Genet 2014
59
8

Opening the psychological black box in genetic counseling. The psychological impact of DNA testing is predicted by the counselees' perception, the medical impact by the pathogenic or uninformative BRCA1/2-result.
Joël Vos, Encarna Gómez-García, Jan C Oosterwijk, Fred H Menko, Reinoud D Stoel, Christi J van Asperen, Anna M Jansen, Anne M Stiggelbout, Aad Tibben. Psychooncology 2012
48
8


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.