A citation-based method for searching scientific literature

Shannon Rego, Orit Dagan-Rosenfeld, Stephanie A Bivona, Michael P Snyder, Kelly E Ormond. J Genet Couns 2019
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Returning negative results to individuals in a genomic screening program: lessons learned.
Rita M Butterfield, James P Evans, Christine Rini, Kristine J Kuczynski, Margaret Waltz, R Jean Cadigan, Katrina A B Goddard, Kristin R Muessig, Gail E Henderson. Genet Med 2019
15
100

Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium.
Emilie S Zoltick, Michael D Linderman, Molly A McGinniss, Erica Ramos, Madeleine P Ball, George M Church, Debra G B Leonard, Stacey Pereira, Amy L McGuire, C Thomas Caskey,[...]. Genome Med 2019
13
100

How Well Do Customers of Direct-to-Consumer Personal Genomic Testing Services Comprehend Genetic Test Results? Findings from the Impact of Personal Genomics Study.
Jenny E Ostergren, Michele C Gornick, Deanna Alexis Carere, Sarah S Kalia, Wendy R Uhlmann, Mack T Ruffin, Joanna L Mountain, Robert C Green, J Scott Roberts. Public Health Genomics 2015
40
50

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
50

Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding.
Susanne B Haga, Rachel Mills, Kathryn I Pollak, Catherine Rehder, Adam H Buchanan, Isaac M Lipkus, Jennifer H Crow, Michael Datto. Genome Med 2014
33
50

Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor, Kim L McBride, Ana Morales, Matthew R G Taylor, Matteo Vatta, Stephanie M Ware. J Card Fail 2018
98
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
41
50

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
740
50

Actionable, pathogenic incidental findings in 1,000 participants' exomes.
Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett,[...]. Am J Hum Genet 2013
262
50

The general public's understanding and perception of direct-to-consumer genetic test results.
J W Leighton, K Valverde, B A Bernhardt. Public Health Genomics 2012
79
50

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
20
50

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
50

Population-Wide Screening for Germline BRCA1 and BRCA2 Mutations: Too Much of a Good Thing?
Matthew B Yurgelun, Elaine Hiller, Judy E Garber. J Clin Oncol 2015
31
50

Creating genetic reports that are understood by nonspecialists: a case study.
Gabriel Recchia, Antonia Chiappi, Gemma Chandratillake, Lucy Raymond, Alexandra L J Freeman. Genet Med 2020
3
50

Primary care patients' views and decisions about, experience of and reactions to direct-to-consumer genetic testing: a longitudinal study.
Katherine Wasson, Tonya Nashay Sanders, Nancy S Hogan, Sara Cherny, Kathy J Helzlsouer. J Community Genet 2013
17
50

Hypertrophic cardiomyopathy genetic test reports: A qualitative study of patient understanding of uninformative genetic test results.
Brooke M Nightingale, Shelly R Hovick, Pamela Brock, Emily Callahan, Elizabeth Jordan, Jennifer Roggenbuck, Amy C Sturm, Ana Morales. J Genet Couns 2019
3
50

Saturation in qualitative research: exploring its conceptualization and operationalization.
Benjamin Saunders, Julius Sim, Tom Kingstone, Shula Baker, Jackie Waterfield, Bernadette Bartlam, Heather Burroughs, Clare Jinks. Qual Quant 2018
986
50

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
50

Australian study on public knowledge of human genetics and health.
C Molster, T Charles, A Samanek, P O'Leary. Public Health Genomics 2009
71
50

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
75
50


Public knowledge of and attitudes toward genetics and genetic testing.
Susanne B Haga, William T Barry, Rachel Mills, Geoffrey S Ginsburg, Laura Svetkey, Jennifer Sullivan, Huntington F Willard. Genet Test Mol Biomarkers 2013
118
50

Application of population screening principles to genetic screening for adult-onset conditions.
W Burke, S S Coughlin, N C Lee, D L Weed, M J Khoury. Genet Test 2001
52
50


Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, George A Diaz, Randi E Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt. Eur J Hum Genet 2016
23
50

False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care.
Stephany Tandy-Connor, Jenna Guiltinan, Kate Krempely, Holly LaDuca, Patrick Reineke, Stephanie Gutierrez, Phillip Gray, Brigette Tippin Davis. Genet Med 2018
95
50






Personal utility in genomic testing: a systematic literature review.
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur J Hum Genet 2017
42
50

Reconciling Opportunistic and Population Screening in Clinical Genomics.
Kyle B Brothers, Jason L Vassy, Robert C Green. Mayo Clin Proc 2019
14
50

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
50

Personal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq Consortium.
Michael D Linderman, Daiva E Nielsen, Robert C Green. J Pers Med 2016
28
50

Increasing confidence and changing behaviors in primary care providers engaged in genetic counselling.
Michael S Wilkes, Frank C Day, Tonya L Fancher, Haley McDermott, Erik Lehman, Robert A Bell, Michael J Green. BMC Med Educ 2017
20
50

Patient perspectives following pharmacogenomics results disclosure in an integrated health system.
Amy A Lemke, Peter J Hulick, Dyson T Wake, Chi Wang, Annette W Sereika, Kristen Dilzell Yu, Nicole S Glaser, Henry M Dunnenberger. Pharmacogenomics 2018
15
50

Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.
Georgia L Wiesner, Alanna Kulchak Rahm, Paul Appelbaum, Sharon Aufox, Sarah T Bland, Carrie L Blout, Kurt D Christensen, Wendy K Chung, Ellen Wright Clayton, Robert C Green,[...]. J Pers Med 2020
6
50

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, D'Andra M Lindbuchler, Miranda L G Hallquist, Kandamurugu Manickam, Adam H Buchanan, Alanna Kulchak Rahm, Monica A Giovanni, Lauren Frisbie,[...]. Am J Hum Genet 2018
50
50

Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.
Laura M Amendola, Jill O Robinson, Ragan Hart, Sawona Biswas, Kaitlyn Lee, Barbara A Bernhardt, Kelly East, Marian J Gilmore, Tia L Kauffman, Katie L Lewis,[...]. J Genet Couns 2018
16
50

Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment.
Amy A Lemke, Laura M Amendola, Kristine Kuchta, Henry M Dunnenberger, Jennifer Thompson, Christian Johnson, Nadim Ilbawi, Lauren Oshman, Peter J Hulick. J Pers Med 2020
2
50

Assessing the implications of positive genomic screening results.
Margaret Waltz, Karen M Meagher, Gail E Henderson, Katrina Ab Goddard, Kristin Muessig, Jonathan S Berg, Karen E Weck, R Jean Cadigan. Per Med 2020
1
100

Reasons for Declining Preconception Expanded Carrier Screening Using Genome Sequencing.
Marian J Gilmore, Jennifer Schneider, James V Davis, Tia L Kauffman, Michael C Leo, Kellene Bergen, Jacob A Reiss, Patricia Himes, Elissa Morris, Carol Young,[...]. J Genet Couns 2017
23
50

The REDCap consortium: Building an international community of software platform partners.
Paul A Harris, Robert Taylor, Brenda L Minor, Veida Elliott, Michelle Fernandez, Lindsay O'Neal, Laura McLeod, Giovanni Delacqua, Francesco Delacqua, Jacqueline Kirby,[...]. J Biomed Inform 2019
50

Genetic Testing: Consent and Result Disclosure for Primary Care Providers.
W Andrew Faucett, Holly Peay, Curtis R Coughlin. Med Clin North Am 2019
1
100

Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, Randi Zinberg, Melissa Wasserstein, Andrew Kasarskis, George A Diaz, Eric E Schadt. Eur J Hum Genet 2017
30
50


Clinical exome sequencing vs. usual care for hereditary colorectal cancer diagnosis: A pilot comparative effectiveness study.
Xin Niu, Laura M Amendola, Ragan Hart, Caroline S Bennette, Patrick Heagerty, Martha Horike-Pyne, Susan B Trinidad, Elisabeth A Rosenthal, Bryan Comstock, Chris Nefcy,[...]. Contemp Clin Trials 2019
4
50

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
Meng Li, Caroline S Bennette, Laura M Amendola, M Ragan Hart, Patrick Heagerty, Bryan Comstock, Peter Tarczy-Hornoch, Stephanie M Fullerton, Dean A Regier, Wylie Burke,[...]. J Genet Couns 2019
13
50

GINA, genetic discrimination, and genomic medicine.
Robert C Green, Denise Lautenbach, Amy L McGuire. N Engl J Med 2015
84
50


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.