A citation-based method for searching scientific literature

Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
617
30

Are you SURE?: Assessing patient decisional conflict with a 4-item screening test.
France Légaré, Stephen Kearing, Kate Clay, Susie Gagnon, Denis D'Amours, Michel Rousseau, Annette O'Connor. Can Fam Physician 2010
123
20


Brazil's Craniofacial Project: genetic evaluation and counseling in the Reference Network for Craniofacial Treatment.
Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes. Cleft Palate Craniofac. J. 2006
13
20


Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children.
J C Sapp, D Dong, C Stark, L E Ivey, G Hooker, L G Biesecker, B B Biesecker. Clin. Genet. 2014
74
20

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

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Carol Jean Saunders, Neil Andrew Miller, Sarah Elizabeth Soden, Darrell Lee Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie LeAnn Patterson, Lisa Ann Krivohlavek, Joel Fellis,[...]. Sci Transl Med 2012
320
20

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
20

Decision coaching using the Ottawa family decision guide with parents and their children: a field testing study.
Bryan Feenstra, Margaret L Lawson, Denise Harrison, Laura Boland, Dawn Stacey. BMC Med Inform Decis Mak 2015
12
20

Life support decisions for extremely premature infants: report of a pilot study.
Karen Kavanaugh, Teresa Savage, Sarah Kilpatrick, Rob Kimura, Patricia Hershberger. J Pediatr Nurs 2005
47
20

The challenge of consent in clinical genome-wide testing.
Katherine Burke, Angus Clarke. Arch. Dis. Child. 2016
10
20

Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit.
Emma E Smith, Christèle du Souich, Nick Dragojlovic, Alison M Elliott. J Genet Couns 2019
8
25

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet. Med. 2017
550
20

Numeracy skill and the communication, comprehension, and use of risk-benefit information.
Ellen Peters, Judith Hibbard, Paul Slovic, Nathan Dieckmann. Health Aff (Millwood) 2007
203
10

Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Nananda F Col, Carol L Bennett, Michael J Barry, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2014
940
10

An interactive computer program can effectively educate potential users of cystic fibrosis carrier tests.
Carlo Castellani, Sandra Perobelli, Vera Bianchi, Manuela Seia, Paola Melotti, Luisa Zanolla, Baroukh Maurice Assael, Faustina Lalatta. Am. J. Med. Genet. A 2011
12
10


"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am. J. Med. Genet. A 2012
109
10

Prenatal whole-genome sequencing--is the quest to know a fetus's future ethical?
Ilana R Yurkiewicz, Bruce R Korf, Lisa Soleymani Lehmann. N. Engl. J. Med. 2014
18
10


Genetic counseling gone awry: miscommunication between prenatal genetic service providers and Mexican-origin clients.
C H Browner, H Mabel Preloran, Maria Christina Casado, Harold N Bass, Ann P Walker. Soc Sci Med 2003
58
10

Whole exome and whole genome sequencing.
David Bick, David Dimmock. Curr. Opin. Pediatr. 2011
81
10


Effect of a computer-based decision aid on knowledge, perceptions, and intentions about genetic testing for breast cancer susceptibility: a randomized controlled trial.
Michael J Green, Susan K Peterson, Maria Wagner Baker, Gregory R Harper, Lois C Friedman, Wendy S Rubinstein, David T Mauger. JAMA 2004
195
10

Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid.
Megan A Lewis, Ryan S Paquin, Myra I Roche, Robert D Furberg, Christine Rini, Jonathan S Berg, Cynthia M Powell, Donald B Bailey. Pediatrics 2016
22
10


A systematic development process for patient decision aids.
Angela Coulter, Diana Stilwell, Jennifer Kryworuchko, Patricia Dolan Mullen, Chirk Jenn Ng, Trudy van der Weijden. BMC Med Inform Decis Mak 2013
158
10


Management of Incidental Findings in the Era of Next-generation Sequencing.
Heather L Blackburn, Bradley Schroeder, Clesson Turner, Craig D Shriver, Darrell L Ellsworth, Rachel E Ellsworth.  2015
20
10



Patients' perceptions of gene expression profiling in breast cancer treatment decisions.
Y Bombard, L Rozmovits, M E Trudeau, N B Leighl, K Deal, D A Marshall. Curr Oncol 2014
16
10

Communicating risk of hereditary breast and ovarian cancer with an interactive decision support tool.
Douglas J Rupert, Linda B Squiers, Jeanette M Renaud, Nedra S Whitehead, Roger J Osborn, Robert D Furberg, Claudia M Squire, Janice P Tzeng. Patient Educ Couns 2013
13
10

Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.
Holly K Tabor, Jacquie Stock, Tracy Brazg, Margaret J McMillin, Karin M Dent, Joon-Ho Yu, Jay Shendure, Michael J Bamshad. Am. J. Med. Genet. A 2012
78
10

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
112
10

Assessment of the content and process of genetic counseling: a critical review of empirical studies.
Bettina Meiser, Jennifer Irle, Elizabeth Lobb, Kristine Barlow-Stewart. J Genet Couns 2008
79
10

Assessing the Costs and Cost-Effectiveness of Genomic Sequencing.
Kurt D Christensen, Dmitry Dukhovny, Uwe Siebert, Robert C Green.  2015
49
10

Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.
Dimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, Sarah Bowdin, Nasim Monfared, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Giovanna Pellecchia, Ryan K C Yuen, Michael J Szego,[...].  2016
125
10

Costs of caring for children with an intellectual developmental disorder.
Dallas Genereaux, Clara D M van Karnebeek, Patricia H Birch. Disabil Health J 2015
10
10


Genetic counselor perceptions of genetic counseling session goals: a validation study of the reciprocal-engagement model.
Julianne E Hartmann, Patricia McCarthy Veach, Ian M MacFarlane, Bonnie S LeRoy. J Genet Couns 2015
23
10

A randomized trial of a prenatal genetic testing interactive computerized information aid.
Lynn M Yee, Michael Wolf, Rebecca Mullen, Ashley R Bergeron, Stacy Cooper Bailey, Robert Levine, William A Grobman. Prenat. Diagn. 2014
22
10

Self-guided management of exome and whole-genome sequencing results: changing the results return model.
Joon-Ho Yu, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Genet. Med. 2013
54
10



Use of an educational computer program before genetic counseling for breast cancer susceptibility: effects on duration and content of counseling sessions.
Michael J Green, Susan K Peterson, Maria Wagner Baker, Lois C Friedman, Gregory R Harper, Wendy S Rubinstein, June A Peters, David T Mauger. Genet. Med. 2005
69
10


An assessment of time involved in pre-test case review and counseling for a whole genome sequencing clinical research program.
Janet L Williams, W Andrew Faucett, Bethanny Smith-Packard, Monisa Wagner, Marc S Williams. J Genet Couns 2014
13
10

Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life.
M Lingen, L Albers, M Borchers, S Haass, J Gärtner, S Schröder, L Goldbeck, R von Kries, K Brockmann, B Zirn. Clin. Genet. 2016
22
10


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.