A citation-based method for searching scientific literature

Rachel Grob, Scott Roberts, Stefan Timmermans. Hastings Cent Rep 2018
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
134
100

Patients-in-waiting: Living between sickness and health in the genomics era.
Stefan Timmermans, Mara Buchbinder. J Health Soc Behav 2010
143
100


Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years.
Anne Andermann, Ingeborg Blancquaert, Sylvie Beauchamp, Véronique Déry. Bull World Health Organ 2008
431
50


Direct-to-Consumer Testing 2.0: Emerging Models of Direct-to-Consumer Genetic Testing.
Megan A Allyse, David H Robinson, Matthew J Ferber, Richard R Sharp. Mayo Clin Proc 2018
54
50

Predictors of genetic testing decisions: a systematic review and critique of the literature.
Kate Sweeny, Arezou Ghane, Angela M Legg, Ho Phi Huynh, Sara E Andrews. J Genet Couns 2014
35
50

Ethics, evidence, and cost in newborn screening.
Mary Ann Baily, Thomas H Murray. Hastings Cent Rep 2008
43
50

From "Personalized" to "Precision" Medicine: The Ethical and Social Implications of Rhetorical Reform in Genomic Medicine.
Eric Juengst, Michelle L McGowan, Jennifer R Fishman, Richard A Settersten. Hastings Cent Rep 2016
42
50

The 'thousand-dollar genome': an ethical exploration.
Wybo J Dondorp, Guido M W R de Wert. Eur J Hum Genet 2013
36
50

Consumers report lower confidence in their genetics knowledge following direct-to-consumer personal genomic testing.
Deanna Alexis Carere, Peter Kraft, Kimberly A Kaphingst, J Scott Roberts, Robert C Green. Genet Med 2016
40
50

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
50

Parents' interest in whole-genome sequencing of newborns.
Aaron J Goldenberg, Daniel S Dodson, Matthew M Davis, Beth A Tarini. Genet Med 2014
54
50


The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
99
50





Whose Odyssey Is It? Family-Centered Care in the Genomic Era.
Jeffrey P Brosco. Hastings Cent Rep 2018
4
50


The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.
Josh E Petrikin, Julie A Cakici, Michelle M Clark, Laurel K Willig, Nathaly M Sweeney, Emily G Farrow, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Lee Zellmer,[...]. NPJ Genom Med 2018
84
50

Current status of newborn screening worldwide: 2015.
Bradford L Therrell, Carmencita David Padilla, J Gerard Loeber, Issam Kneisser, Amal Saadallah, Gustavo J C Borrajo, John Adams. Semin Perinatol 2015
213
50

Genomic sequencing in newborn screening programs.
Wybo J Dondorp, Guido M W R de Wert, Martinus F Niermeijer. JAMA 2012
4
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

Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results.
J Scott Roberts, Michele C Gornick, Deanna Alexis Carere, Wendy R Uhlmann, Mack T Ruffin, Robert C Green. Public Health Genomics 2017
61
50





Whole Genome Sequencing and Newborn Screening.
Jeffrey R Botkin, Erin Rothwell. Curr Genet Med Rep 2016
24
50

Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
259
50

Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome and Cystic Fibrosis Screen Positive, Inconclusive Diagnosis.
Clement L Ren, Drucy S Borowitz, Tanja Gonska, Michelle S Howenstine, Hara Levy, John Massie, Carlos Milla, Anne Munck, Kevin W Southern. J Pediatr 2017
55
50



Cancer, Our Genes, And The Anxiety Of Risk-Based Medicine.
Siddhartha Mukherjee. Health Aff (Millwood) 2018
2
50

Precision Medicine: From Science To Value.
Geoffrey S Ginsburg, Kathryn A Phillips. Health Aff (Millwood) 2018
140
50



The usefulness of whole-exome sequencing in routine clinical practice.
Alejandro Iglesias, Kwame Anyane-Yeboa, Julia Wynn, Ashley Wilson, Megan Truitt Cho, Edwin Guzman, Rebecca Sisson, Claire Egan, Wendy K Chung. Genet Med 2014
129
50

State laws regarding the retention and use of residual newborn screening blood samples.
Michelle H Lewis, Aaron Goldenberg, Rebecca Anderson, Erin Rothwell, Jeffrey Botkin. Pediatrics 2011
59
50

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
Laurel K Willig, Josh E Petrikin, Laurie D Smith, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Sarah E Soden, Julie A Cakici, Suzanne M Herd, Greyson Twist,[...]. Lancet Respir Med 2015
187
50

Genetic research and health disparities.
Pamela Sankar, Mildred K Cho, Celeste M Condit, Linda M Hunt, Barbara Koenig, Patricia Marshall, Sandra Soo-Jin Lee, Paul Spicer. JAMA 2004
158
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
819
50


Uptake rates for breast cancer genetic testing: a systematic review.
Mary E Ropka, Jennifer Wenzel, Elayne K Phillips, Mir Siadaty, John T Philbrick. Cancer Epidemiol Biomarkers Prev 2006
114
50

Genetic tests: clinical validity and clinical utility.
Wylie Burke. Curr Protoc Hum Genet 2014
50
50

Direct-to-consumer personalized genomic testing.
Cinnamon S Bloss, Burcu F Darst, Eric J Topol, Nicholas J Schork. Hum Mol Genet 2011
60
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.