A citation-based method for searching scientific literature

Erin Rothwell, Aaron Goldenberg, Erin Johnson, Naomi Riches, Beth Tarini, Jeffrey R Botkin. J Empir Res Hum Res Ethics 2017
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity



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

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am J Hum Genet 2017
95
50

Broad Consent for Research With Biological Samples: Workshop Conclusions.
Christine Grady, Lisa Eckstein, Ben Berkman, Dan Brock, Robert Cook-Deegan, Stephanie M Fullerton, Hank Greely, Mats G Hansson, Sara Hull, Scott Kim,[...]. Am J Bioeth 2015
141
50


Births: Final Data for 2014.
Brady E Hamilton, Joyce A Martin, Michelle J K Osterman, Sally C Curtin, T J Matthews. Natl Vital Stat Rep 2015
544
25

Relationship of prenatal diagnosis and pregnancy termination to overall infant mortality in Canada.
Shiliang Liu, K S Joseph, Michael S Kramer, Alexander C Allen, Reg Sauve, I D Rusen, Shi Wu Wen. JAMA 2002
87
25


An evaluation of the use of dried blood spots from newborn screening for monitoring the prevalence of cocaine use among childbearing women.
L O Henderson, M K Powell, W H Hannon, J T Bernert, K A Pass, P Fernhoff, C D Ferre, L Martin, E Franko, R W Rochat,[...]. Biochem Mol Med 1997
29
25

Moral concerns and the willingness to donate to a research biobank.
Tom Tomlinson, Raymond De Vries, Kerry Ryan, Hyungjin Myra Kim, Nicole Lehpamer, Scott Y H Kim. JAMA 2015
37
25

Characterizing biobank organizations in the U.S.: results from a national survey.
Gail E Henderson, R Jean Cadigan, Teresa P Edwards, Ian Conlon, Anders G Nelson, James P Evans, Arlene M Davis, Catherine Zimmer, Bryan J Weiner. Genome Med 2013
128
25

Germline Mutations in Predisposition Genes in Pediatric Cancer.
Jinghui Zhang, Michael F Walsh, Gang Wu, Michael N Edmonson, Tanja A Gruber, John Easton, Dale Hedges, Xiaotu Ma, Xin Zhou, Donald A Yergeau,[...]. N Engl J Med 2015
539
25


Informed consent for biobanking: consensus-based guidelines for adequate comprehension.
Laura M Beskow, Carrie B Dombeck, Cole P Thompson, J Kemp Watson-Ormond, Kevin P Weinfurt. Genet Med 2015
38
25



What's in a name? Qualitative description revisited.
Margarete Sandelowski. Res Nurs Health 2010
25

NIPT and Informed Consent: an Assessment of Patient Understanding of a Negative NIPT Result.
Julie L Piechan, Karrie A Hines, Daniel L Koller, Kristyne Stone, Kimberly Quaid, Wilfredo Torres-Martinez, Divya Wilson Mathews, Tatiana Foroud, Lola Cook. J Genet Couns 2016
26
25

Neuropeptides and neurotrophins in neonatal blood of children with autism or mental retardation.
K B Nelson, J K Grether, L A Croen, J M Dambrosia, B F Dickens, L L Jelliffe, R L Hansen, T M Phillips. Ann Neurol 2001
291
25

The qualitative content analysis process.
Satu Elo, Helvi Kyngäs. J Adv Nurs 2008
25

Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials.
Adam Nishimura, Jantey Carey, Patricia J Erwin, Jon C Tilburt, M Hassan Murad, Jennifer B McCormick. BMC Med Ethics 2013
238
25

A measure of informed choice.
T M Marteau, E Dormandy, S Michie. Health Expect 2001
449
25

From newborn screening to population health research: implementation of the Michigan BioTrust for health.
Carrie Langbo, Janice Bach, Mary Kleyn, Frances Pouch Downes. Public Health Rep 2013
11
25

Religious Values and Biobanking Decisions: An Integrative Review.
Elizabeth R Eisenhauer, Cynthia Arslanian-Engoren. Res Theory Nurs Pract 2016
9
25

Informed decision making in the context of prenatal screening.
Matthijs van den Berg, Danielle R M Timmermans, Leo P ten Kate, John M G van Vugt, Gerrit van der Wal. Patient Educ Couns 2006
91
25


Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
96
25

Do people care what's done with their biobanked samples?
Tom Tomlinson, Stan A Kaplowitz, Meghan Faulkner. IRB 2014
7
25


Participants' Understanding of Informed Consent for Biobanking: A Systematic Review.
Elizabeth R Eisenhauer, Alan R Tait, Soo Young Rieh, Cynthia M Arslanian-Engoren. Clin Nurs Res 2019
13
25

Why women say yes to prenatal diagnosis.
N Press, C H Browner. Soc Sci Med 1997
144
25

Prenatal tobacco exposure and cotinine in newborn dried blood spots.
Logan G Spector, Sharon E Murphy, Katherine M Wickham, Bruce Lindgren, Anne M Joseph. Pediatrics 2014
23
25


Informed decision making in the context of childhood immunization.
Birthe A Lehmann, Hester E de Melker, Daniëlle R M Timmermans, Liesbeth Mollema. Patient Educ Couns 2017
9
25

Shared decision making: a model for clinical practice.
Glyn Elwyn, Dominick Frosch, Richard Thomson, Natalie Joseph-Williams, Amy Lloyd, Paul Kinnersley, Emma Cording, Dave Tomson, Carole Dodd, Stephen Rollnick,[...]. J Gen Intern Med 2012
25

Genetic research on stored tissue samples from minors: a systematic review of the ethical literature.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. Am J Med Genet A 2009
34
25

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
25

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
25

A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Nanibaa' A Garrison, Nila A Sathe, Armand H Matheny Antommaria, Ingrid A Holm, Saskia C Sanderson, Maureen E Smith, Melissa L McPheeters, Ellen W Clayton. Genet Med 2016
85
25

Central challenges facing the national clinical research enterprise.
Nancy S Sung, William F Crowley, Myron Genel, Patricia Salber, Lewis Sandy, Louis M Sherwood, Stephen B Johnson, Veronica Catanese, Hugh Tilson, Kenneth Getz,[...]. JAMA 2003
780
25

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
115
25


Evaluating the Efficacy of a Registry linked to a Consent to Re-Contact Program and Communication Strategies for Recruiting and Enrolling Participants into Clinical Trials.
Elizabeth Flood-Grady, Virginia C Clark, Angie Bauer, Lauren Morelli, Patrick Horne, Janice L Krieger, David R Nelson. Contemp Clin Trials Commun 2017
5
25

Experiences among Women with Positive Prenatal Expanded Carrier Screening Results.
Erin Rothwell, Erin Johnson, Amber Mathiesen, Kylie Golden, Audrey Metcalf, Nancy C Rose, Jeffrey R Botkin. J Genet Couns 2017
28
25

A template for broad consent in biobank research. Results and explanation of an evidence and consensus-based development process.
D Strech, S Bein, M Brumhard, W Eisenmenger, C Glinicke, T Herbst, R Jahns, S von Kielmansegg, G Schmidt, J Taupitz,[...]. Eur J Med Genet 2016
29
25


Measuring trust in medical researchers.
Mark A Hall, Fabian Camacho, Janice S Lawlor, Venita Depuy, Jeremy Sugarman, Kevin Weinfurt. Med Care 2006
81
25

Assessing the understanding of biobank participants.
K E Ormond, A L Cirino, I B Helenowski, R L Chisholm, W A Wolf. Am J Med Genet A 2009
105
25


A randomized controlled trial of an electronic informed consent process.
Erin Rothwell, Bob Wong, Nancy C Rose, Rebecca Anderson, Beth Fedor, Louisa A Stark, Jeffrey R Botkin. J Empir Res Hum Res Ethics 2014
23
25


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.