A citation-based method for searching scientific literature

Megan Kasimatis Singleton, Margaret Moon, E Verena Jorgensen. J Pediatr 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Disclosing Study Information to Children and Adolescents: Is What They Want, What Their Parents Think They Want?
Alan R Tait, Michael E Geisser, Lamira Ray, Raymond J Hutchinson, Terri Voepel-Lewis. Acad Pediatr 2018
5
100

Reconsidering the Need for Reconsent at 18.
Benjamin E Berkman, Dana Howard, David Wendler. Pediatrics 2018
4
100

Informed consent instead of assent is appropriate in children from the age of twelve: Policy implications of new findings on children's competence to consent to clinical research.
Irma M Hein, Martine C De Vries, Pieter W Troost, Gerben Meynen, Johannes B Van Goudoever, Ramón J L Lindauer. BMC Med Ethics 2015
47
100

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
123
100

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
13
100

Development of the Precision Link Biobank at Boston Children's Hospital: Challenges and Opportunities.
Florence T Bourgeois, Paul Avillach, Sek Won Kong, Michelle M Heinz, Tram A Tran, Ramkrishna Chakrabarty, Jonathan Bickel, Piotr Sliz, Erin M Borglund, Susan Kornetsky,[...]. J Pers Med 2017
12
100

The limits of autonomy: the Belmont Report and the history of childhood.
Tamar W Carroll, Myron P Gutmann. J Hist Med Allied Sci 2011
6
100


An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics.
Ruth R Faden, Nancy E Kass, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
278
100


Revised 'Common Rule' Shapes Protections For Research Participants.
Barbara E Bierer, Mark Barnes, Holly Fernandez Lynch. Health Aff (Millwood) 2017
11
100

Understanding of informed consent by parents of children enrolled in a genetic biobank.
Jennifer Klima, Sara M Fitzgerald-Butt, Kelly J Kelleher, Deena J Chisolm, R Dawn Comstock, Amy K Ferketich, Kim L McBride. Genet Med 2014
33
100

Parental attitudes and expectations towards receiving genomic test results in healthy children.
Alanna Kulchak Rahm, Lindsay Bailey, Kara Fultz, Audrey Fan, Janet L Williams, Adam Buchanan, F Daniel Davis, Michael F Murray, Marc S Williams. Transl Behav Med 2018
8
100

Implementation of Electronic Consent at a Biobank: An Opportunity for Precision Medicine Research.
Natalie T Boutin, Kathleen Mathieu, Alison G Hoffnagle, Nicole L Allen, Victor M Castro, Megan Morash, P Pearl O'Rourke, Elizabeth L Hohmann, Neil Herring, Lynn Bry,[...]. J Pers Med 2016
27
100

Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents.
Juliann M Savatt, Jennifer K Wagner, Steven Joffe, Alanna Kulchak Rahm, Marc S Williams, Angela R Bradbury, F Daniel Davis, Julie Hergenrather, Yirui Hu, Melissa A Kelly,[...]. BMC Pediatr 2020
3
100

Challenges in creating an opt-in biobank with a registrar-based consent process and a commercial EHR.
Keith Marsolo, Jeremy Corsmo, Michael G Barnes, Carrie Pollick, Jamie Chalfin, Jeremy Nix, Christopher Smith, Rajesh Ganta. J Am Med Inform Assoc 2012
18
100

Anticipatory Waivers of Consent for Pediatric Biobanking.
Jane A Hartsock, Peter H Schwartz, Amy C Waltz, Mary A Ott. Ethics Hum Res 2019
2
100

Giving adolescents a voice: the types of genetic information adolescents choose to learn and why.
Josie Pervola, Melanie F Myers, Michelle L McGowan, Cynthia A Prows. Genet Med 2019
10
100

The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.
David J Carey, Samantha N Fetterolf, F Daniel Davis, William A Faucett, H Lester Kirchner, Uyenlinh Mirshahi, Michael F Murray, Diane T Smelser, Glenn S Gerhard, David H Ledbetter. Genet Med 2016
161
100

Key Implications of Data Sharing in Pediatric Genomics.
Vasiliki Rahimzadeh, Christoph Schickhardt, Bartha M Knoppers, Karine Sénécal, Danya F Vears, Conrad V Fernandez, Stefan Pfister, Sharon Plon, Sharon Terry, Janet Williams,[...]. JAMA Pediatr 2018
15
100

Research Consent at the Age of Majority: Preferable but not Obligatory.
Kyle B Brothers, Benjamin S Wilfond. Pediatrics 2018
3
100

The MICHR Genomic DNA BioLibrary: An Empirical Study of the Ethics of Biorepository Development.
Blake J Roessler, Nicholas H Steneck, Lisa Connally. J Empir Res Hum Res Ethics 2015
3
100

When Children Become Adults: Should Biobanks Re-Contact?
Noor A A Giesbertz, Annelien L Bredenoord, Johannes J M van Delden. PLoS Med 2016
7
100

Improving informed consent: Stakeholder views.
Emily E Anderson, Susan B Newman, Alicia K Matthews. AJOB Empir Bioeth 2017
20
100

Online Pediatric Research: Addressing Consent, Assent, and Parental Permission.
Kyle B Brothers, Ellen Wright Clayton, Aaron J Goldenberg. J Law Med Ethics 2020
3
100

Assessing the stability of biobank donor preferences regarding sample use: evidence supporting the value of dynamic consent.
Joel E Pacyna, Jennifer B McCormick, Janet E Olson, Erin M Winkler, Josh T Bublitz, Matthew A Hathcock, Richard R Sharp. Eur J Hum Genet 2020
2
100

Practical guidance on informed consent for pediatric participants in a biorepository.
Kyle B Brothers, John A Lynch, Sharon A Aufox, John J Connolly, Bruce D Gelb, Ingrid A Holm, Saskia C Sanderson, Jennifer B McCormick, Janet L Williams, Wendy A Wolf,[...]. Mayo Clin Proc 2014
17
100

Raising Genomic Citizens: Adolescents and the Return of Secondary Genomic Findings.
Maya Sabatello, Paul S Appelbaum. J Law Med Ethics 2016
16
100

Testing an online, dynamic consent portal for large population biobank research.
Daniel B Thiel, Jodyn Platt, Tevah Platt, Susan B King, Nicole Fisher, Robert Shelton, Sharon L R Kardia. Public Health Genomics 2015
25
100

At a Moment's Notice: Community Advisory Board Perspectives on Biobank Communication to Supplement Broad Consent.
Karen M Meagher, Susan H Curtis, Kylie O Gamm, Erica J Sutton, Jennifer B McCormick, Richard R Sharp. Public Health Genomics 2020
1
100

Metaphors matter: from biobank to a library of medical information.
Mildred K Cho, Nina Varsava, Stephanie A Kraft, Gary Ashwal, Katie Gillespie, David Magnus, Kelly E Ormond, Alex Thomas, Benjamin S Wilfond, Sandra S-J Lee. Genet Med 2018
5
100

An Observational Study of Children's Involvement in Informed Consent for Exome Sequencing Research.
Victoria A Miller, Allison Werner-Lin, Sarah A Walser, Sawona Biswas, Barbara A Bernhardt. J Empir Res Hum Res Ethics 2017
7
100


Child's assent in research: age threshold or personalisation?
Marcin Waligora, Vilius Dranseika, Jan Piasecki. BMC Med Ethics 2014
25
100

Interactive multimedia consent for biobanking: a randomized trial.
Christian M Simon, David W Klein, Helen A Schartz. Genet Med 2016
26
100

Comparison of Video, App, and Standard Consent Processes on Decision-Making for Biospecimen Research: A Randomized Controlled Trial.
Erin Rothwell, Erin Johnson, Bob Wong, Aaron Goldenberg, Beth A Tarini, Naomi Riches, Louisa A Stark, Christina Pries, Carrie Langbo, Elizabeth Langen,[...]. J Empir Res Hum Res Ethics 2020
3
100

The Catch to Confidentiality: The Use of Electronic Health Records in Adolescent Health Care.
Timothy Stablein, Keith J Loud, Christopher DiCapua, Denise L Anthony. J Adolesc Health 2018
9
100

Incorporating Biobank Consent into a Healthcare Setting: Challenges for Patient Understanding.
T J Kasperbauer, Karen K Schmidt, Ariane Thomas, Susan M Perkins, Peter H Schwartz. AJOB Empir Bioeth 2021
1
100

When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority.
Kyle B Brothers, Ingrid A Holm, Janet E Childerhose, Armand H M Antommaria, Barbara A Bernhardt, Ellen Wright Clayton, Bruce D Gelb, Steven Joffe, John A Lynch, Jennifer B McCormick,[...]. J Pediatr 2016
8
100

Inclusion of pediatric samples in an opt-out biorepository linking DNA to de-identified medical records: pediatric BioVU.
T L McGregor, S L Van Driest, K B Brothers, E A Bowton, L J Muglia, D M Roden. Clin Pharmacol Ther 2013
25
100



Banking the Future: Adolescent Capacity to Consent to Biobank Research.
Kyle A McGregor, Mary A Ott. Ethics Hum Res 2019
1
100

Perspectives of adolescents on decision making about participation in a biobank study: a pilot study.
Petronella Grootens-Wiegers, Eline G Visser, Annemarie M C van Rossum, Claudia N van Waardhuizen, Saskia N de Wildt, Boudewijn Sweep, Jos M van den Broek, Martine C de Vries. BMJ Paediatr Open 2017
10
100

Recontacting Pediatric Research Participants for Consent When They Reach the Age of Majority.
Bartha Maria Knoppers, Karine Sénécal, Joanne Boisjoli, Pascal Borry, Martina C Cornel, Conrad V Fernandez, Jasjote Grewal, Ingrid A Holm, Erin Nelson, Wim Pinxten,[...]. IRB 2016
5
100

Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.
Isabelle Budin-Ljøsne, Harriet J A Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D'Abramo, Heike Felzmann, Teresa Finlay,[...]. BMC Med Ethics 2017
81
100

Informed Consent in Decision-Making in Pediatric Practice.
Aviva L Katz, Sally A Webb. Pediatrics 2016
163
100

Opinions of Adolescents and Parents About Pediatric Biobanking.
Cynthia C Kong, Tamsin E Tarling, Caron Strahlendorf, Michelle Dittrick, Suzanne M Vercauteren. J Adolesc Health 2016
14
100

Design Issues in E-Consent.
John Wilbanks. J Law Med Ethics 2018
20
100

Age-related differences in moral identity across adulthood.
Tobias Krettenauer, Lourdes Andrea Murua, Fanli Jia. Dev Psychol 2016
7
100


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.