A citation-based method for searching scientific literature

Ingrid A Holm, Sarah K Savage, Robert C Green, Eric Juengst, Amy McGuire, Susan Kornetsky, Stephanie J Brewster, Steven Joffe, Patrick Taylor. Genet Med 2014
Times Cited: 39







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



Times Cited
  Times     Co-cited
Similarity


Research Consent at the Age of Majority: Preferable but not Obligatory.
Kyle B Brothers, Benjamin S Wilfond. Pediatrics 2018
3
33

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
33

When Children Become Adults: Should Biobanks Re-Contact?
Noor A A Giesbertz, Annelien L Bredenoord, Johannes J M van Delden. PLoS Med 2016
7
14

Improving informed consent: Stakeholder views.
Emily E Anderson, Susan B Newman, Alicia K Matthews. AJOB Empir Bioeth 2017
20
5

Online Pediatric Research: Addressing Consent, Assent, and Parental Permission.
Kyle B Brothers, Ellen Wright Clayton, Aaron J Goldenberg. J Law Med Ethics 2020
3
33

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
50

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
20


Interactive multimedia consent for biobanking: a randomized trial.
Christian M Simon, David W Klein, Helen A Schartz. Genet Med 2016
26
3

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
33

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
11

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

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
4


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
10

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
20

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
2

Informed Consent in Decision-Making in Pediatric Practice.
Aviva L Katz, Sally A Webb. Pediatrics 2016
157
2

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
7

Design Issues in E-Consent.
John Wilbanks. J Law Med Ethics 2018
20
5

Age-related differences in moral identity across adulthood.
Tobias Krettenauer, Lourdes Andrea Murua, Fanli Jia. Dev Psychol 2016
6
16

Accuracy of the MacArthur competence assessment tool for clinical research (MacCAT-CR) for measuring children's competence to consent to clinical research.
Irma M Hein, Pieter W Troost, Robert Lindeboom, Marc A Benninga, C Michel Zwaan, Johannes B van Goudoever, Ramón J L Lindauer. JAMA Pediatr 2014
63
2

Beyond Biobanking: Future Use of Specimens and Data from Pediatric Participants.
Megan Kasimatis Singleton, Margaret Moon, E Verena Jorgensen. J Pediatr 2020
1
100


'You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research.
Pauline McCormack, Anna Kole, Sabina Gainotti, Deborah Mascalzoni, Caron Molster, Hanns Lochmüller, Simon Woods. Eur J Hum Genet 2016
35
2

Improving readability of informed consents for research at an academic medical institution.
Kristie B Hadden, Latrina Y Prince, Tina D Moore, Laura P James, Jennifer R Holland, Christopher R Trudeau. J Clin Transl Sci 2017
9
11


Biobanking in the Pediatric Critical Care Setting: Adolescent/Young Adult Perspectives.
Erin D Paquette, Sabrina F Derrington, Avani Shukla, Neha Sinha, Sarah Oswald, Lauren Sorce, Kelly N Michelson. J Empir Res Hum Res Ethics 2018
2
50

Opinions of Young Adults on Re-Consenting for Biobanking.
Amanda Rush, Robert Battisti, Belinda Barton, Daniel Catchpoole. J Pediatr 2015
12
8


Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.
Stephanie A Kraft, Mildred K Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E Ormond, Harold S Luft, Benjamin S Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2018
72
2

"I don't want to be Henrietta Lacks": diverse patient perspectives on donating biospecimens for precision medicine research.
Sandra S-J Lee, Mildred K Cho, Stephanie A Kraft, Nina Varsava, Katie Gillespie, Kelly E Ormond, Benjamin S Wilfond, David Magnus. Genet Med 2019
26
3

A qualitative study of adolescents' understanding of biobanks and their attitudes toward participation, re-contact, and data sharing.
Andrea M Murad, Melanie F Myers, Susan D Thompson, Rachel Fisher, Armand H Matheny Antommaria. Am J Med Genet A 2017
8
12

Genomic Contextualism: Shifting the Rhetoric of Genetic Exceptionalism.
Nanibaa' A Garrison, Kyle B Brothers, Aaron J Goldenberg, John A Lynch. Am J Bioeth 2019
29
3

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.
Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
14
7


Whole genomes, small children, big questions.
Jeantine E Lunshof. Per Med 2012
4
25


Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?
Jan M Friedman, Yvonne Bombard, Martina C Cornel, Conrad V Fernandez, Anne K Junker, Sharon E Plon, Zornitza Stark, Bartha Maria Knoppers. Genet Med 2019
25
4






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. Curr Genomics 2015
26
3

Scanning the body, sequencing the genome: Dealing with unsolicited findings.
Roel H P Wouters, Candice Cornelis, Ainsley J Newson, Eline M Bunnik, Annelien L Bredenoord. Bioethics 2017
11
9

Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatrics.
M J Szego, M S Meyn, C Shuman, R Zlotnik Shaul, J A Anderson, S Bowdin, N Monfared, R Z Hayeems. Eur J Med Genet 2019
6
16

Genomics in newborn screening.
Yuval E Landau, Uta Lichter-Konecki, Harvey L Levy. J Pediatr 2014
39
2


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.