A citation-based method for searching scientific literature

Harriet Ja Teare, Michael Morrison, Edgar A Whitley, Jane Kaye. Digit Health 2015
Times Cited: 25







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



Times Cited
  Times     Co-cited
Similarity



Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.
Don Chalmers, Dianne Nicol, Jane Kaye, Jessica Bell, Alastair V Campbell, Calvin W L Ho, Kazuto Kato, Jusaku Minari, Chih-Hsing Ho, Colin Mitchell,[...]. BMC Med Ethics 2016
60
8

Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population.
Anna Fry, Thomas J Littlejohns, Cathie Sudlow, Nicola Doherty, Ligia Adamska, Tim Sprosen, Rory Collins, Naomi E Allen. Am J Epidemiol 2017
915
8

The "vampire project".
B J Crigger. Hastings Cent Rep 1995
3
66


Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
671
8

Quality of informed consent: a new measure of understanding among research subjects.
S Joffe, E F Cook, P D Cleary, J W Clark, J C Weeks. J Natl Cancer Inst 2001
256
8

Audio-visual presentation of information for informed consent for participation in clinical trials.
Anneliese Synnot, Rebecca Ryan, Megan Prictor, Deirdre Fetherstonhaugh, Barbara Parker. Cochrane Database Syst Rev 2014
72
8

Recall of informed consent information by healthy volunteers in clinical trials.
P Fortun, J West, L Chalkley, A Shonde, C Hawkey. QJM 2008
43
8

FHIRChain: Applying Blockchain to Securely and Scalably Share Clinical Data.
Peng Zhang, Jules White, Douglas C Schmidt, Gunther Lenz, S Trent Rosenbloom. Comput Struct Biotechnol J 2018
67
8


Ethics and biobanks.
M G Hansson. Br J Cancer 2009
107
8

Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach.
Menno Mostert, Annelien L Bredenoord, Monique C I H Biesaart, Johannes J M van Delden. Eur J Hum Genet 2016
43
8

Traditional and electronic informed consent for biobanking: a survey of U.S. biobanks.
Christian M Simon, David W Klein, Helen A Schartz. Biopreserv Biobank 2014
20
10


Patient preferences toward an interactive e-consent application for research using electronic health records.
Christopher A Harle, Elizabeth H Golembiewski, Kiarash P Rahmanian, Janice L Krieger, Dorothy Hagmajer, Arch G Mainous, Ray E Moseley. J Am Med Inform Assoc 2018
19
10

An investigation of the efficacy of electronic consenting interfaces of research permissions management system in a hospital setting.
Kapil Chalil Madathil, Reshmi Koikkara, Jihad Obeid, Joel S Greenstein, Iain C Sanderson, Katrina Fryar, Jay Moskowitz, Anand K Gramopadhye. Int J Med Inform 2013
42
8

iCONCUR: informed consent for clinical data and bio-sample use for research.
Hyeoneui Kim, Elizabeth Bell, Jihoon Kim, Amy Sitapati, Joe Ramsdell, Claudiu Farcas, Dexter Friedman, Stephanie Feudjio Feupe, Lucila Ohno-Machado. J Am Med Inform Assoc 2017
24
8


Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
97
8


From consent to institutions: designing adaptive governance for genomic biobanks.
Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
92
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
91
8

Dwarna: a blockchain solution for dynamic consent in biobanking.
Nicholas Mamo, Gillian M Martin, Maria Desira, Bridget Ellul, Jean-Paul Ebejer. Eur J Hum Genet 2020
14
14

Models of consent to return of incidental findings in genomic research.
Paul S Appelbaum, Erik Parens, Cameron R Waldman, Robert Klitzman, Abby Fyer, Josue Martinez, W Nicholson Price, Wendy K Chung. Hastings Cent Rep 2014
51
4

[Genome sequencing for personalized cancer treatment].
Rolf I Skotheim, Leonardo A Meza-Zepeda, Eivind Hovig, Per E Lønning, Ragnhild A Lothe, Ola Myklebost. Tidsskr Nor Laegeforen 2012
2
50

Should genetic findings from genome research be reported back to the participants?
Kristin Solum Steinsbekk, Berge Solberg. Tidsskr Nor Laegeforen 2012
7
14

The ethics of research using biobanks: reason to question the importance attributed to informed consent.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Arch Intern Med 2005
71
4



Prevalence of comorbidities in rheumatoid arthritis and evaluation of their monitoring: results of an international, cross-sectional study (COMORA).
Maxime Dougados, Martin Soubrier, Anna Antunez, Peter Balint, Alejandro Balsa, Maya H Buch, Gustavo Casado, Jacqueline Detert, Bassel El-Zorkany, Paul Emery,[...]. Ann Rheum Dis 2014
418
4

Adoption, non-adoption, and abandonment of a personal electronic health record: case study of HealthSpace.
Trisha Greenhalgh, Susan Hinder, Katja Stramer, Tanja Bratan, Jill Russell. BMJ 2010
168
4


The use of medical records in research: what do patients want?
Nancy E Kass, Marvin R Natowicz, Sara Chandros Hull, Ruth R Faden, Laura Plantinga, Lawrence O Gostin, Julia Slutsman. J Law Med Ethics 2003
52
4


Exploring barriers to participation and adoption of telehealth and telecare within the Whole System Demonstrator trial: a qualitative study.
Caroline Sanders, Anne Rogers, Robert Bowen, Peter Bower, Shashivadan Hirani, Martin Cartwright, Ray Fitzpatrick, Martin Knapp, James Barlow, Jane Hendy,[...]. BMC Health Serv Res 2012
221
4


How to develop patient-centered research: some perspectives based on surveys among people with rheumatic diseases in Scandinavia.
Ingvild Kjeken, Connie Ziegler, Jack Skrolsvik, Jan Bagge, Geir Smedslund, Anne Tøvik, Hanne S Dagfinrud, Ingemar F Petersson, Kåre Birger Hagen. Phys Ther 2010
16
6

Why do people cooperate with medical research? Findings from three studies.
Mary Dixon-Woods, Carolyn Tarrant. Soc Sci Med 2009
47
4

Consent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?
Donald J Willison, Valerie Steeves, Cathy Charles, Lisa Schwartz, Jennifer Ranford, Gina Agarwal, Ji Cheng, Lehana Thabane. BMC Med Ethics 2009
50
4

Patient and public views on electronic health records and their uses in the United kingdom: cross-sectional survey.
Serena A Luchenski, Julie E Reed, Cicely Marston, Chrysanthi Papoutsi, Azeem Majeed, Derek Bell. J Med Internet Res 2013
36
4

Patient confidentiality in a time of care.data.
Julian Sheather, Sophie Brannan. BMJ 2013
12
8


Easier citizen science is better.
Jeffrey Parsons, Roman Lukyanenko, Yolanda Wiersma. Nature 2011
8
12

Scientific research is a moral duty.
John Harris. J Med Ethics 2005
140
4


Governing the postmortem procurement of human body material for research.
Kristof Van Assche, Laura Capitaine, Guido Pennings, Sigrid Sterckx. Kennedy Inst Ethics J 2015
3
33

Open Air Laboratories (OPAL): a community-driven research programme.
L Davies, J N B Bell, J Bone, M Head, L Hill, C Howard, S J Hobbs, D T Jones, S A Power, N Rose,[...]. Environ Pollut 2011
18
5




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.