A citation-based method for searching scientific literature

Elizabeth Bromley, Alexandra Mendoza-Graf, Sandra Berry, Camille Nebeker, Dmitry Khodyakov. J Law Med Ethics 2020
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity



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
156
42

Broad consent for biobanks is best - provided it is also deep.
Rasmus Bjerregaard Mikkelsen, Mickey Gjerris, Gunhild Waldemar, Peter Sandøe. BMC Med Ethics 2019
25
42


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
109
28


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
115
28


Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
98
28

Respecting donors to biobank research.
Tom Tomlinson. Hastings Cent Rep 2013
25
28


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
9
28

A review of the key issues associated with the commercialization of biobanks.
Timothy Caulfield, Sarah Burningham, Yann Joly, Zubin Master, Mahsa Shabani, Pascal Borry, Allan Becker, Michael Burgess, Kathryn Calder, Christine Critchley,[...]. J Law Biosci 2014
52
28

Ethics and clinical research.
H K Beecher. N Engl J Med 1966
928
14

A systematic literature review of individuals' perspectives on privacy and genetic information in the United States.
Ellen W Clayton, Colin M Halverson, Nila A Sathe, Bradley A Malin. PLoS One 2018
54
14

Active choice but not too active: public perspectives on biobank consent models.
Christian M Simon, Jamie L'heureux, Jeffrey C Murray, Patricia Winokur, George Weiner, Elizabeth Newbury, Laura Shinkunas, Bridget Zimmerman. Genet Med 2011
112
14



Returning aggregate results of clinical trials: Empirical data of patient preferences.
Carmen E Aldinger, Jennifer Ligibel, Im Hee Shin, John W Denninger, Barbara E Bierer. J Clin Transl Sci 2018
5
20

Just compensation: a no-fault proposal for research-related injuries.
Leslie Meltzer Henry, Megan E Larkin, Elizabeth R Pike. J Law Biosci 2015
8
14

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
308
14



Understanding Broad Consent.
John W Maloy, Pat F Bass. Ochsner J 2020
12
14

Ethics of genetic research on same-sex sexual behaviour.
Julian Savulescu, Brian D Earp, Udo Schuklenk. Nat Hum Behav 2021
3
33



Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
255
14


Paving the way to a more effective informed consent process: Recommendations from the Clinical Trials Transformation Initiative.
Jennifer Lentz, Michele Kennett, Jane Perlmutter, Annemarie Forrest. Contemp Clin Trials 2016
41
14

Inequalities in health: definitions, concepts, and theories.
Mariana C Arcaya, Alyssa L Arcaya, S V Subramanian. Glob Health Action 2015
171
14

Communicating Identifiability Risks to Biobank Donors.
T J Kasperbauer, Mickey Gjerris, Gunhild Waldemar, Peter Sandøe. Camb Q Healthc Ethics 2018
6
16

A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
62
14

Scientific research is a moral duty.
John Harris. J Med Ethics 2005
141
14


A framework for tiered informed consent for health genomic research in Africa.
Victoria Nembaware, Katherine Johnston, Alpha A Diallo, Maritha J Kotze, Alice Matimba, Keymanthri Moodley, Godfrey B Tangwa, Rispah Torrorey-Sawe, Nicki Tiffin. Nat Genet 2019
18
14

Where Did Informed Consent for Research Come From?
Alexander Morgan Capron. J Law Med Ethics 2018
8
14


Equitable Participation in Biobanks: The Risks and Benefits of a "Dynamic Consent" Approach.
Megan Prictor, Harriet J A Teare, Jane Kaye. Front Public Health 2018
24
14




Dynamic-informed consent: A potential solution for ethical dilemmas in population sequencing initiatives.
Fida K Dankar, Marton Gergely, Bradley Malin, Radja Badji, Samar K Dankar, Khaled Shuaib. Comput Struct Biotechnol J 2020
11
14


Informed consent and routinisation.
Thomas Ploug, Soren Holm. J Med Ethics 2013
23
14


Gender equality in science, medicine, and global health: where are we at and why does it matter?
Geordan Shannon, Melanie Jansen, Kate Williams, Carlos Cáceres, Angelica Motta, Aloyce Odhiambo, Alie Eleveld, Jenevieve Mannell. Lancet 2019
149
14

Banking together. A unified model of informed consent for biobanking.
Elena Salvaterra, Lucilla Lecchi, Silvia Giovanelli, Barbara Butti, Maria Teresa Bardella, Pier Alberto Bertazzi, Silvano Bosari, Guido Coggi, Domenico A Coviello, Faustina Lalatta,[...]. EMBO Rep 2008
64
14

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
108
14



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.