A citation-based method for searching scientific literature

Erica J Sutton, Joel E Pacyna, Matthew Hathcock, Jennifer B McCormick, Katherine Nowakowski, Janet E Olson, Richard R Sharp. Biopreserv Biobank 2019
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Developing Ethical Practices for Public Health Research Data Sharing in South Africa: The Views and Experiences From a Diverse Sample of Research Stakeholders.
Spencer G Denny, Blessing Silaigwana, Douglas Wassenaar, Susan Bull, Michael Parker. J Empir Res Hum Res Ethics 2015
24
50


Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
122
50

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
50
50

A research agenda for helminth diseases of humans: towards control and elimination.
Boakye A Boatin, María-Gloria Basáñez, Roger K Prichard, Kwablah Awadzi, Rashida M Barakat, Héctor H García, Andrea Gazzinelli, Warwick N Grant, James S McCarthy, Eliézer K N'Goran,[...]. PLoS Negl Trop Dis 2012
62
50

Emerging issues in paediatric health research consent forms in Canada: working towards best practices.
Edward S Dove, Denise Avard, Lee Black, Bartha M Knoppers. BMC Med Ethics 2013
13
50


Regulating biobanking with children's tissue: a legal analysis and the experts' view.
Elcke J Kranendonk, M Corrette Ploem, Raoul C M Hennekam. Eur J Hum Genet 2016
8
50


IRB practices and policies regarding the secondary research use of biospecimens.
Aaron J Goldenberg, Karen J Maschke, Steven Joffe, Jeffrey R Botkin, Erin Rothwell, Thomas H Murray, Rebecca Anderson, Nicole Deming, Beth F Rosenthal, Suzanne M Rivera. BMC Med Ethics 2015
15
50

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
50


What makes clinical research in developing countries ethical? The benchmarks of ethical research.
Ezekiel J Emanuel, David Wendler, Jack Killen, Christine Grady. J Infect Dis 2004
436
50

Experiences and attitudes of genome investigators regarding return of individual genetic test results.
Rachel B Ramoni, Amy L McGuire, Jill Oliver Robinson, Debra S Morley, Sharon E Plon, Steven Joffe. Genet Med 2013
39
50

Biobanking Research and Human Subjects Protections: Perspectives of IRB Leaders.
Erin Rothwell, Karen J Maschke, Jeffrey R Botkin, Aaron Goldenberg, Thomas H Murray, Suzanne M Rivera. IRB 2015
5
50


Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience.
Paulina Tindana, Susan Bull, Lucas Amenga-Etego, Jantina de Vries, Raymond Aborigo, Kwadwo Koram, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2012
65
50

Attitudes toward genetic research review: results from a survey of human genetics researchers.
K L Edwards, A A Lemke, S B Trinidad, S M Lewis, H Starks, M T Quinn Griffin, G L Wiesner. Public Health Genomics 2011
28
50

Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat Rev Genet 2015
92
50

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
105
50

Challenges in biobank governance in Sub-Saharan Africa.
Ciara Staunton, Keymanthri Moodley. BMC Med Ethics 2013
38
50

Principal investigator views of the IRB system.
Simon N Whitney, Kirsten Alcser, Carl Schneider, Laurence B McCullough, Amy L McGuire, Robert J Volk. Int J Med Sci 2008
38
50

Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis.
Karen L Edwards, Amy A Lemke, Susan B Trinidad, Susan M Lewis, Helene Starks, Katherine W Snapinn, Mary Quinn Griffin, Georgia L Wiesner, Wylie Burke. Genet Med 2012
28
50

Decentralisation of child tuberculosis services increases case finding and uptake of preventive therapy in Uganda.
S Zawedde-Muyanja, A Nakanwagi, J P Dongo, M P Sekadde, R Nyinoburyo, G Ssentongo, A K Detjen, F Mugabe, J Nakawesi, Y Karamagi,[...]. Int J Tuberc Lung Dis 2018
18
50

Trends in ethical and legal frameworks for the use of human biobanks.
A Cambon-Thomsen, E Rial-Sebbag, B M Knoppers. Eur Respir J 2007
156
50

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
230
50

Children and biobanks: a review of the ethical and legal discussion.
Kristien Hens, Emmanuelle Lévesque, Kris Dierickx. Hum Genet 2011
31
50

Translational research in pediatrics: tissue sampling and biobanking.
Alayne R Brisson, Doreen Matsui, Michael J Rieder, Douglas D Fraser. Pediatrics 2012
47
50

Informed consent, biobank research, and locality: perceptions of breast cancer patients in three European countries.
Imme Petersen, Christine Desmedt, Adrian Harris, Francesca Buffa, Regine Kollek. J Empir Res Hum Res Ethics 2014
13
50



Children, biobanks and the scope of parental consent.
Kristien Hens, Jean-Jacques Cassiman, Herman Nys, Kris Dierickx. Eur J Hum Genet 2011
34
50



Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
Jeffrey R Botkin, John W Belmont, Jonathan S Berg, Benjamin E Berkman, Yvonne Bombard, Ingrid A Holm, Howard P Levy, Kelly E Ormond, Howard M Saal, Nancy B Spinner,[...]. Am J Hum Genet 2015
220
50


Sample and data sharing barriers in biobanking: consent, committees, and compromises.
Flora Colledge, Kirsten Persson, Bernice Elger, David Shaw. Ann Diagn Pathol 2014
13
50

Research on stored biological samples: the views of Ugandans.
David Wendler, Christine Pace, Ambrose O Talisuna, Faustine Maiso, Christine Grady, Ezekiel Emanuel. IRB 2005
22
50

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
54
50

Attitudes toward genetic research review: results from a national survey of professionals involved in human subjects protection.
Amy A Lemke, Susan B Trinidad, Karen L Edwards, Helene Starks, Georgia L Wiesner. J Empir Res Hum Res Ethics 2010
27
50

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
50

Biobanking: shifting the analogy from consent to surrogacy.
Ann M Mongoven, Stephanie Solomon. Genet Med 2012
11
50


Research ethics. Children and population biobanks.
David Gurwitz, Isabel Fortier, Jeantine E Lunshof, Bartha Maria Knoppers. Science 2009
57
50




Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.
Susan M Wolf, Rebecca Branum, Barbara A Koenig, Gloria M Petersen, Susan A Berry, Laura M Beskow, Mary B Daly, Conrad V Fernandez, Robert C Green, Bonnie S LeRoy,[...]. J Law Med Ethics 2015
61
50

Attitudes towards transfers of human tissue samples across borders: an international survey of researchers and policy makers in five countries.
Xinqing Zhang, Kenji Matsui, Benjamin Krohmal, Alaa Abou Zeid, Vasantha Muthuswamy, Young Mo Koo, Yoshikuni Kita, Reidar K Lie. BMC Med Ethics 2010
8
50

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
41
50


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.