A citation-based method for searching scientific literature

Deborah Mascalzoni, Andrew Hicks, Peter Pramstaller, Matthias Wjst. PLoS Med 2008
Times Cited: 47







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



Times Cited
  Times     Co-cited
Similarity


From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
192
29

Ethics. Identifiability in genomic research.
William W Lowrance, Francis S Collins. Science 2007
96
19

Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.
Nils Homer, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V Pearson, Dietrich A Stephan, Stanley F Nelson, David W Craig. PLoS Genet 2008
418
17

Research ethics and the challenge of whole-genome sequencing.
Amy L McGuire, Timothy Caulfield, Mildred K Cho. Nat Rev Genet 2008
131
17

Genetics. No longer de-identified.
Amy L McGuire, Richard A Gibbs. Science 2006
106
17

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
185
17

Data sharing in genomics--re-shaping scientific practice.
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat Rev Genet 2009
129
14

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
198
14

Research ethics recommendations for whole-genome research: consensus statement.
Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh,[...]. PLoS Biol 2008
144
12


Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
123
12

Tailoring the process of informed consent in genetic and genomic research.
Charles N Rotimi, Patricia A Marshall. Genome Med 2010
41
14

From patients to partners: participant-centric initiatives in biomedical research.
Jane Kaye, Liam Curren, Nick Anderson, Kelly Edwards, Stephanie M Fullerton, Nadja Kanellopoulou, David Lund, Daniel G MacArthur, Deborah Mascalzoni, James Shepherd,[...]. Nat Rev Genet 2012
139
12

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
62
12


Valid consent for genomic epidemiology in developing countries.
Dave A Chokshi, Mahamadou A Thera, Michael Parker, Mahamadou Diakite, Julie Makani, Dominic P Kwiatkowski, Ogobara K Doumbo. PLoS Med 2007
30
16

Impact of social stigma on the process of obtaining informed consent for genetic research on podoconiosis: a qualitative study.
Fasil Tekola, Susan Bull, Bobbie Farsides, Melanie J Newport, Adebowale Adeyemo, Charles N Rotimi, Gail Davey. BMC Med Ethics 2009
63
10

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
91
10

Glad you asked: participants' opinions of re-consent for dbGap data submission.
Evette J Ludman, Stephanie M Fullerton, Leslie Spangler, Susan Brown Trinidad, Monica M Fujii, Gail P Jarvik, Eric B Larson, Wylie Burke. J Empir Res Hum Res Ethics 2010
76
10

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
82
10

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
61
10

DNA data sharing: research participants' perspectives.
Amy L McGuire, Jennifer A Hamilton, Rebecca Lunstroth, Laurence B McCullough, Alica Goldman. Genet Med 2008
68
8


Voluntary participation and informed consent to international genetic research.
Patricia A Marshall, Clement A Adebamowo, Adebowale A Adeyemo, Temidayo O Ogundiran, Mirjana Vekich, Teri Strenski, Jie Zhou, T Elaine Prewitt, Richard S Cooper, Charles N Rotimi. Am J Public Health 2006
48
8

Ethical data release in genome-wide association studies in developing countries.
Michael Parker, Susan J Bull, Jantina de Vries, Tsiri Agbenyega, Ogobara K Doumbo, Dominic P Kwiatkowski. PLoS Med 2009
41
9



Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya.
Vicki M Marsh, Dorcas M Kamuya, Albert M Mlamba, Thomas N Williams, Sassy S Molyneux. BMC Med Ethics 2010
54
8

Human genetic research: emerging trends in ethics.
Bartha Maria Knoppers, Ruth Chadwick. Nat Rev Genet 2005
110
8

Research ethics. Research practice and participant preferences: the growing gulf.
S B Trinidad, S M Fullerton, E J Ludman, G P Jarvik, E B Larson, W Burke. Science 2011
65
8

Ethical issues in human genomics research in developing countries.
Jantina de Vries, Susan J Bull, Ogobara Doumbo, Muntaser Ibrahim, Odile Mercereau-Puijalon, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2011
77
8

The complexities of ethical evaluation of genomics research.
R Hoedemaekers, B Gordijn, Y Hekster, F van Agt. HEC Forum 2006
10
30


New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
Teri A Manolio, Laura Lyman Rodriguez, Lisa Brooks, Gonçalo Abecasis, Dennis Ballinger, Mark Daly, Peter Donnelly, Stephen V Faraone, Kelly Frazer, Stacey Gabriel,[...]. Nat Genet 2007
221
6


Taking tissue seriously means taking communities seriously.
Ross E G Upshur, James V Lavery, Paulina O Tindana. BMC Med Ethics 2007
29
10


Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
422
6

Prepublication data sharing.
Ewan Birney, Thomas J Hudson, Eric D Green, Chris Gunter, Sean Eddy, Jane Rogers, Jennifer R Harris, S Dusko Ehrlich, Rolf Apweiler, Christopher P Austin,[...]. Nature 2009
151
6

On Jim Watson's APOE status: genetic information is hard to hide.
Dale R Nyholt, Chang-En Yu, Peter M Visscher. Eur J Hum Genet 2009
39
7


Data sharing and intellectual property in a genomic epidemiology network: policies for large-scale research collaboration.
Dave A Chokshi, Michael Parker, Dominic P Kwiatkowski. Bull World Health Organ 2006
27
11

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
136
6


Human stem cell ethics: beyond the embryo.
Jeremy Sugarman. Cell Stem Cell 2008
26
11

Tailoring consent to context: designing an appropriate consent process for a biomedical study in a low income setting.
Fasil Tekola, Susan J Bull, Bobbie Farsides, Melanie J Newport, Adebowale Adeyemo, Charles N Rotimi, Gail Davey. PLoS Negl Trop Dis 2009
64
6

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
385
6

Informed consent in international health research.
Patricia A Marshall. J Empir Res Hum Res Ethics 2006
43
6




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.