A citation-based method for searching scientific literature

R Hoedemaekers, B Gordijn, Y Hekster, F van Agt. HEC Forum 2006
Times Cited: 10







List of co-cited articles
45 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
217
40

Research ethics and the challenge of whole-genome sequencing.
Amy L McGuire, Timothy Caulfield, Mildred K Cho. Nat Rev Genet 2008
141
40

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
156
40

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
46
40

Genome-wide association studies for complex traits: consensus, uncertainty and challenges.
Mark I McCarthy, Gon├žalo R Abecasis, Lon R Cardon, David B Goldstein, Julian Little, John P A Ioannidis, Joel N Hirschhorn. Nat Rev Genet 2008
30

Informed consent in the genomics era.
Deborah Mascalzoni, Andrew Hicks, Peter Pramstaller, Matthias Wjst. PLoS Med 2008
56
30

Genetics. No longer de-identified.
Amy L McGuire, Richard A Gibbs. Science 2006
119
30



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
469
30

The emergence of an ethical duty to disclose genetic research results: international perspectives.
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur J Hum Genet 2006
196
30

Genomic research and incidental findings.
Brian Van Ness. J Law Med Ethics 2008
34
30

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
30


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
67
30

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
451
20



Taking tissue seriously means taking communities seriously.
Ross E G Upshur, James V Lavery, Paulina O Tindana. BMC Med Ethics 2007
32
20

Ethics. Identifiability in genomic research.
William W Lowrance, Francis S Collins. Science 2007
112
20

Data sharing in genomics--re-shaping scientific practice.
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat Rev Genet 2009
145
20

Incidental findings in genetics research using archived DNA.
Ellen Wright Clayton. J Law Med Ethics 2008
42
20

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
51
20



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
31
20







Sickle cell trait and the risk of Plasmodium falciparum malaria and other childhood diseases.
Thomas N Williams, Tabitha W Mwangi, Sammy Wambua, Neal D Alexander, Moses Kortok, Robert W Snow, Kevin Marsh. J Infect Dis 2005
193
20

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
32
20

Effectiveness of Haemophilus influenzae type b Conjugate vaccine introduction into routine childhood immunization in Kenya.
Karen D Cowgill, Moses Ndiritu, Joyce Nyiro, Mary P E Slack, Salome Chiphatsi, Amina Ismail, Tatu Kamau, Isaiah Mwangi, Mike English, Charles R J C Newton,[...]. JAMA 2006
139
20

Ethical implications of the use of whole genome methods in medical research.
Jane Kaye, Paula Boddington, Jantina de Vries, Naomi Hawkins, Karen Melham. Eur J Hum Genet 2010
59
20



Public access to genome-wide data: five views on balancing research with privacy and protection.
George Church, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington, Jane Kaye, Martin Bobrow, Bruce Weir. PLoS Genet 2009
58
20

Disclosing genetic research results after death of pediatric patients.
Adrienne C Sexton, Sylvia A Metcalfe. JAMA 2008
11
20

Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
221
20



Grand challenges in global health: community engagement in research in developing countries.
Paulina O Tindana, Jerome A Singh, C Shawn Tracy, Ross E G Upshur, Abdallah S Daar, Peter A Singer, Janet Frohlich, James V Lavery. PLoS Med 2007
191
20

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
56
20

Ethical and practical issues associated with aggregating databases.
David R Karp, Shelley Carlin, Robert Cook-Deegan, Daniel E Ford, Gail Geller, David N Glass, Hank Greely, Joel Guthridge, Jeffrey Kahn, Richard Kaslow,[...]. PLoS Med 2008
18
10

Data withholding in academic genetics: evidence from a national survey.
Eric G Campbell, Brian R Clarridge, Manjusha Gokhale, Lauren Birenbaum, Stephen Hilgartner, Neil A Holtzman, David Blumenthal. JAMA 2002
120
10

Assessing the impact of biobanks.
Anne Cambon-Thomsen. Nat Genet 2003
47
10


New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
Teri A Manolio, Laura Lyman Rodriguez, Lisa Brooks, Gon├žalo Abecasis, Dennis Ballinger, Mark Daly, Peter Donnelly, Stephen V Faraone, Kelly Frazer, Stacey Gabriel,[...]. Nat Genet 2007
234
10


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.