A citation-based method for searching scientific literature

Nchangwi Syntia Munung, Patricia Marshall, Megan Campbell, Katherine Littler, Francis Masiye, Odile Ouwe-Missi-Oukem-Boyer, Janet Seeley, D J Stein, Paulina Tindana, Jantina de Vries. J Med Ethics 2016
Times Cited: 30







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



Times Cited
  Times     Co-cited
Similarity


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
43

Research capacity. Enabling the genomic revolution in Africa.
Charles Rotimi, Akin Abayomi, Alash'le Abimiku, Victoria May Adabayeri, Clement Adebamowo, Ezekiel Adebiyi, Adebowale D Ademola, Adebowale Adeyemo, Dwomoa Adu, Dissou Affolabi,[...]. Science 2014
213
36

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
80
33


Ethical issues in genomic research on the African continent: experiences and challenges to ethics review committees.
Michèle Ramsay, Jantina de Vries, Himla Soodyall, Shane A Norris, Osman Sankoh. Hum Genomics 2014
33
26

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
138
23


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
65
20

Regulation of genomic and biobanking research in Africa: a content analysis of ethics guidelines, policies and procedures from 22 African countries.
Jantina de Vries, Syntia Nchangwi Munung, Alice Matimba, Sheryl McCurdy, Odile Ouwe Missi Oukem-Boyer, Ciara Staunton, Aminu Yakubu, Paulina Tindana. BMC Med Ethics 2017
32
20


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
213
16

Understandings of genomic research in developing countries: a qualitative study of the views of MalariaGEN participants in Mali.
Karim Traore, Susan Bull, Alassane Niare, Salimata Konate, Mahamadou A Thera, Dominic Kwiatkowski, Michael Parker, Ogobara K Doumbo. BMC Med Ethics 2015
12
41

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
92
16

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
551
16

Voluntary participation and comprehension of informed consent in a genetic epidemiological study of breast cancer in Nigeria.
Patricia A Marshall, Clement A Adebamowo, Adebowale A Adeyemo, Temidayo O Ogundiran, Teri Strenski, Jie Zhou, Charles N Rotimi. BMC Med Ethics 2014
19
26

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
55
13

The H3Africa policy framework: negotiating fairness in genomics.
Jantina de Vries, Paulina Tindana, Katherine Littler, Michèle Ramsay, Charles Rotimi, Akin Abayomi, Nicola Mulder, Bongani M Mayosi. Trends Genet 2015
41
13


Tailoring the process of informed consent in genetic and genomic research.
Charles N Rotimi, Patricia A Marshall. Genome Med 2010
44
13

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
32
13

Ethical and legal implications of whole genome and whole exome sequencing in African populations.
Galen E B Wright, Pieter G J Koornhof, Adebowale A Adeyemo, Nicki Tiffin. BMC Med Ethics 2013
32
13


Community engagement strategies for genomic studies in Africa: a review of the literature.
Paulina Tindana, Jantina de Vries, Megan Campbell, Katherine Littler, Janet Seeley, Patricia Marshall, Jennifer Troyer, Morisola Ogundipe, Vincent Pius Alibu, Aminu Yakubu,[...]. BMC Med Ethics 2015
44
13



Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
469
13

Using the framework method for the analysis of qualitative data in multi-disciplinary health research.
Nicola K Gale, Gemma Heath, Elaine Cameron, Sabina Rashid, Sabi Redwood. BMC Med Res Methodol 2013
13

Model framework for governance of genomic research and biobanking in Africa - a content description.
Aminu Yakubu, Paulina Tindana, Alice Matimba, Katherine Littler, Nchangwi Syntia Munung, Ebony Madden, Ciara Staunton, Jantina De Vries. AAS Open Res 2018
18
22


Taking tissue seriously means taking communities seriously.
Ross E G Upshur, James V Lavery, Paulina O Tindana. BMC Med Ethics 2007
32
13

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
10
40

Challenges in biobank governance in Sub-Saharan Africa.
Ciara Staunton, Keymanthri Moodley. BMC Med Ethics 2013
37
10


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
45
10




Involving Research Stakeholders in Developing Policy on Sharing Public Health Research Data in Kenya: Views on Fair Process for Informed Consent, Access Oversight, and Community Engagement.
Irene Jao, Francis Kombe, Salim Mwalukore, Susan Bull, Michael Parker, Dorcas Kamuya, Sassy Molyneux, Vicki Marsh. J Empir Res Hum Res Ethics 2015
24
12


Best Practices for Ethical Sharing of Individual-Level Health Research Data From Low- and Middle-Income Settings.
Susan Bull, Phaik Yeong Cheah, Spencer Denny, Irene Jao, Vicki Marsh, Laura Merson, Neena Shah More, Le Nguyen Thanh Nhan, David Osrin, Decha Tangseefa,[...]. J Empir Res Hum Res Ethics 2015
32
10


Why do participants enroll in population biobank studies? A systematic literature review.
Hélène Nobile, Eric Vermeulen, Kristof Thys, Manuela M Bergmann, Pascal Borry. Expert Rev Mol Diagn 2013
31
10

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
64
10

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
281
10

Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
238
10

Informed consent in the genomics era.
Deborah Mascalzoni, Andrew Hicks, Peter Pramstaller, Matthias Wjst. PLoS Med 2008
56
10

Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014
46
10

Exploring researchers' experiences of working with a researcher-driven, population-specific community advisory board in a South African schizophrenia genomics study.
Megan M Campbell, Ezra Susser, Jantina de Vries, Adam Baldinger, Goodman Sibeko, Michael M Mndini, Sibonile G Mqulwana, Odwa A Ntola, Raj S Ramesar, Dan J Stein. BMC Med Ethics 2015
20
15


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
81
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.