A citation-based method for searching scientific literature

Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Times Cited: 60







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



Times Cited
  Times     Co-cited
Similarity


Rethinking counselling in prenatal screening: An ethical analysis of informed consent in the context of non-invasive prenatal testing (NIPT).
Adriana Kater-Kuipers, Inez D de Beaufort, Robert-Jan H Galjaard, Eline M Bunnik. Bioethics 2020
7
14


Birth cohort studies: past, present and future.
Debbie A Lawlor, Anne-Marie Nybo Andersen, G David Batty. Int J Epidemiol 2009
40
2

Reasonable Expectations of Privacy and Disclosure of Health Data.
Mark J Taylor, James Wilson. Med Law Rev 2019
5
20

When can the Child Speak for Herself? The Limits of Parental Consent in Data Protection Law for Health Research.
Mark J Taylor, Edward S Dove, Graeme Laurie, David Townend. Med Law Rev 2018
6
16

Informed consent instead of assent is appropriate in children from the age of twelve: Policy implications of new findings on children's competence to consent to clinical research.
Irma M Hein, Martine C De Vries, Pieter W Troost, Gerben Meynen, Johannes B Van Goudoever, Ramón J L Lindauer. BMC Med Ethics 2015
52
1

Establishing a twin register in Sri Lanka.
A Sumathipala, D J Fernando, S H Siribaddana, M R Abeysingha, R W Jayasekare, V H Dissanayake, N De Silva. Twin Res 2000
10
10

Massive UK baby study cancelled.
Helen Pearson. Nature 2015
19
5


The Danish National Birth Cohort--its background, structure and aim.
J Olsen, M Melbye, S F Olsen, T I Sørensen, P Aaby, A M Andersen, D Taxbøl, K D Hansen, M Juhl, T B Schow,[...]. Scand J Public Health 2001
800
1

Public involvement in the governance of population-level biomedical research: unresolved questions and future directions.
Sonja Erikainen, Phoebe Friesen, Leah Rand, Karin Jongsma, Michael Dunn, Annie Sorbie, Matthew McCoy, Jessica Bell, Michael Burgess, Haidan Chen,[...]. J Med Ethics 2020
7
14

Reflections on dynamic consent in biomedical research: the story so far.
Harriet J A Teare, Megan Prictor, Jane Kaye. Eur J Hum Genet 2021
9
11

Diversity in Clinical and Biomedical Research: A Promise Yet to Be Fulfilled.
Sam S Oh, Joshua Galanter, Neeta Thakur, Maria Pino-Yanes, Nicolas E Barcelo, Marquitta J White, Danielle M de Bruin, Ruth M Greenblatt, Kirsten Bibbins-Domingo, Alan H B Wu,[...]. PLoS Med 2015
239
1


International Data Sharing in Practice: New Technologies Meet Old Governance.
Madeleine J Murtagh, Andrew Turner, Joel T Minion, Michaela Fay, Paul R Burton. Biopreserv Biobank 2016
13
7

The Generation R Study: design and cohort update 2017.
Marjolein N Kooijman, Claudia J Kruithof, Cornelia M van Duijn, Liesbeth Duijts, Oscar H Franco, Marinus H van IJzendoorn, Johan C de Jongste, Caroline C W Klaver, Aad van der Lugt, Johan P Mackenbach,[...]. Eur J Epidemiol 2016
380
1

'CTRL': an online, Dynamic Consent and participant engagement platform working towards solving the complexities of consent in genomic research.
Matilda A Haas, Harriet Teare, Megan Prictor, Gabi Ceregra, Miranda E Vidgen, David Bunker, Jane Kaye, Tiffany Boughtwood. Eur J Hum Genet 2021
6
16

Cohort Profile: Mandela's children: the 1990 Birth to Twenty study in South Africa.
Linda Richter, Shane Norris, John Pettifor, Derek Yach, Noel Cameron. Int J Epidemiol 2007
199
1

Lack Of Diversity In Genomic Databases Is A Barrier To Translating Precision Medicine Research Into Practice.
Latrice G Landry, Nadya Ali, David R Williams, Heidi L Rehm, Vence L Bonham. Health Aff (Millwood) 2018
87
1

Access Governance for Biobanks: The Case of the BioSHaRE-EU Cohorts.
Jane Kaye, Linda Briceño Moraia, Colin Mitchell, Jessica Bell, Jasper Adriaan Bovenberg, Anne-Marie Tassé, Bartha Maria Knoppers. Biopreserv Biobank 2016
13
7

Diversity and inclusion in genomic research: why the uneven progress?
Amy R Bentley, Shawneequa Callier, Charles N Rotimi. J Community Genet 2017
98
1

The discombobulation of de-identification.
Mark Phillips, Bartha M Knoppers. Nat Biotechnol 2016
11
9

Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries.
Richard Milne, Katherine I Morley, Mohamed A Almarri, Shamim Anwer, Jerome Atutornu, Elena E Baranova, Paul Bevan, Maria Cerezo, Yali Cong, Alessia Costa,[...]. Genome Med 2021
5
20


Core Outcome Set-STAndards for Development: The COS-STAD recommendations.
Jamie J Kirkham, Katherine Davis, Douglas G Altman, Jane M Blazeby, Mike Clarke, Sean Tunis, Paula R Williamson. PLoS Med 2017
229
1


The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
1

The governance structure for data access in the DIRECT consortium: an innovative medicines initiative (IMI) project.
Harriet J A Teare, Federico de Masi, Karina Banasik, Anna Barnett, Sanna Herrgard, Bernd Jablonka, Jacqueline W M Postma, Timothy J McDonald, Ian Forgie, Piotr J Chmura,[...]. Life Sci Soc Policy 2018
4
25


An empirical investigation into the effectiveness of genetic genealogy to identify individuals in the UK.
Jim Thomson, Tim Clayton, John Cleary, Maurice Gleeson, Debbie Kennett, Michelle Leonard, Donna Rutherford. Forensic Sci Int Genet 2020
8
12

Crack down on genomic surveillance.
Yves Moreau. Nature 2019
8
12


Privacy and genetic genealogy data.
Ellen M Greytak, David H Kaye, Bruce Budowle, CeCe Moore, Steven L Armentrout. Science 2018
15
6


Accessing medical biobanks to solve crimes: ethical considerations.
Nina F de Groot, Britta C van Beers, Lieven Decock, Gerben Meynen. J Med Ethics 2020
1
100

Four misconceptions about investigative genetic genealogy.
Christi J Guerrini, Ray A Wickenheiser, Blaine Bettinger, Amy L McGuire, Stephanie M Fullerton. J Law Biosci 2021
3
33

Universal DNA databases: a way to improve privacy?
Kirsten Dedrickson. J Law Biosci 2018
10
10

Operationalising forensic genetic genealogy in an Australian context.
Nathan Scudder, Runa Daniel, Jennifer Raymond, Alison Sears. Forensic Sci Int 2020
6
16

Forensic genealogy: Some serious concerns.
Denise Syndercombe Court. Forensic Sci Int Genet 2018
22
4

Identity inference of genomic data using long-range familial searches.
Yaniv Erlich, Tal Shor, Itsik Pe'er, Shai Carmi. Science 2018
98
1

Whole-genome sequencing of human remains to enable genealogy DNA database searches - A case report.
Andreas Tillmar, Peter Sjölund, Bo Lundqvist, Therese Klippmark, Cajsa Älgenäs, Henrik Green. Forensic Sci Int Genet 2020
15
6

Is it time for a universal genetic forensic database?
J W Hazel, E W Clayton, B A Malin, C Slobogin. Science 2018
8
12

Interpol review of forensic biology and forensic DNA typing 2016-2019.
John M Butler, Sheila Willis. Forensic Sci Int Synerg 2020
11
9






Is It Ethical to Use Genealogy Data to Solve Crimes?
Benjamin E Berkman, Wynter K Miller, Christine Grady. Ann Intern Med 2018
11
9

Genealogy databases and the future of criminal investigation.
Natalie Ram, Christi J Guerrini, Amy L McGuire. Science 2018
33
3


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.