Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Times Cited: 60
Times Cited: 60
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
Adriana Kater-Kuipers, Inez D de Beaufort, Robert-Jan H Galjaard, Eline M Bunnik. Bioethics 2020
14
A qualitative study looking at informed choice in the context of non-invasive prenatal testing for aneuploidy.
Celine Lewis, Melissa Hill, Lyn S Chitty. Prenat Diagn 2016
Celine Lewis, Melissa Hill, Lyn S Chitty. Prenat Diagn 2016
4
Birth cohort studies: past, present and future.
Debbie A Lawlor, Anne-Marie Nybo Andersen, G David Batty. Int J Epidemiol 2009
Debbie A Lawlor, Anne-Marie Nybo Andersen, G David Batty. Int J Epidemiol 2009
2
Reasonable Expectations of Privacy and Disclosure of Health Data.
Mark J Taylor, James Wilson. Med Law Rev 2019
Mark J Taylor, James Wilson. Med Law Rev 2019
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
Mark J Taylor, Edward S Dove, Graeme Laurie, David Townend. Med Law Rev 2018
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
Irma M Hein, Martine C De Vries, Pieter W Troost, Gerben Meynen, Johannes B Van Goudoever, Ramón J L Lindauer. BMC Med Ethics 2015
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
A Sumathipala, D J Fernando, S H Siribaddana, M R Abeysingha, R W Jayasekare, V H Dissanayake, N De Silva. Twin Res 2000
10
Problem-solving tools for analyzing system problems. The affinity map and the relationship diagram.
C J Lepley. J Nurs Adm 1998
C J Lepley. J Nurs Adm 1998
33
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
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
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
Sonja Erikainen, Phoebe Friesen, Leah Rand, Karin Jongsma, Michael Dunn, Annie Sorbie, Matthew McCoy, Jessica Bell, Michael Burgess, Haidan Chen,[...]. J Med Ethics 2020
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
Harriet J A Teare, Megan Prictor, Jane Kaye. Eur J Hum Genet 2021
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
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
1
Governing Commercial Access to Health Data for Public Benefit: Charity Law Solutions.
Jessica L Bell. Med Law Rev 2020
Jessica L Bell. Med Law Rev 2020
100
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
Madeleine J Murtagh, Andrew Turner, Joel T Minion, Michaela Fay, Paul R Burton. Biopreserv Biobank 2016
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
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
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
Matilda A Haas, Harriet Teare, Megan Prictor, Gabi Ceregra, Miranda E Vidgen, David Bunker, Jane Kaye, Tiffany Boughtwood. Eur J Hum Genet 2021
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
Linda Richter, Shane Norris, John Pettifor, Derek Yach, Noel Cameron. Int J Epidemiol 2007
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
Latrice G Landry, Nadya Ali, David R Williams, Heidi L Rehm, Vence L Bonham. Health Aff (Millwood) 2018
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
Jane Kaye, Linda Briceño Moraia, Colin Mitchell, Jessica Bell, Jasper Adriaan Bovenberg, Anne-Marie Tassé, Bartha Maria Knoppers. Biopreserv Biobank 2016
7
Diversity and inclusion in genomic research: why the uneven progress?
Amy R Bentley, Shawneequa Callier, Charles N Rotimi. J Community Genet 2017
Amy R Bentley, Shawneequa Callier, Charles N Rotimi. J Community Genet 2017
1
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
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
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
Jamie J Kirkham, Katherine Davis, Douglas G Altman, Jane M Blazeby, Mike Clarke, Sean Tunis, Paula R Williamson. PLoS Med 2017
1
From tokenism to empowerment: progressing patient and public involvement in healthcare improvement.
Josephine Ocloo, Rachel Matthews. BMJ Qual Saf 2016
Josephine Ocloo, Rachel Matthews. BMJ Qual Saf 2016
1
The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
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
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
25
Methods of consumer involvement in developing healthcare policy and research, clinical practice guidelines and patient information material.
E S Nilsen, H T Myrhaug, M Johansen, S Oliver, A D Oxman. Cochrane Database Syst Rev 2006
E S Nilsen, H T Myrhaug, M Johansen, S Oliver, A D Oxman. Cochrane Database Syst Rev 2006
1
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
Jim Thomson, Tim Clayton, John Cleary, Maurice Gleeson, Debbie Kennett, Michelle Leonard, Donna Rutherford. Forensic Sci Int Genet 2020
12
The Golden State Killer investigation and the nascent field of forensic genealogy.
Chris Phillips. Forensic Sci Int Genet 2018
Chris Phillips. Forensic Sci Int Genet 2018
3
Privacy and genetic genealogy data.
Ellen M Greytak, David H Kaye, Bruce Budowle, CeCe Moore, Steven L Armentrout. Science 2018
Ellen M Greytak, David H Kaye, Bruce Budowle, CeCe Moore, Steven L Armentrout. Science 2018
6
Review of policies of companies and databases regarding access to customers' genealogy data for law enforcement purposes.
Sevasti Skeva, Maarten Hd Larmuseau, Mahsa Shabani. Per Med 2020
Sevasti Skeva, Maarten Hd Larmuseau, Mahsa Shabani. Per Med 2020
16
Accessing medical biobanks to solve crimes: ethical considerations.
Nina F de Groot, Britta C van Beers, Lieven Decock, Gerben Meynen. J Med Ethics 2020
Nina F de Groot, Britta C van Beers, Lieven Decock, Gerben Meynen. J Med Ethics 2020
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
Christi J Guerrini, Ray A Wickenheiser, Blaine Bettinger, Amy L McGuire, Stephanie M Fullerton. J Law Biosci 2021
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Operationalising forensic genetic genealogy in an Australian context.
Nathan Scudder, Runa Daniel, Jennifer Raymond, Alison Sears. Forensic Sci Int 2020
Nathan Scudder, Runa Daniel, Jennifer Raymond, Alison Sears. Forensic Sci Int 2020
16
4
Identity inference of genomic data using long-range familial searches.
Yaniv Erlich, Tal Shor, Itsik Pe'er, Shai Carmi. Science 2018
Yaniv Erlich, Tal Shor, Itsik Pe'er, Shai Carmi. Science 2018
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
Andreas Tillmar, Peter Sjölund, Bo Lundqvist, Therese Klippmark, Cajsa Älgenäs, Henrik Green. Forensic Sci Int Genet 2020
6
Is it time for a universal genetic forensic database?
J W Hazel, E W Clayton, B A Malin, C Slobogin. Science 2018
J W Hazel, E W Clayton, B A Malin, C Slobogin. Science 2018
12
Interpol review of forensic biology and forensic DNA typing 2016-2019.
John M Butler, Sheila Willis. Forensic Sci Int Synerg 2020
John M Butler, Sheila Willis. Forensic Sci Int Synerg 2020
9
'Only a click away - DTC genetics for ancestry, health, love…and more: A view of the business and regulatory landscape'.
Andelka M Phillips. Appl Transl Genom 2016
Andelka M Phillips. Appl Transl Genom 2016
1
Consumer genomics will change your life, whether you get tested or not.
Razib Khan, David Mittelman. Genome Biol 2018
Razib Khan, David Mittelman. Genome Biol 2018
2
Direct to consumer genetic testing and the libertarian right to test.
Michele Loi. J Med Ethics 2016
Michele Loi. J Med Ethics 2016
20
WHY WE FEAR GENETIC INFORMANTS: USING GENETIC GENEALOGY TO CATCH SERIAL KILLERS.
Teneille R Brown. Columbia Sci Technol Law Rev 2019
Teneille R Brown. Columbia Sci Technol Law Rev 2019
50
Attacks on genetic privacy via uploads to genealogical databases.
Michael D Edge, Graham Coop. Elife 2020
Michael D Edge, Graham Coop. Elife 2020
7
Is It Ethical to Use Genealogy Data to Solve Crimes?
Benjamin E Berkman, Wynter K Miller, Christine Grady. Ann Intern Med 2018
Benjamin E Berkman, Wynter K Miller, Christine Grady. Ann Intern Med 2018
9
Genealogy databases and the future of criminal investigation.
Natalie Ram, Christi J Guerrini, Amy L McGuire. Science 2018
Natalie Ram, Christi J Guerrini, Amy L McGuire. Science 2018
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.