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: 50







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



Times Cited
  Times     Co-cited
Similarity


The Unbearable Requirement of Informed Consent.
Ellen Wright Clayton. Am J Bioeth 2019
1
100

Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.
Stephanie A Kraft, Mildred K Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E Ormond, Harold S Luft, Benjamin S Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2018
69
2



Informed consent, comparative effectiveness, and learning health care.
Ruth R Faden, Tom L Beauchamp, Nancy E Kass. N Engl J Med 2014
128
2

Confirming comprehension of informed consent as a protection of human subjects.
Jeremy Sugarman, Michael Paasche-Orlow. J Gen Intern Med 2006
17
5

Defining and redefining the scope and goals of genetic counseling.
Robert G Resta. Am J Med Genet C Semin Med Genet 2006
45
2


Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
792
2

Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.
Joon-Ho Yu, Paul S Appelbaum, Kyle B Brothers, Steven Joffe, Tia L Kauffman, Barbara A Koenig, Anya Er Prince, Sarah Scollon, Susan M Wolf, Barbara A Bernhardt,[...]. Per Med 2019
5
20


Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms.
Danya F Vears, Emilia Niemiec, Heidi Carmen Howard, Pascal Borry. Eur J Hum Genet 2018
28
3

Searching for secondary findings: considering actionability and preserving the right not to know.
Bertrand Isidor, Sophie Julia, Pascale Saugier-Veber, Paul-Loup Weil-Dubuc, Stéphane Bézieau, Eric Bieth, Jean-Paul Bonnefont, Arnold Munnich, Franck Bourdeaut, Catherine Bourgain,[...]. Eur J Hum Genet 2019
7
14

An ethical framework for genetic counseling in the genomic era.
Leila Jamal, Will Schupmann, Benjamin E Berkman. J Genet Couns 2020
7
14

Reconceptualizing Autonomy for Bioethics.
Lisa Dive, Ainsley J Newson. Kennedy Inst Ethics J 2018
7
14

Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, Samuel P Strom, Sibel Kantarci, Fabiola Quintero-Rivera, Kingshuk Das, Traci Toy, Bret Harry, Michael Yourshaw,[...]. JAMA 2014
558
2

Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners.
Tanya Dwarte, Kristine Barlow-Stewart, Rosie O'Shea, Marcel E Dinger, Bronwyn Terrill. J Genet Couns 2019
3
33

A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study.
Erin Turbitt, Paola P Chrysostomou, Holly L Peay, Alexis R Heidlebaugh, Lawrence M Nelson, Barbara B Biesecker. Eur J Hum Genet 2018
6
16

Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests.
Christel Thauvin-Robinet, Julien Thevenon, Sophie Nambot, Julian Delanne, Paul Kuentz, Ange-Line Bruel, Aline Chassagne, Elodie Cretin, Aurore Pelissier, Chritine Peyron,[...]. Eur J Hum Genet 2019
6
16

Challenges to informed consent for exome sequencing: A best-worst scaling experiment.
Rachel H Gore, John F P Bridges, Julie S Cohen, Barbara B Biesecker. J Genet Couns 2019
2
50

Why genomics researchers are sometimes morally required to hunt for secondary findings.
Julian J Koplin, Julian Savulescu, Danya F Vears. BMC Med Ethics 2020
4
25

Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.
Amy Nisselle, Ivan Macciocca, Fiona McKenzie, Hannah Vuong, Kate Dunlop, Belinda McClaren, Sylvia Metcalfe, Clara Gaff. J Genet Couns 2019
15
6

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
32
3

Points to consider for laboratories reporting results from diagnostic genomic sequencing.
D F Vears, K Sénécal, A J Clarke, L Jackson, A M Laberge, L Lovrecic, A Piton, K L I Van Gassen, H G Yntema, B M Knoppers,[...]. Eur J Hum Genet 2018
28
3

Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research.
Holly K Tabor, Benjamin E Berkman, Sara Chandros Hull, Michael J Bamshad. Am J Med Genet A 2011
93
2

A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin,[...]. Genet Med 2017
47
2


Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project.
Saskia C Sanderson, Melissa Hill, Christine Patch, Beverly Searle, Celine Lewis, Lyn S Chitty. BMJ Open 2019
10
10


Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results.
Courtney Berrios, Cynthia A James, Karen Raraigh, Juli Bollinger, Brittney Murray, Crystal Tichnell, Carolyn D Applegate, Amanda L Bergner. J Genet Couns 2018
7
14

Genetic health professionals' experiences with initiating reanalysis of genomic sequence data.
Danya F Vears, Karine Sénécal, Pascal Borry. Fam Cancer 2020
4
25

The relationship of nondirectiveness to genetic counseling: report of a workshop at the 2003 NSGC Annual Education Conference.
Jon Weil, Kelly Ormond, June Peters, Kathryn Peters, Barbara Bowles Biesecker, Bonnie LeRoy. J Genet Couns 2006
31
3

Nondirectiveness in genetic counseling: a survey of practitioners.
D M Bartels, B S LeRoy, P McCarthy, A L Caplan. Am J Med Genet 1997
43
2

Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium.
Susan M Wolf, Laura M Amendola, Jonathan S Berg, Wendy K Chung, Ellen Wright Clayton, Robert C Green, Julie Harris-Wai, Gail E Henderson, Gail P Jarvik, Barbara A Koenig,[...]. Genet Med 2018
19
5


Genome sequencing in the clinic: the past, present, and future of genomic medicine.
Jeremy W Prokop, Thomas May, Kim Strong, Stephanie M Bilinovich, Caleb Bupp, Surender Rajasekaran, Elizabeth A Worthey, Jozef Lazar. Physiol Genomics 2018
20
5

Should informed consent be based on rational beliefs?
J Savulescu, R W Momeyer. J Med Ethics 1997
50
2

Freedom of Choice About Incidental Findings Can Frustrate Participants' True Preferences.
Jennifer Viberg, Pär Segerdahl, Sophie Langenskiöld, Mats G Hansson. Bioethics 2016
15
6


Patient Perspectives on Sharing Anonymized Personal Health Data Using a Digital System for Dynamic Consent and Research Feedback: A Qualitative Study.
Karen Spencer, Caroline Sanders, Edgar A Whitley, David Lund, Jane Kaye, William Gregory Dixon. J Med Internet Res 2016
62
2

Health Research with Big Data: Time for Systemic Oversight.
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
31
3


A dynamic model of patient consent to sharing of medical record data.
William G Dixon, Karen Spencer, Hawys Williams, Caroline Sanders, David Lund, Edgar A Whitley, Jane Kaye. BMJ 2014
10
10

Dynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical research.
Hawys Williams, Karen Spencer, Caroline Sanders, David Lund, Edgar A Whitley, Jane Kaye, William G Dixon. JMIR Med Inform 2015
54
2


Prognostic models for identifying risk of poor outcome in people with acute ankle sprains: the SPRAINED development and external validation study.
David J Keene, Michael M Schlüssel, Jacqueline Thompson, Daryl A Hagan, Mark A Williams, Christopher Byrne, Steve Goodacre, Matthew Cooke, Stephen Gwilym, Philip Hormbrey,[...]. Health Technol Assess 2018
2
50

Towards 'Engagement 2.0': Insights from a study of dynamic consent with biobank participants.
Harriet Ja Teare, Michael Morrison, Edgar A Whitley, Jane Kaye. Digit Health 2015
23
4


The Effect of the General Data Protection Regulation on Medical Research.
John Mark Michael Rumbold, Barbara Pierscionek. J Med Internet Res 2017
41
2

Dynamic Consent: An Evaluation and Reporting Framework.
Megan Prictor, Megan A Lewis, Ainsley J Newson, Matilda Haas, Sachiko Baba, Hannah Kim, Minori Kokado, Jusaku Minari, Fruzsina Molnár-Gábor, Beverley Yamamoto,[...]. J Empir Res Hum Res Ethics 2020
7
14


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.