A citation-based method for searching scientific literature

Gaia Barazzetti, Samuele Cavalli, Lazare Benaroyo, Alain Kaufmann. Genet Test Mol Biomarkers 2017
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Pediatric biobanking: a pilot qualitative survey of practices, rules, and researcher opinions in ten European countries.
Elena Salvaterra, Roberto Giorda, Maria T Bassi, Renato Borgatti, Lisbeth E Knudsen, Andrea Martinuzzi, Maria Nobile, Uberto Pozzoli, Gian P Ramelli, Gianl L Reni,[...]. Biopreserv Biobank 2012
17
42

Engaging African-Americans about biobanks and the return of research results.
Colin Me Halverson, Lainie Friedman Ross. J Community Genet 2012
35
42

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
308
42

The development of a preference-setting model for the return of individual genomic research results.
Phoebe L Bacon, Erin D Harris, Sonja I Ziniel, Sarah K Savage, Elissa R Weitzman, Robert C Green, Noelle L Huntington, Ingrid A Holm. J Empir Res Hum Res Ethics 2015
17
42

The return of unexpected research results in a biobank study and referral to health care for heritable long QT syndrome.
A Haukkala, E Kujala, P Alha, V Salomaa, S Koskinen, H Swan, H Kääriäinen. Public Health Genomics 2013
28
42

Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
211
42

Return of "accurate" and "actionable" results: yes!
Bartha Maria Knoppers, Claude Laberge. Am J Bioeth 2009
18
28

Researchers' opinions towards the communication of results of biobank research: a survey study.
Tineke M Meulenkamp, Sjef J K Gevers, Jasper A Bovenberg, Ellen M A Smets. Eur J Hum Genet 2012
13
28

Biobanking, consent, and control: a survey of Albertans on key research ethics issues.
Timothy Caulfield, Christen Rachul, Erin Nelson. Biopreserv Biobank 2012
40
28

Participant Satisfaction With a Preference-Setting Tool for the Return of Individual Research Results in Pediatric Genomic Research.
Ingrid A Holm, Brittany R Iles, Sonja I Ziniel, Phoebe L Bacon, Sarah K Savage, Kurt D Christensen, Elissa R Weitzman, Robert C Green, Noelle L Huntington. J Empir Res Hum Res Ethics 2015
16
28

Return of research results from genomic biobanks: cost matters.
Marianna J Bledsoe, Ellen Wright Clayton, Amy L McGuire, William E Grizzle, P Pearl O'Rourke, Nikolajs Zeps. Genet Med 2013
43
28


Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
28

Allocation of Resources to Communication of Research Result Summaries.
Julie E Richards, Emmi Bane, Stephanie M Fullerton, Evette J Ludman, Gail Jarvik. J Empir Res Hum Res Ethics 2016
5
40

Preferences Regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank.
Carmen Radecki Breitkopf, Gloria M Petersen, Susan M Wolf, Kari G Chaffee, Marguerite E Robinson, Deborah R Gordon, Noralane M Lindor, Barbara A Koenig. J Law Med Ethics 2015
23
28


Adolescent perspectives on the return of individual results in genomic addiction research.
Marilyn E Coors, Kristen M Raymond, Shannon K McWilliams, Christian J Hopfer, Susan K Mikulich-Gilbertson. Psychiatr Genet 2015
7
28

When research seems like clinical care: a qualitative study of the communication of individual cancer genetic research results.
Fiona A Miller, Mita Giacomini, Catherine Ahern, Jason S Robert, Sonya de Laat. BMC Med Ethics 2008
29
28

Return of individual genetic results in a high-risk sample: enthusiasm and positive behavioral change.
Sarah M Hartz, Emily Olfson, Robert Culverhouse, Patricia Cavazos-Rehg, Li-Shiun Chen, James DuBois, Sherri Fisher, Kimberly Kaphingst, David Kaufman, Andrew Plunk,[...]. Genet Med 2015
20
28

Prospective biorepository participants' perspectives on access to research results.
Laura M Beskow, Sondra J Smolek. J Empir Res Hum Res Ethics 2009
34
28

Communication of biobanks' research results: what do (potential) participants want?
Tineke M Meulenkamp, Sjef K Gevers, Jasper A Bovenberg, Gerard H Koppelman, Astrid van Hylckama Vlieg, Ellen M A Smets. Am J Med Genet A 2010
70
28

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
134
28


Population studies: return of research results and incidental findings Policy Statement.
Bartha Maria Knoppers, Mylène Deschênes, Ma'n H Zawati, Anne Marie Tassé. Eur J Hum Genet 2013
73
28


Patients' Attitudes Towards the Return of Incidental Findings After Research with Residual Tissue: A Mixed Methods Study.
Eric Vermeulen, Susanne Rebers, Neil K Aaronson, Alexander P Brandenburg, Flora E van Leeuwen, Marjanka K Schmidt. Genet Test Mol Biomarkers 2018
5
40

Family decision maker perspectives on the return of genetic results in biobanking research.
Laura A Siminoff, Heather M Traino, Maghboeba Mosavel, Laura Barker, Glencora Gudger, Anita Undale. Genet Med 2016
18
28

The responses of research participants and their next of kin to receiving feedback of genetic test results following participation in the Australian Ovarian Cancer Study.
Nina Hallowell, Kathryn Alsop, Margaret Gleeson, Ashley Crook, Loren Plunkett, David Bowtell, Gillian Mitchell, Mary-Anne Young. Genet Med 2013
20
28

Public preferences for the return of research results in genetic research: a conjoint analysis.
Juli Murphy Bollinger, John F P Bridges, Ateesha Mohamed, David Kaufman. Genet Med 2014
37
28

Researchers' views on return of incidental genomic research results: qualitative and quantitative findings.
Robert Klitzman, Paul S Appelbaum, Abby Fyer, Josue Martinez, Brigitte Buquez, Julia Wynn, Cameron R Waldman, Jo Phelan, Erik Parens, Wendy K Chung. Genet Med 2013
87
28


Institutional review board perspectives on obligations to disclose genetic incidental findings to research participants.
Catherine Gliwa, Ilana R Yurkiewicz, Lisa Soleymani Lehmann, Sara Chandros Hull, Nathan Jones, Benjamin E Berkman. Genet Med 2016
18
28

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019
75
28

IRB perspectives on the return of individual results from genomic research.
Lynn G Dressler, Sondra Smolek, Roselle Ponsaran, Janell M Markey, Helene Starks, Nancy Gerson, Susan Lewis, Nancy Press, Eric Juengst, Georgia L Wiesner. Genet Med 2012
51
28



The right to know and genetic testing.
Mark Sheehan. J Med Ethics 2015
5
20

Community engagement for big epidemiology: deliberative democracy as a tool.
Rebekah E McWhirter, Christine R Critchley, Dianne Nicol, Don Chalmers, Tess Whitton, Margaret Otlowski, Michael M Burgess, Joanne L Dickinson. J Pers Med 2014
25
14


Can I be sued for that? Liability risk and the disclosure of clinically significant genetic research findings.
Amy L McGuire, Bartha Maria Knoppers, Ma'n H Zawati, Ellen Wright Clayton. Genome Res 2014
22
14

Development and progress of Ireland's biobank network: Ethical, legal, and social implications (ELSI), standardized documentation, sample and data release, and international perspective.
Blanaid Mee, Eoin Gaffney, Sharon A Glynn, Simona Donatello, Paul Carroll, Elizabeth Connolly, Sarah Mc Garrigle, Terry Boyle, Delia Flannery, Francis J Sullivan,[...]. Biopreserv Biobank 2013
11
14

The Mayo Clinic Biobank: a building block for individualized medicine.
Janet E Olson, Euijung Ryu, Kiley J Johnson, Barbara A Koenig, Karen J Maschke, Jody A Morrisette, Mark Liebow, Paul Y Takahashi, Zachary S Fredericksen, Ruchi G Sharma,[...]. Mayo Clin Proc 2013
150
14


The Tohoku Medical Megabank Project: Design and Mission.
Shinichi Kuriyama, Nobuo Yaegashi, Fuji Nagami, Tomohiko Arai, Yoshio Kawaguchi, Noriko Osumi, Masaki Sakaida, Yoichi Suzuki, Keiko Nakayama, Hiroaki Hashizume,[...]. J Epidemiol 2016
152
14

Stakeholders' perspectives on biobank-based genomic research: systematic review of the literature.
Alma Husedzinovic, Dominik Ose, Christoph Schickhardt, Stefan Fröhling, Eva C Winkler. Eur J Hum Genet 2015
34
14

Funding considerations for the disclosure of genetic incidental findings in biobank research.
L Black, D Avard, M H Zawati, B M Knoppers, J Hébert, G Sauvageau. Clin Genet 2013
19
14

The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.
David J Carey, Samantha N Fetterolf, F Daniel Davis, William A Faucett, H Lester Kirchner, Uyenlinh Mirshahi, Michael F Murray, Diane T Smelser, Glenn S Gerhard, David H Ledbetter. Genet Med 2016
197
14

Offering aggregate results to participants in genomic research: opportunities and challenges.
Laura M Beskow, Wylie Burke, Stephanie M Fullerton, Richard R Sharp. Genet Med 2012
38
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.