A citation-based method for searching scientific literature

Jeffrey Peppercorn, Eric Campbell, Steve Isakoff, Nora K Horick, Julia Rabin, Katharine Quain, Lecia V Sequist, Aditya Bardia, Deborah Collyar, Fay Hlubocky, Debra Mathews. Oncologist 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Shadow health records meet new data privacy laws.
W Nicholson Price, Margot E Kaminski, Timo Minssen, Kayte Spector-Bagdady. Science 2019
15
50


Measuring Understanding and Respecting Trust in Biobank Consent.
T J Kasperbauer, Peter H Schwartz. Am J Bioeth 2019
4
50

Encouraging Participation And Transparency In Biobank Research.
Kayte Spector-Bagdady, Raymond G De Vries, Michele G Gornick, Andrew G Shuman, Sharon Kardia, Jodyn Platt. Health Aff (Millwood) 2018
17
50

Clinical Trial Participants' Views of the Risks and Benefits of Data Sharing.
Michelle M Mello, Van Lieou, Steven N Goodman. N Engl J Med 2018
73
50

Standard Versus Simplified Consent Materials for Biobank Participation: Differences in Patient Knowledge and Trial Accrual.
Sarah B Garrett, Marie Murphy, James Wiley, Daniel Dohan. J Empir Res Hum Res Ethics 2017
8
50

Patient Perspectives About Decisions to Share Medical Data and Biospecimens for Research.
Jihoon Kim, Hyeoneui Kim, Elizabeth Bell, Tyler Bath, Paulina Paul, Anh Pham, Xiaoqian Jiang, Kai Zheng, Lucila Ohno-Machado. JAMA Netw Open 2019
21
50

A systematic literature review of individuals' perspectives on privacy and genetic information in the United States.
Ellen W Clayton, Colin M Halverson, Nila A Sathe, Bradley A Malin. PLoS One 2018
37
50

"I don't want to be Henrietta Lacks": diverse patient perspectives on donating biospecimens for precision medicine research.
Sandra S-J Lee, Mildred K Cho, Stephanie A Kraft, Nina Varsava, Katie Gillespie, Kelly E Ormond, Benjamin S Wilfond, David Magnus. Genet Med 2019
29
50

Neglected ethical issues in biobank management: Results from a U.S. study.
R Jean Cadigan, Dragana Lassiter, Kaaren Haldeman, Ian Conlon, Erik Reavely, Gail E Henderson. Life Sci Soc Policy 2013
48
25

Debunking the Delusion That Precision Oncology Is an Illusion.
Vivek Subbiah, Razelle Kurzrock. Oncologist 2017
13
25

Big Data Analytics for Genomic Medicine.
Karen Y He, Dongliang Ge, Max M He. Int J Mol Sci 2017
47
25

Public Trust in Health Information Sharing: A Measure of System Trust.
Jodyn E Platt, Peter D Jacobson, Sharon L R Kardia. Health Serv Res 2018
18
25

Patient and Provider Perspectives Regarding Enrollment in Head and Neck Cancer Research.
Andrew G Shuman, Michele C Gornick, Collin Brummel, Madison Kent, Kayte Spector-Bagdady, Elliot Biddle, Carol R Bradford, J Chad Brenner. Otolaryngol Head Neck Surg 2020
3
33


Are Patients With Cancer Less Willing to Share Their Health Information? Privacy, Sensitivity, and Social Purpose.
David Grande, David A Asch, Fei Wan, Angela R Bradbury, Reshma Jagsi, Nandita Mitra. J Oncol Pract 2015
16
25

Patient perspectives on compensation for biospecimen donation.
Samuel C Allen, Minisha Lohani, Kristopher A Hendershot, Travis R Deal, Taylor White, Margie D Dixon, Rebecca D Pentz. AJOB Empir Bioeth 2018
5
25

Attitudes Toward Risk and Informed Consent for Research on Medical Practices: A Cross-sectional Survey.
Mildred K Cho, David Magnus, Melissa Constantine, Sandra Soo-Jin Lee, Maureen Kelley, Stephanie Alessi, Diane Korngiebel, Cyan James, Ellen Kuwana, Thomas H Gallagher,[...]. Ann Intern Med 2015
68
25

Revisiting Expectations in an Era of Precision Oncology.
Emily J Marchiano, Andrew C Birkeland, Paul L Swiecicki, Kayte Spector-Bagdady, Andrew G Shuman. Oncologist 2018
14
25

Big Data, Big Tech, and Protecting Patient Privacy.
I Glenn Cohen, Michelle M Mello. JAMA 2019
30
25


Genetic data partnerships: academic publications with privately owned or generated genetic data.
Kayte Spector-Bagdady, Amanda Fakih, Chris Krenz, Erica E Marsh, J Scott Roberts. Genet Med 2019
1
100

Moral concerns and the willingness to donate to a research biobank.
Tom Tomlinson, Raymond De Vries, Kerry Ryan, Hyungjin Myra Kim, Nicole Lehpamer, Scott Y H Kim. JAMA 2015
37
25

A Belmont Report for Health Data.
Efthimios Parasidis, Elizabeth Pike, Deven McGraw. N Engl J Med 2019
16
25

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
141
25

Genomic Privacy.
Abraham P Schwab, Hung S Luu, Jason Wang, Jason Y Park. Clin Chem 2018
5
25

Genomic Contextualism: Shifting the Rhetoric of Genetic Exceptionalism.
Nanibaa' A Garrison, Kyle B Brothers, Aaron J Goldenberg, John A Lynch. Am J Bioeth 2019
30
25

Communicating Identifiability Risks to Biobank Donors.
T J Kasperbauer, Mickey Gjerris, Gunhild Waldemar, Peter Sand√łe. Camb Q Healthc Ethics 2018
5
25


Data sharing practices of medicines related apps and the mobile ecosystem: traffic, content, and network analysis.
Quinn Grundy, Kellia Chiu, Fabian Held, Andrea Continella, Lisa Bero, Ralph Holz. BMJ 2019
45
25

Protecting health privacy even when privacy is lost.
T J Kasperbauer. J Med Ethics 2020
3
33

An Assessment of a Shortened Consent Form for the Storage and Research Use of Residual Newborn Screening Blood Spots.
Erin Rothwell, Aaron Goldenberg, Erin Johnson, Naomi Riches, Beth Tarini, Jeffrey R Botkin. J Empir Res Hum Res Ethics 2017
4
25

Transparency and choice in learning healthcare systems.
Jeffrey R Botkin. Learn Health Syst 2017
6
25

Identity and privacy. Unique in the shopping mall: on the reidentifiability of credit card metadata.
Yves-Alexandre de Montjoye, Laura Radaelli, Vivek Kumar Singh, Alex Sandy Pentland. Science 2015
53
25



Identity inference of genomic data using long-range familial searches.
Yaniv Erlich, Tal Shor, Itsik Pe'er, Shai Carmi. Science 2018
92
25

Privacy Risks from Genomic Data-Sharing Beacons.
Suyash S Shringarpure, Carlos D Bustamante. Am J Hum Genet 2015
80
25

Secure genome-wide association analysis using multiparty computation.
Hyunghoon Cho, David J Wu, Bonnie Berger. Nat Biotechnol 2018
31
25





Routes for breaching and protecting genetic privacy.
Yaniv Erlich, Arvind Narayanan. Nat Rev Genet 2014
143
25


Assessment of the All of Us research program's informed consent process.
Megan Doerr, Sarah Moore, Vanessa Barone, Scott Sutherland, Brian M Bot, Christine Suver, John Wilbanks. AJOB Empir Bioeth 2021
2
50

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am J Hum Genet 2017
95
25


Understanding public reactions to commercialization of biobanks and use of biobank resources.
Dianne Nicol, Christine Critchley, Rebekah McWhirter, Tess Whitton. Soc Sci Med 2016
30
25

Incorporating Biobank Consent into a Healthcare Setting: Challenges for Patient Understanding.
T J Kasperbauer, Karen K Schmidt, Ariane Thomas, Susan M Perkins, Peter H Schwartz. AJOB Empir Bioeth 2021
4
25


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.