A citation-based method for searching scientific literature

Lauren C Milner, Nanibaa' A Garrison, Mildred K Cho, Russ B Altman, Louanne Hudgins, Stephen J Galli, Henry J Lowe, Iris Schrijver, David C Magnus. Per Med 2015
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity



Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
458
100


Genetics. Genomic research and human subject privacy.
Zhen Lin, Art B Owen, Russ B Altman. Science 2004
178
100

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
799
100

Whole genome sequencing in critically ill children.
Danton S Char, Mildred Cho, David Magnus. Lancet Respir Med 2015
8
100

Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing.
Kelly Hitch, Galen Joseph, Jenna Guiltinan, Jessica Kianmahd, Janey Youngblom, Amie Blanco. J Genet Couns 2014
45
100


Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
463
100

Machine learning applications in genetics and genomics.
Maxwell W Libbrecht, William Stafford Noble. Nat Rev Genet 2015
452
100

Unsolicited findings of next-generation sequencing for tumor analysis within a Dutch consortium: clinical daily practice reconsidered.
Rhodé M Bijlsma, Annelien L Bredenoord, Christa G Gadellaa-Hooijdonk, Martijn Pj Lolkema, Stefan Sleijfer, Emile E Voest, Margreet Gem Ausems, Neeltje Steeghs. Eur J Hum Genet 2016
18
100


Artificial intelligence in healthcare.
Kun-Hsing Yu, Andrew L Beam, Isaac S Kohane. Nat Biomed Eng 2018
227
100


Ethics. Identifiability in genomic research.
William W Lowrance, Francis S Collins. Science 2007
112
100




The next-generation sequencing revolution and its impact on genomics.
Daniel C Koboldt, Karyn Meltz Steinberg, David E Larson, Richard K Wilson, Elaine R Mardis. Cell 2013
533
100

Next-Generation Sequencing and the Return of Results.
Bartha Maria Knoppers, Minh Thu Nguyen, Karine Sénécal, Anne Marie Tassé, Ma'n H Zawati. Cold Spring Harb Perspect Med 2016
6
100

Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics.
Tessel Rigter, Lidewij Henneman, Ulf Kristoffersson, Alison Hall, Helger G Yntema, Pascal Borry, Holger Tönnies, Quinten Waisfisz, Mariet W Elting, Wybo J Dondorp,[...]. Hum Mutat 2013
39
100

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
63
100

The therapeutic misconception: informed consent in psychiatric research.
P S Appelbaum, L H Roth, C Lidz. Int J Law Psychiatry 1982
374
100

Next generation sequencing in psychiatric research: what study participants need to know about research findings.
Ghislaine Mathieu, Iris Jaitovich Groisman, Beatrice Godard. Int J Neuropsychopharmacol 2013
10
100

Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat Rev Genet 2015
89
100

The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
213
100

Considerations for ethics review of big data health research: A scoping review.
Marcello Ienca, Agata Ferretti, Samia Hurst, Milo Puhan, Christian Lovis, Effy Vayena. PLoS One 2018
38
100


Learning one's genetic risk changes physiology independent of actual genetic risk.
Bradley P Turnwald, J Parker Goyer, Danielle Z Boles, Amy Silder, Scott L Delp, Alia J Crum. Nat Hum Behav 2019
23
100

Informed Consent.
Christine Grady, Steven R Cummings, Michael C Rowbotham, Michael V McConnell, Euan A Ashley, Gagandeep Kang. N Engl J Med 2017
84
100

Standards and Guidelines for Validating Next-Generation Sequencing Bioinformatics Pipelines: A Joint Recommendation of the Association for Molecular Pathology and the College of American Pathologists.
Somak Roy, Christopher Coldren, Arivarasan Karunamurthy, Nefize S Kip, Eric W Klee, Stephen E Lincoln, Annette Leon, Mrudula Pullambhatla, Robyn L Temple-Smolkin, Karl V Voelkerding,[...]. J Mol Diagn 2018
144
100

Application of next-generation sequencing technology in forensic science.
Yaran Yang, Bingbing Xie, Jiangwei Yan. Genomics Proteomics Bioinformatics 2014
63
100

Assessing the privacy risks of data sharing in genomics.
C Heeney, N Hawkins, J de Vries, P Boddington, J Kaye. Public Health Genomics 2011
60
100


Health privacy in the electronic age.
Mark A Rothstein. J Leg Med 2007
11
100

The future of forensic DNA analysis.
John M Butler. Philos Trans R Soc Lond B Biol Sci 2015
50
100

Research ethics and the challenge of whole-genome sequencing.
Amy L McGuire, Timothy Caulfield, Mildred K Cho. Nat Rev Genet 2008
141
100


Genetics. No longer de-identified.
Amy L McGuire, Richard A Gibbs. Science 2006
118
100

Guidelines for diagnostic next-generation sequencing.
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur J Hum Genet 2016
226
100

Participant identification in genetic association studies: improved methods and practical implications.
Nicholas Masca, Paul R Burton, Nuala A Sheehan. Int J Epidemiol 2011
12
100

A machine learning model to determine the accuracy of variant calls in capture-based next generation sequencing.
Jeroen van den Akker, Gilad Mishne, Anjali D Zimmer, Alicia Y Zhou. BMC Genomics 2018
8
100

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
100

Implementing Machine Learning in Health Care - Addressing Ethical Challenges.
Danton S Char, Nigam H Shah, David Magnus. N Engl J Med 2018
224
100

Why Deep Learning Is Changing the Way to Approach NGS Data Processing: A Review.
Fabrizio Celesti, Antonio Celesti, Jiafu Wan, Massimo Villari. IEEE Rev Biomed Eng 2018
4
100

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
201
100

Clinical Versus Research Sequencing.
Yuriy Shevchenko, Sherri Bale. Cold Spring Harb Perspect Med 2016
9
100

Big Data, Large-Scale Text Analysis, and Public Health Research.
Merlin Chowkwanyun. Am J Public Health 2019
3
100

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
100

Electronic medical records for genetic research: results of the eMERGE consortium.
Abel N Kho, Jennifer A Pacheco, Peggy L Peissig, Luke Rasmussen, Katherine M Newton, Noah Weston, Paul K Crane, Jyotishman Pathak, Christopher G Chute, Suzette J Bielinski,[...]. Sci Transl Med 2011
225
100


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.