A citation-based method for searching scientific literature

Barbara J Evans, Gail Javitt, Ralph Hall, Megan Robertson, Pilar Ossorio, Susan M Wolf, Thomas Morgan, Ellen Wright Clayton. J Law Med Ethics 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


From Genetics to Genomics: Facing the Liability Implications in Clinical Care.
Gary Marchant, Mark Barnes, James P Evans, Bonnie LeRoy, Susan M Wolf. J Law Med Ethics 2020
11
75

The law of genetic privacy: applications, implications, and limitations.
Ellen Wright Clayton, Barbara J Evans, James W Hazel, Mark A Rothstein. J Law Biosci 2019
28
75

Integrating Rules for Genomic Research, Clinical Care, Public Health Screening and DTC Testing: Creating Translational Law for Translational Genomics.
Susan M Wolf, Pilar N Ossorio, Susan A Berry, Henry T Greely, Amy L McGuire, Michelle A Penny, Sharon F Terry. J Law Med Ethics 2020
7
50

Key Expert Stakeholder Perceptions of the Law of Genomics: Identified Problems and Potential Solutions.
Fook Yee Cheung, Lauren Clatch, Susan M Wolf, Ellen Wright Clayton, Frances Lawrenz. J Law Med Ethics 2020
2
100




Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines.
Wylie Burke, Ellen Wright Clayton, Susan M Wolf, Susan A Berry, Barbara J Evans, James P Evans, Ralph Hall, Diane Korngiebel, Anne-Marie Laberge, Bonnie S LeRoy,[...]. Genet Med 2019
6
25



23andMe, the Food and Drug Administration, and the future of genetic testing.
Patricia J Zettler, Jacob S Sherkow, Henry T Greely. JAMA Intern Med 2014
18
25

Direct-to-consumer raw genetic data and third-party interpretation services: more burden than bargain?
Tia Moscarello, Brittney Murray, Chloe M Reuter, Erin Demo. Genet Med 2019
20
25

Paternity testing under the cloak of recreational genetics.
Nathalie Moray, Katherina E Pink, Pascal Borry, Maarten Hd Larmuseau. Eur J Hum Genet 2017
16
25

Banning genetic discrimination.
Henry T Greely. N Engl J Med 2005
29
25

Legislation of direct-to-consumer genetic testing in Europe: a fragmented regulatory landscape.
L Kalokairinou, H C Howard, S Slokenberga, E Fisher, M Flatscher-Thöni, M Hartlev, R van Hellemondt, J Juškevičius, J Kapelenska-Pregowska, P Kováč,[...]. J Community Genet 2018
28
25

Family ties: the use of DNA offender databases to catch offenders' kin.
Henry T Greely, Daniel P Riordan, Nanibaa' A Garrison, Joanna L Mountain. J Law Med Ethics 2006
19
25

Medical genetics and genomic medicine in the United States. Part 2: Reproductive genetics, newborn screening, genetic counseling, training, and registries.
Debra S Regier, Carlos R Ferreira, Suzanne Hart, Donald W Hadley, Maximilian Muenke. Mol Genet Genomic Med 2017
6
25

Regulation: The FDA is overcautious on consumer genomics.
Robert C Green, Nita A Farahany. Nature 2014
49
25

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
17
25

Regulatory changes raise troubling questions for genomic testing.
Barbara J Evans, Michael O Dorschner, Wylie Burke, Gail P Jarvik. Genet Med 2014
18
25

Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years.
Anne Andermann, Ingeborg Blancquaert, Sylvie Beauchamp, Véronique Déry. Bull World Health Organ 2008
414
25

Knowledge integration at the center of genomic medicine.
Muin J Khoury, Marta Gwinn, W David Dotson, Sheri D Schully. Genet Med 2012
18
25

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
25

Relation between malpractice claims and adverse events due to negligence. Results of the Harvard Medical Practice Study III.
A R Localio, A G Lawthers, T A Brennan, N M Laird, L E Hebert, L M Peterson, J P Newhouse, P C Weiler, H H Hiatt. N Engl J Med 1991
486
25

Direct-to-consumer personalized genomic testing.
Cinnamon S Bloss, Burcu F Darst, Eric J Topol, Nicholas J Schork. Hum Mol Genet 2011
60
25

Direct-to-Consumer Testing 2.0: Emerging Models of Direct-to-Consumer Genetic Testing.
Megan A Allyse, David H Robinson, Matthew J Ferber, Richard R Sharp. Mayo Clin Proc 2018
53
25

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
463
25

Emerging issues in public health genomics.
J Scott Roberts, Dana Dolinoy, Beth Tarini. Annu Rev Genomics Hum Genet 2014
23
25


An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics.
Ruth R Faden, Nancy E Kass, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
266
25

Customers or research participants? Guidance for research practices in commercialization of personal genomics.
Sara L Tobin, Mildred K Cho, Sandra S-J Lee, David C Magnus, Megan Allyse, Kelly E Ormond, Nanibaa' A Garrison. Genet Med 2012
10
25



Sharing data under the 21st Century Cures Act.
Mary A Majumder, Christi J Guerrini, Juli M Bollinger, Robert Cook-Deegan, Amy L McGuire. Genet Med 2017
10
25

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.
Laura M Amendola, Gail P Jarvik, Michael C Leo, Heather M McLaughlin, Yassmine Akkari, Michelle D Amaral, Jonathan S Berg, Sawona Biswas, Kevin M Bowling, Laura K Conlin,[...]. Am J Hum Genet 2016
226
25

The role of patient advocacy organizations in shaping genomic science.
Pei P Koay, Richard R Sharp. Annu Rev Genomics Hum Genet 2013
21
25

Values in translation: how asking the right questions can move translational science toward greater health impact.
Maureen Kelley, Kelly Edwards, Helene Starks, Stephanie M Fullerton, Rosalina James, Sara Goering, Suzanne Holland, Mary L Disis, Wylie Burke. Clin Transl Sci 2012
12
25

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
340
25

The current landscape for direct-to-consumer genetic testing: legal, ethical, and policy issues.
Stuart Hogarth, Gail Javitt, David Melzer. Annu Rev Genomics Hum Genet 2008
153
25



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
296
25


Open sharing of genomic data: Who does it and why?
Tobias Haeusermann, Bastian Greshake, Alessandro Blasimme, Darja Irdam, Martin Richards, Effy Vayena. PLoS One 2017
27
25

The historical foundations of the research-practice distinction in bioethics.
Tom L Beauchamp, Yashar Saghai. Theor Med Bioeth 2012
28
25


ClinVar: improving access to variant interpretations and supporting evidence.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth R Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang,[...]. Nucleic Acids Res 2018
815
25

ClinVar: public archive of relationships among sequence variation and human phenotype.
Melissa J Landrum, Jennifer M Lee, George R Riley, Wonhee Jang, Wendy S Rubinstein, Deanna M Church, Donna R Maglott. Nucleic Acids Res 2014
25

The challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations.
Gail E Henderson, Susan M Wolf, Kristine J Kuczynski, Steven Joffe, Richard R Sharp, D Williams Parsons, Bartha M Knoppers, Joon-Ho Yu, Paul S Appelbaum. J Law Med Ethics 2014
46
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.