A citation-based method for searching scientific literature

Fook Yee Cheung, Lauren Clatch, Susan M Wolf, Ellen Wright Clayton, Frances Lawrenz. J Law Med Ethics 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


How Can Law and Policy Advance Quality in Genomic Analysis and Interpretation for Clinical Care?
Barbara J Evans, Gail Javitt, Ralph Hall, Megan Robertson, Pilar Ossorio, Susan M Wolf, Thomas Morgan, Ellen Wright Clayton. J Law Med Ethics 2020
5
100

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
100

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
29
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
7
50

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



Regulatory changes raise troubling questions for genomic testing.
Barbara J Evans, Michael O Dorschner, Wylie Burke, Gail P Jarvik. Genet Med 2014
18
50

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
418
50

Knowledge integration at the center of genomic medicine.
Muin J Khoury, Marta Gwinn, W David Dotson, Sheri D Schully. Genet Med 2012
18
50

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
814
50

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
50

Direct-to-consumer personalized genomic testing.
Cinnamon S Bloss, Burcu F Darst, Eric J Topol, Nicholas J Schork. Hum Mol Genet 2011
60
50

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
55
50

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
466
50

Emerging issues in public health genomics.
J Scott Roberts, Dana Dolinoy, Beth Tarini. Annu Rev Genomics Hum Genet 2014
24
50


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
270
50

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
50



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
50

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
233
50

The role of patient advocacy organizations in shaping genomic science.
Pei P Koay, Richard R Sharp. Annu Rev Genomics Hum Genet 2013
22
50

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
13
50

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
344
50

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
50



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
50


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
50

The historical foundations of the research-practice distinction in bioethics.
Tom L Beauchamp, Yashar Saghai. Theor Med Bioeth 2012
28
50



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
858
50

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
50

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
47
50


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
50


Precision Public Health for the Era of Precision Medicine.
Muin J Khoury, Michael F Iademarco, William T Riley. Am J Prev Med 2016
207
50

Just compensation: a no-fault proposal for research-related injuries.
Leslie Meltzer Henry, Megan E Larkin, Elizabeth R Pike. J Law Biosci 2015
5
50




Assessment of US Hospital Compliance With Regulations for Patients' Requests for Medical Records.
Carolyn T Lye, Howard P Forman, Ruiyi Gao, Jodi G Daniel, Allen L Hsiao, Marilyn K Mann, Dave deBronkart, Hugo O Campos, Harlan M Krumholz. JAMA Netw Open 2018
19
50


Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
256
50


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.