A citation-based method for searching scientific literature

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
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
534
42

Clinical use of current polygenic risk scores may exacerbate health disparities.
Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
418
42

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
40

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
28

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
28

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
32
28

Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia.
Richard Milne, Katherine I Morley, Heidi Howard, Emilia Niemiec, Dianne Nicol, Christine Critchley, Barbara Prainsack, Danya Vears, James Smith, Claire Steed,[...]. Hum Genet 2019
19
28

The FAIR Guiding Principles for scientific data management and stewardship.
Mark D Wilkinson, Michel Dumontier, I Jsbrand Jan Aalbersberg, Gabrielle Appleton, Myles Axton, Arie Baak, Niklas Blomberg, Jan-Willem Boiten, Luiz Bonino da Silva Santos, Philip E Bourne,[...]. Sci Data 2016
28

Return of individual genomic research results: are laws and policies keeping step?
Adrian Thorogood, Gratien Dalpé, Bartha Maria Knoppers. Eur J Hum Genet 2019
34
28

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, D'Andra M Lindbuchler, Miranda L G Hallquist, Kandamurugu Manickam, Adam H Buchanan, Alanna Kulchak Rahm, Monica A Giovanni, Lauren Frisbie,[...]. Am J Hum Genet 2018
59
28

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
14


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
50



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
14

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
14

Paternity testing under the cloak of recreational genetics.
Nathalie Moray, Katherina E Pink, Pascal Borry, Maarten Hd Larmuseau. Eur J Hum Genet 2017
16
14

Banning genetic discrimination.
Henry T Greely. N Engl J Med 2005
29
14

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
14

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
14

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
16

Regulation: The FDA is overcautious on consumer genomics.
Robert C Green, Nita A Farahany. Nature 2014
49
14


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
14

Successful recruitment and retention of diverse participants in a genomics clinical trial: a good invitation to a great party.
Carol R Horowitz, Tatiana Sabin, Michelle Ramos, Lynne D Richardson, Diane Hauser, Mimsie Robinson, Kezhen Fei. Genet Med 2019
8
14

Insights into genetics, human biology and disease gleaned from family based genomic studies.
Jennifer E Posey, Anne H O'Donnell-Luria, Jessica X Chong, Tamar Harel, Shalini N Jhangiani, Zeynep H Coban Akdemir, Steven Buyske, Davut Pehlivan, Claudia M B Carvalho, Samantha Baxter,[...]. Genet Med 2019
62
14

Factors Contributing to the Success of NIH-Designated Underrepresented Minorities in Academic and Nonacademic Research Positions.
Luis R Martinez, Dwayne W Boucaud, Arturo Casadevall, Avery August. CBE Life Sci Educ 2018
14
14

Unraveling the 3D genome: genomics tools for multiscale exploration.
Viviana I Risca, William J Greenleaf. Trends Genet 2015
40
14



The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
14

Data privacy in the age of personal genomics.
Dennis Grishin, Kamal Obbad, George M Church. Nat Biotechnol 2019
11
14

Variable prediction accuracy of polygenic scores within an ancestry group.
Hakhamanesh Mostafavi, Arbel Harpak, Ipsita Agarwal, Dalton Conley, Jonathan K Pritchard, Molly Przeworski. Elife 2020
57
14

The translational potential of research on the ethical, legal, and social implications of genomics.
Wylie Burke, Paul Appelbaum, Lauren Dame, Patricia Marshall, Nancy Press, Reed Pyeritz, Richard Sharp, Eric Juengst. Genet Med 2015
13
14

Ensembl 2019.
Fiona Cunningham, Premanand Achuthan, Wasiu Akanni, James Allen, M Ridwan Amode, Irina M Armean, Ruth Bennett, Jyothish Bhai, Konstantinos Billis, Sanjay Boddu,[...]. Nucleic Acids Res 2019
400
14

Opportunities, resources, and techniques for implementing genomics in clinical care.
Teri A Manolio, Robb Rowley, Marc S Williams, Dan Roden, Geoffrey S Ginsburg, Carol Bult, Rex L Chisholm, Patricia A Deverka, Howard L McLeod, George A Mensah,[...]. Lancet 2019
25
14

Pharmacogenomics.
Dan M Roden, Howard L McLeod, Mary V Relling, Marc S Williams, George A Mensah, Josh F Peterson, Sara L Van Driest. Lancet 2019
86
14

Multi-site investigation of strategies for the clinical implementation of CYP2D6 genotyping to guide drug prescribing.
Larisa H Cavallari, Sara L Van Driest, Cynthia A Prows, Jeffrey R Bishop, Nita A Limdi, Victoria M Pratt, Laura B Ramsey, D Max Smith, Sony Tuteja, Benjamin Q Duong,[...]. Genet Med 2019
34
14

Telomere-to-telomere assembly of a complete human X chromosome.
Karen H Miga, Sergey Koren, Arang Rhie, Mitchell R Vollger, Ariel Gershman, Andrey Bzikadze, Shelise Brooks, Edmund Howe, David Porubsky, Glennis A Logsdon,[...]. Nature 2020
127
14



Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference.
Laura J Corbin, Vanessa Y Tan, David A Hughes, Kaitlin H Wade, Dirk S Paul, Katherine E Tansey, Frances Butcher, Frank Dudbridge, Joanna M Howson, Momodou W Jallow,[...]. Nat Commun 2018
22
14

Role of genomics literacy in reducing the burden of common genetic diseases in Africa.
Gerald Mboowa, Ivan Sserwadda. Mol Genet Genomic Med 2019
8
14

Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes.
David P Steensma, Rafael Bejar, Siddhartha Jaiswal, R Coleman Lindsley, Mikkael A Sekeres, Robert P Hasserjian, Benjamin L Ebert. Blood 2015
805
14

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
773
14

Evolving methodologies and concepts in 4D nucleome research.
Thomas M Sparks, Izabela Harabula, Ana Pombo. Curr Opin Cell Biol 2020
4
25

Earth BioGenome Project: Sequencing life for the future of life.
Harris A Lewin, Gene E Robinson, W John Kress, William J Baker, Jonathan Coddington, Keith A Crandall, Richard Durbin, Scott V Edwards, Félix Forest, M Thomas P Gilbert,[...]. Proc Natl Acad Sci U S A 2018
164
14

Sequencing of Circulating Cell-free DNA during Pregnancy.
Diana W Bianchi, Rossa W K Chiu. N Engl J Med 2018
105
14

Primary care physician experiences utilizing a family health history tool with electronic health record-integrated clinical decision support: an implementation process assessment.
Amy A Lemke, Jennifer Thompson, Peter J Hulick, Annette W Sereika, Christian Johnson, Lauren Oshman, Henry M Dunnenberger. J Community Genet 2020
6
16


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.