A citation-based method for searching scientific literature

Go Yoshizawa, Teguh H Sasongko, Chih-Hsing Ho, Kazuto Kato. Front Genet 2017
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


ELSI practices in genomic research in East Asia: implications for research collaboration and public participation.
Go Yoshizawa, Calvin Wai-Loon Ho, Wei Zhu, Chingli Hu, Yoni Syukriani, Ilhak Lee, Hannah Kim, Daniel Fu Chang Tsai, Jusaku Minari, Kazuto Kato. Genome Med 2014
13
60


Life insurance: genomic stratification and risk classification.
Yann Joly, Hilary Burton, Bartha Maria Knoppers, Ida Ngueng Feze, Tom Dent, Nora Pashayan, Susmita Chowdhury, William Foulkes, Alison Hall, Pavel Hamet,[...]. Eur J Hum Genet 2014
18
40

The emerging need for family-centric initiatives for obtaining consent in personal genome research.
Jusaku Minari, Harriet Teare, Colin Mitchell, Jane Kaye, Kazuto Kato. Genome Med 2014
12
40

Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.
Isabelle Budin-Ljøsne, Harriet J A Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D'Abramo, Heike Felzmann, Teresa Finlay,[...]. BMC Med Ethics 2017
81
40

Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan.
Victoria Coathup, Harriet J A Teare, Jusaku Minari, Go Yoshizawa, Jane Kaye, Masanori P Takahashi, Kazuto Kato. BMC Med Ethics 2016
14
40

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
40

Comparative Approaches to Genetic Discrimination: Chasing Shadows?
Yann Joly, Ida Ngueng Feze, Lingqiao Song, Bartha M Knoppers. Trends Genet 2017
39
40

Genetic discrimination: international perspectives.
M Otlowski, S Taylor, Y Bombard. Annu Rev Genomics Hum Genet 2012
65
40

South Korea: in the midst of a privacy reform centered on data sharing.
Hannah Kim, So Yoon Kim, Yann Joly. Hum Genet 2018
6
40

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
207
20

Actionable, pathogenic incidental findings in 1,000 participants' exomes.
Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett,[...]. Am J Hum Genet 2013
270
20

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
831
20

Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals.
Yumi Yamaguchi-Kabata, Jun Yasuda, Osamu Tanabe, Yoichi Suzuki, Hiroshi Kawame, Nobuo Fuse, Masao Nagasaki, Yosuke Kawai, Kaname Kojima, Fumiki Katsuoka,[...]. J Hum Genet 2018
20
20

The DNA of a nation.
Vivien Marx. Nature 2015
45
20

Industry involvement in publicly funded biobanks.
Timothy Caulfield, Pascal Borry, Herbert Gottweis. Nat Rev Genet 2014
3
33



Funding of US biomedical research, 2003-2008.
E Ray Dorsey, Jason de Roulet, Joel P Thompson, Jason I Reminick, Ashley Thai, Zachary White-Stellato, Christopher A Beck, Benjamin P George, Hamilton Moses. JAMA 2010
195
20

A framework for biobank sustainability.
Peter H Watson, Sara Y Nussbeck, Candace Carter, Sheila O'Donoghue, Stefanie Cheah, Lise A M Matzke, Rebecca O Barnes, John Bartlett, Jane Carpenter, William E Grizzle,[...]. Biopreserv Biobank 2014
69
20

Closure of population biobanks and direct-to-consumer genetic testing companies.
Ma'n H Zawati, Pascal Borry, Heidi Carmen Howard. Hum Genet 2011
24
20

Public-private relationships in biobanking: a still underestimated key component of open innovation.
Paul Hofman, Christian Bréchot, Kurt Zatloukal, Georges Dagher, Bruno Clément. Virchows Arch 2014
21
20


GINA, genetic discrimination, and genomic medicine.
Robert C Green, Denise Lautenbach, Amy L McGuire. N Engl J Med 2015
98
20

Implementing Precision Medicine: The Ethical Challenges.
Diane M Korngiebel, Kenneth E Thummel, Wylie Burke. Trends Pharmacol Sci 2017
18
20


Genetic testing for Alzheimer's and long-term care insurance.
Donald H Taylor, Robert M Cook-Deegan, Susan Hiraki, J Scott Roberts, Dan G Blazer, Robert C Green. Health Aff (Millwood) 2010
38
20

Data analysis: Create a cloud commons.
Lincoln D Stein, Bartha M Knoppers, Peter Campbell, Gad Getz, Jan O Korbel. Nature 2015
53
20

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Robert C Green, Katrina A B Goddard, Gail P Jarvik, Laura M Amendola, Paul S Appelbaum, Jonathan S Berg, Barbara A Bernhardt, Leslie G Biesecker, Sawona Biswas, Carrie L Blout,[...]. Am J Hum Genet 2016
23
20

Policy challenges of clinical genome sequencing.
Caroline F Wright, Anna Middleton, Hilary Burton, Fiona Cunningham, Steve E Humphries, Jane Hurst, Ewan Birney, Helen V Firth. BMJ 2013
38
20


Stratified, precision or personalised medicine? Cancer services in the 'real world' of a London hospital.
Sophie Day, R Charles Coombes, Louise McGrath-Lone, Claudia Schoenborn, Helen Ward. Sociol Health Illn 2017
30
20

Moving closer to a rapid-learning health care system.
Jean R Slutsky. Health Aff (Millwood) 2007
35
20

Genome sequencing for healthy individuals.
Saskia C Sanderson. Trends Genet 2013
6
20

A rapid-learning health system.
Lynn M Etheredge. Health Aff (Millwood) 2007
179
20

My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings.
Holly K Tabor, Seema M Jamal, Joon-Ho Yu, Julia M Crouch, Aditi G Shankar, Karin M Dent, Nick Anderson, Damon A Miller, Brett T Futral, Michael J Bamshad. Genet Med 2017
18
20


How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods study.
Sandi Dheensa, Gillian Crawford, Claire Salter, Michael Parker, Angela Fenwick, Anneke Lucassen. Fam Cancer 2018
7
20


HIPAA Privacy Rule 2.0.
Mark A Rothstein. J Law Med Ethics 2013
7
20


Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
336
20

Achieving a nationwide learning health system.
Charles P Friedman, Adam K Wong, David Blumenthal. Sci Transl Med 2010
250
20

Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature.
Katharina Schwarze, James Buchanan, Jenny C Taylor, Sarah Wordsworth. Genet Med 2018
185
20

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
20

Japan's initiative on rare and undiagnosed diseases (IRUD): towards an end to the diagnostic odyssey.
Takeya Adachi, Kazuo Kawamura, Yoshihiko Furusawa, Yuji Nishizaki, Noriaki Imanishi, Senkei Umehara, Kazuo Izumi, Makoto Suematsu. Eur J Hum Genet 2017
36
20

Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, George A Diaz, Randi E Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt. Eur J Hum Genet 2016
49
20

Public responses to the sharing and linkage of health data for research purposes: a systematic review and thematic synthesis of qualitative studies.
Mhairi Aitken, Jenna de St Jorre, Claudia Pagliari, Ruth Jepson, Sarah Cunningham-Burley. BMC Med Ethics 2016
91
20


Public awareness of genetic nondiscrimination laws in four states and perceived importance of life insurance protections.
Alicia A Parkman, Joan Foland, Beth Anderson, Debra Duquette, Holly Sobotka, Mary Lynn, Shelley Nottingham, William David Dotson, Katherine Kolor, Summer L Cox. J Genet Couns 2015
28
20


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.