A citation-based method for searching scientific literature

Go Yoshizawa, Teguh H Sasongko, Chih-Hsing Ho, Kazuto Kato.  2017
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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
9
66

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
51
66

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
10
66

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N. Engl. J. Med. 2015
66

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
175
33

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
240
33

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
550
33

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
13
33

The DNA of a nation.
Vivien Marx. Nature 2015
39
33

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




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
14
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
155
33

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
58
33

Closure of population biobanks and direct-to-consumer genetic testing companies.
Ma'n H Zawati, Pascal Borry, Heidi Carmen Howard. Hum. Genet. 2011
22
33

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
17
33


GINA, genetic discrimination, and genomic medicine.
Robert C Green, Denise Lautenbach, Amy L McGuire. N. Engl. J. Med. 2015
70
33

Implementing Precision Medicine: The Ethical Challenges.
Diane M Korngiebel, Kenneth E Thummel, Wylie Burke. Trends Pharmacol. Sci. 2017
14
33


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
30
33

Data analysis: Create a cloud commons.
Lincoln D Stein, Bartha M Knoppers, Peter Campbell, Gad Getz, Jan O Korbel. Nature 2015
49
33

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
33

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
35
33


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
20
33

Moving closer to a rapid-learning health care system.
Jean R Slutsky. Health Aff (Millwood) 2007
31
33

Genome sequencing for healthy individuals.
Saskia C Sanderson. Trends Genet. 2013
5
33

A rapid-learning health system.
Lynn M Etheredge. Health Aff (Millwood) 2007
151
33

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
16
33


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
6
33


HIPAA Privacy Rule 2.0.
Mark A Rothstein. J Law Med Ethics 2013
6
33

Large numbers of genetic variants considered to be pathogenic are common in asymptomatic individuals.
Christopher A Cassa, Mark Y Tong, Daniel M Jordan. Hum. Mutat. 2013
49
33

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
299
33

Achieving a nationwide learning health system.
Charles P Friedman, Adam K Wong, David Blumenthal. Sci Transl Med 2010
215
33

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
107
33

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
33

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
22
33

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
34
33

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
58
33


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
23
33


Stratified medicine: strategic and economic implications of combining drugs and clinical biomarkers.
Mark R Trusheim, Ernst R Berndt, Frank L Douglas. Nat Rev Drug Discov 2007
237
33

Comparative Approaches to Genetic Discrimination: Chasing Shadows?
Yann Joly, Ida Ngueng Feze, Lingqiao Song, Bartha M Knoppers. Trends Genet. 2017
31
33

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.
Don Chalmers, Dianne Nicol, Jane Kaye, Jessica Bell, Alastair V Campbell, Calvin W L Ho, Kazuto Kato, Jusaku Minari, Chih-Hsing Ho, Colin Mitchell,[...]. BMC Med Ethics 2016
31
33


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.