A citation-based method for searching scientific literature

Francis S Collins, Harold Varmus. N Engl J Med 2015
Times Cited: 2397







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



Times Cited
  Times     Co-cited
Similarity



The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
178
5

Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
Freddie Bray, Jacques Ferlay, Isabelle Soerjomataram, Rebecca L Siegel, Lindsey A Torre, Ahmedin Jemal. CA Cancer J Clin 2018
5

Precision Medicine: From Science To Value.
Geoffrey S Ginsburg, Kathryn A Phillips. Health Aff (Millwood) 2018
121
4

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
4

Precision Public Health for the Era of Precision Medicine.
Muin J Khoury, Michael F Iademarco, William T Riley. Am J Prev Med 2016
207
4

The path to personalized medicine.
Margaret A Hamburg, Francis S Collins. N Engl J Med 2010
947
3

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
3


Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.
Nina R Sperber, Janet S Carpenter, Larisa H Cavallari, Laura J Damschroder, Rhonda M Cooper-DeHoff, Joshua C Denny, Geoffrey S Ginsburg, Yue Guan, Carol R Horowitz, Kenneth D Levy,[...]. BMC Med Genomics 2017
52
5


Towards precision medicine.
Euan A Ashley. Nat Rev Genet 2016
242
3

Human genomics. The human transcriptome across tissues and individuals.
Marta MelĂ©, Pedro G Ferreira, Ferran Reverter, David S DeLuca, Jean Monlong, Michael Sammeth, Taylor R Young, Jakob M Goldmann, Dmitri D Pervouchine, Timothy J Sullivan,[...]. Science 2015
648
3

Public Health in the Precision-Medicine Era.
Ronald Bayer, Sandro Galea. N Engl J Med 2015
115
3


Induction of pluripotent stem cells from adult human fibroblasts by defined factors.
Kazutoshi Takahashi, Koji Tanabe, Mari Ohnuki, Megumi Narita, Tomoko Ichisaka, Kiichiro Tomoda, Shinya Yamanaka. Cell 2007
3

Hallmarks of cancer: the next generation.
Douglas Hanahan, Robert A Weinberg. Cell 2011
3

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
3

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
3

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
3


The new field of 'precision psychiatry'.
Brisa S Fernandes, Leanne M Williams, Johann Steiner, Marion Leboyer, AndrĂ© F Carvalho, Michael Berk. BMC Med 2017
152
2


Grand challenges in global mental health.
Pamela Y Collins, Vikram Patel, Sarah S Joestl, Dana March, Thomas R Insel, Abdallah S Daar, Warwick Anderson, Muhammad A Dhansay, Anthony Phillips, Susan Shurin,[...]. Nature 2011
2

Rare-disease genetics in the era of next-generation sequencing: discovery to translation.
Kym M Boycott, Megan R Vanstone, Dennis E Bulman, Alex E MacKenzie. Nat Rev Genet 2013
421
2




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
2

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.
Joshua C Denny, Marylyn D Ritchie, Melissa A Basford, Jill M Pulley, Lisa Bastarache, Kristin Brown-Gentry, Deede Wang, Dan R Masys, Dan M Roden, Dana C Crawford. Bioinformatics 2010
536
2

The European Genome-phenome Archive of human data consented for biomedical research.
Ilkka Lappalainen, Jeff Almeida-King, Vasudev Kumanduri, Alexander Senf, John Dylan Spalding, Saif Ur-Rehman, Gary Saunders, Jag Kandasamy, Mario Caccamo, Rasko Leinonen,[...]. Nat Genet 2015
166
2

Integrating Genomics into Healthcare: A Global Responsibility.
Zornitza Stark, Lena Dolman, Teri A Manolio, Brad Ozenberger, Sue L Hill, Mark J Caulfied, Yves Levy, David Glazer, Julia Wilson, Mark Lawler,[...]. Am J Hum Genet 2019
115
2

The UK Biobank resource with deep phenotyping and genomic data.
Clare Bycroft, Colin Freeman, Desislava Petkova, Gavin Band, Lloyd T Elliott, Kevin Sharp, Allan Motyer, Damjan Vukcevic, Olivier Delaneau, Jared O'Connell,[...]. Nature 2018
2

Next-generation DNA sequencing.
Jay Shendure, Hanlee Ji. Nat Biotechnol 2008
2

Harnessing Smartphone-Based Digital Phenotyping to Enhance Behavioral and Mental Health.
Jukka-Pekka Onnela, Scott L Rauch. Neuropsychopharmacology 2016
159
2

The state of the art and future opportunities for using longitudinal n-of-1 methods in health behaviour research: a systematic literature overview.
Suzanne McDonald, Francis Quinn, Rute Vieira, Nicola O'Brien, Martin White, Derek W Johnston, Falko F Sniehotta. Health Psychol Rev 2017
57
3

Microrandomized trials: An experimental design for developing just-in-time adaptive interventions.
Predrag Klasnja, Eric B Hekler, Saul Shiffman, Audrey Boruvka, Daniel Almirall, Ambuj Tewari, Susan A Murphy. Health Psychol 2015
152
2

Developing community-based health education strategies with family history: Assessing the association between community resident family history and interest in health education.
Elizabeth C Prom-Wormley, James S Clifford, Jessica L Bourdon, Peter Barr, Courtney Blondino, Kevin M Ball, Joshua Montgomery, Jonathan K Davis, Joseph E Real, Alexis C Edwards,[...]. Soc Sci Med 2021
7
28

Evaluating genetic counseling for family members of individuals with schizophrenia in the molecular age.
Gregory Costain, Mary Jane Esplen, Brenda Toner, Kathleen A Hodgkinson, Anne S Bassett. Schizophr Bull 2014
28
7

Use of genetic tests among neurologists and psychiatrists: knowledge, attitudes, behaviors, and needs for training.
Melissa Salm, Kristopher Abbate, Paul Appelbaum, Ruth Ottman, Wendy Chung, Karen Marder, Cheng-Shiun Leu, Roy Alcalay, Jill Goldman, Alexander Malik Curtis,[...]. J Genet Couns 2014
55
3

Genetic counseling in psychiatry.
Christine T Finn, Jordan W Smoller. Harv Rev Psychiatry 2006
35
5

Genetic architectures of psychiatric disorders: the emerging picture and its implications.
Patrick F Sullivan, Mark J Daly, Michael O'Donovan. Nat Rev Genet 2012
716
2

Experiences and attitudes of genome investigators regarding return of individual genetic test results.
Rachel B Ramoni, Amy L McGuire, Jill Oliver Robinson, Debra S Morley, Sharon E Plon, Steven Joffe. Genet Med 2013
36
5

Genetics in population health science: strategies and opportunities.
Daniel W Belsky, Terrie E Moffitt, Avshalom Caspi. Am J Public Health 2013
40
5

Attitudes of medical genetics practitioners and psychiatrists toward communicating with patients about genetic risk for psychiatric disorders.
Yi Zhou Zhou, Alex Wilde, Bettina Meiser, Philip B Mitchell, Kristine Barlow-Stewart, Peter R Schofield. Psychiatr Genet 2014
10
20

Researchers' views on return of incidental genomic research results: qualitative and quantitative findings.
Robert Klitzman, Paul S Appelbaum, Abby Fyer, Josue Martinez, Brigitte Buquez, Julia Wynn, Cameron R Waldman, Jo Phelan, Erik Parens, Wendy K Chung. Genet Med 2013
82
2

The Efficacy of Genetic Counseling for Psychiatric Disorders: a Meta-Analysis.
Ramona Moldovan, Sebastian Pintea, Jehannine Austin. J Genet Couns 2017
20
10

Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting.
Conrad V Fernandez, Caron Strahlendorf, Denise Avard, Bartha M Knoppers, Colleen O'Connell, Eric Bouffet, David Malkin, Nada Jabado, Kym Boycott, Poul H Sorensen. Genet Med 2013
35
5


Genomic data in the electronic medical record: perspectives from a biobank community advisory board.
Brittany C Kimball, Katherine E Nowakowski, Karen J Maschke, Jennifer B McCormick. J Empir Res Hum Res Ethics 2014
18
11


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.