A citation-based method for searching scientific literature

Rhonda G Kost, Stephen M Poppel, Barry S Coller. J Clin Transl Sci 2017
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


The Role of Next-Generation Sequencing in Enabling Personalized Oncology Therapy.
C A Cummings, E Peters, L Lacroix, F Andre, M R Lackner. Clin Transl Sci 2016
23
25

Standardization and quality management in next-generation sequencing.
Christoph Endrullat, Jörn Glökler, Philipp Franke, Marcus Frohme. Appl Transl Genom 2016
80
25

Standardized decision support in next generation sequencing reports of somatic cancer variants.
Rodrigo Dienstmann, Fei Dong, Darrell Borger, Dora Dias-Santagata, Leif W Ellisen, Long P Le, A John Iafrate. Mol Oncol 2014
54
25

Comprehensive identification of mutational cancer driver genes across 12 tumor types.
David Tamborero, Abel Gonzalez-Perez, Christian Perez-Llamas, Jordi Deu-Pons, Cyriac Kandoth, Jüri Reimand, Michael S Lawrence, Gad Getz, Gary D Bader, Li Ding,[...]. Sci Rep 2013
308
25

Sequencing depth and coverage: key considerations in genomic analyses.
David Sims, Ian Sudbery, Nicholas E Ilott, Andreas Heger, Chris P Ponting. Nat Rev Genet 2014
591
25

Next-generation sequencing: advances and applications in cancer diagnosis.
Simona Serratì, Simona De Summa, Brunella Pilato, Daniela Petriella, Rosanna Lacalamita, Stefania Tommasi, Rosamaria Pinto. Onco Targets Ther 2016
64
25

Cancer statistics in China, 2015.
Wanqing Chen, Rongshou Zheng, Peter D Baade, Siwei Zhang, Hongmei Zeng, Freddie Bray, Ahmedin Jemal, Xue Qin Yu, Jie He. CA Cancer J Clin 2016
25

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests.
Nazneen Aziz, Qin Zhao, Lynn Bry, Denise K Driscoll, Birgit Funke, Jane S Gibson, Wayne W Grody, Madhuri R Hegde, Gerald A Hoeltge, Debra G B Leonard,[...]. Arch Pathol Lab Med 2015
184
25

Next-Generation Sequencing in Clinical Molecular Diagnostics of Cancer: Advantages and Challenges.
Rajyalakshmi Luthra, Hui Chen, Sinchita Roy-Chowdhuri, R Rajesh Singh. Cancers (Basel) 2015
72
25

Circulating Tumor DNA Analysis in Patients With Cancer: American Society of Clinical Oncology and College of American Pathologists Joint Review.
Jason D Merker, Geoffrey R Oxnard, Carolyn Compton, Maximilian Diehn, Patricia Hurley, Alexander J Lazar, Neal Lindeman, Christina M Lockwood, Alex J Rai, Richard L Schilsky,[...]. J Clin Oncol 2018
318
25

Bioinformatics for clinical next generation sequencing.
Gavin R Oliver, Steven N Hart, Eric W Klee. Clin Chem 2015
49
25

Designing transformative clinical trials in the cancer genome era.
Stefan Sleijfer, Jan Bogaerts, Lillian L Siu. J Clin Oncol 2013
108
25

Next-generation sequencing of cytologic preparations: An analysis of quality metrics.
David H Hwang, Elizabeth P Garcia, Matthew D Ducar, Edmund S Cibas, Lynette M Sholl. Cancer Cytopathol 2017
33
25

Factors affecting the success of next-generation sequencing in cytology specimens.
Sinchita Roy-Chowdhuri, Rashmi S Goswami, Hui Chen, Keyur P Patel, Mark J Routbort, Rajesh R Singh, Russell R Broaddus, Bedia A Barkoh, Jawad Manekia, Hui Yao,[...]. Cancer Cytopathol 2015
80
25

ACMG clinical laboratory standards for next-generation sequencing.
Heidi L Rehm, Sherri J Bale, Pinar Bayrak-Toydemir, Jonathan S Berg, Kerry K Brown, Joshua L Deignan, Michael J Friez, Birgit H Funke, Madhuri R Hegde, Elaine Lyon. Genet Med 2013
508
25


An NGS Workflow Blueprint for DNA Sequencing Data and Its Application in Individualized Molecular Oncology.
Jian Li, Aarif Mohamed Nazeer Batcha, Björn Grüning, Ulrich R Mansmann. Cancer Inform 2016
7
25

The importance of genetic counselling in genome-wide sequencing.
Alison M Elliott, Jan M Friedman. Nat Rev Genet 2018
13
25

Moving Forward on Consent Practices in Australia.
Rebekah E McWhirter, Lisa Eckstein. J Bioeth Inq 2018
5
25

Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children.
J C Sapp, D Dong, C Stark, L E Ivey, G Hooker, L G Biesecker, B B Biesecker. Clin Genet 2014
78
25

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.
Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
12
25

Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions.
Xin Li, Rachel Nusbaum, Constance Smith-Hicks, Leila Jamal, Shannan Dixon, Sonal Mahida. J Genet Couns 2019
8
25

Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
941
25

Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases.
Lotte Krabbenborg, L E L M Vissers, J Schieving, T Kleefstra, E J Kamsteeg, J A Veltman, M A Willemsen, S Van der Burg. J Genet Couns 2016
39
25


Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients.
T Rigter, C J A van Aart, M W Elting, Q Waisfisz, M C Cornel, L Henneman. Clin Genet 2014
30
25

The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders.
Nick Dragojlovic, Clara D M van Karnebeek, Aisha Ghani, Dallas Genereaux, Ellen Kim, Patricia Birch, Alison M Elliott, Jan M Friedman, Larry D Lynd. Genet Med 2020
7
25

Evidence-Based Strategies for Shortening Informed Consent Forms in Clinical Research.
Amy Corneli, Emily Namey, Monique P Mueller, Jenae Tharaldson, Steve Sortijas, Thomas Grey, Jeremy Sugarman. J Empir Res Hum Res Ethics 2017
16
25

Simplifying informed consent for biorepositories: stakeholder perspectives.
Laura M Beskow, Joëlle Y Friedman, N Chantelle Hardy, Li Lin, Kevin P Weinfurt. Genet Med 2010
37
25

Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions.
Shelin Adam, Patricia H Birch, Rachel R Coe, Nick Bansback, Adrian L Jones, Mary B Connolly, Michelle K Demos, Eric B Toyota, Matthew J Farrer, Jan M Friedman. J Genet Couns 2018
5
25

From the Patient Perspective, Consent Forms Fall Short of Providing Information to Guide Decision Making.
Christine J Manta, Jacqueline Ortiz, Benjamin W Moulton, Seema S Sonnad. J Patient Saf 2021
11
25

Development of a consent resource for genomic data sharing in the clinical setting.
Erin Rooney Riggs, Danielle R Azzariti, Annie Niehaus, Scott R Goehringer, Erin M Ramos, Laura Lyman Rodriguez, Bartha Knoppers, Heidi L Rehm, Christa Lese Martin. Genet Med 2019
7
25

A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study.
Erin Turbitt, Paola P Chrysostomou, Holly L Peay, Alexis R Heidlebaugh, Lawrence M Nelson, Barbara B Biesecker. Eur J Hum Genet 2018
5
25

The challenge of consent in clinical genome-wide testing.
Katherine Burke, Angus Clarke. Arch Dis Child 2016
12
25

Challenges to informed consent for exome sequencing: A best-worst scaling experiment.
Rachel H Gore, John F P Bridges, Julie S Cohen, Barbara B Biesecker. J Genet Couns 2019
2
50

IRB perspectives on the return of individual results from genomic research.
Lynn G Dressler, Sondra Smolek, Roselle Ponsaran, Janell M Markey, Helene Starks, Nancy Gerson, Susan Lewis, Nancy Press, Eric Juengst, Georgia L Wiesner. Genet Med 2012
46
25

The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia.
Alison M Elliott, Christèle du Souich, Shelin Adam, Nick Dragojlovic, Clara van Karnebeek, Tanya N Nelson, Anna Lehman, Larry D Lynd, Jan M Friedman. Mol Genet Genomic Med 2018
10
25


Paving the way to a more effective informed consent process: Recommendations from the Clinical Trials Transformation Initiative.
Jennifer Lentz, Michele Kennett, Jane Perlmutter, Annemarie Forrest. Contemp Clin Trials 2016
32
25

Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.
Allyn McConkie Rosell, Loren D M Pena, Kelly Schoch, Rebecca Spillmann, Jennifer Sullivan, Stephen R Hooper, Yong-Hui Jiang, Nicolas Mathey-Andrews, David B Goldstein, Vandana Shashi. J Genet Couns 2016
41
25

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
25

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
45
25


Public participation in genomics research in the Netherlands: validating a measurement scale.
Anne M Dijkstra, Jan M Gutteling, J A A Swart, Nicolien F Wieringa, Henny J van Derwindt, Erwin R Seydel. Public Underst Sci 2012
5
25

"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
Ashley N Tomlinson, Debra Skinner, Denise L Perry, Sarah R Scollon, Myra I Roche, Barbara A Bernhardt. J Genet Couns 2016
36
25

The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking study.
Nick Dragojlovic, Alison M Elliott, Shelin Adam, Clara van Karnebeek, Anna Lehman, Jill C Mwenifumbo, Tanya N Nelson, Christèle du Souich, Jan M Friedman, Larry D Lynd. Genet Med 2018
35
25



Views of clinical trial participants on the readability and their understanding of informed consent documents.
Rita Somers, Cornelius Van Staden, Francois Steffens. AJOB Empir Bioeth 2017
4
25

Participation in genetic testing research varies by social group.
Sharon Hensley Alford, Colleen M McBride, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Public Health Genomics 2011
72
25


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.