A citation-based method for searching scientific literature

Kerry A Ryan, Raymond G De Vries, Wendy R Uhlmann, J Scott Roberts, Michele C Gornick. J Genet Couns 2017
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


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
592
45

Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur. J. Hum. Genet. 2016
90
45

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
45

Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.
Joon-Ho Yu, Tanya M Harrell, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am. J. Hum. Genet. 2014
80
45

Incidental findings in the era of whole genome sequencing?
Erik Parens, Paul Appelbaum, Wendy Chung. Hastings Cent Rep 2013
15
36

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
72
36


To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur. J. Hum. Genet. 2013
97
27

Potential research participants support the return of raw sequence data.
Anna Middleton, Caroline F Wright, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Michael Parker. J. Med. Genet. 2015
24
27

The Danish Blood Donor Study: a large, prospective cohort and biobank for medical research.
O B Pedersen, C Erikstrup, S R Kotzé, E Sørensen, M S Petersen, K Grau, H Ullum. Vox Sang. 2012
50
27

Stakeholders in psychiatry and their attitudes toward receiving pertinent and incident findings in genomic research.
Anna Sundby, Merete W Boolsen, Kristoffer S Burgdorf, Henrik Ullum, Thomas F Hansen, Anna Middleton, Ole Mors. Am. J. Med. Genet. A 2017
12
27

A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin,[...]. Genet. Med. 2017
41
27

Exploring concordance and discordance for return of incidental findings from clinical sequencing.
Robert C Green, Jonathan S Berg, Gerard T Berry, Leslie G Biesecker, David P Dimmock, James P Evans, Wayne W Grody, Madhuri R Hegde, Sarah Kalia, Bruce R Korf,[...]. Genet. Med. 2012
120
27


Effect of Public Deliberation on Attitudes toward Return of Secondary Results in Genomic Sequencing.
Michele C Gornick, Aaron M Scherer, Erica J Sutton, Kerry A Ryan, Nicole L Exe, Ming Li, Wendy R Uhlmann, Scott Y H Kim, J Scott Roberts, Raymond G De Vries. J Genet Couns 2017
12
27

Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.
Stephanie A Kraft, Mildred K Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E Ormond, Harold S Luft, Benjamin S Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2018
48
27

Can I access my personal genome? The current legal position in the UK.
Jane Kaye, Nadja Kanellopoulou, Naomi Hawkins, Heather Gowans, Liam Curren, Karen Melham. Med Law Rev 2014
13
18

Participation rates in epidemiologic studies.
Sandro Galea, Melissa Tracy. Ann Epidemiol 2007
968
18

Using whole-exome sequencing to identify inherited causes of autism.
Timothy W Yu, Maria H Chahrour, Michael E Coulter, Sarn Jiralerspong, Kazuko Okamura-Ikeda, Bulent Ataman, Klaus Schmitz-Abe, David A Harmin, Mazhar Adli, Athar N Malik,[...]. Neuron 2013
231
18

Empirical research on the ethics of genomic research.
Anna Middleton, Michael Parker, Caroline F Wright, Eugene Bragin, Matthew E Hurles. Am. J. Med. Genet. A 2013
10
20

Personal genome research : what should the participant be told?
Amy L McGuire, James R Lupski. Trends Genet. 2010
52
18



The emergence of an ethical duty to disclose genetic research results: international perspectives.
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur. J. Hum. Genet. 2006
165
18


Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.
Kyle B Brothers, Kelly M East, Whitley V Kelley, M Frances Wright, Matthew J Westbrook, Carla A Rich, Kevin M Bowling, Edward J Lose, E Martina Bebin, Shirley Simmons,[...]. Genet. Med. 2017
23
18

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
18

Research Participants' Preferences for Hypothetical Secondary Results from Genomic Research.
Julia Wynn, Josue Martinez, Jimmy Duong, Codruta Chiuzan, Jo C Phelan, Abby Fyer, Robert L Klitzman, Paul S Appelbaum, Wendy K Chung. J Genet Couns 2017
20
18

The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
174
18

Attitudes of parents toward the return of targeted and incidental genomic research findings in children.
Conrad V Fernandez, Eric Bouffet, David Malkin, Nada Jabado, Colleen O'Connell, Denise Avard, Bartha M Knoppers, Meghan Ferguson, Kym M Boycott, Poul H Sorensen,[...]. Genet. Med. 2014
50
18


Assessing hypothetical scenario methodology in genetic susceptibility testing analog studies: a quantitative review.
Susan Persky, Kimberly A Kaphingst, Celeste M Condit, Colleen M McBride. Genet. Med. 2007
57
18

Is "incidental finding" the best term?: a study of patients' preferences.
Nina Tan, Laura M Amendola, Julianne M O'Daniel, Amber Burt, Martha J Horike-Pyne, Lacey Boshe, Gail E Henderson, Christine Rini, Myra I Roche, Fuki M Hisama,[...]. Genet. Med. 2017
20
18

CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
Brian H Shirts, Joseph S Salama, Samuel J Aronson, Wendy K Chung, Stacy W Gray, Lucia A Hindorff, Gail P Jarvik, Sharon E Plon, Elena M Stoffel, Peter Z Tarczy-Hornoch,[...]. J Am Med Inform Assoc 2015
50
18

Circulating Tumor DNA Reveals Clinically Actionable Somatic Genome of Metastatic Bladder Cancer.
Gillian Vandekerkhove, Tilman Todenhöfer, Matti Annala, Werner J Struss, Amanda Wong, Kevin Beja, Elie Ritch, Sonal Brahmbhatt, Stanislav V Volik, Jörg Hennenlotter,[...]. Clin. Cancer Res. 2017
46
18

Mastering genomic terminology.
Gail P Jarvik, James P Evans. Genet. Med. 2017
7
28

Health literacy interventions and outcomes: an updated systematic review.
Nancy D Berkman, Stacey L Sheridan, Katrina E Donahue, David J Halpern, Anthony Viera, Karen Crotty, Audrey Holland, Michelle Brasure, Kathleen N Lohr, Elizabeth Harden,[...]. Evid Rep Technol Assess (Full Rep) 2011
270
18

The impact of the format of graphical presentation on health-related knowledge and treatment choices.
Sarah T Hawley, Brian Zikmund-Fisher, Peter Ubel, Aleksandra Jancovic, Todd Lucas, Angela Fagerlin. Patient Educ Couns 2008
181
18

The Impact of Patient Participation in Health Decisions Within Medical Encounters: A Systematic Review.
Marla L Clayman, Carma L Bylund, Betty Chewning, Gregory Makoul. Med Decis Making 2016
36
18

Characterizing genetic variants for clinical action.
Erin M Ramos, Corina Din-Lovinescu, Jonathan S Berg, Lisa D Brooks, Audrey Duncanson, Michael Dunn, Peter Good, Tim J P Hubbard, Gail P Jarvik, Christopher O'Donnell,[...]. Am J Med Genet C Semin Med Genet 2014
30
18

Comprehensive Characterization of Molecular Differences in Cancer between Male and Female Patients.
Yuan Yuan, Lingxiang Liu, Hu Chen, Yumeng Wang, Yanxun Xu, Huzhang Mao, Jun Li, Gordon B Mills, Yongqian Shu, Liang Li,[...]. Cancer Cell 2016
75
18

Effect of various risk/benefit trade-offs on parents' understanding of a pediatric research study.
Alan R Tait, Brian J Zikmund-Fisher, Angela Fagerlin, Terri Voepel-Lewis. Pediatrics 2010
14
18

Genomic Alterations in Cell-Free DNA and Enzalutamide Resistance in Castration-Resistant Prostate Cancer.
Alexander W Wyatt, Arun A Azad, Stanislav V Volik, Matti Annala, Kevin Beja, Brian McConeghy, Anne Haegert, Evan W Warner, Fan Mo, Sonal Brahmbhatt,[...]. JAMA Oncol 2016
144
18

A framework for genomic biomarker actionability and its use in clinical decision making.
Smruti J Vidwans, Michelle L Turski, Filip Janku, Ignacio Garrido-Laguna, Javier Munoz, Richard Schwab, Vivek Subbiah, Jordi Rodon, Razelle Kurzrock.  2014
18
18

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N. Engl. J. Med. 2014
308
18

Detection rate of actionable mutations in diverse cancers using a biopsy-free (blood) circulating tumor cell DNA assay.
Maria Schwaederle, Hatim Husain, Paul T Fanta, David E Piccioni, Santosh Kesari, Richard B Schwab, Kimberly C Banks, Richard B Lanman, AmirAli Talasaz, Barbara A Parker,[...]. Oncotarget 2016
70
18

From days to hours: reporting clinically actionable variants from whole genome sequencing.
Sumit Middha, Saurabh Baheti, Steven N Hart, Jean-Pierre A Kocher. PLoS ONE 2014
3
66


Exome Sequencing of Cell-Free DNA from Metastatic Cancer Patients Identifies Clinically Actionable Mutations Distinct from Primary Disease.
Timothy M Butler, Katherine Johnson-Camacho, Myron Peto, Nicholas J Wang, Tara A Macey, James E Korkola, Theresa M Koppie, Christopher L Corless, Joe W Gray, Paul T Spellman. PLoS ONE 2015
59
18

Development and validation of the JAX Cancer Treatment Profile™ for detection of clinically actionable mutations in solid tumors.
Guruprasad Ananda, Susan Mockus, Micaela Lundquist, Vanessa Spotlow, Al Simons, Talia Mitchell, Grace Stafford, Vivek Philip, Timothy Stearns, Anuj Srivastava,[...]. Exp. Mol. Pathol. 2015
22
18


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.