A citation-based method for searching scientific literature

Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Times Cited: 57







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



Times Cited
  Times     Co-cited
Similarity


Return of research results from genomic biobanks: cost matters.
Marianna J Bledsoe, Ellen Wright Clayton, Amy L McGuire, William E Grizzle, P Pearl O'Rourke, Nikolajs Zeps. Genet Med 2013
41
2


Use of SNP chips to detect rare pathogenic variants: retrospective, population based diagnostic evaluation.
Weedon Mn, Jackson L, Harrison Jw, Ruth Ks, Tyrrell J, Hattersley At, Wright Cf. BMJ 2021
6
16

Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting.
Caroline F Wright, Ben West, Marcus Tuke, Samuel E Jones, Kashyap Patel, Thomas W Laver, Robin N Beaumont, Jessica Tyrrell, Andrew R Wood, Timothy M Frayling,[...]. Am J Hum Genet 2019
64
1

Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
Eden V Haverfield, Edward D Esplin, Sienna J Aguilar, Kathryn E Hatchell, Kelly E Ormond, Andrea Hanson-Kahn, Paldeep S Atwal, Sarah Macklin-Mantia, Stephanie Hines, Caron W-M Sak,[...]. BMC Med 2021
2
50

Preferences for Return of Genetic Results Among Participants in the Jackson Heart Study and Framingham Heart Study.
Steven Joffe, Deborah E Sellers, Lynette Ekunwe, Donna Antoine-Lavigne, Sarah McGraw, Daniel Levy, Greta Lee Splansky. Circ Genom Precis Med 2019
6
16

Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group.
Elizabeth M Webber, Jessica Ezzell Hunter, Leslie G Biesecker, Adam H Buchanan, Elizabeth V Clarke, Erin Currey, Orit Dagan-Rosenfeld, Kristy Lee, Noralane M Lindor, Christa Lese Martin,[...]. Hum Mutat 2018
16
6

Precision Population Medicine in Primary Care: The Sanford Chip Experience.
Kurt D Christensen, Megan Bell, Carrie L B Zawatsky, Lauren N Galbraith, Robert C Green, Allison M Hutchinson, Leila Jamal, Jessica L LeBlanc, Jennifer R Leonhard, Michelle Moore,[...]. Front Genet 2021
5
20

Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel.
Amy C Sturm, Joshua W Knowles, Samuel S Gidding, Zahid S Ahmad, Catherine D Ahmed, Christie M Ballantyne, Seth J Baum, Mafalda Bourbon, Alain Carri√©, Marina Cuchel,[...]. J Am Coll Cardiol 2018
171
1

The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testing.
Samuel J Aronson, Eugene H Clark, Lawrence J Babb, Samantha Baxter, Lisa M Farwell, Birgit H Funke, Amy Lovelette Hernandez, Victoria A Joshi, Elaine Lyon, Andrew R Parthum,[...]. Hum Mutat 2011
56
1

A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal Method in Clinical Genetic Testing.
Stephen E Lincoln, Rebecca Truty, Chiao-Feng Lin, Justin M Zook, Joshua Paul, Vincent H Ramey, Marc Salit, Heidi L Rehm, Robert L Nussbaum, Matthew S Lebo. J Mol Diagn 2019
19
5

Return of results: ethical and legal distinctions between research and clinical care.
Wylie Burke, Barbara J Evans, Gail P Jarvik. Am J Med Genet C Semin Med Genet 2014
72
1

An international policy on returning genomic research results.
Anna C F Lewis, Bartha Maria Knoppers, Robert C Green. Genome Med 2021
3
33


Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
241
1



Genetic Counseling for Neurofibromatosis 1, Neurofibromatosis 2, and Schwannomatosis-Practice Resource of the National Society of Genetic Counselors.
Heather B Radtke, Amanda L Bergner, Allison L Goetsch, Caroline McGowan, Karin Panzer, Ashley Cannon. J Genet Couns 2020
4
25

Informed Consent and the Reasonable-Patient Standard.
Barry G Main, Angus McNair, Jane M Blazeby. JAMA 2016
4
25

Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor, Kim L McBride, Ana Morales, Matthew R G Taylor, Matteo Vatta, Stephanie M Ware. J Card Fail 2018
128
1

Research guidelines for the Delphi survey technique.
F Hasson, S Keeney, H McKenna. J Adv Nurs 2000
1


Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the national society of genetic counselors.
Brenda Finucane, Liane Abrams, Amy Cronister, Alison D Archibald, Robin L Bennett, Allyn McConkie-Rosell. J Genet Couns 2012
37
2

Information Mismatch: Cancer Risk Counseling with Diverse Underserved Patients.
Galen Joseph, Rena J Pasick, Dean Schillinger, Judith Luce, Claudia Guerra, Janice Ka Yan Cheng. J Genet Couns 2017
58
1

Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association.
Kiran Musunuru, Ray E Hershberger, Sharlene M Day, N Jennifer Klinedinst, Andrew P Landstrom, Victoria N Parikh, Siddharth Prakash, Christopher Semsarian, Amy C Sturm. Circ Genom Precis Med 2020
45
2

Application of a framework to guide genetic testing communication across clinical indications.
Miranda L G Hallquist, Eric P Tricou, Kelly E Ormond, Juliann M Savatt, Curtis R Coughlin, W Andrew Faucett, Laura Hercher, Howard P Levy, Julianne M O'Daniel, Holly L Peay,[...]. Genome Med 2021
2
50

Shortened consent forms for genome-wide sequencing: Parent and provider perspectives.
Emma C Hitchcock, Causes Study, Alison M Elliott. Mol Genet Genomic Med 2020
4
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.