A citation-based method for searching scientific literature

Kelly M East, Meagan Cochran, Whitley V Kelley, Veronica Greve, Kristina Emmerson, Grace Raines, Jesse Nicholas Cochran, Adam M Hott, David Bick. J Genet Couns 2019
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity



Clinical outcomes of a genomic screening program for actionable genetic conditions.
Adam H Buchanan, H Lester Kirchner, Marci L B Schwartz, Melissa A Kelly, Tara Schmidlen, Laney K Jones, Miranda L G Hallquist, Heather Rocha, Megan Betts, Rachel Schwiter,[...]. Genet Med 2020
7
100

Patient assessment of chatbots for the scalable delivery of genetic counseling.
Tara Schmidlen, Marci Schwartz, Kristy DiLoreto, H Lester Kirchner, Amy C Sturm. J Genet Couns 2019
25
100


Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria.
Frank I Marcus, William J McKenna, Duane Sherrill, Cristina Basso, Barbara Bauce, David A Bluemke, Hugh Calkins, Domenico Corrado, Moniek G P J Cox, James P Daubert,[...]. Eur Heart J 2010
648
100

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
Sara L Van Driest, Quinn S Wells, Sarah Stallings, William S Bush, Adam Gordon, Deborah A Nickerson, Jerry H Kim, David R Crosslin, Gail P Jarvik, David S Carrell,[...]. JAMA 2016
100
100

Design and Reporting Considerations for Genetic Screening Tests.
Jill Hagenkord, Birgit Funke, Emily Qian, Madhuri Hegde, Kevin B Jacobs, Matthew Ferber, Matthew Lebo, Adam Buchanan, David Bick. J Mol Diagn 2020
3
100

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation.
Jessica Ezzell Hunter, Stephanie A Irving, Leslie G Biesecker, Adam Buchanan, Brian Jensen, Kristy Lee, Christa Lese Martin, Laura Milko, Kristin Muessig, Annie D Niehaus,[...]. Genet Med 2016
51
100

2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines.
Scott M Grundy, Neil J Stone, Alison L Bailey, Craig Beam, Kim K Birtcher, Roger S Blumenthal, Lynne T Braun, Sarah de Ferranti, Joseph Faiella-Tommasino, Daniel E Forman,[...]. J Am Coll Cardiol 2019
552
100

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
720
100

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, D'Andra M Lindbuchler, Miranda L G Hallquist, Kandamurugu Manickam, Adam H Buchanan, Alanna Kulchak Rahm, Monica A Giovanni, Lauren Frisbie,[...]. Am J Hum Genet 2018
50
100


Teaching genomic counseling: preparing the genetic counseling workforce for the genomic era.
Gillian W Hooker, Kelly E Ormond, Kevin Sweet, Barbara B Biesecker. J Genet Couns 2014
41
100

Managing Secondary Genomic Findings Associated With Arrhythmogenic Right Ventricular Cardiomyopathy: Case Studies and Proposal for Clinical Surveillance.
Christopher M Haggerty, Brittney Murray, Crystal Tichnell, Daniel P Judge, Harikrishna Tandri, Marci Schwartz, Amy C Sturm, Martin E Matsumura, Michael F Murray, Hugh Calkins,[...]. Circ Genom Precis Med 2018
5
100

Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing: Elective Genomic Testing.
James T Lu, Matthew Ferber, Jill Hagenkord, Elissa Levin, Sarah South, Hyunseok P Kang, Kimberly A Strong, David P Bick. J Mol Diagn 2019
10
100

Management of Secondary Genomic Findings.
Alexander E Katz, Robert L Nussbaum, Benjamin D Solomon, Heidi L Rehm, Marc S Williams, Leslie G Biesecker. Am J Hum Genet 2020
3
100

Positive impact of genetic counseling assistants on genetic counseling efficiency, patient volume, and cost in a cancer genetics clinic.
Miranda L G Hallquist, Eric P Tricou, Michael N Hallquist, Juliann M Savatt, Heather Rocha, Alyson E Evans, Nicole Deckard, Yirui Hu, H Lester Kirchner, Josie Pervola,[...]. Genet Med 2020
3
100

Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
Kandamurugu Manickam, Adam H Buchanan, Marci L B Schwartz, Miranda L G Hallquist, Janet L Williams, Alanna Kulchak Rahm, Heather Rocha, Juliann M Savatt, Alyson E Evans, Loren M Butry,[...]. JAMA Netw Open 2018
70
100

Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria.
Robert Pilarski, Randall Burt, Wendy Kohlman, Lana Pho, Kristen M Shannon, Elizabeth Swisher. J Natl Cancer Inst 2013
203
100

Prevalence and Electronic Health Record-Based Phenotype of Loss-of-Function Genetic Variants in Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Genes.
Eric D Carruth, Wilson Young, Dominik Beer, Cynthia A James, Hugh Calkins, Linyuan Jing, Sushravya Raghunath, Dustin N Hartzel, Joseph B Leader, H Lester Kirchner,[...]. Circ Genom Precis Med 2019
7
100

Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society.
Børge G Nordestgaard, M John Chapman, Steve E Humphries, Henry N Ginsberg, Luis Masana, Olivier S Descamps, Olov Wiklund, Robert A Hegele, Frederick J Raal, Joep C Defesche,[...]. Eur Heart J 2013
100

Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
Francis M Giardiello, John I Allen, Jennifer E Axilbund, C Richard Boland, Carol A Burke, Randall W Burt, James M Church, Jason A Dominitz, David A Johnson, Tonya Kaltenbach,[...]. Am J Gastroenterol 2014
244
100

Should pretest genetic counselling be required for patients pursuing genomic sequencing? Results from a survey of participants in a large genomic implementation study.
Joel E Pacyna, Carmen Radecki Breitkopf, Sarah M Jenkins, Erica J Sutton, Caroline Horrow, Iftikhar J Kullo, Richard R Sharp. J Med Genet 2019
11
100

Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors.
Bronson D Riley, Julie O Culver, Cécile Skrzynia, Leigha A Senter, June A Peters, Josephine W Costalas, Faith Callif-Daley, Sherry C Grumet, Katherine S Hunt, Rebecca S Nagy,[...]. J Genet Couns 2012
177
100


Malignant Hyperthermia Susceptibility and Fitness for Duty.
Michael A Lee, Erin B McGlinch, Maria C McGlinch, John F Capacchione. Mil Med 2017
9
100

Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background.
Kelly E Ormond, Miranda L G Hallquist, Adam H Buchanan, Danielle Dondanville, Mildred K Cho, Maureen Smith, Myra Roche, Kyle B Brothers, Curtis R Coughlin, Laura Hercher,[...]. Genet Med 2019
20
100


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.