A citation-based method for searching scientific literature

Douglas B Pet, Ingrid A Holm, Janet L Williams, Melanie F Myers, Laurie L Novak, Kyle B Brothers, Georgia L Wiesner, Ellen W Clayton. Genet Med 2019
Times Cited: 26







List of co-cited articles
79 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
831
30

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
23

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
19


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
238
19

Consumer use and response to online third-party raw DNA interpretation services.
Catharine Wang, Tiernan J Cahill, Andrew Parlato, Blake Wertz, Qiankun Zhong, Tricia Norkunas Cunningham, James J Cummings. Mol Genet Genomic Med 2018
22
18

Gatekeepers or intermediaries? The role of clinicians in commercial genomic testing.
Michelle L McGowan, Jennifer R Fishman, Richard A Settersten, Marcie A Lambrix, Eric T Juengst. PLoS One 2014
23
13


Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018
119
11

Consumer Perceptions of Interactions With Primary Care Providers After Direct-to-Consumer Personal Genomic Testing.
Cathelijne H van der Wouden, Deanna Alexis Carere, Anke H Maitland-van der Zee, Mack T Ruffin, J Scott Roberts, Robert C Green. Ann Intern Med 2016
66
11

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
235
11

Direct-to-Consumer Testing 2.0: Emerging Models of Direct-to-Consumer Genetic Testing.
Megan A Allyse, David H Robinson, Matthew J Ferber, Richard R Sharp. Mayo Clin Proc 2018
55
11

ClinGen--the Clinical Genome Resource.
Heidi L Rehm, Jonathan S Berg, Lisa D Brooks, Carlos D Bustamante, James P Evans, Melissa J Landrum, David H Ledbetter, Donna R Maglott, Christa Lese Martin, Robert L Nussbaum,[...]. N Engl J Med 2015
502
11

Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.
Kurt D Christensen, Barbara A Bernhardt, Gail P Jarvik, Lucia A Hindorff, Jeffrey Ou, Sawona Biswas, Bradford C Powell, Robert W Grundmeier, Kalotina Machini, Dean J Karavite,[...]. Genet Med 2018
8
37

"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project.
Elizabeth Ormondroyd, Michael P Mackley, Edward Blair, Judith Craft, Julian C Knight, Jenny C Taylor, John Taylor, Hugh Watkins. Genet Med 2018
32
11

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
34
11

Are physicians prepared for whole genome sequencing? a qualitative analysis.
K D Christensen, J L Vassy, L Jamal, L S Lehmann, M J Slashinski, D L Perry, J O Robinson, J Blumenthal-Barby, L Z Feuerman, M F Murray,[...]. Clin Genet 2016
76
11

Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, Randi Zinberg, Melissa Wasserstein, Andrew Kasarskis, George A Diaz, Eric E Schadt. Eur J Hum Genet 2017
32
11

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Robert C Green, Katrina A B Goddard, Gail P Jarvik, Laura M Amendola, Paul S Appelbaum, Jonathan S Berg, Barbara A Bernhardt, Leslie G Biesecker, Sawona Biswas, Carrie L Blout,[...]. Am J Hum Genet 2016
97
11

What Results Should Be Returned from Opportunistic Screening in Translational Research?
Colin Me Halverson, Sarah H Jones, Laurie Novak, Christopher Simpson, Digna R Velez Edwards, Sifang Kathy Zhao, Ellen W Clayton. J Pers Med 2020
4
75

Patient and provider perspectives on the development of personalized medicine: a mixed-methods approach.
Lauren Puryear, Natalie Downs, Andrea Nevedal, Eleanor T Lewis, Kelly E Ormond, Maria Bregendahl, Carlos J Suarez, Sean P David, Steven Charlap, Isabella Chu,[...]. J Community Genet 2018
9
22

A systematic review of interventions to provide genetics education for primary care.
Milena Paneque, Daniela Turchetti, Leigh Jackson, Peter Lunt, Elisa Houwink, Heather Skirton. BMC Fam Pract 2016
40
7

Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.
Barbara B Biesecker, Katie L Lewis, Kendall L Umstead, Jennifer J Johnston, Erin Turbitt, Kristen P Fishler, John H Patton, Ilana M Miller, Alexis R Heidlebaugh, Leslie G Biesecker. JAMA Intern Med 2018
46
7

Primary care providers' cancer genetic testing-related knowledge, attitudes, and communication behaviors: A systematic review and research agenda.
Jada G Hamilton, Ekland Abdiwahab, Heather M Edwards, Min-Lin Fang, Andrew Jdayani, Erica S Breslau. J Gen Intern Med 2017
48
7

Physician preparedness for big genomic data: a review of genomic medicine education initiatives in the United States.
Caryn Kseniya Rubanovich, Cynthia Cheung, Jess Mandel, Cinnamon S Bloss. Hum Mol Genet 2018
39
7

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
24
8

Primary care providers' experiences with and perceptions of personalized genomic medicine.
June C Carroll, Tutsirai Makuwaza, Donna P Manca, Nicolette Sopcak, Joanne A Permaul, Mary Ann O'Brien, Ruth Heisey, Elizabeth A Eisenhauer, Julie Easley, Monika K Krzyzanowska,[...]. Can Fam Physician 2016
50
7

Internet-Based Direct-to-Consumer Genetic Testing: A Systematic Review.
Loredana Covolo, Sara Rubinelli, Elisabetta Ceretti, Umberto Gelatti. J Med Internet Res 2015
60
7

Primary care providers' lived experiences of genetics in practice.
Brittany Harding, Colleen Webber, Lucia Ruhland, Nancy Dalgarno, Christine M Armour, Richard Birtwhistle, Glenn Brown, June C Carroll, Michael Flavin, Susan Phillips,[...]. J Community Genet 2019
14
14

The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group.
Steven M Teutsch, Linda A Bradley, Glenn E Palomaki, James E Haddow, Margaret Piper, Ned Calonge, W David Dotson, Michael P Douglas, Alfred O Berg. Genet Med 2009
464
7

Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results.
J Scott Roberts, Michele C Gornick, Deanna Alexis Carere, Wendy R Uhlmann, Mack T Ruffin, Robert C Green. Public Health Genomics 2017
57
7

Prescription medication changes following direct-to-consumer personal genomic testing: findings from the Impact of Personal Genomics (PGen) Study.
Deanna Alexis Carere, Tyler J VanderWeele, Jason L Vassy, Cathelijne H van der Wouden, J Scott Roberts, Peter Kraft, Robert C Green. Genet Med 2017
19
10

Impact of a randomized controlled educational trial to improve physician practice behaviors around screening for inherited breast cancer.
Robert A Bell, Haley McDermott, Tonya L Fancher, Michael J Green, Frank C Day, Michael S Wilkes. J Gen Intern Med 2015
21
9

False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care.
Stephany Tandy-Connor, Jenna Guiltinan, Kate Krempely, Holly LaDuca, Patrick Reineke, Stephanie Gutierrez, Phillip Gray, Brigette Tippin Davis. Genet Med 2018
113
7

Prototype of a Standards-Based EHR and Genetic Test Reporting Tool Coupled with HL7-Compliant Infobuttons.
Jacob K Crump, Guilherme Del Fiol, Marc S Williams, Robert R Freimuth. AMIA Jt Summits Transl Sci Proc 2018
6
33

Third party interpretation of raw genetic data: an ethical exploration.
Lauren Badalato, Louiza Kalokairinou, Pascal Borry. Eur J Hum Genet 2017
31
7

Genomic education for the next generation of health-care providers.
MaryAnn Campion, Constance Goldgar, Robert J Hopkin, Cynthia A Prows, Shoumita Dasgupta. Genet Med 2019
26
7


Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017
71
7

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J Med Genet 2015
118
7

Practical considerations for implementing genomic information resources. Experiences from eMERGE and CSER.
Luke V Rasmussen, Casey L Overby, John Connolly, Christopher G Chute, Joshua C Denny, Robert Freimuth, Andrea L Hartzler, Ingrid A Holm, Shannon Manzi, Jyotishman Pathak,[...]. Appl Clin Inform 2016
17
11

Opportunities for genomic clinical decision support interventions.
Casey Lynnette Overby, Isaac Kohane, Joseph L Kannry, Marc S Williams, Justin Starren, Erwin Bottinger, Omri Gottesman, Joshua C Denny, Chunhua Weng, Peter Tarczy-Hornoch,[...]. Genet Med 2013
44
7

Crossing the omic chasm: a time for omic ancillary systems.
Justin Starren, Marc S Williams, Erwin P Bottinger. JAMA 2013
53
7

Return of results in the genomic medicine projects of the eMERGE network.
Iftikhar J Kullo, Ra'ad Haddad, Cynthia A Prows, Ingrid Holm, Saskia C Sanderson, Nanibaa' A Garrison, Richard R Sharp, Maureen E Smith, Helena Kuivaniemi, Erwin P Bottinger,[...]. Front Genet 2014
31
7

Technical desiderata for the integration of genomic data into Electronic Health Records.
Daniel R Masys, Gail P Jarvik, Neil F Abernethy, Nicholas R Anderson, George J Papanicolaou, Dina N Paltoo, Mark A Hoffman, Isaac S Kohane, Howard P Levy. J Biomed Inform 2012
66
7

Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
463
7

Public perspectives on returning genetics and genomics research results.
J O'Daniel, S B Haga. Public Health Genomics 2011
55
7

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
49
7

Race, Genomics and Chronic Disease: What Patients with African Ancestry Have to Say.
Carol R Horowitz, Kadija Ferryman, Rennie Negron, Tatiana Sabin, Mayra Rodriguez, Randi F Zinberg, Erwin Böttinger, Mimsie Robinson. J Health Care Poor Underserved 2017
17
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.