A citation-based method for searching scientific literature

Catharine Wang, Tiernan J Cahill, Andrew Parlato, Blake Wertz, Qiankun Zhong, Tricia Norkunas Cunningham, James J Cummings. Mol Genet Genomic Med 2018
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity


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
111
50

Third party interpretation of raw genetic data: an ethical exploration.
Lauren Badalato, Louiza Kalokairinou, Pascal Borry. Eur J Hum Genet 2017
31
45

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
36

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
27

Internet-Based Direct-to-Consumer Genetic Testing: A Systematic Review.
Loredana Covolo, Sara Rubinelli, Elisabetta Ceretti, Umberto Gelatti. J Med Internet Res 2015
58
27

The impact of raw DNA availability and corresponding online interpretation services: A mixed-methods study.
Caitlin G Allen, Jazmine Gabriel, Maureen Flynn, Tricia N Cunningham, Catharine Wang. Transl Behav Med 2018
15
33


Direct-to-consumer raw genetic data and third-party interpretation services: more burden than bargain?
Tia Moscarello, Brittney Murray, Chloe M Reuter, Erin Demo. Genet Med 2019
20
25

Effect of direct-to-consumer genomewide profiling to assess disease risk.
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011
345
22

Ancestry Testing and the Practice of Genetic Counseling.
Brianne E Kirkpatrick, Misha D Rashkin. J Genet Couns 2017
19
21

Genealogy databases and the future of criminal investigation.
Natalie Ram, Christi J Guerrini, Amy L McGuire. Science 2018
30
18

APPLaUD: access for patients and participants to individual level uninterpreted genomic data.
Adrian Thorogood, Jason Bobe, Barbara Prainsack, Anna Middleton, Erick Scott, Sarah Nelson, Manuel Corpas, Natasha Bonhomme, Laura Lyman Rodriguez, Madeleine Murtagh,[...]. Hum Genomics 2018
29
18

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
814
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
231
18

Utilization of Genetic Counseling after Direct-to-Consumer Genetic Testing: Findings from the Impact of Personal Genomics (PGen) Study.
Diane R Koeller, Wendy R Uhlmann, Deanna Alexis Carere, Robert C Green, J Scott Roberts. J Genet Couns 2017
20
20

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
18

The dawn of consumer-directed testing.
Erica Ramos, Scott M Weissman. Am J Med Genet C Semin Med Genet 2018
27
18


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
18

Physicians' perspectives on receiving unsolicited genomic results.
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
26
18

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
47
18

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
18

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
21

An exploration of genetic health professionals' experience with direct-to-consumer genetic testing in their clinical practice.
Gemma R Brett, Sylvia A Metcalfe, David J Amor, Jane L Halliday. Eur J Hum Genet 2012
36
13

Behavioural changes, sharing behaviour and psychological responses after receiving direct-to-consumer genetic test results: a systematic review and meta-analysis.
Kelly F J Stewart, Anke Wesselius, Maartje A C Schreurs, Annemie M W J Schols, Maurice P Zeegers. J Community Genet 2018
32
13


The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
100
13


The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
388
13

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
13


Third-Party Genetic Interpretation Tools: A Mixed-Methods Study of Consumer Motivation and Behavior.
Sarah C Nelson, Deborah J Bowen, Stephanie M Fullerton. Am J Hum Genet 2019
14
21

Characteristics of users of online personalized genomic risk assessments: implications for physician-patient interactions.
Colleen M McBride, Sharon Hensley Alford, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2009
87
13

Physician Experience with Direct-To-Consumer Genetic Testing in Kaiser Permanente.
M Cabell Jonas, Pim Suwannarat, Andrea Burnett-Hartman, Nikki Carroll, Michelle Turner, Kristen Janes, Christine Truong, Erica Blum-Barnett, Nazneen Aziz, Elizabeth A McGlynn. J Pers Med 2019
6
50

Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing.
David J Kaufman, Juli M Bollinger, Rachel L Dvoskin, Joan A Scott. J Genet Couns 2012
112
9

Tilting at windmills no longer: a data-driven discussion of DTC DNA ancestry tests.
Jennifer K Wagner, Jill D Cooper, Rene Sterling, Charmaine D Royal. Genet Med 2012
22
9

openSNP--a crowdsourced web resource for personal genomics.
Bastian Greshake, Philipp E Bayer, Helge Rausch, Julia Reda. PLoS One 2014
30
9

Educational needs of primary care physicians regarding direct-to-consumer genetic testing.
Karen P Powell, Carol A Christianson, Whitney A Cogswell, Gaurav Dave, Amit Verma, Sonja Eubanks, Vincent C Henrich. J Genet Couns 2012
39
9


Primary care physicians' awareness, experience and opinions of direct-to-consumer genetic testing.
Karen P Powell, Whitney A Cogswell, Carol A Christianson, Gaurav Dave, Amit Verma, Sonja Eubanks, Vincent C Henrich. J Genet Couns 2012
64
9

Information access. Raw personal data: providing access.
Jeantine E Lunshof, George M Church, Barbara Prainsack. Science 2014
34
9

ClinVar: public archive of interpretations of clinically relevant variants.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Jeffrey Hoover,[...]. Nucleic Acids Res 2016
9

GINA, genetic discrimination, and genomic medicine.
Robert C Green, Denise Lautenbach, Amy L McGuire. N Engl J Med 2015
97
9

Patients' understanding of and responses to multiplex genetic susceptibility test results.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Robert Reid, Eric Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2012
86
9

Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group.
Stacy W Gray, Yolanda Martins, Lindsay Z Feuerman, Barbara A Bernhardt, Barbara B Biesecker, Kurt D Christensen, Steven Joffe, Christine Rini, David Veenstra, Amy L McGuire. Genet Med 2014
45
9

Direct-to-consumer genetic testing: an assessment of genetic counselors' knowledge and beliefs.
Kathryn T Hock, Kurt D Christensen, Beverly M Yashar, J Scott Roberts, Sarah E Gollust, Wendy R Uhlmann. Genet Med 2011
43
9

Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years.
Michael D Linderman, Saskia C Sanderson, Ali Bashir, George A Diaz, Andrew Kasarskis, Randi Zinberg, Milind Mahajan, Sabrina A Suckiel, Micol Zweig, Eric E Schadt. BMC Med Genomics 2018
10
20

Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine.
Keyan Salari, Konrad J Karczewski, Louanne Hudgins, Kelly E Ormond. PLoS One 2013
59
9

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
74
9

Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
80
9


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.