A citation-based method for searching scientific literature

Theresa A Grebe, George Khushf, Margaret Chen, Dawn Bailey, Leslie Manace Brenman, Marc S Williams, Laurie H Seaver. Genet Med 2020
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Clinical genomics in the world of the electronic health record.
Keith Marsolo, S Andrew Spooner. Genet Med 2013
22
30

Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG).
Joshua L Deignan, Wendy K Chung, Hutton M Kearney, Kristin G Monaghan, Catherine W Rehder, Elizabeth C Chao. Genet Med 2019
42
20

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
20

The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
178
20

Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG).
Karen L David, Robert G Best, Leslie Manace Brenman, Lynn Bush, Joshua L Deignan, David Flannery, Jodi D Hoffman, Ingrid Holm, David T Miller, James O'Leary,[...]. Genet Med 2019
45
20

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
20

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
33
20

Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service.
Irena Vrečar, Dimitar Hristovski, Borut Peterlin. J Med Syst 2017
27
20

Integrating cancer genomic data into electronic health records.
Jeremy L Warner, Sandeep K Jain, Mia A Levy. Genome Med 2016
30
20

The genome-enabled electronic medical record.
M A Hoffman. J Biomed Inform 2007
50
20

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
20

An overview of clinical decision support systems: benefits, risks, and strategies for success.
Reed T Sutton, David Pincock, Daniel C Baumgart, Daniel C Sadowski, Richard N Fedorak, Karen I Kroeker. NPJ Digit Med 2020
39
20

An overview of clinical decision support systems: benefits, risks, and strategies for success.
Reed T Sutton, David Pincock, Daniel C Baumgart, Daniel C Sadowski, Richard N Fedorak, Karen I Kroeker. NPJ Digit Med 2020
88
20

Telehealth as a Bright Spot of the COVID-19 Pandemic: Recommendations From the Virtual Frontlines ("Frontweb").
J Nwando Olayiwola, Candy Magaña, Ashley Harmon, Shalina Nair, Erica Esposito, Christine Harsh, L Arick Forrest, Randy Wexler. JMIR Public Health Surveill 2020
23
10

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.
Ozge Ceyhan-Birsoy, Jaclyn B Murry, Kalotina Machini, Matthew S Lebo, Timothy W Yu, Shawn Fayer, Casie A Genetti, Talia S Schwartz, Pankaj B Agrawal, Richard B Parad,[...]. Am J Hum Genet 2019
60
10


Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.
Lainie Friedman Ross, Ellen Wright Clayton. Pediatrics 2019
10
10


Awareness of family health history in a predominantly young adult population.
Sarina Madhavan, Emily Bullis, Rachel Myers, Chris J Zhou, Elise M Cai, Anu Sharma, Shreya Bhatia, Lori A Orlando, Susanne B Haga. PLoS One 2019
3
33


Improving Utilization of the Family History in the Electronic Health Record.
Kathleen T Hickey, Maria C Katapodi, Bernice Coleman, Karin Reuter-Rice, Angela R Starkweather. J Nurs Scholarsh 2017
12
10

Comparing Outcomes of Genetic Counseling Options in Breast and Ovarian Cancer: An Integrative Review
.
Danielle M Fournier, Angela F Bazzell, Joyce E Dains. Oncol Nurs Forum 2018
13
10

Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer.
Jeanna M McCuaig, Susan Randall Armel, Melanie Care, Alexandra Volenik, Raymond H Kim, Kelly A Metcalfe. Cancers (Basel) 2018
32
10

Impact of patient education videos on genetic counseling outcomes after exome sequencing.
Rebecca Hernan, Megan T Cho, Ashley L Wilson, Priyanka Ahimaz, Catherine Au, Sara M Berger, Edwin Guzman, Michelle Primiano, Jessica E Shaw, Meredith Ross,[...]. Patient Educ Couns 2020
6
16

Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies.
Josephine Johnston, John D Lantos, Aaron Goldenberg, Flavia Chen, Erik Parens, Barbara A Koenig. Hastings Cent Rep 2018
33
10

Genetics professionals' opinions of whole-genome sequencing in the newborn period.
Elizabeth Ulm, W Gregory Feero, Richard Dineen, Joel Charrow, Catherine Wicklund. J Genet Couns 2015
8
12

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
39
10

Genetics workforce: distribution of genetics services and challenges to health care in California.
Monica Penon-Portmann, Jiyoo Chang, Mira Cheng, Joseph T Shieh. Genet Med 2020
14
10

Assessment of primary care practitioners' attitudes and interest in pharmacogenomic testing.
D Max Smith, Tarlan Namvar, Ryan P Brown, T Blaise Springfield, Beth N Peshkin, Richard J Walsh, James C Welsh, Bonnie Levin, Nicole Brandt, Sandra M Swain. Pharmacogenomics 2020
7
14

Patient experience with family history tool: analysis of patients' experience sharing their family health history through patient-computer dialogue in a patient portal.
Adarsha S Bajracharya, Bradley H Crotty, Hollis B Kowoloff, Charles Safran, Warner V Slack. J Am Med Inform Assoc 2019
3
33


Parents' interest in whole-genome sequencing of newborns.
Aaron J Goldenberg, Daniel S Dodson, Matthew M Davis, Beth A Tarini. Genet Med 2014
55
10


Developing knowledge resources to support precision medicine: principles from the Clinical Pharmacogenetics Implementation Consortium (CPIC).
James M Hoffman, Henry M Dunnenberger, J Kevin Hicks, Kelly E Caudle, Michelle Whirl Carrillo, Robert R Freimuth, Marc S Williams, Teri E Klein, Josh F Peterson. J Am Med Inform Assoc 2016
50
10


CYP450 genotyping and cumulative drug-gene interactions: an update for precision medicine.
Ranjit K Thirumaran, Jarrod W Heck, Brian T Hocum. Per Med 2016
5
20

Practical considerations in genomic decision support: The eMERGE experience.
Timothy M Herr, Suzette J Bielinski, Erwin Bottinger, Ariel Brautbar, Murray Brilliant, Christopher G Chute, Beth L Cobb, Joshua C Denny, Hakon Hakonarson, Andrea L Hartzler,[...]. J Pathol Inform 2015
31
10



Consensus Guidelines on Genetic` Testing for Hereditary Breast Cancer from the American Society of Breast Surgeons.
Eric R Manahan, Henry M Kuerer, Molly Sebastian, Kevin S Hughes, Judy C Boughey, David M Euhus, Susan K Boolbol, Walton A Taylor. Ann Surg Oncol 2019
53
10

Primary care physician experiences utilizing a family health history tool with electronic health record-integrated clinical decision support: an implementation process assessment.
Amy A Lemke, Jennifer Thompson, Peter J Hulick, Annette W Sereika, Christian Johnson, Lauren Oshman, Henry M Dunnenberger. J Community Genet 2020
6
16

A comparison of genome cohort participants' genetic knowledge and preferences to receive genetic results before and after a genetics workshop.
Kayono Yamamoto, Atsushi Shimizu, Fumie Aizawa, Hiroshi Kawame, Tomoharu Tokutomi, Akimune Fukushima. J Hum Genet 2018
7
14

An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening.
Laura V Milko, Julianne M O'Daniel, Daniela M DeCristo, Stephanie B Crowley, Ann Katherine M Foreman, Kathleen E Wallace, Lonna F Mollison, Natasha T Strande, Zahra S Girnary, Lacey J Boshe,[...]. J Pediatr 2019
15
10

Genetic counseling service delivery models: A study of genetic counselors' interests, needs, and barriers to implementation.
Emily Boothe, Samantha Greenberg, Christine L Delaney, Stephanie A Cohen. J Genet Couns 2021
4
25

Genetic Testing to Guide Risk-Stratified Screens for Breast Cancer.
Ava Willoughby, Paul R Andreassen, Amanda Ewart Toland. J Pers Med 2019
12
10

Reconsidering the family history in primary care.
Eugene C Rich, Wylie Burke, Caryl J Heaton, Susanne Haga, Linda Pinsky, M Priscilla Short, Louise Acheson. J Gen Intern Med 2004
226
10

Expansion of genetic services utilizing a general genetic counseling clinic.
V L Hannig, M P Cohen, J P Pfotenhauer, M D Williams, T M Morgan, J A Phillips. J Genet Couns 2014
13
10

Changing trends in carrier screening for genetic disease in the United States.
Shivani B Nazareth, Gabriel A Lazarin, James D Goldberg. Prenat Diagn 2015
45
10




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.