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: 14







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



Times Cited
  Times     Co-cited
Similarity


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
21

Real-world integration of genomic data into the electronic health record: the PennChart Genomics Initiative.
Kelsey S Lau-Min, Stephanie Byers Asher, Jessica Chen, Susan M Domchek, Michael Feldman, Steven Joffe, Jeffrey Landgraf, Virginia Speare, Lisa A Varughese, Sony Tuteja,[...]. Genet Med 2021
8
37


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
58
14

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
111
14

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
331
14

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
956
14

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
47
14


Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service.
Irena Vrečar, Dimitar Hristovski, Borut Peterlin. J Med Syst 2017
34
14

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
68
14

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
200
14

FHIR Genomics: enabling standardization for precision medicine use cases.
Gil Alterovitz, Bret Heale, James Jones, David Kreda, Fan Lin, Lei Liu, Xin Liu, Kenneth D Mandl, David W Poloway, Rachel Ramoni,[...]. NPJ Genom Med 2020
14
14

SMART on FHIR Genomics: facilitating standardized clinico-genomic apps.
Gil Alterovitz, Jeremy Warner, Peijin Zhang, Yishen Chen, Mollie Ullman-Cullere, David Kreda, Isaac S Kohane. J Am Med Inform Assoc 2015
68
14

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland,[...]. Genet Med 2020
328
14

The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.
Carol R Horowitz, Lori A Orlando, Anne M Slavotinek, Josh Peterson, Frank Angelo, Barbara Biesecker, Vence L Bonham, Linda D Cameron, Stephanie M Fullerton, Bruce D Gelb,[...]. Am J Hum Genet 2019
20
14

Strategic vision for improving human health at The Forefront of Genomics.
Eric D Green, Chris Gunter, Leslie G Biesecker, Valentina Di Francesco, Carla L Easter, Elise A Feingold, Adam L Felsenfeld, David J Kaufman, Elaine A Ostrander, William J Pavan,[...]. Nature 2020
78
14

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
48
7

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
82
7

Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.
Lainie Friedman Ross, Ellen Wright Clayton. Pediatrics 2019
19
7


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
7
14


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
16
7

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
14
7

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
41
7

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
8
12

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
41
7

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
9
11

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
84
7

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
23
7

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
15
7

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
6
16


Parents' interest in whole-genome sequencing of newborns.
Aaron J Goldenberg, Daniel S Dodson, Matthew M Davis, Beth A Tarini. Genet Med 2014
58
7


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
54
7


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
36
7



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
89
7

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
8
12

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
8
12

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
23
7

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
14
7

Genetic Testing to Guide Risk-Stratified Screens for Breast Cancer.
Ava Willoughby, Paul R Andreassen, Amanda Ewart Toland. J Pers Med 2019
14
7

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
239
7

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
14
7


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.