A citation-based method for searching scientific literature

Karina L Brierley, Erica Blouch, Whitney Cogswell, Jeanne P Homer, Debbie Pencarinha, Christine L Stanislaw, Ellen T Matloff. Cancer J 2012
Times Cited: 63







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



Times Cited
  Times     Co-cited
Similarity


A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?
Bernardo Dias Pereira, Tiago Nunes da Silva, Ana Teresa Bernardo, Rui César, Henrique Vara Luiz, Karel Pacak, Luísa Mota-Vieira. Int J Endocrinol 2018
6
16


Genetic testing in endocrine surgery: Opportunities for precision surgery.
Wilson Alobuia, Justin Annes, Electron Kebebew. Surgery 2020
3
33

Next-generation sequencing in the clinical genetic screening of patients with pheochromocytoma and paraganglioma.
Joakim Crona, Alberto Delgado Verdugo, Dan Granberg, Staffan Welin, Peter Stålberg, Per Hellman, Peyman Björklund. Endocr Connect 2013
35
2

When should genetic testing be performed in patients with neuroendocrine tumours?
Triona O'Shea, Maralyn Druce. Rev Endocr Metab Disord 2017
11
9


Bioinformatics for clinical next generation sequencing.
Gavin R Oliver, Steven N Hart, Eric W Klee. Clin Chem 2015
52
1

Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
Samuel A Wells, Sylvia L Asa, Henning Dralle, Rossella Elisei, Douglas B Evans, Robert F Gagel, Nancy Lee, Andreas Machens, Jeffrey F Moley, Furio Pacini,[...]. Thyroid 2015
733
1

Evaluation and comparison of multiple aligners for next-generation sequencing data analysis.
Jing Shang, Fei Zhu, Wanwipa Vongsangnak, Yifei Tang, Wenyu Zhang, Bairong Shen. Biomed Res Int 2014
27
3

ACMG clinical laboratory standards for next-generation sequencing.
Heidi L Rehm, Sherri J Bale, Pinar Bayrak-Toydemir, Jonathan S Berg, Kerry K Brown, Joshua L Deignan, Michael J Friez, Birgit H Funke, Madhuri R Hegde, Elaine Lyon. Genet Med 2013
522
1


Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunities.
Chiara Di Resta, Silvia Galbiati, Paola Carrera, Maurizio Ferrari. EJIFCC 2018
36
2

Genetics of Adrenocortical Development and Tumors.
Maya Lodish. Endocrinol Metab Clin North Am 2017
8
12


Yield and Utility of Germline Testing Following Tumor Sequencing in Patients With Cancer.
Stephen E Lincoln, Robert L Nussbaum, Allison W Kurian, Sarah M Nielsen, Kingshuk Das, Scott Michalski, Shan Yang, Nhu Ngo, Amie Blanco, Edward D Esplin. JAMA Netw Open 2020
2
50

Misconceptions About Genomics Among Nursing Faculty and Students.
Catherine Y Read, Linda D Ward. Nurse Educ 2018
3
33


Implementation of Germline Testing for Prostate Cancer: Philadelphia Prostate Cancer Consensus Conference 2019.
Veda N Giri, Karen E Knudsen, William K Kelly, Heather H Cheng, Kathleen A Cooney, Michael S Cookson, William Dahut, Scott Weissman, Howard R Soule, Daniel P Petrylak,[...]. J Clin Oncol 2020
34
2


Personalized medicine and genetic malpractice.
Gary E Marchant, Rachel A Lindor. Genet Med 2013
14
7


Telehealth technology: Reducing barriers for rural residents seeking genetic counseling.
Sarah Rhoads, Anna Laura Rakes. J Am Assoc Nurse Pract 2020
5
20

Challenges and Opportunities for Genomics Education: Insights from an Institute of Medicine Roundtable Activity.
Michael J Dougherty, Catherine Wicklund, Katherine A Johansen Taber. J Contin Educ Health Prof 2016
10
10


Illustrative case studies in the return of exome and genome sequencing results.
Laura M Amendola, Denise Lautenbach, Sarah Scollon, Barbara Bernhardt, Sawona Biswas, Kelly East, Jessica Everett, Marian J Gilmore, Patricia Himes, Victoria M Raymond,[...]. Per Med 2015
29
3

From helices to health: undergraduate medical education in genetics and genomics.
Katherine Hyland, Kathryn Garber, Shoumita Dasgupta. Per Med 2019
10
10

A toolkit for incorporating genetics into mainstream medical services: Learning from service development pilots in England.
Catherine L Bennett, Sarah E Burke, Hilary Burton, Peter A Farndon. BMC Health Serv Res 2010
17
5

Art and Challenges of Precision Medicine: Interpreting and Integrating Genomic Data Into Clinical Practice.
Subha Madhavan, Somasundaram Subramaniam, Thomas D Brown, James L Chen. Am Soc Clin Oncol Educ Book 2018
14
7


An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Catherine A Brownstein, Alan H Beggs, Nils Homer, Barry Merriman, Timothy W Yu, Katherine C Flannery, Elizabeth T DeChene, Meghan C Towne, Sarah K Savage, Emily N Price,[...]. Genome Biol 2014
73
1

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.
Laura M Amendola, Gail P Jarvik, Michael C Leo, Heather M McLaughlin, Yassmine Akkari, Michelle D Amaral, Jonathan S Berg, Sawona Biswas, Kevin M Bowling, Laura K Conlin,[...]. Am J Hum Genet 2016
72
1

Utilization of health information technology among cancer genetic counselors.
Jordon B Ritchie, Caitlin G Allen, Heath Morrison, Michelle Nichols, Steven D Lauzon, Joshua D Schiffman, Chanita Hughes Halbert, Brandon M Welch. Mol Genet Genomic Med 2020
5
20

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
14
7

Chatbots & artificial intelligence to scale genetic information delivery.
Shivani Nazareth, Robert L Nussbaum, Elen Siglen, Catherine A Wicklund. J Genet Couns 2021
1
100

Generation and Implementation of a Patient-Centered and Patient-Facing Genomic Test Report in the EHR.
Jessica M Goehringer, Michele A Bonhag, Laney K Jones, Tara Schmidlen, Marci Schwartz, Alanna Kulchak Rahm, Janet L Williams, Marc S Williams. EGEMS (Wash DC) 2018
6
16

The future is now: Technology's impact on the practice of genetic counseling.
Erynn S Gordon, Deepti Babu, Dawn A Laney. Am J Med Genet C Semin Med Genet 2018
17
5

Hereditary cancer gene panel test reports: wide heterogeneity suggests need for standardization.
Sukh Makhnoon, Brian H Shirts, Deborah J Bowen, Stephanie M Fullerton. Genet Med 2018
7
14

Recent developments in genetic/genomic medicine.
Rachel H Horton, Anneke M Lucassen. Clin Sci (Lond) 2019
18
5

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
29
3

Retention of medical genetics knowledge and skills by medical students.
Anne E Greb, Simone Brennan, Lori McParlane, Renee Page, Patrick D Bridge. Genet Med 2009
18
5




Genetic Counseling Service Delivery Models in the United States: Assessment of changes in use from 2010 to 2017.
Samantha E Greenberg, Emily Boothe, Christine L Delaney, Ryan Noss, Stephanie A Cohen. J Genet Couns 2020
4
25

Genetic education and nongenetic health professionals: educational providers and curricula in Europe.
Kirsty Challen, Hilary J Harris, Claire Julian-Reynier, Leo P Ten Kate, Ulf Kristoffersson, Irmgard Nippert, Jörg Schmidtke, Caroline Benjamin, Rodney Harris. Genet Med 2005
28
3

JAMA patient page. Genomic medicine.
Denise M Goodman, Cassio Lynm, Edward H Livingston. JAMA 2013
6
16

Enhancing genomic laboratory reports: A qualitative analysis of provider review.
Janet L Williams, Alanna Kulchak Rahm, Heather Stuckey, Jamie Green, Lynn Feldman, Doris T Zallen, Michele Bonhag, Michael M Segal, Audrey L Fan, Marc S Williams. Am J Med Genet A 2016
21
4

Genomic medicine: new frontiers and new challenges.
Maria D Pasic, Sara Samaan, George M Yousef. Clin Chem 2013
41
2

Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education.
Belinda J McClaren, Emily A King, Erin Crellin, Clara Gaff, Sylvia A Metcalfe, Amy Nisselle. Front Genet 2020
6
16

Informing Integration of Genomic Medicine Into Primary Care: An Assessment of Current Practice, Attitudes, and Desired Resources.
June C Carroll, Judith Allanson, Shawna Morrison, Fiona A Miller, Brenda J Wilson, Joanne A Permaul, Deanna Telner. Front Genet 2019
12
8


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.