A citation-based method for searching scientific literature

Ellen Wright Clayton, Susanne Haga, Patricia Kuszler, Emily Bane, Krysta Shutske, Wylie Burke. Genet Med 2013
Times Cited: 45







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



Times Cited
  Times     Co-cited
Similarity


Australian Genomics: A Federated Model for Integrating Genomics into Healthcare.
Zornitza Stark, Tiffany Boughtwood, Peta Phillips, John Christodoulou, David P Hansen, Jeffrey Braithwaite, Ainsley J Newson, Clara L Gaff, Andrew H Sinclair, Kathryn N North. Am J Hum Genet 2019
38
2

Physician-Reported Benefits and Barriers to Clinical Implementation of Genomic Medicine: A Multi-Site IGNITE-Network Survey.
Aniwaa Owusu Obeng, Kezhen Fei, Kenneth D Levy, Amanda R Elsey, Toni I Pollin, Andrea H Ramirez, Kristin W Weitzel, Carol R Horowitz. J Pers Med 2018
65
2

What works in genomics education: outcomes of an evidenced-based instructional model for community-based physicians.
E Kate Reed, Katherine A Johansen Taber, Therese Ingram Nissen, Suzanna Schott, Lynn O Dowling, James C O'Leary, Joan A Scott. Genet Med 2016
23
4

A retrospective review of multiple findings in diagnostic exome sequencing: half are distinct and half are overlapping diagnoses.
Erica D Smith, Kirsten Blanco, Samin A Sajan, Jesse M Hunter, Deepali N Shinde, Bess Wayburn, Mari Rossi, Jennifer Huang, Cathy A Stevens, Candace Muss,[...]. Genet Med 2019
30
3

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
538
2

From hype to reality: data science enabling personalized medicine.
Holger Fröhlich, Rudi Balling, Niko Beerenwinkel, Oliver Kohlbacher, Santosh Kumar, Thomas Lengauer, Marloes H Maathuis, Yves Moreau, Susan A Murphy, Teresa M Przytycka,[...]. BMC Med 2018
109
2

Integrating Genomics into Healthcare: A Global Responsibility.
Zornitza Stark, Lena Dolman, Teri A Manolio, Brad Ozenberger, Sue L Hill, Mark J Caulfied, Yves Levy, David Glazer, Julia Wilson, Mark Lawler,[...]. Am J Hum Genet 2019
154
2

Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer.
Nadine Tung, Nancy U Lin, John Kidd, Brian A Allen, Nanda Singh, Richard J Wenstrup, Anne-Renee Hartman, Eric P Winer, Judy E Garber. J Clin Oncol 2016
287
2

Ethical conundrums in pediatric genomics.
Seth J Rotz, Eric Kodish. Hematology Am Soc Hematol Educ Program 2018
7
14

Communication challenges for nongeneticist physicians relaying clinical genomic results.
Nonie S Arora, J Kelly Davis, Christine Kirby, Amy L McGuire, Robert C Green, J S Blumenthal-Barby, Peter A Ubel. Per Med 2016
22
4

Performance of exome sequencing for pharmacogenomics.
Eric R Londin, Peter Clark, Marialuisa Sponziello, Larry J Kricka, Paolo Fortina, Jason Y Park. Per Med 2014
16
6

Implementation and utilization of genetic testing in personalized medicine.
Noura S Abul-Husn, Aniwaa Owusu Obeng, Saskia C Sanderson, Omri Gottesman, Stuart A Scott. Pharmgenomics Pers Med 2014
49
2

Overview of pharmacogenomic testing in clinical practice.
Tonya Gross, Jeremy Daniel. Ment Health Clin 2018
14
7

Pitfalls in genetic testing: a case of a SNP in primer-annealing region leading to allele dropout in BRCA1.
Felipe Carneiro Silva, Giovana Tardin Torrezan, Rafael Canfield Brianese, Raquel Stabellini, Dirce Maria Carraro. Mol Genet Genomic Med 2017
9
11

NIH working group report-using genomic information to guide weight management: From universal to precision treatment.
Molly S Bray, Ruth J F Loos, Jeanne M McCaffery, Charlotte Ling, Paul W Franks, George M Weinstock, Michael P Snyder, Jason L Vassy, Tanya Agurs-Collins. Obesity (Silver Spring) 2016
72
2

Evidence-based medicine and big genomic data.
John P A Ioannidis, Muin J Khoury. Hum Mol Genet 2018
20
5



Clinical use of current polygenic risk scores may exacerbate health disparities.
Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
660
2

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
47
2


Integrating Pharmacogenomics into Clinical Practice: Promise vs Reality.
Jennifer L St Sauver, Suzette J Bielinski, Janet E Olson, Elizabeth J Bell, Michaela E Mc Gree, Debra J Jacobson, Jennifer B McCormick, Pedro J Caraballo, Paul Y Takahashi, Veronique L Roger,[...]. Am J Med 2016
39
2


At Preeclampsia Diagnosis, Total Cell-Free DNA Concentration is Elevated and Correlates With Disease Severity.
Teodora R Kolarova, Hilary S Gammill, J Lee Nelson, Christina M Lockwood, Raj Shree. J Am Heart Assoc 2021
5
20

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
Karuna R M van der Meij, Erik A Sistermans, Merryn V E Macville, Servi J C Stevens, Caroline J Bax, Mireille N Bekker, Caterina M Bilardo, Elles M J Boon, Marjan Boter, Karin E M Diderich,[...]. Am J Hum Genet 2019
98
2

Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease.
C Michael Osborne, Emily Hardisty, Patricia Devers, Kathleen Kaiser-Rogers, Melissa A Hayden, William Goodnight, Neeta L Vora. Prenat Diagn 2013
131
2


Incidental Detection of Maternal Neoplasia in Noninvasive Prenatal Testing.
Nilesh G Dharajiya, Daniel S Grosu, Daniel H Farkas, Ron M McCullough, Eyad Almasri, Youting Sun, Sung K Kim, Taylor J Jensen, Juan-Sebastian Saldivar, Eric J Topol,[...]. Clin Chem 2018
51
2

Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis.
Francesca Malvestiti, Cristina Agrati, Beatrice Grimi, Eva Pompilii, Claudia Izzi, Lorenza Martinoni, Elisa Gaetani, Maria Rosaria Liuti, Anna Trotta, Federico Maggi,[...]. Prenat Diagn 2015
81
2

Unsuspected extracolonic findings at screening CT colonography: clinical and economic impact.
Perry J Pickhardt, Meghan E Hanson, David J Vanness, Justin Y Lo, David H Kim, Andrew J Taylor, Thomas C Winter, J Louis Hinshaw. Radiology 2008
144
2

Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies.
Diana W Bianchi, Darya Chudova, Amy J Sehnert, Sucheta Bhatt, Kathryn Murray, Tracy L Prosen, Judy E Garber, Louise Wilkins-Haug, Neeta L Vora, Stephen Warsof,[...]. JAMA 2015
231
2

Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests.
Xing Ji, Jia Li, Yonghua Huang, Pi-Lin Sung, Yuying Yuan, Qiang Liu, Yan Chen, Jia Ju, Yafeng Zhou, Shujia Huang,[...]. Genet Med 2019
20
5

Outcome of publicly funded nationwide first-tier noninvasive prenatal screening.
Kris Van Den Bogaert, Lore Lannoo, Nathalie Brison, Vincent Gatinois, Machteld Baetens, Bettina Blaumeiser, François Boemer, Laura Bourlard, Vincent Bours, Anne De Leener,[...]. Genet Med 2021
19
5


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.