A citation-based method for searching scientific literature

Alison M Elliott, Christèle du Souich, Anna Lehman, Ilaria Guella, Daniel M Evans, Tara Candido, Leah Tooman, Linlea Armstrong, Lorne Clarke, William Gibson, Harinder Gill, Pascal M Lavoie, Suzanne Lewis, Margaret L McKinnon, Sarah M Nikkel, Millan Patel, Alfonso Solimano, Anne Synnes, Joseph Ting, Margot van Allen, Jan Christilaw, Matthew J Farrer, Jan M Friedman, Horacio Osiovich. Eur J Pediatr 2019
Times Cited: 19



Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin Perinatol 2015
Times Cited: 103




List of shared articles



Times cited

Clinical Utility of Rapid Exome Sequencing Combined With Mitochondrial DNA Sequencing in Critically Ill Pediatric Patients With Suspected Genetic Disorders.
Xuejun Ouyang, Yu Zhang, Lijuan Zhang, Jixuan Luo, Ting Zhang, Hui Hu, Lin Liu, Lieqiang Zhong, Shaoying Zeng, Pingyi Xu,[...]. Front Genet 2021
0

Rapid genome-wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences.
Caitlin E Aldridge, Horacio Osiovich, Harold Hal Siden, Alison M Elliott. J Genet Couns 2021
3

The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children.
Amanda S Freed, Sarah V Clowes Candadai, Megan C Sikes, Jenny Thies, Heather M Byers, Jennifer N Dines, Mesaki Kenneth Ndugga-Kabuye, Mallory B Smith, Katie Fogus, Heather C Mefford,[...]. J Pediatr 2020
4

Genetic testing strategies in the newborn.
Jeanne Carroll, Kristen Wigby, Sarah Murray. J Perinatol 2020
2

Neonatal Presentations of Metabolic Disorders.
Anna-Kaisa Niemi Md. Neoreviews 2020
1

Rapid whole-exome sequencing facilitates precision medicine in paediatric rare disease patients and reduces healthcare costs.
Claudia C Y Chung, Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, Mianne Lee, Steven L C Pei, Mullin H C Yu, Vivian C C Hui, Joshua C K Chan, Jeffrey F T Chau,[...]. Lancet Reg Health West Pac 2020
1

Genetic testing for unexplained perinatal disorders.
Thomas Hays, Ronald J Wapner. Curr Opin Pediatr 2021
1

Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield.
Cynthia S Gubbels, Grace E VanNoy, Jill A Madden, Deborah Copenheaver, Sandra Yang, Monica H Wojcik, Nina B Gold, Casie A Genetti, Joan Stoler, Richard B Parad,[...]. Genet Med 2020
27

Rapid Phenotype-Driven Gene Sequencing with the NeoSeq Panel: A Diagnostic Tool for Critically Ill Newborns with Suspected Genetic Disease.
María José de Castro, Emiliano González-Vioque, Sofía Barbosa-Gouveia, Enrique Salguero, Segundo Rite, Olalla López-Suárez, Alejandro Pérez-Muñuzuri, María-Luz Couce. J Clin Med 2020
1