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: 21



Kyle Retterer, Jane Juusola, Megan T Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G Monaghan, Dianalee McKnight, Renkui Bai, Sharon Suchy, Bethany Friedman, Jackie Tahiliani, Daniel Pineda-Alvarez, Gabriele Richard, Tracy Brandt, Eden Haverfield, Wendy K Chung, Sherri Bale. Genet Med 2016
Times Cited: 459




List of shared articles



Times cited

Improving diagnostics of rare genetic diseases with NGS approaches.
Mateja Vinkšel, Karin Writzl, Aleš Maver, Borut Peterlin. J Community Genet 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

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
30