A citation-based method for searching scientific literature

Monica H Wojcik, Talia S Schwartz, Inbar Yamin, Heather L Edward, Casie A Genetti, Meghan C Towne, Pankaj B Agrawal. Genet Med 2018
Times Cited: 24



Laurie D Smith, Laurel K Willig, Stephen F Kingsmore. Cold Spring Harb Perspect Med 2015
Times Cited: 56




List of shared articles



Times cited


Peri-mortem evaluation of infants who die without a diagnosis: focus on advances in genomic technology.
Monica H Wojcik, Dara Brodsky, Jane E Stewart, Jonathan Picker. J Perinatol 2018
5

Developmental Support for Infants With Genetic Disorders.
Monica H Wojcik, Jane E Stewart, Susan E Waisbren, Jonathan S Litt. Pediatrics 2020
2

Infant mortality: the contribution of genetic disorders.
Monica H Wojcik, Talia S Schwartz, Katri E Thiele, Heather Paterson, Rachel Stadelmaier, Thomas E Mullen, Grace E VanNoy, Casie A Genetti, Jill A Madden, Cynthia S Gubbels,[...]. J Perinatol 2019
12

Application of Full-Spectrum Rapid Clinical Genome Sequencing Improves Diagnostic Rate and Clinical Outcomes in Critically Ill Infants in the China Neonatal Genomes Project.
Bingbing Wu, Wenqing Kang, Yingyuan Wang, Deyi Zhuang, Liping Chen, Long Li, Yajie Su, Xinnian Pan, Qiufen Wei, Zezhong Tang,[...]. Crit Care Med 2021
0

Congenital anomalies and genetic disorders in neonates and infants: a single-center observational cohort study.
A Marouane, R A C M Olde Keizer, G W J Frederix, L E L M Vissers, W P de Boode, W A G van Zelst-Stams. Eur J Pediatr 2021
0

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