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: 22



Laurel K Willig, Josh E Petrikin, Laurie D Smith, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Sarah E Soden, Julie A Cakici, Suzanne M Herd, Greyson Twist, Aaron Noll, Mitchell Creed, Patria M Alba, Shannon L Carpenter, Mark A Clements, Ryan T Fischer, J Allyson Hays, Howard Kilbride, Ryan J McDonough, Jamie L Rosterman, Sarah L Tsai, Lee Zellmer, Emily G Farrow, Stephen F Kingsmore. Lancet Respir Med 2015
Times Cited: 182




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

Application of Next-Generation Sequencing for Genetic Diagnosis in Neonatal Intensive Care Units: Results of a Multicenter Study in China.
Tianwen Zhu, Xiaohui Gong, Fei Bei, Li Ma, Yan Chen, Yonghong Zhang, Xia Wang, Jingjing Sun, Jian Wang, Gang Qiu,[...]. Front Genet 2020
1

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

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

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 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

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

Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditions.
Hadley Stevens Smith, John M Swint, Seema R Lalani, Marcia C de Oliveira Otto, Jose-Miguel Yamal, Heidi V Russell, Brendan H Lee. Genet Med 2020
4

Diagnostic and service impact of genomic testing technologies in a neonatal intensive care unit.
Natalie B Tan, Tiong Yang Tan, Melissa M Martyn, Ravi Savarirayan, David J Amor, Amanda Moody, Susan M White, Zornitza Stark. J Paediatr Child Health 2019
6