Whole genome methylation and transcriptome analyses to identify risk for cerebral palsy (CP) in extremely low gestational age neonates (ELGAN)
Abstract Preterm birth remains the leading identifiable risk factor for cerebral palsy (CP), a devastating form of motor impairment due to developmental brain injury occurring around the time of birth. We performed genome wide methylation and whole transcriptome analyses to elucidate the early patho...
Saved in:
Main Authors: | An N. Massaro, Theo K. Bammler, James W. MacDonald, Krystle M. Perez, Bryan Comstock, Sandra E. Juul |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2021
|
Subjects: | |
Online Access: | https://doaj.org/article/fcea0f7077dc4ee3b7e684612a03d384 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Clinical patterns of cerebral palsy with complications and neurodisabilities associated with cerebral palsy
by: Anmar jumaa Ghali, et al.
Published: (2021) -
Nanomedicine in cerebral palsy
by: Balakrishnan B, et al.
Published: (2013) -
Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencing
by: C. L. van Eyk, et al.
Published: (2021) -
ELBW and ELGAN outcomes in developing nations-Systematic review and meta-analysis.
by: Viraraghavan Vadakkencherry Ramaswamy, et al.
Published: (2021) -
The habilitation of the cerebral palsied child
by: F. M. Tragott-Vorwerg, et al.
Published: (1954)