Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants.

Brain and behavior - 1 Jul 2016

Krishnan Michelle L, Wang Zi, Silver Matt, Boardman James P, Ball Gareth, Counsell Serena J, Walley Andrew J, Montana Giovanni, Edwards Anthony David

Abstract excerpt

BACKGROUND: The consequences of preterm birth are a major public health concern with high rates of ensuing multisystem morbidity, and uncertain biological mechanisms. Common genetic variation may mediate vulnerability to the insult of prematurity and provide opportunities to predict and modify risk. OBJECTIVE: To gain novel biological and therapeutic insights from the integrated analysis of magnetic resonance...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Brain Injuries
Share to Diffusion Magnetic Resonance Imaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Infant, Newborn

Share to Infant, Premature

Share to Lipid Metabolism

Share to Pilot Projects

Share to White Matter

Source

Open in PubMed Open full text

Identifiers

PMID: 27110435
DOI: 10.1002/brb3.434
PMCID: PMC4821839

Genes

ACAA1
AQP7
PLIN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants.PMID 27110435Read ↗

Machine learning shows association between genetic variability in PPARG and cerebral connectivity in preterm infants.Semantic proximity Read ↗

Prediction of short-term neonatal complications in preterm infants using exome-wide genetic variation and gestational age: a pilot study.Semantic proximity Read ↗

Common genetic variants and risk of brain injury after preterm birth.Semantic proximity Read ↗

Investigating the Interplay Between Prematurity and Genetic Variation in the Context of Rare Developmental DisordersSemantic proximity Read ↗

Cerebral palsy: causes, pathways, and the role of genetic variants.Semantic proximity Read ↗

Investigating the interplay between prematurity and genetic variation in the context of rare developmental disorders.Semantic proximity Read ↗

Genetic Predisposition to Adverse Neurodevelopmental Outcome of Extremely Low Birth Weight Infants.Semantic proximity Read ↗

Maternal plasma lipids are involved in the pathogenesis of preterm birthSemantic proximity Read ↗

Complex genetic dependencies among growth and neurological phenotypes in healthy children: Towards deciphering developmental mechanisms.Semantic proximity Read ↗

Placental-brain axis in females detected within broadly impacted metabolic gene networks protects against prenatal PCB exposureSemantic proximity Read ↗

Pathway-based genetic analysis of preterm birth.Semantic proximity Read ↗

Epigenomic profiling of preterm infants reveals DNA methylation differences at sites associated with neural functionSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.