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Pediatric Research|March 14, 2024
Epigenetic associations in HPA axis genes related to bronchopulmonary dysplasia and antenatal steroidsKenyaita M Hodge, Vasyl Zhabotynsky, Amber A Burt, et al.
Journal of Lipid Research|April 9, 2014
Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing ProjectDaniel Seung Kim, David R Crosslin, Paul L Auer, et al.
Scientific Reports|August 5, 2024
Epigenetic associations with neonatal age in infants born very preterm, particularly among genes involved in neurodevelopmentKenyaita M Hodge, Amber A Burt, Marie Camerota, et al.
Pediatric Research|September 23, 2020
Epigenome-wide analysis identifies genes and pathways linked to acoustic cry variation in preterm infantsGhazal Aghagoli, Stephen J Sheinkopf, Todd M Everson, et al.
The Journal of Thoracic and Cardiovascular Surgery|October 6, 2014
Validation of association of the apolipoprotein E ε2 allele with neurodevelopmental dysfunction after cardiac surgery in neonates and infantsJ William Gaynor, Daniel Seung Kim, Cammon B Arrington, et al.
Nature Genetics|February 20, 2019
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distributionAnne E Justice, Tugce Karaderi, Heather M Highland, et al.
Nature|February 2, 2017
Rare and low-frequency coding variants alter human adult heightEirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, et al.
Nature Genetics|December 24, 2017
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesityValérie Turcot, Yingchang Lu, Heather M Highland, et al.
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