2022
Discovery of 42 genome-wide significant loci associated with dyslexia
Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B, Pourcain B, Francks C, Marioni R, Zhao J, Paracchini S, Talcott J, Monaco A, Stein J, Gruen J, Olson R, Willcutt E, DeFries J, Pennington B, Smith S, Wright M, Martin N, Auton A, Bates T, Fisher S, Luciano M. Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics 2022, 54: 1621-1629. PMID: 36266505, PMCID: PMC9649434, DOI: 10.1038/s41588-022-01192-y.Peer-Reviewed Original ResearchConceptsGenome-wide significant lociSignificant lociIndependent genome-wide significant lociWide association studyGenetic covarianceAssociation studiesGenetic markersLociGenetic etiologyEuropean ancestryTraitsPolygenic scoresCrucial life skillGenesHeritabilityIndependent cohortAncestryFamily studiesDiscovery
2014
The Genetics of Disorders Affecting the Premature Newborn
Prosnitz A, Gruen J, Bhandari V. The Genetics of Disorders Affecting the Premature Newborn. 2014 DOI: 10.1016/b978-0-12-801238-3.05514-8.Peer-Reviewed Original ResearchPatent ductus arteriosusRespiratory distress syndromeRetinopathy of prematurityBronchopulmonary dysplasiaIntraventricular hemorrhageNecrotizing enterocolitisDistress syndromeDuctus arteriosusPremature newbornsCommon disorderGenetics of disordersGenetic etiologyDisordersEnterocolitisArteriosusPrematurityHemorrhageRetinopathyNewbornsDysplasiaInfantsSyndromeEtiology