Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2712
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dc.contributor.authorMiddeldorp, C. M.en
dc.contributor.authorMcCarthy, M. I.en
dc.contributor.authorMahajan, A.en
dc.contributor.authorFelix, J. F.en
dc.date.accessioned2022-11-07T23:34:28Z-
dc.date.available2022-11-07T23:34:28Z-
dc.date.issued2019en
dc.identifier.citation34, (3), 2019, p. 279-300en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/2712-
dc.description.abstractThe impact of many unfavorable childhood traits or diseases, such as low birth weight and mental disorders, is not limited to childhood and adolescence, as they are also associated with poor outcomes in adulthood, such as cardiovascular disease. Insight into the genetic etiology of childhood and adolescent traits and disorders may therefore provide new perspectives, not only on how to improve wellbeing during childhood, but also how to prevent later adverse outcomes. To achieve the sample sizes required for genetic research, the Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia were established. The majority of the participating cohorts are longitudinal population-based samples, but other cohorts with data on early childhood phenotypes are also involved. Cohorts often have a broad focus and collect(ed) data on various somatic and psychiatric traits as well as environmental factors. Genetic variants have been suc-cessfully identified for multiple traits, for example, birth weight, atopic dermatitis, childhood BMI, allergic sensitization, and pubertal growth. Furthermore, the results have shown that genetic factors also partly underlie the association with adult traits. As sample sizes are still increasing, it is expected that future analyses will identify additional variants. This, in com-bination with the development of innovative statistical methods, will provide detailed insight on the mechanisms underlying the transition from childhood to adult disorders. Both consortia welcome new collaborations. Policies and contact details are available from the corresponding authors of this manuscript and/or the consortium websites.L6268900332019-03-28 <br />2020-12-22 <br />en
dc.language.isoenen
dc.relation.ispartofEuropean Journal of Epidemiologyen
dc.titleThe early growth genetics (Egg) and early genetics and lifecourse epidemiology (eagle) consortia: Design, results and future prospectsen
dc.typeArticleen
dc.identifier.doi10.1007/s10654-019-00502-9en
dc.subject.keywordschildhooden
dc.subject.keywordschildhood diseaseen
dc.subject.keywordsdevelopmental geneticsen
dc.subject.keywordsenvironmental factoren
dc.subject.keywordsepidemiologyen
dc.subject.keywordsgenetic variabilityen
dc.subject.keywordsgroups by ageen
dc.subject.keywordshumanen
dc.subject.keywordsphenotypeen
dc.subject.keywordsarticleen
dc.subject.keywordspubertyen
dc.subject.keywordssample sizeen
dc.subject.keywordssensitizationen
dc.subject.keywordsstatistical analysisen
dc.subject.keywordsadolescenceadverse outcomeen
dc.subject.keywordspolicyen
dc.subject.keywordsatopic dermatitisen
dc.subject.keywordsbirth weighten
dc.subject.keywordsbody massen
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L626890033&from=exporthttp://dx.doi.org/10.1007/s10654-019-00502-9 |en
dc.identifier.risid1788en
dc.description.pages279-300en
local.message.claim2024-06-13T14:28:53.052+1000|||rp04980|||submit_approve|||dc_contributor_author|||None*
local.message.claim2024-06-13T14:29:04.755+1000|||rp04980|||submit_approve|||dc_contributor_author|||None*
local.message.claim2024-06-13T14:29:04.755+1000|||rp04980|||submit_approve|||dc_contributor_author|||None*
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Sites:Children's Health Queensland Publications
Queensland Health Publications
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