Publication
miRNA and lncRNA gene variants in Autism Spectrum Disorder
| dc.contributor.author | Marques, Ana Rita | |
| dc.contributor.author | Martiniano, H. | |
| dc.contributor.author | Santos, J.X. | |
| dc.contributor.author | Vilela, J. | |
| dc.contributor.author | Asif, M. | |
| dc.contributor.author | Oliveira, G. | |
| dc.contributor.author | Enguita, F.J. | |
| dc.contributor.author | Romão, L. | |
| dc.contributor.author | Vicente, A.M. | |
| dc.date.accessioned | 2018-10-22T15:31:59Z | |
| dc.date.available | 2018-10-22T15:31:59Z | |
| dc.date.issued | 2018-06 | |
| dc.description | A.R.Marques is recipiente of a fellowship from BioSys PhD programme (Ref PD/BD/113773/2015 from FCT (Portugal). Patients and parents were genotyped in the context of the Autism Genome Project (AGP), funded by NIMH, HRB, MRC, Autism Speaks, Hilibrand Foundation, Genome Canada, OGI, CIHR, and the Simons Simplex Collection (SSC), a core project of the Simons Foundation Autism Research Initiative (SFARI). | pt_PT |
| dc.description | Prémio melhor poster | pt_PT |
| dc.description.abstract | Introduction: Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder: Characterized by deficits in social communication/interaction and by unusual repetitive and restricted behaviors and interests; Median estimated prevalence worldwide is 17/10000; Male to female ratio: ~4:1; Comorbidities: intellectual disability, anxiety, epilepsy, (…). | pt_PT |
| dc.description.sponsorship | A.R.Marques is recipient of a fellowship from BioSys PhD programme (Ref PD/BD/113773/2015 from FCT (Portugal). Patients and parents were genotyped in the context of the Autism Genome Project (AGP), funded by NIMH, HRB, MRC, Autism Speaks, Hilibrand Foundation, Genome Canada, OGI, CIHR, and the Simons Simplex Collection (SSC), a core project of the Simons Foundation Autism Research Initiative (SFARI). | pt_PT |
| dc.description.version | N/A | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.18/5623 | |
| dc.language.iso | eng | pt_PT |
| dc.publisher | Instituto Nacional de Saúde Doutor Ricardo Jorge, IP | pt_PT |
| dc.subject | Autism Spectrum Disorder | pt_PT |
| dc.subject | Perturbações do Desenvolvimento Infantil e Saúde Mental | pt_PT |
| dc.subject | miRNA Gene | pt_PT |
| dc.subject | lncRNA Gene | pt_PT |
| dc.title | miRNA and lncRNA gene variants in Autism Spectrum Disorder | pt_PT |
| dc.type | conference object | |
| dspace.entity.type | Publication | |
| oaire.citation.conferencePlace | Milão, itália | pt_PT |
| oaire.citation.title | 52nd European Human Genetics Conference (ESHG), 16-19 Jun 2018 | pt_PT |
| rcaap.rights | embargoedAccess | pt_PT |
| rcaap.type | conferenceObject | pt_PT |
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