👤 Debora Pérez-García

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3
Articles
3
Name variants
Also published as: Cristian Pérez-García, Miguel Pérez-García
articles
Raquel Rodríguez-López, Javier García-Planells, Marina Martínez-Matilla +7 more · 2022 · Life (Basel, Switzerland) · MDPI · added 2026-04-24
đź“„ PDF DOI: 10.3390/life12071035
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Cristina Campoy, Hatim Azaryah, Francisco J Torres-Espínola +13 more · 2020 · Nutrients · MDPI · added 2026-04-24
Both pre- and early postnatal supplementation with docosahexaenoic acid (DHA), arachidonic acid (AA) and folate have been related to neural development, but their long-term effects on later neural fun Show more
Both pre- and early postnatal supplementation with docosahexaenoic acid (DHA), arachidonic acid (AA) and folate have been related to neural development, but their long-term effects on later neural function remain unclear. We evaluated the long-term effects of maternal prenatal supplementation with fish-oil (FO), 5-methyltetrahydrofolate (5-MTHF), placebo or FO + 5-MTHF, as well as the role of fatty acid desaturase ( Show less
đź“„ PDF DOI: 10.3390/nu13010131
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Marta Codina-Sola, Mar Costa-Roger, Debora Pérez-García +4 more · 2019 · Journal of medical genetics · added 2026-04-24
The hallmark of the neurobehavioural phenotype of Williams-Beuren syndrome (WBS) is increased sociability and relatively preserved language skills, often described as opposite to autism spectrum disor Show more
The hallmark of the neurobehavioural phenotype of Williams-Beuren syndrome (WBS) is increased sociability and relatively preserved language skills, often described as opposite to autism spectrum disorders (ASD). However, the prevalence of ASD in WBS is 6-10 times higher than in the general population. We have investigated the genetic factors that could contribute to the ASD phenotype in individuals with WBS. We studied four males and four females with WBS and a confirmed diagnosis of ASD by the Autism Diagnostic Interview-Revised. We performed a detailed molecular characterisation of the deletion and searched for genomic variants using exome sequencing. A de novo deletion of 1.55 Mb (6 cases) or 1.83 Mb (2 cases) at 7q11.23 was detected, being in 7/8 patients of paternal origin. No common breakpoint, deletion mechanism or size was found. Two cases were hemizygous for the rare T allele at rs12539160 in The increased susceptibility to ASD in patients with WBS might be due to additive effects of the common WBS deletion, inherited and de novo rare sequence variants in ASD-related genes elsewhere in the genome, with higher burden of deleterious mutations required for females, and possible hypomorphic variants in the hemizygous allele or Show less
đź“„ PDF DOI: 10.1136/jmedgenet-2019-106080
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