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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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How personalised medicine will transform healthcare by 2030: the ICPerMed visionJournal of translational medicine, 2020-04, Vol.18 (1), p.180-180, Article 180 [Peer Reviewed Journal]COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1479-5876 ;EISSN: 1479-5876 ;DOI: 10.1186/s12967-020-02316-w ;PMID: 32345312Full text available |
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Identifying disease genes using machine learning and gene functional similarities, assessed through Gene OntologyPloS one, 2018-12, Vol.13 (12), p.e0208626-e0208626 [Peer Reviewed Journal]COPYRIGHT 2018 Public Library of Science ;COPYRIGHT 2018 Public Library of Science ;2018 Asif et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2018 Asif et al 2018 Asif et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0208626 ;PMID: 30532199Full text available |
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Protein interaction networks reveal novel autism risk genes within GWAS statistical noisePloS one, 2014-11, Vol.9 (11), p.e112399-e112399 [Peer Reviewed Journal]2014 Correia et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2014 Correia et al 2014 Correia et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0112399 ;PMID: 25409314Full text available |
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A Role for Gene-Environment Interactions in Autism Spectrum Disorder Is Supported by Variants in Genes Regulating the Effects of Exposure to XenobioticsFrontiers in neuroscience, 2022-05, Vol.16, p.862315-862315 [Peer Reviewed Journal]Copyright © 2022 Santos, Rasga, Marques, Martiniano, Asif, Vilela, Oliveira, Sousa, Nunes and Vicente. ;Copyright © 2022 Santos, Rasga, Marques, Martiniano, Asif, Vilela, Oliveira, Sousa, Nunes and Vicente. 2022 Santos, Rasga, Marques, Martiniano, Asif, Vilela, Oliveira, Sousa, Nunes and Vicente ;ISSN: 1662-4548 ;ISSN: 1662-453X ;EISSN: 1662-453X ;DOI: 10.3389/fnins.2022.862315 ;PMID: 35663546Full text available |
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Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaborationNeurology, 2016-03, Vol.86 (13), p.1217-1226 [Peer Reviewed Journal]2016 American Academy of Neurology ;2016 American Academy of Neurology. ;2016 American Academy of Neurology 2016 American Academy of Neurology ;ISSN: 0028-3878 ;ISSN: 1526-632X ;EISSN: 1526-632X ;DOI: 10.1212/WNL.0000000000002528 ;PMID: 26935894Full text available |
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Are we PREPAREd? Concerning the “PREemptive Pharmacogenomics Testing for Preventing Adverse Drug Reactions (PREPARE) Study”Acta médica portuguesa, 2023-10, Vol.36 (10), p.689-690ISSN: 0870-399X ;EISSN: 1646-0758 ;DOI: 10.20344/amp.20170Full text available |
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Identification of biological mechanisms underlying a multidimensional ASD phenotype using machine learningTranslational psychiatry, 2020-01, Vol.10 (1), p.43-43, Article 43 [Peer Reviewed Journal]This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2158-3188 ;EISSN: 2158-3188 ;DOI: 10.1038/s41398-020-0721-1 ;PMID: 32066720Full text available |
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TTC7B Emerges as a Novel Risk Factor for Ischemic Stroke Through the Convergence of Several Genome-Wide ApproachesJournal of cerebral blood flow and metabolism, 2012-06, Vol.32 (6), p.1061-1072 [Peer Reviewed Journal]2012 ISCBFM ;2015 INIST-CNRS ;Copyright © 2012 International Society for Cerebral Blood Flow & Metabolism, Inc. 2012 International Society for Cerebral Blood Flow & Metabolism, Inc. ;ISSN: 0271-678X ;EISSN: 1559-7016 ;DOI: 10.1038/jcbfm.2012.24 ;PMID: 22453632 ;CODEN: JCBMDNFull text available |
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Variants of the Matrix Metalloproteinase-2 but not the Matrix Metalloproteinase-9 genes significantly influence functional outcome after strokeBMC genetics, 2010-03, Vol.11 (1), p.40-40, Article 40 [Peer Reviewed Journal]COPYRIGHT 2010 BioMed Central Ltd. ;COPYRIGHT 2010 BioMed Central Ltd. ;2010 Manso et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright ©2010 Manso et al; licensee BioMed Central Ltd. 2010 Manso et al; licensee BioMed Central Ltd. ;ISSN: 1471-2350 ;ISSN: 1471-2156 ;EISSN: 1471-2350 ;EISSN: 1471-2156 ;DOI: 10.1186/1471-2350-11-40 ;PMID: 20222942Full text available |
| 10 |
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Evidence for epistasis between SLC6a4 and ITGB3 in autism etiology and in the determination of platelet serotonin levelsHuman genetics, 2007-04, Vol.121 (2), p.243-256 [Peer Reviewed Journal]2007 INIST-CNRS ;COPYRIGHT 2007 Springer ;Springer-Verlag 2007 ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-006-0301-3 ;PMID: 17203304 ;CODEN: HUGEDQFull text available |
| 11 |
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Hope for GWAS: relevant risk genes uncovered from GWAS statistical noiseInternational journal of molecular sciences, 2014-09, Vol.15 (10), p.17601-17621 [Peer Reviewed Journal]Copyright MDPI AG 2014 ;2014 by the authors; licensee MDPI, Basel, Switzerland. 2014 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms151017601 ;PMID: 25268625Full text available |
| 12 |
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Bridging Genetic Insights with Neuroimaging in Autism Spectrum Disorder-A Systematic ReviewInternational journal of molecular sciences, 2024-05, Vol.25 (9), p.4938 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms25094938 ;PMID: 38732157Full text available |
| 13 |
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The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analysesMolecular autism, 2014-05, Vol.5 (1), p.34-34 [Peer Reviewed Journal]COPYRIGHT 2014 BioMed Central Ltd. ;COPYRIGHT 2014 BioMed Central Ltd. ;Copyright © 2014 Buxbaum et al.; licensee BioMed Central Ltd. 2014 Buxbaum et al.; licensee BioMed Central Ltd. ;ISSN: 2040-2392 ;EISSN: 2040-2392 ;DOI: 10.1186/2040-2392-5-34 ;PMID: 25392729Full text available |
| 14 |
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Mental Health of Healthcare Professionals: Two Years of the COVID-19 Pandemic in PortugalInternational journal of environmental research and public health, 2023-02, Vol.20 (4), p.3131 [Peer Reviewed Journal]COPYRIGHT 2023 MDPI AG ;2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 by the authors. 2023 ;ISSN: 1660-4601 ;ISSN: 1661-7827 ;EISSN: 1660-4601 ;DOI: 10.3390/ijerph20043131 ;PMID: 36833822Full text available |
| 15 |
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Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum DisordersFrontiers in genetics, 2013, Vol.4, p.54-54 [Peer Reviewed Journal]Copyright © 2013 Gilling, Rasmussen, Calloe, Sequeira, Baretto, Oliveira, Almeida, Lauritsen, Ullmann, Boonen, Brondum-Nielsen, Kalscheuer, Tümer, Vicente, Schmitt and Tommerup. 2013 ;ISSN: 1664-8021 ;EISSN: 1664-8021 ;DOI: 10.3389/fgene.2013.00054 ;PMID: 23596459Full text available |
| 16 |
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Compensatory T-cell regulation in unaffected relatives of SLE patients, and opposite IL-2/CD25-mediated effects suggested by coreferentiality modelingPloS one, 2012-03, Vol.7 (3), p.e33992-e33992 [Peer Reviewed Journal]COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;2012 Fesel et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Fesel et al. 2012 ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0033992 ;PMID: 22479496Full text available |
| 17 |
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Brief Report: High Frequency of Biochemical Markers for Mitochondrial Dysfunction in Autism: No Association with the Mitochondrial Aspartate/Glutamate Carrier "SLC25A12" GeneJournal of autism and developmental disorders, 2006-11, Vol.36 (8), p.1137-1140 [Peer Reviewed Journal]2007 INIST-CNRS ;Springer Science+Business Media, LLC 2006 ;ISSN: 0162-3257 ;EISSN: 1573-3432 ;DOI: 10.1007/s10803-006-0138-6 ;PMID: 17151801 ;CODEN: JADDDQFull text available |
| 18 |
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Variants in the Inflammatory IL6 and MPO Genes Modulate Stroke Susceptibility Through Main Effects and Gene—Gene InteractionsJournal of cerebral blood flow and metabolism, 2011-08, Vol.31 (8), p.1751-1759 [Peer Reviewed Journal]2011 ISCBFM ;2015 INIST-CNRS ;Copyright © 2011 International Society for Cerebral Blood Flow & Metabolism, Inc. 2011 International Society for Cerebral Blood Flow & Metabolism, Inc. ;ISSN: 0271-678X ;EISSN: 1559-7016 ;DOI: 10.1038/jcbfm.2011.27 ;PMID: 21407237 ;CODEN: JCBMDNFull text available |
| 19 |
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Association of a Genetic Variant in the ALOX5AP with Higher Risk of Ischemic Stroke: A Case-Control, Meta-Analysis and Functional StudyCerebrovascular diseases (Basel, Switzerland), 2010-01, Vol.29 (6), p.528-537 [Peer Reviewed Journal]2010 S. Karger AG, Basel ;Copyright 2010 S. Karger AG, Basel. ;ISSN: 1015-9770 ;EISSN: 1421-9786 ;DOI: 10.1159/000302738 ;PMID: 20357438Full text available |
| 20 |
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Disease similarity network analysis of Autism Spectrum Disorder and comorbid brain disordersFrontiers in molecular neuroscience, 2022-08, Vol.15, p.932305-932305 [Peer Reviewed Journal]2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2022 Vilela, Martiniano, Marques, Santos, Rasga, Oliveira and Vicente. 2022 Vilela, Martiniano, Marques, Santos, Rasga, Oliveira and Vicente ;ISSN: 1662-5099 ;EISSN: 1662-5099 ;DOI: 10.3389/fnmol.2022.932305 ;PMID: 36061363Full text available |
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