Found: 34
Select item for more details and to access through your institution.
Association of a Genetic Variant in the ALOX5AP with Higher Risk of Ischemic Stroke: A Case-Control, Meta-Analysis and Functional Study.
- Published in:
- Cerebrovascular Diseases, 2010, v. 29, n. 6, p. 528, doi. 10.1159/000302738
- By:
- Publication type:
- Article
Prevalence of Autism Spectrum Disorder in the Centro region of Portugal: a population based study of school age children within the ASDEU project.
- Published in:
- Frontiers in Psychiatry, 2023, p. 1, doi. 10.3389/fpsyt.2023.1148184
- By:
- Publication type:
- Article
Hope for GWAS: Relevant Risk Genes Uncovered from GWAS Statistical Noise.
- Published in:
- International Journal of Molecular Sciences, 2014, v. 15, n. 10, p. 17601, doi. 10.3390/ijms151017601
- By:
- Publication type:
- Article
The role of rare compound heterozygous events in autism spectrum disorder.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-00866-7
- By:
- Publication type:
- Article
Pharmacogenetic Profile of a South Portuguese Population: Results from the Pilot Study of the European Health Examination Survey in Portugal.
- Published in:
- Public Health Genomics, 2015, v. 18, n. 3, p. 139, doi. 10.1159/000373920
- By:
- Publication type:
- Article
Low frequency of CD4<sup>+</sup> CD25<sup>+</sup> Treg in SLE patients: a heritable trait associated with CTLA4 and TGF gene variants.
- Published in:
- BMC Immunology, 2009, v. 10, p. 1, doi. 10.1186/1471-2172-10-5
- By:
- Publication type:
- Article
Protein Interaction Networks Reveal Novel Autism Risk Genes within GWAS Statistical Noise.
- Published in:
- PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0112399
- By:
- Publication type:
- Article
Compensatory T-Cell Regulation in Unaffected Relatives of SLE Patients, and Opposite IL-2/CD25-Mediated Effects Suggested by Coreferentiality Modeling.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0033992
- By:
- Publication type:
- Article
Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions.
- Published in:
- Developmental Medicine & Child Neurology, 2007, v. 49, n. 10, p. 726, doi. 10.1111/j.1469-8749.2007.00726.x
- By:
- Publication type:
- Article
Mental Health of Healthcare Professionals: Two Years of the COVID-19 Pandemic in Portugal.
- Published in:
- International Journal of Environmental Research & Public Health, 2023, v. 20, n. 4, p. 3131, doi. 10.3390/ijerph20043131
- By:
- Publication type:
- Article
Kalirin: a novel genetic risk factor for ischemic stroke.
- Published in:
- Human Genetics, 2010, v. 127, n. 5, p. 513, doi. 10.1007/s00439-010-0790-y
- By:
- Publication type:
- Article
Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels.
- Published in:
- Human Genetics, 2007, v. 121, n. 2, p. 243, doi. 10.1007/s00439-006-0301-3
- By:
- Publication type:
- Article
Brief Report: High Frequency of Biochemical Markers for Mitochondrial Dysfunction in Autism: No Association with the Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene.
- Published in:
- Journal of Autism & Developmental Disorders, 2006, v. 36, n. 8, p. 1137, doi. 10.1007/s10803-006-0138-6
- By:
- Publication type:
- Article
Partial Tetrasomy of Chromosome 3q and Mosaicism in a Child with Autism.
- Published in:
- Journal of Autism & Developmental Disorders, 2003, v. 33, n. 2, p. 177, doi. 10.1023/A:1022943627660
- By:
- Publication type:
- Article
CNVs leading to fusion transcripts in individuals with autism spectrum disorder.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 11, p. 1141, doi. 10.1038/ejhg.2012.73
- By:
- Publication type:
- Article
A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 3, p. 312, doi. 10.1038/sj.ejhg.5201985
- By:
- Publication type:
- Article
Evidence for CTLA4 as a susceptibility gene for systemic lupus erythematosus.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 8, p. 620, doi. 10.1038/sj.ejhg.5201214
- By:
- Publication type:
- Article
TTC7B emerges as a novel risk factor for ischemic stroke through the convergence of several genome-wide approaches.
- Published in:
- Journal of Cerebral Blood Flow & Metabolism, 2012, v. 32, n. 6, p. 1061, doi. 10.1038/jcbfm.2012.24
- By:
- Publication type:
- Article
Variants in the inflammatory IL6 and MPO genes modulate stroke susceptibility through main effects and gene-gene interactions.
- Published in:
- Journal of Cerebral Blood Flow & Metabolism, 2011, v. 31, n. 8, p. 1751, doi. 10.1038/jcbfm.2011.27
- By:
- Publication type:
- Article
Identification of biological mechanisms underlying a multidimensional ASD phenotype using machine learning.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-0721-1
- By:
- Publication type:
- Article
Evaluation of Linkage Disequilibrium on the Xq13.3 Region: Comparison Between the Azores Islands and Mainland Portugal.
- Published in:
- American Journal of Human Biology, 2008, v. 20, n. 3, p. 364, doi. 10.1002/ajhb.20734
- By:
- Publication type:
- Article
Genetic Signature of the São Miguel Island Population (Azores) Assessed by 21 Microsatellite Loci.
- Published in:
- American Journal of Human Biology, 2008, v. 20, n. 1, p. 118, doi. 10.1002/ajhb.20692
- By:
- Publication type:
- Article
Disease similarity network analysis of Autism Spectrum Disorder and comorbid brain disorders.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.932305
- By:
- Publication type:
- Article
Identification of Neurotransmission and Synaptic Biological Processes Disrupted in Autism Spectrum Disorder Using Interaction Networks and Community Detection Analysis.
- Published in:
- Biomedicines, 2023, v. 11, n. 11, p. 2971, doi. 10.3390/biomedicines11112971
- By:
- Publication type:
- Article
Gene Variants Involved in Nonsense-Mediated mRNA Decay Suggest a Role in Autism Spectrum Disorder.
- Published in:
- Biomedicines, 2022, v. 10, n. 3, p. 665, doi. 10.3390/biomedicines10030665
- By:
- Publication type:
- Article
Biomedical knowledge graph embeddings for personalized medicine: Predicting disease‐gene associations.
- Published in:
- Expert Systems, 2023, v. 40, n. 5, p. 1, doi. 10.1111/exsy.13181
- By:
- Publication type:
- Article
Genetic variation at the CYP2C19 gene associated with metabolic syndrome susceptibility in a South Portuguese population: results from the pilot study of the European health examination survey in Portugal.
- Published in:
- Diabetology & Metabolic Syndrome, 2014, v. 6, n. 1, p. 1, doi. 10.1186/1758-5996-6-23
- By:
- Publication type:
- Article
Are we PREPAREd? Concerning the "PREemptive Pharmacogenomics Testing for Preventing Adverse Drug Reactions (PREPARE) Study".
- Published in:
- 2023
- By:
- Publication type:
- Letter to the Editor
Identifying disease genes using machine learning and gene functional similarities, assessed through Gene Ontology.
- Published in:
- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208626
- By:
- Publication type:
- Article
Bridging Genetic Insights with Neuroimaging in Autism Spectrum Disorder—A Systematic Review.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 9, p. 4938, doi. 10.3390/ijms25094938
- By:
- Publication type:
- Article
A Role for Gene-Environment Interactions in Autism Spectrum Disorder Is Supported by Variants in Genes Regulating the Effects of Exposure to Xenobiotics.
- Published in:
- Frontiers in Neuroscience, 2022, p. 1, doi. 10.3389/fnins.2022.862315
- By:
- Publication type:
- Article
How personalised medicine will transform healthcare by 2030: the ICPerMed vision.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Variants of the Matrix Metalloproteinase-2 but not the Matrix Metalloproteinase-9 genes significantly influence functional outcome after stroke.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 40, doi. 10.1186/1471-2350-11-40
- By:
- Publication type:
- Article
Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-57
- By:
- Publication type:
- Article