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Multi-omics profiling of DNA methylation and gene expression alterations in human cocaine use disorder.
- Published in:
- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-03139-9
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- Publication type:
- Article
Disentangling heterogeneity in substance use disorder: Insights from genome-wide polygenic scores.
- Published in:
- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-02923-x
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- Publication type:
- Article
The pleiotropic contribution of genes in dopaminergic and serotonergic pathways to addiction and related behavioral traits.
- Published in:
- Frontiers in Psychiatry, 2023, p. 1, doi. 10.3389/fpsyt.2023.1293663
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- Publication type:
- Article
Decreased Brain Serotonin in rbfox1 Mutant Zebrafish and Partial Reversion of Behavioural Alterations by the SSRI Fluoxetine.
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- Pharmaceuticals (14248247), 2024, v. 17, n. 2, p. 254, doi. 10.3390/ph17020254
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- Publication type:
- Article
Differential expression of miR-1249-3p and miR-34b-5p between vulnerable and resilient phenotypes of cocaine addiction.
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- 2022
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- Publication type:
- journal article
Frustrated expected reward induces differential transcriptional changes in the mouse brain.
- Published in:
- Addiction Biology, 2015, v. 20, n. 1, p. 22, doi. 10.1111/adb.12188
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- Publication type:
- Article
Replication study of previous migraine genome-wide association study findings in a Spanish sample of migraine with aura.
- Published in:
- Cephalalgia, 2015, v. 35, n. 9, p. 776, doi. 10.1177/0333102414557841
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- Publication type:
- Article
A replication study of a GWAS finding in migraine does not identify association in a Spanish case-control sample.
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- Cephalalgia, 2012, v. 32, n. 14, p. 1076, doi. 10.1177/0333102412457090
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- Publication type:
- Article
Genomics and epigenomics of substance use disorders: An introduction.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2021, v. 186, n. 3, p. 125, doi. 10.1002/ajmg.b.32844
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- Publication type:
- Article
Cover Image, Volume 171B, Number 5, July 2016.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 5, p. i, doi. 10.1002/ajmg.b.32513
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- Publication type:
- Article
Aggressive behavior in humans: Genes and pathways identified through association studies.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 5, p. 676, doi. 10.1002/ajmg.b.32419
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- Publication type:
- Article
Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 5, p. 733, doi. 10.1002/ajmg.b.32434
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- Publication type:
- Article
The genetics of aggression: Where are we now?
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 5, p. 559, doi. 10.1002/ajmg.b.32450
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- Publication type:
- Article
Genetics of Aggressive Behavior: An Overview.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 1, p. 3, doi. 10.1002/ajmg.b.32364
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- Publication type:
- Article
On the role of NOS1 ex1f-VNTR in ADHD-allelic, subgroup, and meta-analysis.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 6, p. 445, doi. 10.1002/ajmg.b.32326
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- Publication type:
- Article
Dopamine receptor DRD4 gene and stressful life events in persistent attention deficit hyperactivity disorder.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 6, p. 480, doi. 10.1002/ajmg.b.32340
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- Publication type:
- Article
New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 6, p. 459, doi. 10.1002/ajmg.b.32341
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- Publication type:
- Article
DISC1 in Adult ADHD Patients: An Association Study in Two European Samples.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 3, p. 227, doi. 10.1002/ajmg.b.32136
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- Publication type:
- Article
Screening of CD96 and ASXL1 in 11 Patients with Opitz C or Bohring-Opitz Syndromes.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 1, p. 24, doi. 10.1002/ajmg.a.37418
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- Publication type:
- Article
Pleiotropic contribution of rbfox1 to psychiatric and neurodevelopmental phenotypes in two zebrafish models.
- Published in:
- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-02801-6
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- Publication type:
- Article
A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes.
- Published in:
- Scientific Reports, 2017, p. 44138, doi. 10.1038/srep44138
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- Publication type:
- Article
A Highly Polymorphic Copy Number Variant in the NSF Gene is Associated with Cocaine Dependence.
- Published in:
- Scientific Reports, 2016, p. 31033, doi. 10.1038/srep31033
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- Publication type:
- Article
Characterization of an eutherian gene cluster generated after transposon domestication identifies Bex3 as relevant for advanced neurological functions.
- Published in:
- Genome Biology, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s13059-020-02172-3
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- Publication type:
- Article
Evaluation of Aminoglycoside and Non-Aminoglycoside Compounds for Stop-Codon Readthrough Therapy in Four Lysosomal Storage Diseases.
- Published in:
- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0135873
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- Publication type:
- Article
Chiari Malformation Type I: A Case-Control Association Study of 58 Developmental Genes.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0057241
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- Publication type:
- Article
Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
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- Journal of Psychiatry & Neuroscience, 2019, v. 44, n. 5, p. 350, doi. 10.1503/jpn.180184
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- Publication type:
- Article
Homovanillic acid in cerebrospinal fluid of 1388 children with neurological disorders.
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- Developmental Medicine & Child Neurology, 2013, v. 55, n. 6, p. 559, doi. 10.1111/dmcn.12116
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- Publication type:
- Article
A mutation within the saposin D domain in a Gaucher disease patient with normal glucocerebrosidase activity.
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- Human Genetics, 2005, v. 117, n. 2/3, p. 275, doi. 10.1007/s00439-005-1288-x
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- Publication type:
- Article
Gene rearrangements in the glucocerebrosidase-metaxin region giving rise to disease-causing mutations and polymorphisms. Analysis of 25 RecNciI alleles in Gaucher disease patients.
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- Human Genetics, 2003, v. 112, n. 4, p. 426, doi. 10.1007/s00439-002-0894-0
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- Publication type:
- Article
Comprehensive exploration of the genetic contribution of the dopaminergic and serotonergic pathways to psychiatric disorders.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-021-01771-3
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- Publication type:
- Article
Reduced cue-induced reinstatement of cocaine-seeking behavior in Plcb1 +/− mice.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01396-6
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- Publication type:
- Article
HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-61628-9
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- Publication type:
- Article
Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability.
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- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1694, doi. 10.1038/ejhg.2015.37
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- Publication type:
- Article
A causal effects of gut microbiota in the development of migraine.
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- Journal of Headache & Pain, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s10194-023-01609-x
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- Publication type:
- Article
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study.
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- Journal of Headache & Pain, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s10194-023-01550-z
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- Publication type:
- Article
The hemiplegic migraine-associated Y1245C mutation in CACNA1A results in a gain of channel function due to its effect on the voltage sensor and G-protein-mediated inhibition.
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- Pflügers Archiv: European Journal of Physiology, 2009, v. 458, n. 3, p. 489, doi. 10.1007/s00424-009-0637-3
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- Publication type:
- Article
Exploring genetic variation that influences brain methylation in attention-deficit/hyperactivity disorder.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41398-019-0574-7
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- Publication type:
- Article
ADGRL3 (LPHN3) variants predict substance use disorder.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-019-0396-7
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- Publication type:
- Article
MiR-9, miR-153 and miR-124 are down-regulated by acute exposure to cocaine in a dopaminergic cell model and may contribute to cocaine dependence.
- Published in:
- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0224-5
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- Publication type:
- Article
Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-65322-4
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- Publication type:
- Article
Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarization.
- Published in:
- Cephalalgia, 2023, v. 43, n. 2, p. 1, doi. 10.1177/03331024221146317
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- Publication type:
- Article
Cerebrospinal fluid alterations of the serotonin product, 5-hydroxyindolacetic acid, in neurological disorders.
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- Journal of Inherited Metabolic Disease, 2010, v. 33, n. 6, p. 803, doi. 10.1007/s10545-010-9200-9
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- Publication type:
- Article
Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 gene.
- Published in:
- Journal of Inherited Metabolic Disease, 2010, v. 33, n. 6, p. 795, doi. 10.1007/s10545-010-9196-1
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- Publication type:
- Article
Variants of the Aggression-Related RBFOX1 Gene in a Population Representative Birth Cohort Study: Aggressiveness, Personality, and Alcohol Use Disorder.
- Published in:
- Frontiers in Psychiatry, 2020, v. 11, p. N.PAG, doi. 10.3389/fpsyt.2020.501847
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- Publication type:
- Article
Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing.
- Published in:
- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0168966
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- Publication type:
- Article
Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or Inattention.
- Published in:
- Genes, 2022, v. 13, n. 1, p. 93, doi. 10.3390/genes13010093
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- Publication type:
- Article
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred.
- Published in:
- Neurogenetics, 2009, v. 10, n. 3, p. 191, doi. 10.1007/s10048-008-0169-6
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- Publication type:
- Article
Levodopa-induced dyskinesias in tyrosine hydroxylase deficiency.
- Published in:
- Movement Disorders, 2013, v. 28, n. 8, p. 1058, doi. 10.1002/mds.25382
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- Publication type:
- Article
Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype.
- Published in:
- Movement Disorders, 2011, v. 26, n. 8, p. 1558, doi. 10.1002/mds.23564
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- Publication type:
- Article
Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation.
- Published in:
- Movement Disorders, 2010, v. 25, n. 8, p. 1086, doi. 10.1002/mds.23002
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- Publication type:
- Article