Detalhe da pesquisa
1.
MicroRNA Profiling of the Inflammatory Response after Early and Late Asthmatic Reaction.
Int J Mol Sci;
25(2)2024 Jan 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38279356
2.
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype.
Am J Hum Genet;
107(3): 555-563, 2020 09 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32758449
3.
Association between Polyunsaturated Fatty Acid Profile and Bronchial Inflammation in Bronchiolitis Obliterans.
Mediators Inflamm;
2023: 3406399, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37448886
4.
DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan.
Mol Psychiatry;
26(6): 2148-2162, 2021 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33420481
5.
Effects of Hypoxia on RNA Cargo in Extracellular Vesicles from Human Adipose-Derived Stromal/Stem Cells.
Int J Mol Sci;
23(13)2022 Jul 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35806391
6.
ADHD-associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient-derived cell lines.
Am J Med Genet B Neuropsychiatr Genet;
189(7-8): 257-270, 2022 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35971782
7.
Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.
Am J Hum Genet;
102(5): 744-759, 2018 05 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29656859
8.
The MiR-320 Family Is Strongly Downregulated in Patients with COVID-19 Induced Severe Respiratory Failure.
Int J Mol Sci;
22(19)2021 Sep 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34638691
9.
[Genetic risk factors and their influence on neural development in autism spectrum disorders]. / Genetische Risikofaktoren und ihre Auswirkungen auf die neurale Entwicklung bei Autismus-Spektrum-Störungen.
Z Kinder Jugendpsychiatr Psychother;
50(3): 187-202, 2021 May.
Artigo
em Alemão
| MEDLINE
| ID: mdl-34128703
10.
Synaptic, transcriptional and chromatin genes disrupted in autism.
Nature;
515(7526): 209-15, 2014 Nov 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25363760
11.
Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot study.
J Neural Transm (Vienna);
126(12): 1679-1693, 2019 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31707462
12.
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities.
J Neural Transm (Vienna);
125(2): 259-271, 2018 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29147782
13.
Conduct disorder in adolescent females: current state of research and study design of the FemNAT-CD consortium.
Eur Child Adolesc Psychiatry;
27(9): 1077-1093, 2018 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29948230
14.
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Am J Hum Genet;
94(5): 677-94, 2014 May 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24768552
15.
The neurobiological basis of human aggression: A review on genetic and epigenetic mechanisms.
Am J Med Genet B Neuropsychiatr Genet;
171(5): 650-75, 2016 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26494515
16.
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
Hum Genet;
133(6): 781-92, 2014 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24442360
17.
Glutamatergic candidate genes in autism spectrum disorder: an overview.
J Neural Transm (Vienna);
121(9): 1081-106, 2014 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24493018
18.
Common EIF4E variants modulate risk for autism spectrum disorders in the high-functioning range.
J Neural Transm (Vienna);
121(9): 1107-16, 2014 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24818597
19.
Interferon regulatory factor 4 plays a pivotal role in the development of aGVHD-associated colitis.
Oncoimmunology;
13(1): 2296712, 2024.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38170159
20.
Generation of four human induced pluripotent stem cells derived from ADHD patients carrying different genotypes for the risk SNP rs1397547 in the ADHD-associated gene ADGRL3.
Stem Cell Res;
67: 103016, 2023 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36640473