Detalhe da pesquisa
1.
Genetic and genomic signatures in ethanol withdrawal seizure-prone and seizure-resistant mice implicate genes involved in epilepsy and neuronal excitability.
Mol Psychiatry
; 27(11): 4611-4623, 2022 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-36198764
2.
Strong and weak cross-inheritance of substance use disorders in a nationally representative sample.
Mol Psychiatry
; 27(3): 1742-1753, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34759357
3.
Multi-omics analysis of alcohol effects on the liver in young and aged mice.
Addict Biol
; 28(12): e13342, 2023 12.
Artigo
Inglês
| MEDLINE | ID: mdl-38017640
4.
Epigenome-wide association study and multi-tissue replication of individuals with alcohol use disorder: evidence for abnormal glucocorticoid signaling pathway gene regulation.
Mol Psychiatry
; 26(6): 2224-2237, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-32398718
5.
Exploratory locomotion, a predictor of addiction vulnerability, is oligogenic in rats selected for this phenotype.
Proc Natl Acad Sci U S A
; 116(26): 13107-13115, 2019 06 25.
Artigo
Inglês
| MEDLINE | ID: mdl-31182603
6.
Host-parasite interaction associated with major mental illness.
Mol Psychiatry
; 25(1): 194-205, 2020 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30127472
7.
Network Meta-Analysis on the Mechanisms Underlying Alcohol Augmentation of COVID-19 Pathologies.
Alcohol Clin Exp Res
; 45(4): 675-688, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33583045
8.
TSPO polymorphism in individuals with alcohol use disorder: Association with cholesterol levels and withdrawal severity.
Addict Biol
; 26(1): e12838, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31713961
9.
Effects of TPH2 gene variation and childhood trauma on the clinical and circuit-level phenotype of functional movement disorders.
J Neurol Neurosurg Psychiatry
; 91(8): 814-821, 2020 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32576619
10.
Relations between catechol-O-methyltransferase Val158Met genotype and inhibitory control development in childhood.
Dev Psychobiol
; 62(2): 181-190, 2020 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31372986
11.
Early-Life Adversity and Blunted Stress Reactivity as Predictors of Alcohol and Drug use in Persons With COMT (rs4680) Val158Met Genotypes.
Alcohol Clin Exp Res
; 43(7): 1519-1527, 2019 07.
Artigo
Inglês
| MEDLINE | ID: mdl-31150143
12.
New Repeat Polymorphism in the AKT1 Gene Predicts Striatal Dopamine D2/D3 Receptor Availability and Stimulant-Induced Dopamine Release in the Healthy Human Brain.
J Neurosci
; 37(19): 4982-4991, 2017 05 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28416594
13.
Severity of alcohol dependence is associated with the fatty acid amide hydrolase Pro129Thr missense variant.
Addict Biol
; 23(1): 474-484, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28150397
14.
Heightened amygdala responsiveness in s-carriers of 5-HTTLPR genetic polymorphism reflects enhanced cortical rather than subcortical inputs: An MEG study.
Hum Brain Mapp
; 38(9): 4313-4321, 2017 09.
Artigo
Inglês
| MEDLINE | ID: mdl-28580622
15.
Joint Impact of Early Life Adversity and COMT Val158Met (rs4680) Genotypes on the Adult Cortisol Response to Psychological Stress.
Psychosom Med
; 79(6): 631-637, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28452825
16.
Genome-wide association study in essential tremor identifies three new loci.
Brain
; 139(Pt 12): 3163-3169, 2016 12.
Artigo
Inglês
| MEDLINE | ID: mdl-27797806
17.
The Leu72Met Polymorphism of the Prepro-ghrelin Gene is Associated With Alcohol Consumption and Subjective Responses to Alcohol: Preliminary Findings.
Alcohol Alcohol
; 52(4): 425-430, 2017 Jul 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28481975
18.
The abundance of cis-acting loci leading to differential allele expression in F1 mice and their relationship to loci harboring genes affecting complex traits.
BMC Genomics
; 17(1): 620, 2016 08 11.
Artigo
Inglês
| MEDLINE | ID: mdl-27515598
19.
Association of Superoxide Dismutase 2 (SOD2) Genotype with Gray Matter Volume Shrinkage in Chronic Alcohol Users: Replication and Further Evaluation of an Addiction Gene Panel.
Int J Neuropsychopharmacol
; 19(9)2016 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-27207918
20.
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts.
Behav Genet
; 46(2): 151-69, 2016 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-26392368