Detalhe da pesquisa
1.
Whole blood transcriptome analysis in bipolar disorder reveals strong lithium effect.
Psychol Med
; 50(15): 2575-2586, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31589133
2.
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy.
Hum Mol Genet
; 24(24): 7111-20, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26427606
3.
GIGYF2 mutation in late-onset Parkinson's disease with cognitive impairment.
J Hum Genet
; 60(10): 637-40, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26134514
4.
Mitigating animal methods bias to reduce animal use and improve biomedical translation.
Sci Prog
; 107(2): 368504241253693, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38752259
5.
The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures.
Hum Mutat
; 34(9): 1200-7, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23804563
6.
Identification of COL6A2 mutations in progressive myoclonus epilepsy syndrome.
Hum Genet
; 132(3): 275-83, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23138527
7.
A survey to assess animal methods bias in scientific publishing.
ALTEX
; 40(4): 665-676, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37463512
8.
Author Guide for Addressing Animal Methods Bias in Publishing.
Adv Sci (Weinh)
; 10(30): e2303226, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37649154
9.
Proceedings of a workshop to address animal methods bias in scientific publishing.
ALTEX
; 40(4): 677-688, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36317507
10.
COVID-19 through Adverse Outcome Pathways: Building networks to better understand the disease - 3rd CIAO AOP Design Workshop.
ALTEX
; 39(2): 322335, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35032963
11.
Systematic Organization of COVID-19 Data Supported by the Adverse Outcome Pathway Framework.
Front Public Health
; 9: 638605, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34095051
12.
SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor.
ASN Neuro
; 7(4)2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26297037
13.
The use of next-generation sequencing in movement disorders.
Front Genet
; 3: 75, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22593763
14.
Variable phenotypic expression in families with early-onset Parkinsonism due to PRKN mutations.
J Neurol
; 261(6): 1223-6, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24781841