Detalhe da pesquisa
1.
Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat allele.
Ann Hum Genet
; 2024 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38624263
2.
Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications.
Epilepsia
; 63(4): 936-949, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35170024
3.
The potential role of human multidrug resistance protein 1 (MDR1) and multidrug resistance-associated protein 2 (MRP2) in the transport of Huperzine A in vitro.
Xenobiotica
; 50(3): 354-362, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31132291
4.
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.
Eur Heart J
; 38(1): 27-34, 2017 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27742809
5.
Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population.
Am J Med Genet B Neuropsychiatr Genet
; 177(1): 86-92, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29150900
6.
Genome-wide copy number variation study in anorectal malformations.
Hum Mol Genet
; 22(3): 621-31, 2013 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23108157
7.
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
Hum Mol Genet
; 21(5): 1184-9, 2012 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22116939
8.
Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy.
Hum Genet
; 133(5): 651-9, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24337656
9.
ELF1 is associated with systemic lupus erythematosus in Asian populations.
Hum Mol Genet
; 20(3): 601-7, 2011 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21044949
10.
Potential role for human P-glycoprotein in the transport of lacosamide.
Epilepsia
; 54(7): 1154-60, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23551115
11.
Variants conferring risk of atrial fibrillation on chromosome 4q25.
Nature
; 448(7151): 353-7, 2007 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-17603472
12.
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data.
Nat Commun
; 14(1): 1131, 2023 02 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36854672
13.
Effects of Deferasirox in Alzheimer's Disease and Tauopathy Animal Models.
Biomolecules
; 12(3)2022 02 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35327557
14.
Third-generation genome sequencing implicates medium-sized structural variants in chronic schizophrenia.
Front Neurosci
; 16: 1058359, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36711134
15.
In vitro transport profile of carbamazepine, oxcarbazepine, eslicarbazepine acetate, and their active metabolites by human P-glycoprotein.
Epilepsia
; 52(10): 1894-904, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21692796
16.
Association of 8q24.21 loci with the risk of colorectal cancer: a systematic review and meta-analysis.
J Gastroenterol Hepatol
; 26(10): 1475-84, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21722176
17.
Preservation of Retinal Function Through Synaptic Stabilization in Alzheimer's Disease Model Mouse Retina by Lycium Barbarum Extracts.
Front Aging Neurosci
; 13: 788798, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35095474
18.
Pharmacogenetic analysis of lipid responses to rosuvastatin in Chinese patients.
Pharmacogenet Genomics
; 20(10): 634-7, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20679960
19.
Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy.
Epilepsia
; 51(9): 1878-81, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20477842
20.
Serum zinc is decreased in Alzheimer's disease and serum arsenic correlates positively with cognitive ability.
Biometals
; 23(1): 173-9, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19911117