Detalhe da pesquisa
1.
An exploration of the genetics of the mutant Huntingtin (mHtt) gene in a cohort of patients with chorea from different ethnic groups in sub-Saharan Africa.
Ann Hum Genet
; 2024 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38563088
2.
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians.
Mov Disord
; 39(4): 728-733, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38390630
3.
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions.
Mov Disord
; 37(8): 1593-1604, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35867623
4.
Central European Group on Genetics of Movement Disorders.
Eur J Neurol
; 31(4): e16165, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38059386
5.
Metabolomic profiling reveals altered phenylalanine metabolism in Parkinson's disease in an Egyptian cohort.
Front Mol Biosci
; 11: 1341950, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38516193
6.
The non-coding GBA1 rs3115534 variant is associated with REM sleep behavior disorder in Nigerians.
medRxiv
; 2023 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38076854
7.
MAPT allele and haplotype frequencies in Nigerian Africans: population distribution and association with Parkinson's disease risk and age at onset.
medRxiv
; 2023 Mar 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36993627
8.
Evaluating the performance of polygenic risk profiling across diverse ancestry populations in Parkinson's disease.
medRxiv
; 2023 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38076954
9.
MAPT allele and haplotype frequencies in Nigerian Africans: Population distribution and association with Parkinson's disease risk and age at onset.
Parkinsonism Relat Disord
; 113: 105517, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37467655
10.
Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed Populations.
medRxiv
; 2023 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37398408
11.
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study.
Lancet Neurol
; 22(11): 1015-1025, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37633302
12.
Spectrum of movement disorders: Experience of a one and half year of existence of the first specialized center in Senegal.
Parkinsonism Relat Disord
; 98: 13-15, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35421779
13.
Prevalence of Fabry Disease among Patients with Parkinson's Disease.
Parkinsons Dis
; 2022: 1014950, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35111290
14.
WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxia.
Parkinsonism Relat Disord
; 94: 54-61, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34890876
15.
Comparing fluid biomarkers of Alzheimer's disease between African American or Black African and white groups: A systematic review and meta-analysis.
J Neurol Sci
; 421: 117270, 2021 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33349466
16.
Negative screening for 12 rare LRRK2 pathogenic variants in a cohort of Nigerians with Parkinson's disease.
Neurobiol Aging
; 99: 101.e15-101.e19, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33158606
17.
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease.
Neurobiol Aging
; 97: 148.e17-148.e24, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32873436
18.
A Cross-Sectional Comprehensive Assessment of the Profile and Burden of Non-motor Symptoms in Relation to Motor Phenotype in the Nigeria Parkinson Disease Registry Cohort.
Mov Disord Clin Pract
; 8(8): 1206-1215, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34765688
19.
Novel fluid biomarkers to differentiate frontotemporal dementia and dementia with Lewy bodies from Alzheimer's disease: A systematic review.
J Neurol Sci
; 415: 116886, 2020 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32428759
20.
LRRK2 Mutations and Asian Disease-Associated Variants in the First Parkinson's Disease Cohort from Kazakhstan.
Parkinsons Dis
; 2020: 2763838, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32148752