Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study
出版年份 2023 全文链接
标题
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study
作者
关键词
-
出版物
LANCET NEUROLOGY
Volume 22, Issue 11, Pages 1015-1025
出版商
Elsevier BV
发表日期
2023-08-24
DOI
10.1016/s1474-4422(23)00283-1
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Genetic risk factor clustering within and across neurodegenerative diseases
- (2023) Mathew J Koretsky et al. BRAIN
- Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture
- (2023) Linda Kachuri et al. NATURE GENETICS
- Comprehensive short and long read sequencing analysis for the Gaucher and Parkinson’s disease-associated GBA gene
- (2022) Marco Toffoli et al. Communications Biology
- Characterizing the Genetic Architecture of Parkinson's Disease in Latinos
- (2021) Douglas P. Loesch et al. ANNALS OF NEUROLOGY
- Screening of GBA Mutations in Nigerian Patients with Parkinson's Disease
- (2021) Lukasz M. Milanowski et al. MOVEMENT DISORDERS
- Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans
- (2020) Jia Nee Foo et al. JAMA Neurology
- The genetic architecture of Parkinson's disease
- (2019) Cornelis Blauwendraat et al. LANCET NEUROLOGY
- Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
- (2019) Mike A Nalls et al. LANCET NEUROLOGY
- Screening of the glucocerebrosidase (GBA) gene in South Africans of African ancestry with Parkinson's disease
- (2019) Amokelani C. Mahungu et al. NEUROBIOLOGY OF AGING
- Leucine rich repeat kinase 2 (LRRK2) GLY2019SER mutation is absent in a second cohort of Nigerian Africans with Parkinson disease
- (2018) Njideka U. Okubadejo et al. PLoS One
- NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
- (2017) Cornelis Blauwendraat et al. NEUROBIOLOGY OF AGING
- Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel
- (2017) Ahmed Bouhouche et al. Frontiers in Neurology
- DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study
- (2016) Joanne Trinh et al. LANCET NEUROLOGY
- Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease
- (2012) Ekaterina Yonova-Doing et al. PARKINSONISM & RELATED DISORDERS
- G2019S Mutation of the Leucine-Rich Repeat Kinase 2 Gene in a Cohort of Egyptian Patients with Parkinson's Disease
- (2011) Doaa I. Hashad et al. Genetic Testing and Molecular Biomarkers
- A generalizable hypothesis for the genetic architecture of disease: pleomorphic risk loci
- (2011) A. Singleton et al. HUMAN MOLECULAR GENETICS
- Screening LRRK2 gene mutations in patients with Parkinson’s disease in Ghana
- (2011) Roberto Cilia et al. JOURNAL OF NEUROLOGY
- METAL: fast and efficient meta-analysis of genomewide association scans
- (2010) C. J. Willer et al. BIOINFORMATICS
- LRRK2 variation and Parkinson's disease in African Americans
- (2010) Owen A. Ross et al. MOVEMENT DISORDERS
- Glucocerebrosidase mutations in diffuse Lewy body disease
- (2010) Kenya Nishioka et al. PARKINSONISM & RELATED DISORDERS
- Genome-wide association study reveals genetic risk underlying Parkinson's disease
- (2009) Javier Simón-Sánchez et al. NATURE GENETICS
- Analysis of exon dosage using MLPA in South African Parkinson's disease patients
- (2009) Rowena J. Keyser et al. NEUROGENETICS
- LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study
- (2008) Mary M Hulihan et al. LANCET NEUROLOGY
- PINK1 mutations and parkinsonism
- (2008) L. Ishihara-Paul et al. NEUROLOGY
- Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's disease
- (2008) Soraya Bardien et al. PARKINSONISM & RELATED DISORDERS
- Analysis of Nigerians with Apparently Sporadic Parkinson Disease for Mutations in LRRK2, PRKN and ATXN3
- (2008) Njideka Okubadejo et al. PLoS One
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