Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease
出版年份 2020 全文链接
标题
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease
作者
关键词
Parkinson's disease, DNAJC13, UCHL1, HTRA2, GIGYF2, EIF4G1, Ashkenazi-Jewish, French-Canadian, SKAT-O
出版物
NEUROBIOLOGY OF AGING
Volume 100, Issue -, Pages 119.e7-119.e13
出版商
Elsevier BV
发表日期
2020-10-31
DOI
10.1016/j.neurobiolaging.2020.10.019
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。- 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
- A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing
- (2019) Chin-Hsien Lin et al. MOVEMENT DISORDERS
- 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
- The genetics of Parkinson disease
- (2018) Hao Deng et al. AGEING RESEARCH REVIEWS
- DNAJC13 mutation screening in patients with Parkinson's disease from South Italy
- (2018) Monica Gagliardi et al. PARKINSONISM & RELATED DISORDERS
- Drosophila Ubiquitin C-Terminal Hydrolase Knockdown Model of Parkinson’s Disease
- (2018) Hiep H. Tran et al. Scientific Reports
- Mitochondrial HTRA2 Plays a Positive, Protective Role in Dictyostelium discoideum but Is Cytotoxic When Overexpressed
- (2018) Suwei Chen et al. Genes
- Systematically analyzing rare variants of autosomal-dominant genes for sporadic Parkinson's disease in a Chinese cohort
- (2018) Nannan Yang et al. NEUROBIOLOGY OF AGING
- Genetic analysis of indel markers in three loci associated with Parkinson's disease
- (2017) Zhixin Huo et al. PLoS One
- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- Identification of TMEM230 mutations in familial Parkinson's disease
- (2016) Han-Xiang Deng et al. NATURE GENETICS
- Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease
- (2016) Jay P. Ross et al. NEUROBIOLOGY OF AGING
- DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients
- (2015) O. Lorenzo-Betancor et al. EUROPEAN JOURNAL OF NEUROLOGY
- EIF4G1 mutations do not cause Parkinson's disease
- (2015) Noah Nichols et al. NEUROBIOLOGY OF AGING
- The contribution of GIGYF2 to Parkinson’s disease: a meta-analysis
- (2015) Yuan Zhang et al. NEUROLOGICAL SCIENCES
- Lack of association between UCHL1 S18Y gene polymorphism and Parkinson’s disease in the Asian population: a meta-analysis
- (2014) Shuang Sun et al. NEUROLOGICAL SCIENCES
- EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population
- (2014) Kenya Nishioka et al. PARKINSONISM & RELATED DISORDERS
- Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease
- (2014) Hilal Unal Gulsuner et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Analysis of EIF4G1 in ethnic Chinese
- (2013) Kai Li et al. BMC Neurology
- Mutations inEIF4G1are not a common cause of Parkinson's disease
- (2013) A. Siitonen et al. EUROPEAN JOURNAL OF NEUROLOGY
- DNAJC13 mutations in Parkinson disease
- (2013) Carles Vilariño-Güell et al. HUMAN MOLECULAR GENETICS
- VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians
- (2013) Sumedha Sudhaman et al. NEUROBIOLOGY OF AGING
- DNAJ mutations are rare in Chinese Parkinson's disease patients and controls
- (2013) Jia Nee Foo et al. NEUROBIOLOGY OF AGING
- Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease
- (2013) K. Nuytemans et al. NEUROLOGY
- Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies
- (2012) Seunggeun Lee et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Analysis of EIF4G1 in Parkinson's disease among Asians
- (2012) Yi Zhao et al. NEUROBIOLOGY OF AGING
- VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from Southwest China
- (2012) YongPing Chen et al. NEUROBIOLOGY OF AGING
- Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson’s disease
- (2012) Eva C. Schulte et al. NEUROGENETICS
- Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease
- (2012) Jin-yong Tian et al. NEUROSCIENCE LETTERS
- Study of the genetic variability in a Parkinson's Disease gene: EIF4G1
- (2012) Arianna Tucci et al. NEUROSCIENCE LETTERS
- Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
- (2011) Marie-Christine Chartier-Harlin et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genetic variations of Omi/HTRA2 in Chinese patients with Parkinson's disease
- (2011) Chun-yu Wang et al. BRAIN RESEARCH
- Novel variant Pro143Ala in HTRA2 contributes to Parkinson’s disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria
- (2011) Chin-Hsien Lin et al. HUMAN GENETICS
- Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease
- (2011) Lei Wang et al. JOURNAL OF CLINICAL NEUROSCIENCE
- No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients
- (2010) Lin Li et al. NEUROSCIENCE LETTERS
- Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population
- (2010) Lei Wang et al. NEUROSCIENCE LETTERS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Association Between the Ubiquitin Carboxyl-Terminal Esterase L1 Gene (UCHL1) S18Y Variant and Parkinson's Disease: A HuGE Review and Meta-Analysis
- (2009) M. Ragland et al. AMERICAN JOURNAL OF EPIDEMIOLOGY
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- Analysis of the GIGYF2 gene in familial and sporadic Parkinson disease in the Spanish population
- (2009) L. Samaranch et al. EUROPEAN JOURNAL OF NEUROLOGY
- Summary of GIGYF2 studies in Parkinson’s disease: the burden of proof
- (2009) E. K. Tan et al. EUROPEAN JOURNAL OF NEUROLOGY
- Non-synonymous GIGYF2 variants in Parkinson’s disease from two Asian populations
- (2009) Eng-King Tan et al. HUMAN GENETICS
- GIGYF2 variants are not associated with Parkinson's disease in Italy
- (2009) Monica Bonetti et al. MOVEMENT DISORDERS
- Reported mutations inGIGYF2are not a common cause of Parkinson's disease
- (2009) Carles Vilariño-Güell et al. MOVEMENT DISORDERS
- Follow-up study of the GIGYF2 gene in French families with Parkinson's disease
- (2009) Suzanne Lesage et al. NEUROBIOLOGY OF AGING
- GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population
- (2009) Bram Meeus et al. NEUROBIOLOGY OF AGING
- A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
- (2009) Rejko Krüger et al. NEUROBIOLOGY OF AGING
- Variation in GIGYF2 is not associated with Parkinson disease
- (2009) W. C. Nichols et al. NEUROLOGY
- GIGYF2 Asn56Ser and Asn457Thr mutations in Parkinson disease patients
- (2009) Yi Guo et al. NEUROSCIENCE LETTERS
- GIGYF2 Asn56Ser mutation is rare in Chinese Parkinson's disease patients
- (2009) Yu Zhang et al. NEUROSCIENCE LETTERS
- GIGYF2 mutations are not a frequent cause of familial Parkinson's disease
- (2009) Alessio Di Fonzo et al. PARKINSONISM & RELATED DISORDERS
- PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease
- (2009) Alexander Zimprich et al. PARKINSONISM & RELATED DISORDERS
- Mutations in the GIGYF2 (TNRC15) Gene at the PARK11 Locus in Familial Parkinson Disease
- (2008) Corinne Lautier et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Lack of replication of association between GIGYF2 variants and Parkinson disease
- (2008) J. Bras et al. HUMAN MOLECULAR GENETICS
- Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls
- (2008) J. Simon-Sanchez et al. HUMAN MOLECULAR GENETICS
- Genetic variability in the mitochondrial serine proteaseHTRA2contributes to risk for Parkinson disease
- (2008) Veerle Bogaerts et al. HUMAN MUTATION
- Genetic variation of Omi/HtrA2 and Parkinson's disease
- (2008) Owen A. Ross et al. PARKINSONISM & RELATED DISORDERS
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