Rare genetic variation in mitochondrial pathways influences the risk for parkinson's disease
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Title
Rare genetic variation in mitochondrial pathways influences the risk for parkinson's disease
Authors
Keywords
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Journal
MOVEMENT DISORDERS
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2018-09-05
DOI
10.1002/mds.64
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- (2016) Anne Grünewald et al. ANNALS OF NEUROLOGY
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- (2016) Charalampos Tzoulis et al. MITOCHONDRION
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- (2016) Christian Dölle et al. Nature Communications
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- (2015) Sarah E. Calvo et al. NUCLEIC ACIDS RESEARCH
- Second-generation PLINK: rising to the challenge of larger and richer datasets
- (2015) Christopher C Chang et al. GigaScience
- A new pathway for mitochondrial quality control: mitochondrial-derived vesicles
- (2014) A. Sugiura et al. EMBO JOURNAL
- A polygenic burden of rare disruptive mutations in schizophrenia
- (2014) Shaun M. Purcell et al. NATURE
- Loss-of-Function Mutations in APOC3 and Risk of Ischemic Vascular Disease
- (2014) Anders Berg Jørgensen et al. NEW ENGLAND JOURNAL OF MEDICINE
- STRING v10: protein–protein interaction networks, integrated over the tree of life
- (2014) Damian Szklarczyk et al. NUCLEIC ACIDS RESEARCH
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- (2014) Laura Fejerman et al. Nature Communications
- Mesencephalic complex I deficiency does not correlate with parkinsonism in mitochondrial DNA maintenance disorders
- (2013) Eino J. H. Palin et al. BRAIN
- Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations
- (2013) Charalampos Tzoulis et al. BRAIN
- Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanisms
- (2013) Celine Perier et al. BRAIN
- Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
- (2013) G. Hudson 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
- LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1
- (2012) X. Wang et al. HUMAN MOLECULAR GENETICS
- Number of CAG repeats in POLG1 and its association with Parkinson disease in the Norwegian population
- (2012) Novin Balafkan et al. MITOCHONDRION
- A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline
- (2012) Thorlakur Jonsson et al. NATURE
- Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
- (2011) Michael C. Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The variant call format and VCFtools
- (2011) P. Danecek et al. BIOINFORMATICS
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
- (2011) H. Li BIOINFORMATICS
- Optimally weighted Z-test is a powerful method for combining probabilities in meta-analysis
- (2011) D. V. ZAYKIN JOURNAL OF EVOLUTIONARY BIOLOGY
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
- The Parkinson Progression Marker Initiative (PPMI)
- (2011) Kenneth Marek et al. PROGRESS IN NEUROBIOLOGY
- Inhibition of mitochondrial fusion by α-synuclein is rescued by PINK1, Parkin and DJ-1
- (2010) Frits Kamp et al. EMBO JOURNAL
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- DJ-1 acts in parallel to the PINK1/parkin pathway to control mitochondrial function and autophagy
- (2010) Kelly Jean Thomas et al. HUMAN MOLECULAR GENETICS
- Oxidant stress evoked by pacemaking in dopaminergic neurons is attenuated by DJ-1
- (2010) Jaime N. Guzman et al. NATURE
- Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease
- (2010) Yukihide Momozawa et al. NATURE GENETICS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- Incidence of Parkinson's disease in Norway: the Norwegian ParkWest study
- (2009) G Alves et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Mitochondrial transcription factor A variants and the risk of Parkinson's disease
- (2009) Katarzyna Gaweda-Walerych et al. NEUROSCIENCE LETTERS
- The PINK1–Parkin pathway is involved in the regulation of mitochondrial remodeling process
- (2008) Jeehye Park et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
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