362(top 1%)
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35.8K(top 0.1%)
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96(top 0.1%)
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182(top 0.1%)
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39.7K
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3.2K
citing journals

Top Articles

#TitleJournalYearCitations
1A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTDNeuron20113,833
2Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseNature Genetics20141,685
3Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagationNature Medicine20081,595
4Analysis of shared heritability in common disorders of the brainScience20181,085
5Serum Neurofilament light: A biomarker of neuronal damage in multiple sclerosisAnnals of Neurology2017768
6Direct Observation of the Interconversion of Normal and Toxic Forms of α-SynucleinCell2012755
7Magnetization transfer ratio and myelin in postmortem multiple sclerosis brainAnnals of Neurology2004678
8Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's diseaseBrain2009612
9Identification of common variants associated with human hippocampal and intracranial volumesNature Genetics2012594
10Genome-wide Analyses Identify KIF5A as a Novel ALS GeneNeuron2018517
11Identification of common variants influencing risk of the tauopathy progressive supranuclear palsyNature Genetics2011502
12Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene DatabasePLoS Genetics2012495
13Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisNature Genetics2016494
14Glucocerebrosidase deficiency in substantia nigra of parkinson disease brainsAnnals of Neurology2012473
15A genetic cause of Alzheimer disease: mechanistic insights from Down syndromeNature Reviews Neuroscience2015404
16Maternal Diet-Induced Obesity Alters Mitochondrial Activity and Redox Status in Mouse Oocytes and ZygotesPLoS ONE2010401
17Characterization of PLA2G6 as a locus for dystonia‐parkinsonismAnnals of Neurology2009399
18Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisNature Neuroscience2014398
19Structural characterization of toxic oligomers that are kinetically trapped during α-synuclein fibril formationProceedings of the National Academy of Sciences of the United States of America2015384
20Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic strokeNature Genetics2012375
21Diffusion tensor imaging of post mortem multiple sclerosis brainNeuroImage2007347
22Genome-wide meta-analysis identifies new susceptibility loci for migraineNature Genetics2013338
23The β-Secretase BACE1 in Alzheimer’s DiseaseBiological Psychiatry2021336
24Hereditary Sensory Neuropathy Type 1 Is Caused by the Accumulation of Two Neurotoxic SphingolipidsJournal of Biological Chemistry2010320
25Neuropathology of variants of progressive supranuclear palsyCurrent Opinion in Neurology2010312
26Genome-wide association study of obsessive-compulsive disorderMolecular Psychiatry2013312
27Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard scorePLoS Medicine2017311
28Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related DementiasPLoS Genetics2014305
29Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK PopulationAmerican Journal of Human Genetics2013297
30Research in motion: the enigma of Parkinson's disease pathology spreadNature Reviews Neuroscience2008296
31Proposed neuropathological criteria for the post mortem diagnosis of multiple system atrophyNeuropathology and Applied Neurobiology2007278
32Mitochondria and Quality Control Defects in a Mouse Model of Gaucher Disease—Links to Parkinson’s DiseaseCell Metabolism2013277
33The age factor in Alzheimer’s diseaseGenome Medicine2015271
34Reliability of the CMT neuropathy score (second version) in Charcot‐Marie‐Tooth diseaseJournal of the Peripheral Nervous System2011269
35Glucocerebrosidase mutations influence the natural history of Parkinson’s disease in a community-based incident cohortBrain2013266
36Ambroxol improves lysosomal biochemistry in glucocerebrosidase mutation-linked Parkinson disease cellsBrain2014258
37SNCA variants are associated with increased risk for multiple system atrophyAnnals of Neurology2009257
38Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathiesActa Neuropathologica2009255
39An additional k-means clustering step improves the biological features of WGCNA gene co-expression networksBMC Systems Biology2017253
40Quantitative magnetization transfer imaging in postmortem multiple sclerosis brainJournal of Magnetic Resonance Imaging2007241
41Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in PathogenesisAmerican Journal of Human Genetics2012224
42Paroxysmal dyskinesias revisited: A review of 500 genetically proven cases and a new classificationMovement Disorders2014224
43Molecular nexopathies: a new paradigm of neurodegenerative diseaseTrends in Neurosciences2013223
44Microglial genes regulating neuroinflammation in the progression of Alzheimer's diseaseCurrent Opinion in Neurobiology2016223
45Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyNature Genetics2021223
46 2-Chimaerin, Cyclin-Dependent Kinase 5/p35, and Its Target Collapsin Response Mediator Protein-2 Are Essential Components in Semaphorin 3A-Induced Growth-Cone CollapseJournal of Neuroscience2004195
47Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association studyLancet Neurology, The2018195
48Nrf2 affects the efficiency of mitochondrial fatty acid oxidationBiochemical Journal2014192
49Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxiaBrain2004191
50The interaction of PRC2 with RNA or chromatin is mutually antagonisticGenome Research2016191