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exaly
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Department of Molecular Neuroscience
›
top-articles
Department of Molecular Neuroscience
362
(top 1%)
papers
35.8K
(top 0.1%)
citations
96
(top 0.1%)
h
-index
182
(top 0.1%)
g
-index
390
all documents
39.7K
doc citations
3.2K
citing journals
Top Articles
#
Title
Journal
Year
Citations
1
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Neuron
2011
3,833
2
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nature Genetics
2014
1,685
3
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation
Nature Medicine
2008
1,595
4
Analysis of shared heritability in common disorders of the brain
Science
2018
1,085
5
Serum Neurofilament light: A biomarker of neuronal damage in multiple sclerosis
Annals of Neurology
2017
768
6
Direct Observation of the Interconversion of Normal and Toxic Forms of α-Synuclein
Cell
2012
755
7
Magnetization transfer ratio and myelin in postmortem multiple sclerosis brain
Annals of Neurology
2004
678
8
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease
Brain
2009
612
9
Identification of common variants associated with human hippocampal and intracranial volumes
Nature Genetics
2012
594
10
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Neuron
2018
517
11
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
Nature Genetics
2011
502
12
Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database
PLoS Genetics
2012
495
13
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Nature Genetics
2016
494
14
Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains
Annals of Neurology
2012
473
15
A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome
Nature Reviews Neuroscience
2015
404
16
Maternal Diet-Induced Obesity Alters Mitochondrial Activity and Redox Status in Mouse Oocytes and Zygotes
PLoS ONE
2010
401
17
Characterization of PLA2G6 as a locus for dystonia‐parkinsonism
Annals of Neurology
2009
399
18
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Nature Neuroscience
2014
398
19
Structural characterization of toxic oligomers that are kinetically trapped during α-synuclein fibril formation
Proceedings of the National Academy of Sciences of the United States of America
2015
384
20
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
Nature Genetics
2012
375
21
Diffusion tensor imaging of post mortem multiple sclerosis brain
NeuroImage
2007
347
22
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Nature Genetics
2013
338
23
The β-Secretase BACE1 in Alzheimer’s Disease
Biological Psychiatry
2021
336
24
Hereditary Sensory Neuropathy Type 1 Is Caused by the Accumulation of Two Neurotoxic Sphingolipids
Journal of Biological Chemistry
2010
320
25
Neuropathology of variants of progressive supranuclear palsy
Current Opinion in Neurology
2010
312
26
Genome-wide association study of obsessive-compulsive disorder
Molecular Psychiatry
2013
312
27
Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score
PLoS Medicine
2017
311
28
Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias
PLoS Genetics
2014
305
29
Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population
American Journal of Human Genetics
2013
297
30
Research in motion: the enigma of Parkinson's disease pathology spread
Nature Reviews Neuroscience
2008
296
31
Proposed neuropathological criteria for the
post mortem
diagnosis of multiple system atrophy
Neuropathology and Applied Neurobiology
2007
278
32
Mitochondria and Quality Control Defects in a Mouse Model of Gaucher Disease—Links to Parkinson’s Disease
Cell Metabolism
2013
277
33
The age factor in Alzheimer’s disease
Genome Medicine
2015
271
34
Reliability of the CMT neuropathy score (second version) in Charcot‐Marie‐Tooth disease
Journal of the Peripheral Nervous System
2011
269
35
Glucocerebrosidase mutations influence the natural history of Parkinson’s disease in a community-based incident cohort
Brain
2013
266
36
Ambroxol improves lysosomal biochemistry in glucocerebrosidase mutation-linked Parkinson disease cells
Brain
2014
258
37
SNCA
variants are associated with increased risk for multiple system atrophy
Annals of Neurology
2009
257
38
Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies
Acta Neuropathologica
2009
255
39
An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks
BMC Systems Biology
2017
253
40
Quantitative magnetization transfer imaging in postmortem multiple sclerosis brain
Journal of Magnetic Resonance Imaging
2007
241
41
Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis
American Journal of Human Genetics
2012
224
42
Paroxysmal dyskinesias revisited: A review of 500 genetically proven cases and a new classification
Movement Disorders
2014
224
43
Molecular nexopathies: a new paradigm of neurodegenerative disease
Trends in Neurosciences
2013
223
44
Microglial genes regulating neuroinflammation in the progression of Alzheimer's disease
Current Opinion in Neurobiology
2016
223
45
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Nature Genetics
2021
223
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 Collapse
Journal of Neuroscience
2004
195
47
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
Lancet Neurology, The
2018
195
48
Nrf2 affects the efficiency of mitochondrial fatty acid oxidation
Biochemical Journal
2014
192
49
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia
Brain
2004
191
50
The interaction of PRC2 with RNA or chromatin is mutually antagonistic
Genome Research
2016
191
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