Daniela Berg

Author PubWeight™ 175.20‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 2009 10.34
2 Loss-of-function of human PINK1 results in mitochondrial pathology and can be rescued by parkin. J Neurosci 2007 5.68
3 Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. PLoS Genet 2012 4.27
4 SNCA variants are associated with increased risk for multiple system atrophy. Ann Neurol 2009 3.55
5 The specificity and sensitivity of transcranial ultrasound in the differential diagnosis of Parkinson's disease: a prospective blinded study. Lancet Neurol 2008 2.42
6 Multiple regions of alpha-synuclein are associated with Parkinson's disease. Ann Neurol 2005 2.40
7 A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies. JAMA Neurol 2013 2.32
8 Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease. Hum Mol Genet 2005 2.28
9 Olfactory dysfunction: common in later life and early warning of neurodegenerative disease. Dtsch Arztebl Int 2013 2.22
10 Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expression. Cell Stem Cell 2013 2.22
11 Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain. FASEB J 2007 1.94
12 Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet 2010 1.86
13 Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*. Brain 2005 1.85
14 Molecular analysis of HER2 signaling in human breast cancer by functional protein pathway activation mapping. Clin Cancer Res 2012 1.74
15 Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair. Hum Mol Genet 2009 1.59
16 Progression of Parkinson's disease in the clinical phase: potential markers. Lancet Neurol 2009 1.58
17 GBA-associated PD. Neurodegeneration, altered membrane metabolism, and lack of energy failure. Neurology 2012 1.51
18 Poor effect of guideline based treatment of restless legs syndrome in clinical practice. J Neurol Neurosurg Psychiatry 2010 1.49
19 SNCA: major genetic modifier of age at onset of Parkinson's disease. Mov Disord 2013 1.48
20 Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Ann Neurol 2011 1.45
21 Transcranial sonography as a diagnostic tool for Parkinson's disease: a pilot study in the city of Rio de Janeiro, Brazil. Arq Neuropsiquiatr 2011 1.40
22 Cortical PIB binding in Lewy body disease is associated with Alzheimer-like characteristics. Neurobiol Dis 2008 1.39
23 Transcranial brain parenchyma sonography in movement disorders: state of the art. Ultrasound Med Biol 2007 1.37
24 Higher frequency of regulatory T cells in the elderly and increased suppressive activity in neurodegeneration. J Neuroimmunol 2007 1.34
25 Phosphorylated α-synuclein in Parkinson's disease. Sci Transl Med 2012 1.29
26 Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease. Proc Natl Acad Sci U S A 2004 1.29
27 [11C]PIB binding in Parkinson's disease dementia. Neuroimage 2007 1.24
28 In vivo detection of iron and neuromelanin by transcranial sonography: a new approach for early detection of substantia nigra damage. Mov Disord 2005 1.23
29 Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7). Hum Mutat 2004 1.22
30 Cellular FLICE-inhibitory protein (cFLIP) isoforms block CD95- and TRAIL death receptor-induced gene induction irrespective of processing of caspase-8 or cFLIP in the death-inducing signaling complex. J Biol Chem 2011 1.19
31 ATP13A2 variants in early-onset Parkinson's disease patients and controls. Mov Disord 2009 1.12
32 The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect. Neurobiol Dis 2011 1.12
33 The patients' perception of prodromal symptoms before the initial diagnosis of Parkinson's disease. Mov Disord 2011 1.10
34 14-3-3 protein is a component of Lewy bodies in Parkinson's disease-mutation analysis and association studies of 14-3-3 eta. Brain Res Mol Brain Res 2002 1.09
35 The transcription factor PITX3 is associated with sporadic Parkinson's disease. Neurobiol Aging 2007 1.09
36 Common variants of LRRK2 are not associated with sporadic Parkinson's disease. Ann Neurol 2005 1.08
37 Poor trail making test performance is directly associated with altered dual task prioritization in the elderly--baseline results from the TREND study. PLoS One 2011 1.07
38 S100B is increased in Parkinson's disease and ablation protects against MPTP-induced toxicity through the RAGE and TNF-α pathway. Brain 2012 1.07
39 Synergism between Hedgehog-GLI and EGFR signaling in Hedgehog-responsive human medulloblastoma cells induces downregulation of canonical Hedgehog-target genes and stabilized expression of GLI1. PLoS One 2013 1.04
40 Biomarker candidates of neurodegeneration in Parkinson's disease for the evaluation of disease-modifying therapeutics. J Neural Transm (Vienna) 2011 1.04
41 Osteopontin is elevated in Parkinson's disease and its absence leads to reduced neurodegeneration in the MPTP model. Neurobiol Dis 2006 1.03
42 Specification of 14-3-3 proteins in Lewy bodies. Ann Neurol 2003 1.02
43 Loss of nocturnal blood pressure fall in various extrapyramidal syndromes. Mov Disord 2009 1.02
44 Functional relevance of ceruloplasmin mutations in Parkinson's disease. FASEB J 2005 1.00
45 Multiregional brain iron deficiency in restless legs syndrome. Mov Disord 2008 1.00
46 Maltose and maltodextrin utilization by Listeria monocytogenes depend on an inducible ABC transporter which is repressed by glucose. PLoS One 2010 1.00
47 LINGO1 is not associated with Parkinson's disease in German patients. Am J Med Genet B Neuropsychiatr Genet 2010 0.99
48 Signalling networks associated with urokinase-type plasminogen activator (uPA) and its inhibitor PAI-1 in breast cancer tissues: new insights from protein microarray analysis. J Pathol 2010 0.99
49 GBA-associated Parkinson's disease: reduced survival and more rapid progression in a prospective longitudinal study. Mov Disord 2014 0.99
50 Substantia nigra hypoechogenicity: definition and findings in restless legs syndrome. Mov Disord 2007 0.99
51 Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis. J Neurol 2009 0.96
52 The proteasomal subunit S6 ATPase is a novel synphilin-1 interacting protein--implications for Parkinson's disease. FASEB J 2007 0.96
53 Impaired trunk stability in individuals at high risk for Parkinson's disease. PLoS One 2012 0.95
54 Autoantibodies against amyloid and glial-derived antigens are increased in serum and cerebrospinal fluid of Lewy body-associated dementias. J Alzheimers Dis 2011 0.94
55 Characterizing POLG ataxia: clinics, electrophysiology and imaging. Cerebellum 2012 0.94
56 Genetic factors influencing age at onset in LRRK2-linked Parkinson disease. Parkinsonism Relat Disord 2008 0.94
57 Clinical and dual-tasking aspects in frequent and infrequent fallers with progressive supranuclear palsy. Mov Disord 2010 0.93
58 Reduced but not oxidized cerebrospinal fluid glutathione levels are lowered in Lewy body diseases. Mov Disord 2010 0.92
59 Influence of different cut-off values on the diagnosis of mild cognitive impairment in Parkinson's disease. Parkinsons Dis 2011 0.91
60 Apoptosis is not required for acantholysis in pemphigus vulgaris. Am J Physiol Cell Physiol 2008 0.91
61 Predictive value of transcranial sonography in the diagnosis of Parkinson's disease. Mov Disord 2006 0.91
62 Echogenicity of the substantia nigra in relatives of patients with sporadic Parkinson's disease. Neuroimage 2003 0.90
63 Comprehensive autonomic assessment does not differentiate between Parkinson's disease, multiple system atrophy and progressive supranuclear palsy. J Neural Transm (Vienna) 2009 0.90
64 Aging-related cortical reorganization of verbal fluency processing: a functional near-infrared spectroscopy study. Neurobiol Aging 2012 0.90
65 Plasma ceramide and glucosylceramide metabolism is altered in sporadic Parkinson's disease and associated with cognitive impairment: a pilot study. PLoS One 2013 0.90
66 Analysis of ACTA2 in European Moyamoya disease patients. Eur J Paediatr Neurol 2010 0.90
67 Three-dimensional magnetic resonance spectroscopic imaging in the substantia nigra of healthy controls and patients with Parkinson's disease. Eur Radiol 2011 0.89
68 Transcranial sonography findings related to non-motor features of Parkinson's disease. J Neurol Sci 2009 0.89
69 Producing reverse phase protein microarrays from formalin-fixed tissues. Methods Mol Biol 2011 0.89
70 uPA and PAI-1-Related Signaling Pathways Differ between Primary Breast Cancers and Lymph Node Metastases. Transl Oncol 2012 0.89
71 Sustained dopaminergic response of parkinsonism and depression in POLG-associated parkinsonism. Mov Disord 2010 0.89
72 Assessment of idiopathic rapid-eye-movement sleep behavior disorder by transcranial sonography, olfactory function test, and FP-CIT-SPECT. Mov Disord 2008 0.88
73 Cortical hypometabolism assessed by a metabolic ratio in Parkinson's disease primarily reflects cognitive deterioration-[18F]FDG-PET. Mov Disord 2009 0.88
74 Clinical and brain imaging characteristics in leucine-rich repeat kinase 2-associated PD and asymptomatic mutation carriers. Mov Disord 2011 0.88
75 Evidence for shoulder girdle dystonia in selected patients with cervical disc prolapse. Mov Disord 2002 0.87
76 Methods in Neuroepidemiology Characterization of European Longitudinal Cohort Studies in Parkinson's Disease - Report of the JPND Working Group BioLoC-PD. Neuroepidemiology 2015 0.87
77 Evidence of prognostic relevant expression profiles of heat-shock proteins and glucose-regulated proteins in oesophageal adenocarcinomas. PLoS One 2012 0.87
78 The CST3 BB genotype and low cystatin C cerebrospinal fluid levels are associated with dementia in Lewy body disease. J Alzheimers Dis 2010 0.87
79 Increased serum insulin-like growth factor 1 in early idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 2010 0.87
80 Retinal nerve fiber layer loss in multiple system atrophy. Mov Disord 2011 0.87
81 No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort. Neurobiol Aging 2009 0.86
82 Neprilysin activity in cerebrospinal fluid is associated with dementia and amyloid-β42 levels in Lewy body disease. J Alzheimers Dis 2010 0.86
83 Effect of 6-hydroxydopamine (6-OHDA) on proliferation of glial cells in the rat cortex and striatum: evidence for de-differentiation of resident astrocytes. Cell Tissue Res 2010 0.86
84 Pre-motor signs of PD are related to SN hyperechogenicity assessed by TCS in an elderly population. Neurobiol Aging 2009 0.85
85 Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans. Childs Nerv Syst 2010 0.85
86 Antibody validation by combining immunohistochemistry and protein extraction from formalin-fixed paraffin-embedded tissues. Histopathology 2012 0.85
87 Immune profiling in blood identifies sTNF-R1 performing comparably well as biomarker panels for classification of Alzheimer's disease patients. J Alzheimers Dis 2013 0.85
88 Risk factors and prodromal markers and the development of Parkinson's disease. J Neurol 2013 0.85
89 Serum insulinlike growth factor 1 as possible marker for risk and early diagnosis of Parkinson disease. Arch Neurol 2011 0.84
90 Substantia nigra hyperechogenicity assessed by transcranial sonography is related to neuropsychological impairment in the elderly population. J Neural Transm (Vienna) 2008 0.84
91 Interaction of Snail and p38 mitogen-activated protein kinase results in shorter overall survival of ovarian cancer patients. Virchows Arch 2010 0.84
92 Substantia nigra hyperechogenicity as a marker of predisposition and slower progression in Parkinson's disease. Mov Disord 2006 0.84
93 Parkinson's disease and dementia: a longitudinal study (DEMPARK). Neuroepidemiology 2011 0.84
94 Effect of genetic variation in Kv1.3 on olfactory function. Diabetes Metab Res Rev 2009 0.84
95 Genetics and iron in the systems biology of Parkinson's disease and some related disorders. Neurochem Int 2012 0.84
96 Serum and cerebrospinal fluid uric acid levels in lewy body disorders: associations with disease occurrence and amyloid-β pathway. J Alzheimers Dis 2011 0.84
97 Detection of MPTP-induced substantia nigra hyperechogenicity in Rhesus monkeys by transcranial ultrasound. Ultrasound Med Biol 2010 0.84
98 Reproducibility and diagnostic accuracy of substantia nigra sonography for the diagnosis of Parkinson's disease. J Neurol Neurosurg Psychiatry 2010 0.84
99 Autonomic dysfunction in patients with progressive supranuclear palsy. Mov Disord 2008 0.84
100 Baroreflex sensitivity and power spectral analysis during autonomic testing in different extrapyramidal syndromes. Mov Disord 2010 0.84
101 Rivastigmine for the treatment of dementia in patients with progressive supranuclear palsy: Clinical observations as a basis for power calculations and safety analysis. Alzheimers Dement 2010 0.84
102 Serum and cerebrospinal fluid levels of transthyretin in Lewy body disorders with and without dementia. PLoS One 2012 0.83
103 Genetic analysis of heme oxygenase-1 (HO-1) in German Parkinson's disease patients. J Neural Transm (Vienna) 2009 0.83
104 Time- and frequency-domain parameters of heart rate variability and sympathetic skin response in Parkinson's disease. J Neural Transm (Vienna) 2014 0.83
105 Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease. J Neurol 2007 0.83
106 Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patients. Acta Neurochir (Wien) 2010 0.83
107 Illicit stimulant use is associated with abnormal substantia nigra morphology in humans. PLoS One 2013 0.83
108 Differentiation between idiopathic and atypical parkinsonian syndromes using three-dimensional magnetic resonance spectroscopic imaging. J Neurol Neurosurg Psychiatry 2013 0.83
109 Evaluation of progression markers in the premotor phase of Parkinson's disease: the progression markers in the premotor phase study. Neuroepidemiology 2013 0.82
110 Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation. J Neurol 2008 0.82
111 Postnatal decrease in substantia nigra echogenicity. Implications for the pathogenesis of Parkinson's disease. J Neurol 2004 0.82
112 Decreased α-synuclein serum levels in patients with Lewy body dementia compared to Alzheimer's disease patients and control subjects. Dement Geriatr Cogn Disord 2011 0.82
113 Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra. Neurosci Lett 2006 0.82
114 Early diagnosis of Parkinson's disease. Int Rev Neurobiol 2010 0.82
115 Parenchymal imaging in movement disorders. Front Neurol Neurosci 2014 0.81
116 How precise are activities of daily living scales for the diagnosis of Parkinson's disease dementia? A pilot study. Parkinsonism Relat Disord 2012 0.81
117 Lowered serum amyloid-β1-42 autoantibodies in individuals with lifetime depression. J Alzheimers Dis 2012 0.81
118 Developments in the role of transcranial sonography for the differential diagnosis of parkinsonism. Curr Neurol Neurosci Rep 2015 0.80
119 The significance of GBA for Parkinson's disease. J Inherit Metab Dis 2014 0.80
120 Progressive secondary neurodegeneration and microcalcification co-occur in osteopontin-deficient mice. Am J Pathol 2010 0.80
121 Mutation analysis of the neurofilament M gene in Parkinson's disease. Neurosci Lett 2003 0.80
122 A single-nucleotide polymorphism of the osteopontin gene may contribute to a susceptibility to Lewy body disease. J Neural Transm (Vienna) 2009 0.80
123 Long-term follow-up of subthalamic nucleus stimulation in glucocerebrosidase-associated Parkinson's disease. J Neurol 2012 0.80
124 Does structural neuroimaging reveal a disturbance of iron metabolism in Parkinson's disease? Implications from MRI and TCS studies. J Neural Transm (Vienna) 2012 0.80
125 No differences of butyrylcholinesterase protein activity and allele frequency in Lewy body diseases. Neurobiol Dis 2009 0.80
126 The regional distribution of T2-relaxation times in MR images of the substantia nigra and crus cerebri. Neuroradiology 2009 0.80
127 Sonographic substantia nigra hypoechogenicity in polyneuropathy and restless legs syndrome. Mov Disord 2009 0.80
128 Cerebrospinal fluid fatty acids in glucocerebrosidase-associated Parkinson's disease. Mov Disord 2011 0.80
129 Friedreich ataxia: dysarthria profile and clinical data. Cerebellum 2013 0.80
130 Cognitive profiles in Parkinson's disease and their relation to dementia: a data-driven approach. Int J Alzheimers Dis 2012 0.79
131 Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patients. J Neural Transm (Vienna) 2009 0.79
132 In vivo comparison of Richardson's syndrome and progressive supranuclear palsy-parkinsonism. J Neural Transm (Vienna) 2011 0.79
133 Sonographic abnormalities of brainstem structures in restless legs syndrome. Sleep Med 2007 0.79
134 Clock test deficits related to the global cognitive state in Alzheimer's and Parkinson's disease. Dement Geriatr Cogn Disord 2012 0.79
135 Biomarkers for PD: How can we approach complexity? Neurology 2013 0.78
136 Treatment of dementia in parkinsonian syndromes with cholinesterase inhibitors. Dement Geriatr Cogn Disord 2007 0.78
137 Fluorodeoxyglucose positron emission tomography in Richardson’s syndrome and progressive supranuclear palsy-parkinsonism. Mov Disord 2012 0.78
138 Clinical, genetic, and brain sonographic features related to Parkinson's disease in Gaucher disease. J Neurol 2013 0.78
139 Analysis of TGFB1 in European and Japanese Moyamoya disease patients. Eur J Med Genet 2012 0.78
140 Transcranial sonography in the premotor diagnosis of Parkinson's disease. Int Rev Neurobiol 2010 0.78
141 Pharmacological strategies for the management of levodopa-induced dyskinesia in patients with Parkinson's disease. CNS Drugs 2014 0.78
142 Substantia nigra hyperechogenicity correlates with subtle motor dysfunction in tap dancers. Parkinsonism Relat Disord 2006 0.78
143 In vivo markers of Parkinson's disease and dementia with Lewy bodies: current value of the 5G4 α-synuclein antibody. Acta Neuropathol 2014 0.78
144 Decreased retinal sensitivity and loss of retinal nerve fibers in multiple system atrophy. Graefes Arch Clin Exp Ophthalmol 2012 0.77
145 Stepwise isolation of human peripheral erythrocytes, T lymphocytes, and monocytes for blood cell proteomics. Proteomics Clin Appl 2012 0.77
146 6-Hydroxydopamine leads to T2 hyperintensity, decreased claudin-3 immunoreactivity and altered aquaporin 4 expression in the striatum. Behav Brain Res 2012 0.77
147 Evaluation of the ventricular system in children using transcranial ultrasound: reference values for routine diagnostics. Ultrasound Med Biol 2004 0.77
148 Hand function is impaired in healthy older adults at risk of Parkinson's disease. J Neural Transm (Vienna) 2014 0.76
149 Pupil diameter in darkness differentiates progressive supranuclear palsy (PSP) from other extrapyramidal syndromes. Mov Disord 2007 0.76
150 Transcranial sonography reveals cerebellar, nigral, and forebrain abnormalities in Friedreich's ataxia. Neurodegener Dis 2011 0.76
151 Parkinson's disease with and without preceding essential tremor-similar phenotypes: a pilot study. J Neurol 2014 0.76
152 Substantia nigra hyperechogenicity in healthy controls: a [¹⁸Fluoro] Dopa-PET follow-up study. J Neurol 2013 0.76
153 Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease. Neurogenetics 2010 0.76
154 Restless legs and substantia nigra hypoechogenicity are common features in Friedreich's ataxia. Cerebellum 2011 0.76
155 Autonomic dysfunction in different subtypes of multiple system atrophy. Mov Disord 2008 0.76
156 Effectiveness and tolerability of rotigotine transdermal patch for the treatment of restless legs syndrome in a routine clinical practice setting in Germany. Sleep Med 2013 0.76
157 No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease. Mov Disord 2013 0.75
158 Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigra. Neurosci Lett 2003 0.75
159 Nutrition and the risk for Parkinson's disease: review of the literature. J Neural Transm (Vienna) 2008 0.75
160 Rotigotine in the Long-Term Treatment of Severe RLS with Augmentation: A Series of 28 Cases. Sleep Disord 2011 0.75
161 High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's disease. J Mol Diagn 2008 0.75
162 Therapeutic strategies for Parkinson's disease based on data derived from genetic research. J Neurol 2003 0.75
163 In reply. Dtsch Arztebl Int 2013 0.75
164 No association between NOD2 variants and Parkinson's disease. Mov Disord 2012 0.75
165 Role of transcranial ultrasound in the diagnosis of movement disorders. Neuroimaging Clin N Am 2010 0.75
166 Quantitative motor assessment of dyskinesias in Parkinson's disease. J Neural Transm (Vienna) 2015 0.75
167 Cerebrotendinous xanthomatosis. Neurology 2006 0.75
168 Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease. Neurobiol Aging 2008 0.75
169 Clinical characteristics related to worsening of motor function assessed by the Unified Parkinson's Disease Rating Scale in the elderly population. J Neurol 2014 0.75
170 POLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism: a preliminary screening study. J Neurol 2012 0.75
171 Home-Based Physical Behavior in Late Stage Parkinson Disease Dementia: Differences between Cognitive Subtypes. Neurodegener Dis 2017 0.75
172 Self estimated quality of life in monogenetic Parkinson's disease. Mov Disord 2010 0.75
173 Preface. Summary of content--TCS in the diagnosis of movement disorders. Int Rev Neurobiol 2010 0.75
174 The relation of SMI and the VSEP in a risk sample for neurodegenerative disorders. J Neural Transm (Vienna) 2014 0.75