Martin Dichgans

Martin Dichgans's AcademicInfluence.com Rankings

Martin Dichgans

Biology

#5770

World Rank

#8330

Historical Rank

Molecular Biology

#551

World Rank

#564

Historical Rank

Neuroscience

#668

World Rank

#698

Historical Rank

biology Degrees

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Biology

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Martin Dichgans's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Neuroimaging standards for research into small vessel disease and its contribution to ageing and neurodegeneration (2013) (3466)
Common variants in ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease (2011) (1701)
Letter abstract - Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's Disease (2009) (1644)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease, and shows evidence for additional susceptibility genes (2009) (1441)
National Institute of Neurological Disorders and Stroke–Canadian Stroke Network Vascular Cognitive Impairment Harmonization Standards (2006) (1436)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2013) (1388)
Mechanisms of sporadic cerebral small vessel disease: insights from neuroimaging (2013) (1192)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (1073)
Global, regional, and national burden of stroke and its risk factors, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 (2021) (822)
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine (2005) (796)
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (2017) (693)
The phenotypic spectrum of CADASIL: Clinical findings in 102 cases (1998) (689)
Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2010) (587)
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) (578)
Small vessel disease: mechanisms and clinical implications (2019) (553)
CADASIL (2009) (551)
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke (2009) (466)
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies (2012) (446)
Shrinkage-mediated imaging of entire organs and organisms using uDISCO (2016) (433)
Multi-ethnic genome-wide association study for atrial fibrillation (2018) (425)
Erratum: Detection and interpretation of shared genetic influences on 42 human traits (2016) (417)
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke (2012) (392)
Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients. (2000) (381)
Microbiota Dysbiosis Controls the Neuroinflammatory Response after Stroke (2016) (375)
Prevalence of superficial siderosis in patients with cerebral amyloid angiopathy (2010) (371)
Vascular dysfunction—The disregarded partner of Alzheimer's disease (2019) (361)
C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy (2007) (356)
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1 (2010) (350)
Genome-wide meta-analysis identifies new susceptibility loci for migraine (2013) (336)
Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog. [corrected]. (2013) (327)
Genetic Heritability of Ischemic Stroke and the Contribution of Previously Reported Candidate Gene and Genomewide Associations (2012) (314)
Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease: A Genome-Wide Analysis of Common Variants (2014) (303)
Five insights from the Global Burden of Disease Study 2019 (2020) (291)
Genome-wide association analysis identifies susceptibility loci for migraine without aura (2012) (286)
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke (2008) (284)
Meta-analysis and systematic review of the predictive value of carotid plaque hemorrhage on cerebrovascular events by magnetic resonance imaging. (2013) (281)
Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients. (2004) (275)
Vascular Cognitive Impairment and Dementia: JACC Scientific Expert Panel. (2019) (266)
Cerebral Microbleeds in CADASIL: A Gradient-Echo Magnetic Resonance Imaging and Autopsy Study (2002) (265)
New insights into the genetic etiology of Alzheimer’s disease and related dementias (2022) (246)
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families (2002) (245)
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (2017) (243)
Genetics of ischaemic stroke (2007) (235)
Action Plan for Stroke in Europe 2018–2030 (2018) (233)
Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine (2004) (223)
Defining Optimal Brain Health in Adults: A Presidential Advisory From the American Heart Association/American Stroke Association. (2017) (217)
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. (2014) (217)
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke (2009) (213)
Donepezil in patients with subcortical vascular cognitive impairment: a randomised double-blind trial in CADASIL (2008) (211)
Modifiable pathways in Alzheimer’s disease: Mendelian randomisation analysis (2017) (207)
A Novel Imaging Marker for Small Vessel Disease Based on Skeletonization of White Matter Tracts and Diffusion Histograms (2016) (206)
Variant in the sequence of the LINGO1 gene confers risk of essential tremor (2009) (204)
Acute Cerebrovascular Disease in the Young: The Stroke in Young Fabry Patients Study (2013) (199)
Acute Cerebrovascular Disease in the Young: The Stroke in Young Fabry Patients Study (2013) (199)
ALOX5AP Gene and the PDE4D Gene in a Central European Population of Stroke Patients (2005) (199)
Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison. (2001) (192)
Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine (2000) (191)
The global burden of neurological disorders: translating evidence into policy (2019) (188)
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects (2017) (188)
Incident subcortical infarcts induce focal thinning in connected cortical regions (2012) (186)
Prevalence of nonstenosing, complicated atherosclerotic plaques in cryptogenic stroke. (2012) (184)
Vascular Cognitive Impairment (2017) (183)
The Causative Classification of Stroke system (2010) (182)
Recommendations for the emergency management of complications associated with the new direct oral anticoagulants (DOACs), apixaban, dabigatran and rivaroxaban (2013) (179)
Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategies. (2005) (178)
Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation (2014) (177)
Preventing dementia by preventing stroke: The Berlin Manifesto (2019) (176)
Blood pressure and haemoglobin A1c are associated with microhaemorrhage in CADASIL: a two-centre cohort study. (2006) (175)
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection (2014) (173)
Convergent genetic and expression data implicate immunity in Alzheimer's disease (2014) (172)
Strategic role of frontal white matter tracts in vascular cognitive impairment: a voxel-based lesion-symptom mapping study in CADASIL. (2011) (169)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Phenotypic and mutational spectrum (2002) (169)
Understanding the role of the perivascular space in cerebral small vessel disease (2018) (168)
RNA-Seq Identifies Circulating miR-125a-5p, miR-125b-5p, and miR-143-3p as Potential Biomarkers for Acute Ischemic Stroke (2017) (165)
Consensus statement for diagnosis of subcortical small vessel disease (2016) (163)
Lifestyle Risk Factors for Ischemic Stroke and Transient Ischemic Attack in Young Adults in the Stroke in Young Fabry Patients Study (2013) (162)
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias (2011) (159)
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. (2012) (158)
Acute infarcts cause focal thinning in remote cortex via degeneration of connecting fiber tracts (2015) (157)
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke (2012) (156)
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants (2004) (156)
Incident lacunes preferentially localize to the edge of white matter hyperintensities: insights into the pathophysiology of cerebral small vessel disease. (2013) (152)
Genetic Association Studies in Stroke: Methodological Issues and Proposed Standard Criteria (2005) (150)
Machine learning analysis of whole mouse brain vasculature (2020) (150)
Increased soluble TREM2 in cerebrospinal fluid is associated with reduced cognitive and clinical decline in Alzheimer’s disease (2019) (150)
The pattern of cognitive performance in CADASIL: a monogenic condition leading to subcortical ischemic vascular dementia. (2005) (147)
Ischemic Stroke Is Associated with the ABO Locus: The EuroCLOT Study (2013) (142)
Subarachnoid Hemosiderosis and Superficial Cortical Hemosiderosis in Cerebral Amyloid Angiopathy (2008) (142)
Lacunar lesions are independently associated with disability and cognitive impairment in CADASIL (2007) (141)
Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3v EGF-like repeat domains (2000) (140)
Diffusion Magnetic Resonance Histograms as a Surrogate Marker and Predictor of Disease Progression in CADASIL: A Two-Year Follow-Up Study (2005) (140)
Reduced Cerebrovascular CO2 Reactivity in CADASIL: A Transcranial Doppler Sonography Study (2001) (137)
Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease. (2015) (136)
Functional Outcome Following Stroke Thrombectomy in Clinical Practice. (2019) (134)
Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study. (2016) (134)
Two Common Mitochondrial DNA Polymorphisms are Highly Associated with Migraine Headache and Cyclic Vomiting Syndrome (2009) (133)
Multiethnic Meta-Analysis of Genome-Wide Association Studies in >100 000 Subjects Identifies 23 Fibrinogen-Associated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease (2013) (133)
CADASIL: A Monogenic Condition Causing Stroke and Subcortical Vascular Dementia (2002) (131)
Short-Chain Fatty Acids Improve Poststroke Recovery via Immunological Mechanisms (2019) (128)
Impact of MRI markers in subcortical vascular dementia: A multi-modal analysis in CADASIL (2010) (126)
Genetic risk, incident stroke, and the benefits of adhering to a healthy lifestyle: cohort study of 306 473 UK Biobank participants (2018) (119)
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies (2016) (118)
Differential Diagnosis of CNS Lesions in AIDS Patients by FDG‐PET (1995) (117)
Divergent sodium channel defects in familial hemiplegic migraine (2008) (113)
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain. (2009) (112)
Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease (2015) (111)
R2* mapping for brain iron: associations with cognition in normal aging (2015) (110)
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine (2007) (108)
Noncontrast CT in Deep Cerebral Venous Thrombosis and Sinus Thrombosis: Comparison of its Diagnostic Value for Both Entities (2009) (108)
Strategic white matter tracts for processing speed deficits in age-related small vessel disease (2014) (107)
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies (2007) (106)
CADASIL: skin biopsy allows diagnosis in early stages (1997) (106)
High-risk plaque features can be detected in non-stenotic carotid plaques of patients with ischaemic stroke classified as cryptogenic using combined 18F-FDG PET/MR imaging (2015) (105)
Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL (1999) (104)
Quantifying blood-brain barrier leakage in small vessel disease: Review and consensus recommendations (2019) (103)
WMH and long-term outcomes in ischemic stroke (2019) (103)
Low-frequency and common genetic variation in ischemic stroke (2016) (102)
A high-density association screen of 155 ion transport genes for involvement with common migraine. (2008) (102)
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations. (2016) (99)
Apathy: A major symptom in CADASIL (2009) (99)
Genetically Determined Levels of Circulating Cytokines and Risk of Stroke: Role of Monocyte Chemoattractant Protein-1 (2019) (98)
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2015) (98)
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (98)
Long-Term Outcome After Suboccipital Decompressive Craniectomy for Malignant Cerebellar Infarction (2009) (97)
Tackling challenges in care of Alzheimer's disease and other dementias amid the COVID‐19 pandemic, now and in the future (2020) (97)
Left frontal cortex connectivity underlies cognitive reserve in prodromal Alzheimer disease (2017) (97)
A Two-Year Clinical Follow-Up Study in 80 CADASIL Subjects: Progression Patterns and Implications for Clinical Trials (2004) (96)
Cerebral small vessel disease-related protease HtrA1 processes latent TGF-β binding protein 1 and facilitates TGF-β signaling (2014) (96)
CADASIL-associated Notch3 mutations have differential effects both on ligand binding and ligand-induced Notch3 receptor signaling through RBP-Jk. (2004) (93)
White matter diffusion alterations precede symptom onset in autosomal dominant Alzheimer’s disease (2018) (93)
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (2020) (92)
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis. (2016) (92)
Pericytes are involved in the pathogenesis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (2015) (91)
Cerebral venous thrombosis: Correlation between recanalization and clinical outcome — a long-term follow-up of 40 patients (2002) (91)
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12 (2014) (90)
Prevention of vascular cognitive impairment. (2012) (89)
Shared genetic basis for migraine and ischemic stroke (2015) (89)
Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke (2019) (88)
Drip, Ship, and Retrieve: Cooperative Recanalization Therapy in Acute Basilar Artery Occlusion (2010) (87)
Opening of the blood-brain barrier preceding cortical edema in a severe attack of FHM type II (2005) (87)
Superficial siderosis is a warning sign for future intracranial hemorrhage (2012) (86)
Staged Escalation Therapy in Acute Basilar Artery Occlusion: Intravenous Thrombolysis and On-Demand Consecutive Endovascular Mechanical Thrombectomy: Preliminary Experience in 16 Patients (2008) (86)
Brain Atrophy Is Related to Lacunar Lesions and Tissue Microstructural Changes in CADASIL (2007) (86)
Serum neurofilament light (2018) (85)
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores (2021) (85)
Stroke genetics: discovery, biology, and clinical applications (2019) (85)
Brain volume changes in CADASIL (2006) (85)
Rare missense variants in ATP1A2 in families with clustering of common forms of migraine (2005) (84)
Reproducibility and variability of quantitative magnetic resonance imaging markers in cerebral small vessel disease (2016) (84)
Co-aggregate formation of CADASIL-mutant NOTCH3: a single-particle analysis. (2011) (84)
Free water determines diffusion alterations and clinical status in cerebral small vessel disease (2018) (84)
Current concepts and clinical applications of stroke genetics (2014) (84)
Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke (2016) (83)
Diverse Functional Consequences of Mutations in the Na+/K+-ATPase α2-Subunit Causing Familial Hemiplegic Migraine Type 2* (2008) (83)
Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy. (2016) (83)
Genetic factors in cerebral small vessel disease and their impact on stroke and dementia (2016) (82)
Characteristic MR lesion pattern and correlation of T1 and T2 lesion volume with neurologic and neuropsychological findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). (1999) (82)
The pathogenesis of CADASIL: an update (2004) (81)
Quantitative MRI in CADASIL (1999) (81)
Microbiota-derived short chain fatty acids modulate microglia and promote Aβ plaque deposition (2021) (81)
METACOHORTS for the study of vascular disease and its contribution to cognitive decline and neurodegeneration: An initiative of the Joint Programme for Neurodegenerative Disease Research (2016) (81)
Cortical changes in cerebral small vessel diseases: a 3D MRI study of cortical morphology in CADASIL. (2008) (80)
Advances in Genomic Analysis of Stroke: What Have We Learned and Where Are We Headed? (2010) (80)
The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1–6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7–34 pathogenic variant (2018) (79)
CADASIL mutations enhance spontaneous multimerization of NOTCH3. (2009) (79)
Pericytes are involved in the pathogenesis of CADASIL (2015) (79)
Genetic Variation in Soluble Epoxide Hydrolase (EPHX2) Is Associated With an Increased Risk of Ischemic Stroke in White Europeans (2008) (78)
Serum Neurofilament Light Chain Levels Are Related to Small Vessel Disease Burden (2018) (78)
Early MoCA predicts long-term cognitive and functional outcome and mortality after stroke (2018) (78)
1H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1 (2005) (77)
Predictors of Clinical Worsening in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Prospective Cohort Study (2016) (75)
Motor Cortex Excitability in Patients with Migraine with Aura and Hemiplegic Migraine (2000) (74)
Variation in the PDE4D Gene and Ischemic Stroke Risk: A Systematic Review and Meta-analysis on 5200 Cases and 6600 Controls (2008) (74)
A Novel MMP12 Locus Is Associated with Large Artery Atherosclerotic Stroke Using a Genome-Wide Age-at-Onset Informed Approach (2014) (74)
Identification of a strategic brain network underlying processing speed deficits in vascular cognitive impairment (2013) (73)
Clinical features, course and outcome in deep cerebral venous system thrombosis: an analysis of 32 cases (2009) (73)
Left frontal hub connectivity delays cognitive impairment in autosomal-dominant and sporadic Alzheimer’s disease (2018) (71)
Hippocampal volume is an independent predictor of cognitive performance in CADASIL (2009) (70)
Genome‐wide meta‐analysis identifies 3 novel loci associated with stroke (2018) (69)
A sequence variant in ZFHX 3 on 16 q 22 associates with atrial fibrillation and ischemic stroke (2009) (68)
Cystatin C and Cardiovascular Disease (2016) (68)
NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL (2001) (68)
Genomic sequences of aldolase C (Zebrin II) direct lacZ expression exclusively in non-neuronal cells of transgenic mice. (1998) (67)
Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes (2019) (66)
Circulating Monocyte Chemoattractant Protein-1 and Risk of Stroke: A Meta-Analysis of Population-Based Studies Involving 17,180 Individuals. (2019) (65)
Prevalence and characteristics of migraine in CADASIL (2016) (65)
Deficiency of the Stroke Relevant HDAC9 Gene Attenuates Atherosclerosis in Accord With Allele-Specific Effects at 7p21.1 (2015) (65)
Use of Genetic Variants Related to Antihypertensive Drugs to Inform on Efficacy and Side Effects (2019) (65)
Genetic analysis for a shared biological basis between migraine and coronary artery disease (2015) (64)
Harmonizing brain magnetic resonance imaging methods for vascular contributions to neurodegeneration (2019) (64)
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2009) (64)
New insights on the genetic etiology of Alzheimer’s and related dementia (2020) (64)
Genome-wide association study of migraine implicates a common susceptibility variant on 8 q 22 . 1 (2010) (64)
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles (2021) (64)
Multilocus Genetic Risk Score Associates With Ischemic Stroke in Case–Control and Prospective Cohort Studies (2014) (63)
Intra-arterial application of nimodipine in reversible cerebral vasoconstriction syndrome: A diagnostic tool in select cases? (2011) (63)
Genetic variation at 16q24.2 is associated with small vessel stroke (2017) (61)
The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. (2012) (61)
Systematic evaluation of stroke thrombectomy in clinical practice: The German Stroke Registry Endovascular Treatment (2018) (60)
Genome-wide association study of cerebral small vessel disease reveals established and novel loci. (2019) (60)
Stroke Genetics Network (SiGN) Study: Design and Rationale for a Genome-Wide Association Study of Ischemic Stroke Subtypes (2013) (60)
Genetic Variation in Members of the Leukotriene Biosynthesis Pathway Confer an Increased Risk of Ischemic Stroke: A Replication Study in Two Independent Populations (2008) (59)
Education modifies the relation of vascular pathology to cognitive function: cognitive reserve in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (2013) (59)
Determinants of iron accumulation in the normal aging brain (2016) (59)
Prevalence of cortical superficial siderosis in patients with cognitive impairment (2014) (59)
Vessel Wall Inflammation in Spontaneous Cervical Artery Dissection: A Prospective, Observational Positron Emission Tomography, Computed Tomography, and Magnetic Resonance Imaging Study (2011) (59)
Agreement between TOAST and CCS ischemic stroke classification (2014) (58)
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans (2015) (58)
Correlations Between Clinical Findings and Magnetization Transfer Imaging Metrics of Tissue Damage in Individuals With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (2001) (58)
Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226) (2019) (57)
Cerebral small vessel disease genomics and its implications across the lifespan (2020) (56)
Genome-Wide Association Study of Vascular Dementia (2012) (56)
Association of SORL1 gene variants with Alzheimer's disease (2009) (56)
Black Blood MRI in Suspected Large Artery Primary Angiitis of the Central Nervous System (2013) (56)
Primary stroke prevention worldwide: translating evidence into action (2021) (56)
Predicting Stroke Through Genetic Risk Functions: The CHARGE Risk Score Project (2014) (56)
High-resolution black-blood contrast-enhanced T1 weighted images for the diagnosis and follow-up of intracranial arteritis. (2010) (56)
Cognitive reserve moderates the association between functional network anti-correlations and memory in MCI (2017) (55)
Shared genetic contribution to ischemic stroke and Alzheimer's disease (2016) (55)
Cortical hypometabolism and crossed cerebellar diaschisis suggest subcortically induced disconnection in CADASIL: an 18F-FDG PET study. (2003) (55)
Left Frontal Hub Connectivity during Memory Performance Supports Reserve in Aging and Mild Cognitive Impairment (2017) (55)
Patient-centered connectivity-based prediction of tau pathology spread in Alzheimer’s disease (2020) (54)
STROKOG (stroke and cognition consortium): An international consortium to examine the epidemiology, diagnosis, and treatment of neurocognitive disorders in relation to cerebrovascular disease (2016) (53)
Detection of Deleterious On-Target Effects after HDR-Mediated CRISPR Editing. (2020) (53)
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies (2021) (52)
Inherited myoclonus‐dystonia syndrome: Narrowing the 7q21‐q31 locus in German families (2001) (52)
Cortical vein thrombosis: the diagnostic value of different imaging modalities (2010) (52)
Higher CSF sTREM2 and microglia activation are associated with slower rates of beta‐amyloid accumulation (2020) (52)
COL4A2 is associated with lacunar ischemic stroke and deep ICH (2017) (51)
Brain-released alarmins and stress response synergize in accelerating atherosclerosis progression after stroke (2018) (51)
Angiographic complications in CADASIL (1997) (51)
Impact of regional cortical and subcortical changes on processing speed in cerebral small vessel disease☆ (2013) (51)
CTA for Screening of Complicated Atherosclerotic Carotid Plaque—American Heart Association Type VI Lesions as Defined by MRI (2013) (51)
Parkin interacts with the proteasome subunit α4 (2005) (50)
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (2018) (50)
Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia (2018) (49)
Genomic duplications mediate overexpression of lamin B1 in adult-onset autosomal dominant leukodystrophy (ADLD) with autonomic symptoms (2011) (49)
Altered white and gray matter metabolism in CADASIL (2001) (48)
Validation of the Telephone Interview of Cognitive Status and Telephone Montreal Cognitive Assessment Against Detailed Cognitive Testing and Clinical Diagnosis of Mild Cognitive Impairment After Stroke (2017) (48)
Complicated Carotid Artery Plaques as a Cause of Cryptogenic Stroke. (2020) (48)
Admission Facility Is Associated With Outcome of Basilar Artery Occlusion (2007) (48)
Sequestration of latent TGF-β binding protein 1 into CADASIL-related Notch3-ECD deposits (2014) (47)
Moyamoya Disease Susceptibility Variant RNF213 p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis. (2019) (46)
The BDNFVal66Met SNP modulates the association between beta-amyloid and hippocampal disconnection in Alzheimer’s disease (2019) (46)
Association of MTHFR C677T Genotype With Ischemic Stroke Is Confined to Cerebral Small Vessel Disease Subtype (2016) (46)
Subclinical Hyperthyroidism Is a Risk Factor for Poor Functional Outcome After Ischemic Stroke (2013) (45)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: decrease in regional cerebral blood volume in hyperintense subcortical lesions inversely correlates with disability and cognitive performance. (2001) (45)
Cognition in CADASIL. (2009) (45)
Retinal vascular abnormalities in CADASIL (2004) (45)
Doxycycline inhibits MMPs via modulation of plasminogen activators in focal cerebral ischemia (2007) (45)
MRI in acute cerebral ischemia of the young (2013) (45)
Preceding Intravenous Thrombolysis Facilitates Endovascular Mechanical Recanalization in Large Intracranial Artery Occlusion (2012) (45)
Reversible coma with raised intracranial pressure: an unusual clinical manifestation of CADASIL (2002) (44)
RLS3: Fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity (2006) (44)
Mendelian Randomization Study of Obesity and Cerebrovascular Disease (2020) (44)
Effects of Gender on the Phenotype of CADASIL (2012) (44)
Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers. (2006) (44)
Dilated Perivascular Spaces in Small-Vessel Disease: A Study in CADASIL (2014) (44)
Common coding variant in SERPINA1 increases the risk for large artery stroke (2017) (44)
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2 (2016) (44)
The left frontal cortex supports reserve in aging by enhancing functional network efficiency (2018) (44)
Gene-based pleiotropy across migraine with aura and migraine without aura patient groups (2016) (44)
Post-Stroke Cognitive Impairment and Dementia. (2022) (44)
Enhanced L-arginine-induced vasoreactivity suggests endothelial dysfunction in CADASIL (2008) (43)
Intrafamilial variability in fragile X–associated tremor/ataxia syndrome (2006) (43)
17q25 Locus Is Associated With White Matter Hyperintensity Volume in Ischemic Stroke, But Not With Lacunar Stroke Status (2013) (43)
Histone Deacetylase 9 Activates IKK to Regulate Atherosclerotic Plaque Vulnerability (2020) (42)
Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set (2016) (42)
Tract-specific white matter hyperintensities disrupt neural network function in Alzheimer's disease (2017) (42)
Pathogenic Ischemic Stroke Phenotypes in the NINDS-Stroke Genetics Network (2014) (42)
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities (2020) (41)
Vascular contributions to cognitive impairment and dementia: Research consortia that focus on etiology and treatable targets to lessen the burden of dementia worldwide (2019) (41)
Segregation of functional networks is associated with cognitive resilience in Alzheimer's disease. (2021) (41)
The D2 receptor Nco I allele: Absence of allelic association with migraine with aura (1998) (41)
CADASIL brain vessels show a HTRA1 loss-of-function profile (2018) (40)
Influence of SORL1 gene variants: Association with CSF amyloid-β products in probable Alzheimer's disease (2008) (40)
In vivo widefield calcium imaging of the mouse cortex for analysis of network connectivity in health and brain disease (2018) (40)
Prolonged Cerebral Transit Time in CADASIL: A Transcranial Ultrasound Study (2002) (40)
Peripheral nerve and skeletal muscle involvement in CADASIL (2005) (40)
The Boston criteria version 2.0 for cerebral amyloid angiopathy: a multicentre, retrospective, MRI–neuropathology diagnostic accuracy study (2022) (40)
The carotid plaque imaging in acute stroke (CAPIAS) study: protocol and initial baseline data (2013) (39)
Midlife vascular risk factors and risk of incident dementia: Longitudinal cohort and Mendelian randomization analyses in the UK Biobank (2021) (39)
Spinocerebellar ataxia type 6: Evidence for a strong founder effect among German families (1999) (38)
Familial Hemiplegic Migraine with Cerebellar Ataxia and Paroxysmal Psychosis (1999) (38)
Cysteine-Sparing CADASIL Mutations in NOTCH3 Show Proaggregatory Properties In Vitro (2015) (38)
Gene polymorphisms in prodynorphin (PDYN) are associated with episodic memory in the elderly (2009) (37)
Global, regional, and national burden of diseases and injuries for adults 70 years and older: systematic analysis for the Global Burden of Disease 2019 Study (2022) (37)
Verbal memory impairment in subcortical ischemic vascular disease A descriptive analysis in CADASIL (2011) (37)
Genetic Overlap Between Diagnostic Subtypes of Ischemic Stroke (2015) (37)
Human Validation of Genes Associated With a Murine Atherosclerotic Phenotype (2014) (37)
Longitudinal changes of cortical morphology in CADASIL (2012) (37)
Post-injury immunosuppression and secondary infections are caused by an AIM2 inflammasome-driven signaling cascade. (2021) (37)
Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing (2018) (36)
Predictive Value of the Velocity of Collateral Filling in Patients with Acute Ischemic Stroke (2015) (36)
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas (2016) (36)
Genome-Wide Genotyping Demonstrates a Polygenic Risk Score Associated With White Matter Hyperintensity Volume in CADASIL (2014) (36)
Histopathological abnormalities in ocular blood vessels of CADASIL patients. (2004) (36)
Genetic determinants of blood lipids and cerebral small vessel disease: role of high-density lipoprotein cholesterol. (2020) (35)
Ischemic stroke of the cortical “hand knob” area: stroke mechanisms and prognosis (2009) (35)
Parkin interacts with the proteasome subunit alpha4. (2005) (35)
Apathy is related to cortex morphology in CADASIL (2011) (35)
Predicting sporadic Alzheimer’s disease progression via inherited Alzheimer’s disease-informed machine-learning (2020) (35)
A genome-wide survey of human short-term memory (2009) (34)
CHLAMYDIA INFECTION (2001) (34)
A prospective study of serum metabolites and risk of ischemic stroke (2019) (34)
Cerebrospinal fluid findings in CADASIL (1999) (33)
Extensive White Matter Hyperintensities May Increase Brain Volume in Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (2012) (33)
Continuous Intra-Arterial Nimodipine for the Treatment of Cerebral Vasospasm (2008) (33)
Cortical Superficial Siderosis in Different Types of Cerebral Small Vessel Disease (2017) (33)
Magnetization Transfer Ratio Relates to Cognitive Impairment in Normal Elderly (2014) (33)
Challenges and opportunities in stroke genetics. (2018) (33)
Effect of Genetic Variants Associated With Plasma Homocysteine Levels on Stroke Risk (2014) (33)
Neuroimmune cardiovascular interfaces control atherosclerosis (2022) (33)
Prognostic relevance of cortical superficial siderosis in cerebral amyloid angiopathy (2019) (33)
Mendelian randomization for studying the effects of perturbing drug targets (2021) (32)
Genetically determined blood pressure, antihypertensive drug classes, and risk of stroke subtypes (2020) (31)
Common variation in PHACTR 1 is associated with susceptibility to cervical artery dissection (2014) (31)
Intracerebral haemorrhage in CADASIL (2005) (31)
Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine (2009) (31)
Comparison of symptomatic and asymptomatic atherosclerotic carotid plaques using parallel imaging and 3 T black-blood in vivo CMR (2013) (31)
Measurement of brain atrophy in subcortical vascular disease: A comparison of different approaches and the impact of ischaemic lesions (2008) (30)
Role of Non-Coding RNAs in Stroke. (2018) (30)
Inhibition of atherogenesis by the COP9 signalosome subunit 5 in vivo (2017) (30)
Successful bilateral pallidal stimulation for Meige syndrome and spasmodic torticollis (2006) (30)
Diagnostic Criteria of Vascular Dementia in CADASIL (2008) (30)
Higher CSF sTREM2 attenuates ApoE4-related risk for cognitive decline and neurodegeneration (2020) (30)
The Determinants of Dementia after Stroke (DEDEMAS) Study: Protocol and Pilot Data (2014) (29)
Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes (2018) (29)
Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes (2018) (29)
A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine (2020) (29)
Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine. (1996) (29)
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies (2015) (29)
The Atherosclerosis Risk Variant rs2107595 Mediates Allele-Specific Transcriptional Regulation of HDAC9 via E2F3 and Rb1. (2019) (28)
Endovascular Treatment of Very Elderly Patients Aged ≥90 With Acute Ischemic Stroke (2020) (28)
Compartment-resolved Proteomic Analysis of Mouse Aorta during Atherosclerotic Plaque Formation Reveals Osteoclast-specific Protein Expression* (2017) (28)
The Meta VCI Map consortium for meta-analyses on strategic lesion locations for vascular cognitive impairment using lesion-symptom mapping: Design and multicenter pilot study (2019) (28)
Genome-Wide Association Analysis of Young Onset Stroke Identifies a Locus on Chromosome 10 q 25 Near HABP 2 (2015) (28)
Broad phenotype of cysteine-altering NOTCH3 variants in UK Biobank (2020) (27)
Enhanced resting-state functional connectivity between core memory-task activation peaks is associated with memory impairment in MCI (2016) (27)
Tau-PET and in vivo Braak-staging as prognostic markers of future cognitive decline in cognitively normal to demented individuals (2021) (27)
Atrial Fibrillation Genetic Risk and Ischemic Stroke Mechanisms (2017) (27)
Cerebral Microbleeds and the Risk of Incident Ischemic Stroke in CADASIL (Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy) (2017) (27)
Small vessel disease more than Alzheimer's disease determines diffusion MRI alterations in memory clinic patients (2020) (27)
Monocyte-Chemoattractant Protein-1 Levels in Human Atherosclerotic Lesions Associate With Plaque Vulnerability (2021) (27)
Stroke Etiology Modifies the Effect of Endovascular Treatment in Acute Stroke (2019) (27)
Bacterial meningitis in adults (1999) (27)
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) (26)
Expansion of the Phenotypic Spectrum of the CACNA1A T666M Mutation: A Family with Familial Hemiplegic Migraine Type 1, Cerebellar Atrophy and Mental Retardation (2008) (26)
Differences in Common Genetic Predisposition to Ischemic Stroke by Age and Sex (2015) (26)
Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (26)
Kidney Function and White Matter Disease in Young Stroke Patients: Analysis of the Stroke in Young Fabry Patients Study Population (2012) (26)
Advances in Stroke 2017 (2018) (26)
Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (26)
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) (26)
APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL (2016) (26)
Genome-Wide Analysis of Blood Pressure Variability and Ischemic Stroke (2013) (26)
Three-Dimensional MRI Analysis of Individual Volume of Lacunes in CADASIL (2009) (26)
Genetic Architecture of White Matter Hyperintensities Differs in Hypertensive and Nonhypertensive Ischemic Stroke (2015) (26)
Matrix metalloproteinase induction by EMMPRIN in experimental focal cerebral ischemia (2005) (26)
A magnetic resonance imaging study of the cervical cord of patients with CADASIL (2001) (25)
Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2016) (25)
Heritability of MRI Lesion Volume in CADASIL: Evidence for Genetic Modifiers (2006) (25)
Age‐dependent amyloid deposition is associated with white matter alterations in cognitively normal adults during the adult life span (2020) (25)
Mendelian randomization for studying the effects of perturbing drug targets. (2021) (24)
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting (2019) (24)
Diabetes mellitus, glycemic traits, and cerebrovascular disease: a Mendelian randomization study (2019) (24)
The novel p . L 1649 Q mutation in the SCN 1 A epilepsy gene is associated with familial hemiplegic migraine : genetic and functional studies (2011) (24)
Contribution of acute infarcts to cerebral small vessel disease progression (2019) (24)
Genetic Imbalance in Patients with Cervical Artery Dissection (2017) (24)
Predictors and Clinical Impact of Incident Lacunes in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (2017) (24)
Effects of short term atorvastatin treatment on cerebral hemodynamics in CADASIL (2007) (24)
Mapping 3-year changes in gray matter and metabolism in Aβ-positive nondemented subjects (2015) (24)
Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache (2020) (23)
Association of Circulating Monocyte Chemoattractant Protein-1 Levels With Cardiovascular Mortality: A Meta-analysis of Population-Based Studies. (2020) (23)
What Is the Best Mix of Population‐Wide and High‐Risk Targeted Strategies of Primary Stroke and Cardiovascular Disease Prevention? (2020) (23)
Polygenic Overlap Between Kidney Function and Large Artery Atherosclerotic Stroke (2014) (23)
Protection of cerebral microvasculature after moderate hypothermia following experimental focal cerebral ischemia in mice (2008) (23)
Multimodal Recanalization Therapy in Acute Basilar Artery Occlusion: Long-Term Functional Outcome and Quality of Life (2012) (23)
Parkin Modulates Gene Expression in Control and Ceramide-Treated PC12 Cells (2006) (23)
Heritable and non-heritable uncommon causes of stroke (2020) (22)
Genetic Variation in the Lymphotoxin-Alpha Pathway and the Risk of Ischemic Stroke in European Populations (2009) (22)
Clinical correlates of longitudinal MRI changes in CADASIL (2019) (22)
A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline (2011) (22)
Genetic overlap and causal inferences between kidney function and cerebrovascular disease (2020) (21)
A new cause of hereditary small vessel disease (2003) (21)
The migraine–stroke connection: A genetic perspective (2016) (21)
EFNS task force on molecular diagnosis of neurologic disorders Guidelines for the molecular diagnosis of inherited neurologic diseases First of two parts (2001) (21)
White-matter lesions without lacunar infarcts in CADASIL. (2012) (21)
ADC Histograms from Routine DWI for Longitudinal Studies in Cerebral Small Vessel Disease: A Field Study in CADASIL (2014) (21)
Prevalence of Amyloid Positron Emission Tomographic Positivity in Poststroke Mild Cognitive Impairment (2016) (20)
Designed CXCR4 mimic acts as a soluble chemokine receptor that blocks atherogenic inflammation by agonist-specific targeting (2020) (20)
Common NOTCH3 Variants and Cerebral Small-Vessel Disease (2015) (20)
Next generation sequencing analysis of patients with familial cervical artery dissection (2017) (20)
Prioritizing the Role of Major Lipoproteins and Subfractions as Risk Factors for Peripheral Artery Disease (2021) (20)
Pravastatin reduces microvascular basal lamina damage following focal cerebral ischemia and reperfusion. (2004) (20)
Genetic Associations With White Matter Hyperintensities Confer Risk of Lacunar Stroke (2016) (20)
Characteristics of carotid atherosclerotic plaques of chronic lipid apheresis patients as assessed by In Vivo High-Resolution CMR - a comparative analysis (2012) (20)
Headache as a symptom at stroke onset in 4,431 young ischaemic stroke patients. Results from the “stroke in young fabry patients (SIFAP1) study” (2013) (20)
rt-PA causes a dose-dependent increase in the extravasation of cellular and non-cellular blood elements after focal cerebral ischemia (2007) (20)
KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease (2021) (19)
Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques (2018) (19)
GIANT CELL ARTERITIS OF THE BASAL CEREBRAL ARTERIES: CORRELATION OF MRI, DSA, AND HISTOPATHOLOGY (2010) (19)
Matrix metalloproteinase (MMP) induction and inhibition at different doses of recombinant tissue plasminogen activator following experimental stroke (2007) (19)
Prediction of 3-year clinical course in CADASIL (2016) (19)
Quantification of Supra-Aortic Arterial Wall Inflammation in Patients With Arteritis Using High Resolution Dynamic Contrast-Enhanced Magnetic Resonance Imaging: Initial Results in Correlation to [18F]-FDG PET/CT (2011) (18)
Sex Differences in Outcome After Thrombectomy for Acute Ischemic Stroke are Explained by Confounding Factors (2020) (18)
Endovascular Mechanical Recanalisation of Acute Carotid-T Occlusions: A Single-Center Retrospective Analysis (2011) (18)
Detection of deleterious on-target effects after HDR-mediated CRISPR editing (2020) (18)
Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke (2016) (18)
Automated analysis of whole brain vasculature using machine learning (2019) (18)
Genetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke (2015) (18)
[Diagnostic evaluation of the craniocervical vascular system with a 16-slice multi-detector row spiral CT. Protocols and first experiences]. (2002) (17)
Pravastatin reduces microvascular basal lamina damage following focal cerebral ischemia and reperfusion (2006) (17)
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke (2020) (17)
Prediction of Vascular Risk after Stroke — Protocol and Pilot Data of the Prospective Cohort with Incident Stroke (PROSCIS) (2013) (17)
Update on the genetics of stroke and cerebrovascular disease 2006. (2007) (17)
Carotid Atherosclerotic Markers in CADASIL (2010) (17)
Update on the genetics of stroke and cerebrovascular disease 2007. (2008) (17)
Cardiometabolic traits mediating the effect of education on osteoarthritis risk: a Mendelian randomization study (2021) (16)
Factors Associated with Failure of Reperfusion in Endovascular Therapy for Acute Ischemic Stroke (2020) (16)
Genetically downregulated interleukin-6 signaling is associated with a favorable cardiometabolic profile: a phenome-wide association study (2020) (16)
European Stroke Organisation (ESO) guideline on pharmacological interventions for long-term secondary prevention after ischaemic stroke or transient ischaemic attack (2022) (15)
Different Types of White Matter Hyperintensities in CADASIL (2018) (15)
Genetically Predicted Blood Pressure Across the Lifespan (2020) (15)
Circulating Metabolites Differentiate Acute Ischemic Stroke from Stroke Mimics (2020) (15)
Circulating Interleukin-6 Levels and Incident Ischemic Stroke (2021) (15)
Cortical folding influences migraine aura symptoms in CADASIL (2011) (15)
Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease. (2022) (15)
NIHSS Scores in Ischemic Small Vessel Disease: A Study in CADASIL (2012) (15)
Familial carpal tunnel syndrome: further evidence for a genetic contribution (2005) (15)
Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model (2021) (15)
Serial carotid MRI identifies rupture of a vulnerable plaque resulting in amaurosis fugax (2013) (15)
Apathy (2009) (15)
Cardiological evaluation after cerebral ischaemia (2010) (15)
Association of the novel single-nucleotide polymorphism which increases oxidized low-density lipoprotein levels with cerebrovascular disease events. (2014) (14)
Advances in stroke 2009: update on the genetics of stroke and cerebrovascular disease 2009. (2010) (14)
Circadian Biology and Stroke. (2021) (14)
Dementia risk after transient ischaemic attack and stroke (2019) (14)
Subjective cognitive decline and stage 2 of Alzheimer disease in patients from memory centers (2022) (13)
Thrombolysis of basilar artery occlusion--intra-arterial or intravenous: is there really no difference? (2007) (13)
Confluent Thalamic Hyperintensities in CADASIL (2010) (13)
A novel HTRA1 exon 2 mutation causes loss of protease activity in a Pakistani CARASIL patient (2015) (13)
Ischemic stroke and peripheral arterial thromboembolism in a patient with Crohn's disease: A case presentation (2008) (13)
Involvement of astrocyte and oligodendrocyte gene sets in migraine (2016) (13)
CADASIL presenting with a movement disorder: A clinical study of a Chilean kindred (2006) (13)
Diabetes Mellitus, Glycemic Traits, and Cerebrovascular Disease (2021) (13)
[Variants of Todd's paralysis: postictal apraxia and prolonged postictal hemineglect]. (1994) (13)
Special topic section: linkages among cerebrovascular, cardiovascular, and cognitive disorders: Preventing dementia by preventing stroke: The Berlin Manifesto. (2019) (13)
Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensities. (2021) (13)
Simple and reliable detection of CRISPR-induced on-target effects by qgPCR and SNP genotyping (2021) (12)
The BIN1 rs744373 Alzheimer's disease risk SNP is associated with faster Aβ‐associated tau accumulation and cognitive decline (2021) (12)
Prediction of Long-term Cognitive Function After Minor Stroke Using Functional Connectivity (2021) (12)
Circulating biomarkers of immunity and inflammation, risk of Alzheimer’s disease, and hippocampal volume: a Mendelian randomization study (2021) (12)
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (12)
Cardiovascular Risk and Atherosclerosis Progression in Hypertensive Persons Treated to Blood Pressure Targets. (2019) (12)
Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke (2017) (12)
Correction: The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1–6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7–34 pathogenic variant (2018) (12)
Family History in Young Patients With Stroke (2015) (12)
[Cardiac workup after cerebral ischemia. Consensus paper of the Working Group on Heart and Brain of the German Cardiac Society and German Stroke Society]. (2010) (12)
Stroke Research Priorities for the Next Decade – A Supplement Statement on Intracranial Haemorrhage (2007) (12)
Impact of the COVID-19-pandemic on thrombectomy services in Germany (2020) (12)
Erratum: National Institute of Neurological Disorders and Stroke-Canadian Stroke Network Vascular Cognitive Impairment Harmonization Standards (Stroke (2006) 37, 9, (2220-2241)) (2007) (12)
Carotid endarterectomy or stenting or best medical treatment alone for moderate-to-severe asymptomatic carotid artery stenosis: 5-year results of a multicentre, randomised controlled trial (2022) (12)
Late Thrombectomy in Clinical Practice (2021) (11)
Effects of intravitreal bevacizumab treatment on proliferative retinopathy in a patient with cerebroretinal vasculopathy (2010) (11)
Shared Genetic Aetiology of Coronary Artery Disease and Atherosclerotic Stroke—2015 (2015) (11)
A Mendelian randomization of γ' and total fibrinogen levels in relation to venous thromboembolism and ischemic stroke. (2020) (11)
EFNS task force on molecular diagnosis of neurologic disorders Guidelines for the molecular diagnosis of inherited neurologic diseases Second of two parts (2001) (11)
Third nerve palsy with contralateral ocular torsion and binocular tilt of visual vertical, indicating a midbrain lesion (1995) (11)
Soluble TAM receptors sAXL and sTyro3 predict structural and functional protection in Alzheimer’s disease (2021) (11)
Role of subvoxel free fluid on diffusion parameters in brain tissue with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and its correlation with physical disability: histogram analysis of standard and fluid-attenuated MR diffusion. (2003) (11)
Malignant hemispheric infarction in Takayasu arteritis (2008) (11)
Using Phenotypic Heterogeneity to Increase the Power of Genome‐Wide Association Studies: Application to Age at Onset of Ischaemic Stroke Subphenotypes (2013) (11)
Effects of Age, APOE ÃÂµ4, Cognitive Reserve and Hippocampal Volume onCognitive Intervention Outcome in Amnestic Mild Cognitive Impairment (2016) (10)
Features and Determinants of Lacune Shape: Relationship With Fiber Tracts and Perforating Arteries (2016) (10)
Dose–response relationship between genetically proxied average blood glucose levels and incident coronary heart disease in individuals without diabetes mellitus (2021) (10)
Prediction of dementia using diffusion tensor MRI measures: the OPTIMAL collaboration (2021) (10)
Statins and Cerebral Perfusion in Patients with Leukoaraiosis – a Translational Proof-of-Principal MRI Study (2012) (10)
Clinically Relevant Depressive Symptoms in Young Stroke Patients - Results of the sifap1 Study (2015) (10)
Genetically Predicted Midlife Blood Pressure and Coronary Artery Disease Risk: Mendelian Randomization Analysis (2020) (10)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (vol 41, pg 1088, 2009) (2013) (10)
Spatial Patterns of Longitudinal Gray Matter Change as Predictors of Concurrent Cognitive Decline in Amyloid Positive Healthy Subjects. (2016) (10)
PRediction of acute coronary syndrome in acute ischemic StrokE (PRAISE) – protocol of a prospective, multicenter trial with central reading and predefined endpoints (2020) (10)
Vascular integrin immunoreactivity is selectively lost on capillaries during rat focal cerebral ischemia and reperfusion (2008) (9)
Internal Carotid Artery Dissection and Ischemic Cerebral Infarction in the Setting of Essential Thrombocythemia (2011) (9)
Shape of the Central Sulcus and Disability After Subcortical Stroke: A Motor Reserve Hypothesis (2016) (9)
A proteomic atlas of the neointima identifies novel druggable targets for preventive therapy (2021) (9)
Cerebral small vessel disease-related protease HtrA1 processes latent TGF-beta binding protein 1 and facilitates TGF-beta signalling (2016) (9)
Erratum: Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (Neuron (2018) 98(4) (743–753.e4), (S0896627318303222) (10.1016/j.neuron.2018.04.014)) (2018) (9)
[Genetics of ischemic stroke]. (2013) (9)
Complicated Carotid Artery Plaques and Risk of Recurrent Ischemic Stroke or TIA. (2022) (9)
Monocyte-chemoattractant protein-1 Levels in Human Atherosclerosis Associate with Plaque Vulnerability (2020) (8)
Within-lesion heterogeneity of subcortical DWI lesion evolution, and stroke outcome: A voxel-based analysis (2020) (8)
Zooming in on cerebral small vessel function in small vessel diseases with 7T MRI: Rationale and design of the “ZOOM@SVDs” study (2021) (8)
A new approach to reduce the number of animals used in experimental focal cerebral ischemia models (2005) (8)
International stroke genetics consortium recommendations for studies of genetics of stroke outcome and recovery (2021) (8)
Additive Effects of Genetic Interleukin‐6 Signaling Downregulation and Low‐Density Lipoprotein Cholesterol Lowering on Cardiovascular Disease: A 2×2 Factorial Mendelian Randomization Analysis (2021) (8)
Modifiable lifestyle factors and risk of stroke: a Mendelian randomization analysis (2020) (8)
Circadian rhythm of ischaemic core progression in human stroke (2021) (8)
APP expression in primary neuronal cell cultures from P6 mice during in vitro differentiation. (1993) (8)
Imaging neurovascular, endothelial and structural integrity in preparation to treat small vessel diseases. The INVESTIGATE-SVDs study protocol. Part of the SVDs@Target project (2021) (7)
Erratum: Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog (Cell Stem Cell (2013) 12 426-439)) (2013) (7)
Update on the genetics of stroke and cerebrovascular disease 2008. (2009) (7)
Reversible cerebral vasoconstriction syndrome with concurrent bilateral carotid artery dissection (2013) (7)
Meningoradiculitis with severe tetraparesis, and unusual manifestation of infection due to Cryptococcus neoformans variety gattii. (1998) (7)
The Subtype Specificity of Genetic Loci Associated with Stroke in 16,664 cases and 32,792 controls (2018) (7)
Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany (2010) (6)
Proteomic profiling in cerebral amyloid angiopathy reveals an overlap with CADASIL highlighting accumulation of HTRA1 and its substrates (2022) (6)
European Stroke Organisation (ESO) standard operating procedure for the preparation and publishing of guidelines (2021) (6)
Earlier Alzheimer’s disease onset is associated with tau pathology in brain hub regions and facilitated tau spreading (2022) (6)
Peripheral glucose levels and cognitive outcome after ischemic stroke—Results from the Munich Stroke Cohort (2016) (6)
[Hereditary CADASIL cerebral arteriopathy. Report of a family]. (1995) (6)
Relationship Between Blood Pressure and Incident Cardiovascular Disease (2021) (6)
Time-of-flight angiography: a viable alternative to contrast-enhanced MR angiography and fat-suppressed T1w images for the diagnosis of cervical artery dissection? (2013) (6)
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia--a comment. (2005) (6)
Multi-omics and 3D-imaging reveal bone heterogeneity and unique calvaria cells in neuroinflammation (2021) (6)
A Mendelian randomization of γ' and total fibrinogen levels on venous thromboembolism and ischemic stroke. (2020) (6)
Microbleeds in cerebral small vessel disease – Authors' reply (2013) (6)
Subarachnoid Hemorrhage and Diplopia as Initial Presentation of Polycythemia vera (2005) (6)
Genetically Proxied Inhibition of Coagulation Factors and Risk of Cardiovascular Disease: A Mendelian Randomization Study (2021) (5)
Associations of genetically predicted IL-6 signaling with cardiovascular disease risk across population subgroups (2022) (5)
Investigating the impact of a mutation in PDE5A on myocardial infarction (2015) (5)
Genetically predicted on-statin LDL response is associated with higher intracerebral haemorrhage risk. (2022) (5)
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Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls. (2019) (5)
Different Imaging Strategies in Patients With Possible Basilar Artery Occlusion (2015) (5)
Stroke while squeezing a pimple (2011) (5)
The neurovascular unit and systemic biology in stroke — implications for translation and treatment (2022) (4)
Microbiota-derived short chain fatty acids promote Aβ plaque deposition (2020) (4)
Genetic study of circulating cytokines offers insight into the determinants, cascades and effects of systemic inflammation (2020) (4)
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Modifiable Lifestyle Factors and Risk of Stroke: A Mendelian Randomization Analysis. (2021) (4)
Endovascular thrombectomy for basilar artery occlusion stroke: Analysis of the German Stroke Registry‐Endovascular Treatment (2023) (4)
Determining the OPTIMAL DTI analysis method for application in cerebral small vessel disease (2022) (3)
Assessing brain atrophy in subcortical vascular disease: A comparison of 3 methods and the impact of lesions on volume measurements in CADASIL (2007) (3)
Population impact of different hypertension management guidelines based on the prospective population-based Heinz Nixdorf Recall study (2021) (3)
Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke (2022) (3)
Pharmacological Targeting of the CCL2/CCR2 Axis for Atheroprotection: A Meta-Analysis of Preclinical Studies (2022) (3)
Targeting the CCL2-CCR2 axis for atheroprotection. (2022) (3)
Disentangling the effects of Alzheimer’s and small vessel disease on white matter fibre tracts (2022) (3)
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Multi-ethnic genome-wide association study for atrial fibrillation (2018) (3)
Cerebral small vessel disease burden and cognitive and functional outcomes after stroke: A multicenter prospective cohort study (2022) (3)
Tau-PET and in vivo Braak-staging as a prognostic marker in Alzheimer's disease (2021) (3)
Genetic variants link lower segregation of brain networks to higher blood pressure and worse cognition within the general aging population (2021) (3)
Monogenic Causes of Stroke (2003) (3)
The BIN1 rs744373 Alzheimer’s disease risk SNP is associated with faster Aβ‐associated tau accumulation and cognitive decline (2021) (3)
Influence of Genetic Variation in PDE3A on Endothelial Function and Stroke (2019) (3)
Dementia after stroke due to intracerebral haemorrhage (2016) (2)
Framework for Clinical Trials in Cerebral Small Vessel Disease (FINESSE): A Review. (2022) (2)
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Letter by Dichgans et al regarding article, "Peripheral artery disease as a manifestation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and practical implications". (2013) (2)
GIANT CELL ARTERITIS OF THE BASAL CEREBRAL ARTERIES (2010) (2)
[Genetics of migraine]. (2006) (2)
Arterial branching and basal ganglia lacunes: A study in pure small vessel disease (2017) (2)
Second European Stroke Science Workshop. (2014) (2)
Between new genetic discoveries and large randomized trials—neurological research in the era of systems medicine (2013) (2)
CCL2/CCR2 inhibition in atherosclerosis: a meta-analysis of preclinical studies (2021) (2)
[Susac syndrome: case reports and review of the literature]. (2006) (2)
[Molecular diagnosis of hereditary neurologic diseases. Position paper]. (2000) (2)
Genetic variants related to antihypertensive targets inform drug efficacy and side effects (2018) (2)
Correction to: Heritable and non-heritable uncommon causes of stroke (2020) (2)
Sequence Variants on Chromosome 9p21 Confer Risk of Large Vessel Stroke. (2009) (2)
Contents, Vol. 4, 1993 (1993) (2)
Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (2017) (2)
Author Correction: Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke (2020) (2)
Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2011) (2)
A magnetization transfer imaging study of individuals with CADASIL (2000) (2)
Prevalence and Significance of the Vessel-Cluster Sign on Susceptibility-Weighted Imaging in Patients With Severe Small Vessel Disease (2022) (2)
Spatial orientation deficits in mild cognitive impairment (2013) (2)
Blurring of the vessels of the interhemispheric fissure in multislice CT angiography: a sign of meningeal carcinomatosis (2004) (2)
Genetic variation in the lymphotoxin alpha pathway and the risk of ischaemic stroke (2007) (2)
Serum IL-6, sAXL, and YKL-40 as systemic correlates of reduced brain structure and function in Alzheimer’s disease: results from the DELCODE study (2023) (1)
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies | NOVA. The University of Newcastle's Digital Repository (2012) (1)
The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1–6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7–34 pathogenic variant (2018) (1)
Migraine without aura: genome-wide association analysis identifies several novel susceptibility (2013) (1)
IKKβ binds NLRP3 providing a shortcut to inflammasome activation for rapid immune responses (2022) (1)
[Tracer diagnosis stroke]. (2017) (1)
Family History in Young Patients With Stroke Brief Reports (2015) (1)
Fourth European stroke science workshop (2018) (1)
CADASIL Affects Multiple Aspects of Cerebral Small Vessel Function on 7T‐MRI (2022) (1)
[CADASIL: clinical aspects and diagnosis]. (1998) (1)
A novel mouse model for familial hemiplegic migraine type 3 reveals increased susceptibility for cortical spreading depression (2017) (1)
Hippocampal volume is an independent predictor of global cognitive performance in pure cerebral small vessel disease (2007) (1)
Subject Index Vol. 13, Suppl. 2, 2002 (2002) (1)
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (2020) (1)
Protective effects of HLA-DRB1*04 subtypes in Parkinson's and Alzheimer's diseases implicate acetylated Tau PHF6 sequences (2021) (1)
Cerebral Microbleeds: Cerebral microbleeds in CADASIL (2011) (1)
Tau-PET and in vivo Braak-staging as prognostic markers of future cognitive decline in cognitively normal to demented individuals (2021) (1)
Absence of the Autophagy Adaptor SQSTM 1 / p 62 Causes Childhood-Onset Neurodegeneration with Ataxia , Dystonia , and Gaze Palsy Haack (1)
[Current aspects of therapy studies of acute stroke]. (2012) (1)
Tau spreads across connected brain regions in progressive supranuclear palsy and corticobasal syndrome (2021) (1)
Machine learning analysis of whole mouse brain vasculature (2020) (1)
Cardiac Risk Factors for Stroke: A Comprehensive Mendelian Randomization Study (2021) (1)
Retinal Vessel Analysis in Cerebral Stroke Patients versus Normals (2009) (1)
Physician-Confirmed and Administrative Definitions of Stroke in UK Biobank Reflect the Same Underlying Genetic Trait (2021) (1)
Polygenic Effect on Tau Pathology Progression in Alzheimer's Disease (2022) (1)
Measurement of meaningful treatment effects in CADASIL – Authors' reply (2008) (1)
Genetic proxies for PCSK9 inhibition associate with lipoprotein(a): Effects on coronary artery disease and ischemic stroke. (2022) (1)
Abstract TP132: Vascular HDAC9 Modulates Atherogenic Processes and Enhances NF-kB Activation (2018) (1)
Disease 2009 Advances in Stroke 2009: Update on the Genetics of Stroke and Cerebrovascular (2010) (1)
Reply to Liu et al.: Loss of TGF-β signaling in CARASIL pathogenesis (2015) (1)
The BS variant of C4 protects against age-related loss of white matter microstructural integrity. (2021) (1)
Genetics, Genomics, and Precision Medicine. (2021) (1)
Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor (2009) (1)
Shared genetic background between SARS-CoV-2 infection and large artery stroke (2022) (1)
Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's disease (2008) (1)
The interplay between inflammatory cytokines and cardiometabolic disease: bi-directional mendelian randomisation study (2023) (1)
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
Common NOTCH 3 Variants and Cerebral Small-Vessel Disease (2015) (1)
Investigating the impact of a mutation in PDE5A on myocardial infarction (2015) (1)
Polygenic score is associated with accelerated tau pathology accumulation in Alzheimer’s disease (2022) (0)
Genetic factors associated with higher segregation of brain networks and cognition mediated by cardiovascular health: GWAS and Mendelian randomization analyses in the UK Biobank and Rotterdam Study (2021) (0)
Spontaneous aggregation of CADASIL-mutated Notch3 (2008) (0)
Advances in Stroke: Genetics, Genomics, Precision Medicine. (2022) (0)
Blood-brain barrier leakage hotspots collocating with brain lesions due to sporadic and monogenic small vessel disease. (2023) (0)
Future Perspectives in Stroke Management (2015) (0)
Neuroimaging Correlates of Cognitive Decline (2009) (0)
CONNECTIVITY OF THE LEFT FRONTAL CORTEX ATTENUATES DETRIMENTAL EFFECTS OF CSF-TAU ON MEMORY IN PRECLINICAL AND CLINICAL ALZHEIMER’S DISEASE (2017) (0)
Cerebral Small Vessel Disease: Hereditary cerebral small vessel disease and the role of genetic factors (2014) (0)
51 A common mtDNA control region polymorphism 16519T is associated with migraine without aura and cyclic vomiting (2007) (0)
Genome-Wide Analysis of Blood Pressure Variability and Ischemic Stroke Clinical Sciences (2013) (0)
Erratum (1992) (0)
A magnetic resonance imaging study of the cervical spinal cord of cadasil patients (2000) (0)
Microplasmin reduces microvascular damage and blood brain barrier disruption following experimental stroke (2005) (0)
Year : 2011 A genome-wide survey of human short-term memory (2010) (0)
Targeting the CCL2-CCR2 axis for atheroprotection. (2022) (0)
Functional cerebrovascular abnormalities in CADASIL (2005) (0)
Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategies (2005) (0)
Author Correction: Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke (2020) (0)
Clinical importance of brain atrophy and brain volume changes in CADASIL: A serial MRI study (2006) (0)
FACE NAME ASSOCIATIVE RECOGNITION IS ASSOCIATED WITH ALZHEIMER’S DISEASE BIOMARKERS IN PATIENTS WITH SUBJECTIVE COGNITIVE DECLINE (2016) (0)
The EffecTs of Amlodipine and other Blood PREssure Lowering Agents on Microvascular FuncTion in Small Vessel Diseases (TREAT-SVDs) trial: Study protocol for a randomised crossover trial (2022) (0)
Hereditary causes of stroke (2002) (0)
Papassotiropoulos 2010 MolPsychiat Supplementary (2014) (0)
Prevalence of complicated carotid atherosclerotic plaques ispilateral to ischemic cryptogenic stroke using high-resolution mri (2011) (0)
Matrix metalloproteinase-inhibitor causes an activation of urokinase after experimental cerebral ischemia (2005) (0)
Higher fiber‐tract myelin levels predict lower longitudinal rates of fibrillar tau independent of amyloid (2022) (0)
Molecular genetic overlap between migraine and major depressive disorder (2018) (0)
Reduction of regional cerebral blood volume (rCBV) in subcortical lesions in CADASIL negatively correlates to disability and cognitive performance (2000) (0)
Erratum: Ischemic stroke is associated with the ABO locus: The EuroCLOT study (2014) (0)
Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease (2018) (0)
Human Genetic Evidence that Common Variants near PIK3CG are Associated with Atherosclerotic Plaque Hemorrhage and Vessel Density (2013) (0)
Postoperative amnesic state with impairment of static visual perception (2008) (0)
optimization study The Causative Classification of Stroke system: An international reliability and (2010) (0)
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (0)
Sequestration of latent TGF-β binding protein 1 into CADASIL-related Notch3-ECD deposits (2014) (0)
White-matter T2-hyperintensities without lacunar infarcts are associated with cognitive impairment but not with dementia in CADASIL (2011) (0)
Abstract P771: Monocyte-Chemoattractant Protein-1 Levels in Human Carotid Atherosclerosis Associate With Hallmarks of Plaque Vulnerability (2021) (0)
A Mendelian Randomization Study (0)
Cost-Effectiveness Analysis (2020) (0)
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (0)
Depression as a confounding factor in subcortical ischaemic vascular dementia: results from a cross-sectional study in CADASIL (2009) (0)
Intravenous thrombolysis during inter-hospital transfer of acute stroke patients is safe and efficient (2008) (0)
2 Stroke July 2015 Methods The details and methods of the Stroke in Fabry Patients (2015) (0)
Author response: WMH and long-term outcomes in ischemic stroke: A systematic review and meta-analysis (2020) (0)
Genetically predicted on-statin LDL response is associated with higher intracerebral hemorrhage risk (2022) (0)
Reproducibility and variability of quantitative MRI markers in cerebral small vessel disease (2016) (0)
Brain network segregation attenuates tau spreading in Alzheimer’s disease (2022) (0)
Targeting the CCL2-CCR2 axis for atheroprotection. (2022) (0)
Reply: Comparison of Different Plaque Imaging Techniques to Detect Complicated Carotid Artery Plaques. (2021) (0)
Functional network segregation is associated with attenuated tau spreading in Alzheimer's disease. (2022) (0)
Prospective Cohort Studies Control and - Multilocus Genetic Risk Score Associates With Ischemic Stroke in Case (2014) (0)
CONNECTIVITY OF THE LEFT FRONTAL CORTEX ATTENUATES DETRIMENTAL EFFECTS OF CSF-TAU ON MEMORY IN PRECLINICAL AND CLINICAL ALZHEIMER’S DISEASE (2017) (0)
Whole-exome sequencing in 16,511 individuals reveals a role of the HTRA1 protease and its substrate EGFL8 in brain white matter hyperintensities (2021) (0)
The role of callosal volume as a MRI marker in subcortical ischaemic vascular dementia: a study in CADASIL (2009) (0)
[Basic research for clinicians : A new rubric for Der Nervenarzt]. (2017) (0)
Abstract T P408: Suboptimal Quality of Reporting of Neuroimaging Methods for Studies of Cerebral Small Vessel Disease (2015) (0)
Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores (2023) (0)
The stroke relevant gene HDAC9 has pro-inflammatory roles in multiple cell types (2017) (0)
Decrease of cerebral blood volumein subcortical lesions correlateswith low cognitive performanceand increasing disability in cadasil (2008) (0)
Epilepsies, IMSGC consortium, IPDGC consortium, METASTROKE and Intracerebral Hemorrhage Studies of the International Stroke Genetics Consortium, Attention-Deficit Hyperactivity Disorder Working Group of the Psychiatric Genomics Consortium, Anorexia Nervosa Working Group of the Psychiatric Genomics C (2016) (0)
[Difficult decisions in stroke therapy]. (2011) (0)
Novel substrates of the small vessel disease related HTRA1 protease identified by proteomics (2017) (0)
Determinants of dementia after stroke: Amyloid-PET findings (2014) (0)
Transcriptional effects of conditional parkin-overexpression in PC12-cells (2007) (0)
Stroke induces early recurrent vascular events by inflammasome-dependent atherosclerotic plaque rupture (2023) (0)
Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a German family with FHM1, cerebellar atrophy and mental retardation (2007) (0)
the Role of the Lectin Pathway of Complement Activation on Stroke Outcome (0)
Diffusion tensor imaging derived metrics and brain volume changes correlate with clinical progression in CADASIL: a serial MRI study in pure subcortical ischaemic vascular disease (2006) (0)
Proteomic profiling in cerebral amyloid angiopathy reveals an overlap with CADASIL highlighting accumulation of HTRA1 and its substrates (2022) (0)
Higher CSF sTREM2 attenuates ApoE4-related risk for cognitive decline and neurodegeneration (2020) (0)
Circulating miR-126-3p and miR-126-5p are increased after acute ischemic stroke and expressed in platelets and T cells (2017) (0)
Effect of HDAC9 deficiency on ischemic stroke outcome (2016) (0)
Impact of educational level and lesion volume on cognitive performance in subcortical ischaemic vascular dementia: a study in CADASIL (2009) (0)
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
Contents Vol. 34, 2012 (2012) (0)
Abstract 2590: Supratentorial Superficial Siderosis is a Warning Sign of Subsequent Intracerebral Hemorrhage (2012) (0)
How High Is Too High? Population Impact of Different Hypertension Management Guidelines (2019) (0)
P4-084 GENOME-WIDE ASSOCIATION STUDY USING CEREBROSPINAL FLUID BIOMARKERS BETA- AMYLOID-42 AND PTAU181 IN GERMAN SAMPLES OFALZHEIMER’S DISEASE (2012) (0)
Multimodal diagnosis of cortical vein thrombosis (2007) (0)
Association of MTHFR genotype with lacunar stroke supports causal role for homocysteine (2015) (0)
Polygenic effect on accelerated tau pathology accumulation in Alzheimer's disease: Implications for patient selection in clinical trials (2021) (0)
Etiologic Stroke Subtypes in the NINDS Stroke Genetics Network Study (S32.001) (2013) (0)
In vivo Braak‐staging using 18F‐Flortaucipir‐tau‐PET as a predictive marker for future cognitive decline in Alzheimer’s disease (2021) (0)
The pattern of cognitive performance in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) (2004) (0)
Erratum: October 2016 cover caption (2016) (0)
Brain network segregation attenuates tau spreading in Alzheimer’s disease (2022) (0)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (0)
LEFT FRONTAL HUB CONNECTIVITY PROBED DURING MEMORY TASK SUPPORTS RESERVE IN HEALTHY AGING (2017) (0)
Neuroimmune cardiovascular interfaces control atherosclerosis (2022) (0)
Intravenous phosphocreatine improves neurological outcome in focal cerebral ischaemia and reperfusion (2007) (0)
Carotid Plaque Imaging in Acute Stroke (CAPIAS): Eine multizentrische Studie (www.clinicaltrials.gov NCT01284933) (2012) (0)
Higher levels of myelin are associated with higher resistance against tau pathology in Alzheimer’s disease (2022) (0)
Abstract TMP99: Genetics Of Stroke Of Undetermined Source: Overlap With Known Stroke Etiologies And Associations With Modifiable Risk Factors (2022) (0)
Evaluation der Karotis-CTA als Screening Methode für die Detektion komplizierter American Heart Association Typ VI Plaques (2014) (0)
Serum Monocyte-Chemoattractant Protein-1 Could be an Indicator of Coronary Artery Calcium Score-Reply. (2021) (0)
Third European Stroke Science Workshop. (2016) (0)
Characterization of cerebrovascular function in mice with cerebral small vessel disease (2016) (0)
P4-335: Donepezil in subcortical vascular cognitive impairment: A randomised double-blind trial in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (cadasil) (2008) (0)
Ischaemic stroke of the cortical „hand knob“ area: pathomechanisms and clinical course (2007) (0)
Differential MRI pattern in CADASIL and hypertensive leukoencephalopathy. (1999) (0)
Genetic Contributions to Early and Late Onset Ischemic Stroke (2021) (0)
Genome-wide association study using cerebrospinal fluid biomarkers beta-amyloid-42 and pTau181 in German samples of Alzheimer's disease (2012) (0)
Increasing use of rt-PA does not affect safety in acute stroke (2005) (0)
Cornea Farinata and other Variants (2009) (0)
Earlier Alzheimer's disease onset is associated with a shift of tau pathology towards brain hubs which facilitates tau spreading (2022) (0)
KL-VS heterozygosity is associated with reduced tau accumulation and lower memory impairment in Alzheimer's disease (2020) (0)
Last-Minute Poster Presentations (2005) (0)
Sequence variation in the gene encoding soluble epoxide hydrolase (EPHX2) is associated with increased susceptibility to ischemic stroke in a central european population (2007) (0)
Shared inflammatory glial cell signature after brain injury, revealed by spatial, temporal and cell-type-specific profiling of the murine cerebral cortex (2023) (0)
What to do for the neurologist who has a screw loose: Glue and the art of tuning fork maintenance (2004) (0)
ERRATUM. (2021) (0)
Genetic Association Studies in Stroke (2005) (0)
A unified classification approach rating clinical utility of protein biomarkers across neurologic diseases (2023) (0)
Second European Stroke Science Workshop Special Report (2014) (0)
Microangiopathic Diseases of the Brain (2003) (0)
Abstract 154: Sex-specific Genome Wide Association Study Of Early-onset Ischemic Stroke (2022) (0)
DEFICIENCY OF THE STROKE-RELEVANT HDAC9 GENE IS ATHEROPROTECTIVE (2015) (0)
Stroke Genetics (2021) (0)
Rare missense variant (R251G) on APOE counterbalances the Alzheimer’s disease risk associated with APOE‐ε4 (2022) (0)
CROSS-NETWORK COUPLING OF THE FRONTO-PARIETAL CONTROL NETWORK DURING MEMORY PERFORMANCE SUPPORTS PROTECTIVE EFFECTS OF EDUCATION IN AGING (2017) (0)
Contralesional cortical atrophy and molecular cortical circuit reorganization after cerebral ischemia (2017) (0)
Organizational Update From the European Stroke Organisation. (2021) (0)
Impaired assembly of HTRA1 oligomers as a pathogenic mechanism in cerebral small vessel disease (2017) (0)
What is CADASIL (2009) (0)
Correction: The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1–6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7–34 pathogenic variant (2018) (0)
Neurofilament light chain as a serum marker for cerebral small vessel disease (P2.096) (2017) (0)
Proteogenomic integration reveals CXCL10 as a potentially downstream causal mediator for IL-6 signaling on atherosclerosis (2023) (0)
Plasma interleukin-6 predicts carotid plaque severity, vulnerability, and progression in the cardiovascular health study (2022) (0)
The Carotid Plaque Imaging in Acute Stroke (CAPIAS) study: initial baseline data (2013) (0)
Abstract TMP15: Penumbral Rescue by Normobaric O2 in Ischemic Stroke With Target Mismatch ProFile (PROOF) (2018) (0)
Graphical Abstract CG 18-2-MS (2017) (0)
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas (2016) (0)
Sporadic hemiplegic migraine associated with a novel mutation in ATP1A2 (2006) (0)
CROSS-NETWORK COUPLING OF THE FRONTOPARIETAL CONTROL NETWORK DURING MEMORY PERFORMANCE SUPPORTS PROTECTIVE EFFECTS OF EDUCATION IN AGING (2017) (0)
Subject Index Vol. 4, 1993 (1993) (0)
Tract-specific white matter hyperintensities disrupt the default mode network in Alzheimer’s disease (2015) (0)
Proton magnetic resonance spectroscopic imaging in CADASIL. (1999) (0)
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (0)
Response to letter by Prof Christian Nolte and colleagues (2022) (0)
[Update on stroke]. (2019) (0)
Abstract WMP99: Proteomics Study Of Stroke In Young Adults (2022) (0)
Tract-specific white matter hyperintensities disrupt the default mode network in Alzheimer’s disease (2015) (0)
Hemiplegic and Basilar-type Migraine: Epidemiology, Genetics, and Mechanism(s) (2006) (0)
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study (2023) (0)
Erratum (2012) (0)
Migraine without aura: genome-wide association analysis identifies several novel susceptibility (2013) (0)
[Treatment and late results of 33 fractures of the pilon tibialis (author's transl)]. (1980) (0)
Abstract 152: Genome-wide Association Study of Early-Onset Ischemic Stroke Identifies Novel Locus on Chromosome 12 Near BCL7A/MLXIP (2020) (0)
CADASIL presenting study with a movement disorder: A clinical of a Chilean kindred (2006) (0)
Earlier Alzheimer's disease onset is associated with a shift of tau pathology towards brain hubs which facilitates tau spreading (2022) (0)
Abstract 181: Meta-Analysis of Genome-Wide Association Studies Identifies Two New Susceptibility Loci for Intracerebral Hemorrhage (2014) (0)
Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets (2018) (0)
Organizational Update From the European Stroke Organization. (2022) (0)
The left frontal cortex supports reserve in aging by enhancing functional network efficiency (2018) (0)
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (2020) (0)
1976 Stroke July 2015 Methods The details and methods of the Stroke in Fabry Patients ( SIFAP (2015) (0)
Klotho‐VS heterozygosity modifies amyloid‐dependent tau accumulation and memory impairment in Alzheimer’s disease (2021) (0)
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (2020) (0)
Evidence for a shared genetic determination of Ischemic Stroke And Coronary Artery Disease - a genome-wide analysis (2013) (0)
Donepezil in Subcortical Vascular Cognitive Impairment: A Randomized Double-Blind Trial in CADASIL (2008) (0)
A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine (2020) (0)
Impaired L-arginine induced vasoreactivity suggests endothelial dysfunction in CADASIL (2005) (0)
Relevance for Stroke of Genes Associated with Other Vascular Phenotypes (2016) (0)

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What Schools Are Affiliated With Martin Dichgans?

Martin Dichgans is affiliated with the following schools:

Fudan University
University of Cambridge
Harvard University
Medical University of Graz
University of Western Ontario
University of Calgary
University of Oslo
University of Oxford
Ludwig Maximilian University of Munich
University of Newcastle
University of Regensburg

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