Area of research
Genetics · Neurology
Research interest
Research interests include Genetic Associations and Epidemiology, Dementia and Cognitive Impairment Research, Acute Ischemic Stroke Management, and Cerebrovascular and genetic disorders.
ABSTRACT NUMBER: ESOC2026A2044 CONTEXT-DEPENDENT PQTLS REVEAL BLOOD PRESSURE–SPECIFIC MOLECULAR MECHANISMS LINKED TO VASCULAR BRAIN DISEASES
Direct oral anticoagulants versus no anticoagulation for the prevention of stroke in survivors of intracerebral haemorrhage with atrial fibrillation (PRESTIGE-AF): a multicentre, open-label, randomised, phase 3 trial
Machine learning in Alzheimer’s disease genetics
Molecular determinants of thrombosis recurrence risk across venous thromboembolism subtypes
The brain neurovascular epigenome and its association with dementia
Burden of intracerebral haemorrhage in Europe: forecasting incidence and mortality between 2019 and 2050
Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia
Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries
Genetic risk factors underlying white matter hyperintensities and cortical atrophy
Cohort Profile: Dementia Risk Prediction Project (DRPP)
Neuroimaging standards for research into small vessel disease—advances since 2013
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation
Large multi-ethnic genetic analyses of amyloid imaging identify new genes for Alzheimer disease
Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by <i>HLA-DRB1*04</i> subtypes
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity
Identification of circulating proteins associated with general cognitive function among middle-aged and older adults
Genetic Insights on the Relation of Vascular Risk Factors and Cervical Artery Dissection
New insights into the genetic etiology of Alzheimer’s disease and related dementias
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
Association of Rare <i>APOE</i> Missense Variants V236E and R251G With Risk of Alzheimer Disease
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse
Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels
Circulating Metabolome and White Matter Hyperintensities in Women and Men
Stroke-associated intergenic variants modulate a human FOXF2 transcriptional enhancer
Stroke genetics informs drug discovery and risk prediction across ancestries
Protective association of <i>HLA‐DRB1</i>*04 subtypes in neurodegenerative diseases implicates acetylated tau PHF6 sequences
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