Lista de obras - Rainer Malik - Dominio Público Uruguay

17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status

artículo científico publicado en 2013

A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach

artículo científico publicado en 2014

APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL

artículo científico publicado en 2015

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of shared heritability in common disorders of the brain

Association of Circulating Monocyte Chemoattractant Protein-1 Levels With Cardiovascular Mortality: A Meta-analysis of Population-Based Studies

artículo científico publicado en 2020

Atrial Fibrillation Genetic Risk and Ischemic Stroke Mechanisms

artículo científico publicado en 2017

Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

artículo científico publicado en 2020

Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study

artículo científico publicado en 2016

Cerebrovascular Disease Knowledge Portal: An Open-Access Data Resource to Accelerate Genomic Discoveries in Stroke

artículo científico publicado en 2018

Challenges and Opportunities in Stroke Genetics

artículo científico publicado en 2018

Circulating Monocyte Chemoattractant Protein-1 and Risk of Stroke: Meta-Analysis of Population-Based Studies Involving 17 180 Individuals

scientific article published on 03 September 2019

Clinical spectrum, underlying etiologies and radiological characteristics of cortical superficial siderosis

artículo científico publicado en 2015

Combination of text-mining algorithms increases the performance

artículo científico

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

artículo científico publicado en 2020

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

Common coding variant in SERPINA1 increases the risk for large artery stroke

artículo científico publicado en 2017

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

artículo científico publicado en 2012

Comparative conservation analysis of the human mitotic phosphoproteome

artículo científico publicado en 2008

Compartment-resolved Proteomic Analysis of Mouse Aorta during Atherosclerotic Plaque Formation Reveals Osteoclast-specific Protein Expression

artículo científico publicado en 2017

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

artículo científico publicado en 2014

Current concepts and clinical applications of stroke genetics

artículo científico

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

artículo científico publicado en 2016

Cysteine-sparing CADASIL mutations in NOTCH3 show proaggregatory properties in vitro

artículo científico publicado en 2015

Decreased CSF Levels of ß-Amyloid in Patients With Cortical Superficial Siderosis

article published in 2019

Deficiency of the stroke relevant HDAC9 gene attenuates atherosclerosis in accord with allele-specific effects at 7p21.1.

artículo científico publicado en 2014

Diabetes Mellitus, Glycemic Traits, and Cerebrovascular Disease

artículo científico publicado en 2021

Differences in Common Genetic Predisposition to Ischemic Stroke by Age and Sex

artículo científico publicado en 2015

Differential effects of PCSK9 variants on risk of coronary disease and ischaemic stroke

artículo científico publicado en 2017

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

artículo científico publicado en 2017

Evaluation of the Low-Specificity Protease Elastase for Large-Scale Phosphoproteome Analysis

article

Free water determines diffusion alterations and clinical status in cerebral small vessel disease

artículo científico publicado en 2018

From proteome lists to biological impact--tools and strategies for the analysis of large MS data sets

artículo científico publicado en 2010

GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

artículo científico publicado en 2018

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

artículo científico publicado en 2015

Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia.

artículo científico publicado en 2018

Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques

Genetic analysis for a shared biological basis between migraine and coronary artery disease

artículo científico publicado en 2015

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

Genetic factors in cerebral small vessel disease and their impact on stroke and dementia

artículo científico

Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations

artículo científico publicado en 2012

Genetic overlap between diagnostic subtypes of ischemic stroke

artículo científico publicado en 2015

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

artículo científico publicado en 2012

Genetic risk, incident stroke, and the benefits of adhering to a healthy lifestyle: cohort study of 306 473 UK Biobank participants

artículo científico publicado en 2018

Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke

artículo científico publicado en 2017

Genetic variants related to antihypertensive targets inform drug efficacy and side effects

Genetic variation at 16q24.2 is associated with small vessel stroke

artículo científico publicado en 2016

Genetically predicted on-statin LDL response is associated with higher intracerebral haemorrhage risk

artículo científico publicado en 2022

Genetically predicted on-statin LDL response is associated with higher intracerebral hemorrhage risk

artículo científico publicado en 2022

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

artículo científico publicado en 2018

Genome-wide analysis of blood pressure variability and ischemic stroke

artículo científico publicado en 2013

Genome-wide association analysis identifies susceptibility loci for migraine without aura

artículo científico publicado en 2012

Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis

artículo científico publicado en 2016

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

artículo científico publicado en 2012

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

artículo científico publicado en 2020

Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.

artículo científico publicado en 2014

Genome-wide meta-analysis identifies new susceptibility loci for migraine

artículo científico publicado en 2013

Human Validation of Genes Associated With a Murine Atherosclerotic Phenotype

artículo científico publicado en 2016

Identification of a strategic brain network underlying processing speed deficits in vascular cognitive impairment

artículo científico publicado en 2012

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

artículo científico publicado en 2014

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

Loci influencing blood pressure identified using a cardiovascular gene-centric array

artículo científico publicado en 2013

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

artículo científico publicado en 2013

Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.

artículo científico publicado en 2016

Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans

artículo científico publicado en 2015

Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.

artículo científico publicado en 2014

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage

artículo científico publicado en 2014

Modifiable pathways in Alzheimer's disease: Mendelian randomisation analysis

artículo científico publicado en 2017

Multi-ethnic genome-wide association study for atrial fibrillation

article

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2018

Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies

artículo científico publicado en 2014

Polygenic overlap between kidney function and large artery atherosclerotic stroke

artículo científico publicado en 2014

Polygenic risk of ischemic stroke is associated with cognitive ability

artículo científico publicado en 2015

Predicting stroke through genetic risk functions: the CHARGE Risk Score Project

artículo científico publicado en 2014

Prevalence of Amyloid Positron Emission Tomographic Positivity in Poststroke Mild Cognitive Impairment

artículo científico

Prevalence of cortical superficial siderosis in patients with cognitive impairment

artículo científico publicado en 2013

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2019

Quantitative analysis of the human spindle phosphoproteome at distinct mitotic stages

artículo científico publicado en 2009

RNA-Seq Identifies Circulating miR-125a-5p, miR-125b-5p, and miR-143-3p as Potential Biomarkers for Acute Ischemic Stroke

artículo científico publicado en 2017

Shared genetic aetiology between cognitive functions and physical and mental health in UK Biobank (N = 112 151) and 24 GWAS consortia

article

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.

artículo científico publicado en 2015

Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke

artículo científico publicado en 2015

Single nucleotide polymorphisms associated with rat expressed sequences

artículo científico publicado en 2004

Text mining and protein annotations: the construction and use of protein description sentences.

artículo científico publicado en 2006

The Plk1-dependent phosphoproteome of the early mitotic spindle

artículo científico publicado en 2010

The Subtype Specificity of Genetic Loci Associated with Stroke in 16,664 cases and 32,792 controls

The causal effect of vitamin D binding protein (DBP) levels on calcemic and cardiometabolic diseases: a Mendelian randomization study

artículo científico publicado en 2014

The migraine-stroke connection: A genetic perspective.

artículo científico publicado en 2015

Uncovering the molecular machinery of the human spindle--an integration of wet and dry systems biology

artículo científico publicado en 2012

What explains the effect of education on cardiovascular disease? Applying Mendelian randomization to identify the consequences of education inequality:

Lista de obras de Rainer Malik

17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status

A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach

APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL

Analysis of shared heritability in common disorders of the brain

Analysis of shared heritability in common disorders of the brain

Association of Circulating Monocyte Chemoattractant Protein-1 Levels With Cardiovascular Mortality: A Meta-analysis of Population-Based Studies

Atrial Fibrillation Genetic Risk and Ischemic Stroke Mechanisms

Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study

Cerebrovascular Disease Knowledge Portal: An Open-Access Data Resource to Accelerate Genomic Discoveries in Stroke

Challenges and Opportunities in Stroke Genetics

Circulating Monocyte Chemoattractant Protein-1 and Risk of Stroke: Meta-Analysis of Population-Based Studies Involving 17 180 Individuals

Clinical spectrum, underlying etiologies and radiological characteristics of cortical superficial siderosis

Combination of text-mining algorithms increases the performance

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

Common coding variant in SERPINA1 increases the risk for large artery stroke

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

Comparative conservation analysis of the human mitotic phosphoproteome

Compartment-resolved Proteomic Analysis of Mouse Aorta during Atherosclerotic Plaque Formation Reveals Osteoclast-specific Protein Expression

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

Current concepts and clinical applications of stroke genetics

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

Cysteine-sparing CADASIL mutations in NOTCH3 show proaggregatory properties in vitro

Decreased CSF Levels of ß-Amyloid in Patients With Cortical Superficial Siderosis

Deficiency of the stroke relevant HDAC9 gene attenuates atherosclerosis in accord with allele-specific effects at 7p21.1.

Diabetes Mellitus, Glycemic Traits, and Cerebrovascular Disease

Differences in Common Genetic Predisposition to Ischemic Stroke by Age and Sex

Differential effects of PCSK9 variants on risk of coronary disease and ischaemic stroke

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Evaluation of the Low-Specificity Protease Elastase for Large-Scale Phosphoproteome Analysis

Free water determines diffusion alterations and clinical status in cerebral small vessel disease

From proteome lists to biological impact--tools and strategies for the analysis of large MS data sets

GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia.

Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

Genetic factors in cerebral small vessel disease and their impact on stroke and dementia

Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations

Genetic overlap between diagnostic subtypes of ischemic stroke

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

Genetic risk, incident stroke, and the benefits of adhering to a healthy lifestyle: cohort study of 306 473 UK Biobank participants

Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke

Genetic variants related to antihypertensive targets inform drug efficacy and side effects

Genetic variation at 16q24.2 is associated with small vessel stroke

Genetically predicted on-statin LDL response is associated with higher intracerebral haemorrhage risk

Genetically predicted on-statin LDL response is associated with higher intracerebral hemorrhage risk

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

Genome-wide analysis of blood pressure variability and ischemic stroke

Genome-wide association analysis identifies susceptibility loci for migraine without aura

Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Human Validation of Genes Associated With a Murine Atherosclerotic Phenotype

Identification of a strategic brain network underlying processing speed deficits in vascular cognitive impairment

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

Loci influencing blood pressure identified using a cardiovascular gene-centric array

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.

Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans

Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage

Modifiable pathways in Alzheimer's disease: Mendelian randomisation analysis

Multi-ethnic genome-wide association study for atrial fibrillation

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies

Polygenic overlap between kidney function and large artery atherosclerotic stroke

Polygenic risk of ischemic stroke is associated with cognitive ability

Predicting stroke through genetic risk functions: the CHARGE Risk Score Project

Prevalence of Amyloid Positron Emission Tomographic Positivity in Poststroke Mild Cognitive Impairment

Prevalence of cortical superficial siderosis in patients with cognitive impairment

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes