Lista de obras -

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

artículo científico publicado en 2013

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

artículo científico publicado en 2007

A survey of the SWISS researchers on the impact of sibling privacy protections on pedigree recruitment

artículo científico publicado en 2005

APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: a genetic association study

artículo científico publicado en 2011

Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?

artículo científico publicado en 2012

Association of integrin alpha2 gene variants with ischemic stroke

artículo científico publicado en 2007

Author response: Ischemic Lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage

artículo científico publicado en 2017

Burden of blood pressure-related alleles is associated with larger hematoma volume and worse outcome in intracerebral hemorrhage

artículo científico publicado en 2013

Burden of risk alleles for hypertension increases risk of intracerebral hemorrhage

artículo científico publicado en 2012

Candidate gene polymorphisms for ischemic stroke

artículo científico publicado en 2009

Common mitochondrial sequence variants in ischemic stroke

artículo científico publicado en 2010

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

artículo científico publicado en 2012

Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage

artículo científico publicado en 2013

Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trials

artículo científico publicado en 2011

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

artículo científico publicado en 2017

GISCOME - Genetics of Ischaemic Stroke Functional Outcome network: A protocol for an international multicentre genetic association study

article

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

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

artículo científico publicado en 2016

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome-wide association analysis of ischemic stroke in young adults

artículo científico publicado en 2011

Genome-wide association meta-analysis of functional outcome after ischemic stroke

artículo científico publicado en 2019

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

artículo científico publicado en 2012

Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.

artículo científico publicado en 2015

Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis

artículo científico publicado en 2011

Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhage

artículo científico publicado en 2013

IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations

artículo científico publicado en 2007

Impact of restricting enrollment in stroke genetics research to adults able to provide informed consent

artículo científico publicado en 2008

Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage

article by Sandro Marini et al published July 2018 in Stroke Journal

Interobserver agreement in the trial of org 10172 in acute stroke treatment classification of stroke based on retrospective medical record review

artículo científico publicado en 2006

Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage

artículo científico publicado en 2017

Joint Commission primary stroke center certification does not affect proband enrollment: the siblings with ischemic stroke study

artículo científico publicado en 2009

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

artículo científico publicado en 2022

NOTCH3 variants and risk of ischemic stroke

artículo científico publicado en 2013

Novel insights into the genetics of intracerebral hemorrhage

artículo científico publicado en 2013

Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke

artículo científico publicado en 2005

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

Rare Coding Variation and Risk of Intracerebral Hemorrhage

artículo científico publicado en 2015

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project

artículo científico publicado en 2015

Sex differences in stroke evaluations in the Ischemic Stroke Genetics Study

artículo científico publicado en 2007

Sex differences in stroke severity, symptoms, and deficits after first-ever ischemic stroke

artículo científico publicado en 2007

Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci

artículo científico publicado en 2011

Spouses and unrelated friends of probands as controls for stroke genetics studies

artículo científico publicado en 2003

Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes

artículo científico publicado en 2013

Stroke genetic research and adults with impaired decision-making capacity: a survey of IRB and investigator practices

artículo científico publicado en 2008

Structural genomic variation in ischemic stroke

artículo científico publicado en 2008

The Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) study protocol

artículo científico publicado en 2013

The Ischemic Stroke Genetics Study (ISGS) Protocol

artículo científico publicado en 2003

The Siblings With Ischemic Stroke Study (SWISS): a progress report

artículo científico publicado en 2006

Variants at APOE influence risk of deep and lobar intracerebral hemorrhage

artículo científico publicado en 2010

White matter hyperintensity quantification in large-scale clinical acute ischemic stroke cohorts - The MRI-GENIE study.

artículo científico publicado en 2019

Lista de obras de

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

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

A survey of the SWISS researchers on the impact of sibling privacy protections on pedigree recruitment

APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: a genetic association study

Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?

Association of integrin alpha2 gene variants with ischemic stroke

Author response: Ischemic Lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage

Burden of blood pressure-related alleles is associated with larger hematoma volume and worse outcome in intracerebral hemorrhage

Burden of risk alleles for hypertension increases risk of intracerebral hemorrhage

Candidate gene polymorphisms for ischemic stroke

Common mitochondrial sequence variants in ischemic stroke

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

Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage

Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trials

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

GISCOME - Genetics of Ischaemic Stroke Functional Outcome network: A protocol for an international multicentre genetic association study

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

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

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

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

Genome-wide association analysis of ischemic stroke in young adults

Genome-wide association meta-analysis of functional outcome after ischemic stroke

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

Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.

Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis

Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhage

IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations

Impact of restricting enrollment in stroke genetics research to adults able to provide informed consent

Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage

Interobserver agreement in the trial of org 10172 in acute stroke treatment classification of stroke based on retrospective medical record review

Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage

Joint Commission primary stroke center certification does not affect proband enrollment: the siblings with ischemic stroke study

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

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

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

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

NOTCH3 variants and risk of ischemic stroke

Novel insights into the genetics of intracerebral hemorrhage

Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke

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

Rare Coding Variation and Risk of Intracerebral Hemorrhage

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project

Sex differences in stroke evaluations in the Ischemic Stroke Genetics Study

Sex differences in stroke severity, symptoms, and deficits after first-ever ischemic stroke

Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci

Spouses and unrelated friends of probands as controls for stroke genetics studies

Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes

Stroke genetic research and adults with impaired decision-making capacity: a survey of IRB and investigator practices

Structural genomic variation in ischemic stroke

The Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) study protocol

The Ischemic Stroke Genetics Study (ISGS) Protocol

The Siblings With Ischemic Stroke Study (SWISS): a progress report

Variants at APOE influence risk of deep and lobar intracerebral hemorrhage

White matter hyperintensity quantification in large-scale clinical acute ischemic stroke cohorts - The MRI-GENIE study.