Lista de obras - Steve Bevan - 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 Comprehensive Analysis ofMNG1,TCO1,fPTC,PTEN,TSHR, and TRKA in Familial Nonmedullary Thyroid Cancer: Confirmation of Linkage to TCO1

article

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

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

artículo científico publicado en 2009

APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL

artículo científico publicado en 2015

Adiponectin level as a consequence of genetic variation, but not leptin level or leptin: adiponectin ratio, is a risk factor for carotid intima-media thickness

artículo científico publicado en 2011

Altered expression and coregulation of dopamine signalling genes in schizophrenia and bipolar disorder ⬇️

artículo científico publicado el 1 de febrero de 2011

Analysis of genetic and phenotypic heterogeneity in juvenile polyposis

artículo científico publicado en 2000

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of the CTLA4 gene in Swedish coeliac disease patients

article

Analysis of the Fanconi anaemia complementation group A gene in acute myeloid leukaemia.

artículo científico publicado en 2002

Association of MTHFR C677T Genotype With Ischemic Stroke Is Confined to Cerebral Small Vessel Disease Subtype.

artículo científico publicado en 2016

Association of the novel single-nucleotide polymorphism which increases oxidized low-density lipoprotein levels with cerebrovascular disease events

Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke

artículo científico publicado en 2016

Ataxia telangiectasia gene mutations and chronic lymphocytic leukaemia

artículo científico publicado en 1999

CDX2 mutations do not account for juvenile polyposis or Peutz-Jeghers syndrome and occur infrequently in sporadic colorectal cancers

artículo científico publicado en 2001

CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours

artículo científico publicado en 2002

Common NOTCH3 Variants and Cerebral Small-Vessel Disease

artículo científico publicado en 2015

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

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease

artículo científico publicado en 2015

Demonstration of epidermal transfer from a polymer membrane using genetically marked porcine keratinocytes

artículo científico publicado en 2001

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

artículo científico publicado en 2015

Dominantly inherited cutaneous small-vessel lymphocytic vasculitis maps to chromosome 6q26-q27.

artículo científico publicado en 2005

EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2003

Evidence HDAC9 genetic variant associated with ischemic stroke increases risk via promoting carotid atherosclerosis.

artículo científico publicado en 2013

Fractalkine receptor/ligand genetic variants and carotid intima-media thickness

artículo científico publicado en 2009

From Linkage to Genes: Positional Cloning

article

Genetic Architecture of Lacunar Stroke

artículo científico publicado en 2015

Genetic Associations With White Matter Hyperintensities Confer Risk of Lacunar Stroke

artículo científico publicado en 2016

Genetic and Acquired Inflammatory Conditions Are Synergistically Associated With Early Carotid Atherosclerosis

article

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

Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke.

artículo científico publicado en 2014

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 variation in members of the leukotriene biosynthesis pathway confer an increased risk of ischemic stroke: a replication study in two independent populations

artículo científico publicado en 2008

Genetic variation in the leukotriene pathway and carotid intima-media thickness: a 2-stage replication study

artículo científico publicado en 2009

Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations

artículo científico publicado en 2009

Genome screening of coeliac disease.

artículo científico publicado en 2002

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

artículo científico publicado en 2013

Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2

artículo científico publicado en 2016

Genome-wide analysis of blood pressure variability and ischemic stroke

artículo científico publicado en 2013

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

artículo científico publicado en 2012

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 of cerebral white matter hyperintensities in patients with stroke.

artículo científico publicado en 2015

Genotyping Methodologies

artículo científico publicado en 2001

Genotyping methodologies

artículo científico publicado en 2000

Germline mutations in fumarate hydratase (FH) do not predispose to prostate cancer

artículo científico publicado en 2003

Identification of novel Tapasin polymorphisms and linkage disequilibrium to MHC class I alleles

artículo científico publicado en 2000

Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study

artículo científico publicado en 2016

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

artículo científico publicado en 2013

Linkage analysis for ATM in familial B cell chronic lymphocytic leukaemia

artículo científico publicado en 1999

Linkage analysis for major histocompatibility complex-related genetic susceptibility in familial chronic lymphocytic leukemia

scientific article published on 01 December 2000

Linkage and the Transmission Disequilibrium Test in Complex Traits: Celiac Disease as a Case Study

article

Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.

artículo científico publicado en 2001

Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas

artículo científico publicado en 2002

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

artículo científico publicado en 2016

Mechanisms and treatment of ischaemic stroke--insights from genetic associations.

artículo científico publicado en 2014

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 genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

artículo científico publicado en 2011

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

artículo científico publicado en 2018

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

artículo científico publicado en 2013

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

artículo científico publicado en 2014

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

artículo científico publicado en 2022

Mutational analysis of CD28 in coeliac disease.

artículo científico publicado en 2002

Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases

artículo científico publicado en 1998

Mutations in the candidate tumour suppressor gene FLJ12973 on chromosome 15q15 are rare in colorectal cancer

scientific article published on 01 June 2003

Nociceptive Sensitizers Are Regulated in Damaged Joint Tissues, Including Articular Cartilage, When Osteoarthritic Mice Display Pain Behavior

artículo científico publicado en 2015

Novel associations for coronary artery disease derived from genome wide association studies are not associated with increased carotid intima-media thickness, suggesting they do not act via early atherosclerosis or vessel remodeling

artículo científico publicado en 2011

Oxidative phosphorylation and lacunar stroke: Genome-wide enrichment analysis of common variants

artículo científico publicado en 2015

PTEN mutations are uncommon in Proteus syndrome.

artículo científico publicado en 2001

Phosphodiesterase 4D gene, ischemic stroke, and asymptomatic carotid atherosclerosis

artículo científico publicado en 2005

Polymorphisms in genes of the endothelin system and cerebral small-vessel disease

artículo científico publicado en 2005

Polymorphisms in genes of the renin-angiotensin system and cerebral small vessel disease

artículo científico publicado en 2006

Prevalence of CADASIL and Fabry Disease in a Cohort of MRI Defined Younger Onset Lacunar Stroke

artículo científico publicado en 2015

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

Retroviral gene transfer into porcine keratinocytes following improved methods of cultivation ⬇️

artículo científico publicado el 1 de noviembre de 1997

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke

artículo científico publicado en 2008

Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke

artículo científico publicado en 2009

The role of genetic variants of matrix metalloproteinases in coronary and carotid atherosclerosis.

artículo científico publicado en 2006

Tissue plasminogen activator -7351C/T polymorphism and lacunar stroke

artículo científico publicado en 2005

Toll receptor polymorphisms and carotid artery intima-media thickness

scientific article published on 01 March 2007

Using phenotypic heterogeneity to increase the power of genome-wide association studies: application to age at onset of ischaemic stroke subphenotypes

artículo científico publicado en 2013

Lista de obras de Steve Bevan

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

A Comprehensive Analysis ofMNG1,TCO1,fPTC,PTEN,TSHR, and TRKA in Familial Nonmedullary Thyroid Cancer: Confirmation of Linkage to TCO1

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

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL

Adiponectin level as a consequence of genetic variation, but not leptin level or leptin: adiponectin ratio, is a risk factor for carotid intima-media thickness

Altered expression and coregulation of dopamine signalling genes in schizophrenia and bipolar disorder ⬇️

Analysis of genetic and phenotypic heterogeneity in juvenile polyposis

Analysis of shared heritability in common disorders of the brain

Analysis of the CTLA4 gene in Swedish coeliac disease patients

Analysis of the Fanconi anaemia complementation group A gene in acute myeloid leukaemia.

Association of MTHFR C677T Genotype With Ischemic Stroke Is Confined to Cerebral Small Vessel Disease Subtype.

Association of the novel single-nucleotide polymorphism which increases oxidized low-density lipoprotein levels with cerebrovascular disease events

Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke

Ataxia telangiectasia gene mutations and chronic lymphocytic leukaemia

CDX2 mutations do not account for juvenile polyposis or Peutz-Jeghers syndrome and occur infrequently in sporadic colorectal cancers

CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours

Common NOTCH3 Variants and Cerebral Small-Vessel Disease

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

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

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease

Demonstration of epidermal transfer from a polymer membrane using genetically marked porcine keratinocytes

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

Dominantly inherited cutaneous small-vessel lymphocytic vasculitis maps to chromosome 6q26-q27.

EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer

Evidence HDAC9 genetic variant associated with ischemic stroke increases risk via promoting carotid atherosclerosis.

Fractalkine receptor/ligand genetic variants and carotid intima-media thickness

From Linkage to Genes: Positional Cloning

Genetic Architecture of Lacunar Stroke

Genetic Associations With White Matter Hyperintensities Confer Risk of Lacunar Stroke

Genetic and Acquired Inflammatory Conditions Are Synergistically Associated With Early Carotid Atherosclerosis

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

Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke.

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 variation in members of the leukotriene biosynthesis pathway confer an increased risk of ischemic stroke: a replication study in two independent populations

Genetic variation in the leukotriene pathway and carotid intima-media thickness: a 2-stage replication study

Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations

Genome screening of coeliac disease.

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2

Genome-wide analysis of blood pressure variability and ischemic stroke

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

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

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

Genotyping Methodologies

Genotyping methodologies

Germline mutations in fumarate hydratase (FH) do not predispose to prostate cancer

Identification of novel Tapasin polymorphisms and linkage disequilibrium to MHC class I alleles

Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

Linkage analysis for ATM in familial B cell chronic lymphocytic leukaemia

Linkage analysis for major histocompatibility complex-related genetic susceptibility in familial chronic lymphocytic leukemia

Linkage and the Transmission Disequilibrium Test in Complex Traits: Celiac Disease as a Case Study

Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.

Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas

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

Mechanisms and treatment of ischaemic stroke--insights from genetic associations.

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

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

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

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

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

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

Mutational analysis of CD28 in coeliac disease.

Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases

Mutations in the candidate tumour suppressor gene FLJ12973 on chromosome 15q15 are rare in colorectal cancer

Nociceptive Sensitizers Are Regulated in Damaged Joint Tissues, Including Articular Cartilage, When Osteoarthritic Mice Display Pain Behavior

Novel associations for coronary artery disease derived from genome wide association studies are not associated with increased carotid intima-media thickness, suggesting they do not act via early atherosclerosis or vessel remodeling

Oxidative phosphorylation and lacunar stroke: Genome-wide enrichment analysis of common variants

PTEN mutations are uncommon in Proteus syndrome.

Phosphodiesterase 4D gene, ischemic stroke, and asymptomatic carotid atherosclerosis

Polymorphisms in genes of the endothelin system and cerebral small-vessel disease

Polymorphisms in genes of the renin-angiotensin system and cerebral small vessel disease

Prevalence of CADASIL and Fabry Disease in a Cohort of MRI Defined Younger Onset Lacunar Stroke

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

Retroviral gene transfer into porcine keratinocytes following improved methods of cultivation ⬇️

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke