Lista de obras - Ludmila Pawlikowska - Dominio Público Uruguay

A common variant in the telomerase RNA component is associated with short telomere length

artículo científico publicado en 2010

A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation

artículo científico publicado en 2013

A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion

scientific journal article

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X.

artículo científico publicado en 2009

Admixture mapping of an allele affecting interleukin 6 soluble receptor and interleukin 6 levels

artículo científico publicado en 2007

Adrenoceptor polymorphisms and the risk of cardiac injury and dysfunction after subarachnoid hemorrhage

artículo científico publicado en 2006

Angiopoietin-like 4 (ANGPTL4) gene polymorphisms and risk of brain arteriovenous malformations

artículo científico publicado en 2011

Apolipoprotein E epsilon 2 is associated with new hemorrhage risk in brain arteriovenous malformations

artículo científico publicado en 2006

Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease

scientific article published on 28 August 2009

Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation

artículo científico publicado en 2013

Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity

artículo científico publicado en 2009

Association of tumor necrosis factor-alpha-238G>A and apolipoprotein E2 polymorphisms with intracranial hemorrhage after brain arteriovenous malformation treatment

artículo científico publicado en 2007

Brain Arteriovenous Malformation Pathogenesis: A Response-to-Injury Paradigm ⬇️

artículo científico publicado el 1 de enero de 2011

Brain arteriovenous malformation biology relevant to hemorrhage and implication for therapeutic development

artículo científico publicado en 2008

Brain arteriovenous malformation multiplicity predicts the diagnosis of hereditary hemorrhagic telangiectasia: quantitative assessment

artículo científico publicado en 2011

Brain-derived neurotrophic factor Val66Met polymorphism predicts worse functional outcome after surgery in patients with unruptured brain arteriovenous malformation

artículo científico publicado en 2012

Common beta-adrenergic receptor polymorphisms are not associated with risk of sudden cardiac death in patients with coronary artery disease

artículo científico publicado en 2008

Common variants in interleukin-1-Beta gene are associated with intracranial hemorrhage and susceptibility to brain arteriovenous malformation

artículo científico publicado en 2008

Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms

artículo científico publicado en 2014

Contemporary human genetic strategies in aging research

artículo científico publicado en 2010

Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1.

artículo científico publicado en 2016

Differences in presentation and progression between severe FIC1 and BSEP deficiencies

artículo científico publicado en 2010

EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations

artículo científico publicado en 2009

Endothelial nitric oxide synthase polymorphism (-786T->C) and increased risk of angiographic vasospasm after aneurysmal subarachnoid hemorrhage

artículo científico publicado en 2008

G Protein-Coupled Receptor 124 (GPR124) Gene Polymorphisms and Risk of Brain Arteriovenous Malformation

artículo científico publicado en 2012

GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease

artículo científico publicado en 2011

Gene expression profiling of blood in brain arteriovenous malformation patients

artículo científico publicado en 2011

Gene-trapped mouse embryonic stem cell-derived cardiac myocytes and human genetics implicate AKAP10 in heart rhythm regulation

artículo científico publicado en 2007

Genome-wide association study of sporadic brain arteriovenous malformations

artículo científico publicado en 2016

Genome-wide detection and characterization of positive selection in human populations

artículo científico publicado en 2007

Glucocorticoid receptor gene and depression in patients with coronary heart disease: the Heart and Soul Study-2009 Curt Richter Award Winner

artículo científico publicado en 2009

Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency

artículo científico publicado en 2006

Inflammation and stress-related candidate genes, plasma interleukin-6 levels, and longevity in older adults

artículo científico publicado en 2009

Interleukin-6 and atrial fibrillation in patients with coronary artery disease: data from the Heart and Soul Study

artículo científico publicado en 2007

Is altered expression of hepatic insulin-related genes in growth hormone receptor knockout mice due to GH resistance or a difference in biological life spans?

artículo científico publicado en 2009

Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults

artículo científico publicado en 2015

Mitochondrial DNA sequence variation and risk of pancreatic cancer

artículo científico publicado en 2011

Mitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderly

artículo científico publicado en 2012

Molecular basis of intrahepatic cholestasis

artículo científico publicado en 2004

Plasma soluble thrombomodulin levels are associated with mortality in the acute respiratory distress syndrome.

artículo científico publicado en 2015

Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity

artículo científico publicado en 2014

Population stratification in a case-control study of brain arteriovenous malformation in Latinos

artículo científico publicado en 2008

Reduced expression of integrin alphavbeta8 is associated with brain arteriovenous malformation pathogenesis

artículo científico publicado en 2009

Serum insulin-like growth factor-1 binding proteins 1 and 2 and mortality in older adults: the Health, Aging, and Body Composition Study

artículo científico publicado en 2009

Severity score for hereditary hemorrhagic telangiectasia

artículo científico publicado en 2014

Single-nucleotide polymorphisms in the β-adrenergic receptor genes are associated with lung allograft utilization

artículo científico publicado en 2011

Strain background modifies phenotypes in the ATP8B1-deficient mouse

artículo científico publicado en 2010

The association between a Darc gene polymorphism and clinical outcomes in African American patients with acute lung injury

artículo científico publicado en 2011

Lista de obras de Ludmila Pawlikowska

A common variant in the telomerase RNA component is associated with short telomere length

A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation

A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion

A second generation human haplotype map of over 3.1 million SNPs

Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X.

Admixture mapping of an allele affecting interleukin 6 soluble receptor and interleukin 6 levels

Adrenoceptor polymorphisms and the risk of cardiac injury and dysfunction after subarachnoid hemorrhage

Angiopoietin-like 4 (ANGPTL4) gene polymorphisms and risk of brain arteriovenous malformations

Apolipoprotein E epsilon 2 is associated with new hemorrhage risk in brain arteriovenous malformations

Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease

Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation

Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity

Association of tumor necrosis factor-alpha-238G>A and apolipoprotein E2 polymorphisms with intracranial hemorrhage after brain arteriovenous malformation treatment

Brain Arteriovenous Malformation Pathogenesis: A Response-to-Injury Paradigm ⬇️

Brain arteriovenous malformation biology relevant to hemorrhage and implication for therapeutic development

Brain arteriovenous malformation multiplicity predicts the diagnosis of hereditary hemorrhagic telangiectasia: quantitative assessment

Brain-derived neurotrophic factor Val66Met polymorphism predicts worse functional outcome after surgery in patients with unruptured brain arteriovenous malformation

Common beta-adrenergic receptor polymorphisms are not associated with risk of sudden cardiac death in patients with coronary artery disease

Common variants in interleukin-1-Beta gene are associated with intracranial hemorrhage and susceptibility to brain arteriovenous malformation

Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms

Contemporary human genetic strategies in aging research

Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1.

Differences in presentation and progression between severe FIC1 and BSEP deficiencies

EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations

Endothelial nitric oxide synthase polymorphism (-786T->C) and increased risk of angiographic vasospasm after aneurysmal subarachnoid hemorrhage

G Protein-Coupled Receptor 124 (GPR124) Gene Polymorphisms and Risk of Brain Arteriovenous Malformation

GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease

Gene expression profiling of blood in brain arteriovenous malformation patients

Gene-trapped mouse embryonic stem cell-derived cardiac myocytes and human genetics implicate AKAP10 in heart rhythm regulation

Genome-wide association study of sporadic brain arteriovenous malformations

Genome-wide detection and characterization of positive selection in human populations

Glucocorticoid receptor gene and depression in patients with coronary heart disease: the Heart and Soul Study-2009 Curt Richter Award Winner

Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency

Inflammation and stress-related candidate genes, plasma interleukin-6 levels, and longevity in older adults

Interleukin-6 and atrial fibrillation in patients with coronary artery disease: data from the Heart and Soul Study

Is altered expression of hepatic insulin-related genes in growth hormone receptor knockout mice due to GH resistance or a difference in biological life spans?

Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults

Mitochondrial DNA sequence variation and risk of pancreatic cancer

Mitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderly

Molecular basis of intrahepatic cholestasis

Plasma soluble thrombomodulin levels are associated with mortality in the acute respiratory distress syndrome.

Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity

Population stratification in a case-control study of brain arteriovenous malformation in Latinos

Reduced expression of integrin alphavbeta8 is associated with brain arteriovenous malformation pathogenesis

Serum insulin-like growth factor-1 binding proteins 1 and 2 and mortality in older adults: the Health, Aging, and Body Composition Study

Severity score for hereditary hemorrhagic telangiectasia

Single-nucleotide polymorphisms in the β-adrenergic receptor genes are associated with lung allograft utilization

Strain background modifies phenotypes in the ATP8B1-deficient mouse

The association between a Darc gene polymorphism and clinical outcomes in African American patients with acute lung injury