Lista de obras - Katrina Scurrah - Dominio Público Uruguay

A loss-of-function polymorphism in the human P2X4 receptor is associated with increased pulse pressure.

artículo científico publicado en 2011

Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure.

artículo científico publicado en 2005

Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia.

artículo científico publicado en 2007

Comprehensive multi-stage linkage analyses identify a locus for adult height on chromosome 3p in a healthy Caucasian population.

artículo científico publicado en 2006

Contribution of genes and environment to variation in postural changes in mean arterial and pulse pressure

article

Covariance components models for longitudinal family data

artículo científico publicado en 2005

Effect of birth parameters on retinal vascular caliber: the Twins Eye Study in Tasmania

artículo científico publicado en 2009

Epistasis amongst PTPN2 and genes of the vitamin D pathway contributes to risk of juvenile idiopathic arthritis

artículo científico publicado en 2014

Estimation of genetic and environmental factors for binary traits using family data by Y. Pawitan, M. Reilly, E. Nilsson, S. Cnattingius and P. Lichtenstein,Statistics in Medicine 2004;23:449–465

Etiology of molar incisor hypomineralization - A systematic review

artículo científico publicado en 2016

Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene.

artículo científico publicado en 2010

Exposure to ionizing radiation and brain cancer incidence: The Life Span Study cohort.

artículo científico publicado en 2016

Familial Analysis of Epistatic and Sex-Dependent Association of Genes of the Renin-Angiotensin-Aldosterone System and Blood Pressure

artículo científico publicado en 2017

Genes controlling postural changes in blood pressure: comprehensive association analysis of ATP-sensitive potassium channel genes KCNJ8 and ABCC9.

artículo científico publicado en 2009

Genetic Mapping of Myopia Susceptibility Loci

artículo científico publicado en 2007

Genetic factors contribute more to hip than knee surgery due to osteoarthritis - a population-based twin registry study of joint arthroplasty.

artículo científico publicado en 2016

Genome-wide linkage analysis of population variation in high-density lipoprotein cholesterol

artículo científico publicado en 2006

Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study

artículo científico publicado en 2007

Linkage Replication of theMYP12Locus in Common Myopia

artículo científico publicado en 2007

Longitudinal data analysis in pedigree studies

artículo científico publicado en 2003

Longitudinal variance components models for systolic blood pressure, fitted using Gibbs sampling

artículo científico publicado en 2003

Measurement of absolute copy number variation reveals association with essential hypertension

artículo científico publicado en 2014

Non-proportional odds multivariate logistic regression of ordinal family data.

artículo científico publicado en 2014

Risk of Wrist Fracture in Women Is Heritable and Is Influenced by Genes That Are Largely Independent of Those Influencing BMD

article

Selective Genotyping Reveals Association Between the Epithelial Sodium Channel γ-Subunit and Systolic Blood Pressure

artículo científico publicado en 2007

Sex differences in genetic and environmental determinants of pulse pressure.

artículo científico publicado en 2006

Socioeconomic position in young adulthood is associated with BMI in Australian families

artículo científico publicado en 2015

The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females.

artículo científico publicado en 2015

The epithelial sodium channel γ-subunit gene and blood pressure: family based association, renal gene expression, and physiological analyses

artículo científico publicado en 2011

Tutorial in biostatistics: spline smoothing with linear mixed models

artículo científico publicado en 2005

Lista de obras de Katrina Scurrah

A loss-of-function polymorphism in the human P2X4 receptor is associated with increased pulse pressure.

Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure.

Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia.

Comprehensive multi-stage linkage analyses identify a locus for adult height on chromosome 3p in a healthy Caucasian population.

Contribution of genes and environment to variation in postural changes in mean arterial and pulse pressure

Covariance components models for longitudinal family data

Effect of birth parameters on retinal vascular caliber: the Twins Eye Study in Tasmania

Epistasis amongst PTPN2 and genes of the vitamin D pathway contributes to risk of juvenile idiopathic arthritis

Estimation of genetic and environmental factors for binary traits using family data by Y. Pawitan, M. Reilly, E. Nilsson, S. Cnattingius and P. Lichtenstein,Statistics in Medicine 2004;23:449–465

Etiology of molar incisor hypomineralization - A systematic review

Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene.

Exposure to ionizing radiation and brain cancer incidence: The Life Span Study cohort.

Familial Analysis of Epistatic and Sex-Dependent Association of Genes of the Renin-Angiotensin-Aldosterone System and Blood Pressure

Genes controlling postural changes in blood pressure: comprehensive association analysis of ATP-sensitive potassium channel genes KCNJ8 and ABCC9.

Genetic Mapping of Myopia Susceptibility Loci

Genetic factors contribute more to hip than knee surgery due to osteoarthritis - a population-based twin registry study of joint arthroplasty.

Genome-wide linkage analysis of population variation in high-density lipoprotein cholesterol

Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study

Linkage Replication of theMYP12Locus in Common Myopia

Longitudinal data analysis in pedigree studies

Longitudinal variance components models for systolic blood pressure, fitted using Gibbs sampling

Measurement of absolute copy number variation reveals association with essential hypertension

Non-proportional odds multivariate logistic regression of ordinal family data.

Risk of Wrist Fracture in Women Is Heritable and Is Influenced by Genes That Are Largely Independent of Those Influencing BMD

Selective Genotyping Reveals Association Between the Epithelial Sodium Channel γ-Subunit and Systolic Blood Pressure

Sex differences in genetic and environmental determinants of pulse pressure.

Socioeconomic position in young adulthood is associated with BMI in Australian families

The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females.

The epithelial sodium channel γ-subunit gene and blood pressure: family based association, renal gene expression, and physiological analyses

Tutorial in biostatistics: spline smoothing with linear mixed models