Lista de obras - Felicity Payne - Dominio Público Uruguay

A Comprehensive, Statistically Powered Analysis of GAD2 in Type 1 Diabetes

scientific article published on 01 September 2002

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

A two-stage inter-rater approach for enrichment testing of variants associated with multiple traits

artículo científico publicado en 2016

An activating mutation of AKT2 and human hypoglycemia.

artículo científico publicado en 2011

Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases

artículo científico publicado en 2006

Analysis of the type 2 diabetes-associated single nucleotide polymorphisms in the genes IRS1, KCNJ11, and PPARG2 in type 1 diabetes

artículo científico publicado en 2004

Association of IL13 with total IgE: evidence against an inverse association of atopy and diabetes

artículo científico publicado en 2006

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

artículo científico publicado en 2003

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

artículo científico publicado en 2010

Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study

artículo científico publicado en 2015

Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes

artículo científico publicado en 2005

Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution.

artículo científico publicado en 2009

Corrigendum: Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance

artículo científico publicado en 2017

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scholarly article published in Nature Genetics

Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans

artículo científico publicado en 2010

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics

artículo científico publicado en 2004

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population

artículo científico publicado en 2010

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

artículo científico publicado en 2009

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

scientific journal article

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

artículo científico publicado en 2011

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

artículo científico publicado en 2009

Haplotype tag single nucleotide polymorphism analysis of the human orthologues of the rat type 1 diabetes genes Ian4 (Lyp/Iddm1) and Cblb

artículo científico publicado en 2004

Haplotype tagging for the identification of common disease genes

article

Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression

artículo científico publicado en 2017

Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase.

artículo científico publicado en 2017

Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance

artículo científico publicado en 2014

Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity

artículo científico publicado en 2013

Insulin resistance uncoupled from dyslipidemia due to C-terminal PIK3R1 mutations

artículo científico publicado en 2016

Interaction analysis of the CBLB and CTLA4 genes in type 1 diabetes

article

Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes

artículo científico publicado en 2003

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

artículo científico publicado en 2008

Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA

artículo científico publicado en 2012

Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease

artículo científico publicado en 2014

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

No evidence for association of the TATA-box binding protein glutamine repeat sequence or the flanking chromosome 6q27 region with type 1 diabetes

artículo científico publicado en 2005

No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels

artículo científico publicado en 2012

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

Polymorphism discovery and association analyses of the interferon genes in type 1 diabetes

artículo científico publicado en 2006

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes

artículo científico publicado en 2012

Remapping the insulin gene/IDDM2 locus in type 1 diabetes

artículo científico publicado en 2004

Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden

artículo científico publicado en 2009

Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

artículo científico publicado en 2007

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

artículo científico publicado en 2007

Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.

artículo científico publicado en 2007

The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes

artículo científico publicado en 2007

The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion.

artículo científico publicado en 2017

Truncation of POC1A associated with short stature and extreme insulin resistance

artículo científico publicado en 2015

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

artículo científico publicado en 2010

Underlying genetic models of inheritance in established type 2 diabetes associations

artículo científico publicado en 2009

Lista de obras de Felicity Payne

A Comprehensive, Statistically Powered Analysis of GAD2 in Type 1 Diabetes

A genome-wide association search for type 2 diabetes genes in African Americans

A two-stage inter-rater approach for enrichment testing of variants associated with multiple traits

An activating mutation of AKT2 and human hypoglycemia.

Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases

Analysis of the type 2 diabetes-associated single nucleotide polymorphisms in the genes IRS1, KCNJ11, and PPARG2 in type 1 diabetes

Association of IL13 with total IgE: evidence against an inverse association of atopy and diabetes

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study

Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes

Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution.

Corrigendum: Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

Haplotype tag single nucleotide polymorphism analysis of the human orthologues of the rat type 1 diabetes genes Ian4 (Lyp/Iddm1) and Cblb

Haplotype tagging for the identification of common disease genes

Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression

Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase.

Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance

Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity

Insulin resistance uncoupled from dyslipidemia due to C-terminal PIK3R1 mutations

Interaction analysis of the CBLB and CTLA4 genes in type 1 diabetes

Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA

Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

No evidence for association of the TATA-box binding protein glutamine repeat sequence or the flanking chromosome 6q27 region with type 1 diabetes

No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

Polymorphism discovery and association analyses of the interferon genes in type 1 diabetes

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes

Remapping the insulin gene/IDDM2 locus in type 1 diabetes

Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden

Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.

The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes

The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion.

Truncation of POC1A associated with short stature and extreme insulin resistance

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Underlying genetic models of inheritance in established type 2 diabetes associations