Lista de obras - Nabila Bouatia-Naji - Dominio Público Uruguay

6C.02: EXOME SEQUENCING IN SEVEN FAMILIES AND GENE-BASED ASSOCIATION STUDIES SUPPORT GENETIC HETEROGENEITY AND SUGGEST POSSIBLE CANDIDATES FOR FIBROMUSCULAR DYSPLASIA.

artículo científico publicado en 2015

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

artículo científico publicado en 2012

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

artículo científico publicado en 2012

A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels

artículo científico publicado en 2012

A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels

artículo científico publicado en 2008

A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk

artículo científico publicado en 2008

ACDC/Adiponectin Polymorphisms Are Associated With Severe Childhood and Adult Obesity

artículo científico publicado en 2006

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

artículo científico publicado en 2010

Association analysis of the IGF1 gene with childhood growth, IGF-1 concentrations and type 1 diabetes

artículo científico publicado en 2008

Association between FTO variant and change in body weight and its interaction with dietary factors: the DiOGenes study

artículo científico publicado en 2012

Association of genetic Loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 children ⬇️

artículo científico publicado en 2011

Association of the ENPP1 K121Q polymorphism with type 2 diabetes and obesity in the Moroccan population

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Dietary factors impact on the association between CTSS variants and obesity related traits

artículo científico publicado en 2012

ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study

article by D. Meyre et al published 18 August 2007 in Diabetologia

Early detrimental metabolic outcomes of rs17300539-A allele of ADIPOQ gene despite higher adiponectinemia

artículo científico publicado en 2009

Erratum: KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

article

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2011

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

artículo científico publicado en 2010

Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia

artículo científico publicado en 2015

Fibromuscular Dysplasia and Its Neurologic Manifestations: A Systematic Review

artículo científico publicado en 2019

G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans

artículo científico publicado en 2009

Genetic Study of PHACTR1 and Fibromuscular Dysplasia, Meta-Analysis and Effects on Clinical Features of Patients: The ARCADIA-POL Study

artículo científico publicado en 2020

Genetic and functional assessment of the role of the rs13431652-A and rs573225-A alleles in the G6PC2 promoter that are strongly associated with elevated fasting glucose levels.

artículo científico publicado en 2010

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

artículo científico publicado en 2015

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

artículo científico publicado en 2016

Genetic evidence of assortative mating in humans

scholarly article

Genetic polymorphisms in the hypothalamic pathway in relation to subsequent weight change--the DiOGenes study

artículo científico publicado en 2011

Genetic risk of type 2 diabetes in populations of the African continent: A systematic review and meta-analyses

artículo científico publicado en 2016

Genetic variant in HK1 is associated with a proanemic state and A1C but not other glycemic control-related traits

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 Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals

scientific article published on 01 July 2019

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

artículo científico publicado en 2013

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 study identifies five loci associated with lung function

artículo científico publicado en 2010

INS VNTR is not associated with childhood obesity in 1,023 families: a family-based study

artículo científico publicado en 2008

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

artículo científico publicado en 2013

Impact of common variation in bone-related genes on type 2 diabetes and related traits

artículo científico publicado en 2012

Inputs from the genetics of fasting glucose: lessons for diabetes

artículo científico publicado en 2009

Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse

artículo científico publicado en 2015

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

artículo científico publicado en 2012

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

artículo científico publicado en 2012

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2010

Mitral valve disease--morphology and mechanisms

artículo científico publicado en 2015

Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels

artículo científico publicado en 2013

Mutations in DCHS1 cause mitral valve prolapse

scientific journal article

Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction

artículo científico publicado en 2009

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

artículo científico publicado en 2010

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

Nouveaux déterminants génétiques des traits glycémiques

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

O97 Des variants du gène MTNR1B du récepteur 2 à la mélatonine augmentent la glycémie et le risque de DT2 : un lien entre le rythme circadien et le diabète ?

artículo científico publicado en 2009

O98 Des variants du promoteur du gène G6PC2 pourraient expliquer la contribution de ce locus au contrôle génétique de la glycémie

artículo científico publicado en 2009

Primary cilia defects causing mitral valve prolapse

artículo científico publicado en 2019

Rare Loss-of-function Mutations of PTGIR are enriched in Fibromuscular Dysplasia

artículo científico publicado en 2020

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

artículo científico publicado en 2012

Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity

artículo científico publicado en 2007

Smallness for gestational age interacts with high mobility group A2 gene genetic variation to modulate height

artículo científico publicado en 2009

The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma

artículo científico publicado en 2016

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

artículo científico publicado en 2016

The relationship between MTHFR C677T gene polymorphism and essential hypertension in a sample of an Algerian population of Oran city

artículo científico publicado en 2016

Transcriptome Analysis of lncRNAs in Pheochromocytomas and Paragangliomas

scientific article published on 01 March 2020

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

artículo científico publicado en 2010

Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes

artículo científico publicado en 2005

Lista de obras de Nabila Bouatia-Naji

6C.02: EXOME SEQUENCING IN SEVEN FAMILIES AND GENE-BASED ASSOCIATION STUDIES SUPPORT GENETIC HETEROGENEITY AND SUGGEST POSSIBLE CANDIDATES FOR FIBROMUSCULAR DYSPLASIA.

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

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

A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels

A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels

A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk

ACDC/Adiponectin Polymorphisms Are Associated With Severe Childhood and Adult Obesity

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Association analysis of the IGF1 gene with childhood growth, IGF-1 concentrations and type 1 diabetes

Association between FTO variant and change in body weight and its interaction with dietary factors: the DiOGenes study

Association of genetic Loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 children ⬇️

Association of the ENPP1 K121Q polymorphism with type 2 diabetes and obesity in the Moroccan population

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

Dietary factors impact on the association between CTSS variants and obesity related traits

ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study

Early detrimental metabolic outcomes of rs17300539-A allele of ADIPOQ gene despite higher adiponectinemia

Erratum: KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

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

Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia

Fibromuscular Dysplasia and Its Neurologic Manifestations: A Systematic Review

G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans

Genetic Study of PHACTR1 and Fibromuscular Dysplasia, Meta-Analysis and Effects on Clinical Features of Patients: The ARCADIA-POL Study

Genetic and functional assessment of the role of the rs13431652-A and rs573225-A alleles in the G6PC2 promoter that are strongly associated with elevated fasting glucose levels.

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Genetic evidence of assortative mating in humans

Genetic polymorphisms in the hypothalamic pathway in relation to subsequent weight change--the DiOGenes study

Genetic risk of type 2 diabetes in populations of the African continent: A systematic review and meta-analyses

Genetic variant in HK1 is associated with a proanemic state and A1C but not other glycemic control-related traits

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

Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

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 study identifies five loci associated with lung function

INS VNTR is not associated with childhood obesity in 1,023 families: a family-based study

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Impact of common variation in bone-related genes on type 2 diabetes and related traits

Inputs from the genetics of fasting glucose: lessons for diabetes

Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Mitral valve disease--morphology and mechanisms

Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels

Mutations in DCHS1 cause mitral valve prolapse

Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction

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

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

Nouveaux déterminants génétiques des traits glycémiques

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

O97 Des variants du gène MTNR1B du récepteur 2 à la mélatonine augmentent la glycémie et le risque de DT2 : un lien entre le rythme circadien et le diabète ?

O98 Des variants du promoteur du gène G6PC2 pourraient expliquer la contribution de ce locus au contrôle génétique de la glycémie

Primary cilia defects causing mitral valve prolapse

Rare Loss-of-function Mutations of PTGIR are enriched in Fibromuscular Dysplasia

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

Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity

Smallness for gestational age interacts with high mobility group A2 gene genetic variation to modulate height

The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

The relationship between MTHFR C677T gene polymorphism and essential hypertension in a sample of an Algerian population of Oran city

Transcriptome Analysis of lncRNAs in Pheochromocytomas and Paragangliomas

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes