Lista de obras - Richa Saxena - Dominio Público Uruguay

A Loss-Of-Function Splice Acceptor Variant in IGF2 is Protective for Type 2 Diabetes

artículo científico publicado en 2017

A common variant of HMGA2 is associated with adult and childhood height in the general population

artículo científico publicado en 2007

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

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 reveals variants in ARL15 that influence adiponectin levels

artículo científico publicado en 2009

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans

scientific article published on 01 February 2019

Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study

artículo científico publicado en 2022

Assessment of MTNR1B Type 2 Diabetes Genetic Risk Modification by Shift Work and Morningness-Eveningness Preference in the UK Biobank

scientific article published on 22 November 2019

Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort

artículo científico publicado en 2015

Associations Between Sleep Health and Amygdala Reactivity to Negative Facial Expressions in the UK Biobank Cohort

scientific article published in 2022

Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep

artículo científico publicado en 2019

Biological and clinical insights from genetics of insomnia symptoms

article

Biological and clinical insights from genetics of insomnia symptoms

scientific article published on 25 February 2019

CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids

artículo científico publicado en 2016

CT Angiographic Evaluation of Pattern and Distribution of Stenosis and its Association with Risk Factors Among Indian Ischemic Stroke Patients

artículo científico publicado en 2016

Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome

artículo científico publicado en 2015

Chronotype Genetic Variant in PER2 is Associated with Intrinsic Circadian Period in Humans

scientific article published on 29 March 2019

Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations

artículo científico publicado en 2008

Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion

artículo científico publicado en 2008

Common variants associated with plasma triglycerides and risk for coronary artery disease

artículo científico publicado en 2013

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

artículo científico publicado en 2010

Common variants in 40 genes assessed for diabetes incidence and response to metformin and lifestyle intervention in the diabetes prevention program

artículo científico publicado en 2010

Common variants in DRD2 are associated with sleep duration: the CARe consortium

artículo científico publicado en 2015

Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage

artículo científico publicado en 2013

Comparison of Heritability Estimation and Linkage Analysis for Multiple Traits Using Principal Component Analyses

artículo científico publicado en 2016

Comprehensive association testing of common mitochondrial DNA variation in metabolic disease

artículo científico publicado en 2006

DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation

artículo científico publicado en 2011

Dimensionality reduction reveals fine-scale structure in the Japanese population with consequences for polygenic risk prediction

artículo científico publicado en 2020

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Discovery and refinement of loci associated with lipid levels

artículo científico publicado en 2013

Environmental and genetic factors influence age at menarche in women with polycystic ovary syndrome ⬇️

artículo científico publicado el 1 de enero de 2012

Evaluating reported candidate gene associations with polycystic ovary syndrome ⬇️

artículo científico publicado el 30 de enero de 2013

Evolutionarily conserved regulation of sleep by epidermal growth factor receptor signaling

artículo científico publicado en 2019

Extension of type 2 diabetes genome-wide association scan results in the diabetes prevention program

artículo científico publicado en 2008

Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans

artículo científico publicado en 2016

Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia

artículo científico publicado en 2014

Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia

artículo científico publicado en 2015

Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits

artículo científico publicado en 2021

Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines

artículo científico publicado en 2008

Genetic predisposition to elevated levels of C-reactive protein is associated with a decreased risk for preeclampsia

artículo científico publicado en 2016

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

scientific journal article

Genetics of circadian rhythms and sleep in human health and disease

artículo científico publicado en 2022

Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms

artículo científico publicado en 2019

Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits

artículo científico publicado en 2016

Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank

artículo científico publicado en 2016

Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups

Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes

artículo científico publicado en 2019

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

artículo científico publicado en 2016

Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India

artículo científico publicado en 2013

Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates

article

Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort

artículo científico publicado en 2014

Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study

artículo científico publicado en 2015

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

artículo científico publicado en 2007

IBC CARe Microarray Allelic Population Prevalences in an American Indian Population ⬇️

artículo científico publicado el 6 de septiembre de 2013

Impact of sleep and circadian disruption on energy balance and diabetes: a summary of workshop discussions

artículo científico publicado en 2015

Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene

artículo científico publicado en 2014

Investigation of Genetic Variation Underlying Central Obesity amongst South Asians

artículo científico publicado en 2016

Large Scale Metabolic Profiling identifies Novel Steroids linked to Rheumatoid Arthritis

artículo científico publicado en 2017

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

artículo científico publicado en 2010

No Association between the Mitochondrial Genome and Prostate Cancer Risk: The Multiethnic Cohort

artículo científico publicado en 2016

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

Phenotype and Tissue Expression as a Function of Genetic Risk in Polycystic Ovary Syndrome

artículo científico publicado en 2017

Pleiotropic effects of GIP on islet function involve osteopontin

artículo científico publicado en 2011

Population Genetic Structure and Origins of Native Hawaiians in the Multiethnic Cohort Study ⬇️

artículo científico publicado el 7 de noviembre de 2012

Principal-component analysis for assessment of population stratification in mitochondrial medical genetics

artículo científico publicado en 2010

RD-1 encoded EspJ protein gets phosphorylated prior to affect the growth and intracellular survival of mycobacteria

artículo científico publicado en 2015

Relationship between polycystic ovary syndrome and ancestry in European Americans

artículo científico publicado en 2016

Surgical Intensive Care Unit Optimal Mobilisation Score (SOMS) trial: a protocol for an international, multicentre, randomised controlled trial focused on goal-directed early mobilisation of surgical ICU patients

artículo científico publicado en 2013

TXNIP regulates peripheral glucose metabolism in humans

artículo científico publicado en 2007

The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people

artículo científico publicado en 2006

The M. tuberculosis HAD phosphatase (Rv3042c) interacts with host proteins and is inhibited by Clofazimine

scientific journal article

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

artículo científico publicado en 2012

Tissue-specific alternative splicing of TCF7L2.

artículo científico publicado en 2009

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

artículo científico publicado en 2015

Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study

artículo científico publicado en 2012

Triglyceride response to an intensive lifestyle intervention is enhanced in carriers of the GCKR Pro446Leu polymorphism

artículo científico publicado en 2011

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

artículo científico publicado en 2010

Two variants of the C-reactive protein gene are associated with risk of pre-eclampsia in an American Indian population

artículo científico publicado en 2013

Updated genetic score based on 34 confirmed type 2 diabetes Loci is associated with diabetes incidence and regression to normoglycemia in the diabetes prevention program

artículo científico publicado en 2011

Variants in DENND1A are associated with polycystic ovary syndrome in women of European ancestry

artículo científico publicado en 2012

Variants in MTNR1B influence fasting glucose levels

artículo científico publicado en 2008

Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level

artículo científico publicado en 2016

Lista de obras de Richa Saxena

A Loss-Of-Function Splice Acceptor Variant in IGF2 is Protective for Type 2 Diabetes

A common variant of HMGA2 is associated with adult and childhood height in the general population

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

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 reveals variants in ARL15 that influence adiponectin levels

A second generation human haplotype map of over 3.1 million SNPs

Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans

Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study

Assessment of MTNR1B Type 2 Diabetes Genetic Risk Modification by Shift Work and Morningness-Eveningness Preference in the UK Biobank

Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort

Associations Between Sleep Health and Amygdala Reactivity to Negative Facial Expressions in the UK Biobank Cohort

Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep

Biological and clinical insights from genetics of insomnia symptoms

Biological and clinical insights from genetics of insomnia symptoms

CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids

CT Angiographic Evaluation of Pattern and Distribution of Stenosis and its Association with Risk Factors Among Indian Ischemic Stroke Patients

Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome

Chronotype Genetic Variant in PER2 is Associated with Intrinsic Circadian Period in Humans

Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations

Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion

Common variants associated with plasma triglycerides and risk for coronary artery disease

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

Common variants in 40 genes assessed for diabetes incidence and response to metformin and lifestyle intervention in the diabetes prevention program

Common variants in DRD2 are associated with sleep duration: the CARe consortium

Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage

Comparison of Heritability Estimation and Linkage Analysis for Multiple Traits Using Principal Component Analyses

Comprehensive association testing of common mitochondrial DNA variation in metabolic disease

DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation

Dimensionality reduction reveals fine-scale structure in the Japanese population with consequences for polygenic risk prediction

Directional dominance on stature and cognition in diverse human populations

Discovery and refinement of loci associated with lipid levels

Environmental and genetic factors influence age at menarche in women with polycystic ovary syndrome ⬇️

Evaluating reported candidate gene associations with polycystic ovary syndrome ⬇️

Evolutionarily conserved regulation of sleep by epidermal growth factor receptor signaling

Extension of type 2 diabetes genome-wide association scan results in the diabetes prevention program

Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans

Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia

Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia

Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits

Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines

Genetic predisposition to elevated levels of C-reactive protein is associated with a decreased risk for preeclampsia

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

Genetics of circadian rhythms and sleep in human health and disease

Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms

Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits

Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank

Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups

Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India

Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates

Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort

Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study

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

IBC CARe Microarray Allelic Population Prevalences in an American Indian Population ⬇️

Impact of sleep and circadian disruption on energy balance and diabetes: a summary of workshop discussions

Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene

Investigation of Genetic Variation Underlying Central Obesity amongst South Asians

Large Scale Metabolic Profiling identifies Novel Steroids linked to Rheumatoid Arthritis

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

No Association between the Mitochondrial Genome and Prostate Cancer Risk: The Multiethnic Cohort

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

Phenotype and Tissue Expression as a Function of Genetic Risk in Polycystic Ovary Syndrome

Pleiotropic effects of GIP on islet function involve osteopontin

Population Genetic Structure and Origins of Native Hawaiians in the Multiethnic Cohort Study ⬇️

Principal-component analysis for assessment of population stratification in mitochondrial medical genetics

RD-1 encoded EspJ protein gets phosphorylated prior to affect the growth and intracellular survival of mycobacteria

Relationship between polycystic ovary syndrome and ancestry in European Americans

Surgical Intensive Care Unit Optimal Mobilisation Score (SOMS) trial: a protocol for an international, multicentre, randomised controlled trial focused on goal-directed early mobilisation of surgical ICU patients

TXNIP regulates peripheral glucose metabolism in humans

The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people

The M. tuberculosis HAD phosphatase (Rv3042c) interacts with host proteins and is inhibited by Clofazimine

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

Tissue-specific alternative splicing of TCF7L2.

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study

Triglyceride response to an intensive lifestyle intervention is enhanced in carriers of the GCKR Pro446Leu polymorphism

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