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1,5-Anhydroglucitol in saliva is a noninvasive marker of short-term glycemic control.

artículo científico publicado en 2014

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

artículo científico publicado en 2018

A Workflow for Missing Values Imputation of Untargeted Metabolomics Data

scientific article published on 26 November 2020

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A genome-wide association meta-analysis identifies new childhood obesity loci

artículo científico publicado en 2012

A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium

artículo científico publicado en 2016

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019

A single night of sleep curtailment increases plasma acylcarnitines: Novel insights in the relationship between sleep and insulin resistance

artículo científico publicado en 2015

A systems view of type 2 diabetes-associated metabolic perturbations in saliva, blood and urine at different timescales of glycaemic control

artículo científico publicado en 2015

A variant of the IGF-I gene is associated with blood pressure but not with left heart dimensions at the age of 2 years: the Generation R Study

scientific article published on 10 June 2008

Advanced glycation end products among patients maintained on antipsychotics

artículo científico

Assessment of reproducibility and biological variability of fasting and postprandial plasma metabolite concentrations using 1H NMR spectroscopy

scientific article published on 20 June 2019

Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: the complex nature of genetic association through growth and development

artículo científico publicado en 2011

Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study

scientific article published on 04 September 2019

Association of alcohol consumption with allergic disease and asthma: a multi-centre Mendelian randomization analysis

scientific article published on 30 October 2018

Associations between Lifestyle Factors and Vitamin E Metabolites in the General Population

scientific article published on 15 December 2020

Associations between outdoor temperature and bright sunlight with metabolites in two population-based European cohorts

scientific article published on 28 July 2020

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

article

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Blood metabolomic measures associate with present and future glycemic control in type 2 diabetes

Breast-feeding modifies the association of PPARgamma2 polymorphism Pro12Ala with growth in early life: the Generation R Study

artículo científico publicado en 2009

CETP (Cholesteryl Ester Transfer Protein) Concentration: A Genome-Wide Association Study Followed by Mendelian Randomization on Coronary Artery Disease

artículo científico publicado en 2018

Causal Associations of Adiposity and Body Fat Distribution with Coronary Heart Disease, Stroke Subtypes and Type 2 Diabetes: A Mendelian Randomization Analysis

artículo científico publicado en 2017

Causes and consequences of the opioid epidemic in the Netherlands: a population-based cohort study

scientific article published on 17 September 2020

Characterization of Bulk Phosphatidylcholine Compositions in Human Plasma Using Side-Chain Resolving Lipidomics

artículo científico publicado en 2019

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Common variants at 12q15 and 12q24 are associated with infant head circumference

artículo científico publicado en 2012

Common variants at 6q22 and 17q21 are associated with intracranial volume

artículo científico publicado en 2012

Connecting genetic risk to disease end points through the human blood plasma proteome

scientific article published on 27 February 2017

Connecting genetic risk to disease endpoints through the human blood plasma proteome

Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

artículo científico publicado en 2016

Deep molecular phenotypes link complex disorders and physiological insult to CpG methylation.

artículo científico publicado en 2018

Discovery of novel heart rate-associated loci using the Exome Chip

artículo científico publicado en 2017

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

artículo científico publicado en 2020

Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals

artículo científico publicado en 2019

Effects of Technology Use on Ageing in Place: The iZi Pilots

artículo científico publicado en 2020

Elevated HbA1c levels in individuals not diagnosed with type 2 diabetes in Qatar: a pilot study

artículo científico publicado en 2014

Epigenetics meets proteomics in an epigenome-wide association study with circulating blood plasma protein traits

artículo científico publicado en 2020

Erratum to: A systems view of type 2 diabetes-associated metabolic perturbations in saliva, blood and urine at different timescales of glycaemic control

artículo científico publicado en 2015

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

scholarly article published in Nature Genetics

Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume

article

Erratum: Connecting genetic risk to disease end points through the human blood plasma proteome

artículo científico publicado en 2017

Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses

article

Ethnic and gender differences in advanced glycation end products measured by skin auto-fluorescence

artículo científico publicado en 2013

Ethnicity and skin autofluorescence-based risk-engines for cardiovascular disease and diabetes mellitus

artículo científico publicado en 2017

Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

artículo científico publicado en 2019

Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

scientific article published on 01 September 2019

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

Exploring the role of low-frequency and rare exonic variants in alcohol and tobacco use

artículo científico publicado en 2018

FFP2-mondmasker of chirurgisch mondkapje bij COVID-19

artículo científico publicado en 2020

Fetal and infant growth and the risk of obesity during early childhood: the Generation R Study

artículo científico publicado en 2011

Fine-Mapping of the Human Blood Plasma N-Glycome onto Its Proteome

scientific article published on 26 June 2019

GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

artículo científico publicado en 2018

Gender-specific pathway differences in the human serum metabolome

artículo científico publicado en 2015

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

scientific article published on 05 May 2020

Genetic Determinants of Electrocardiographic P-wave Duration and Relation to Atrial Fibrillation

artículo científico publicado en 2020

Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

scientific article published on 11 September 2020

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

artículo científico publicado en 2016

Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group

artículo científico publicado en 2019

Genome-Wide Association Study on the Early-Phase Insulin Response to a Liquid Mixed Meal: Results From the NEO Study

artículo científico publicado en 2019

Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent

artículo científico publicado en 2017

Genome-Wide and Abdominal MRI-Imaging Data Provides Evidence that a Genetically Determined Favourable Adiposity Phenotype is Characterized by Lower Ectopic Liver Fat and Lower Risk of Type 2 Diabetes, Heart Disease and Hypertension

scientific article published on 23 October 2018

Genome-wide Association Study of the Postprandial Triglyceride Response Yields Common Genetic Variation in Hepatic Lipase (LIPC)

artículo científico publicado en 2020

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

artículo científico publicado en 2016

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

artículo científico publicado en 2019

Genome-wide association study of breakfast skipping links clock regulation with food timing

artículo científico publicado en 2019

Genome-wide associations for birth weight and correlations with adult disease

artículo científico publicado en 2016

Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry

artículo científico publicado en 2018

Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium

artículo científico publicado en 2018

Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

artículo científico publicado en 2016

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

artículo científico publicado en 2017

Growth in foetal life and infancy is associated with abdominal adiposity at the age of 2 years: the generation R study

artículo científico publicado en 2009

Healthcare and disease burden among refugees in long-stay refugee camps at Lesbos, Greece.

artículo científico publicado en 2017

Heritability estimates of body size in fetal life and early childhood

artículo científico publicado en 2012

Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation

artículo científico publicado en 2017

Insulin VNTR and IGF-1 promoter region polymorphisms are not associated with body composition in early childhood: the generation R study.

artículo científico publicado en 2010

Insulin gene variable number of tandem repeats is not associated with weight from fetal life until infancy: the Generation R Study

artículo científico publicado en 2007

Integration of epidemiologic, pharmacologic, genetic and gut microbiome data in a drug-metabolite atlas

scientific article published on 13 January 2020

Interactions between TCF7L2 genotype and growth hormone-induced changes in glucose homeostasis in small for gestational age children.

artículo científico publicado en 2009

Investigating the causal effect of smoking on hay fever and asthma: a Mendelian randomization meta-analysis in the CARTA consortium

artículo científico publicado en 2017

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

artículo científico publicado en 2018

Low Birth Weight and Kidney Function in Middle-Aged Men and Women: The Netherlands Epidemiology of Obesity Study

artículo científico publicado en 2019

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

artículo científico publicado en 2017

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

scientific article published on 01 December 2018

LysoPC-acyl C16:0 is associated with brown adipose tissue activity in men

scientific article published on 03 March 2017

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

artículo científico publicado en 2019

Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood

artículo científico publicado en 2020

Mendelian randomization reveals unexpected effects of CETP on the lipoprotein profile

scientific article published on 12 November 2018

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

artículo científico publicado en 2016

Meta-analysis of exome array data identifies six novel genetic loci for lung function

scientific article published on 12 January 2018

Meta-analysis of exome array data identifies six novel genetic loci for lung function

Metabolomics Profile in Depression: A Pooled Analysis of 230 Metabolic Markers in 5283 Cases With Depression and 10,145 Controls

artículo científico publicado en 2019

Metabolomics Profiling of Visceral Adipose Tissue: Results From MESA and the NEO Study

artículo científico publicado en 2019

Metabolomics analyses in non-diabetic middle-aged individuals reveal metabolites impacting early glucose disturbances and insulin sensitivity

artículo científico publicado en 2020

Metabolomics: a search for biomarkers of visceral fat and liver fat content

scientific article published on 05 October 2019

Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

scientific article published on 21 May 2020

Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

article

Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

artículo científico publicado en 2019

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

artículo científico publicado en 2019

Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis.

artículo científico publicado en 2016

Multiethnic Meta-analysis Identifies New Loci for Pulmonary Function

Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function

scientific article published in Nature Communications

Network-based approach for analyzing intra- and interfluid metabolite associations in human blood, urine, and saliva

artículo científico publicado en 2014

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

artículo científico publicado en 2012

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

artículo científico publicado en 2017

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

artículo científico publicado en 2018

Ovarian function during puberty in girls with type 1 diabetes mellitus: response to leuprolide

artículo científico publicado en 2005

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

artículo científico publicado en 2016

PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

article

Phenotype-driven identification of modules in a hierarchical map of multifluid metabolic correlations

artículo científico publicado en 2017

Physiological changes due to mild cooling in healthy lean males of white Caucasian and South Asian descent: A metabolomics study.

artículo científico publicado en 2015

Plasma metabolomics identifies markers of impaired renal function: A meta-analysis of 3,089 persons with type 2 diabetes

artículo científico publicado en 2020

Ponderal gain, waist-to-hip ratio, and pubertal development in girls with type-1 diabetes mellitus

scientific article published on 01 December 2004

Postprandial metabolite profiles associated with type 2 diabetes clearly stratify individuals with impaired fasting glucose

artículo científico publicado en 2017

Potential Interplay between Dietary Saturated Fats and Genetic Variants of the NLRP3 Inflammasome to Modulate Insulin Resistance and Diabetes Risk: Insights from a Meta-Analysis of 19 005 Individuals

scientific article published on 12 September 2019

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2017

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

article

Proteome-wide assessment of diabetes mellitus in Qatari identifies IGFBP-2 as a risk factor already with early glycaemic disturbances

artículo científico publicado en 2020

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2019

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

artículo científico publicado en 2018

Rare and low-frequency coding variants alter human adult height

artículo científico publicado en 2017

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

article

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.

artículo científico publicado en 2018

Relationships between sleep patterns and metabolic profile in patients maintained on antipsychotics: a cross-sectional comparative study

scientific article published on 19 July 2019

Replication of type 2 diabetes associated variants in a Saudi Arabian population

artículo científico publicado en 2018

Risk factors and outcomes associated with first-trimester fetal growth restriction

artículo científico publicado en 2010

Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

artículo científico publicado en 2020

SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function

artículo científico publicado en 2016

Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

artículo científico publicado en 2020

Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis

artículo científico publicado en 2017

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

artículo científico publicado en 2019

The association between overall and abdominal adiposity and depressive mood: A cross-sectional analysis in 6459 participants

scientific article published on 04 September 2019

The association between various smoking behaviors, cotinine biomarkers and skin autofluorescence, a marker for advanced glycation end product accumulation.

artículo científico publicado en 2017

The association of genetic variants in the cholesteryl ester transfer protein gene with hemostatic factors and a first venous thrombosis

scientific article published on 21 June 2019

The genetics of fasting and postprandial metabolite levels are overlapping.

artículo científico publicado en 2018

The prevalence of metabolic syndrome in patients receiving antipsychotics in Qatar: a cross sectional comparative study.

artículo científico publicado en 2018

Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies

artículo científico publicado en 2009

Type 2 diabetes is associated with postprandial amino acid measures

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Variants nearCCNL1/LEKR1and inADCY5and Fetal Growth Characteristics in Different Trimesters

article

Variation in the IGF-1 gene is associated with lymphocyte subset counts in neonates: the Generation R Study.

artículo científico publicado en 2008

Variation in the IGF1 gene and growth in foetal life and infancy. The Generation R Study

scientific article published on 19 September 2007

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

artículo científico publicado en 2016

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

article

[Age of pubertal events in Chilean school age girls and its relationship with socioeconomic status and body mass index]

artículo científico publicado en 2004

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