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Lista de obras de John Blangero

'Mutiny on the Bounty': the genetic history of Norfolk Island reveals extreme gender-biased admixture

artículo científico publicado en 2015

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

artículo científico publicado en 2021

3069 Characterizing the Neural Signature of Metabolic Syndrome

artículo científico publicado en 2019

A Genome Search for Genetic Determinants That Influence Plasma Fibrinogen Levels

scientific article published on 10 March 2005

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

artículo científico publicado en 2017

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

artículo científico publicado en 2017

A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers

artículo científico publicado en 2015

A QTL for genotype by sex interaction for anthropometric measurements in Alaskan Eskimos (GOCADAN Study) on chromosome 19q12-13.

artículo científico publicado en 2011

A QTL on chromosome 3q23 influences processing speed in humans

scientific article published on 16 November 2018

A Quantitative Trait Locus Influencing Free Plasma Protein S Levels on Human Chromosome 1q

artículo científico publicado en 2003

A Variant in the LRRFIP1 Gene Is Associated With Adiposity and Inflammation

article

A White Matter Connection of Schizophrenia and Alzheimer's Disease

artículo científico publicado en 2020

A chromosome 11q quantitative-trait locus influences change of blood-pressure measurements over time in Mexican Americans of the San Antonio Family Heart Study

artículo científico publicado en 2007

A comparison of univariate, bivariate, and trivariate whole-genome linkage screens of genetically correlated electrophysiological endophenotypes

artículo científico publicado en 2005

A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and system

artículo científico publicado en 2013

A comprehensive linkage analysis for myocardial infarction and its related risk factors

artículo científico publicado en 2002

A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies ⬇️

artículo científico publicado en 2022

A gene expression signature for insulin resistance

artículo científico publicado en 2010

A genetic association study of carotid intima-media thickness (CIMT) and plaque in Mexican Americans and European Americans with rheumatoid arthritis

artículo científico publicado en 2017

A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility

artículo científico publicado en 2012

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 exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels

artículo científico publicado en 2008

A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).

artículo científico publicado en 2013

A genome-wide linkage scan for quantitative trait loci influencing the craniofacial complex in humans (Homo sapiens sapiens) ⬇️

artículo científico publicado el 15 de febrero de 2011

A genome-wide search for linkage to chronic kidney disease in a community-based sample: the SAFHS.

artículo científico publicado en 2008

A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project

artículo científico publicado en 2005

A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans

artículo científico publicado en 2006

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

artículo científico publicado en 2021

A kernel of truth: statistical advances in polygenic variance component models for complex human pedigrees

artículo científico publicado en 2013

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

artículo científico publicado en 2015

A linkage analysis of cigarette and alcohol consumption in an unselected Mexican American population

artículo científico publicado en 2008

A multimodal assessment of the genetic control over working memory

artículo científico publicado en 2010

A neural signature of metabolic syndrome

scientific article published on 07 May 2019

A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibility.

artículo científico publicado en 2002

A novel missense mutation in ADRB3 increases risk for type 2 diabetes in a Mexican American family

artículo científico publicado en 2006

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

artículo científico publicado en 2016

A quantitative trait locus (QTL) on chromosome 6q influences birth weight in two independent family studies

artículo científico publicado en 2006

A quantitative trait locus influences coordinated variation in measures of ApoB-containing lipoproteins

artículo científico publicado en 2004

A quantitative trait locus influencing type 2 diabetes susceptibility maps to a region on 5q in an extended French family

artículo científico publicado en 2002

A quantitative trait locus on chromosome 22 for serum leptin levels adjusted for serum testosterone

artículo científico publicado en 2002

A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease

artículo científico publicado en 2002

A retrospective examination of mean relative telomere length in the Tasmanian Familial Hematological Malignancies Study

artículo científico publicado en 2014

A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels

artículo científico publicado en 2007

A single nucleotide polymorphism in MGEA5 encoding O-GlcNAc-selective N-acetyl-beta-D glucosaminidase is associated with type 2 diabetes in Mexican Americans

artículo científico publicado en 2005

A transcriptional profile of the decidua in preeclampsia

artículo científico publicado en 2011

A variance component method for integrated pathway analysis of gene expression data

artículo científico publicado en 2016

A variance component-based gene burden test

artículo científico publicado en 2014

A variant in the LRRFIP1 gene is associated with adiposity and inflammation

artículo científico publicado en 2013

ADAM19: A Novel Target for Metabolic Syndrome in Humans and Mice.

artículo científico publicado en 2017

ADAM28 is elevated in humans with the metabolic syndrome and is a novel sheddase of human tumour necrosis factor-α.

artículo científico publicado en 2012

Acanthosis nigricans as a composite marker of cardiometabolic risk and its complex association with obesity and insulin resistance in Mexican American children

artículo científico publicado en 2020

Adjudicating neurocognitive endophenotypes for schizophrenia

scientific article published on 01 March 2007

Amygdalar and hippocampal substrates of anxious temperament differ in their heritability

artículo científico publicado en 2010

An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12.

artículo científico publicado en 2012

An epigenetic map of age-associated autosomal loci in northern European families at high risk for the metabolic syndrome

artículo científico publicado en 2015

Analysis of SLC16A11 Variants in 12,811 American Indians: Genotype-Obesity Interaction for Type 2 Diabetes and an Association With RNASEK Expression

artículo científico publicado en 2015

Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study

artículo científico publicado en 2017

Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume

artículo científico publicado en 2009

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

artículo científico publicado en 2022

Arguments for the sake of endophenotypes: examining common misconceptions about the use of endophenotypes in psychiatric genetics

artículo científico publicado en 2014

Assessment of Cognition and Personality as Potential Endophenotypes in the Western Australian Family Study of Schizophrenia

artículo científico publicado en 2017

Assessment of gene-by-sex interaction effect on bone mineral density

artículo científico publicado en 2012

Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study).

artículo científico publicado en 2008

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

artículo científico publicado en 2019

Association of POAG risk factors and the Thr377Met MYOC mutation in an isolated Greek population

artículo científico publicado en 2010

Association of Urinary Phthalates with Self-Reported Eye Affliction/Retinopathy in Individuals with Diabetes: National Health and Nutrition Examination Survey, 2001-2010.

artículo científico publicado en 2015

Association of differential gene expression with imatinib mesylate and omacetaxine mepesuccinate toxicity in lymphoblastoid cell lines

artículo científico publicado en 2012

Association of genetic variation in ENPP1 with obesity-related phenotypes

artículo científico publicado en 2008

Association of genetic variation within UBL5 with phenotypes of metabolic syndrome.

artículo científico publicado en 2006

Association of neuropeptide Y receptor Y5 polymorphisms with dyslipidemia in Mexican Americans

artículo científico publicado en 2007

Associations of cannabis use disorder with cognition, brain structure, and brain function in African Americans

scientific article published on 19 December 2020

Autosomal genome-wide linkage analysis to identify loci for gallbladder wall thickness in Mexican Americans

artículo científico publicado en 2008

Benchmarking Relatedness Inference Methods with Genome-Wide Data from Thousands of Relatives

artículo científico publicado en 2017

Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study

artículo científico publicado en 2010

Bivariate linkage analysis of the insulin resistance syndrome phenotypes on chromosome 7q.

artículo científico publicado en 2005

Bivariate linkage between acylation-stimulating protein and BMI and high-density lipoproteins

artículo científico publicado en 2004

Blood pressure and cerebral white matter share common genetic factors in Mexican Americans

artículo científico publicado en 2010

Burden of Type 2 Diabetes and Associated Cardiometabolic Traits and Their Heritability Estimates in Endogamous Ethnic Groups of India: Findings From the INDIGENIUS Consortium

artículo científico publicado en 2022

Characterizing the Extent of Human Genetic Variation for Performance-Related Traits

article

Chemerin is associated with metabolic syndrome phenotypes in a Mexican-American population

artículo científico publicado en 2009

Chemerin, A Novel Adipokine in the Regulation of Angiogenesis.

artículo científico publicado en 2010

Chemerin, a novel adipokine in the regulation of angiogenesis

artículo científico publicado en 2010

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

artículo científico publicado en 2021

Cognitive impairment from early to middle adulthood in patients with affective and nonaffective psychotic disorders

scientific article published on 04 January 2019

Collection of pedigree data for genetic analysis in isolate populations

artículo científico publicado en 2006

Combined cis-regulator elements as important mechanism affecting FXII plasma levels

artículo científico publicado en 2009

Common genetic variants and gene expression associated with white matter microstructure in the human brain

artículo científico publicado en 2014

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Common polygenic variation contributes to risk of migraine in the Norfolk Island population

artículo científico publicado en 2015

Comparing empirical kinship derived heritability for imaging genetics traits in the UK biobank and human connectome project

artículo científico publicado en 2021

Comparison of heritability estimates on resting state fMRI connectivity phenotypes using the ENIGMA analysis pipeline

article

Complex rare variation and its role in endophenotypic variation in schizophrenia

artículo científico publicado en 2013

Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility

artículo científico publicado en 2014

Conceptualizing Major Depression

Contemporary model-free methods for linkage analysis

scientific article published on January 2008

Contribution of Inbred Singletons to Variance Component Estimation of Heritability and Linkage

artículo científico publicado en 2018

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

artículo científico publicado en 2020

Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2016

Correction: Waist Circumference Independently Associates with the Risk of Insulin Resistance and Type 2 Diabetes in Mexican American Families.

artículo científico publicado en 2013

Corrigendum to “Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA–DTI working group” [NeuroImage 81 (2013) 455–469]

scholarly article published in NeuroImage

Cortical bone health shows significant linkage to chromosomes 2p, 3p, and 17q in 10-year-old children ⬇️

artículo científico publicado el 31 de agosto de 2011

Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies

artículo científico publicado en 2009

Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives

artículo científico publicado en 2019

Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees

artículo científico publicado en 2014

Data on genetic associations of carotid atherosclerosis markers in Mexican American and European American rheumatoid arthritis subjects.

artículo científico publicado en 2018

Deficits in visual working-memory capacity and general cognition in African Americans with psychosis

artículo científico

Defining the role of common variation in the genomic and biological architecture of adult human height

artículo científico publicado en 2014

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

artículo científico publicado en 2020

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Differences in the heritability of growth and growth velocity during infancy and associations with FTO variants

artículo científico publicado en 2011

Discovering schizophrenia endophenotypes in randomly ascertained pedigrees ⬇️

artículo científico publicado en 2014

Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes

artículo científico publicado en 2007

Disentangling the genetic overlap between cholesterol and suicide risk

scientific article published on 23 July 2018

Diverse biological activities of the vascular non-inflammatory molecules – The Vanin pantetheinases ⬇️

artículo científico publicado el 13 de enero de 2012

Do Candidate Genes Affect the Brain's White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans

article

Do rare variant genotypes predict common variant genotypes?

artículo científico publicado en 2011

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

artículo científico publicado en 2020

Effects of copy number variable regions on local gene expression in white blood cells of Mexican Americans

artículo científico publicado en 2015

Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies

scientific article published on 10 January 2019

Endothelial nitric oxide synthase (eNOS) gene polymorphisms and their association with type 2 diabetes-related traits in Mexican Americans

artículo científico publicado en 2008

Epidemiologic investigation of tuberculosis in a Mexican population from Chihuahua State, Mexico: a pilot study

artículo científico publicado en 2013

Epigenetic Age Acceleration Assessed with Human White-Matter Images.

artículo científico publicado en 2017

Erratum to: 'Mutiny on the Bounty': the genetic history of Norfolk Island reveals extreme gender-biased admixture

artículo científico publicado en 2015

Erratum to: Multi-region hemispheric specialization differentiates human from nonhuman primate brain function

artículo científico publicado en 2013

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2018

Estimating the additive genetic effect of the X chromosome

artículo científico publicado en 2005

Evaluating a CLL susceptibility variant in ITGB2 in families with multiple subtypes of hematological malignancies

artículo científico publicado en 2017

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

artículo científico publicado en 2017

Evaluation of estimated genetic values and their application to genome-wide investigation of systolic blood pressure

artículo científico publicado en 2014

Evaluation of gremlin 1 (GREM1) as a candidate susceptibility gene for albuminuria-related traits in Mexican Americans with type 2 diabetes mellitus

artículo científico publicado en 2009

Evaluation of neurotrophic tyrosine receptor kinase 2 (NTRK2) as a positional candidate gene for variation in estimated glomerular filtration rate (eGFR) in Mexican American participants of San Antonio Family Heart study

artículo científico publicado en 2015

Evaluation of polymorphisms in paraoxonase 2 (PON2) gene and their association with cardiovascular-renal disease risk in Mexican Americans

artículo científico publicado en 2009

Evaluation of qualitative methods for phenotyping brachymesophalangia‐V from radiographs of children ⬇️

artículo científico publicado el 1 de enero de 2012

Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q.

artículo científico publicado en 2004

Evidence for a gene on chromosome 13 influencing postural systolic blood pressure change and body mass index

artículo científico publicado en 2004

Evidence for bivariate linkage of obesity and HDL-C levels in the Framingham Heart Study

artículo científico publicado en 2003

Evidence for genetic correlation between human cerebral white matter microstructure and inflammation

artículo científico publicado en 2019

Evidence for genetic susceptibility to developing early childhood diarrhea among shantytown children living in northeastern Brazil

artículo científico publicado en 2011

Evidence of a novel quantitative-trait locus for obesity on chromosome 4p in Mexican Americans

artículo científico publicado en 2004

Evidence that multiple genetic variants of MC4R play a functional role in the regulation of energy expenditure and appetite in Hispanic children

artículo científico publicado en 2009

Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk

artículo científico publicado en 2015

Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS).

artículo científico publicado en 2018

Exome array analysis suggests an increased variant burden in families with schizophrenia.

artículo científico publicado en 2016

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

article by Jason Flannick et al published 22 May 2019 in Nature

Exposure to Schistosoma mansoni infection in a rural area in Brazil. II: Household risk factors

artículo científico publicado en 2001

F145. Extremely Weak Relationship Between Gyrification and Intelligence

scientific article published in 2019

Factors of insulin resistance syndrome--related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic mexican-americans

artículo científico publicado en 2002

Family-based analyses reveal novel genetic overlap between cytokine interleukin-8 and risk for suicide attempt

artículo científico publicado en 2019

Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data

artículo científico publicado en 2016

Fast and powerful genome wide association of dense genetic data with high dimensional imaging phenotypes

scientific article published in Nature Communications

Fast and powerful heritability inference for family-based neuroimaging studies

artículo científico publicado en 2015

Fasting insulin and obesity-related phenotypes are linked to chromosome 2p: the Strong Heart Family Study

artículo científico publicado en 2006

Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a Northern European family population

artículo científico publicado en 2013

Finding potential cis-regulatory loci using allele-specific chromatin accessibility as weights in a kernel-based variance component test

artículo científico publicado en 2016

Functional analysis of the genetic variability in the F7 gene promoter

artículo científico publicado en 2007

Further evidence for a type 2 diabetes susceptibility locus on chromosome 11q

article

Further evidence supporting a potential role for ADH1B in obesity

artículo científico

GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans

artículo científico publicado en 2016

Gene Expression Differences Between Offspring of Long-Lived Individuals and Controls in Candidate Longevity Regions: Evidence for PAPSS2 as a Longevity Gene

artículo científico publicado en 2016

Gene by smoking interaction: evidence for effects on low-density lipoprotein size and plasma levels of triglyceride and high-density lipoprotein cholesterol.

artículo científico publicado en 2004

Gene-by-age effects on BMI from birth to adulthood: the Fels Longitudinal Study

artículo científico publicado en 2013

Genes on chromosomes 1 and 13 have significant effects on Ascaris infection

artículo científico publicado en 2002

Genetic Analysis Workshop 17 mini-exome simulation

artículo científico publicado en 2011

Genetic Epidemiology of Chagas Disease ⬇️

artículo científico publicado el 1 de enero de 2011

Genetic Influence on the Human Brain

Genetic Variants Influencing Joint Damage in Mexican Americans and European Americans With Rheumatoid Arthritis

artículo científico publicado en 2015

Genetic Variants in Toll-Like Receptor 4 Gene and Their Association Analysis with Estimated Glomerular Filtration Rate in Mexican American Families

artículo científico publicado en 2016

Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain

artículo científico publicado en 2011

Genetic analysis of sexual dimorphism in serum apo AI and HDL-C concentrations in baboons

artículo científico publicado en 1992

Genetic and environmental (physical fitness and sedentary activity) interaction effects on cardiometabolic risk factors in Mexican American children and adolescents

artículo científico publicado en 2018

Genetic and environmental factors influencing the human factor H plasma levels

artículo científico publicado en 2004

Genetic and environmental influences on infant weight and weight change: the Fels Longitudinal Study

artículo científico publicado en 2007

Genetic and environmental influences on thyroid hormone variation in Mexican Americans

artículo científico publicado en 2004

Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13q

artículo científico publicado en 2010

Genetic architecture of carotid artery intima-media thickness in Mexican Americans

artículo científico publicado en 2013

Genetic association of preeclampsia to the inflammatory response gene SEPS1

article

Genetic basis for the increased expression of vacuolar H+ translocating ATPase genes upon imatinib treatment in human lymphoblastoid cells

artículo científico publicado en 2013

Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging

artículo científico publicado en 2013

Genetic basis of variation in carotid artery plaque in the San Antonio Family Heart Study

artículo científico publicado en 2002

Genetic component to susceptibility to Trichuris trichiura: evidence from two Asian populations

artículo científico publicado en 2002

Genetic correlation of the plasma lipidome with type 2 diabetes, prediabetes and insulin resistance in Mexican American families

artículo científico publicado en 2017

Genetic determinants of iron metabolism plasma phenotypes and their relationship with risk of thrombosis

scientific article published on 01 December 2003

Genetic determinants of metabolic biomarkers and their associations with cardiometabolic traits in Hispanic/Latino adolescents

artículo científico publicado en 2021

Genetic determinants of mitochondrial content

article

Genetic determinants of obesity-related lipid traits

scientific article published on February 2004

Genetic determinants of variation in gallbladder disease in the Mexican-American population

Genetic determinants of variation in the plasma levels of the C4b-binding protein (C4BP) in Spanish families

article

Genetic determination of biological age in the Mennonites of the Midwestern United States

artículo científico publicado en 2002

Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease

artículo científico publicado en 2013

Genetic effects on DNA methylation and its potential relevance for obesity in Mexican Americans

artículo científico publicado en 2013

Genetic epidemiology of cardiometabolic risk factors and their clustering patterns in Mexican American children and adolescents: the SAFARI Study

artículo científico publicado en 2013

Genetic epidemiology of trypanosoma cruzi infection and Chagas disease

artículo científico publicado el 1 de mayo de 2003

Genetic factors influence serological measures of common infections ⬇️

artículo científico publicado el 11 de octubre de 2011

Genetic influence on cognitive development between childhood and adulthood

scientific article published on 19 October 2018

Genetic influences on plasma cytokine variation in a parasitized population.

artículo científico publicado en 2004

Genetic influences on type 2 diabetes and metabolic syndrome related quantitative traits in Mauritius

artículo científico publicado en 2009

Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis

artículo científico publicado en 2016

Genetic polymorphisms in the renin-angiotensin system (RAS) genes and their association analysis with type 2 diabetes and related traits in Mexican Americans

artículo científico publicado en 2007

Genetic risk for earlier menarche also influences peripubertal body mass index

artículo científico publicado en 2013

Genetic signal maximization using environmental regression

artículo científico publicado en 2011

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variants in Transient Receptor Potential cation channel, subfamily M 1 (TRPM1) and their risk of albuminuria-related traits in Mexican Americans ⬇️

artículo científico publicado el 20 de noviembre de 2011

Genetic variants in the renin-angiotensin system genes are associated with cardiovascular-renal-related risk factors in Mexican Americans

artículo científico publicado en 2008

Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate

article

Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate

artículo científico publicado en 2017

Genetic variation at the FTO locus influences RBL2 gene expression

artículo científico publicado en 2009

Genetic variation in BEACON influences quantitative variation in metabolic syndrome-related phenotypes

artículo científico publicado en 2004

Genetic variation in PARL influences mitochondrial content

artículo científico publicado en 2009

Genetic variation in selenoprotein S influences inflammatory response

artículo científico publicado en 2005

Genetics of serum carotenoid concentrations and their correlation with obesity-related traits in Mexican American children

artículo científico publicado en 2017

Genetics of variation in HOMA-IR and cardiovascular risk factors in Mexican-Americans

artículo científico publicado en 2008

Genetics of variation in serum uric acid and cardiovascular risk factors in Mexican Americans

artículo científico publicado en 2008

Genome scan for determinants of serum uric acid variability

artículo científico publicado en 2007

Genome- and epigenome-wide association study of hypertriglyceridemic waist in Mexican American families

artículo científico publicado en 2016

Genome-Wide Analyses of Working-Memory Ability: A Review

artículo científico publicado en 2014

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention ⬇️

artículo científico publicado en 2022

Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans

artículo científico publicado en 2013

Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.

artículo científico publicado en 2011

Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene

artículo científico publicado en 2012

Genome-wide discovery of maternal effect variants

artículo científico publicado en 2009

Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens

artículo científico publicado en 2014

Genome-wide genetic investigation of serological measures of common infections

artículo científico publicado en 2015

Genome-wide linkage analyses of type 2 diabetes in Mexican Americans: the San Antonio Family Diabetes/Gallbladder Study

artículo científico publicado en 2005

Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels

artículo científico publicado en 2008

Genome-wide linkage analysis of von Willebrand factor plasma levels: results from the GAIT project

artículo científico publicado en 2003

Genome-wide linkage on chromosome 10q26 for a dimensional scale of major depression

artículo científico publicado en 2016

Genome-wide linkage scan for genes influencing plasma triglyceride levels in the Veterans Administration Genetic Epidemiology Study

artículo científico publicado en 2008

Genome-wide linkage scan for loci influencing plasma triglyceride levels

Genome-wide linkage screen for systolic blood pressure in the Veterans Administration Genetic Epidemiology Study (VAGES) of Mexican-Americans and confirmation of a major susceptibility locus on chromosome 6q14.1.

artículo científico publicado en 2011

Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.

artículo científico publicado en 2017

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

Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

artículo científico publicado en 2016

Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Genome-wide scan identifies a quantitative trait locus at 4p15.3 for serum urate

artículo científico publicado en 2010

Genome-wide scans for microalbuminuria in Mexican Americans: the San Antonio Family Heart Study

scientific article published on 01 February 2007

Genome-wide scans reveal quantitative trait Loci on 8p and 13q related to insulin action and glucose metabolism: the San Antonio Family Heart Study

artículo científico publicado en 2004

Genome-wide significant linkage of schizophrenia-related neuroanatomical trait to 12q24.

artículo científico publicado en 2015

Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition

artículo científico publicado en 2013

Genomewide linkage analysis of soluble transferrin receptor plasma levels

artículo científico publicado en 2005

Genomic kinship construction to enhance genetic analyses in the human connectome project data

scientific article published on 29 November 2018

Genotype by diabetes interaction effects on the detection of linkage of glomerular filtration rate to a region on chromosome 2q in Mexican Americans

artículo científico publicado en 2007

Genotype by energy expenditure interaction with metabolic syndrome traits: the Portuguese healthy family study.

artículo científico publicado en 2013

Genotype by sex and genotype by age interactions with sedentary behavior: the Portuguese Healthy Family Study

artículo científico publicado en 2014

Genotype by smoking interaction for leptin levels in the San Antonio family heart study

artículo científico publicado en 2002

Genotype phasing in pedigrees using whole-genome sequence data

scientific article published on 29 January 2020

Genotype x adiposity interaction linkage analyses reveal a locus on chromosome 1 for lipoprotein-associated phospholipase A2, a marker of inflammation and oxidative stress

artículo científico publicado en 2006

Genotype×age interaction in human transcriptional ageing

artículo científico publicado en 2012

Gestational Age and the Cord Blood Lipidomic Profile in Late Preterm and Term Infants.

artículo científico publicado en 2018

Glycated Serum Protein Genetics and Pleiotropy with Cardiometabolic Risk Factors

article

Haplotypes of transcription factor 7-like 2 (TCF7L2) gene and its upstream region are associated with type 2 diabetes and age of onset in Mexican Americans

artículo científico publicado en 2007

Hemoglobin concentration of high-altitude Tibetans and Bolivian Aymara

artículo científico publicado en 1998

Hepatic gene networks in morbidly obese patients with nonalcoholic fatty liver disease

artículo científico publicado en 2010

Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships

Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island.

artículo científico publicado en 2011

Heritability estimates on resting state fMRI data using ENIGMA analysis pipeline

artículo científico publicado en 2018

Heritability of 596 lipid species and genetic correlation with cardiovascular traits in the Busselton Family Heart Study

artículo científico publicado en 2020

Heritability of age at menarche in girls from the Fels Longitudinal Study

artículo científico publicado en 2005

Heritability of brachydactyly type A3 in children, adolescents, and young adults from an endogamous population in eastern Nepal

artículo científico publicado en 2007

Heritability of brain volume, surface area and shape: an MRI study in an extended pedigree of baboons

artículo científico publicado en 2007

Heritability of fractional anisotropy in human white matter: a comparison of Human Connectome Project and ENIGMA-DTI data

artículo científico publicado en 2015

Heritability of hemostasis phenotypes and their correlation with type 2 diabetes status in Mexican Americans

scientific article published on 01 February 2005

Heritable changes in regional cortical thickness with age

artículo científico publicado en 2014

High dimensional endophenotype ranking in the search for major depression risk genes

artículo científico publicado en 2011

Highly efficient induced pluripotent stem cell reprogramming of cryopreserved lymphoblastoid cell lines

scientific article published on 08 January 2020

Host genetics and population structure effects on parasitic disease

artículo científico publicado en 2012

Human Cortical Thickness Organized into Genetically-determined Communities across Spatial Resolutions.

artículo científico publicado en 2017

Human F7 sequence is split into three deep clades that are related to FVII plasma levels

artículo científico publicado en 2005

Human QTL linkage mapping

scientific article published on 31 July 2008

Human plasma lipidome is pleiotropically associated with cardiovascular risk factors and death

artículo científico publicado en 2014

Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex.

artículo científico publicado en 2016

Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus

artículo científico publicado en 2015

Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease

artículo científico publicado en 2011

Identification of a large deletion and three novel mutations in exon 13 of the factor V gene in a Spanish family with normal factor V coagulant and anticoagulant properties

artículo científico publicado en 2002

Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

artículo científico publicado en 2013

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Identification of pleiotropic genetic effects on obesity and brain anatomy

artículo científico publicado en 2013

Imaging local genetic influences on cortical folding

artículo científico publicado en 2020

Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

artículo científico publicado en 2019

Impact of family structure and common environment on heritability estimation for neuroimaging genetics studies using Sequential Oligogenic Linkage Analysis Routines

artículo científico publicado en 2014

Increased waist circumference is independently associated with hypothyroidism in Mexican Americans: replicative evidence from two large, population-based studies

artículo científico publicado en 2014

Independent test assessment using the extreme value distribution theory

artículo científico publicado en 2016

Induced Pluripotent Stem Cells in Disease Modeling and Gene Identification

artículo científico publicado en 2018

Inferring Identical-by-Descent Sharing of Sample Ancestors Promotes High-Resolution Relative Detection

article published in 2018

Influence of Processing Pipeline on Cortical Thickness Measurement

artículo científico publicado en 2020

Influence of age, sex and genetic factors on the human brain

artículo científico publicado en 2014

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

artículo científico publicado en 2020

Integrating genomic analysis with the genetic basis of gene expression: preliminary evidence of the identification of causal genes for cardiovascular and metabolic traits related to nutrition in Mexicans.

artículo científico publicado en 2012

Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study

Intercellular adhesion molecule-1 concentration is genetically correlated with insulin resistance, obesity, and HDL concentration in Mexican Americans

artículo científico publicado en 2004

Intergenerational neural mediators of early-life anxious temperament

artículo científico publicado en 2015

Introduction to genetic analysis workshop 17 summaries

artículo científico publicado en 2011

Joint linkage and association analysis of the hepatic lipase promoter polymorphism and lipoprotein size phenotypes.

artículo científico publicado en 2005

Lack of Association between SLC30A8 Variants and Type 2 Diabetes in Mexican American Families

artículo científico publicado en 2016

Large scale mitochondrial sequencing in Mexican Americans suggests a reappraisal of Native American origins

artículo científico publicado en 2011

Legacy of mutiny on the Bounty: founder effect and admixture on Norfolk Island

artículo científico publicado en 2010

Leptin's sexual dimorphism results from genotype by sex interactions mediated by testosterone

artículo científico publicado en 2002

Linkage analysis without defined pedigrees

artículo científico publicado en 2011

Linkage disequilibrium across two different single-nucleotide polymorphism genome scans

artículo científico publicado en 2005

Linkage of high-density lipoprotein-cholesterol concentrations to a locus on chromosome 9p in Mexican Americans

artículo científico publicado en 2001

Linkage of type 2 diabetes on chromosome 9p24 in Mexican Americans: additional evidence from the Veterans Administration Genetic Epidemiology Study (VAGES).

artículo científico publicado en 2013

Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree

artículo científico publicado en 2005

Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts

artículo científico publicado en 2016

Lipidomics in the Study of Hypertension in Metabolic Syndrome

artículo científico publicado en 2017

Localization and identification of human quantitative trait loci: king harvest has surely come

artículo científico publicado en 2004

Localization of multiple quantitative trait loci influencing susceptibility to infection with Ascaris lumbricoides

scientific article published on 01 January 2008

Long-term changes in adiposity and glycemic control are associated with past adenovirus infection

artículo científico publicado en 2012

Long-term neural and physiological phenotyping of a single human

artículo científico publicado en 2015

Longitudinal familial analysis of blood pressure involving parametric (co)variance functions

artículo científico publicado en 2003

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

artículo científico publicado en 2014

MACROD2 gene associated with autistic-like traits in a general population sample

artículo científico publicado en 2014

Major quantitative trait locus for resting heart rate maps to a region on chromosome 4.

artículo científico publicado en 2004

Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits.

artículo científico publicado en 2013

Measuring and comparing brain cortical surface area and other areal quantities

artículo científico publicado en 2012

Meta-Analysis of Genome-wide Linkage Studies in BMI and Obesity*

article

Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm

artículo científico publicado en 2013

Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

artículo científico publicado en 2013

Metabolic syndrome is linked to chromosome 7q21 and associated with genetic variants in CD36 and GNAT3 in Mexican Americans

artículo científico publicado en 2012

Methylation of SOCS3 is inversely associated with metabolic syndrome in an epigenome-wide association study of obesity

artículo científico publicado en 2016

Minimal Relationship between Local Gyrification and General Cognitive Ability in Humans

scientific article published on 09 February 2020

Modeling methylation data as an additional genetic variance component

Molecular prioritization strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1.

artículo científico publicado en 2013

Multi-region hemispheric specialization differentiates human from nonhuman primate brain function

artículo científico publicado en 2013

Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA-DTI working group

artículo científico publicado en 2013

Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling

artículo científico publicado en 2014

Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

artículo científico publicado en 2016

Multiple QTLs influence variation in paraoxonase 1 activity in Mexican Americans

artículo científico publicado en 2006

Neurocognitive endophenotypes in a multiplex multigenerational family study of schizophrenia

artículo científico publicado en 2007

Neurocognitive impairment in type 2 diabetes: evidence for shared genetic aetiology

artículo científico publicado en 2020

Neurodegenerative disease biomarkers Aβ1-40, Aβ1-42, tau, and p-tau181 in the vervet monkey cerebrospinal fluid: Relation to normal aging, genetic influences, and cerebral amyloid angiopathy

artículo científico publicado en 2018

Neuroimaging endophenotypes: strategies for finding genes influencing brain structure and function

artículo científico publicado en 2007

Neurostructural subgroup in 4291 individuals with schizophrenia identified using the subtype and stage inference algorithm

artículo científico publicado en 2024

New approaches for the discovery of lipid‑related genes

scientific article published on 01 January 2011

New genetic loci link adipose and insulin biology to body fat distribution

artículo científico publicado en 2015

New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk ⬇️

artículo científico publicado en 2016

Non-crossover gene conversions show strong GC bias and unexpected clustering in humans

artículo científico publicado en 2015

Nonsyndromic brachydactyly type D and type E mapped to 7p15 in healthy children and adults from the Jirel ethnic group in eastern Nepal

artículo científico publicado en 2013

Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders

artículo científico publicado en 2014

Novel associations of nonstructural Loci with paraoxonase activity

artículo científico publicado en 2012

Novel epigenetic determinants of type 2 diabetes in Mexican-American families

artículo científico publicado en 2015

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

OP004. A SNP associated with susceptibility to preeclampsia near the inhibin, beta B gene, is also associated with cardiovascular disease risk traits

artículo científico publicado en 2013

Obesity, central adiposity and cardiometabolic risk factors in children and adolescents: a family-based study

artículo científico publicado en 2014

Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19.

artículo científico publicado en 2016

On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis

artículo científico publicado en 2003

On study design in neuroimaging heritability analyses

On the genetic architecture of cortical folding and brain volume in primates

artículo científico publicado en 2010

P2 Promoter Variants of the Hepatocyte Nuclear Factor 4 Gene Are Associated With Type 2 Diabetes in Mexican Americans

article

Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model

artículo científico publicado en 2010

Pedigree-based random effect tests to screen gene pathways

artículo científico publicado en 2014

Percent of oxygen saturation of arterial hemoglobin among Bolivian Aymara at 3,900-4,000 m

artículo científico publicado en 1999

Phenotypic, genetic, and genome-wide structure in the metabolic syndrome

artículo científico publicado en 2003

Phenotypical characterisation of the isolated norfolk island population focusing on epidemiological indicators of cardiovascular disease.

artículo científico publicado en 2005

Plasma dihydroceramide species associate with waist circumference in Mexican American families

artículo científico publicado en 2013

Plasma levels of soluble interleukin 1 receptor accessory protein are reduced in obesity

artículo científico publicado en 2014

Plasma lipid profiling in a large population-based cohort

artículo científico publicado en 2013

Plasma lipid profiling shows similar associations with prediabetes and type 2 diabetes

artículo científico publicado en 2013

Plasma lipidome is independently associated with variability in metabolic syndrome in Mexican American families

artículo científico publicado en 2014

Plasma lipidomic profile signature of hypertension in Mexican American families: specific role of diacylglycerols

scientific article published on 24 June 2013

Pleiotropic QTL on chromosome 12q23-q24 influences triglyceride and high-density lipoprotein cholesterol levels: the HERITAGE family study

artículo científico publicado en 2006

Pleiotropic QTL on chromosome 19q13 for triglycerides and adiposity: the HERITAGE Family Study

artículo científico publicado en 2005

Pleiotropic effects of genes for insulin resistance on adiposity in baboons

artículo científico publicado en 2004

Pleiotropic locus for emotion recognition and amygdala volume identified using univariate and bivariate linkage

artículo científico publicado en 2014

Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study

artículo científico publicado en 2017

Power Estimates for Voxel-Based Genetic Association Studies Using Diffusion Imaging

article

Power of variance component linkage analysis to detect epistasis

artículo científico publicado en 1997

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

artículo científico publicado en 2023

Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22.

artículo científico publicado en 2014

Presentation, heritability, and genome-wide linkage analysis of the midchildhood growth spurt in healthy children from the Fels Longitudinal Study

artículo científico publicado en 2008

Principal component and linkage analysis of cardiovascular risk traits in the Norfolk isolate

artículo científico publicado en 2009

Principal component for metabolic syndrome risk maps to chromosome 4p in Mexican Americans: the San Antonio Family Heart Study.

artículo científico publicado en 2004

Progressive Bidirectional Age-Related Changes in Default Mode Network Effective Connectivity across Six Decades

artículo científico publicado en 2016

Prosaposin is a regulator of progranulin levels and oligomerization

artículo científico publicado en 2016

Protein C levels are regulated by a quantitative trait locus on chromosome 16: results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project

artículo científico publicado en 2004

Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

artículo científico publicado en 2018

Quantitative HLA-class-II/factor VIII (FVIII) peptidomic variation in dendritic cells correlates with the immunogenic potential of therapeutic FVIII proteins in hemophilia A

artículo científico publicado en 2020

Quantitative genetic analysis of glucose transporter 4 mRNA levels in baboon adipose

artículo científico publicado en 2004

Quantitative genetics of sexual dimorphism in body fat measurements

article

Quantitative physical activity assessment of children and adolescents in a rural population from Eastern Nepal

artículo científico publicado en 2015

Quantitative trait loci on chromosomes 2p, 4p, and 13q influence bone mineral density of the forearm and hip in Mexican Americans

artículo científico publicado en 2003

Quantitative trait locus determining dietary macronutrient intakes is located on human chromosome 2p22

artículo científico publicado en 2004

Quantitative trait locus on Chromosome 19 for circulating levels of intercellular adhesion molecule-1 in Mexican Americans

artículo científico publicado en 2006

Quantitative trait locus on chromosome 1q influences bone loss in young Mexican American adults

artículo científico publicado en 2008

Quantitative trait nucleotide analysis using Bayesian model selection

artículo científico publicado en 2005

Quantitative trait nucleotide analysis using Bayesian model selection. 2005.

artículo científico publicado en 2009

Rapid, Phase-free Detection of Long Identity-by-Descent Segments Enables Effective Relationship Classification

scientific article published on 19 March 2020

Rare DEGS1 variant significantly alters de novo ceramide synthesis pathway

artículo científico publicado en 2019

Recurrent major depression and right hippocampal volume: A bivariate linkage and association study

artículo científico publicado en 2015

Rediscovering the value of families for psychiatric genetics research

article

Reliability of genomic predictions of complex human phenotypes

Response to Comment on: Lin et al. Long-term changes in adiposity and glycemic control are associated with past adenovirus infection. Diabetes Care 2013;36:701-707.

artículo científico publicado en 2013

Role of miRNA-mRNA Interaction in Neural Stem Cell Differentiation of Induced Pluripotent Stem Cells

scientific article published on 23 September 2020

SORCS1: a novel human type 2 diabetes susceptibility gene suggested by the mouse

artículo científico publicado en 2007

SU74THE POTENTIAL OF LOCAL GYRIFICATION INDEX AS A NEUROPHENOTYPE

artículo científico publicado en 2019

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2017

Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels

artículo científico publicado en 2009

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

artículo científico publicado en 2019

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

artículo científico publicado en 2021

Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits

artículo científico publicado en 2015

Seroprevalence of 13 common pathogens in a rapidly growing U.S. minority population: Mexican Americans from San Antonio, TX

artículo científico publicado en 2011

Serum phosphatidylinositol as a biomarker for bipolar disorder liability

artículo científico publicado en 2017

Sex-specific QTL effects on variation in paraoxonase 1 (PON1) activity in Mexican Americans

artículo científico publicado en 2007

Sex-specific genetic effects in physical activity: results from a quantitative genetic analysis

artículo científico publicado en 2015

Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait loci

artículo científico publicado en 2012

Shared Genetic Factors Influence Head Motion During MRI and Body Mass Index

artículo científico publicado en 2016

Shared genetic factors influence amygdala volumes and risk for alcoholism

artículo científico publicado en 2014

Shared genetic variance between obesity and white matter integrity in Mexican Americans

artículo científico publicado en 2015

Smoothing of the bivariate LOD score for non-normal quantitative traits

artículo científico publicado en 2005

Soluble Forms of Intercellular and Vascular Cell Adhesion Molecules Independently Predict Progression to Type 2 Diabetes in Mexican American Families

artículo científico publicado en 2016

Statin action favors normalization of the plasma lipidome in the atherogenic mixed dyslipidemia of MetS: potential relevance to statin-associated dysglycemia

artículo científico publicado en 2015

Strategy and model building in the fourth dimension: a null model for genotype x age interaction as a Gaussian stationary stochastic process

artículo científico publicado en 2003

Sulcal depth-position profile is a genetically mediated neuroscientific trait: description and characterization in the central sulcus

scientific article published on September 2013

Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs

artículo científico publicado en 2014

Systems genetics of the nuclear factor-κB signal transduction network. I. Detection of several quantitative trait loci potentially relevant to aging

artículo científico publicado en 2011

TRAK2, a novel regulator of ABCA1 expression, cholesterol efflux and HDL biogenesis.

artículo científico publicado en 2017

Testing the hypothesis of accelerated cerebral white matter aging in schizophrenia and major depression

artículo científico publicado en 2012

The 27-bp repeat polymorphism in intron 4 (27 bp-VNTR) of endothelial nitric oxide synthase (eNOS) gene is associated with albumin to creatinine ratio in Mexican Americans

artículo científico publicado en 2009

The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cells

artículo científico publicado en 2011

The Arg59Trp variant in ANGPTL8 (betatrophin) is associated with total and HDL-cholesterol in American Indians and Mexican Americans and differentially affects cleavage of ANGPTL3.

artículo científico publicado en 2016

The Cys(311)Ser polymorphism of paraoxonase 2 (PON2) is associated with albumin-to-creatinine ratio (ACR) in Mexican Americans

artículo científico publicado en 2007

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

artículo científico publicado en 2014

The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations

artículo científico publicado en 2009

The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus.

artículo científico publicado en 2005

The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus. 2005.

artículo científico publicado en 2009

The Factor II (FII) Expression Quantitative Trait Locus (eQTL) Prothrombin G20210A Is Pleiotropically Associated with Plasma Fibrinogen Levels and Has a Profound Effect on Obesity in Mexican Americans of South Texas

artículo científico publicado en 2021

The Genetic Basis of Plasma Variation in Adiponectin, a Global Endophenotype for Obesity and the Metabolic Syndrome

artículo científico publicado en 2001

The Gly(972)Arg variant of human IRS1 gene is associated with variation in glomerular filtration rate likely through impaired insulin receptor signaling

artículo científico publicado en 2012

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2015

The Processing-Speed Impairment in Psychosis Is More Than Just Accelerated Aging

artículo científico publicado en 2017

The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions

artículo científico publicado en 2015

The Ser(326)Cys polymorphism of 8-oxoguanine glycosylase 1 (OGG1) is associated with type 2 diabetes in Mexican Americans

artículo científico publicado en 2010

The baboon as a nonhuman primate model for the study of the genetics of obesity

artículo científico publicado en 2003

The characterization of Abelson helper integration site-1 in skeletal muscle and its links to the metabolic syndrome

scientific journal article

The functional connectivity of the human caudate: an application of meta-analytic connectivity modeling with behavioral filtering

artículo científico publicado en 2011

The genes influencing adiponectin levels also influence risk factors for metabolic syndrome and type 2 diabetes

artículo científico publicado en 2007

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

The genetic architecture of type 2 diabetes

artículo científico publicado en 2016

The genetic basis of the comorbidity between cannabis use and major depression

artículo científico publicado en 2016

The genetics of obesity in Mexican Americans: the evidence from genome scanning efforts in the San Antonio family heart study

scientific article published on 01 October 2003

The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness

artículo científico publicado en 2010

The positive association of obesity variants with adulthood adiposity strengthens over an 80-year period: a gene-by-birth year interaction

artículo científico publicado en 2013

The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratification

artículo científico publicado en 2005

The reliability and heritability of cortical folds and their genetic correlations across hemispheres

artículo científico publicado en 2020

The transcriptional landscape of age in human peripheral blood

artículo científico publicado en 2015

Thromboplastin-thrombomodulin-mediated time and serum folate levels are genetically correlated with the risk of thromboembolic disease: results from the GAIT project.

artículo científico publicado en 2002

Toward the identification of causal genes in complex diseases: a gene-centric joint test of significance combining genomic and transcriptomic data

artículo científico publicado en 2009

Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms

artículo científico publicado en 2016

Transcriptomic Profiling of Fibropapillomatosis in Green Sea Turtles (<i>Chelonia mydas</i>) From South Texas

artículo científico publicado en 2021

Transcriptomic epidemiology of smoking: the effect of smoking on gene expression in lymphocytes

artículo científico publicado en 2010

Transcriptomic identification of ADH1B as a novel candidate gene for obesity and insulin resistance in human adipose tissue in Mexican Americans from the Veterans Administration Genetic Epidemiology Study (VAGES)

artículo científico publicado en 2015

Transcriptomics in type 2 diabetes: Bridging the gap between genotype and phenotype

artículo científico publicado en 2015

Two quantitative trait loci influence whipworm (Trichuris trichiura) infection in a Nepalese population

artículo científico publicado en 2008

Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis

artículo científico publicado en 2023

Type I error rates in association versus joint linkage/association tests in related individuals

artículo científico publicado en 2007

UniMóvil: A Mobile Health Clinic Providing Primary Care to the Colonias of the Rio Grande Valley, South Texas

scientific article published on 21 August 2019

Unifying ideas for non-parametric linkage analysis

artículo científico publicado en 2011

Update to Blangero et al.'s "Quantitative trait nucleotide analysis using Bayesian model selection" (2005): from QTL localization to functional variant identification

artículo científico publicado en 2009

Update to Blangero's "Statistical genetic approaches to human adaptability" (1993): a unified theory of genotype x environment interaction

artículo científico publicado en 2009

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

artículo científico publicado en 2019

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

artículo científico publicado en 2019

Using the Schmahmann Syndrome Scale to Assess Cognitive Impairment in Young Adults with Metabolic Syndrome: a Hypothesis-Generating Report

artículo científico publicado en 2020

Utility of Lymphoblastoid Cell Lines for Induced Pluripotent Stem Cell Generation

artículo científico publicado en 2016

Utilizing extended pedigree information for discovery and confirmation of copy number variable regions among Mexican Americans

artículo científico publicado en 2012

Variability in associations of phosphatidylcholine molecular species with metabolic syndrome in Mexican-American families

artículo científico publicado en 2013

Variance component methods for analysis of complex phenotypes

artículo científico publicado en 2010

Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos

artículo científico publicado en 2012

Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate

artículo científico publicado en 2011

Ventilation and hypoxic ventilatory response of Tibetan and Aymara high altitude natives

artículo científico publicado en 1997

Waist circumference independently associates with the risk of insulin resistance and type 2 diabetes in mexican american families

artículo científico publicado en 2013

Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses

artículo científico publicado en 2010

Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

artículo científico publicado en 2017

Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity.

artículo científico publicado en 2018

Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes

scientific article published on 01 May 2019

Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

artículo científico publicado en 2021

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes

artículo científico publicado en 2014

Why endophenotype development requires families

article

X chromosome effects and their interactions with mitochondrial effects

artículo científico publicado en 2005

microRNA and mRNA interactions in induced pluripotent stem cell reprogramming of lymphoblastoid cell lines

scientific article published on 15 August 2019

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