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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 bias-ed assessment of the use of SNPs in human complex traits

artículo científico publicado en 2002

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

artículo científico publicado en 2006

A novel obesity locus on chromosome 4q: the Strong Heart Family Study

scientific article published on 01 July 2007

A quantitative trait loci-specific gene-by-sex interaction on systolic blood pressure among American Indians: the Strong Heart Family Study

article

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

artículo científico publicado en 2006

A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5.

artículo científico publicado en 2008

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

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

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

Association of TMTC2 With Human Nonsyndromic Sensorineural Hearing Loss

scientific article published on 16 June 2016

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

artículo científico publicado en 2012

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

artículo científico publicado en 2010

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

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

Comparison of strategies for identification of regulatory quantitative trait loci of transcript expression traits

artículo científico publicado en 2007

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

artículo científico publicado en 2018

Detection of a quantitative trait locus associated with resistance to Ascaris suum infection in pigs

artículo científico publicado en 2012

Diabetes-specific genetic effects on obesity traits in American Indian populations: the Strong Heart Family Study

artículo científico publicado en 2008

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

Do rare variant genotypes predict common variant genotypes?

artículo científico publicado en 2011

Dopamine perturbation of gene co-expression networks reveals differential response in schizophrenia for translational machinery

article

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

artículo científico publicado en 2015

Epigenetic Age Acceleration Assessed with Human White-Matter Images.

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

Evidence for a founder effect for pseudoxanthoma elasticum in the Afrikaner population of South Africa

artículo científico publicado en 2002

Exome sequences of multiplex, multigenerational families reveal schizophrenia risk loci with potential implications for neurocognitive performance

artículo científico publicado en 2017

F145. Extremely Weak Relationship Between Gyrification and Intelligence

scientific article published in 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2006

Functional study of a genetic marker allele associated with resistance to Ascaris suum in pigs

artículo científico publicado en 2014

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 mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design. 2000.

artículo científico publicado en 2009

Genetic and environmental factors in familial clustering in physical activity

artículo científico publicado en 2008

Genetic and environmental influences on thyroid hormone variation in Mexican Americans

artículo científico publicado en 2004

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

artículo científico publicado en 2013

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 determinants of mitochondrial content

article

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

artículo científico publicado en 2013

Genetic factors influence serological measures of common infections ⬇️

artículo científico publicado el 11 de octubre de 2011

Genetic influence on variation in serum uric acid in American Indians: the strong heart family study

artículo científico publicado en 2009

Genetic influences of sports participation in Portuguese families

artículo científico publicado en 2013

Genetic influences on serum bilirubin in American Indians: The Strong Heart Family Study

artículo científico publicado en 2011

Genetic variation at the FTO locus influences RBL2 gene expression

artículo científico publicado en 2009

Genetic variation in APOJ, LPL, and TNFRSF10B affects plasma fatty acid distribution in Alaskan Eskimos

artículo científico publicado en 2010

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

artículo científico publicado en 2016

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

artículo científico publicado en 2012

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 of carotid artery lumen diameter: the strong heart family study

artículo científico publicado en 2013

Genome-wide linkage analysis of pulse pressure in American Indians: the Strong Heart Study

artículo científico publicado en 2008

Genome-wide scan for serum ghrelin detects linkage on chromosome 1p36 in Hispanic children: results from the Viva La Familia study

artículo científico publicado en 2007

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

Genotype phasing in pedigrees using whole-genome sequence data

scientific article published on 29 January 2020

Genotype×age interaction in human transcriptional ageing

artículo científico publicado en 2012

Global metabolomic profiling targeting childhood obesity in the Hispanic population

artículo científico publicado en 2015

Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

artículo científico publicado en 2009

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

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

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Identity-by-Descent Mapping Identifies Major Locus for Serum Triglycerides in Amerindians Largely Explained by an APOC3 Founder Mutation

artículo científico publicado en 2017

Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle

artículo científico publicado en 2002

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

artículo científico publicado en 2014

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

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

artículo científico publicado en 2016

Linkage analysis of albuminuria

scientific article published on 15 April 2009

Linkage analysis of factors underlying insulin resistance: Strong Heart Family Study

artículo científico publicado en 2005

Linkage analysis of glomerular filtration rate in American Indians.

artículo científico publicado en 2008

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 study of fibrinogen levels: the Strong Heart Family Study

artículo científico publicado en 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

Mapping of a blood pressure QTL on chromosome 17 in American Indians of the strong heart family study

artículo científico publicado en 2014

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

Mother-to-child transmission of HIV-1: strong association with certain maternal HLA-B alleles independent of viral load implicates innate immune mechanisms

artículo científico publicado en 2004

Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa

artículo científico publicado en 2009

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

artículo científico publicado en 2020

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

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 the statistical properties of family-based association tests in datasets containing both pedigrees and unrelated case-control samples

artículo científico publicado en 2011

On the validity of the likelihood ratio test and consistency of resulting parameter estimates in joint linkage and linkage disequilibrium analysis under improperly specified parametric models

artículo científico publicado en 2011

PSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus

artículo científico publicado en 2005

Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expression

artículo científico publicado en 2012

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

artículo científico publicado en 2006

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

Radiologic Phenotypes in Lumbar MR Imaging for a Gene Defect in theCOL9A3Gene of Type IX Collagen

artículo científico publicado en 2003

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

artículo científico publicado en 2015

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

Serum phosphatidylinositol as a biomarker for bipolar disorder liability

artículo científico publicado en 2017

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

Social- and behavioral-specific genetic effects on blood pressure traits: the Strong Heart Family Study

scientific article published on 16 June 2009

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

Statistical Genetic Analysis of Serological Measures of Common, Chronic Infections in Alaska Native Participants in the GOCADAN Study ⬇️

artículo científico publicado el 24 de junio de 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

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

artículo científico publicado en 2014

The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study

artículo científico publicado en 2010

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

artículo científico publicado en 2016

The transcriptional landscape of age in human peripheral blood

artículo científico publicado en 2015

Tissue specificity of genetic regulation of gene expression ⬇️

artículo científico publicado el 1 de octubre de 2012

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

Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants

artículo científico publicado en 2015

Transcriptome study of differential expression in schizophrenia ⬇️

artículo científico publicado el 30 de julio de 2013

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

Transcriptomic signatures of schizophrenia revealed by dopamine perturbation in an ex vivo model

scholarly article by Jubao Duan et al published 16 August 2018 in Translational Psychiatry

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

artículo científico publicado en 2015

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

artículo científico publicado en 2007

Update to Terwilliger and Göring's "Gene mapping in the 20th and 21st centuries" (2000): gene mapping when rare variants are common and common variants are rare

scientific article published on 01 December 2009

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

artículo científico publicado en 2012

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

Whole Genome Sequence Data From Captive Baboons Implicate <i>RBFOX1</i> in Epileptic Seizure Risk

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

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