Lista de obras -

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

artículo científico publicado en 2013

A variance component-based gene burden test

artículo científico publicado en 2014

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

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

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

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

artículo científico publicado en 2015

Epigenetics, heritability and longitudinal analysis

scientific article published on 17 September 2018

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

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

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Filtering genetic variants and placing informative priors based on putative biological function.

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Genetic and Molecular Basis of Drug Resistance and Species-Specific Drug Action in Schistosome Parasites

artículo científico publicado en 2013

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

artículo científico publicado en 2021

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

artículo científico publicado en 2016

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

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

artículo científico publicado en 2014

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Independent test assessment using the extreme value distribution theory

artículo científico publicado en 2016

Modeling methylation data as an additional genetic variance component

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

artículo científico publicado en 2016

Pathway analysis approaches for rare and common variants: insights from Genetic Analysis Workshop 18.

artículo científico publicado en 2014

Pedigree-based random effect tests to screen gene pathways

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

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

artículo científico publicado en 2017

Prosaposin is a regulator of progranulin levels and oligomerization

artículo científico publicado en 2016

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

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

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

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

artículo científico publicado en 2017

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

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

artículo científico publicado en 2014

Lista de obras de

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

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

A variance component-based gene burden test

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

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

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

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

Epigenetics, heritability and longitudinal analysis

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

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

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

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

Filtering genetic variants and placing informative priors based on putative biological function.

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

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

Genetic and Molecular Basis of Drug Resistance and Species-Specific Drug Action in Schistosome Parasites

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

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

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

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

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

Identification of common variants associated with human hippocampal and intracranial volumes

Independent test assessment using the extreme value distribution theory

Modeling methylation data as an additional genetic variance component

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

Pathway analysis approaches for rare and common variants: insights from Genetic Analysis Workshop 18.

Pedigree-based random effect tests to screen gene pathways

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

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

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

Prosaposin is a regulator of progranulin levels and oligomerization

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

Rare DEGS1 variant significantly alters de novo ceramide synthesis pathway

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

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

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

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

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