Lista de obras -

A Novel Test for Detecting SNP-SNP Interactions in Case-Only Trio Studies

artículo científico publicado en 2016

A model and test for coordinated polygenic epistasis in complex traits

artículo científico publicado en 2021

A nonparametric test to detect quantitative trait loci where the phenotypic distribution differs by genotypes

artículo científico publicado en 2013

Accurate estimation of expression levels of homologous genes in RNA-seq experiments.

artículo científico publicado en 2011

Adapt-Mix: learning local genetic correlation structure improves summary statistics-based analyses

artículo científico publicado en 2015

An ancestry-based approach for detecting interactions

artículo científico publicado en 2017

Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation

artículo científico publicado en 2013

Analysis of case-control association studies with known risk variants

artículo científico publicado en 2012

Author Correction: Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing

scientific article published on 04 September 2020

COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis

artículo científico publicado en 2015

CRISPR-Cas9-mediated functional dissection of 3'-UTRs

artículo científico publicado en 2017

Combining effects from rare and common genetic variants in an exome-wide association study of sequence data

artículo científico publicado en 2011

Comprehensive cell type decomposition of circulating cell-free DNA with CelFiE

artículo científico publicado en 2021

Correcting for cell-type heterogeneity in DNA methylation: a comprehensive evaluation

artículo científico publicado en 2017

Correction: Pleiotropic Mechanisms Indicated for Sex Differences in Autism

artículo científico publicado en 2017

Creating ethnicity-specific reference intervals for lab tests from EHR data

DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome

artículo científico publicado en 2016

Differential methylation between ethnic sub-groups reflects the effect of genetic ancestry and environmental exposures

article

Dual gene activation and knockout screen reveals directional dependencies in genetic networks

artículo científico publicado en 2018

Efficient estimation and applications of cross-validated genetic predictions

Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium

artículo científico publicado en 2011

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

artículo científico publicado en 2012

Fast and accurate imputation of summary statistics enhances evidence of functional enrichment

artículo científico publicado en 2014

GLINT: a user-friendly toolset for the analysis of high-throughput DNA-methylation array data

artículo científico publicado en 2017

Genetic Mechanisms Leading to Sex Differences Across Common Diseases and Anthropometric Traits

artículo científico publicado en 2016

Genetic and environmental components of family history in type 2 diabetes

artículo científico publicado en 2014

Genetic and socioeconomic study of mate choice in Latinos reveals novel assortment patterns

artículo científico publicado en 2015

Genome-wide association study of ancestry-specific TB risk in the South African Coloured population

scientific journal article

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection

artículo científico publicado en 2011

Genome-wide methylation data mirror ancestry information

artículo científico publicado en 2017

Genotyping common and rare variation using overlapping pool sequencing

artículo científico publicado en 2011

Heritability in the genome-wide association era

artículo científico publicado en 2012

Heritable natural variation of an anxiety-like behavior in larval zebrafish

artículo científico publicado en 2017

Imputation aware meta-analysis of genome-wide association studies

artículo científico publicado en 2010

Informed conditioning on clinical covariates increases power in case-control association studies

artículo científico publicado en 2012

Intersection of population variation and autoimmunity genetics in human T cell activation

artículo científico publicado en 2014

Leveraging genetic variability across populations for the identification of causal variants.

artículo científico publicado en 2010

Leveraging population admixture to characterize the heritability of complex traits

artículo científico publicado en 2014

Leveraging the HapMap correlation structure in association studies

artículo científico publicado en 2007

Linkage effects and analysis of finite sample errors in the HapMap

artículo científico publicado en 2009

Local Joint Testing Improves Power and Identifies Hidden Heritability in Association Studies

artículo científico publicado en 2016

Massively Parallel Identification of Regulatory Variants in Asthma

artículo científico publicado en 2016

Massively parallel functional annotation of 3' untranslated regions

artículo científico publicado en 2014

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

artículo científico publicado en 2015

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Modeling epistasis in mice and yeast using the proportion of two or more distinct genetic backgrounds: Evidence for "polygenic epistasis"

scientific article published on 26 October 2020

Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression.

artículo científico publicado en 2018

Multi-marker tagging single nucleotide polymorphism selection using estimation of distribution algorithms

artículo científico publicado en 2010

Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors

artículo científico publicado en 2015

Multiplexed droplet single-cell RNA-sequencing using natural genetic variation

artículo científico publicado en 2017

PIGS: improved estimates of identity-by-descent probabilities by probabilistic IBD graph sampling

artículo científico publicado en 2015

Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing

scientific article published on 19 June 2020

Quantifying missing heritability at known GWAS loci

artículo científico publicado en 2013

ROP: dumpster diving in RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues.

artículo científico publicado en 2018

Reverse GWAS: Using genetics to identify and model phenotypic subtypes

article

Shift-invariant adaptive double threading: learning MHC II-peptide binding

artículo científico publicado en 2008

Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies

artículo científico publicado en 2016

The Effects of Migration and Assortative Mating on Admixture Linkage Disequilibrium

artículo científico publicado en 2016

Transethnic Genetic-Correlation Estimates from Summary Statistics

artículo científico publicado en 2016

Ultrarare variants drive substantial cis heritability of human gene expression

artículo científico publicado en 2019

Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits

artículo científico publicado en 2013

Variation in predictive ability of common genetic variants by established strata: the example of breast cancer and age.

artículo científico publicado en 2015

Lista de obras de

A Novel Test for Detecting SNP-SNP Interactions in Case-Only Trio Studies

A model and test for coordinated polygenic epistasis in complex traits

A nonparametric test to detect quantitative trait loci where the phenotypic distribution differs by genotypes

Accurate estimation of expression levels of homologous genes in RNA-seq experiments.

Adapt-Mix: learning local genetic correlation structure improves summary statistics-based analyses

An ancestry-based approach for detecting interactions

Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation

Analysis of case-control association studies with known risk variants

Author Correction: Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing

COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis

CRISPR-Cas9-mediated functional dissection of 3'-UTRs

Combining effects from rare and common genetic variants in an exome-wide association study of sequence data

Comprehensive cell type decomposition of circulating cell-free DNA with CelFiE

Correcting for cell-type heterogeneity in DNA methylation: a comprehensive evaluation

Correction: Pleiotropic Mechanisms Indicated for Sex Differences in Autism

Creating ethnicity-specific reference intervals for lab tests from EHR data

DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome

Differential methylation between ethnic sub-groups reflects the effect of genetic ancestry and environmental exposures

Dual gene activation and knockout screen reveals directional dependencies in genetic networks

Efficient estimation and applications of cross-validated genetic predictions

Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

Fast and accurate imputation of summary statistics enhances evidence of functional enrichment

GLINT: a user-friendly toolset for the analysis of high-throughput DNA-methylation array data

Genetic Mechanisms Leading to Sex Differences Across Common Diseases and Anthropometric Traits

Genetic and environmental components of family history in type 2 diabetes

Genetic and socioeconomic study of mate choice in Latinos reveals novel assortment patterns

Genome-wide association study of ancestry-specific TB risk in the South African Coloured population

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection

Genome-wide methylation data mirror ancestry information

Genotyping common and rare variation using overlapping pool sequencing

Heritability in the genome-wide association era

Heritable natural variation of an anxiety-like behavior in larval zebrafish

Imputation aware meta-analysis of genome-wide association studies

Informed conditioning on clinical covariates increases power in case-control association studies

Intersection of population variation and autoimmunity genetics in human T cell activation

Leveraging genetic variability across populations for the identification of causal variants.

Leveraging population admixture to characterize the heritability of complex traits

Leveraging the HapMap correlation structure in association studies

Linkage effects and analysis of finite sample errors in the HapMap

Local Joint Testing Improves Power and Identifies Hidden Heritability in Association Studies

Massively Parallel Identification of Regulatory Variants in Asthma

Massively parallel functional annotation of 3' untranslated regions

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Modeling epistasis in mice and yeast using the proportion of two or more distinct genetic backgrounds: Evidence for "polygenic epistasis"

Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression.

Multi-marker tagging single nucleotide polymorphism selection using estimation of distribution algorithms

Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors

Multiplexed droplet single-cell RNA-sequencing using natural genetic variation

PIGS: improved estimates of identity-by-descent probabilities by probabilistic IBD graph sampling

Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing

Quantifying missing heritability at known GWAS loci

ROP: dumpster diving in RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues.

Reverse GWAS: Using genetics to identify and model phenotypic subtypes

Shift-invariant adaptive double threading: learning MHC II-peptide binding

Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies

The Effects of Migration and Assortative Mating on Admixture Linkage Disequilibrium

Transethnic Genetic-Correlation Estimates from Summary Statistics

Ultrarare variants drive substantial cis heritability of human gene expression

Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits

Variation in predictive ability of common genetic variants by established strata: the example of breast cancer and age.