List of works - Juan Peralta

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

scientific article published on 22 March 2021

A genome screen for quantitative trait loci influencing schizophrenia and neurocognitive phenotypes

scientific article published on 15 July 2008

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

scientific article

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

scientific article

A variance component-based gene burden test

scientific article

Constrained multivariate association with longitudinal phenotypes

scientific article

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

scientific article

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

scientific article published on 24 August 2020

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

scientific article

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

scientific article published on 17 June 2014

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

scientific article

Genetic Analysis Workshop 17 mini-exome simulation

scientific article

Genotype phasing in pedigrees using whole-genome sequence data

scientific article published on 29 January 2020

Independent test assessment using the extreme value distribution theory

scientific article published on 18 October 2016

Investigation of Genetic Variation Underlying Central Obesity amongst South Asians

scientific article

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

scientific article

Linkage disequilibrium across two different single-nucleotide polymorphism genome scans

scientific article published on 30 December 2005

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

scientific article published on 05 December 2016

Neurocognitive endophenotypes for bipolar disorder identified in multiplex multigenerational families

scientific article

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

scientific article

Pedigree-based random effect tests to screen gene pathways

scientific article published on 17 June 2014

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

scientific article published on 13 March 2014

Prosaposin is a regulator of progranulin levels and oligomerization

scientific article published on 30 June 2016

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

scientific article published on 01 May 2019

List of works by Juan Peralta

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

A genome screen for quantitative trait loci influencing schizophrenia and neurocognitive phenotypes

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

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

A variance component-based gene burden test

Constrained multivariate association with longitudinal phenotypes

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

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

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

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

Genetic Analysis Workshop 17 mini-exome simulation

Genotype phasing in pedigrees using whole-genome sequence data

Independent test assessment using the extreme value distribution theory

Investigation of Genetic Variation Underlying Central Obesity amongst South Asians

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

Linkage disequilibrium across two different single-nucleotide polymorphism genome scans

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

Neurocognitive endophenotypes for bipolar disorder identified in multiplex multigenerational families

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

Pedigree-based random effect tests to screen gene pathways

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

Prosaposin is a regulator of progranulin levels and oligomerization

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