List of works - Alejandro Q Nato

Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP

scientific article published on 03 June 2018

Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees

scientific article published on 04 December 2018

Estimating relationships between phenotypes and subjects drawn from admixed families

scientific article

GIGI-Quick: A Fast Approach to Impute Missing Genotypes in Genome-Wide Association Family Data

scientific article published on 18 December 2017

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

scientific article

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project

scientific article published on 27 February 2018

Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) study

scientific article

Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data.

scientific article

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

scientific article published on 17 June 2014

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.

scientific article

No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population

scientific article published on 08 October 2013

PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers

scientific article

Post-genome-wide association study challenges for lipid traits: describing age as a modifier of gene-lipid associations in the Population Architecture using Genomics and Epidemiology (PAGE) study

scientific article published on 28 June 2013

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project

article

Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error.

scientific article published on January 2012

The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation

scientific article

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes

scientific article

List of works by Alejandro Q Nato

Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP

Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees

Estimating relationships between phenotypes and subjects drawn from admixed families

GIGI-Quick: A Fast Approach to Impute Missing Genotypes in Genome-Wide Association Family Data

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project

Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) study

Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data.

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.

No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population

PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers

Post-genome-wide association study challenges for lipid traits: describing age as a modifier of gene-lipid associations in the Population Architecture using Genomics and Epidemiology (PAGE) study

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project

Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error.

The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes