Lista de obras - Julian Maller - Dominio Público Uruguay

A fine-scale chimpanzee genetic map from population sequencing

artículo científico publicado en 2012

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

ASD and ADHD have a similar burden of rare protein-truncating variants

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

artículo científico publicado en 2019

Bayesian refinement of association signals for 14 loci in 3 common diseases

artículo científico publicado en 2012

Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13

artículo científico publicado en 2008

Common risk variants identified in autism spectrum disorder

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration

artículo científico publicado en 2006

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

scholarly article published 3 June 2017

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

artículo científico publicado en 2018

Evaluating and improving power in whole-genome association studies using fixed marker sets

artículo científico publicado en 2006

Evoker: a visualization tool for genotype intensity data

artículo científico publicado en 2010

Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approach

artículo científico publicado en 2009

Genome-wide association scan of attention deficit hyperactivity disorder

artículo científico publicado en 2008

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

scientific journal article

Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder

artículo científico publicado en 2008

Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae

artículo científico publicado en 2009

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

artículo científico publicado en 2010

Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae

scientific article published on 15 February 2009

Genome-wide detection and characterization of positive selection in human populations

artículo científico publicado en 2007

Haploview: analysis and visualization of LD and haplotype maps

artículo científico publicado en 2005

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.

artículo científico publicado en 2016

Identification of common genetic risk variants for autism spectrum disorder

artículo científico publicado en 2019

Integrated detection and population-genetic analysis of SNPs and copy number variation

artículo científico publicado en 2008

PLINK: a tool set for whole-genome association and population-based linkage analyses

artículo científico publicado en 2007

Prediction model for prevalence and incidence of advanced age-related macular degeneration based on genetic, demographic, and environmental variables

artículo científico publicado en 2008

Reply to Cipriani et al.

artículo científico publicado en 2011

Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae

artículo científico publicado en 2009

Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

artículo científico publicado en 2007

Variation in complement factor 3 is associated with risk of age-related macular degeneration

artículo científico publicado en 2007

Variation near complement factor I is associated with risk of advanced AMD

artículo científico publicado en 2009

Lista de obras de Julian Maller

A fine-scale chimpanzee genetic map from population sequencing

A second generation human haplotype map of over 3.1 million SNPs

ASD and ADHD have a similar burden of rare protein-truncating variants

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Bayesian refinement of association signals for 14 loci in 3 common diseases

Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13

Common risk variants identified in autism spectrum disorder

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Evaluating and improving power in whole-genome association studies using fixed marker sets

Evoker: a visualization tool for genotype intensity data

Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approach

Genome-wide association scan of attention deficit hyperactivity disorder

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder

Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae

Genome-wide detection and characterization of positive selection in human populations

Haploview: analysis and visualization of LD and haplotype maps

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.

Identification of common genetic risk variants for autism spectrum disorder

Integrated detection and population-genetic analysis of SNPs and copy number variation

PLINK: a tool set for whole-genome association and population-based linkage analyses

Prediction model for prevalence and incidence of advanced age-related macular degeneration based on genetic, demographic, and environmental variables

Reply to Cipriani et al.

Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae

Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

Variation in complement factor 3 is associated with risk of age-related macular degeneration

Variation near complement factor I is associated with risk of advanced AMD