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Full Name
Julian B Maller
Affiliation
Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
ORCID
Career Start Year
2005
Papers
31
H Index
26
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
30478444
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Nat Genet
2019
30478444
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Nat Genet
2019
28044064
ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties.
Mol Psychiatry
2018
29279374
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Proc Natl Acad Sci U S A
2018
28044064
ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties.
Mol Psychiatry
2018
29279374
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Proc Natl Acad Sci U S A
2018
26998691
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
Nat Genet
2016
27089011
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.
PLoS One
2016
27367377
Measurement of the Radiation Energy in the Radio Signal of Extensive Air Showers as a Universal Estimator of Cosmic-Ray Energy.
Phys Rev Lett
2016
26998691
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
Nat Genet
2016
27367377
Measurement of the Radiation Energy in the Radio Signal of Extensive Air Showers as a Universal Estimator of Cosmic-Ray Energy.
Phys Rev Lett
2016
27089011
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.
PLoS One
2016
25954003
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.
Science
2015
25954003
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.
Science
2015
26120280
Search for patterns by combining cosmic-ray energy and arrival directions at the Pierre Auger Observatory.
Eur Phys J C Part Fields
2015
26120280
Search for patterns by combining cosmic-ray energy and arrival directions at the Pierre Auger Observatory.
Eur Phys J C Part Fields
2015
22422862
A fine-scale chimpanzee genetic map from population sequencing.
Science
2012
22422862
A fine-scale chimpanzee genetic map from population sequencing.
Science
2012
23104008
Bayesian refinement of association signals for 14 loci in 3 common diseases.
Nat Genet
2012
23104008
Bayesian refinement of association signals for 14 loci in 3 common diseases.
Nat Genet
2012
19844262
Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approach.
Eur J Hum Genet
2010
19844262
Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approach.
Eur J Hum Genet
2010
20507892
Evoker: a visualization tool for genotype intensity data.
Bioinformatics
2010
20360734
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
Nature
2010
20507892
Evoker: a visualization tool for genotype intensity data.
Bioinformatics
2010
20360734
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
Nature
2010
18685559
Variation near complement factor I is associated with risk of advanced AMD.
Eur J Hum Genet
2009
19389651
Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae.
Heart Rhythm
2009
19117936
Prediction model for prevalence and incidence of advanced age-related macular degeneration based on genetic, demographic, and environmental variables.
Invest Ophthalmol Vis Sci
2009
19667188
Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae.
Proc Natl Acad Sci U S A
2009
19197348
Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
PLoS Genet
2009
18685559
Variation near complement factor I is associated with risk of advanced AMD.
Eur J Hum Genet
2009
19667188
Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae.
Proc Natl Acad Sci U S A
2009
19389651
Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae.
Heart Rhythm
2009
19117936
Prediction model for prevalence and incidence of advanced age-related macular degeneration based on genetic, demographic, and environmental variables.
Invest Ophthalmol Vis Sci
2009
19197348
Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
PLoS Genet
2009
18937294
Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.
Am J Med Genet B Neuropsychiatr Genet
2008
18980221
Genome-wide association scan of attention deficit hyperactivity disorder.
Am J Med Genet B Neuropsychiatr Genet
2008
18802019
Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13.
Arterioscler Thromb Vasc Biol
2008
18776908
Integrated detection and population-genetic analysis of SNPs and copy number variation.
Nat Genet
2008
18937294
Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.
Am J Med Genet B Neuropsychiatr Genet
2008
18821565
Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.
Am J Med Genet B Neuropsychiatr Genet
2008
18821565
Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.
Am J Med Genet B Neuropsychiatr Genet
2008
18776908
Integrated detection and population-genetic analysis of SNPs and copy number variation.
Nat Genet
2008
18802019
Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13.
Arterioscler Thromb Vasc Biol
2008
18980221
Genome-wide association scan of attention deficit hyperactivity disorder.
Am J Med Genet B Neuropsychiatr Genet
2008
17701901
PLINK: a tool set for whole-genome association and population-based linkage analyses.
Am J Hum Genet
2007
17701901
PLINK: a tool set for whole-genome association and population-based linkage analyses.
Am J Hum Genet
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
1 - 50 of 62
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