List of works by Daniel P Howrigan

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

Analysis of protein-coding genetic variation in 60,706 humans

scientific article (publication date: 17 August 2016)

Common risk variants identified in autism spectrum disorder

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

scientific article

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

scientific article published on 21 October 2019

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

scientific article published on 26 November 2018

Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein

scientific article published on 25 November 2019

Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations

scientific article published on 13 January 2020

Human genetic analyses of organelles highlight the nucleus in age-related trait heritability

scientific article published in 2021

Identification of common genetic risk variants for autism spectrum disorder

scientific article published on 25 February 2019

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

scientific article

Paternal-age-related de novo mutations and risk for five disorders

scientific article published on 10 July 2019

Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein

scientific article published on 01 February 2020

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

scientific article published on 03 October 2016

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

article

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