Author details

Full Name

Daniel P Howrigan

Affiliation

ORCID

Career Start Year

2011

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35410376	Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia.	Nat Genet	2022
35396580	Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Nature	2022
35396579	Rare coding variants in ten genes confer substantial risk for schizophrenia.	Nature	2022
34467851	Human genetic analyses of organelles highlight the nucleus in age-related trait heritability.	Elife	2021
31932770	Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.	Nat Neurosci	2020
31857710	Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein.	Nat Neurosci	2020
31171447	SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse.	Neuron	2019
31768050	Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein.	Nat Neurosci	2019
30392412	Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.	Am J Psychiatry	2019
30478444	Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.	Nat Genet	2019
31292440	Paternal-age-related de novo mutations and risk for five disorders.	Nat Commun	2019
30279509	Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.	Nat Commun	2018
28191890	Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.	Nat Genet	2017
28756411	Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies.	J Med Genet	2017
28671696	Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders.	Nat Neurosci	2017
29042551	Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder.	Nat Commun	2017
27869829	Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.	Nat Genet	2017
27535533	Analysis of protein-coding genetic variation in 60,706 humans.	Nature	2016
26390830	Genome-wide autozygosity is associated with lower general cognitive ability.	Mol Psychiatry	2016
27694993	Ultra-rare disruptive and damaging mutations influence educational attainment in the general population.	Nat Neurosci	2016
27792727	No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.	PLoS Genet	2016
26196440	Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.	Transl Psychiatry	2015
25637581	Genome-Wide Association Study of Behavioral Disinhibition in a Selected Adolescent Sample.	Behavior Genetics	2015
24145379	Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'.	Mol Psychiatry	2014
22511889	Runs of homozygosity implicate autozygosity as a schizophrenia risk factor.	PLoS Genet	2012
21943305	Detecting autozygosity through runs of homozygosity: a comparison of three autozygosity detection algorithms.	BMC Genomics	2011
21480485	Using linkage information to weight a genome-wide association of bipolar disorder.	Am J Med Genet B Neuropsychiatr Genet	2011
22373138	Mutational load analysis of unrelated individuals.	BMC Proceedings	2011