Daniel P. Howrigan, Ph.D.
Affiliations: | 2012 | Psychology | University of Colorado, Boulder, Boulder, CO, United States |
Area:
Genetics, Clinical PsychologyGoogle:
"Daniel Howrigan"Mean distance: 42746.4
Parents
Sign in to add mentor| Matthew B. McQueen | grad student | 2012 | CU Boulder | |
| (Non-Traditional Approaches to Interrogating Genome-Wide SNP Data.) | ||||
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Publications
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| Karczewski KJ, Solomonson M, Chao KR, et al. (2022) Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes. Cell Genomics. 2: 100168 |
| Palmer DS, Howrigan DP, Chapman SB, et al. (2022) Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia. Nature Genetics |
| Trubetskoy V, Pardiñas AF, Qi T, et al. (2022) Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature |
| Niestroj LM, Perez-Palma E, Howrigan DP, et al. (2020) Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects. Brain : a Journal of Neurology |
| Howrigan DP, Rose SA, Samocha KE, et al. (2020) Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations. Nature Neuroscience |
| Farhan SMK, Howrigan DP, Abbott LE, et al. (2019) Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. Nature Neuroscience |
| Taylor JL, Debost JPG, Morton SU, et al. (2019) Paternal-age-related de novo mutations and risk for five disorders. Nature Communications. 10: 3043 |
| Grove J, Ripke S, Als TD, et al. (2019) Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics |
| Carey C, Shafee R, Walters R, et al. (2019) 29GENETIC ASSOCIATIONS BETWEEN PSYCHIATRIC DISORDER RISK AND PHENOTYPIC FACTORS IN THE UK BIOBANK European Neuropsychopharmacology. 29: S1082-S1083 |
| Zayats T, Martin J, Thiruvahindrapuram B, et al. (2019) A Contribution Of Rare Copy Number Variations To The Development Of Attention Deficit Hyperactivity Disorder: Genome-Wide Meta-Analyses In 12548 Individuals European Neuropsychopharmacology. 29 |