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Daniel P. Howrigan, Ph.D. - Publications

Affiliations: 
2012 Psychology University of Colorado, Boulder, Boulder, CO, United States 
Area:
Genetics, Clinical Psychology
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30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Boltz TA, Chu BB, Liao C, Sealock JM, Ye R, Majara L, Fu JM, Service S, Zhan L, Medland SE, Chapman SB, Rubinacci S, DeFelice M, Grimsby JL, Abebe T, ... ... Howrigan DP, et al. A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner. Biorxiv : the Preprint Server For Biology. PMID 39282356 DOI: 10.1101/2024.09.06.611689  0.343
2022 Karczewski KJ, Solomonson M, Chao KR, Goodrich JK, Tiao G, Lu W, Riley-Gillis BM, Tsai EA, Kim HI, Zheng X, Rahimov F, Esmaeeli S, Grundstad AJ, Reppell M, Waring J, ... ... Howrigan DP, et al. Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes. Cell Genomics. 2: 100168. PMID 36778668 DOI: 10.1016/j.xgen.2022.100168  0.334
2022 Palmer DS, Howrigan DP, Chapman SB, Adolfsson R, Bass N, Blackwood D, Boks MPM, Chen CY, Churchhouse C, Corvin AP, Craddock N, Curtis D, Di Florio A, Dickerson F, Freimer NB, et al. Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia. Nature Genetics. PMID 35410376 DOI: 10.1038/s41588-022-01034-x  0.312
2022 Trubetskoy V, Pardiñas AF, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli TB, Bryois J, Chen CY, Dennison CA, Hall LS, Lam M, Watanabe K, Frei O, Ge T, Harwood JC, ... ... Howrigan DP, et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. PMID 35396580 DOI: 10.1038/s41586-022-04434-5  0.37
2020 Niestroj LM, Perez-Palma E, Howrigan DP, Zhou Y, Cheng F, Saarentaus E, Nürnberg P, Stevelink R, Daly MJ, Palotie A, Lal D. Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects. Brain : a Journal of Neurology. PMID 32568404 DOI: 10.1093/Brain/Awaa171  0.337
2020 Howrigan DP, Rose SA, Samocha KE, Fromer M, Cerrato F, Chen WJ, Churchhouse C, Chambert K, Chandler SD, Daly MJ, Dumont A, Genovese G, Hwu HG, Laird N, Kosmicki JA, et al. Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations. Nature Neuroscience. PMID 31932770 DOI: 10.1038/S41593-019-0564-3  0.385
2019 Farhan SMK, Howrigan DP, Abbott LE, Klim JR, Topp SD, Byrnes AE, Churchhouse C, Phatnani H, Smith BN, Rampersaud E, Wu G, Wuu J, Shatunov A, Iacoangeli A, Al Khleifat A, et al. Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. Nature Neuroscience. PMID 31768050 DOI: 10.1038/S41593-019-0530-0  0.304
2019 Taylor JL, Debost JPG, Morton SU, Wigdor EM, Heyne HO, Lal D, Howrigan DP, Bloemendal A, Larsen JT, Kosmicki JA, Weiner DJ, Homsy J, Seidman JG, Seidman CE, Agerbo E, et al. Paternal-age-related de novo mutations and risk for five disorders. Nature Communications. 10: 3043. PMID 31292440 DOI: 10.1097/Ogx.0000000000000775  0.34
2019 Grove J, Ripke S, Als TD, Mattheisen M, Walters RK, Won H, Pallesen J, Agerbo E, Andreassen OA, Anney R, Awashti S, Belliveau R, Bettella F, Buxbaum JD, Bybjerg-Grauholm J, ... ... Howrigan DP, et al. Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics. PMID 30804558 DOI: 10.1038/S41588-019-0344-8  0.444
2019 Carey C, Shafee R, Walters R, Palmer D, Abbott L, Howrigan D, Churchhouse C, Neale B, Robinson E. 29GENETIC ASSOCIATIONS BETWEEN PSYCHIATRIC DISORDER RISK AND PHENOTYPIC FACTORS IN THE UK BIOBANK European Neuropsychopharmacology. 29: S1082-S1083. DOI: 10.1016/J.Euroneuro.2018.08.036  0.343
2019 Zayats T, Martin J, Thiruvahindrapuram B, Wang Z, Howrigan D, Shanta O, Neale B, Sebat J. 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. DOI: 10.1016/J.Euroneuro.2018.07.045  0.384
2018 Demontis D, Walters RK, Martin J, Mattheisen M, Als TD, Agerbo E, Baldursson G, Belliveau R, Bybjerg-Grauholm J, Bækvad-Hansen M, Cerrato F, Chambert K, Churchhouse C, Dumont A, Eriksson N, ... ... Howrigan DP, et al. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature Genetics. PMID 30478444 DOI: 10.1038/S41588-018-0269-7  0.341
2018 Bergen SE, Ploner A, Howrigan D, O'Donovan MC, Smoller JW, Sullivan PF, Sebat J, Neale B, Kendler KS. Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia. The American Journal of Psychiatry. appiajp201817040467. PMID 30392412 DOI: 10.1176/Appi.Ajp.2018.17040467  0.451
2018 Regier AA, Farjoun Y, Larson DE, Krasheninina O, Kang HM, Howrigan DP, Chen BJ, Kher M, Banks E, Ames DC, English AC, Li H, Xing J, Zhang Y, Matise T, et al. Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects. Nature Communications. 9: 4038. PMID 30279509 DOI: 10.1038/S41467-018-06159-4  0.392
2018 Bis JC, Jian X, Kunkle BW, Chen Y, Hamilton-Nelson KL, Bush WS, Salerno WJ, Lancour D, Ma Y, Renton AE, Marcora E, Farrell JJ, Zhao Y, Qu L, Ahmad S, ... ... Howrigan DP, et al. Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry. PMID 30108311 DOI: 10.1038/S41380-018-0112-7  0.389
2017 Noh HJ, Tang R, Flannick J, O'Dushlaine C, Swofford R, Howrigan D, Genereux DP, Johnson J, van Grootheest G, Grünblatt E, Andersson E, Djurfeldt DR, Patel PD, Koltookian M, M Hultman C, et al. Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder. Nature Communications. 8: 774. PMID 29042551 DOI: 10.1038/S41467-017-00831-X  0.38
2017 Pérez-Palma E, Helbig I, Klein KM, Anttila V, Horn H, Reinthaler EM, Gormley P, Ganna A, Byrnes A, Pernhorst K, Toliat MR, Saarentaus E, Howrigan DP, Hoffman P, Miquel JF, et al. Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies. Journal of Medical Genetics. PMID 28756411 DOI: 10.1136/Jmedgenet-2016-104495  0.318
2017 Kosmicki JA, Samocha KE, Howrigan DP, Sanders SJ, Slowikowski K, Lek M, Karczewski KJ, Cutler DJ, Devlin B, Roeder K, Buxbaum JD, Neale BM, MacArthur DG, Wall DP, Robinson EB, et al. Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples. Nature Genetics. PMID 28191890 DOI: 10.1038/Ng.3789  0.386
2017 Howrigan D, Samocha K, Kosmicki J, Moran J, Chambert K, Fromer M, Chandler S, Laird N, Hwu H, Chen WJ, Faraone S, Glatt S, Tsuang M, McCarroll S, Neale B. Damaging Missense De Novo Coding Mutations Contribute To Schizophrenia Risk European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.481  0.333
2016 Johnson EC, Bjelland DW, Howrigan DP, Abdellaoui A, Breen G, Borglum A, Cichon S, Degenhardt F, Forstner AJ, Frank J, Genovese G, Heilmann-Heimbach S, Herms S, Hoffman P, Maier W, et al. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. Plos Genetics. 12: e1006343. PMID 27792727 DOI: 10.1371/Journal.Pgen.1006343  0.718
2016 Ganna A, Genovese G, Howrigan DP, Byrnes A, Kurki MI, Zekavat SM, Whelan CW, Kals M, Nivard MG, Bloemendal A, Bloom JM, Goldstein JI, Poterba T, Seed C, Handsaker RE, et al. Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nature Neuroscience. PMID 27694993 DOI: 10.1038/Nn.4404  0.356
2016 Lek M, Karczewski KJ, Minikel EV, Samocha KE, Banks E, Fennell T, O'Donnell-Luria AH, Ware JS, Hill AJ, Cummings BB, Tukiainen T, Birnbaum DP, Kosmicki JA, Duncan LE, Estrada K, ... ... Howrigan D, et al. Analysis of protein-coding genetic variation in 60,706 humans. Nature. 536: 285-291. PMID 27535533 DOI: 10.1038/Nature19057  0.37
2015 Howrigan DP, Simonson MA, Davies G, Harris SE, Tenesa A, Starr JM, Liewald DC, Deary IJ, McRae A, Wright MJ, Montgomery GW, Hansell N, Martin NG, Payton A, Horan M, et al. Genome-wide autozygosity is associated with lower general cognitive ability. Molecular Psychiatry. PMID 26390830 DOI: 10.1038/Mp.2015.120  0.724
2015 Rees E, Kirov G, Walters JT, Richards AL, Howrigan D, Kavanagh DH, Pocklington AJ, Fromer M, Ruderfer DM, Georgieva L, Carrera N, Gormley P, Palta P, Williams H, Dwyer S, et al. Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia. Translational Psychiatry. 5: e607. PMID 26196440 DOI: 10.1038/Tp.2015.99  0.477
2015 Derringer J, Corley RP, Haberstick BC, Young SE, Demmitt BA, Howrigan DP, Kirkpatrick RM, Iacono WG, McGue M, Keller MC, Brown S, Tapert S, Hopfer CJ, Stallings MC, Crowley TJ, et al. Genome-Wide Association Study of Behavioral Disinhibition in a Selected Adolescent Sample. Behavior Genetics. 45: 375-81. PMID 25637581 DOI: 10.1007/S10519-015-9705-Y  0.643
2012 Keller MC, Simonson MA, Ripke S, Neale BM, Gejman PV, Howrigan DP, Lee SH, Lencz T, Levinson DF, Sullivan PF. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. Plos Genetics. 8: e1002656. PMID 22511889 DOI: 10.1371/Journal.Pgen.1002656  0.724
2011 Howrigan DP, Simonson MA, Kamens HM, Stephens SH, Wills AG, Ehringer MA, Keller MC, McQueen MB. Mutational load analysis of unrelated individuals. Bmc Proceedings. 5: S55. PMID 22373138 DOI: 10.1186/1753-6561-5-S9-S55  0.687
2011 Howrigan DP, Simonson MA, Keller MC. Detecting autozygosity through runs of homozygosity: a comparison of three autozygosity detection algorithms. Bmc Genomics. 12: 460. PMID 21943305 DOI: 10.1186/1471-2164-12-460  0.7
2011 Howrigan DP, Laird NM, Smoller JW, Devlin B, McQueen MB. Using linkage information to weight a genome-wide association of bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 462-71. PMID 21480485 DOI: 10.1002/Ajmg.B.31183  0.641
2011 Keller MC, Howrigan DP, Simonson MA. Theory and Methods in Evolutionary Behavioral Genetics The Evolution of Personality and Individual Differences. DOI: 10.1093/acprof:oso/9780195372090.003.0010  0.668
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