Daniel Howrigan
Daniel Howrigan
Group Leader
Verified email at broadinstitute.org
Title
Cited by
Cited by
Year
Analysis of protein-coding genetic variation in 60,706 humans
M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ...
Nature 536 (7616), 285-291, 2016
67342016
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ...
Nature genetics 51 (1), 63-75, 2019
5982019
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
Nature genetics 49 (1), 27-35, 2017
3812017
Identification of common genetic risk variants for autism spectrum disorder
J Grove, S Ripke, TD Als, M Mattheisen, RK Walters, H Won, J Pallesen, ...
Nature genetics 51 (3), 431-444, 2019
3652019
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
EB Robinson, B St Pourcain, V Anttila, JA Kosmicki, B Bulik-Sullivan, ...
Nature genetics 48 (5), 552-555, 2016
2672016
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
2252017
Detecting autozygosity through runs of homozygosity: a comparison of three autozygosity detection algorithms
DP Howrigan, MA Simonson, MC Keller
BMC genomics 12 (1), 460, 2011
2032011
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
JA Kosmicki, KE Samocha, DP Howrigan, SJ Sanders, K Slowikowski, ...
Nature genetics 49 (4), 504, 2017
1782017
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
1682020
Humor as a mental fitness indicator
DP Howrigan, KB MacDonald
Evolutionary Psychology 6 (4), 147470490800600411, 2008
1102008
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
109*2019
Runs of homozygosity implicate autozygosity as a schizophrenia risk factor
MC Keller, MA Simonson, S Ripke, BM Neale, PV Gejman, DP Howrigan, ...
PLoS Genet 8 (4), e1002656, 2012
1042012
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder
J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ...
Biological psychiatry 83 (12), 1044-1053, 2018
852018
The psychometric assessment of human life history strategy: A meta-analytic construct validation.
AJ Figueredo, PSA Wolf, SG Olderbak, PR Gladden, HBF Fernandes, ...
Evolutionary Behavioral Sciences 8 (3), 148, 2014
852014
Ultra-rare disruptive and damaging mutations influence educational attainment in the general population
A Ganna, G Genovese, DP Howrigan, A Byrnes, MI Kurki, SM Zekavat, ...
Nature neuroscience 19 (12), 1563-1565, 2016
792016
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ...
Molecular psychiatry, 1-17, 2018
772018
Common risk variants identified in autism spectrum disorder
J Grove, S Ripke, TD Als, M Mattheisen, R Walters, H Won, J Pallesen, ...
BioRxiv, 224774, 2017
692017
SynGO: an evidence-based, expert-curated knowledge base for the synapse
F Koopmans, P van Nierop, M Andres-Alonso, A Byrnes, T Cijsouw, ...
Neuron 103 (2), 217-234. e4, 2019
542019
Genome-wide association study of behavioral disinhibition in a selected adolescent sample
J Derringer, RP Corley, BC Haberstick, SE Young, BA Demmitt, ...
Behavior genetics 45 (4), 375-381, 2015
502015
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects
AA Regier, Y Farjoun, DE Larson, O Krasheninina, HM Kang, ...
Nature communications 9 (1), 1-8, 2018
492018
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Articles 1–20