עקוב אחר
Daniel Howrigan
Daniel Howrigan
Group Leader
כתובת אימייל מאומתת בדומיין broadinstitute.org
כותרת
צוטט על ידי
צוטט על ידי
שנה
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
105632016
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
22732019
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
20982019
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
V Trubetskoy, AF Pardiñas, T Qi, G Panagiotaropoulou, S Awasthi, ...
Nature 604 (7906), 502-508, 2022
16172022
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
11512019
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
9812017
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
6872019
Rare coding variants in ten genes confer substantial risk for schizophrenia
T Singh, T Poterba, D Curtis, H Akil, M Al Eissa, JD Barchas, N Bass, ...
Nature 604 (7906), 509-516, 2022
5602022
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
4942017
Detecting autozygosity through runs of homozygosity: a comparison of three autozygosity detection algorithms
DP Howrigan, MA Simonson, MC Keller
BMC genomics 12, 1-15, 2011
3882011
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
D Demontis, GB Walters, G Athanasiadis, R Walters, K Therrien, ...
Nature genetics 55 (2), 198-208, 2023
3572023
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), 504-510, 2017
3492017
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
2612019
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 25 (8), 1859-1875, 2020
2582020
A cross-disorder dosage sensitivity map of the human genome
RL Collins, JT Glessner, E Porcu, M Lepamets, R Brandon, C Lauricella, ...
Cell 185 (16), 3041-3055. e25, 2022
2152022
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), 4038, 2018
2082018
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
1942018
Humor as a mental fitness indicator
DP Howrigan, KB MacDonald
Evolutionary Psychology 6 (4), 147470490800600411, 2008
1702008
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes
KJ Karczewski, M Solomonson, KR Chao, JK Goodrich, G Tiao, W Lu, ...
Cell Genomics 2 (9), 2022
1572022
Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations
DP Howrigan, SA Rose, KE Samocha, M Fromer, F Cerrato, WJ Chen, ...
Nature neuroscience 23 (2), 185-193, 2020
1472020
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מאמרים 1–20