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Daniel Howrigan
Daniel Howrigan
Group Leader
在 broadinstitute.org 的电子邮件经过验证
标题
引用次数
年份
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays
M DeFelice, JL Grimsby, D Howrigan, K Yuan, SB Chapman, C Stevens, ...
bioRxiv, 2024.04. 03.587209, 2024
2024
INSIGHTS FROM> 80 LOCI ASSOCIATED WITH ATTENTION-DEFICIT/HYPERACTIVITY DISORDER
R Walters, D Demontis, G Athanasiadis, GB Walters, T Zayats, ...
European Neuropsychopharmacology 75, S21, 2023
2023
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
EA Maury, MA Sherman, G Genovese, TG Gilgenast, T Kamath, SJ Burris, ...
Cell Genomics 3 (8), 2023
42023
Author Correction: 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 (4), 730-730, 2023
22023
Genome-wide analyses of attention deficit hyperactivity disorder 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, 2023
2023
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
2122023
EXOME SEQUENCING TECHNOLOGY AND ANALYSIS
D Howrigan
European Neuropsychopharmacology 63, e312, 2022
2022
REPLACING GWAS ARRAYS: CAPTURING GENOMIC DIVERSITY WITH A NOVEL WHOLE-EXOME PLUS LOW-PASS WHOLE GENOME PRODUCT
D Howrigan, M DeFelice, J Grimsby, B Blumenstiel, L Holmes, S Ferriera, ...
European Neuropsychopharmacology 63, e25-e26, 2022
12022
CONTEXTUALIZING PSYCHIATRIC CONSTRUCTS AND THEIR RELATIONSHIPS TO PUBLIC HEALTH VIA BIOBANK-SCALE FACTOR ANALYSIS
C Carey, R Shafee, R Wedow, D Palmer, L Abbott, D Howrigan, ...
European Neuropsychopharmacology 63, e112-e113, 2022
2022
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
1072022
Principled distillation of multidimensional UK Biobank data reveals insights into the correlated human phenome
CE Carey, R Shafee, A Elliott, DS Palmer, J Compitello, M Kanai, L Abbott, ...
medRxiv, 2022.09. 02.22279546, 2022
12022
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
1582022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia
DS Palmer, DP Howrigan, SB Chapman, R Adolfsson, N Bass, ...
Nature genetics 54 (5), 541-547, 2022
862022
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
4342022
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
12022022
Distinct gene-set burden patterns underlie common generalized and focal epilepsies
M Koko, R Krause, T Sander, DR Bobbili, M Nothnagel, P May, H Lerche, ...
EBioMedicine 72, 2021
112021
6. CONTRIBUTION OF COPY NUMBER VARIANTS TO SCHIZOPHRENIA IN EAST ASIAN POPULATIONS
Q Feng, B Thiruvahindrapuram, D Howrigan, J Sebat, T Ge, H Huang
European Neuropsychopharmacology 51, e42-e43, 2021
2021
Human genetic analyses of organelles highlight the nucleus in age-related trait heritability
R Gupta, KJ Karczewski, D Howrigan, BM Neale, VK Mootha
Elife 10, e68610, 2021
82021
Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations
R Stevelink, JJ Luykx, BD Lin, C Leu, D Lal, AW Smith, D Schijven, ...
Epilepsia 62 (7), 1518-1527, 2021
72021
Systematic single-variant and gene-based association testing of thousands of phenotypes in 426,370 UK Biobank exomes
KJ Karczewski, M Solomonson, KR Chao, JK Goodrich, G Tiao, W Lu, ...
Medrxiv, 2021.06. 19.21259117, 2021
272021
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