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Matthew Aguirre
Matthew Aguirre
Verified email at stanford.edu
Title
Cited by
Cited by
Year
Landscape of X chromosome inactivation across human tissues
T Tukiainen, AC Villani, A Yen, MA Rivas, JL Marshall, R Satija, M Aguirre, ...
Nature 550 (7675), 244-248, 2017
8352017
Genetics of 35 blood and urine biomarkers in the UK Biobank
N Sinnott-Armstrong, Y Tanigawa, D Amar, N Mars, C Benner, M Aguirre, ...
Nature Genetics 53 (2), 185-194, 2021
4742021
Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide
DM Ruderfer, CG Walsh, MW Aguirre, Y Tanigawa, JD Ribeiro, ...
Molecular psychiatry, 1-9, 2019
1212019
A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank
J Qian, Y Tanigawa, W Du, M Aguirre, C Chang, R Tibshirani, MA Rivas, ...
PLoS genetics 16 (10), e1009141, 2020
113*2020
Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics
G McInnes, Y Tanigawa, C DeBoever, A Lavertu, J Olivieri, M Aguirre, ...
Bioinformatics, 2018
982018
Phenome-wide burden of copy-number variation in the UK biobank
M Aguirre, MA Rivas, J Priest
The American Journal of Human Genetics 105 (2), 373-383, 2019
632019
Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology
Y Tanigawa, J Li, JM Justesen, H Horn, M Aguirre, C DeBoever, C Chang, ...
Nature Communications 10 (1), 1-14, 2019
572019
Assessing digital phenotyping to enhance genetic studies of human diseases
C DeBoever, Y Tanigawa, M Aguirre, G McInnes, A Lavertu, MA Rivas
The American Journal of Human Genetics 106 (5), 611-622, 2020
532020
Polygenic risk modeling with latent trait-related genetic components
M Aguirre, Y Tanigawa, GR Venkataraman, R Tibshirani, T Hastie, ...
European Journal of Human Genetics, 1-11, 2021
162021
A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population
C Tcheandjieu, M Aguirre, S Gustafsson, P Saha, P Potiny, M Haendel, ...
PLoS genetics 16 (11), e1008802, 2020
15*2020
Integration of rare expression outlier-associated variants improves polygenic risk prediction
C Smail, NM Ferraro, Q Hui, MG Durrant, M Aguirre, Y Tanigawa, ...
The American Journal of Human Genetics 109 (6), 1055-1064, 2022
12*2022
Bayesian model comparison for rare-variant association studies
GR Venkataraman, C DeBoever, Y Tanigawa, M Aguirre, AG Ioannidis, ...
The American Journal of Human Genetics 108 (12), 2354-2367, 2021
9*2021
Learning epistatic polygenic phenotypes with Boolean interactions
M Behr, K Kumbier, A Cordova-Palomera, M Aguirre, O Ronen, C Ye, ...
Plos one 19 (4), e0298906, 2024
72024
Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy
M Yu, AR Harper, M Aguirre, M Pittman, C Tcheandjieu, D Amgalan, ...
Circulation: Genomic and Precision Medicine, e003708, 2023
22023
Transcriptomics and chromatin accessibility in multiple African population samples
MK DeGorter, PC Goddard, E Karakoc, S Kundu, SM Yan, D Nachun, ...
bioRxiv, 2023
12023
Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes
M Yu, M Aguirre, M Jia, K Gjoni, A Cordova-Palomera, C Munger, ...
Circulation: Genomic and Precision Medicine, e003968, 2023
12023
Assessment of Polygenic Trait Risk via Trait Components and Applications Thereof
MA Rivas, MW Aguirre
US Patent App. 17/005,241, 2021
2021
A deep learning classifier for local ancestry inference
M Aguirre, J Sokol, G Venkataraman, A Ioannidis
arXiv preprint arXiv:2011.02081, 2020
2020
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Articles 1–18