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Author Details
Full Name
Yosuke Tanigawa
Affiliation
USA Broad Institute of MIT and Harvard
ORCID
Career Start Year
2018
Papers
28
H Index
12
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37774678
Human microglial state dynamics in Alzheimer's disease progression.
Cell
2023
37890495
Power of inclusion: Enhancing polygenic prediction with admixed individuals.
Am J Hum Genet
2023
32989444
Fast Lasso method for large-scale and ultrahigh-dimensional Cox model with applications to UK Biobank.
Biostatistics
2022
35588732
Integration of rare expression outlier-associated variants improves polygenic risk prediction.
Am J Hum Genet
2022
36042219
Deconvoluting complex correlates of COVID-19 severity with a multi-omic pandemic tracking strategy.
Nat Commun
2022
36040971
WhichTF is functionally important in your open chromatin data?
PLoS Comput Biol
2022
36198295
Single-cell dissection of the obesity-exercise axis in adipose-muscle tissues implies a critical role for mesenchymal stem cells.
Cell Metab
2022
36091495
LARGE-SCALE MULTIVARIATE SPARSE REGRESSION WITH APPLICATIONS TO UK BIOBANK.
Ann Appl Stat
2022
35324888
Significant sparse polygenic risk scores across 813 traits in UK Biobank.
PLoS Genet
2022
34269393
Corrigendum to: Fast Lasso method for large-scale and ultrahigh-dimensional Cox model with applications to UK Biobank.
Biostatistics
2022
32873964
Sex-specific genetic effects across biomarkers.
Eur J Hum Genet
2021
33560296
Survival analysis on rare events using group-regularized multi-response Cox regression.
Bioinformatics
2021
33558700
Polygenic risk modeling with latent trait-related genetic components.
Eur J Hum Genet
2021
34822764
Bayesian model comparison for rare-variant association studies.
Am J Hum Genet
2021
34608296
Author Correction: Genetics of 35 blood and urine biomarkers in the UK Biobank.
Nat Genet
2021
34548093
APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups.
Lipids Health Dis
2021
34594039
A cross-population atlas of genetic associations for 220 human phenotypes.
Nat Genet
2021
34146108
Fast numerical optimization for genome sequencing data in population biobanks.
Bioinformatics
2021
30610202
Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide.
Mol Psychiatry
2020
33125279
Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease Phenotypes.
Circ Genom Precis Med
2020
33095761
A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank.
PLoS Genet
2020
32766602
High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabs.
medRxiv
2020
32275883
Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases.
Am J Hum Genet
2020
30520965
Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics.
Bioinformatics
2019
31492854
Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology.
Nat Commun
2019
30864321
SNPs2ChIP: Latent Factors of ChIP-seq to infer functions of non-coding SNPs.
Pac Symp Biocomput
2019
29460198
Collaborative environmental DNA sampling from petal surfaces of flowering cherry Cerasus⿿ÿ⿿yedoensis 'Somei-yoshino' across the Japanese archipelago.
J Plant Res
2018
29691392
Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study.
Nat Commun
2018
1 - 28 of 28
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