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/vufind/Search/Results?lookfor=%22Chatterjee%2C+Nilanjan%22&type=Person&sort=year
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PubPharm (694)
1
MEGSA: A powerful and flexible framework for analyzing mutual exclusivity of tumor mutations
enthalten in:
bioRxiv.org
| 2024
von
Hua, X.
|
Hyland, P.
|
Huang, J.
| +5
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2
A Powerful Procedure for Pathway-based Meta-Analysis Using Summary Statistics Identifies 43 Pathways Associated with Type II Diabetes in European Populations
enthalten in:
bioRxiv.org
| 2024
von
Zhang, H.
|
Wheeler, W.
|
Hyland, P.
| +4
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3
Post-selection Inference Following Aggregate Level Hypothesis Testing in Large Scale Genomic Data
enthalten in:
bioRxiv.org
| 2024
von
Heller, R.
|
Chatterjee, N.
|
Krieger, A.
| +1
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4
Using imputed genotype data in the joint score tests for genetic association and gene-environment interactions in case-control studies
enthalten in:
bioRxiv.org
| 2024
von
Song, M.
|
Wheeler, W.
|
Caporaso, N.
| +2
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5
iCARE: R package to build, validate and apply absolute risk models
enthalten in:
bioRxiv.org
| 2024
von
Choudhury, P.
|
Maas, P.
|
Wilcox, A.
| +5
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6
Power Analysis Provides Bounds for Genetic Architecture and Insights to Challenges for Rare Variant Association Studies
enthalten in:
bioRxiv.org
| 2024
von
Derkach, A.
|
Zhang, H.
|
Chatterjee, N.
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7
Estimation of complex effect-size distributions using summary-level statistics from genome-wide association studies across 32 complex traits and implications for the future
enthalten in:
bioRxiv.org
| 2024
von
Zhang, Y.
|
Qi, G.
|
Park, J.
| +1
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8
A Mixed-Model Approach for Powerful Testing of Genetic Associations with Cancer Risk Incorporating Tumor Characteristics
enthalten in:
bioRxiv.org
| 2024
von
Zhang, H.
|
Zhao, N.
|
Ahearn, T.
| +3
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9
A Powerful Method for Pleiotropic Analysis under Composite Null Hypothesis Identifies Novel Shared Loci Between Type 2 Diabetes and Prostate Cancer
enthalten in:
bioRxiv.org
| 2024
von
Ray, D.
|
Chatterjee, N.
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10
Germline determinants of the somatic mutation landscape in 2,642 cancer genomes
enthalten in:
bioRxiv.org
| 2024
von
Waszak, S.
|
Tiao, G.
|
Zhu, B.
| +88
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