Shefali S. Verma

According to our database1, Shefali S. Verma authored at least 23 papers between 2010 and 2023.

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Bibliography

2023
Leveraging electronic health record data for endometriosis research.
Frontiers Digit. Health, May, 2023

A radiomics-based model for the outcome prediction in COVID-19 positive patients through deep learning with both longitudinal chest x-ray and chest computed tomography images.
Proceedings of the Medical Imaging 2023: Computer-Aided Diagnosis, 2023

2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.
npj Digit. Medicine, 2021

What about the environment? Leveraging multi-omic datasets to characterize the environment's role in human health.
Proceedings of the Biocomputing 2021: Proceedings of the Pacific Symposium, 2021

2019
Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43, 870 individuals from the eMERGE network.
Proceedings of the Biocomputing 2019: Proceedings of the Pacific Symposium, 2019

Session Introduction.
Proceedings of the Biocomputing 2019: Proceedings of the Pacific Symposium, 2019

Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies.
Proceedings of the Biocomputing 2019: Proceedings of the Pacific Symposium, 2019

Neural network-based multiomics data integration in Alzheimer's disease.
Proceedings of the Genetic and Evolutionary Computation Conference Companion, 2019

2018
A simulation study investigating power estimates in phenome-wide association studies.
BMC Bioinform., 2018

Collective feature selection to identify crucial epistatic variants.
BioData Min., 2018

Session Introduction.
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018

Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression.
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018

2017
Using knowledge-driven genomic interactions for multi-omics data analysis: metadimensional models for predicting clinical outcomes in ovarian carcinoma.
J. Am. Medical Informatics Assoc., 2017

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.
BioData Min., 2017

Identifying Genetic Associations with Variability in Metabolic Health and Blood Count Laboratory Values: Diving into the Quantitative Traits by Leveraging Longitudinal Data from an EHR.
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017

2016
Integrating Clinical Laboratory Measures and ICD-9 Code Diagnoses in Phenome-Wide Association Studies.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

Phenome-Wide Interaction Study (PheWIS) in Aids Clinical Trials Group Data (ACTG).
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

Biofilter as a Functional Annotation Pipeline for Common and Rare Copy Number Burden.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

2015
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR).
BioData Min., 2015

Session Introduction.
Proceedings of the Biocomputing 2015: Proceedings of the Pacific Symposium, 2015

2014
Benefits of Accurate Imputations in GWAS.
Proceedings of the Applications of Evolutionary Computation - 17th European Conference, 2014

2013
Next-Generation Analysis of Cataracts: Determining Knowledge Driven Gene-Gene Interactions Using Biofilter, and Gene-Environment Interactions Using the PhenX Toolkit.
Proceedings of the Biocomputing 2013: Proceedings of the Pacific Symposium, 2013

2010
On Comparing Two Structured RNA Multiple alignments.
J. Bioinform. Comput. Biol., 2010


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