Author

Krutik Patel

Newcastle UniversityORCID 0000-0001-6806-8675Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Krutik Patel2 papers · Rubicon Biotechnology (United States)

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:human· 1 Approach:machine learning (classical)· 1 Organism:mouse· 1

Frequent Co-Authors

A. ZygmuntiD· 1 shared Alan H. BeggsiD· 1 shared Andoni Echaniz‐LagunaiD· 1 shared Anna LaGroon· 1 shared C Sheridan· 1 shared Carina Wallgren‐PetterssoniD· 1 shared Carole J. ProctoriD· 1 shared Carsten G. BönnemanniD· 1 shared

Activity by Year

2022-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. ZygmuntORCID

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3 papers

Recent·Most cited

Systems BiologyeLifePeer-reviewedOct 14, 2024

Systems analysis of miR-199a/b-5p and multiple miR-199a/b-5p targets during chondrogenesis

Krutik Patel, Matt J. Barter, Jamie Soul…·Daryl P. Shanley

The paper identifies miR-199a/b-5p as pro-chondrogenic regulators and constructs a multi-miRNA kinetic model of chondrogenesis.

5 citations

statistical modelgene regulatory network inference

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintOct 4, 2024

Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions

Lydia Sagath, K. Kiiski, Kireshnee Naidu…·Vilma‐Lotta Lehtokari

The paper identifies structural variants in the NEB gene across 35 families, showing large deletions cause dominant distal myopathy while recessive variants show no severity correlation.

DOI 10.1101/2024.10.04.24313542

humanwhole-exome sequencing

𝕏 PostBluesky

BioinformaticsbioRxivPreprintAug 16, 2022

Using Machine Learning to identify microRNA biomarkers for predisposition to Huntington's Disease

Krutik Patel, C Sheridan, DP Shanley

The paper uses machine learning to identify microRNA biomarkers for Huntington's Disease predisposition by analyzing miRNA-mRNA expression data from mouse cortex samples.

4 citations

mousebulk RNA-seq

𝕏 PostBluesky