Author

Bálint Mészáros

St. Jude Children's Research HospitalORCID 0000-0002-9913-4994Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Besian I. Sejdiu1 paper · St. Jude Children's Research Hospital

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Assay:protein structure· 1 Organism:rat· 1

Frequent Co-Authors

M. Madan BabuiD· 2 shared Benjamin LangiD· 1 shared Benshang Li· 1 shared Besian I. Sejdiu· 1 shared Catherine E. WelshiD· 1 shared Charles GawadiD· 1 shared Gang WuiD· 1 shared Huiyun WuiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersBioinformatics

M. Madan BabuORCID

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2 papers

Recent·Most cited

AlphaSync is an enhanced AlphaFold structure database synchronized with UniProt

Benjamin Lang, Bálint Mészáros, Besian I. Sejdiu, Jaimin N Patel, M. Madan Babu

AlphaSync provides updated AlphaFold structure models for 39,961 UniProt proteins and enhances 2.6 million structures with residue-level features.

Nature Structural & Molecular Biology · Nov 11, 2025Peer-reviewedBioinformatics

Somatic mitochondrial DNA mutations are a source of heterogeneity among primary leukemic cells

Kelly McCastlain, Catherine E. Welsh, Yonghui Ni, Liang Ding, Melissa Franco, Robert J. Autry, Besian I. Sejdiu, Ti‐Cheng Chang, Wenan Chen, Huiyun Wu, Qingfei Pan, Veronica Gonzalez-Pena, Patrick A. Schreiner, Sasi Arunachalam, Joung Hyuck Joo, , Mondira Kundu

The paper identifies differences in mtDNA mutation accumulation and selective pressures in pediatric leukemias using bulk and single-cell sequencing, linking these to functional heterogeneity among leukemic cells.

medRxiv · Sep 26, 2024 · PreprintGenetic & Genomic Medicine