Author

Aniko Sabo

Baylor College of MedicineORCID 0000-0002-9667-8072Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Donna Marie MuznyiD· 3 shared Richard A. GibbsiD· 3 shared Christine M. EngiD· 2 shared Eric VenneriD· 2 shared Wendy K. ChungiD· 2 shared Adithya BalasubramanianiD· 1 shared Ahmad S. Chatha· 1 shared Akhila BalasubramanianiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Donna Marie MuznyORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 30, 2026

Integrated Clinical-Genomic Reanalysis Identifies Diagnostic Gaps and Candidate Genes in a Pediatric Rare Disease Cohort

Hyunjung Gu, Aniko Sabo, Sharayu V. Jangam…·Katherine Y. King

DOI 10.64898/2026.09.24.26363679

humanwhole-exome sequencing

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BioinformaticsGenetics in MedicinePeer-reviewedJul 13, 2021

Neptune: An environment for the delivery of genomic medicine

Eric Venner, Victoria Yi, David R. Murdock…·Andrea L. Hartzler

Neptune delivers structured genomic data to EHR systems through customizable reports and variant reanalysis, supporting over 15,000 clinical reports.

7 citations

experimental assaydatabase / resource

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Geneticsnpj Genomic MedicinePeer-reviewedAug 23, 2019

Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes

Pamela Feliciano, Xueya Zhou, Irina Astrovskaya…·Brenda Hauf

The paper reports exome sequencing of 457 ASD families, identifying 10.4% with known ASD genes and 3.4% with possibly associated variants, and provides statistical support for 34 ASD risk genes using the TADA framework.

247 citationstop 1%

humanwhole-exome sequencing

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