Mohammad Marhabaie
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
32
Citations
223
Est. group size
~8
Recurring co-author estimate
Active years
15
Publishing since 2012
This researcher works at the intersection of clinical genomics and molecular biology, focusing on using genome sequencing to diagnose rare genetic and neurometabolic disorders, including newborn screening and pediatric cancer variant classification. They also contribute to more basic research on RNA-binding proteins (Pumilio and Nanos) that regulate gene expression during early development in fruit flies. The work combines clinical diagnostic applications with fundamental studies of gene regulation.
Publication output was minimal or absent from 2017-2020, then increased substantially from 2021 onward, peaking in 2024 with continued activity through 2025-2026.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Whole genome sequencing from dried blood spots for newborn screening of Menkes disease and 36 other actionable inherited neurometabolic disorders
Molecular Genetics and Metabolism · 2026
- The velvet spiders: an atlas of the Eresidae (Arachnida, Araneae)
Data Archiving and Networked Services (DANS) · 2026
- P605: Enhancement of variant classification tools in support of pediatric cancer genomic analysis at an academic clinical laboratory
Genetics in Medicine Open · 2026
- Abstract 1508: A large-scale resource of standardized pediatric somatic cancer variant classifications
Cancer Research · 2026
- VarCat Demonstration Platform
Open MIND · 2026
- VarCat Demonstration Platform
Zenodo (CERN European Organization for Nuclear Research) · 2026
- Significant roles in RNA-binding for the amino-terminal regions of Drosophila Pumilio and Nanos
PLoS Genetics · 2025
- Whole genome sequencing from dried blood spots for newborn screening of Menkes disease and 36 other actionable inherited neurometabolic disorders
SSRN Electronic Journal · 2025
- 30. Enhancing data standardization and structure to improve clinical variant classification
Cancer Genetics · 2025
- Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromes
npj Genomic Medicine · 2024
- Widespread regulation of the maternal transcriptome by Nanos in Drosophila
PLoS Biology · 2024
- A novel IKZF1 variant in a family with autosomal dominant CVID: A case for expanding exon coverage in inborn errors of immunity
Clinical Immunology · 2024
- Expanding the phenotypic spectrum of CSNK2A1-associated Okur-Chung neurodevelopmental syndrome
Human Genetics and Genomics Advances · 2024
- Biallelic variants in HTRA2 cause 3-methylglutaconic aciduria mitochondrial disorder: case report and literature review
Frontiers in Genetics · 2024
- P183: Genome sequencing increases the diagnostic yield in exome-negative individuals with rare genetic disorders
Genetics in Medicine Open · 2024
- Molecular Case Studies×2
- bioRxiv (Cold Spring Harbor Laboratory)×2
- Zenodo (CERN European Organization for Nuclear Research)×2
- Genetics in Medicine Open×2
- npj Genomic Medicine×1
- Kayla Treat
Biochemistry, Genetics and Molecular Biology · Indiana University
- Ying‐Chen Claire Hou
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Danielle Mouhlas
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Francesco Vetrini
Biochemistry, Genetics and Molecular Biology · Indiana University
- Jesse M. Hunter
Biochemistry, Genetics and Molecular Biology · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile