Author

Heather Fisher

Children's Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Research Focus:database / resource· 2 Assay:metabolomics· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Angela E. ScheuerleiD· 3 shared Luis Alfredo UmañaiD· 3 shared Sarah Montgomery· 3 shared Bookyung KoiD· 2 shared Bushra AfrozeiD· 2 shared Callie Hornbuckle· 2 shared Chendong YangiD· 2 shared Christine M. QuinniD· 2 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Angela E. ScheuerleORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Metabolic landscape of inborn errors of metabolism

Min Ni, Ling Cai, Hieu Vu, Hongli Chen, Margaret Cervantes, Wen Gu, Lea Abou Haidar, Zheng Wu, Chunxiao Pan, Feng Cai, Phong T. Nguyen, Yan Jin, Jin Wang, Bookyung Ko, Chendong Yang, , Ralph J. DeBerardinis

This study uses metabolomics to analyze 474 subjects with inborn errors of metabolism, identifying genotype-specific metabolic alterations and providing diagnostic tools and a database of metabolomic features.

medRxiv · Oct 29, 2026 · PreprintGenetic & Genomic Medicine

An interactive web application for exploring human plasma and fibroblast metabolomics data from patients with inborn errors of metabolism

Ling Cai, Hieu Vu, Wen Gu, Hongli Chen, Jordan Franklin, Lea Abou Haidar, Zheng Wu, Chunxiao Pan, Feng Cai, Phong Nguyen, Bookyung Ko, Chendong Yang, Lauren G. Zacharias, Jessica Sudderth, Sarah Montgomery, , Ralph J. DeBerardinis

The paper introduces a web application for exploring metabolomics data from plasma and fibroblasts of patients with inborn errors of metabolism, enabling analysis of metabolic deviations and relationships.

bioRxiv · Dec 11, 2023 · PreprintBioinformatics

Deleterious, protein-altering variants in the X-linked transcriptional coregulator ZMYM3 in 22 individuals with a neurodevelopmental delay phenotype

Susan M. Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano, E. Christopher Partridge, Fatima Abidi, Ashlyn G. Anderson, Muhammad Ansar, Stylianos E. Antonarakis, Azadeh Azadi, Ruxandra Bachmann‐Gagescu, Andrea Bartuli, Caroline Bénech, Jennifer L. Berkowitz, Michael J. Betti, Alfredo Brusco, , Gregory M. Cooper

The paper identifies ZMYM3 variants in 22 individuals with neurodevelopmental delay, showing recurrent mutations, phenotypic overlap, and functional effects, supporting ZMYM3 as a novel NDD gene.

medRxiv · Sep 29, 2022 · PreprintGenetic & Genomic Medicine