Author

Kyle P. Flannery

Rutgers, The State University of New Jersey

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

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:zebrafish· 2 Research Focus:cell type annotation· 1 Organism:human· 1 Research Focus:protein structure prediction· 1 Approach:statistical model· 1

Frequent Co-Authors

M. Chiara ManziniiD· 3 shared Brittany F. KarasiD· 2 shared Kristin R. Terez· 2 shared Namarata BattulaiD· 2 shared Shorbon MowlaiD· 2 shared Alison M. MaleiD· 1 shared Amir BahreiniiD· 1 shared Brian M. Gural· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 26 mutual co-author links

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3 shared papersGenetics

M. Chiara ManziniORCID

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Author profile →

3 papers

Recent·Most cited

Impact of maternal compensation on developmental phenotypes in a zebrafish model of severe congenital muscular dystrophy

Kyle P. Flannery, Shorbon Mowla, Namarata Battula, L. Rose Clark, Deze Liu, Callista D Oliveira, Cynthia Venkatesan, Lillian M Simhon, Brittany F. Karas, Kristin R. Terez, Daniel Alberto Burbano-L., M. Chiara Manzini

This study examines the impact of maternal compensation on developmental phenotypes in a zebrafish model of congenital muscular dystrophy, showing distinct effects between zygotic and maternal-zygotic knockouts.

bioRxiv · May 13, 2025 · PreprintGenetics

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders

Daniel G. Calame, Jovi Huixin Wong, Puravi Panda, Dat Nguyen, Nancy C.P. Leong, Riccardo Sangermano, Sohil G Patankar, Mohamed S. Abdel‐Hamid, Lama AlAbdi, Sylvia Safwat, Kyle P. Flannery, Zain Dardas, Jawid M. Fatih, Chaya Nautiyal Murali, Varun Kannan, , Long Nam Nguyen

The paper identifies biallelic FLVCR1 variants causing a range of neurodevelopmental and neurodegenerative disorders, linking them to choline and ethanolamine transport dysfunction.

medRxiv · Feb 9, 2024 · PreprintGenetic & Genomic Medicine

Removal of pomt1 in zebrafish leads to loss of α-dystroglycan glycosylation and dystroglycanopathy phenotypes

Brittany F. Karas, Kristin R. Terez, Shorbon Mowla, Namarata Battula, Kyle P. Flannery, Brian M. Gural, Grace Aboussleman, Numa Mubin, M. Chiara Manzini

This study shows that removing pomt1 in zebrafish leads to dystroglycanopathy phenotypes, including muscle disease and retinal defects, and highlights the role of maternal pomt1 mRNA in development.

Human Molecular Genetics · Jan 25, 2024Peer-reviewedNeuroscience