Author

Leena Panwala

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· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:Drosophila· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:metabolomics· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

Amanda Hope· 2 shared Agnes JH Liang· 1 shared Akhilesh PandeyiD· 1 shared Amina Kurtović-KozarićiD· 1 shared Burak TepeiD· 1 shared Emily G. EvangelistaiD· 1 shared Geoff McGrane· 1 shared Gist F. CroftiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 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

2 shared papersGenetic & Genomic Medicine

Amanda Hope

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

An estimation of global genetic prevalence of PLA2G6-associated neurodegeneration

Amina Kurtović-Kozarić, Moriel Singer‐Berk, Jordan C. Wood, Emily G. Evangelista, Leena Panwala, Amanda Hope, Stefanie M. Heinrich, Samantha M. Baxter, Mark J. Kiel

The paper estimates the genetic prevalence of PLA2G6-associated neurodegeneration using database and literature-based approaches, finding higher prevalence in African/African-American and Asian populations.

Orphanet Journal of Rare Diseases · Oct 18, 2024Peer-reviewedGenetic & Genomic Medicine

Exploring therapeutic strategies for Infantile Neuronal Axonal Dystrophy (INAD/PARK14)

Guang Lin, Burak Tepe, Geoff McGrane, Regine C. Tipon, Gist F. Croft, Leena Panwala, Amanda Hope, Agnes JH Liang, Zhongyuan Zuo, Seul Kee Byeon, Lily Wang, Akhilesh Pandey, Hugo Jozef Bellen

The paper identifies ceramide accumulation, lysosomal expansion, and mitochondrial defects as root causes of INAD/PARK14 and tests therapeutic strategies including drugs and gene therapy.

eLife · Jan 16, 2023Peer-reviewedNeuroscience