Author

Hongling Pan

Baylor College of Medicine

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

Signature Assays, Organisms & Methods

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Organism:Drosophila· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Jonathan C. AndrewsiD· 2 shared Michael F. WangleriD· 2 shared Oguz KancaiD· 2 shared Ryan J. GermaniD· 2 shared Sharayu V. JangamiD· 2 shared Shinya YamamotoiD· 2 shared Alfredo BruscoiD· 1 shared Amanda GerardiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jonathan C. AndrewsORCID

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2 papers

Recent·Most cited

Resolution of SLC6A1 variable expressivity in a multi-generational family using deep clinical phenotyping and Drosophila models

Kristy L. Jay, Nikhita Gogate, Kimberly M. Ezell, Jonathan C. Andrews, Sharayu V. Jangam, Paige I. Hall, Hongling Pan, Kelvin Pham, Ryan J. German, Vanessa Gomez, Emily R. Jellinek, Eric A. Storch, Undiagnosed Diseases Network, Shinya Yamamoto, Oguz Kanca, , Michael F. Wangler

The paper identifies a hypomorphic SLC6A1 variant causing variable expressivity in neurodevelopmental disorders using clinical phenotyping and Drosophila models.

medRxiv · Sep 27, 2024 · PreprintGenetic & Genomic Medicine

Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases

Paul C. Marcogliese, Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves, Sharayu V. Jangam, Xi Luo, Ning Liu, Danqing Bei, Yu-Hsin Chao, Brooke Hull, Pei-Tseng Lee, Hongling Pan, Pradnya Bhadane, , Shinya Yamamoto

The paper functionally tests ASD missense variants in Drosophila, finding 38% caused functional alterations and identifying GLRA2 as a cause of neurodevelopmental phenotypes.

Cell Reports · Mar 1, 2022Peer-reviewedGenetics