Author

Kaifang Pang

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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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

Li WangiD· 2 shared Zhandong LiuiD· 2 shared Alex A. PolleniD· 1 shared Arantxa Cebrián‐SillaiD· 1 shared Arnold R. KriegsteiniD· 1 shared Arturo Álvarez-BuyllaiD· 1 shared Brandon Ho· 1 shared Chao ChengiD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersNeuroscience

Li WangORCID

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2 papers

Recent·Most cited

A cross-species proteomic map reveals neoteny of human synapse development

Li Wang, Kaifang Pang, Li Zhou, Arantxa Cebrián‐Silla, Susana González-Granero, Shaohui Wang, Qiuli Bi, Matthew L. White, Brandon Ho, Jiani Li, Tao Li, Yonatan Perez, Eric Jinsheng Huang, Ethan A. Winkler, Mercedes F. Paredes, , Arnold R. Kriegstein

This study creates a cross-species proteomic map of synapse development in human, macaque, and mouse neocortex, revealing slower human PSD maturation and its potential link to neoteny.

Nature · Sep 13, 2023Peer-reviewedNeuroscience

Co-expression enrichment analysis at the single-cell level reveals convergent defects in neural progenitor cells and their cell-type transitions in neurodevelopmental disorders

Kaifang Pang, Li Wang, Wei Wang, Jian Zhou, Chao Cheng, Kihoon Han, Huda Yahya Zoghbi, Zhandong Liu

The paper identifies a convergent defect in neural progenitor cell transitions during fetal development associated with autism and epilepsy using single-cell RNA sequencing and gene co-expression analysis.

Genome Research · Jun 1, 2020Peer-reviewedGenetics