Author

Hina Khan

Michigan State University

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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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

Aiden Eliot SheareriD· 1 shared Allyson Cole-Strauss· 1 shared Arash Kordbacheh· 1 shared Artur A. IndzhykulianiD· 1 shared Asher Bury· 1 shared Barbara VonaiD· 1 shared Bohan CheniD· 1 shared Caryl E. SortwelliD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aiden Eliot ShearerORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Complement Dysregulation During the Early Phases of Synucleinopathy

Hina Khan, Mary Gifford, Arash Kordbacheh, Asher Bury, Spencer Panoushek, Allyson Cole-Strauss, Christopher J. Kemp, Kelvin C. Luk, Kathy Steece‐Collier, Nathan C. Kuhn, Nicholas M. Kanaan, Caryl E. Sortwell, Joseph R. Patterson, Matthew J. Benskey

This study shows that synucleinopathy triggers complement activation and dysregulation before neurodegeneration in a rat model and human Parkinson's disease tissue.

Acta Neuropathologica · Jul 20, 2026Peer-reviewedNeuroscience

Extended culture of 2D gastruloids to model human mesoderm development

Bohan Chen, Hina Khan, Zhiyuan Yu, LiAng Yao, Emily Freeburne, Kyoung Jo, Craig N. Johnson, Idse Heemskerk

The paper extends the culture of 2D gastruloids to 96h, revealing a phase of mesoderm differentiation with spatial organization similar to embryos.

Nature Methods · May 7, 2025Peer-reviewedDevelopmental Biology

PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss

Shelby E. Redfield, Pedro De‐la‐Torre, Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris, Gholamreza Shariati, Majid Karimi, Margaret A. Kenna, Go Hun Seo, Hongen Xu, Wei Lu, Sadaf Naz, Hamid Galehdari, Artur A. Indzhykulian, , Barbara Vona

This study identifies PKHD1L1 as a cause of autosomal recessive nonsyndromic hearing loss through exome sequencing and functional analysis in human families and animal models.

Human Genetics · Mar 1, 2024Peer-reviewedGenetic & Genomic Medicine