Author

Samuel Kim

Stanford MedicinePrimary ORCID profile (0000-0002-1814-4032 · 2 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Samuel KimiD2 papers · Columbia University

Biology Disciplines

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Genetic & Genomic Medicine· 1 Immunology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:flow cytometry· 1 Research Focus:gene regulatory network inference· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

Allyssa L. DaughertyiD· 1 shared Alyssa MonterrosoiD· 1 shared Andre L. M. ReisiD· 1 shared Andrew J. MartiniD· 1 shared Andrew M. SorniD· 1 shared Andrew P. HannafordiD· 1 shared Anna BadneriD· 1 shared Arjun Nair· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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1 shared paperImmunology

Allyssa L. DaughertyORCID

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3 papers

Recent·Most cited

Divergent phenotypic and functional roles of human T follicular helper cells from infancy to adulthood

Suhas Sureshchandra, Jenna M. Kastenschmidt, Erika M. Joloya, Zachary W. Wagoner, Arjun Nair, Samuel Kim, Natalie Zane, Gargee Bhattacharya, Alyssa Monterroso, Evien Cheng, Andrew M. Sorn, Mahina Tabassum Mitul, Haven Beares, Germaine Mendez, Timothy B. Yates, , Lisa E. Wagar

This study examines age-related differences in T follicular helper cell function and their impact on antibody responses across human development.

bioRxiv · Feb 9, 2026 · PreprintImmunology

Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders

Laura Ivete Rudaks, Igor Stevanovski, Dennis Yeow, Andre L. M. Reis, Sanjog R. Chintalaphani, Pak Leng Cheong, Hasindu Gamaarachchi, Lisa C. Worgan, Kate E. Ahmad, Michael Hayes, Andrew P. Hannaford, Samuel Kim, Victor S.C. Fung, Gabor Michael Halmagyi, Andrew J. Martin, , Kishore Raj Kumar

This paper demonstrates that targeted long-read sequencing improves genetic diagnosis of spastic-ataxia disorders by identifying causative variants in 41% of undiagnosed cases using a single assay.

Annals of Clinical and Translational Neurology · Feb 25, 2025Peer-reviewedGenetic & Genomic Medicine

BMAL1 loss in oligodendroglial lineage cells dysregulates myelination and sleep

Daniela Rojo, Anna Badner, Louisa Dal Cengio, Samuel Kim, Noriaki Sakai, Jacob J. Greene, Ella C. Eisinger, Caroline Arellano-Garcia, Lindsey Catherine Mehl, Mohammad Elmojtaba F Gumma, Rebecca L. Soyk, Julia Ransom, Maya K. Weigel, Belgin Yalçın, Samuel E. Jones, , Erin M. Gibson

The paper shows BMAL1 regulates oligodendroglial maintenance and myelination, which affects sleep, and links this to MS pathology.

bioRxiv · Apr 28, 2022 · PreprintNeuroscience