Author

Navjot Kaur

Yale UniversityORCID 0000-0001-8514-203XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 3 Approach:statistical model· 3 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:eQTL / molecular QTL mapping· 1

Frequent Co-Authors

Forrest O. GuldeniD· 3 shared Gabriel SantpereiD· 3 shared Nenad ŠestaniD· 3 shared Akemi ShibataiD· 2 shared André M. M. SousaiD· 2 shared Andrew T.N. TebbenkampiD· 2 shared Hyesun ChoiD· 2 shared Shaojie MaiD· 2 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersNeuroscience

Forrest O. GuldenORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintMay 20, 2025

Adaptive Evolution of Gene Regulatory Networks in Mammalian Neocortical Neurons

Zhuo Li, Navjot Kaur, Gabriel Santpere…·Nenad Šestan

The paper identifies mammalian-specific gene regulatory elements and their role in neocortical neuron subtype diversity and connectivity, linking them to neurodevelopmental disorders.

1 citation

mousebulk RNA-seq

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NeurosciencebioRxivPreprintOct 20, 2024

Molecular Specification of Claustro-Amygdalar and Paleocortical Neurons and Connectivity

Navjot Kaur, Rothem Kovner, Forrest O. Gulden…·Nenad Šestan

This study identifies SOX4, SOX11, and TFAP2D as critical regulators of ventropallial excitatory neuron development and PFC connectivity in mice, with conserved roles in humans.

1 citation

mousehuman

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NeuroscienceCell ReportsPeer-reviewedApr 1, 2020

Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex

Donna M. Werling, Sirisha Pochareddy, Jinmyung Choi…·Nenad Šestan

The paper uses whole-genome and RNA sequencing from the human prefrontal cortex to identify genetic variants and transcriptomic changes associated with neurodevelopment and neuropsychiatric disorders.

145 citationstop 1%

humanwhole-genome sequencing

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