Author

Muhammad Nadeem Anjum

University of Child Health SciencesORCID 0009-0000-0059-3297Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Henry HouldeniD· 2 shared Huma Arshad CheemaiD· 2 shared Peter BaueriD· 2 shared Reza MaroofianiD· 2 shared Abraham José Paredes-FuentesiD· 1 shared Afshin FayaziiD· 1 shared Aida Maria Bertoli‐AvellaiD· 1 shared Alex KentsisiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersNeuroscience

Henry HouldenORCID

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2 papers

Recent·Most cited

NeuroscienceScience AdvancesPeer-reviewedJan 14, 2026

A transposase-derived gene required for human brain development

Luz Jubierre, Sara A. Lewis, Rodrigo Lopez Gutierrez…·Alex Kentsis

This study identifies PGBD5 as a transposase-derived gene essential for brain development in humans and mice, with deficiency causing intellectual disability and seizures.

9 citationstop 2%

humanmouse

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Genetic & Genomic MedicinemedRxivPreprintNov 27, 2024

CLINICAL AND MOLECULAR CHARACTERISATION OF SLC31A1-RELATED NEURODEVELOPMENTAL DISORDER.

Natalia Juliá‐Palacios, Gerard Muñoz‐Pujol, Reza Maroofian…·Roser Urreizti

This study characterizes a neurodevelopmental disorder caused by bi-allelic SLC31A1 mutations, showing severe clinical features and mitochondrial dysfunction.

DOI 10.1101/2024.11.27.24317634

humanbulk RNA-seq

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