Author

Jeffrey Lorenz Neul

Vanderbilt University Medical CenterORCID 0000-0002-5628-5872Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Developmental Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Organism:mouse· 2 Approach:statistical model· 2 Research Focus:clustering· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Jonathan K. Merritt· 2 shared Alan K. PercyiD· 1 shared Aryn KnightiD· 1 shared Bennett A. LandmaniD· 1 shared Bernd WilkeniD· 1 shared Beth Ann MalowiD· 1 shared Carlos A. BacinoiD· 1 shared Christa EinspieleriD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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2 shared papersNeuroscience

Jonathan K. Merritt

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

NeurosciencebioRxivPreprintFeb 17, 2025

In vitro cellular phenotypes of cortical neurons from R255X MECP2 knock-in mice are improved by either expression of wildtype MeCP2 or read-through with G418

Xin Xu, Jonathan K. Merritt, Steven James Gray…·Lucas D. Pozzo‐Miller

The paper shows that expressing wildtype MeCP2 or using G418 treatment in R255X MECP2 knock-in neurons restores cellular phenotypes to wildtype levels.

DOI 10.1101/2025.02.17.638700

mouseexperimental assay

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Developmental BiologyResearch in Developmental DisabilitiesPeer-reviewedApr 25, 2023

Learning about neurodiversity from parents - auditory gestalt perception of prelinguistic vocalisations

Dajie Zhang, Sigrun Lang, Bernd Wilken…·Peter B. Marschik

This study examines how parents of children with Rett syndrome perceive prelinguistic vocalizations, finding they can distinguish RTT vocalizations from typically developing ones, even when the RTT vocalizations are considered inconspicuous by experts.

2 citations

humanproteomics

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NeurosciencebioRxivPreprintMar 29, 2022

Behavioral and imaging analysis of Foxg1 heterozygous mice

Kirsty R. Erickson, Rebekah Lifer, Jonathan K. Merritt…·Jeffrey Lorenz Neul

This study characterizes behavioral and structural brain phenotypes in Foxg1 heterozygous mice, showing abnormalities similar to FOXG1 Syndrome in humans.

DOI 10.1101/2022.03.29.486318

mouseimaging

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GeneticsPediatric NeurologyPeer-reviewedJul 24, 2021

Evaluating Sleep Disturbances in Children with Rare Genetic Neurodevelopmental Syndromes

Olivia J. Veatch, Beth Ann Malow, Hye‐Seung Lee…·Daniel G. Glaze

This study evaluates sleep disturbances in children with Rett, Angelman, and Prader-Willi syndromes compared to typically developing controls, identifying common sleep issues and their associations.

38 citationstop 3%

humanstatistical model

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