Harrison W Gabel
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Explore the profile of Harrison W Gabel including associated specialties, affiliations and a list of published articles.
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37
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2581
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Recent Articles
1.
Dougherty J, Sarafinovska S, Chaturvedi S, Law T, Akinwe T, Gabel H
Curr Opin Neurobiol
. 2025 Mar;
92:102990.
PMID: 40036988
The identification of hundreds of neurodevelopmental disorder (NDD) genes in the last decade led to numerous genetic models for understanding NDD gene mutation consequences and delineating putative neurobiological mediators of...
2.
Hamagami N, Kapadia D, Abduljawad N, Cheng Z, McLaughlin L, Singhania D, et al.
bioRxiv
. 2025 Feb;
PMID: 39975390
Single-cell transcriptomic studies have identified distinct microglial subpopulations with shared and divergent gene signatures across development, aging and disease. Whether these microglial subsets represent ontogenically separate lineages of cells, or...
3.
Grens K, Weisenberg J, Ryther R, Gabel H
Mo Med
. 2025 Feb;
122(1):53-59.
PMID: 39958601
As the rate of diagnosis for rare disease increases, so does the need to develop scalable solutions to address patient community needs. Drawing upon our experiences in rare intellectual and...
4.
Chen J, Lambo M, Ge X, Dearborn J, Liu Y, McCullough K, et al.
Neuron
. 2024 Jun;
112(13):2257.
PMID: 38906150
No abstract available.
5.
Moore J, Nemera M, DSouza R, Hamagami N, Clemens A, Beard D, et al.
bioRxiv
. 2024 Feb;
PMID: 38352532
The extraordinary diversity of neuron types in the mammalian brain is delineated at the highest resolution by subtle gene expression differences that may require specialized molecular mechanisms to be maintained....
6.
Nettles S, Ikeuchi Y, Lefton K, Abbasi L, Erickson A, Agwu C, et al.
Cell Rep
. 2023 Dec;
42(12):113538.
PMID: 38096051
A unique signature of neurons is the high expression of the longest genes in the genome. These genes have essential neuronal functions, and disruption of their expression has been implicated...
7.
Beard D, Zhang X, Wu D, Martin J, Erickson A, Boua J, et al.
Cell Rep
. 2023 Nov;
42(11):113411.
PMID: 37952155
Phenotypic heterogeneity in monogenic neurodevelopmental disorders can arise from differential severity of variants underlying disease, but how distinct alleles drive variable disease presentation is not well understood. Here, we investigate...
8.
Mangetti Goncalves T, Stewart C, Baxley S, Xu J, Li D, Gabel H, et al.
Res Sq
. 2023 Oct;
PMID: 37841836
Genome mapping studies have generated a nearly complete collection of genes for the human genome, but we still lack an equivalently vetted inventory of human regulatory sequences. Cis-regulatory modules (CRMs)...
9.
Hamagami N, Wu D, Clemens A, Nettles S, Li A, Gabel H
Mol Cell
. 2023 Apr;
83(9):1412-1428.e7.
PMID: 37098340
During postnatal development, the DNA methyltransferase DNMT3A deposits high levels of non-CG cytosine methylation in neurons. This methylation is critical for transcriptional regulation, and loss of this mark is implicated...
10.
Beard D, Zhang X, Wu D, Martin J, Hamagami N, Swift R, et al.
bioRxiv
. 2023 Mar;
PMID: 36909558
Phenotypic heterogeneity is a common feature of monogenic neurodevelopmental disorders that can arise from differential severity of missense variants underlying disease, but how distinct alleles impact molecular mechanisms to drive...