Joseph D Dougherty
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Explore the profile of Joseph D Dougherty including associated specialties, affiliations and a list of published articles.
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133
Citations
3544
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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.
Chaturvedi S, Sarafinovska S, Selmanovic D, McCullough K, Swift R, Maloney S, et al.
Biol Sex Differ
. 2025 Feb;
16(1):13.
PMID: 39966983
Background: Sex differences in brain development are thought to lead to sex variation in social behavior. Sex differences are fundamentally driven by both gonadal hormones and sex chromosomes, yet little...
3.
Schreiber A, Swift R, Wilson L, Kroll K, Dougherty J, Maloney S
Sci Rep
. 2025 Feb;
15(1):4998.
PMID: 39930023
MYT1L syndrome is a newly recognized disorder characterized by intellectual disability, speech and motor delay, neuroendocrine disruptions, ADHD, and autism. In order to study this gene and its association with...
4.
Schreiber A, Swift R, Wilson L, Kroll K, Dougherty J, Maloney S
Res Sq
. 2025 Jan;
PMID: 39764117
MYT1L syndrome is a newly recognized disorder characterized by intellectual disability, speech and motor delay, neuroendocrine disruptions, ADHD, and autism. In order to study this gene and its association with...
5.
Maloney S, McCullough K, Chaturvedi S, Selmanovic D, Chase R, Chen J, et al.
bioRxiv
. 2024 Dec;
PMID: 39651298
The transcription factor MYT1L supports proper neuronal differentiation and maturation during brain development. MYT1L haploinsufficiency results in a neurodevelopmental disorder characterized by intellectual disability, developmental delay, autism, behavioral disruptions, aggression,...
6.
Yen A, Sarafinovska S, Chen X, Skinner D, Leti F, Crosby M, et al.
Nat Commun
. 2024 Nov;
15(1):10308.
PMID: 39604385
Mutations reducing the function of MYT1L, a neuron-specific transcription factor, are associated with a syndromic neurodevelopmental disorder. MYT1L is used as a pro-neural factor in fibroblast-to-neuron transdifferentiation and is hypothesized...
7.
Chaturvedi S, Sarafinovska S, Selmanovic D, McCullough K, Swift R, Maloney S, et al.
bioRxiv
. 2024 Nov;
PMID: 39554131
Background: Sex differences in brain development are thought to lead to sex variation in social behavior. Sex differences are fundamentally driven by both gonadal (i.e., hormonal) and chromosomal sex, yet...
8.
Hanzel M, Fernando K, Maloney S, Horn Z, Gong S, Matlik K, et al.
Proc Natl Acad Sci U S A
. 2024 Aug;
121(34):e2405901121.
PMID: 39150780
Astrotactin 2 (ASTN2) is a transmembrane neuronal protein highly expressed in the cerebellum that functions in receptor trafficking and modulates cerebellar Purkinje cell (PC) synaptic activity. Individuals with mutations exhibit...
9.
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.
10.
Shallow M, Tian L, Lin H, Lefton K, Chen S, Dougherty J, et al.
bioRxiv
. 2024 Jun;
PMID: 38895408
The development of motor control over sensory organs is a critical milestone in sensory processing, enabling active exploration and shaping of the sensory environment. However, whether the onset of sensory...