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P Joel Ross

Explore the profile of P Joel Ross including associated specialties, affiliations and a list of published articles. Areas
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Articles 25
Citations 1470
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Recent Articles
1.
Faheem M, Deneault E, Alexandrova R, Rodrigues D, Pellecchia G, Shum C, et al.
BMC Med Genomics . 2023 Jan; 16(1):5. PMID: 36635662
Background: The X-linked PTCHD1 locus is strongly associated with autism spectrum disorder (ASD). Males who carry chromosome microdeletions of PTCHD1 antisense long non-coding RNA (PTCHD1-AS)/DEAD-box helicase 53 (DDX53) have ASD,...
2.
Zhang W, Ross P, Ellis J, Salter M
Transl Psychiatry . 2022 Jun; 12(1):243. PMID: 35680847
NMDA receptors (NMDARs), a prominent subtype of glutamatergic receptors, are implicated in the pathogenesis and development of neuropsychiatric disorders such as epilepsy, intellectual disability, autism spectrum disorder, and schizophrenia, and...
3.
Ross P, Mok R, Smith B, Rodrigues D, Mufteev M, Scherer S, et al.
Mol Autism . 2020 May; 11(1):33. PMID: 32398033
Genetic factors contribute to the development of autism spectrum disorder (ASD), and although non-protein-coding regions of the genome are being increasingly implicated in ASD, the functional consequences of these variants...
4.
Rodrigues D, Mufteev M, Weatheritt R, Djuric U, Ha K, Ross P, et al.
Cell Rep . 2020 Mar; 30(12):4179-4196.e11. PMID: 32209477
Regulation of translation during human development is poorly understood, and its dysregulation is associated with Rett syndrome (RTT). To discover shifts in mRNA ribosomal engagement (RE) during human neurodevelopment, we...
5.
Sengar A, Li H, Zhang W, Leung C, Ramani A, Saw N, et al.
Cell Rep . 2019 Dec; 29(13):4285-4294.e5. PMID: 31875540
NMDA receptors (NMDARs) are critical for physiological synaptic plasticity, learning, and memory and for pathological plasticity and neuronal death. The GluN1 subunit is encoded by a single gene, GRIN1, with...
6.
Ross P, Zhang W, Mok R, Zaslavsky K, Deneault E, DAbate L, et al.
Biol Psychiatry . 2019 Sep; 87(2):139-149. PMID: 31540669
Background: The Xp22.11 locus that encompasses PTCHD1, DDX53, and the long noncoding RNA PTCHD1-AS is frequently disrupted in male subjects with autism spectrum disorder (ASD), but the functional consequences of...
7.
Zaslavsky K, Zhang W, McCready F, Rodrigues D, Deneault E, Loo C, et al.
Nat Neurosci . 2019 Mar; 22(4):556-564. PMID: 30911184
Heterozygous loss-of-function mutations in SHANK2 are associated with autism spectrum disorder (ASD). We generated cortical neurons from induced pluripotent stem cells derived from neurotypic and ASD-affected donors. We developed sparse...
8.
Deneault E, White S, Rodrigues D, Ross P, Faheem M, Zaslavsky K, et al.
Stem Cell Reports . 2019 Feb; 12(2):427-429. PMID: 30759379
No abstract available.
9.
Deneault E, White S, Rodrigues D, Ross P, Faheem M, Zaslavsky K, et al.
Stem Cell Reports . 2018 Nov; 11(5):1211-1225. PMID: 30392976
Autism spectrum disorder (ASD) is phenotypically and genetically heterogeneous. We present a CRISPR gene editing strategy to insert a protein tag and premature termination sites creating an induced pluripotent stem...
10.
Rodrigues D, Kim D, Yang G, Zaslavsky K, Ha K, Mok R, et al.
Cell Rep . 2016 Oct; 17(3):720-734. PMID: 27732849
A progressive increase in MECP2 protein levels is a crucial and precisely regulated event during neurodevelopment, but the underlying mechanism is unclear. We report that MECP2 is regulated post-transcriptionally during...