David J Picketts
Overview
Explore the profile of David J Picketts including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
53
Citations
1322
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Danussi C, Bose P, Parthasarathy P, Silberman P, Van Arnam J, Vitucci M, et al.
Nat Commun
. 2022 Jan;
13(1):190.
PMID: 34987156
No abstract available.
12.
Goodwin L, Zapata G, Timpano S, Marenger J, Picketts D
Front Mol Neurosci
. 2021 Jul;
14:680280.
PMID: 34295220
Chromatin remodeling proteins utilize the energy from ATP hydrolysis to mobilize nucleosomes often creating accessibility for transcription factors within gene regulatory elements. Aberrant chromatin remodeling has diverse effects on neuroprogenitor...
13.
Ahmed R, Sarwar S, Hu J, Cardin V, Qiu L, Zapata G, et al.
Hum Mol Genet
. 2021 Mar;
30(7):575-594.
PMID: 33772537
The PHF6 mutation c.1024C > T; p.R342X, is a recurrent cause of Börjeson-Forssman-Lehmann Syndrome (BFLS), a neurodevelopmental disorder characterized by moderate-severe intellectual disability, truncal obesity, gynecomastia, hypogonadism, long tapering fingers...
14.
Lagali P, Zhao B, Yan K, Baker A, Coupland S, Tsilfidis C, et al.
Neuroscience
. 2020 Nov;
452:169-180.
PMID: 33197500
Mutation of the α-thalassemia/mental retardation syndrome X-linked protein, ATRX, causes intellectual disability and is associated with pleiotropic defects including ophthalmological abnormalities. We have previously demonstrated that Atrx deficiency in the...
15.
Timpano S, Picketts D
Front Genet
. 2020 Aug;
11:885.
PMID: 32849845
The ability to determine the genetic etiology of intellectual disability (ID) and neurodevelopmental disorders (NDD) has improved immensely over the last decade. One prevailing metric from these studies is the...
16.
Correction to: C3aR signaling and gliosis in response to neurodevelopmental damage in the cerebellum
Young K, Yan K, Picketts D
J Neuroinflammation
. 2020 Jan;
17(1):32.
PMID: 31973732
Following publication of the original article, the authors noticed missing labels in Fig. 1a.
17.
Lovejoy C, Takai K, Huh M, Picketts D, de Lange T
PLoS Biol
. 2020 Jan;
18(1):e3000594.
PMID: 31895940
Alpha thalassemia/mental retardation syndrome X-linked chromatin remodeler (ATRX), a DAXX (death domain-associated protein) interacting protein, is often lost in cells using the alternative lengthening of telomeres (ALT) pathway, but it...
18.
Alvarez-Saavedra M, Yan K, De Repentigny Y, Hashem L, Chaudary N, Sarwar S, et al.
Front Mol Neurosci
. 2019 Nov;
12:243.
PMID: 31680852
Alterations in the homeostasis of either cortical progenitor pool, namely the apically located radial glial (RG) cells or the basal intermediate progenitors (IPCs) can severely impair cortical neuron production. Such...
19.
Young K, Yan K, Picketts D
J Neuroinflammation
. 2019 Jul;
16(1):135.
PMID: 31272467
Background: Conditional ablation of the Smarca5 gene in mice severely impairs the postnatal growth of the cerebellum and causes an ataxic phenotype. Comparative gene expression studies indicated that complement-related proteins...
20.
Danussi C, Bose P, Parthasarathy P, Silberman P, Van Arnam J, Vitucci M, et al.
Nat Commun
. 2018 Mar;
9(1):1057.
PMID: 29535300
Mutational inactivation of the SWI/SNF chromatin regulator ATRX occurs frequently in gliomas, the most common primary brain tumors. Whether and how ATRX deficiency promotes oncogenesis by epigenomic dysregulation remains unclear,...