June-Anne Gold
Overview
Explore the profile of June-Anne Gold including associated specialties, affiliations and a list of published articles.
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28
Citations
643
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Recent Articles
1.
Schmok T, Surampalli A, Khare M, Zandihaghighi S, Baghbaninogourani R, Patolia B, et al.
Am J Med Genet A
. 2024 Jun;
194(10):e63724.
PMID: 38837660
Prader-Willi syndrome (PWS) is the most common genetic syndrome with obesity and results from loss of expression of paternally inherited genes on chromosome 15q11-q13 by a variety of mechanisms which...
2.
Mahmoud R, Swanson H, Butler M, Flodman P, Gold J, Miller J, et al.
J Clin Med
. 2022 May;
11(9).
PMID: 35566699
Prader-Willi syndrome (PWS) is a complex genetic disorder with three genetic classes. Patients with PWS are characterized by severe hypotonia, developmental delay, behavioral problems, learning disabilities and morbid obesity in...
3.
Veatch O, Malow B, Lee H, Knight A, Barrish J, Neul J, et al.
Pediatr Neurol
. 2021 Aug;
123:30-37.
PMID: 34388423
Background: Adequate sleep is important for proper neurodevelopment and positive health outcomes. Sleep disturbances are more prevalent in children with genetically determined neurodevelopmental syndromes compared with typically developing counterparts. We...
4.
Mahmoud R, Leonenko A, Butler M, Flodman P, Gold J, Miller J, et al.
Clin Genet
. 2021 Feb;
100(1):29-39.
PMID: 33615449
Prader-Willi syndrome (PWS) is a complex genetic disorder with three molecular classes but clinical ascertainment is based on distinctive features. The prevalence of dysmorphic features was studied in 355 PWS...
5.
Oldzej J, Manazir J, Gold J, Mahmoud R, Osann K, Flodman P, et al.
Am J Med Genet A
. 2019 Nov;
182(1):169-175.
PMID: 31782896
Prader-Willi syndrome (PWS) affects 1/15,000-1/30,000 live births and is characterized by lack of expression of paternally inherited genes on 15q11.2-15q13 caused by paternal deletions, maternal uniparental disomy (UPD), or imprinting...
6.
Kimonis V, Tamura R, Gold J, Patel N, Surampalli A, Manazir J, et al.
Genes (Basel)
. 2019 Nov;
10(11).
PMID: 31698873
Prader-Willi syndrome (PWS) is an imprinting genetic disorder characterized by lack of expression of genes on the paternal chromosome 15q11-q13 region. Growth hormone (GH) replacement positively influences stature and body...
7.
Kimonis V, Surampalli A, Wencel M, Gold J, Cowen N
PLoS One
. 2019 Sep;
14(9):e0221615.
PMID: 31545799
Introduction: Prader-Willi syndrome (PWS) is a complex genetic condition characterized by hyperphagia, hypotonia, low muscle mass, excess body fat, developmental delays, intellectual disability, behavioral problems, and growth hormone deficiency. This...
8.
Butler M, Matthews N, Patel N, Surampalli A, Gold J, Khare M, et al.
Am J Med Genet A
. 2019 Jul;
179(9):1826-1835.
PMID: 31313492
Prader-Willi syndrome (PWS) is a genomic imprinting disorder characterized by infantile hypotonia with a poor suck and failure to thrive, hypogenitalism/hypogonadism, behavior and cognitive problems, hormone deficiencies, hyperphagia, and obesity....
9.
Vetrini F, McKee S, Rosenfeld J, Suri M, Lewis A, Nugent K, et al.
Genome Med
. 2019 Mar;
11(1):16.
PMID: 30909959
It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised...
10.
Vetrini F, McKee S, Rosenfeld J, Suri M, Lewis A, Nugent K, et al.
Genome Med
. 2019 Mar;
11(1):12.
PMID: 30819258
Background: Neurodevelopmental disorders are genetically and phenotypically heterogeneous encompassing developmental delay (DD), intellectual disability (ID), autism spectrum disorders (ASDs), structural brain abnormalities, and neurological manifestations with variants in a large...