Alexander Kolevzon
Overview
Explore the profile of Alexander Kolevzon including associated specialties, affiliations and a list of published articles.
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Articles
115
Citations
6939
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Recent Articles
1.
Levy T, Silver H, Soufer R, Rouhandeh A, Kolevzon A, Buxbaum J, et al.
Front Psychiatry
. 2025 Mar;
16:1526383.
PMID: 40066139
Background: FOXP1 syndrome is a genetic neurodevelopmental disorder associated with complex clinical presentations including global developmental delay, mild to profound intellectual disability, speech and language impairment, autism traits, attention-deficit/hyperactivity disorder...
2.
Verdes A, Bhattachan S, Kolevzon A, King B, McDougle C, Sanders K, et al.
J Child Adolesc Psychopharmacol
. 2025 Feb;
PMID: 39970017
Although randomized clinical trials (RCTs) have investigated several treatments for social communication difficulties and repetitive behavior in autism, none has yet shown consistent superiority over placebo. Placebo response in autism...
3.
Avila M, Jung S, Satterstrom F, Fu J, Levy T, Sloofman L, et al.
medRxiv
. 2025 Jan;
PMID: 39830258
The past decade has seen remarkable progress in identifying genes that, when impacted by deleterious coding variation, confer high risk for autism spectrum disorder (ASD), intellectual disability, and other developmental...
4.
Levy T, Lloyd Holder Jr J, Horrigan J, Snape M, McMorn A, Layton C, et al.
HGG Adv
. 2024 Dec;
6(2):100393.
PMID: 39690738
Phelan-McDermid syndrome (PMS) is a neurodevelopmental disorder caused by haploinsufficiency of the SHANK3 gene. Approximately 25% of individuals with PMS have epilepsy. Treatment of epilepsy in PMS may require multiple...
5.
Frazier T, Busch R, Klaas P, Lachlan K, Jeste S, Kolevzon A, et al.
Autism Res
. 2024 Dec;
18(2):334-348.
PMID: 39643599
Social attention is a key aspect of neurodevelopment and is significantly altered in neurodevelopmental genetic syndromes and many individuals with idiopathic autism spectrum disorder (ASD). The primary aim of the...
6.
San Jose Caceres A, Wilkinson E, Cooke J, Baskett V, Blackmore C, Crawley D, et al.
J Neurodev Disord
. 2024 Nov;
16(1):64.
PMID: 39563223
Background: Phelan-McDermid syndrome (PMS) is a rare genetic syndrome characterized by developmental delay/intellectual disability, absent or delayed speech, physical dysmorphic features and high rates of autistic features. However, it is...
7.
Gluckman J, Levy T, Friedman K, Garces F, Filip-Dhima R, Quinlan A, et al.
Am J Med Genet A
. 2024 Sep;
197(1):e63872.
PMID: 39257296
Phelan-McDermid syndrome (PMS) is a rare genetic neurodevelopmental disorder that results from the loss of one functional copy of the SHANK3 gene. While many clinical features of PMS are well-understood,...
8.
Buxbaum Grice A, Sloofman L, Levy T, Walker H, Ganesh G, de Los Santos M, et al.
Transl Psychiatry
. 2024 Jul;
14(1):307.
PMID: 39054328
Activity-dependent neuroprotective protein (ADNP) syndrome is a rare neurodevelopmental disorder resulting in intellectual disability, developmental delay and autism spectrum disorder (ASD) and is due to mutations in the ADNP gene....
9.
Gallin Z, Kolevzon A, Reichenberg A, Hankerson S, Kolevzon A
J Autism Dev Disord
. 2024 Jun;
PMID: 38941049
Purpose: Racial differences in prevalence rates of autism spectrum disorder (ASD) have shifted in the United States (US) since the 1990s. This review addresses the nature and context of this...
10.
Levy T, Gluckman J, Siper P, Halpern D, Zweifach J, Filip-Dhima R, et al.
J Neurodev Disord
. 2024 May;
16(1):25.
PMID: 38730350
Background: Phelan-McDermid syndrome (PMS) is a genetic neurodevelopmental disorder caused by SHANK3 haploinsufficiency and is associated with an increased risk for seizures. Previous literature indicates that around one third of...