Serkan Erdin
Overview
Explore the profile of Serkan Erdin including associated specialties, affiliations and a list of published articles.
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65
Citations
4973
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Recent Articles
1.
Martin P, Szkop K, Robert F, Bhattacharyya S, Beauchamp R, Brenner J, et al.
Brain
. 2025 Mar;
PMID: 40037376
Tuberous sclerosis complex (TSC) is an inherited multi-system neurocutaneous disorder where patients often present with neurodevelopmental manifestations such as epilepsy and TSC-associated neuropsychiatric disorder (TAND) that includes autism spectrum disorder...
2.
Martin P, Szkop K, Robert F, Bhattacharyya S, Beauchamp R, Brenner J, et al.
bioRxiv
. 2024 Jun;
PMID: 38895292
Tuberous sclerosis complex (TSC) is an inherited neurodevelopmental disorder (NDD) with frequent manifestations of epilepsy and autism spectrum disorder (ASD). TSC is caused by inactivating mutations in or tumor suppressor...
3.
Harripaul R, Morini E, Salani M, Logan E, Kirchner E, Bolduc J, et al.
Sci Rep
. 2024 May;
14(1):10103.
PMID: 38698036
No abstract available.
4.
Tai D, Razaz P, Erdin S, Gao D, Wang J, Nuttle X, et al.
Am J Hum Genet
. 2024 Mar;
111(3):619.
PMID: 38458168
No abstract available.
5.
Harripaul R, Morini E, Salani M, Logan E, Kirchner E, Bolduc J, et al.
Sci Rep
. 2024 Jan;
14(1):570.
PMID: 38177237
Familial dysautonomia (FD) is a rare recessive neurodevelopmental disease caused by a splice mutation in the Elongator acetyltransferase complex subunit 1 (ELP1) gene. This mutation results in a tissue-specific reduction...
6.
Harripaul R, Morini E, Salani M, Logan E, Kirchner E, Bolduc J, et al.
bioRxiv
. 2023 Oct;
PMID: 37808686
Familial dysautonomia (FD) is a rare recessive neurodevelopmental disease caused by a splice mutation in the Elongator acetyltransferase complex subunit 1 ( ) gene. This mutation results in a tissue-specific...
7.
Liao C, Moyses-Oliveira M, De Esch C, Bhavsar R, Nuttle X, Li A, et al.
Cell Genom
. 2023 Apr;
3(4):100277.
PMID: 37082147
Autism spectrum disorder (ASD) is a heritable neurodevelopmental disorder characterized by deficits in social interactions and communication. Protein-altering variants in many genes have been shown to contribute to ASD; however,...
8.
Bhattacharyya S, Oblinger J, Beauchamp R, Yin Z, Erdin S, Koundinya P, et al.
Neuro Oncol
. 2023 Feb;
25(9):1617-1630.
PMID: 36806881
Background: Neurofibromatosis 2 (NF2) is an inherited disorder caused by bi-allelic inactivation of the NF2 tumor suppressor gene. NF2-associated tumors, including schwannoma and meningioma, are resistant to chemotherapy, often recurring...
9.
Kerschbamer E, Arnoldi M, Tripathi T, Pellegrini M, Maturi S, Erdin S, et al.
Nucleic Acids Res
. 2022 Dec;
50(22):12809-12828.
PMID: 36537238
Disruptive mutations in the chromodomain helicase DNA-binding protein 8 gene (CHD8) have been recurrently associated with autism spectrum disorders (ASDs). Here we investigated how chromatin reacts to CHD8 suppression by...
10.
Mohajeri K, Yadav R, Dhaene E, Boone P, Erdin S, Gao D, et al.
Am J Hum Genet
. 2022 Oct;
109(11):2049-2067.
PMID: 36283406
Point mutations and structural variants that directly disrupt the coding sequence of MEF2C have been associated with a spectrum of neurodevelopmental disorders (NDDs). However, the impact of MEF2C haploinsufficiency on...