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T

Thomas Besnard

Nantes Université
H指数:31
被引数:2,736

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De novo variants in the poly(rC)-binding protein gene PCBP1 cause a neurodevelopmental disorder

PCBP1基因中的全新变异导致神经发育障碍

2026-09-160
PRE
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies

snRNA基因的系统分析揭示了显性和隐性发育性和癫痫性脑病中常见的RNU2-2变异

2026-03-300
OAAI
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders

剪接因子基因SF3B1的从头变异与神经发育障碍有关

2026-01-230
OA
Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies

研究蛋白酶体ATP酶亚基基因PSMC5在神经发育性蛋白酶体病理学中的神经元作用

2025-11-260
OA
Heterozygous pathogenic variants in the splicing factor SF1 lead to a large spectrum of neurodevelopmental disorders

SF1剪接因子的杂合致病性变异导致一系列神经发育障碍。

2025-09-220
PRE
De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder

Bradbrook, S.M.; Graham, G.; Carter, M.T.; Kibaek, M.; Fagerberg, C.; Larsen, M.J.; Dawson, K.; Meuter, C.; Pepler, A.; Besnard, T.; et al. ZNF865基因中的新发截短突变导致一种新型神经发育障碍。Am. J. Med. Genet. A 2025, 11, e64242. [Google Scholar] [CrossRef] [PubMed]

2025-09-011
PRE
Ubiquitin-proteasome system dysregulation in FAM111B-related poikiloderma and phenotypic spectrum expansion: new case reports and long-term follow-up

FAM111B相关性异色性皮病中泛素-蛋白酶体系统失调及表型谱扩展:新病例报告与长期随访

2025-08-200
PREAI
Bi-allelic variants in TM2D3 cause a severe syndromic neurodevelopmental disorder associated with endoplasmic reticulum and mitochondrial abnormalities

TM2D3基因的双等位基因变异会导致一种与内质网和线粒体异常相关的严重综合征性神经发育障碍。

2025-05-300
PRE
Clinical and Neurodevelopmental Characteristics of Paralogous Gain-of-Function Variants at GRIA2 p.Gly792 and GRIA3 p.Gly803

GRIA2 p.Gly792和GRIA3 p.Gly803旁系同源获得功能变异的临床及神经发育特征

2025-05-200
OA
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders
2025-02-010
OAAI
Further delineation of the SCAF4-associated neurodevelopmental disorder
2024-12-120
OAAI
LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder
2024-10-010
OAAI
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes

KMT2C的致病变异导致与Kleefstra和Kabuki综合征不同的神经发育障碍

2024-08-014
PRE
PSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response

PSMD11功能丧失变体与神经行为表型,肥胖和干扰素反应增加相关

2024-07-013
OAAI
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes
BRAIN
IF11.7
2023-12-012
OA
PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production
2023-05-3111
OA
SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation
2023-02-1072
OAAI
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects
2022-12-014
OAAI
Bi-allelic loss-of-function variants in TMEM147 cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huet anomaly
2022-10-017
OAAI