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Wallid Deb

Nantes Université
H指数:17
被引数:1,042

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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
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
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

SMARCA1的致病变异引起由NURF复合物组成调节的X连锁神经发育障碍

2025-11-100
OAAI
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder

KDM6B相关的神经发育障碍的临床与分子谱

2025-10-180
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
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
Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder

CUL3中的功能丧失变体导致综合征性神经发育障碍

2024-09-202
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
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder

KDM6B-related神经发育障碍的临床和分子谱

2023-06-0111
OAAI
PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production
2023-05-3111
OA
Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases
2022-09-2222
OA
Rare pathogenic variants in WNK3 cause X-linked intellectual disability

WNK3中罕见的致病变异导致X连锁智力障碍

2022-09-015
OAAI
Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder
2022-08-0114
OAAI
THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder
2022-04-0131
OAAI
Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder
2022-02-0114
OAAI