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C

Caroline Nava

Inria
H指数:51
被引数:8,755

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Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

作者更正:非编码RNA基因RNU4-2中的biallelic变异导致一种具有独特白质变化的隐性神经发育综合征

2026-05-180
OAAI
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

RNU4-2非编码RNA基因的双等位基因变异导致一种具有独特白质变化的隐性神经发育综合征。

2026-04-080
OAAI
Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders

RNU4-2的饱和编辑揭示了不同的显性和隐性障碍

Nature
IF48.5
2026-04-080
OAAI
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
Loss of DOT1L disrupts neuronal transcription and leads to a neurodevelopmental disorder

DOT1L的缺失破坏了神经元转录,并导致神经发育障碍

BRAIN
IF11.7
2025-12-010
PRE
A large cohort study of prenatal exome sequencing redefines diagnosis in fetal corpus callosum anomalies

一项大型队列研究重新定义了产前外显子测序在胎儿胼胝体畸形诊断中的应用。

BRAIN
IF11.7
2025-11-010
PRE
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function

致病性UNC13A变异通过损害突触功能导致神经发育综合征

2025-10-220
OAAI
The Clinical and Genetic Landscape of a French Multicenter Cohort of 2563 Epilepsy Patients Referred for Genetic Diagnosis

法国多中心队列2563例接受遗传诊断的癫痫患者的临床与遗传特征图谱

2025-08-080
OAAI
Further characterisation of ARX-related disorders in females due to inherited or de novo variants
2023-10-253
PRE
Loss-of-function variants in ZEB1 cause dominant anomalies of the corpus callosum with favourable cognitive prognosis
2023-10-190
PRE
A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism
2022-12-0119
OAAI
Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X

人类X染色体单基因疾病相关基因的系统分析和预测

2022-11-0221
OAAI
A reverse genetics and genomics approach to gene paralog function and disease: Myokymia and the juxtaparanode
2022-09-016
OAAI
GM3 synthase deficiency in non-Amish patients
2022-02-019
PRE
PURA-Related Developmental and Epileptic Encephalopathy

紫癜相关性发育性和癫痫性脑病

2021-12-0126
OAAI
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
2021-09-0129
OAAI
KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum

KCNT1-related癫痫和癫痫性脑病: 表型和突变谱

BRAIN
IF11.7
2021-06-1140
OA
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity

CSNK2B: 广泛的神经发育障碍和癫痫严重程度

2021-05-2620
OAAI
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

在具有智力障碍,行为障碍和癫痫的显性神经发育障碍中,CHD5的错觉和截断变异

2021-05-0425
OAAI
Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy
2021-05-0120
OAAI