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Stephanie DiTroia

university college london
H指数:16
被引数:1,030

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De Novo Variants Associated With Autosomal Recessive Conditions: Case Series and Implications for Genetic Testing and Counseling

常染色体隐性条件相关的全新变异:病例系列及其对遗传检测和咨询的启示

2026-09-010
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
Multi-omics approach identifies a novel recessive pathogenic variant in the TNNT3 gene in two siblings with congenital myopathy

多组学方法在两名先天性肌病患者同胞中鉴定出一个新型隐性致病性变异体,位于TNNT3基因。

2025-06-030
PRE
Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

通过对超过6,500个罕见病家庭的外显子组和基因组测序数据进行系统分析,实现了线粒体DNA变异的检测,从而解决了未确诊病例。

2025-04-150
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
Genome Sequencing for Diagnosing Rare Diseases
2024-06-0610
PRE
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease
2024-05-017
OAAI
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project
2024-04-293
OAAI
Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features
2024-04-012
OAAI
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

基因组尸检以确定妊娠丢失和围产儿死亡的根本原因

2023-01-1924
OAAI
GGPS1-associated muscular dystrophy with and without hearing loss
2022-07-238
OA
seqr: A web-based analysis and collaboration tool for rare disease genomics
2022-03-2163
OA
Recessive variants in COL25A1 gene as novel cause of arthrogryposis multiplex congenita with ocular congenital cranial dysinnervation disorder
2022-02-039
OA
The importance of automation in genetic diagnosis: Lessons from analyzing an inherited retinal degeneration cohort with the Mendelian Analysis Toolkit (MATK)
2022-02-017
OAAI
Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency

与PAX5单倍体不足相关的新型神经发育综合征的描述

2022-01-308
OA
KCND2 variants associated with global developmental delay differentially impair Kv4.2 channel gating
2021-07-1015
OA