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Sian Ellard

Stanford University
H指数:118
被引数:5.5万

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CIROZ is dispensable in ancestral vertebrates but essential for left in humans
2025-02-010
PRE
Congenital Titinopathy: Comprehensive Characterization of the Most Severe End of the Disease Spectrum
2025-01-240
OAAI
Pathogenic PDE12 variants impair mitochondrial RNA processing causing neonatal mitochondrial disease
2024-11-201
PRE
Primate-specific ZNF808 is essential for pancreatic development in humans
2023-11-166
OAAI
Detailed Analysis of ITPR1 Missense Variants Guides Diagnostics and Therapeutic Design
2023-11-143
OAAI
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5
2023-02-0710
OA
Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications

CLDN5的变异引起以癫痫、小头畸形和脑钙化为特征的综合征

BRAIN
IF11.7
2022-12-089
OA
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis
2022-12-019
OAAI
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism

破坏HK1组织特异性调控元件的非编码变异导致先天性高胰岛素血症

2022-11-0423
OAAI
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria
2022-09-068
OAAI
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations
2022-09-014
OAAI
Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK)
2022-09-0117
OAAI
De novo putative loss-of-function variants in TAF4 are associated with a neuro-developmental disorder
2022-08-105
OAAI
Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhood
2022-07-0113
OAAI
Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome
2022-07-0120
OAAI
Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans
2022-04-093
PRE
THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder
2022-04-0131
OAAI