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Francisca Millan

Duke University
H指数:30
被引数:3,313

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Multiscore, a gene ranker powered by artificial intelligence and real-world clinical data, shows high sensitivity for the molecular diagnosis of Mendelian disorders in nearly 10,000 exomes and genomes

Multiscore,一种由人工智能和真实世界临床数据驱动的基因排序器,在近10,000个外显子和基因组中对孟德尔疾病的分子诊断显示出高敏感性。

2026-02-160
OAAI
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals
2023-11-014
OAAI
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
2023-08-0114
OAAI
Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts
2023-03-066
PRE
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders
BRAIN
IF11.7
2023-02-094
OAAI
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder
2023-01-017
OAAI
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants

由CTNNB1变体引起的神经发育障碍的404个个体的基因组和表型特征

2022-11-0122
OA
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling
2022-10-016
OAAI
Highlighting the Dystonic Phenotype Related to GNAO1

突出显示与ginao1相关的肌张力障碍表型

2022-06-2027
OA
Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome
2022-04-0120
OAAI
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (vol 23, pg 740, 2021)
2021-12-011
OAAI
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia (vol 144, pg 1422, 2021)
BRAIN
IF11.7
2021-08-312
OA
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
2021-06-0145
OAAI
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia

HPDL中的双等位基因变体导致纯的和复杂的遗传性痉挛性截瘫

BRAIN
IF11.7
2021-05-1029
OAAI
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids
2021-04-0130
OAAI