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Sebastiano Cavallaro

consiglio nazionale delle ricerche (cnr)

H指数:43

被引数:6,856

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Unraveling the missing heritability of amyotrophic lateral sclerosis: Should we focus more on copy number variations?

揭示肌萎缩侧索硬化症的缺失遗传力：我们是否应更关注拷贝数变异？

Neural Regeneration Research

IF6.7

2026-05-010

PRE

Artificial Intelligence in Transcriptomics: From Human-in-the-Loop to Agentic AI

转录组学中的人工智能：从人机协同到智能体AI

Journal of Personalized Medicine

IF3

2026-04-050

OAAI

Multi-Omics Integration for Advancing Glioma Precision Medicine

多组学整合以推进胶质瘤精准医学

Annals of Clinical and Translational Neurology

IF3.9

2025-11-170

OAAI

Artificial Intelligence-Driven Multi-Omics Approaches in Glioblastoma

人工智能驱动的多组学方法在胶质母细胞瘤中的应用

International Journal of Molecular Sciences 2025, Vol. 26, Page 9362

IF4.9

2025-09-260

OAAI

Predicting amyotrophic lateral sclerosis in the pre-symptomatic phase: Insights from SOD1G93A mouse gene expression profiles

预测前驱症状期肌萎缩侧索硬化症：来自SOD1G93A小鼠基因表达谱的见解

Experimental Neurology

IF4.2

2025-06-060

OA

Increased copy-number variant load of associated risk genes in sporadic cases of amyotrophic lateral sclerosis

散发性肌萎缩性侧索硬化症相关危险基因拷贝数变异负荷增加

CELLULAR AND MOLECULAR LIFE SCIENCES

IF6.2

2024-07-270

OAAI

The multifaceted role of the CXC chemokines and receptors signaling axes in ALS pathophysiology

PROGRESS IN NEUROBIOLOGY

IF6.1

2024-04-010

OAAI

In vitro exposure to PM2.5 of olfactory Ensheathing cells and SH-SY5Y cells and possible association with neurodegenerative processes

ENVIRONMENTAL RESEARCH

IF7.7

2024-01-014

PRE

Transcriptomic Analysis in the Hippocampus and Retina of Tg2576 AD Mice Reveals Defective Mitochondrial Oxidative Phosphorylation and Recovery by Tau 12A12mAb Treatment

IF5.2

2023-09-121

OAAI

A Diagnostic Gene-Expression Signature in Fibroblasts of Amyotrophic Lateral Sclerosis

IF5.2

2023-07-183

OAAI

CXCR2 Is Deregulated in ALS Spinal Cord and Its Activation Triggers Apoptosis in Motor Neuron-Like Cells Overexpressing hSOD1-G93A

CXCR2在ALS脊髓中被解除调节，其激活触发过表达hSOD1-G93A的运动神经元样细胞凋亡

IF5.2

2023-07-095

OAAI

Detection of Single-Nucleotide and Copy Number Defects Underlying Hyperphenylalaninemia by Next-Generation Sequencing

IF3.9

2023-07-041

OAAI

Cracking the Code of Neuronal Cell Fate

破解神经元细胞命运的密码

IF5.2

2023-03-300

OAAI

Detection of Structural Variants by NGS: Revealing Missing Alleles in Lysosomal Storage Diseases

IF3.9

2022-07-291

OAAI

A Targeted Next-Generation Sequencing Panel to Genotype Gliomas

靶向下一代测序小组对胶质瘤进行基因分型

IF3.4

2022-06-244

OAAI

Dysregulated miRNAs as Biomarkers and Therapeutical Targets in Neurodegenerative Diseases

JOURNAL OF PERSONALIZED MEDICINE

IF3

2022-05-1046

OAAI

The Advent of Omics Sciences in Clinical Trials of Motor Neuron Diseases

JOURNAL OF PERSONALIZED MEDICINE

IF3

2022-05-078

OAAI

The Utility of Genomic Testing for Hyperphenylalaninemia

JOURNAL OF CLINICAL MEDICINE

IF2.9

2022-02-185

OAAI

CXCR2 increases in ALS cortical neurons and its inhibition prevents motor neuron degeneration in vitro and improves neuromuscular function in SOD1G93A mice

NEUROBIOLOGY OF DISEASE

IF5.6

2021-12-019

OAAI

Transcriptional Profiles of Cell Fate Transitions Reveal Early Drivers of Neuronal Apoptosis and Survival

细胞命运转换的转录谱揭示了神经元凋亡和存活的早期驱动因素

IF5.2

2021-11-194

OAAI