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Antonio Musio

University of Ferrara · IT
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Area of research
Molecular Biology · Genetics
Research interest
Research interests include Medicine, Biology, Surgery, Genetics, Phenotype, and Cohesin.
h-index
citations
255
works
11
NIH funding
primary concept
email

Recent publications

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, <scp>genotype–phenotype</scp> correlations and common mechanisms
American Journal of Medical Genetics Part A 2023cited by 39position: middledoi
A novel, reusable, realistic neurosurgical training simulator for cerebrovascular bypass surgery: Iatrotek® bypass simulator validation study and literature review
Frontiers in Surgery 2023cited by 0position: middledoi
Transpars approach for L5-S1 foraminal and extra-foraminal lumbar disc herniations: technical note
Journal of Neurosurgical Sciences 2022cited by 4position: middledoi
Vermian subtentorial arteriovenous malformation supplied by the artery of Wollschlaeger and Wollschlaeger
Clinical Neurology and Neurosurgery 2021cited by 4position: middledoi
The Infratemporal Retro-Eustachian Transposition of the Temporoparietal Fascial Flap for Clival Reconstruction After Endoscopic Endonasal Approach: An Anatomic Conceptual Technique
Operative Neurosurgery 2021cited by 2position: middledoi
Epidermoid cyst of the anterior clinoid process: report of a unique finding and literature review of the middle cranial fossa locations
Clinical Neurology and Neurosurgery 2020cited by 7position: middledoi
Filthy operative rooms and other mistakes during movies on neurosurgical procedures
Clinical Neurology and Neurosurgery 2020cited by 1position: firstdoi
Reciprocal Regulation of TRPS1 and miR-221 in Intervertebral Disc Cells
Cells 2019cited by 20position: middledoi
Functional Outcome After Odontoid Fractures in the Elderly
Acta neurochirurgica. Supplementum 2019cited by 5position: middledoi
Separase prevents genomic instability by controlling replication fork speed
Nucleic Acids Research 2017cited by 23position: lastdoi
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Human Molecular Genetics 2014cited by 150position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Lorenzo Mongardi · University of Ferrara5 papers (2019–2023)Michele Alessandro Cavallo · University of Ferrara4 papers (2019–2022)Pasquale De Bonis · Neurological Surgery4 papers (2019–2022)Luigino Tosatto · University of Ferrara3 papers (2020–2023) · 3 papers (2020–2023) · 3 papers (2020–2023)Giorgio Lofrese · University of Ferrara3 papers (2019–2023)Alba Scerrati · The Ohio State University Wexner Medical Center2 papers (2020–2022)Letizia Penolazzi · University of Ferrara1 papers (2019–2019) · 1 papers (2019–2019)Jacopo Visani · University of Ferrara1 papers (2022–2022) · 1 papers (2017–2017)Elisabetta Lambertini · University of California, Davis1 papers (2019–2019)Elisa Palumbo · University of Padua1 papers (2017–2017)Carlotta Gandini · University of Ferrara1 papers (2019–2019)Franco Servadei · Tulane University1 papers (2019–2019) · 1 papers (2017–2017)Roberto Colasanti · The Ohio State University Wexner Medical Center1 papers (2023–2023)Antonella Russo · University of Padua1 papers (2017–2017) · 1 papers (2019–2019)
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