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Corrado Angelini

Corrado Angelini

D-Index & Metrics

Medicine

D-Index
110
Citations
48675
World Ranking
5521
National Ranking
174

Overview

Corrado Angelini is affiliated with the University of Padua in Italy. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, and Medicine, with a focus on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology, and Cardiology and Cardiovascular Medicine.

Their scientific contributions have largely centered on topics such as Muscle Physiology and Disorders, Genetic Neurodegenerative Diseases, Neurogenetic and Muscular Disorders Research, Cardiomyopathy and Myosin Studies, Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, as well as Nuclear Structure and Function.

Frequent co-authors collaborating with Corrado Angelini include:

  • Gabriele Siciliano
  • Valentina Pegoraro
  • Massimiliano Filosto
  • Daniela Tavian
  • Roberta Marozzo

Angelini has published extensively in several journals, with notable frequent publication venues being:

  • Muscles
  • Neurology
  • European Journal of Translational Myology
  • Frontiers in Neurology
  • PubMed

Among the recent papers associated with Corrado Angelini are:

  • "Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy," published in 2020 in JAMA Network Open
  • "LGMD. Identification, description and classification," published in 2020 in PubMed
  • "Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis," published in 2020 in Scientific Reports
  • "ETF dehydrogenase advances in molecular genetics and impact on treatment," published in 2021 in Critical Reviews in Biochemistry and Molecular Biology
  • "MicroRNAs and HDAC4 protein expression in the skeletal muscle of ALS patients," published in 2020 in Clinical Neuropathology

This body of work reflects a consistent involvement in neurogenetic and muscular disorder research, molecular mechanisms underlying muscle pathology, and related genetic studies.

Best Publications

  • The BABAR detector

    B. Aubert;A. Bazan;A. Boucham;D. Boutigny

  • ATLAS: Technical proposal for a general-purpose p p experiment at the Large Hadron Collider at CERN

    W.W. Armstrong;W. Burris;D.M. Gingrich;P. Green

  • Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

    Jing Liu;Masashi Aoki;Isabel Illa;Chenyan Wu

  • Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells

    Marco Spinazzi;Alberto Casarin;Vanessa Pertegato;Leonardo Salviati

  • Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind, placebo-controlled, multicentre study

    James F Howard;Kimiaki Utsugisawa;Michael Benatar;Hiroyuki Murai

  • MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.

    A. Chomyn;A. Martinuzzi;M. Yoneda;A. Daga

  • Carnitine Deficiency of Human Skeletal Muscle with Associated Lipid Storage Myopathy: A New Syndrome

    Andrew G. Engel;Corrado Angelini

  • MELAS: Clinical features, biochemistry, and molecular genetics

    E. Ciafaloni;E. Ricci;S. Shanske;C. T. Moraes

  • β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

    Carsten G. Bönnemann;Raju Modi;Satoru Noguchi;Yuji Mizuno

  • EXPLORING THE MOLECULAR-BASIS FOR VARIABILITY AMONG PATIENTS WITH BECKER MUSCULAR-DYSTROPHY - DYSTROPHIN GENE AND PROTEIN STUDIES

    Alan H. Beggs;Eric P. Hoffman;Judith R. Snyder;Kiichi Arahata

  • Gene for Chronic Proximal Spinal Muscular Atrophies Maps To Chromosome-5q

    J. Melki;S. Abdelhak;Peter Sheth;M. F. Bachelot

  • Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb–MyoD pathways in muscle regeneration

    Marina Bakay;Zuyi Wang;Zuyi Wang;Gisela Melcon;Louis Schiltz

  • Improved diagnosis of Becker muscular dystrophy by dystrophin testing.

    E. P. Hoffman;L. M. Kunkel;C. Angelini;A. Clarke

  • 229th ENMC international workshop: Limb girdle muscular dystrophies - Nomenclature and reformed classification Naarden, the Netherlands, 17-19 March 2017.

    Volker Straub;Alexander Murphy;Bjarne Udd;Angelini Corrado

  • Correlating phenotype and genotype in the periodic paralyses

    T. M. Miller;M. R. Dias da Silva;H. A. Miller;H. Kwiecinski

  • Systemic Carnitine Deficiency — A Treatable Inherited Lipid-Storage Disease Presenting as Reye's Syndrome

    P R Chapoy;C Angelini;W J Brown;J E Stiff

  • Mutations in the sarcoglycan genes in patients with myopathy.

    David J. Duggan;J. Rafael Gorospe;Marina Fanin;Eric P. Hoffman

  • Increases in walking distance in patients with peripheral vascular disease treated with L-carnitine: a double-blind, cross-over study.

    G Brevetti;M Chiariello;G Ferulano;A Policicchio

  • A multicenter, double-blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophy

    Marco Domenico Bonifati;Giampietro Ruzza;Piero Bonometto;Angela Berardinelli

  • Myocardial Involvement Is Very Frequent Among Patients Affected With Subclinical Becker's Muscular Dystrophy

    Paola Melacini;M. Fanin;G. A. Danieli;C. Villanova

Frequent Co-Authors

A. Seiden
A. Seiden University of California, Santa Cruz
J. D. Richman
J. D. Richman University of California, Santa Barbara
W. H. Toki
W. H. Toki Colorado State University
R. Waldi
R. Waldi University of Rostock
F. C. Porter
F. C. Porter California Institute of Technology
A. Roodman
A. Roodman Stanford University
C. Hearty
C. Hearty University of British Columbia
B. N. Ratcliff
B. N. Ratcliff Stanford University
J. M. Roney
J. M. Roney University of Victoria
D. G. Hitlin
D. G. Hitlin California Institute of Technology

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