Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

E. Gazzerro · SciRah

Researcher profile · Semantic Scholar

E. Gazzerro

Share profile

E. Gazzerro — researcher profile on SciRah

h-index: 30
Works: 75
Citations: 3,516

Most-cited papers

Bone morphogenetic proteins and their antagonists
E. Gazzerro, E. Canalis
2007Reviews in Endocrine & Metabolic Disorders376 citations
Semantic Scholar
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors.
F. Cetani, E. Pardi, S. Borsari, P. Viacava +9 more
2004Journal of Clinical Endocrinology and Metabolism244 citations
Semantic Scholar
Notch 1 Overexpression Inhibits Osteoblastogenesis by Suppressing Wnt/β-Catenin but Not Bone Morphogenetic Protein Signaling*
V. Deregowski, E. Gazzerro, Leah Priest, S. Rydziel +1 more
2006Journal of Biological Chemistry234 citations Open access
Semantic Scholar
Notch 1 impairs osteoblastic cell differentiation.
Maria Sciaudone, E. Gazzerro, Leah Priest, A. Delany +1 more
2003Endocrinology191 citations
Semantic Scholar
Caveolinopathies: from the biology of caveolin-3 to human diseases
E. Gazzerro, F. Sotgia, C. Bruno, M. Lisanti +1 more
2010European Journal of Human Genetics190 citations Open access
Semantic Scholar
Skeletal overexpression of gremlin impairs bone formation and causes osteopenia.
E. Gazzerro, R. Pereira, V. Jorgetti, S. Olson +2 more
2005Endocrinology186 citations
Semantic Scholar
Relationship between Cognitive Function, Growth Hormone and Insulin-Like Growth Factor I Plasma Levels in Aged Subjects
A. Rollero, G. Murialdo, S. Fonzi, S. Garrone +4 more
1998Neuropsychobiology134 citations
Semantic Scholar
Menstrual cycle and ovary alterations in women with epilepsy on antiepileptic therapy
G. Murialdo, C. A. Galimberti, F. Magri, P. Sampaolo +9 more
1997Journal of Endocrinological Investigation129 citations
Semantic Scholar
The leukodystrophy protein FAM126A/Hyccin regulates PI4P synthesis at the plasma membrane
J. Baskin, Xudong Wu, Romain Christiano, M. Oh +13 more
2015Nature Cell Biology122 citations Open access
Semantic Scholar
Conditional Deletion of Gremlin Causes a Transient Increase in Bone Formation and Bone Mass*
E. Gazzerro, A. Smerdel-Ramoya, Stefano Zanotti, L. Stadmeyer +3 more
2007Journal of Biological Chemistry119 citations Open access
Semantic Scholar
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract
F. Zara, R. Biancheri, C. Bruno, L. Bordo +14 more
2006Nature Genetics99 citations Open access
Semantic Scholar
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy
N. Vanni, Floriana Fruscione, E. Ferlazzo, P. Striano +11 more
2014Annals of Neurology87 citations
Semantic Scholar
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy
L. Bello, L. Piva, A. Barp, A. Taglia +33 more
2012Neurology84 citations Open access
Semantic Scholar
Therapeutic potential of proteasome inhibition in Duchenne and Becker muscular dystrophies.
E. Gazzerro, S. Assereto, A. Bonetto, F. Sotgia +8 more
2010American Journal of Pathology79 citations Open access
Semantic Scholar
Localized Treatment with a Novel FDA-Approved Proteasome Inhibitor Blocks the Degradation of Dystrophin and Dystrophin-Associated Proteins in mdx Mice
G. Bonuccelli, F. Sotgia, F. Capozza, E. Gazzerro +2 more
2007Cell Cycle79 citations Open access
Semantic Scholar
Targeting gut dysbiosis against inflammation and impaired autophagy in Duchenne muscular dystrophy
Hilal Kalkan, E. Pagano, D. Paris, E. Panza +11 more
2023EMBO Molecular Medicine72 citations Open access
Semantic Scholar
Effects of non‐euphoric plant cannabinoids on muscle quality and performance of dystrophic mdx mice
F. Iannotti, E. Pagano, A. S. Moriello, F. Alvino +7 more
2018British Journal of Pharmacology71 citations Open access
Semantic Scholar
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
P. Striano, A. Coppola, R. Paravidino, M. Malacarne +28 more
2012Archives of Neurology71 citations Open access
Semantic Scholar
A reappraisal of the Rb1 gene abnormalities in the diagnosis of parathyroid cancer
F. Cetani, E. Pardi, P. Viacava, Giada Di Pollina +8 more
2004Clinical Endocrinology71 citations
Semantic Scholar
Genetic and pharmacological regulation of the endocannabinoid CB1 receptor in Duchenne muscular dystrophy
F. Iannotti, E. Pagano, O. Guardiola, S. Adinolfi +10 more
2018Nature Communications55 citations Open access
Semantic Scholar
Caveolinopathies: translational implications of caveolin-3 in skeletal and cardiac muscle disorders.
E. Gazzerro, A. Bonetto, C. Minetti
2011Handbook of Clinical Neurology52 citations
Semantic Scholar
The epidemiology of partialandrogen deficiency in aging men (PADAM).
E. Canalis, V. Deregowski, R. C. Pereira, E. Gazzerro
200552 citations
Semantic Scholar
Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X Axis.
E. Gazzerro, S. Baldassari, S. Assereto, Floriana Fruscione +9 more
2015American Journal of Pathology50 citations Open access
Semantic Scholar
Potentiating role of IGFBP-2 on IGF-II-stimulated alkaline phosphatase activity in differentiating osteoblasts.
C. Palermo, P. Manduca, E. Gazzerro, L. Foppiani +2 more
2004American Journal of Physiology. Endocrinology and Metabolism47 citations
Semantic Scholar
Phenotypic characterization of hypomyelination and congenital cataract
R. Biancheri, F. Zara, C. Bruno, A. Rossi +16 more
2007Annals of Neurology44 citations
Semantic Scholar
Potential drug targets within bone morphogenetic protein signaling pathways.
E. Gazzerro, C. Minetti
2007Current opinion in pharmacology (Print)41 citations
Semantic Scholar
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitro
M. Traverso, E. Gazzerro, S. Assereto, F. Sotgia +12 more
2008Laboratory Investigation40 citations Open access
Semantic Scholar
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene.
C. Fiorillo, Giacomo Brisca, D. Cassandrini, S. Scapolan +11 more
2013Biochemical and Biophysical Research Communications - BBRC34 citations
Semantic Scholar
Signals that determine the fate of osteoblastic cells.
E. Canalis, V. Deregowski, R. Pereira, E. Gazzerro
2005Journal of Endocrinological Investigation33 citations
Semantic Scholar
Zidovudine ameliorates pathology in the mouse model of Duchenne muscular dystrophy via P2RX7 purinoceptor antagonism
R. Al-khalidi, C. Panicucci, P. Cox, Natalia Chira +10 more
2018Acta Neuropathologica Communications32 citations Open access
Semantic Scholar
Hypomyelination and congenital cataract: broadening the clinical phenotype.
R. Biancheri, F. Zara, A. Rossi, M. Mathot +12 more
2011Archives of Neurology27 citations Open access
Semantic Scholar
Overexpression of twisted gastrulation inhibits bone morphogenetic protein action and prevents osteoblast cell differentiation in vitro.
E. Gazzerro, V. Deregowski, S. Vaira, E. Canalis
2005Endocrinology27 citations Open access
Semantic Scholar
Role of the Ram Domain and Ankyrin Repeats on Notch Signaling and Activity in Cells of Osteoblastic Lineage
V. Deregowski, E. Gazzerro, Leah Priest, S. Rydziel +1 more
2006Journal of Bone and Mineral Research26 citations Open access
Semantic Scholar
Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein
E. Gazzerro, S. Baldassari, Caterina Giacomini, V. Musante +13 more
2012PLoS ONE25 citations Open access
Semantic Scholar
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular Dystrophy
Lizzia Raffaghello, E. Principi, S. Baratto, C. Panicucci +9 more
2022Pharmaceuticals24 citations Open access
Semantic Scholar
Twisted gastrulation, a bone morphogenetic protein agonist/antagonist, is not required for post-natal skeletal function.
E. Gazzerro, V. Deregowski, L. Stadmeyer, N. Gale +2 more
2006Bone23 citations
Semantic Scholar
Skeletal actions of insulin-like growth factors
E. Gazzerro, E. Canalis
2006Expert Review of Endocrinology & Metabolism23 citations
Semantic Scholar
eATP/P2X7R Axis: An Orchestrated Pathway Triggering Inflammasome Activation in Muscle Diseases
C. Panicucci, Lizzia Raffaghello, Santina Bruzzone, S. Baratto +4 more
2020International Journal of Molecular Sciences22 citations Open access
Semantic Scholar
Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies
S. Assereto, Mauro Mastrototaro, S. Stringara, E. Gazzerro +8 more
2008Cell Cycle22 citations Open access
Semantic Scholar
The spectrum of GNE mutations: allelic heterogeneity for a common phenotype
M. Grandis, Rossella Gulli, D. Cassandrini, E. Gazzerro +10 more
2010Neurological Sciences21 citations
Semantic Scholar
Neuromuscular Disorders of Glycogen Metabolism
E. Gazzerro, A. Andreu, C. Bruno
2013Current Neurology and Neuroscience Reports20 citations
Semantic Scholar
Caveolinopathies: from the biology of caveolin-3 to human diseases
E. Gazzerro, F. Sotgia, C. Bruno, M. Lisanti +1 more
2009European Journal of Human Genetics20 citations Open access
Semantic Scholar
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease
M. Traverso, C. Bruno, A. Broccolini, F. Sotgia +11 more
2007Journal of Neurology Neurosurgery & Psychiatry20 citations
Semantic Scholar
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy
S. Assereto, R. Piccirillo, S. Baratto, P. Scudieri +8 more
2016Laboratory Investigation19 citations Open access
Semantic Scholar
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular Dystrophy.
E. Gazzerro, S. Baratto, S. Assereto, S. Baldassari +14 more
2019American Journal of Pathology14 citations Open access
Semantic Scholar
Novel FAM126A mutations in hypomyelination and congenital cataract disease.
M. Traverso, S. Assereto, E. Gazzerro, S. Savasta +10 more
2013Biochemical and Biophysical Research Communications - BBRC14 citations Open access
Semantic Scholar
Hypomyelination and congenital cataract: identification of novel mutations in two unrelated families.
M. Traverso, O. O. Yuregir, A. Mimouni-Bloch, A. Rossi +7 more
2013European journal of paediatric neurology12 citations
Semantic Scholar
Clinical and molecular consequences of exon 78 deletion in DMD gene
M. Traverso, S. Assereto, S. Baratto, M. Iacomino +10 more
2018Journal of Human Genetics9 citations Open access
Semantic Scholar
Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey
Lynda El‐Hassar, Ahmed Amara, B. Sanson, Oana Lăcătuș +46 more
2022Journal of Neuromuscular Diseases8 citations Open access
Semantic Scholar
Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I
S. Assereto, Angela Robbiano, M. Dirocco, A. Rossi +10 more
2014Clinical Genetics6 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

C. Minetti×27
Invite
C. Minetti — researcher profile on SciRah
C. Bruno×19
Invite
C. Bruno — researcher profile on SciRah
F. Zara×15
Invite
F. Zara — researcher profile on SciRah
S. Assereto×12
Invite
S. Assereto — researcher profile on SciRah

×11

Invite

E. Canalis — researcher profile on SciRah

R. Biancheri×9

Invite

R. Biancheri — researcher profile on SciRah

Invite

F. Sotgia — researcher profile on SciRah

Invite

M. Traverso — researcher profile on SciRah

Invite

M. Lisanti — researcher profile on SciRah

V. Deregowski×6

Invite

V. Deregowski — researcher profile on SciRah

S. Baldassari×6

Invite

S. Baldassari — researcher profile on SciRah

C. Panicucci×6

Invite

C. Panicucci — researcher profile on SciRah