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M. Godi · SciRah

Researcher profile · Semantic Scholar

M. Godi

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M. Godi — researcher profile on SciRah

h-index: 14
Works: 19
Citations: 492

Most-cited papers

The natural history of Cri du Chat Syndrome. A report from the Italian Register.
P. Mainardi, G. Pastore, C. Castronovo, M. Godi +5 more
2006European Journal of Medical Genetics90 citations
Semantic Scholar
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient.
L. Corrado, Y. Carlomagno, Luca Falasco, Simona Mellone +6 more
2011Neurobiology of Aging80 citations
Semantic Scholar
ATXN-2 CAG repeat expansions are interrupted in ALS patients
L. Corrado, L. Mazzini, G. Oggioni, B. Luciano +3 more
2011Human Genetics71 citations
Semantic Scholar
Rare Variants in the TREX1 Gene and Susceptibility to Autoimmune Diseases
N. Barizzone, S. Monti, Simona Mellone, M. Godi +4 more
2013BioMed Research International35 citations Open access
Semantic Scholar
A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency.
M. Godi, Simona Mellone, A. Petri, T. Arrigo +7 more
2009Journal of Clinical Endocrinology and Metabolism28 citations
Semantic Scholar
Growth hormone (GH) deficiency type II: a novel GH-1 gene mutation (GH-R178H) affecting secretion and action.
Vibor Petkovic, M. Godi, A. Pandey, Didier Lochmatter +5 more
2010Journal of Clinical Endocrinology and Metabolism25 citations Open access
Semantic Scholar
A novel deletion in the GH1 gene including the IVS3 branch site responsible for autosomal dominant isolated growth hormone deficiency.
D. Vivenza, L. Guazzarotti, M. Godi, D. Frasca +4 more
2006Journal of Clinical Endocrinology and Metabolism25 citations Open access
Semantic Scholar
A functional common polymorphism in the vitamin D-responsive element of the GH1 promoter contributes to isolated growth hormone deficiency.
M. Giordano, M. Godi, Simona Mellone, A. Petri +11 more
2008Journal of Clinical Endocrinology and Metabolism24 citations
Semantic Scholar
Genitourinary Anomalies in Mowat-Wilson Syndrome with Deletion/Mutation in the Zinc Finger Homeo Box 1B Gene (ZFHX1B)
L. Garavelli, P. Cerruti-Mainardi, R. Virdis, S. Pedori +11 more
2005Hormone Research in Paediatrics23 citations Open access
Semantic Scholar
Topical nerve growth factor prevents neurodegenerative and vascular stages of diabetic retinopathy
G. Zerbini, S. Maestroni, L. Leocani, A. Mosca +11 more
2022Frontiers in Pharmacology19 citations Open access
Semantic Scholar
A variation in a Pit-1 site in the growth hormone gene (GH1) promoter induces a differential transcriptional activity.
M. Giordano, M. Godi, Francesca Giacopelli, M. Lessi +7 more
2006Molecular and Cellular Endocrinology16 citations
Semantic Scholar
A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing.
D. Vivenza, M. Godi, M. Faienza, Simona Mellone +8 more
2011European Journal of Endocrinology15 citations Open access
Semantic Scholar
Growth hormone (GH)-releasing hormone increases the expression of the dominant-negative GH isoform in cases of isolated GH deficiency due to GH splice-site mutations.
Vibor Petkovic, M. Godi, Didier Lochmatter, A. Eblé +3 more
2010Endocrinology15 citations
Semantic Scholar
A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency
Y. Carlomagno, M. Salerno, D. Vivenza, D. Capalbo +7 more
2009Journal of Endocrinological Investigation14 citations
Semantic Scholar
The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism
S. Moia, M. Godi, Ge Walker, M. Roccio +7 more
2013Journal of Endocrinological Investigation8 citations
Semantic Scholar
Functional SNPs within the intron 1 of the PROP1 gene contribute to combined growth hormone deficiency (CPHD).
M. Godi, Simona Mellone, L. Tiradani, Rita Marabese +8 more
2012Journal of Clinical Endocrinology and Metabolism4 citations
Semantic Scholar
Analisi molecolare del gene HESX1 in soggetti affetti da ipopituitarismo e deficit di GH.
Daniela Vivenza, G. Corneli, M. Godi, Simonetta Bellone +9 more
20070 citations
Semantic Scholar
Idiopathic isolated GH deficiency (IGHD) and combined pituitary hormone deficiency (CPHD) in Italy: genetic screening and clinical correlates
G. Corneli, D. Vivenza, Simona Mellone, L. Tiradani +7 more
20070 citations
Semantic Scholar
[Genetics of low stature].
G. Bona, G. Corneli, D. Vivenza, S. Bellone +4 more
2007Minerva Pediatrica0 citations
Semantic Scholar

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