Michela Godi - Concepedia

Author

Michela Godi

Università degli Studi del Piemonte Orientale “Amedeo Avogadro”

Also Known As

M Godi, M. Godi, Michela Godi

Publications

463

Citations

H-Index

Concepts

All Affiliations

Università degli Studi del Piemonte Orientale “Amedeo Avogadro”University of Milan University of Messina University Hospital of Bern University Children’s Hospital Bern

About

Michela Godi is an author at Università degli Studi del Piemonte Orientale “Amedeo Avogadro” specializing in medicine, genetics, and endocrinology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	161
2	Endocrinology	3	3	47
3	Cell Biology	2	2	31
4	Communicative Disorders	1	1	94
5	Diabetes	1	1	15

Michela Godi

Publications

384

Citations

H-Index

Page 1

	Year	Citations
The natural history of Cri du Chat Syndrome. A report from the Italian Register Paola Cerruti Mainardi, Guido Pastore, Chiara Castronovo, European Journal of Medical Genetics Natural HistoryItalian RegisterCommunicative DisordersChat Syndrome	2006	94
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient Lucia Corrado, Yari Carlomagno, Luca Falasco, Neurobiology of Aging Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMendelian DisorderGeneticsNovel Peripherin Gene	2010	67
Rare Variants in the<i>TREX1</i>Gene and Susceptibility to Autoimmune Diseases Nadia Barizzone, Sara Monti, Simona Mellone, BioMed Research International Autoimmune DiseaseSystemic Lupus ErythematosusTrex1 GeneLupusImmunodeficiencies	2013	32
A Recurrent Signal Peptide Mutation in the Growth Hormone Releasing Hormone Receptor with Defective Translocation to the Cell Surface and Isolated Growth Hormone Deficiency Michela Godi, Simona Mellone, Antonella Petri, The Journal of Clinical Endocrinology & Metabolism	2009	26
Growth Hormone (GH) Deficiency Type II: A Novel GH-1 Gene Mutation (GH-R178H) Affecting Secretion and Action Vibor Petkovic, Michela Godi, Amit V. Pandey, The Journal of Clinical Endocrinology & Metabolism	2009	26
A Novel Deletion in the<i>GH1</i>Gene Including the IVS3 Branch Site Responsible for Autosomal Dominant Isolated Growth Hormone Deficiency Daniela Vivenza, Laura Guazzarotti, Michela Godi, The Journal of Clinical Endocrinology & Metabolism	2006	22
A Functional Common Polymorphism in the Vitamin D-Responsive Element of the<i>GH1</i>Promoter Contributes to Isolated Growth Hormone Deficiency Mara Giordano, Michela Godi, Simona Mellone, The Journal of Clinical Endocrinology & Metabolism	2007	21
Genitourinary Anomalies in Mowat-Wilson Syndrome with Deletion/Mutation in the Zinc Finger Homeo Box 1B Gene (ZFHX1B) Livia Garavelli, P. Cerruti-Mainardi, R Virdis, Hormone Research in Paediatrics	2005	18
A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency Yari Carlomagno, Mariacarolina Salerno, Daniela Vivenza, Journal of Endocrinological Investigation Transcriptional RegulationDevelopmental BiologyPituitary GlandGenetic DisorderGenetics	2009	16
A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing Daniela Vivenza, Michela Godi, Maria Felicia Faienza, European Journal of Endocrinology	2011	16

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