Marco Di Duca - Concepedia

Author

Marco Di Duca

Also Known As

Alessia Omenetti, Antonella Insalaco, M Di Duca, M. DI DUCA, M. Di Duca, MARCO DI DUCA, MARCO Di DUCA, Marco DI Duca, Marco Di Duca, Marco Di Duca

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Istituto Giannina Gaslini University of Genoa Istituti di Ricovero e Cura a Carattere Scientifico University of Padua Bambino Gesù Children's Hospital

About

Marco Di Duca is an author at Istituto Giannina Gaslini specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	24	1.3K
2	Allergy	2	2	138
3	Biochemistry	2	2	78
4	Natural Sciences	1	1	17
5	Biology	1	1	32

Marco Di Duca

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma Hamid Azzedine, Alessandra Bolino, T. Taïeb, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyEarly-onset Glaucoma	2003	301
Broadening the Spectrum of Diseases Related to Podocin Mutations Gianluca Caridi, Roberta Bertelli, Marco Di Duca, Journal of the American Society of Nephrology	2003	183
Clinical presentation and pathogenesis of cold-induced autoinflammatory disease in a family with recurrence of an NLRP12 mutation Silvia Borghini, Sara Tassi, Sabrina Chiesa, Arthritis & Rheumatism	2010	182
Prevalence, Genetics, and Clinical Features of Patients Carrying Podocin Mutations in Steroid-Resistant Nonfamilial Focal Segmental Glomerulosclerosis Gianluca Caridi, Roberta Bertelli, Alba Carrea, Journal of the American Society of Nephrology	2001	179
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin Roberta Bertelli, Fabrizio Ginevri, Gianluca Caridi, American Journal of Kidney Diseases Glomerular DiseaseGlomerulonephritisTransplantation SurgeryUrologyRenal Function	2003	154
Neutrophils from patients with <i>TNFRSF1A</i> mutations display resistance to tumor necrosis factor–induced apoptosis: Pathogenetic and clinical implications Andrea D’Osualdo, Francesca Ferlito, Ignazia Prigione, Arthritis & Rheumatism	2006	143
Distinct pathogenetic mechanisms for PHOX2B associated polyalanine expansions and frameshift mutations in congenital central hypoventilation syndrome Tiziana Bachetti, Ivana Matera, Silvia Borghini, Human Molecular Genetics GeneticsDistinct Pathogenetic MechanismsTranscriptional RegulationAbnormal DevelopmentNeurogenetics	2005	118
Lysyl Oxidase Activates the Transcription Activity of Human Collagene III Promoter Monia Giampuzzi, Gerardo Botti, Marco Di Duca, Journal of Biological Chemistry	2000	117
Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements Renata Bocciardi, Domenico Bordo, Marco Di Duca, European Journal of Human Genetics FibrosisMutational AnalysisGeneticsPathogenesisPathology	2008	102
Parental origin and somatic mosaicism of PHOX2B mutations in Congenital Central Hypoventilation Syndrome Sara Parodi, Tiziana Bachetti, Francesca Lantieri, Human Mutation	2007	59

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