Rita Genesio - Concepedia

Author

Rita Genesio

University of Naples Federico II ORCID

Also Known As

Floriana Fabbrini, Genesio Rita, Genesio, Rita, Lucio Nitsch, R Genesio, R. Genesio, RITA GENESIO, Rita Genesio

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

University of Naples Federico II Federico II University Hospital Institute for Experimental Endocrinology and Oncology National Research Council Istituti di Ricovero e Cura a Carattere Scientifico

About

Rita Genesio is an author at University of Naples Federico II specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	339
2	Cell Biology	3	3	175
3	Health Sciences	2	2	48
4	Cellular Physiology	2	2	79
5	Public Health	1	1	19

Rita Genesio

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies Francesca Romana Grati, D. Molina Gomes, José Carlos Ferreira, Prenatal Diagnosis	2015	303
Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy A. Conti, Floriana Fabbrini, Paola D'Agostino, BMC Genomics	2007	142
Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells Antonella Izzo, Maria Nitti, Nunzia Mollo, Human Molecular Genetics MitophagyMitochondrial ActivityMitochondrial DysfunctionDown Syndrome CellsMitochondrial Biology	2017	96
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2 Enza Mozzillo, Maurizio Delvecchio, Massimo Carella, BMC Medical Genetics	2014	75
Clinical description of a patient carrying the smallest reported deletion involving 10p14 region Daniela Melis, Rita Genesio, Pasquale Boemio, American Journal of Medical Genetics Part A	2012	62
Genetic and molecular analysis of a new unbalanced X;18 rearrangement: localization of the diminished ovarian reserve disease locus in the distal Xq POF1 region Francesca Fusco, Mariateresa Paciolla, Emily Chen, Human Reproduction	2011	54
Constitutional chromothripsis involving the critical region of 9q21.13 microdeletion syndrome Rita Genesio, Paolo Fontana, Angela Mormile, Molecular Cytogenetics	2015	48
Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation Rita Genesio, Angela Mormile, Maria Rosaria Licenziati, Molecular Cytogenetics	2015	46
Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype Rita Genesio, Daniela Melis, Sole Gatto, Epigenetics Large Xq RegionChromatinUrologyDevelopmental BiologyGenetic Disorder	2011	46
Loss-of-function variants in myocardin cause congenital megabladder in humans and mice Arjan C. Houweling, Glenda M. Beaman, Alex V. Postma, Journal of Clinical Investigation Cardiac MuscleCardiomyopathyDevelopmental BiologyMyocd ResultGenetic Disorder	2019	46

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