Fernando Gianfrancesco

Author

Institute of Genetics and Biophysics ORCID

Also Known As

F Gianfrancesco, F. Gianfrancesco, F., Gianfrancesco, Fernando Gianfrancesco, Jean-Pierre Devogelaer, F. Gianfrancesco

102

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Institute of Genetics and Biophysics National Research Council Istituto Neurologico Mediterraneo University of Campania "Luigi Vanvitelli"University of Siena

About

Fernando Gianfrancesco is an author at Institute of Genetics and Biophysics specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	21	1.4K
2	Natural Sciences	5	5	173
3	Public Health	2	2	23
4	Language Studies	1	1	40
5	Social Sciences	1	1	40

Fernando Gianfrancesco

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti Asma Smahi, Nina S. Heiss, Petra Kioschis, Nature Transcriptional RegulationGeneticsGenomic MechanismPathologyMolecular Genetics	2000	736
FSHR gene polymorphisms influence bone mineral density and bone turnover in postmenopausal women Domenico Rendina, Fernando Gianfrancesco, Gianpaolo De Filippo, European Journal of Endocrinology	2010	99
Identification of a novel candidate gene,<i>CASC2</i>, in a region of common allelic loss at chromosome 10q26 in human endometrial cancer Paola Baldinu, Antonio Cossu, Antonella Manca, Human Mutation	2004	92
A synaptobrevin–like gene in the Xq28 pseudoautosomal region undergoes X inactivation Mark D’Esposito, Alfredo Ciccodicola, Fernando Gianfrancesco, Nature Genetics Natural SciencesMolecular BiologyMolecular GeneticsIntracellular TraffickingGene Expression	1996	89
Identification of sixteen novel candidate genes for late onset Parkinson’s disease Alessandro Gialluisi, Mafalda Giovanna Reccia, Nicola Modugno, Molecular Neurodegeneration	2021	83
piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene Teresa Esposito, Sara Magliocca, Daniela Formicola, PLoS ONE Systems BiologyFunctional GenomicsDevelopmental BiologyPirnas ConsistGenetics	2011	79
SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone Luigi Gennari, Fernando Gianfrancesco, Marco Di Stefano, Journal of Bone and Mineral Research SclerostinConsecutive Pdb PatientsGeneticsPathologySqstm1 Gene Mutations	2010	76
ZNF687 Mutations in Severe Paget Disease of Bone Associated with Giant Cell Tumor Giuseppina Divisato, Daniela Formicola, Teresa Esposito, The American Journal of Human Genetics	2016	76
Identification of a Novel Gene and a Common Variant Associated with Uric Acid Nephrolithiasis in a Sardinian Genetic Isolate Fernando Gianfrancesco, Teresa Esposito, Maria Neve Ombra, The American Journal of Human Genetics Urological ResearchUrologySardinian Genetic IsolateKidney ResearchMedicine	2003	75
Common susceptibility alleles and <i>SQSTM1</i> mutations predict disease extent and severity in a multinational study of patients with Paget's disease Omar Albagha, Micaela Rios Visconti, Nerea Alonso, Journal of Bone and Mineral Research	2013	55

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