Sara Magliocca

- sara.magliocca@na.icar.cnr.it
Sara Magliocca

Dr.ssa Sara Magliocca is Postdoctoral Fellow, Institute for High Performance Computing and Networking (ICAR), CNR, Naples, Italy, 2014. PhD, Cellular and Molecula Biotechnology, “seconda Università degli Studi di Napoli (SUN), Caserta, Italy, 2013. Master Degree in Biotechnology, “Seconda Università degli Studi di Napoli” (SUN), Caserta, Italy, 2010.


Publications

Order by year - citations - title

Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene Cited 3 times. Human molecular genetics 2013
TNFRSF11A GENE ALLELIC VARIANTS ARE ASSOCIATED WITH PAGET'S DISEASE OF BONE AND INTERACT WITH SQSTM1 MUTATIONS TO CAUSE THE SEVERITY OF THE DISORDER Cited 1 times. OSTEOPOROSIS INTERNATIONAL 22, 276-276 2011
Interaction between FGF23 R176W mutation and C716T nonsynonymous change (T239M, rs7955866) in FGF23 on the clinical phenotype in a family with autosomal dominant hypophosphatemic rickets BioScientifica 2013
piR_015520 belongs to Piwi-associated RNAs regulates expression of the human melatonin receptor 1A gene Cited 25 times. PloS one 6 (7), e22727 2011
A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease Cited 17 times. Journal of Bone and Mineral Research 27 (2), 443-452 2012
A Functional Allelic Variant of the FGF23 Gene Is Associated with Renal Phosphate Leak in Calcium Nephrolithiasis Cited 6 times. Journal of Clinical Endocrinology & Metabolism 97 (5), E840-E844 2012
The melatonin receptor 1A (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis Cited 5 times. Nephrology Dialysis Transplantation 27 (1), 210-218 2012