Filomena Baorda - Concepedia

Author

Filomena Baorda

Istituti di Ricovero e Cura a Carattere Scientifico

Also Known As

F. Baorda, Filomena Baorda

Publications

384

Citations

H-Index

Concepts

All Affiliations

Istituti di Ricovero e Cura a Carattere Scientifico Casa Sollievo della Sofferenza University of Toronto McGill University University of Milan

About

Filomena Baorda is an author at Istituti di Ricovero e Cura a Carattere Scientifico specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	200
2	Cell Biology	2	2	42
3	Natural Sciences	1	1	20
4	Clinical Nutrition	1	1	29
5	Molecular Biology	1	1	20

Filomena Baorda

Publications

358

Citations

H-Index

Page 1

	Year	Citations
CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort Vito Guarnieri, Claudia Battista, Lucia Anna Muscarella, Cellular Oncology MedicineParathyroid DiseasePathologyCdc73 MutationsMolecular Oncology	2012	85
20 novel point mutations and one large deletion in EXT1 and EXT2 genes: Report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis Michele Ciavarella, Michelina Coco, Filomena Baorda, Gene Genetic DisorderMedicineGeneticsPathologyHereditary Multiple Exostosis	2012	29
Vitamin D status in primary hyperparathyroidism: effect of genetic background Claudia Battista, Vito Guarnieri, Vincenzo Carnevale, Endocrine Parathyroid HormoneClinical NutritionParathyroid DiseaseVitamin D StatusParathyroid Gland	2016	29
Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism Luigia Cinque, Angelo Sparaneo, Laura Penta, The Journal of Clinical Endocrinology & Metabolism	2017	27
Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family Vito Guarnieri, Raewyn M. Seaberg, Catherine A. Kelly, BMC Medical Genetics	2017	26
Spectrum ofPTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: Identification of thirteen novel alleles Maria D’Apolito, Vincenza Formica, Filomena Baorda, Human Mutation	2004	24
EZH2 and ZFX oncogenes in malignant behaviour of parathyroid neoplasms Eliana Sanpaolo, Mattia Miroballo, Sabrina Corbetta, Endocrine Tumor BiologyMalignant DiseaseMedicineZfx OncogenesPathology	2016	22
Identification and Functional Characterization of Three NoLS (Nucleolar Localisation Signals) Mutations of the CDC73 Gene Valerio Pazienza, Annamaria la Torre, Filomena Baorda, PLoS ONE Three NolsHyperparathyroidism Jaw-tumour SyndromeNucleolar Localisation SignalsGeneticsParathyroid Disease	2013	20
Calcium-sensing-related gene mutations in hypercalcaemic hypocalciuric patients as differential diagnosis from primary hyperparathyroidism: detection of two novel inactivating mutations in an Italian population Paolo Stratta, Guido Merlotti, Claudio Musetti, Nephrology Dialysis Transplantation	2014	19
A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome Maria Grazia Chiofalo, Angelo Sparaneo, Massimiliano Chetta, Cellular Oncology Mendelian DisorderItalian FamilyGenetic DisorderGeneticsParathyroid Disease	2014	18

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