Claudia Santoro

InstitutionUniversity of Campania "Luigi Vanvitelli"
AddressNaples
Italy
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    Publication Timeline
    COVID-19 publications
    Bar chart showing 1 Covid-19 publications, with a maximum of 1 publications in June 2021
    All Publications
    Bar chart showing 14 publications over 9 distinct years, with a maximum of 3 publications in 2017 and 2018
    These graphs show COVID-19 publications by month since August 2019 and all publications written by authors of COVID-19 publications over the past 30 years.

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    Publication Field Summary
    This graph shows the number and percent of publications by field. Fields are based on how the National Library of Medicine (NLM) classifies the publications' journals and might not represent the specific topics of the publications. Note that an individual publication can be assigned to more than one field. As a result, the publication counts in this graph might add up to more than the number of publications the person has written. To see the data as text, click here.
    Publication List
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Piccolo V, Russo T, Di Pinto D, Pota E, Di Martino M, Piluso G, Ronchi A, Argenziano G, Di Brizzi EV, Santoro C. Poikiloderma With Neutropenia and Mastocytosis: A Case Report and a Review of Dermatological Signs. Front Med (Lausanne). 2021; 8:680363. PMID: 34179048.
      Citations: Article has an altmetric score of 2    
    2. Piccolo V, Corneli P, Ferrara G, Russo T, Santoro C, Ronchi A, Zalaudek I, Alfano R, Argenziano G. Superimposed Blaschkoid lichen planus pigmentosus. Ital J Dermatol Venerol. 2021 Dec; 156(Suppl. 1 to No. 6):69-70. PMID: 31210466.
      Fields:    
    3. Santoro C, Giugliano T, Kraemer M, Torella A, Schwitalla JC, Cirillo M, Melis D, Berlit P, Nigro V, Perrotta S, Piluso G. Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1. PLoS One. 2018; 13(7):e0200446. PMID: 30001348.
      Citations: 3   Article has an altmetric score of 1    Fields:    Translation:Humans
    4. Santoro C, Bernardo P, Coppola A, Pugliese U, Cirillo M, Giugliano T, Piluso G, Cinalli G, Striano S, Bravaccio C, Perrotta S. Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough? Ital J Pediatr. 2018 Mar 22; 44(1):41. PMID: 29566708.
      Citations: 5   Article has an altmetric score of 1    Fields:    Translation:Humans
    5. D'Amico A, Mazio F, Ugga L, Cuocolo R, Cirillo M, Santoro C, Perrotta S, Melis D, Brunetti A. Medullary unidentified bright objects in Neurofibromatosis type 1: a case series. BMC Pediatr. 2018 02 28; 18(1):91. PMID: 29490631.
      Citations: 5   Article has an altmetric score of 9    Fields:    Translation:Humans
    6. Roth J, Ber R, Wisoff JH, Hidalgo ET, Limbrick DD, Berger DS, Thomale UW, Schulz M, Cinalli G, Santoro C, Constantini S. Endoscopic Third Ventriculostomy in Patients with Neurofibromatosis Type 1: A Multicenter International Experience. World Neurosurg. 2017 Nov; 107:623-629. PMID: 28842232.
      Citations: 4   Fields:    Translation:Humans
    7. Santoro C, Giugliano T, Bifano D, D'Anna C, D'Onofrio V, Perrotta S. From Gardner fibroma diagnosis to constitutional APC mutation detection: a one-way street. Clin Case Rep. 2017 10; 5(10):1557-1560. PMID: 29026543.
      Citations: 1   Article has an altmetric score of 1    
    8. Santoro C, Di Rocco F, Kossorotoff M, Zerah M, Boddaert N, Calmon R, Vidaud D, Cirillo M, Cinalli G, Mirone G, Giugliano T, Piluso G, D'Amico A, Capra V, Pavanello M, Cama A, Nobili B, Lyonnet S, Perrotta S. Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience. Am J Med Genet A. 2017 Jun; 173(6):1521-1530. PMID: 28422438.
      Citations: 9   Translation:HumansCells
    9. Santoro C, Apicella A, Casale F, La Manna A, Di Martino M, Di Pinto D, Indolfi C, Perrotta S. Unusual association of non-anaplastic Wilms tumor and Cornelia de Lange syndrome: case report. BMC Cancer. 2016 06 13; 16:365. PMID: 27291393.
      Citations: 1   Article has an altmetric score of 2    Fields:    Translation:Humans
    10. Santoro C, Maietta A, Giugliano T, Melis D, Perrotta S, Nigro V, Piluso G. Arg(1809) substitution in neurofibromin: further evidence of a genotype-phenotype correlation in neurofibromatosis type 1. Eur J Hum Genet. 2015 Nov; 23(11):1460-1. PMID: 25966637.
      Citations: 13   Article has an altmetric score of 12    Fields:    Translation:Humans
    11. Perrotta S, Di Iorgi N, Ragione FD, Scianguetta S, Borriello A, Allegri AE, Ferraro M, Santoro C, Napoli F, Calcagno A, Giaccardi M, Cappa M, Salerno MC, Cozzolino D, Maghnie M. Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations. Eur J Endocrinol. 2015 Apr; 172(4):461-72. PMID: 25740874.
      Citations: 6   Fields:    Translation:HumansCells
    12. Santoro C, Pacileo G, Limongelli G, Scianguetta S, Giugliano T, Piluso G, Ragione FD, Cirillo M, Mirone G, Perrotta S. LEOPARD syndrome: clinical dilemmas in differential diagnosis of RASopathies. BMC Med Genet. 2014 Apr 26; 15:44. PMID: 24767283.
      Citations: 7   Article has an altmetric score of 1    Fields:    Translation:Humans
    13. Santoro C, Malan V, Bertoli M, Boddaert N, Vidaud D, Lyonnet S. Sporadic NF1 mutation associated with a de-novo 20q11.3 deletion explains the association of unusual facies, Moyamoya vasculopathy, and developmental delay, reported by Bertoli et al. in 2009. Clin Dysmorphol. 2013 Jan; 22(1):42-3. PMID: 23207425.
      Citations: 1   Article has an altmetric score of 1    Fields:    Translation:Humans
    14. Accetturo M, Creanza TM, Santoro C, Tria G, Giordano A, Battagliero S, Vaccina A, Scioscia G, Leo P. Finding new genes for non-syndromic hearing loss through an in silico prioritization study. PLoS One. 2010 Sep 28; 5(9). PMID: 20927407.
      Citations: 8   Fields:    Translation:Humans