Roberto Della Casa

811 total citations
34 papers, 536 citations indexed

About

Roberto Della Casa is a scholar working on Rheumatology, Genetics and Physiology. According to data from OpenAlex, Roberto Della Casa has authored 34 papers receiving a total of 536 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Rheumatology, 11 papers in Genetics and 10 papers in Physiology. Recurrent topics in Roberto Della Casa's work include Glycogen Storage Diseases and Myoclonus (16 papers), Metabolism and Genetic Disorders (7 papers) and Lysosomal Storage Disorders Research (7 papers). Roberto Della Casa is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (16 papers), Metabolism and Genetic Disorders (7 papers) and Lysosomal Storage Disorders Research (7 papers). Roberto Della Casa collaborates with scholars based in Italy, Finland and Brazil. Roberto Della Casa's co-authors include Generoso Andria, Giancarlo Parenti, Daniela Melis, Rossella Parini, Rosario Pivonello, Mariacarolina Salerno, Angelo Benedetti, Paola Marcolongo, Michelina Sibilio and Pietro Strisciuglio and has published in prestigious journals such as The Journal of Pediatrics, Clinical Endocrinology and Acta Paediatrica.

In The Last Decade

Roberto Della Casa

34 papers receiving 522 citations

Peers

Roberto Della Casa

RHEUM

GENET

PHYSI

John Fernandes Netherlands

Miriam Rigoldi Italy

Fatih Süheyl Ezgü Türkiye

Anne Boney United States

Komudi Siriwardena Canada

Anke Schumann Germany

Roberta Taurisano Italy

Arthur Hays United States

Joanna Taybert Poland

Merçè Pineda Spain

John Fernandes Netherlands

Roberto Della Casa

268 ×0.9

RHEUM

148 ×0.9

GENET

164 ×1.2

PHYSI

179 ×1.3

205 ×2.0

Citations per year, relative to Roberto Della Casa Roberto Della Casa (= 1×) peers John Fernandes

Countries citing papers authored by Roberto Della Casa

Since Specialization

Citations

This map shows the geographic impact of Roberto Della Casa's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Roberto Della Casa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberto Della Casa more than expected).

Fields of papers citing papers by Roberto Della Casa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roberto Della Casa. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Roberto Della Casa. The network helps show where Roberto Della Casa may publish in the future.

Co-authorship network of co-authors of Roberto Della Casa

This figure shows the co-authorship network connecting the top 25 collaborators of Roberto Della Casa. A scholar is included among the top collaborators of Roberto Della Casa based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Roberto Della Casa. Roberto Della Casa is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Rossi, Alessandro, Chiara Simeoli, Mariacarolina Salerno, et al.. (2020). Imbalanced cortisol concentrations in glycogen storage disease type I: evidence for a possible link between endocrine regulation and metabolic derangement. Orphanet Journal of Rare Diseases. 15(1). 99–99. 17 indexed citations

Fecarotta, Simona, Vincenza Gragnaniello, Roberto Della Casa, et al.. (2018). Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case report. Neuromuscular Disorders. 28(11). 956–960. 4 indexed citations

Cappuccio, Gerarda, Pia Bernardo, Michele Pinelli, et al.. (2018). Pain and sleep disturbances in Rett syndrome and other neurodevelopmental disorders. Acta Paediatrica. 108(1). 171–172. 6 indexed citations

Cappuccio, Gerarda, Silvia Di Tommaso, Claudio Bruno, et al.. (2017). Gait disturbance and lower limb pain in a patient with PIK3CA-related disorder. European Journal of Medical Genetics. 60(12). 655–657. 1 indexed citations

Melis, Daniela, Paola Marcolongo, Rossella Parini, et al.. (2015). Vitamin E Improves Clinical Outcome of Patients Affected by Glycogen Storage Disease Type Ib. JIMD Reports. 25. 39–45. 11 indexed citations

Melis, Daniela, Alessandro Rossi, Rosario Pivonello, et al.. (2015). Glycogen storage disease type Ia (GSDIa) but not Glycogen storage disease type Ib (GSDIb) is associated to an increased risk of metabolic syndrome: possible role of microsomal glucose 6-phosphate accumulation. Orphanet Journal of Rare Diseases. 10(1). 91–91. 21 indexed citations

Melis, Daniela, Roberto Della Casa, Alessandro Rossi, et al.. (2014). Involvement of endocrine system in a patient affected by Glycogen storage disease 1b: speculation on the role of autoimmunity. The Italian Journal of Pediatrics/Italian journal of pediatrics. 40(1). 30–30. 13 indexed citations

Melis, Daniela, Rosario Pivonello, Mario Cozzolino, et al.. (2013). Impaired Bone Metabolism in Glycogen Storage Disease Type 1 Is Associated with Poor Metabolic Control in Type 1a and with Granulocyte Colony-Stimulating Factor Therapy in Type 1b. Hormone Research in Paediatrics. 81(1). 55–62. 19 indexed citations

Rosa, Michelino Di, Antonia Pascarella, Giancarlo Parenti, et al.. (2011). Developmental evolution in a patient with multiple acyl-coenzymeA dehydrogenase deficiency under pharmacological treatment. European Journal of Paediatric Neurology. 16(2). 203–205. 7 indexed citations

10.

Melis, Daniela, Rita Genesio, Gerarda Cappuccio, et al.. (2011). Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22. American Journal of Medical Genetics Part A. 155(7). 1697–1705. 14 indexed citations

11.

Melis, Daniela, Rosario Pivonello, Giancarlo Parenti, et al.. (2009). The Growth Hormone-Insulin-like Growth Factor Axis in Glycogen Storage Disease Type 1: Evidence of Different Growth Patterns and Insulin-like Growth Factor Levels in Patients with Glycogen Storage Disease Type 1a and 1b. The Journal of Pediatrics. 156(4). 663–670.e1. 16 indexed citations

12.

Melis, Daniela, Roberto Della Casa, Rossella Parini, et al.. (2008). Vitamin E supplementation improves neutropenia and reduces the frequency of infections in patients with glycogen storage disease type 1b. European Journal of Pediatrics. 168(9). 1069–1074. 21 indexed citations

13.

Brasi, Daniele De, Rita Genesio, Roberto Ciccone, et al.. (2008). Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephaly. European Journal of Medical Genetics. 51(6). 658–665. 12 indexed citations

14.

Melis, Daniela, Rosario Pivonello, Giancarlo Parenti, et al.. (2007). Increased Prevalence of Thyroid Autoimmunity and Hypothyroidism in Patients with Glycogen Storage Disease Type I. The Journal of Pediatrics. 150(3). 300–305.e1. 31 indexed citations

15.

Melis, Daniela, Giancarlo Parenti, Paola Marcolongo, et al.. (2005). Genotype/phenotype correlation in glycogen storage disease type 1b: a multicentre study and review of the literature. European Journal of Pediatrics. 164(8). 501–508. 64 indexed citations

16.

Melis, Daniela, Giancarlo Parenti, R. Gatti, et al.. (2005). Efficacy of ACE‐inhibitor therapy on renal disease in glycogen storage disease type 1: a multicentre retrospective study. Clinical Endocrinology. 63(1). 19–25. 32 indexed citations

17.

Melis, Daniela, Giancarlo Parenti, Roberto Della Casa, et al.. (2004). Brain damage in glycogen storage disease type I. The Journal of Pediatrics. 144(5). 637–642. 31 indexed citations

18.

Melis, Daniela, Giancarlo Parenti, Roberto Della Casa, et al.. (2003). Crohn's-like ileo-colitis in patients affected by glycogen storage disease Ib: two years' follow-up of patients with a wide spectrum of gastrointestinal signs. Acta Paediatrica. 92(12). 1415–1421. 30 indexed citations

19.

Toscano, Evelina, Roberto Della Casa, Sek Mardy, et al.. (2000). Multisystem Involvement in Congenital Insensitivity to Pain with Anhidrosis (CIPA), a Nerve Growth Factor Receptor(Trk A)-Related Disorder. Neuropediatrics. 31(1). 39–41. 33 indexed citations

20.

Sebastio, Gianfranco, Lucia Perone, Vito Guzzetta, et al.. (1996). Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21) (p16.3;q22.1): Relevance to the Wolf-Hirschhorn and Down syndrome critical regions. American Journal of Medical Genetics. 63(2). 366–372. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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