Miriam Rigoldi

1.3k total citations
29 papers, 544 citations indexed

About

Miriam Rigoldi is a scholar working on Physiology, Rheumatology and Epidemiology. According to data from OpenAlex, Miriam Rigoldi has authored 29 papers receiving a total of 544 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Physiology, 13 papers in Rheumatology and 7 papers in Epidemiology. Recurrent topics in Miriam Rigoldi's work include Lysosomal Storage Disorders Research (14 papers), Glycogen Storage Diseases and Myoclonus (10 papers) and Trypanosoma species research and implications (6 papers). Miriam Rigoldi is often cited by papers focused on Lysosomal Storage Disorders Research (14 papers), Glycogen Storage Diseases and Myoclonus (10 papers) and Trypanosoma species research and implications (6 papers). Miriam Rigoldi collaborates with scholars based in Italy, United States and Netherlands. Miriam Rigoldi's co-authors include Rossella Parini, Amelia Morrone, Francesca Furlan, Daniela Melis, Leda Dalprà, Sabrina Paci, Raffaele Manna, Giancarlo Parenti, Maria Teresa Mascia and Pietro Strisciuglio and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Miriam Rigoldi

29 papers receiving 537 citations

Peers

Miriam Rigoldi

PHYSI

RHEUM

EPIDE

Stephanie DeArmey United States

Norberto Guelbert Argentina

Johanna M. P. van den Hout Netherlands

Ana Marcão Portugal

Susana Teijeira Spain

Hana Vlášková Czechia

Joyce A. Kobori United States

Roberto Della Casa Italy

Andrea M. Atherton United States

Eugênia Ribeiro Valadares Brazil

Stephanie DeArmey United States

Miriam Rigoldi

467 ×1.6

PHYSI

319 ×1.4

RHEUM

99 ×0.8

128 ×1.1

EPIDE

117 ×1.3

Citations per year, relative to Miriam Rigoldi Miriam Rigoldi (= 1×) peers Stephanie DeArmey

Countries citing papers authored by Miriam Rigoldi

Since Specialization

Citations

This map shows the geographic impact of Miriam Rigoldi'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 Miriam Rigoldi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Miriam Rigoldi more than expected).

Fields of papers citing papers by Miriam Rigoldi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Miriam Rigoldi. 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 Miriam Rigoldi. The network helps show where Miriam Rigoldi may publish in the future.

Co-authorship network of co-authors of Miriam Rigoldi

This figure shows the co-authorship network connecting the top 25 collaborators of Miriam Rigoldi. A scholar is included among the top collaborators of Miriam Rigoldi 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 Miriam Rigoldi. Miriam Rigoldi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Piras, Rossella, Elisabetta Valoti, Marta Alberti, et al.. (2023). CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome. Frontiers in Immunology. 13. 1011580–1011580. 9 indexed citations

Orisio, Silvia, Marina Noris, Miriam Rigoldi, et al.. (2023). Mutation Analysis of <i>PKD1</i> and <i>PKD2</i> Genes in a Large Italian Cohort Reveals Novel Pathogenic Variants Including a Novel Complex Rearrangement. The Nephron journals/Nephron journals. 148(5). 273–291. 3 indexed citations

Bertolini, Anna, Miriam Rigoldi, Raffaella Mariani, et al.. (2023). Long-term outcome of a cohort of Italian patients affected with alpha-Mannosidosis. Clinical Dysmorphology. 33(1). 1–8. 3 indexed citations

Caciotti, Anna, Lucrezia Cellai, Davide Mei, et al.. (2021). Morquio B disease: From pathophysiology towards diagnosis. Molecular Genetics and Metabolism. 132(3). 180–188. 5 indexed citations

Rossi, Alessandro, Foekje de Boer, C Montanari, et al.. (2020). Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations. Journal of Inherited Metabolic Disease. 43(4). 770–777. 21 indexed citations

Redaelli, Serena, Silvia Maitz, Francesca Crosti, et al.. (2019). Refining the Phenotype of Recurrent Rearrangements of Chromosome 16. International Journal of Molecular Sciences. 20(5). 1095–1095. 28 indexed citations

Rovelli, Valentina, Sabrina Paci, Miriam Rigoldi, et al.. (2019). Novel mutations in two unrelated Italian patients with SSADH deficiency. Metabolic Brain Disease. 34(5). 1515–1518. 3 indexed citations

Caciotti, Anna, Matthew Mort, D.N. Cooper, et al.. (2018). Mis-splicing of the GALNS gene resulting from deep intronic mutations as a cause of Morquio a disease. BMC Medical Genetics. 19(1). 183–183. 15 indexed citations

Conconi, Donatella, Nicoletta Villa, Serena Redaelli, et al.. (2018). Familiar unbalanced complex rearrangements involving 13 p-arm: description of two cases. Molecular Cytogenetics. 11(1). 52–52. 1 indexed citations

10.

Furlan, Francesca, Attilio Rovelli, Miriam Rigoldi, et al.. (2018). A new case report of severe mucopolysaccharidosis type VII: diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancy. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(S2). 128–128. 11 indexed citations

11.

Rigoldi, Miriam, Elena Verrecchia, Raffaele Manna, & Maria Teresa Mascia. (2018). Clinical hints to diagnosis of attenuated forms of Mucopolysaccharidoses. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(S2). 132–132. 28 indexed citations

12.

Melis, Daniela, Rossella Parini, Miriam Rigoldi, et al.. (2015). Progression of Renal Damage in Glycogen Storage Disease Type I Is Associated to Hyperlipidemia: A Multicenter Prospective Italian Study. The Journal of Pediatrics. 166(4). 1079–1082. 17 indexed citations

13.

Sechi, Annalisa, Laura Deroma, Sabrina Paci, et al.. (2013). Quality of Life in Adult Patients with Glycogen Storage Disease Type I: Results of a Multicenter Italian Study. JIMD Reports. 14. 47–53. 18 indexed citations

14.

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

15.

Rigoldi, Miriam, Daniela Concolino, Amelia Morrone, et al.. (2013). Intrafamilial phenotypic variability in four families with Anderson‐Fabry disease. Clinical Genetics. 86(3). 258–263. 43 indexed citations

16.

Ferri, Lorenzo, Anna Caciotti, Catia Cavicchi, et al.. (2012). Integration of PCR-Sequencing Analysis with Multiplex Ligation-Dependent Probe Amplification for Diagnosis of Hereditary Fructose Intolerance. JIMD Reports. 6. 31–37. 8 indexed citations

17.

Bembi, Bruno, Federica Pisa, Marco Confalonieri, et al.. (2010). Long‐term observational, non‐randomized study of enzyme replacement therapy in late‐onset glycogenosis type II. Journal of Inherited Metabolic Disease. 33(6). 727–735. 74 indexed citations

18.

Parini, Rossella, Miriam Rigoldi, Francesca Furlan, et al.. (2008). Enzyme replacement therapy with agalsidase alfa in a cohort of Italian patients with Anderson–Fabry disease: testing the effects with the Mainz Severity Score Index. Clinical Genetics. 74(3). 260–266. 24 indexed citations

19.

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

20.

Ferrarese, Carlo, Lucio Tremolizzo, Miriam Rigoldi, et al.. (2001). Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease. Neurological Sciences. 22(1). 65–66. 28 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.

Explore authors with similar magnitude of impact