Daniela Melis

4.3k total citations
107 papers, 1.8k citations indexed

About

Daniela Melis is a scholar working on Rheumatology, Genetics and Molecular Biology. According to data from OpenAlex, Daniela Melis has authored 107 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Rheumatology, 41 papers in Genetics and 38 papers in Molecular Biology. Recurrent topics in Daniela Melis's work include Glycogen Storage Diseases and Myoclonus (35 papers), Lysosomal Storage Disorders Research (17 papers) and Genomic variations and chromosomal abnormalities (13 papers). Daniela Melis is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (35 papers), Lysosomal Storage Disorders Research (17 papers) and Genomic variations and chromosomal abnormalities (13 papers). Daniela Melis collaborates with scholars based in Italy, United States and Netherlands. Daniela Melis's co-authors include Generoso Andria, Giancarlo Parenti, Roberto Della Casa, Rosario Pivonello, Rossella Parini, Annamaria Colao, Gaetano Lombardi, Lucio Nitsch, Antongiulio Faggiano and Mariacarolina Salerno and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and PLoS ONE.

In The Last Decade

Daniela Melis

105 papers receiving 1.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Daniela Melis Italy 25 691 651 580 224 200 107 1.8k
Gu-Hwan Kim South Korea 26 591 0.9× 301 0.5× 1.1k 1.9× 313 1.4× 153 0.8× 180 2.2k
Stephanie Austin United States 25 622 0.9× 1.4k 2.2× 375 0.6× 776 3.5× 233 1.2× 72 2.0k
Kanya Suphapeetiporn Thailand 23 714 1.0× 403 0.6× 804 1.4× 144 0.6× 130 0.7× 131 2.0k
Jung Min Ko South Korea 22 677 1.0× 123 0.2× 767 1.3× 120 0.5× 78 0.4× 156 1.6k
Vito Guarnieri Italy 23 456 0.7× 111 0.2× 617 1.1× 93 0.4× 133 0.7× 78 1.8k
N E Skakkebæk Denmark 25 657 1.0× 283 0.4× 1.3k 2.3× 137 0.6× 73 0.4× 45 2.8k
Atsuko Sato Japan 19 193 0.3× 86 0.1× 333 0.6× 216 1.0× 43 0.2× 62 1.1k
Sebastiano Grasso Italy 22 351 0.5× 169 0.3× 308 0.5× 146 0.7× 47 0.2× 75 1.4k
Anya Rothenbühler France 23 422 0.6× 268 0.4× 348 0.6× 95 0.4× 41 0.2× 83 1.6k
Sławomir Jeka Poland 22 203 0.3× 1.1k 1.8× 159 0.3× 120 0.5× 37 0.2× 98 2.2k

Countries citing papers authored by Daniela Melis

Since Specialization
Citations

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

Fields of papers citing papers by Daniela Melis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Melis

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

All Works

20 of 20 papers shown
1.
Rossi, Alessandro, Chiara Simeoli, Rosario Pivonello, et al.. (2024). Endocrine involvement in hepatic glycogen storage diseases: pathophysiology and implications for care. Reviews in Endocrine and Metabolic Disorders. 25(4). 707–725. 4 indexed citations
2.
Priolo, Manuela, Francesca Clementina Radio, Andrea Ciolfi, et al.. (2023). Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants. European Journal of Human Genetics. 31(7). 805–814. 4 indexed citations
3.
D’Amico, Alessandra, Carmen L. Rosano, Luca Pannone, et al.. (2021). Clinical variability of neurofibromatosis 1: A modifying role of cooccurring PTPN11 variants and atypical brain MRI findings. Clinical Genetics. 100(5). 563–572. 5 indexed citations
4.
Melis, Daniela, et al.. (2021). Liver Involvement in Congenital Disorders of Glycosylation. Journal of Pediatric Gastroenterology and Nutrition. 73(4). 444–454. 4 indexed citations
5.
D’Amico, Alessandra, et al.. (2021). Clinical report of a brain magnetic resonance imaging finding in Noonan syndrome. Child s Nervous System. 37(12). 3963–3966. 3 indexed citations
6.
Giugliano, Teresa, Claudia Santoro, Annalaura Torella, et al.. (2019). Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders. Genes. 10(8). 580–580. 29 indexed citations
7.
Santoro, Claudia, Teresa Giugliano, Markus Kraemer, et al.. (2018). Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1. PLoS ONE. 13(7). e0200446–e0200446. 22 indexed citations
8.
Casertano, Alberto, Paolo Fontana, Raoul C. M. Hennekam, et al.. (2017). Alterations in metabolic patterns have a key role in diagnosis and progression of primrose syndrome. American Journal of Medical Genetics Part A. 173(7). 1896–1902. 7 indexed citations
9.
Piccolo, Pasquale, Pratibha Mithbaokar, John Tolmie, et al.. (2014). SMAD4 mutations causing Myhre syndrome result in disorganization of extracellular matrix improved by losartan. European Journal of Human Genetics. 22(8). 988–994. 32 indexed citations
10.
Fontana, Paolo, Rita Genesio, Alberto Casertano, et al.. (2014). Loeys–Dietz syndrome type 4, caused by chromothripsis, involving the TGFB2 gene. Gene. 538(1). 69–73. 13 indexed citations
11.
Cappuccio, Gerarda, Alessandro Rossi, Paolo Fontana, et al.. (2014). Bronchial isomerism in a Kabuki syndrome patient with a novel mutation in MLL2gene. BMC Medical Genetics. 15(1). 15–15. 5 indexed citations
12.
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 œItalian Journal of Pediatrics/Italian journal of pediatrics. 40(1). 30–30. 13 indexed citations
13.
Cappuccio, Gerarda, Rita Genesio, Alberto Casertano, et al.. (2013). Complex chromosomal rearrangements causing Langer–Giedion syndrome atypical phenotype: Genotype–phenotype correlation and literature review. American Journal of Medical Genetics Part A. 164(3). 753–759. 10 indexed citations
14.
Gervasini, Cristina, Silvia Russo, Anna Cereda, et al.. (2013). Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrum. American Journal of Medical Genetics Part A. 161(11). 2909–2919. 24 indexed citations
15.
Capalbo, Donatella, Daniela Melis, Lucia De Martino, et al.. (2012). Noonan‐like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurological manifestations. American Journal of Medical Genetics Part A. 158A(4). 856–860. 17 indexed citations
16.
Melis, Daniela, Rita Genesio, Ennio Del Giudice, et al.. (2012). Clinical description of a patient carrying the smallest reported deletion involving 10p14 region. American Journal of Medical Genetics Part A. 158A(4). 832–835. 34 indexed citations
17.
Gritti, Antonella, et al.. (2011). A case of Klinefelter syndrome, mosaicism (46,XY/47,XXY), associated with anorexia nervosa. Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity. 16(1). e69–e71. 2 indexed citations
18.
Rocco, Maja Di, et al.. (2008). Hepatocellular adenoma and metabolic balance in patients with type Ia glycogen storage disease. Molecular Genetics and Metabolism. 93(4). 398–402. 28 indexed citations
19.
Garavelli, Livia, Daniele De Brasi, Filomena Cariola, et al.. (2008). Holt–Oram syndrome associated with anomalies of the feet. American Journal of Medical Genetics Part A. 146A(9). 1185–1189. 11 indexed citations
20.
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

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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