Adriana Carando

921 total citations
16 papers, 627 citations indexed

About

Adriana Carando is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Oncology. According to data from OpenAlex, Adriana Carando has authored 16 papers receiving a total of 627 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 3 papers in Pulmonary and Respiratory Medicine and 3 papers in Oncology. Recurrent topics in Adriana Carando's work include RNA modifications and cancer (10 papers), Cancer-related gene regulation (9 papers) and Epigenetics and DNA Methylation (5 papers). Adriana Carando is often cited by papers focused on RNA modifications and cancer (10 papers), Cancer-related gene regulation (9 papers) and Epigenetics and DNA Methylation (5 papers). Adriana Carando collaborates with scholars based in Italy, United States and Belarus. Adriana Carando's co-authors include Emanuela Garelli, Irma Dianzani, Ugo Ramenghi, Paola Quarello, Anna Aspesi, Alfredo Brusco, Elisa Pavesi, Maria Francesca Campagnoli, Daniela Longoni and Carlo Dufour and has published in prestigious journals such as British Journal of Haematology, Journal of Clinical Pathology and Human Mutation.

In The Last Decade

Adriana Carando

16 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adriana Carando Italy 15 480 113 96 67 58 16 627
Javier Suela Spain 13 268 0.6× 145 1.3× 61 0.6× 52 0.8× 158 2.7× 31 539
Nuo Si China 12 288 0.6× 85 0.8× 47 0.5× 160 2.4× 42 0.7× 37 505
Jamil Al-Alami Jordan 6 302 0.6× 132 1.2× 29 0.3× 105 1.6× 28 0.5× 13 419
Elisabeth Salzer Austria 10 114 0.2× 121 1.1× 83 0.9× 347 5.2× 57 1.0× 18 511
Francesca Rucci United States 12 216 0.5× 94 0.8× 124 1.3× 238 3.6× 17 0.3× 14 469
Thomas P. Howard United States 8 460 1.0× 28 0.2× 64 0.7× 42 0.6× 34 0.6× 12 549
Lesley Everett United States 9 167 0.3× 61 0.5× 43 0.4× 43 0.6× 136 2.3× 39 478
Rajan K. Mannari United States 3 693 1.4× 71 0.6× 86 0.9× 42 0.6× 384 6.6× 3 847
Naïs Prade France 7 197 0.4× 78 0.7× 95 1.0× 90 1.3× 176 3.0× 8 395
Qian-Fei Wang United States 13 327 0.7× 41 0.4× 64 0.7× 116 1.7× 233 4.0× 15 561

Countries citing papers authored by Adriana Carando

Since Specialization
Citations

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

Fields of papers citing papers by Adriana Carando

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adriana Carando

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

All Works

16 of 16 papers shown
1.
Quarello, Paola, Emanuela Garelli, Adriana Carando, et al.. (2020). A 20‐year long term experience of the Italian Diamond‐Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease?. British Journal of Haematology. 190(1). 93–104. 18 indexed citations
2.
Giorgio, Elisa, Emanuela Garelli, Adriana Carando, et al.. (2019). Design of a multiplex ligation-dependent probe amplification assay for SLC20A2: identification of two novel deletions in primary familial brain calcification. Journal of Human Genetics. 64(11). 1083–1090. 4 indexed citations
3.
Garelli, Emanuela, Paola Quarello, Elisa Giorgio, et al.. (2018). Spontaneous remission in a Diamond‐Blackfan anaemia patient due to a revertant uniparental disomy ablating a de novo RPS19 mutation. British Journal of Haematology. 185(5). 994–998. 19 indexed citations
4.
Quarello, Paola, Emanuela Garelli, Adriana Carando, et al.. (2016). Ribosomal RNA analysis in the diagnosis of Diamond‐Blackfan Anaemia. British Journal of Haematology. 172(5). 782–785. 22 indexed citations
5.
Aspesi, Anna, Paola Quarello, Emanuela Garelli, et al.. (2014). Loss of GATA‐1 full length as a cause of Diamond–Blackfan anemia phenotype. Pediatric Blood & Cancer. 61(7). 1319–1321. 60 indexed citations
6.
Garelli, Emanuela, Alfredo Brusco, Adriana Carando, et al.. (2012). High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay. Haematologica. 97(12). 1813–1817. 44 indexed citations
7.
Prontera, Paolo, Emanuela Garelli, Amedea Mencarelli, et al.. (2011). Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome. American Journal of Medical Genetics Part A. 155(11). 2746–2749. 21 indexed citations
8.
Quarello, Paola, Emanuela Garelli, Adriana Carando, et al.. (2009). Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations. Haematologica. 95(2). 206–213. 65 indexed citations
9.
Ferraris, Silvio, Emanuela Garelli, Adriana Carando, et al.. (2009). HDR syndrome: A novel “de novo” mutation in GATA3 gene. American Journal of Medical Genetics Part A. 149A(4). 770–775. 36 indexed citations
10.
Campagnoli, Maria Francesca, Ugo Ramenghi, Paola Quarello, et al.. (2008). RPS19 mutations in patients with Diamond-Blackfan anemia. Human Mutation. 29(7). 911–920. 83 indexed citations
11.
Quarello, Paola, Emanuela Garelli, Anna Aspesi, et al.. (2008). A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia. Human Mutation. 29(11). E263–E270. 30 indexed citations
12.
Quarello, Paola, Emanuela Garelli, Adriana Carando, et al.. (2006). The broad spectrum of autoimmune lymphoproliferative disease: molecular bases, clinical features and long-term follow-up in 31 patients.. PubMed. 91(4). 538–41. 34 indexed citations
13.
Campagnoli, Maria Francesca, Angela Pucci, Emanuela Garelli, et al.. (2006). Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family. Journal of Clinical Pathology. 59(4). 440–442. 50 indexed citations
14.
Chiocchetti, Annalisa, Adriana Carando, Anna Aspesi, et al.. (2005). Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein.. PubMed. 90(11). 1453–62. 38 indexed citations
15.
Garelli, Emanuela, Paola Quarello, Adriana Carando, et al.. (2004). Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature.. PubMed. 89(4). 480–9. 71 indexed citations
16.
Ramenghi, Ugo, Emanuela Garelli, Adriana Carando, et al.. (2000). Diamond-Blackfan Anemia: Report of Seven Further Mutations in the RPS19 Gene and Evidence of Mutation Heterogeneity in the Italian Population. Blood Cells Molecules and Diseases. 26(5). 417–422. 32 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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