Aldo Giannotti

5.0k total citations
104 papers, 3.0k citations indexed

About

Aldo Giannotti is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Aldo Giannotti has authored 104 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 40 papers in Genetics and 33 papers in Epidemiology. Recurrent topics in Aldo Giannotti's work include Congenital heart defects research (42 papers), Congenital Heart Disease Studies (29 papers) and Genomic variations and chromosomal abnormalities (22 papers). Aldo Giannotti is often cited by papers focused on Congenital heart defects research (42 papers), Congenital Heart Disease Studies (29 papers) and Genomic variations and chromosomal abnormalities (22 papers). Aldo Giannotti collaborates with scholars based in Italy, United States and Germany. Aldo Giannotti's co-authors include Bruno Dallapiccola, M. Cristina Digilio, Bruno Marino, Alessandra Toscano, Bruno Marino, Maria Cristina Digilio, Rita Mingarelli, Giuseppe Novelli, M. Cristina Digilio and Francesca Amati and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and CHEST Journal.

In The Last Decade

Aldo Giannotti

102 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aldo Giannotti Italy 31 1.9k 1.1k 1.0k 678 512 104 3.0k
Michael Silberbach United States 25 1.3k 0.7× 677 0.6× 1.3k 1.3× 867 1.3× 481 0.9× 67 3.3k
Stephanie M. Ware United States 35 3.1k 1.6× 1.5k 1.4× 1.1k 1.1× 597 0.9× 900 1.8× 141 4.9k
Margherita Lerone Italy 25 1.1k 0.6× 285 0.3× 827 0.8× 169 0.2× 1.3k 2.6× 101 2.8k
Margherita Silengo Italy 29 2.0k 1.1× 273 0.3× 1.7k 1.7× 146 0.2× 489 1.0× 114 3.3k
Paul Grossfeld United States 22 1.7k 0.9× 893 0.8× 716 0.7× 680 1.0× 343 0.7× 53 2.9k
Cecilia Camacho‐Hübner United Kingdom 38 1.8k 0.9× 283 0.3× 1.5k 1.5× 168 0.2× 627 1.2× 103 5.0k
Susan Holder United Kingdom 21 1.1k 0.6× 176 0.2× 1.2k 1.2× 94 0.1× 525 1.0× 43 2.2k
Kwame Anyane‐Yeboa United States 26 1.3k 0.7× 270 0.3× 1.2k 1.2× 233 0.3× 277 0.5× 66 2.3k
Kirstine Stochholm Denmark 30 1.3k 0.7× 230 0.2× 2.1k 2.0× 435 0.6× 515 1.0× 84 3.6k
Clarisse Baumann France 26 969 0.5× 101 0.1× 853 0.8× 330 0.5× 495 1.0× 73 2.1k

Countries citing papers authored by Aldo Giannotti

Since Specialization
Citations

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

Fields of papers citing papers by Aldo Giannotti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aldo Giannotti

This figure shows the co-authorship network connecting the top 25 collaborators of Aldo Giannotti. A scholar is included among the top collaborators of Aldo Giannotti 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 Aldo Giannotti. Aldo Giannotti 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.
Pastore, Anna, Giulia Tozzi, Laura Gaeta, et al.. (2003). Glutathione metabolism and antioxidant enzymes in children with down syndrome. The Journal of Pediatrics. 142(5). 583–585. 51 indexed citations
2.
Angioni, Adriano, et al.. (2003). Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies. Clinical Genetics. 63(4). 308–313. 75 indexed citations
3.
Marino, Bruno, Vincenzo Di Ciommo, Lucilla Ravà, et al.. (2002). Prevalence of major malformations in infants with Down's syndrome. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 28(6). 488–493. 1 indexed citations
4.
Mangino, Massimo, Elisabetta Flex, M. Cristina Digilio, Aldo Giannotti, & Bruno Dallapiccola. (2002). Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism. Human Mutation. 19(3). 308–308. 30 indexed citations
5.
Patrono, Carlo, Carlo Dionisi‐Vici, Aldo Giannotti, et al.. (2002). Two novel mutations of the human Δ7-sterol reductase (DHCR7) gene in children with Smith–Lemli–Opitz syndrome. Molecular and Cellular Probes. 16(4). 315–318. 13 indexed citations
6.
Bonamico, Margherita, P. Mariani, Pinella Failla, et al.. (2001). Prevalence and Clinical Picture of Celiac Disease in Italian Down Syndrome Patients: A Multicenter Study. Journal of Pediatric Gastroenterology and Nutrition. 33(2). 139–143. 108 indexed citations
7.
Gigante, Maddalena, Maria G. Matera, Davide Seripa, et al.. (2001). Ext-mutation analysis in Italian sporadic and hereditary osteochondromas. International Journal of Cancer. 95(6). 378–383. 14 indexed citations
8.
Marino, Bruno, M. Cristina Digilio, Alessandra Toscano, et al.. (2001). Anatomic patterns of conotruncal defects associated with deletion 22q11. Genetics in Medicine. 3(1). 45–48. 96 indexed citations
9.
Giannotti, Aldo, Alessandra Tessa, Clarice Patrono, et al.. (2000). A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia. Human Mutation. 16(3). 277–277. 7 indexed citations
10.
Marino, Bruno, et al.. (2000). Clinical and Cardiorespiratory Assessment in Children With Down Syndrome Without Congenital Heart Disease. Archives of Pediatrics and Adolescent Medicine. 154(4). 408–408. 41 indexed citations
11.
Digilio, M. Cristina, Bruno Marino, Salvatore Giannico, Aldo Giannotti, & Bruno Dallapiccola. (1999). Atrioventricular canal defect and hypoplastic left heart syndrome as discordant congenital heart defects in twins. Teratology. 60(4). 206–208. 6 indexed citations
12.
Digilio, Maria Cristina, et al.. (1998). Congenital heart defect in sibs with discordant karyotypes. American Journal of Medical Genetics. 80(2). 169–172. 8 indexed citations
13.
Formigari, Roberto, et al.. (1996). Associated cardiac anomalies in isolated and syndromic patients with tetralogy of fallot. The American Journal of Cardiology. 77(7). 505–508. 45 indexed citations
14.
Digilio, M. Cristina, Bruno Marino, Rita Mingarelli, et al.. (1996). Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11?. Journal of the American College of Cardiology. 27(2). 93–93. 1 indexed citations
15.
Giannotti, Aldo, M. Cristina Digilio, Giuseppe Albertini, Rita Mingarelli, & Bruno Dallapiccola. (1995). Sporadic trichodental dysplasia with microcephaly and mental retardation. Clinical Dysmorphology. 4(4). 334–337. 2 indexed citations
16.
Giannotti, Aldo, et al.. (1992). New case of Bartsocas‐Papas syndrome surviving at 20 months. American Journal of Medical Genetics. 42(5). 733–735. 11 indexed citations
17.
Marino, Bruno, Maria Cristina Digilio, Aldo Giannotti, & Bruno Dallapiccola. (1989). Atrioventricular Canal Associated with Trisomy 9. CHEST Journal. 96(6). 1420–1421. 13 indexed citations
18.
Dallapiccola, Bruno, Giuseppe Novelli, & Aldo Giannotti. (1988). Deletion 2q31.3?2q33.3: gene dosage effect of ribulose 5-phosphate 3-epimerase. Human Genetics. 79(1). 92–92. 10 indexed citations
19.
Forabosco, Antonino, Anna Baroncini, Leda Dalprà, et al.. (1988). The phenotype of partial dup(7q) reconsidered: a report of five new cases. Clinical Genetics. 34(1). 48–59. 34 indexed citations
20.
Novelli, Giuseppe, Vilberto Stocchi, Aldo Giannotti, Mauro Magnani, & Bruno Dallapiccola. (1986). Increased Erythrocyte Adenosine Deaminase Activity without Haemolytic Anaemia. Human Heredity. 36(1). 37–40. 5 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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