Romeo Carrozzo

2.9k total citations · 1 hit paper
37 papers, 1.8k citations indexed

About

Romeo Carrozzo is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Romeo Carrozzo has authored 37 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 18 papers in Genetics and 8 papers in Epidemiology. Recurrent topics in Romeo Carrozzo's work include Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Romeo Carrozzo is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Romeo Carrozzo collaborates with scholars based in Italy, United States and United Kingdom. Romeo Carrozzo's co-authors include Renzo Guerrini, Andrea Ballabio, Barbara Bardoni, Rossana Tonlorenzi, Patricia Taillon‐Miller, Elena Maestrini, Brunella Franco, Antonella Pragliola, Giovanna Camerino and Charles B. Lawrence and has published in prestigious journals such as Nature, Circulation and The EMBO Journal.

In The Last Decade

Romeo Carrozzo

36 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1991 638 citations Barbara Bardoni, Rossana Tonlorenzi et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Romeo Carrozzo Italy	20	828	743	360	313	222	37	1.8k
Kimia Kahrizi Iran	30	835 1.0×	1.8k 2.4×	271 0.8×	203 0.6×	105 0.5×	141	3.0k
Guntram Borck Germany	27	681 0.8×	876 1.2×	31 0.1×	133 0.4×	103 0.5×	65	1.7k
Kazunari Yuri Japan	22	369 0.4×	306 0.4×	186 0.5×	276 0.9×	56 0.3×	72	1.6k
Tsuyoshi Takagi Japan	25	230 0.3×	1.1k 1.5×	133 0.4×	170 0.5×	55 0.2×	78	2.1k
Tullio Barni Italy	25	211 0.3×	476 0.6×	545 1.5×	107 0.3×	50 0.2×	66	1.6k
Hope O. Sweet United States	21	440 0.5×	1.0k 1.4×	65 0.2×	264 0.8×	80 0.4×	32	1.9k
J. Hikke van Doorninck Netherlands	15	249 0.3×	971 1.3×	33 0.1×	328 1.0×	81 0.4×	17	1.8k
Lacey Plummer United States	24	1.0k 1.2×	1.1k 1.5×	1.6k 4.5×	115 0.4×	41 0.2×	54	2.3k
Christophe Philippe France	30	1.6k 1.9×	1.5k 2.0×	48 0.1×	135 0.4×	207 0.9×	77	2.7k
Emeka K. Enwere Canada	14	126 0.2×	824 1.1×	84 0.2×	321 1.0×	116 0.5×	22	2.1k

Countries citing papers authored by Romeo Carrozzo

Since Specialization

Citations

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

Fields of papers citing papers by Romeo Carrozzo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Romeo Carrozzo

This figure shows the co-authorship network connecting the top 25 collaborators of Romeo Carrozzo. A scholar is included among the top collaborators of Romeo Carrozzo 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 Romeo Carrozzo. Romeo Carrozzo 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

Corsello, Antonio, Gregorio P. Milani, Marina Picca, et al.. (2024). Recurrent upper respiratory tract infections in early childhood: a newly defined clinical condition. The Italian Journal of Pediatrics/Italian journal of pediatrics. 50(1). 30–30. 4 indexed citations

Picca, Marina, Romeo Carrozzo, Carlo Agostoni, et al.. (2024). Factors behind Antibiotic Therapy: A Survey of Primary Care Pediatricians in Lombardy. International Journal of Environmental Research and Public Health. 21(8). 1091–1091. 1 indexed citations

Picca, Marina, Romeo Carrozzo, Gregorio P. Milani, et al.. (2023). Leading reasons for antibiotic prescriptions in pediatric respiratory infections: influence of fever in a primary care setting. The Italian Journal of Pediatrics/Italian journal of pediatrics. 49(1). 131–131. 3 indexed citations

Bettio, Daniela, et al.. (2007). Molecular cytogenetic and clinical findings in a patient with a small supernumerary r(8) mosaicism. American Journal of Medical Genetics Part A. 146A(2). 247–250. 19 indexed citations

Ciccone, Roberto, Roberto Giorda, Giuliana Gregato, et al.. (2005). Reciprocal translocations: a trap for cytogenetists?. Human Genetics. 117(6). 571–582. 40 indexed citations

Cosma, Maria Pia, Stefano Pepe, Giancarlo Parenti, et al.. (2004). Molecular and functional analysis ofSUMF1 mutations in multiple sulfatase deficiency. Human Mutation. 23(6). 576–581. 52 indexed citations

Guerrini, Renzo, Francesca Moro, Eva Andermann, et al.. (2003). Nonsyndromic mental retardation and cryptogenic epilepsy in women with Doublecortin gene mutations. Annals of Neurology. 54(1). 30–37. 43 indexed citations

Guerrini, Renzo, Romeo Carrozzo, Roberta Rinaldi, & Paolo Bonanni. (2003). Angelman Syndrome. Pediatric Drugs. 5(10). 647–661. 56 indexed citations

Bonaglia, María Clara, Roberto Giorda, Romeo Carrozzo, et al.. (2002). 20‐Mb duplication of chromosome 9p in a girl with minimal physical findings and normal IQ: Narrowing of the 9p duplication critical region to 6 Mb. American Journal of Medical Genetics. 112(2). 154–159. 21 indexed citations

10.

Syrris, Petros, Kirsten Heathcote, Romeo Carrozzo, et al.. (2002). Human piebaldism: six novel mutations of the proto-oncogene KIT. Human Mutation. 20(3). 234–234. 20 indexed citations

11.

Guerrini, Renzo, et al.. (2000). A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy. Annals of Neurology. 47(1). 117–121. 7 indexed citations

12.

Giglio, Sabrina, Giulia Arrigo, Gian Paolo Dagrada, et al.. (2000). Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements. European Journal of Human Genetics. 8(1). 63–70. 26 indexed citations

13.

Moro, Francesca, et al.. (1998). The β and γ Subunits of the Human Platelet-Activating Factor Acetyl Hydrolase Isoform Ib (PAFAH1B2 and PAFAH1B3) Map to Chromosome 11q23 and 19q13.1, Respectively. Genomics. 51(1). 157–159. 4 indexed citations

14.

Canevini, Maria Paola, V. Sgrò, Orsetta Zuffardi, et al.. (1998). Chromosome 20 Ring: A Chromosomal Disorder Associated with a Particular Electroclinical Pattern. Epilepsia. 39(9). 942–951. 71 indexed citations

15.

Meroni, Germana, Alexandre Reymond, Myriam Alcalay, et al.. (1997). Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor. The EMBO Journal. 16(19). 6055–6055. 4 indexed citations

16.

Carrozzo, Romeo, Rossana Tonlorenzi, Fabio Corsolini, & Rosanna Gatti. (1996). Two New Nonsense mutations (Q80X; Q389X) in patients with severe hunter syndrome ( mucopolysaccharidosis type II). Human Mutation. 7(2). 184–185. 6 indexed citations

17.

Lindsay, Elizabeth A., Lisa G. Shaffer, Romeo Carrozzo, Frank Greenberg, & Antonio Baldini. (1995). De novo tandem duplication of chromosome segment 22q11‐q12: Clinical, cytogenetic, and molecular characterization. American Journal of Medical Genetics. 56(3). 296–299. 28 indexed citations

18.

Carrozzo, Romeo, Jay W. Ellison, Pauline H. Yen, et al.. (1992). Isolation and characterization of a yeast artificial chromosome (YAC) contig around the human steroid sulfatase gene. Genomics. 12(1). 7–12. 10 indexed citations

19.

Rubba, Paolo, Paolo Pauciullo, Luciano Carbone, et al.. (1990). Early signs of vascular disease in homocystinuria: A noninvasive study by ultrasound methods in eight families with cystathionine-β-synthase deficiency. Metabolism. 39(11). 1191–1195. 40 indexed citations

20.

Greco, Luigi, et al.. (1988). A simplified test to detect PKU heterozygotes by discriminant analysis in mentally retarded children and their mothers. Clinical Genetics. 33(4). 241–245. 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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