G. Cara Romeo

24.9k total citations
114 papers, 3.0k citations indexed

About

G. Cara Romeo is a scholar working on Molecular Biology, Genetics and Nuclear and High Energy Physics. According to data from OpenAlex, G. Cara Romeo has authored 114 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 32 papers in Genetics and 31 papers in Nuclear and High Energy Physics. Recurrent topics in G. Cara Romeo's work include High-Energy Particle Collisions Research (27 papers), Particle physics theoretical and experimental studies (27 papers) and Quantum Chromodynamics and Particle Interactions (24 papers). G. Cara Romeo is often cited by papers focused on High-Energy Particle Collisions Research (27 papers), Particle physics theoretical and experimental studies (27 papers) and Quantum Chromodynamics and Particle Interactions (24 papers). G. Cara Romeo collaborates with scholars based in Italy, Switzerland and United States. G. Cara Romeo's co-authors include Giuseppe Gasparre, Anna Maria Porcelli, Michela Rugolo, Elena Bonora, Giovanni Tallini, Marcella Devoto, T. Mohandas, Larry J. Shapiro, Giorgio Lenaz and Valério Carelli and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Bioinformatics.

In The Last Decade

G. Cara Romeo

112 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
G. Cara Romeo Italy 28 1.4k 798 568 483 311 114 3.0k
E. Polli Italy 30 1.3k 0.9× 214 0.3× 174 0.3× 609 1.3× 119 0.4× 145 3.6k
Carolyn E. Mountford Australia 40 1.4k 1.0× 75 0.1× 422 0.7× 318 0.7× 174 0.6× 137 3.9k
Phillip A. Wilmarth United States 29 1.9k 1.3× 237 0.3× 213 0.4× 263 0.5× 40 0.1× 112 3.3k
G. Swarup India 35 2.4k 1.6× 116 0.1× 175 0.3× 599 1.2× 214 0.7× 146 4.7k
Rex Moats United States 33 1.7k 1.2× 259 0.3× 177 0.3× 69 0.1× 75 0.2× 83 4.1k
William E. Sweeney United States 37 2.7k 1.9× 2.7k 3.4× 90 0.2× 155 0.3× 62 0.2× 96 4.1k
J. Wauters Belgium 33 1.0k 0.7× 710 0.9× 153 0.3× 916 1.9× 32 0.1× 107 3.5k
Alex S. Nord United States 37 2.5k 1.8× 1.7k 2.1× 756 1.3× 562 1.2× 52 0.2× 85 5.3k
Shin Nakamura Japan 32 993 0.7× 151 0.2× 201 0.4× 358 0.7× 53 0.2× 138 3.5k
Shu Zhang China 26 1.3k 0.9× 186 0.2× 330 0.6× 47 0.1× 147 0.5× 85 2.3k

Countries citing papers authored by G. Cara Romeo

Since Specialization
Citations

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

Fields of papers citing papers by G. Cara Romeo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Cara Romeo

This figure shows the co-authorship network connecting the top 25 collaborators of G. Cara Romeo. A scholar is included among the top collaborators of G. Cara Romeo 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 G. Cara Romeo. G. Cara Romeo 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.
Farjadian, Shirin, Francesco Bonatti, Alessandra Soriano, et al.. (2019). A new MEFV gene mutation in an Iranian patient with familial Mediterranean fever. Reumatismo. 71(2). 85–87. 1 indexed citations
2.
Giuliani, Cristina, David Biggs, Elena Marasco, et al.. (2018). First evidence of association between past environmental exposure to dioxin and DNA methylation of CYP1A1 and IGF2 genes in present day Vietnamese population. Environmental Pollution. 242(Pt A). 976–985. 8 indexed citations
3.
Nagara, Majdi, Gregory Papagregoriou, Zied Landoulsi, et al.. (2017). Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance. European Journal of Medical Genetics. 61(1). 1–7. 7 indexed citations
4.
Fanti, Sara De, Saverio Vicario, Martin Lang, et al.. (2017). Intra-individual purifying selection on mitochondrial DNA variants during human oogenesis. Human Reproduction. 32(5). 1100–1107. 20 indexed citations
5.
Magini, Pamela, Monica Poscente, Simona Ferrari, et al.. (2015). Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration. Molecular Cytogenetics. 8(1). 58–58. 15 indexed citations
6.
Fontanesi, Luca, Manuela Vargiolu, Emilio Scotti, et al.. (2014). The KIT Gene Is Associated with the English Spotting Coat Color Locus and Congenital Megacolon in Checkered Giant Rabbits (Oryctolagus cuniculus). PLoS ONE. 9(4). e93750–e93750. 29 indexed citations
7.
Gasparre, Giuseppe, Ivana Kurelac, Mariantonietta Capristo, et al.. (2011). A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1 , an Oncojanus Function. Cancer Research. 71(19). 6220–6229. 81 indexed citations
8.
Gialluisi, Alessandro, Tommaso Pippucci, Yair Anikster, et al.. (2011). Estimating the Allele Frequency of Autosomal Recessive Disorders through Mutational Records and Consanguinity: The Homozygosity Index (HI). Annals of Human Genetics. 76(2). 159–167. 13 indexed citations
9.
Romeo, G. Cara. (2010). Confessione dei peccati e confessori nell'Italia della Controriforma: cosa dire del Seicento?. Studi storici. 51(4). 967–1002. 1 indexed citations
10.
Castellana, Stefano, et al.. (2008). The RHNumtS compilation: Features and bioinformatics approaches to locate and quantify Human NumtS. BMC Genomics. 9(1). 267–267. 30 indexed citations
11.
Graziano, Claudio, Angela D’Elia, Laura Mazzanti, et al.. (2007). A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation. American Journal of Medical Genetics Part A. 143A(15). 1802–1805. 25 indexed citations
12.
Bonora, Elena, Anna Maria Porcelli, Giuseppe Gasparre, et al.. (2006). Defective Oxidative Phosphorylation in Thyroid Oncocytic Carcinoma Is Associated with Pathogenic Mitochondrial DNA Mutations Affecting Complexes I and III. Cancer Research. 66(12). 6087–6096. 184 indexed citations
13.
Romeo, G. Cara. (2001). Roberto Bellarmino tra Inquisizione e indice. Studi storici. 42(2). 529–535.
14.
Harach, H R, Fabienne Lesueur, Patrizia Amati, et al.. (1999). Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2. The Journal of Pathology. 189(3). 387–393. 25 indexed citations
15.
Ferlini, Alessandra, et al.. (1988). Discrimination of peripheral polyneuropathies caused by TTR variant or diabetes in the same pedigree through protein studies.. PubMed. 48. 201–8. 7 indexed citations
16.
Saraiva, Maria João, Pedro P. Costa, Maria Rosário Almeida, et al.. (1988). Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin. Human Genetics. 80(4). 341–343. 8 indexed citations
17.
Ballabio, Andrea, Giancarlo Parenti, Rosalba Carrozzo, et al.. (1987). Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.. Proceedings of the National Academy of Sciences. 84(13). 4519–4523. 115 indexed citations
18.
Basile, M., G. Cara Romeo, L. Cifarelli, et al.. (1984). The leading effect explains the charged-particle multiplicity distributions observed at the cern pp collider. Lettere al nuovo cimento della societa italiana di fisica/Lettere al nuovo cimento. 41(9). 298–304. 7 indexed citations
19.
Sangiorgi, Simonetta, et al.. (1982). Genetic and Demographic Characterization of a Population with High Incidence of Fucosidosis. Human Heredity. 32(2). 100–105. 3 indexed citations
20.
Basile, M., G. Cara Romeo, L. Cifarelli, et al.. (1980). Evidence of the same multiparticle production mechanism in p−p collisions as in e+e− annihilation. Physics Letters B. 92(3-4). 367–370. 65 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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