G Venti

467 total citations
25 papers, 253 citations indexed

About

G Venti is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, G Venti has authored 25 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in G Venti's work include Genomic variations and chromosomal abnormalities (6 papers), Acute Myeloid Leukemia Research (4 papers) and Chronic Myeloid Leukemia Treatments (4 papers). G Venti is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Acute Myeloid Leukemia Research (4 papers) and Chronic Myeloid Leukemia Treatments (4 papers). G Venti collaborates with scholars based in Italy, Japan and United States. G Venti's co-authors include Emilio Donti, Maria Bodo, Ennio Becchetti, Gaetano Paludetti, Gabriella Rosi, Antonio Tabilio, Monica Giammarioli, Francesco Carinci, V. Bocchini and Tiziano Baroni and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and Cells Tissues Organs.

In The Last Decade

G Venti

24 papers receiving 233 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G Venti Italy	11	131	118	39	35	24	25	253
M. Alkan Switzerland	8	207 1.6×	90 0.8×	56 1.4×	18 0.5×	43 1.8×	13	317
Iskra Petković Croatia	11	179 1.4×	164 1.4×	53 1.4×	24 0.7×	20 0.8×	31	305
Ursula Giussani Italy	9	124 0.9×	90 0.8×	54 1.4×	18 0.5×	28 1.2×	16	226
V. D. Marković Canada	8	258 2.0×	183 1.6×	31 0.8×	76 2.2×	18 0.8×	10	419
M.-F. de Tand France	7	201 1.5×	131 1.1×	32 0.8×	11 0.3×	14 0.6×	10	346
Donatella Fantasia Italy	11	158 1.2×	108 0.9×	20 0.5×	72 2.1×	11 0.5×	19	311
R.L. Stallings Ireland	8	97 0.7×	81 0.7×	42 1.1×	24 0.7×	26 1.1×	9	269
Juan Cota United States	6	198 1.5×	74 0.6×	28 0.7×	69 2.0×	11 0.5×	8	384
M.H. Breuning Netherlands	8	219 1.7×	157 1.3×	34 0.9×	43 1.2×	27 1.1×	13	385
Lara Cresswell United Kingdom	8	83 0.6×	134 1.1×	21 0.5×	28 0.8×	14 0.6×	9	317

Countries citing papers authored by G Venti

Since Specialization

Citations

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

Fields of papers citing papers by G Venti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G Venti

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Prontera, Paolo, Vincenzo Aiello, G Venti, et al.. (2006). Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis. Prenatal Diagnosis. 26(6). 571–576. 20 indexed citations

Sainati, Laura, Anna Leszl, Maria Caterina Putti, et al.. (1998). Centralized cytogenetic analysis of pediatric acute leukemia: results of an Italian collaborative experience.. PubMed. 82(6). 654–9. 2 indexed citations

Locci, Paola, Ennio Becchetti, G Venti, et al.. (1996). Glycosaminoglycan metabolism in otosclerotic bone cells. Biology of the Cell. 86(1). 73–78. 13 indexed citations

Palka, Giandomenico, G Calabrese, Liborio Stuppia, et al.. (1995). Molecular characterization of an unusual variant t(15;17) detected in an APL patient.. PubMed. 9(10). 1787–9. 3 indexed citations

Bodo, Maria, G Venti, Tiziano Baroni, et al.. (1995). Phenotype of in vitro human otosclerotic cells and its modulation by TGF beta.. PubMed. 41(8). 1039–49. 21 indexed citations

Venti, G, Mariantonietta Colozza, Berardino Porfirio, et al.. (1993). Expression of aphidicolin-induced fragile sites in lymphocytes of patients with breast cancer. Cancer Genetics and Cytogenetics. 67(2). 113–116. 23 indexed citations

Locci, Paola, G Venti, Cinzia Lilli, et al.. (1993). Synthesis and secretion of glycosaminoglycans and proteins in human normal and otosclerotic bone cells.. PubMed. 38(5-6). 635–42. 6 indexed citations

Bodo, Maria, Tiziano Baroni, Mario Calvitti, et al.. (1992). Modulation of Phenotype and Cytoskeleton Architecture by lnterleukin-1 Alpha in Human Osteoblast-Like Cells in vitro. Cells Tissues Organs. 145(2). 156–161. 7 indexed citations

Donti, Emilio, et al.. (1991). Myelodysplastic syndromes: Cytogenetic studies of 130 cases. Leukemia Research. 15. 21–21. 2 indexed citations

10.

Venti, G, et al.. (1991). Characterization of the Cytoskeleton in Human Normal and Otosclerotic Osteoblast-Like Cells. Cells Tissues Organs. 141(4). 311–315. 6 indexed citations

11.

Donti, Emilio, Luisa Lanfrancone, Kay Huebner, et al.. (1990). Localization of the human HF.10 finger gene on a chromosome region (3p21?22) frequently deleted in human cancers. Human Genetics. 84(5). 391–5. 12 indexed citations

12.

Longo, Letizia, Emilio Donti, Amedea Mencarelli, et al.. (1990). Mapping of chromosome 17 breakpoints in acute myeloid leukemias.. PubMed. 5(10). 1557–63. 29 indexed citations

13.

Donti, Emilio, Ildo Nicoletti, G Venti, et al.. (1989). X-ring Turner’s syndrome with combined immunodeficiency and selective gonadotropin defect. Journal of Endocrinological Investigation. 12(4). 257–263. 10 indexed citations

14.

Donti, Emilio, et al.. (1985). 5q− in a case of blastic phase chronic myeloid leukemia. Cancer Genetics and Cytogenetics. 16(4). 365–367. 3 indexed citations

15.

Donti, Emilio, et al.. (1982). DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminisation).. Journal of Medical Genetics. 19(5). 349–353. 2 indexed citations

16.

Rosi, Gabriella, et al.. (1980). [Karyotype 47,XXY in a subject with complete testicular feminization].. PubMed. 71(1013). 388–9. 3 indexed citations

17.

Donti, Emilio, et al.. (1979). The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(qh?,RHG,GAG,CBG). Human Genetics. 48(1). 53–59. 12 indexed citations

18.

Venti, G, et al.. (1979). A case of complete testicular feminisation and 47,XXY karyotype.. Journal of Medical Genetics. 16(6). 480–483. 14 indexed citations

19.

Rosi, Gabriella, et al.. (1979). Trisomy 6p22?6pter due to familial t(6;13)(p22;q34 or 33) translocation. Human Genetics. 51(1). 67–72. 12 indexed citations

20.

Furbetta, M., et al.. (1978). [Karyotype 46,XY,22p+ in a male patient (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 26(2). 177–84. 2 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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