V. Ventruto

1.1k total citations
48 papers, 792 citations indexed

About

V. Ventruto is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, V. Ventruto has authored 48 papers receiving a total of 792 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 18 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in V. Ventruto's work include Hemoglobinopathies and Related Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). V. Ventruto is often cited by papers focused on Hemoglobinopathies and Related Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). V. Ventruto collaborates with scholars based in Italy, United States and Spain. V. Ventruto's co-authors include Barkur S. Shastry, Xiaodong Jiao, J. Fielding Hejtmancik, Michael T. Trese, Corrado Baglioni, M Stabile, Michele D’Urso, Maria Giuseppina Miano, Maria Luigia Cavaliere and Gioacchino Scarano and has published in prestigious journals such as Science, Annals of the New York Academy of Sciences and The American Journal of Human Genetics.

In The Last Decade

V. Ventruto

46 papers receiving 756 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. Ventruto Italy 17 479 288 87 81 79 48 792
K. O. J. Simola Finland 20 863 1.8× 472 1.6× 42 0.5× 95 1.2× 166 2.1× 36 1.2k
Rudolf A. Pfeiffer Germany 13 438 0.9× 383 1.3× 38 0.4× 25 0.3× 75 0.9× 18 672
Florence Niel France 17 879 1.8× 241 0.8× 94 1.1× 82 1.0× 34 0.4× 24 1.3k
E. M. Bleeker‐Wagemakers Netherlands 17 719 1.5× 235 0.8× 104 1.2× 36 0.4× 46 0.6× 50 904
Abdulrahman Alswaid Saudi Arabia 16 509 1.1× 698 2.4× 155 1.8× 55 0.7× 67 0.8× 29 1.1k
Silvestre Oltra Spain 20 626 1.3× 478 1.7× 48 0.6× 84 1.0× 109 1.4× 69 1.1k
Regine Witköwski Germany 12 246 0.5× 203 0.7× 64 0.7× 209 2.6× 46 0.6× 43 539
Anneke I. den Hollander Netherlands 13 537 1.1× 301 1.0× 86 1.0× 14 0.2× 39 0.5× 15 673
Ghislaine Plessis France 18 431 0.9× 341 1.2× 46 0.5× 129 1.6× 55 0.7× 31 810
Carol A. Crowe United States 17 582 1.2× 318 1.1× 100 1.1× 70 0.9× 136 1.7× 28 904

Countries citing papers authored by V. Ventruto

Since Specialization
Citations

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

Fields of papers citing papers by V. Ventruto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Ventruto

This figure shows the co-authorship network connecting the top 25 collaborators of V. Ventruto. A scholar is included among the top collaborators of V. Ventruto 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 V. Ventruto. V. Ventruto 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.
Crecchio, Giuseppe de, et al.. (2013). Severe Myopia with Unusual Retinal Anomalies and Dandy-Walker Sequence in Two Sibs. A Distinct New Neuro-ocular Disorder. Ophthalmic Genetics. 34(4). 254–257. 3 indexed citations
2.
Spizzichino, L., Pio D’Adamo, Jlenia Monfregola, et al.. (2007). MRX87 family with Aristaless Xdup24bp mutation and implication for polyAlanine expansions. BMC Medical Genetics. 8(1). 25–25. 23 indexed citations
3.
Falco, Geppino, et al.. (2005). Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2–q28 associated with ovarian dysfunction. Human Reproduction. 21(2). 529–535. 24 indexed citations
4.
Jiao, Xiaodong, V. Ventruto, Michael T. Trese, Barkur S. Shastry, & J. Fielding Hejtmancik. (2004). Autosomal Recessive Familial Exudative Vitreoretinopathy Is Associated with Mutations in LRP5. The American Journal of Human Genetics. 75(5). 878–884. 152 indexed citations
5.
Annunziata, Ida, Carmela Lanzara, Iván Conte, et al.. (2003). Mapping of MRX81 in Xp11.2‐Xq12 suggests the presence of a new gene involved in nonspecific X‐linked mental retardation. American Journal of Medical Genetics Part A. 118A(3). 217–222. 10 indexed citations
6.
Spitz, François, Thomas Montavon, Michael A. Morris, et al.. (2002). A t(2;8) Balanced Translocation with Breakpoints Near the Human HOXD Complex Causes Mesomelic Dysplasia and Vertebral Defects. Genomics. 79(4). 493–498. 36 indexed citations
7.
Miano, Maria Giuseppina, Francesco Testa, Francesco Filippini, et al.. (2001). Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains. Human Mutation. 18(2). 109–119. 34 indexed citations
8.
Miano, Maria Giuseppina, Francesco Testa, Maria Strazzullo, et al.. (1999). Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa. European Journal of Human Genetics. 7(6). 687–694. 29 indexed citations
9.
Fujimoto, Masahiro, Piranit Nik Kantaputra, Shiro Ikegawa, et al.. (1998). The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32. Journal of Human Genetics. 43(1). 32–36. 31 indexed citations
10.
Magli, Adriano, et al.. (1997). A further observation of corneal dystrophy and perceptive deafness in two siblings. Ophthalmic Genetics. 18(2). 87–91. 7 indexed citations
11.
Ferrara, Felicetto, Luigi Del Vecchio, Fabrizio Pane, et al.. (1995). Simultaneous occurrence of tetrasomy 21 and trisomy 8 in a patient with early blastic metamorphosis of chronic myeloproliferative disorder. American Journal of Hematology. 50(1). 49–52. 8 indexed citations
12.
Russo, Rosa, Maria DʼArmiento, Pasquale Martinelli, et al.. (1989). Neu‐Laxova syndrome: Pathological, radiological, and prenatal findings in a stillborn female. American Journal of Medical Genetics. 32(1). 136–139. 22 indexed citations
13.
Cobellis, Giovanni, et al.. (1988). Prenatal ultrasound diagnosis of macroglossia in the Wiedemann‐Beckwith syndrome. Prenatal Diagnosis. 8(1). 79–81. 20 indexed citations
14.
Ventruto, V., et al.. (1982). Familial Laryngeal Abductor Paralysis with Presumed Autosomal Dominant Inheritance. Annals of Otology Rhinology & Laryngology. 91(3). 323–324. 16 indexed citations
15.
Dallapiccola, Bruno, et al.. (1982). t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome.. PubMed. 25(1). 56–8. 8 indexed citations
16.
Pagano, Livio, et al.. (1980). Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter.. PubMed. 23(3). 173–5. 4 indexed citations
17.
Koo, Gloria C., Stephen S. Wachtel, Paul Saenger, et al.. (1977). H-Y Antigen: Expression in Human Subjects with the Testicular Feminization Syndrome. Science. 196(4290). 655–656. 16 indexed citations
18.
Ventruto, V., et al.. (1974). Hemoglobin Lepore: Its significance for thalassemia and clinical manifestations. Annals of Hematology. 28(5). 327–336. 6 indexed citations
19.
Ventruto, V., et al.. (1970). Hemoglobinopathies in Campania with particular reference to the rare and new types. Annals of Hematology. 20(5). 292–295. 4 indexed citations
20.

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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