Nenad Bukvić

881 total citations
40 papers, 520 citations indexed

About

Nenad Bukvić is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Nenad Bukvić has authored 40 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Genetics and 12 papers in Cancer Research. Recurrent topics in Nenad Bukvić's work include Carcinogens and Genotoxicity Assessment (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Nenad Bukvić is often cited by papers focused on Carcinogens and Genotoxicity Assessment (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Nenad Bukvić collaborates with scholars based in Italy, Serbia and Canada. Nenad Bukvić's co-authors include Ginevra Guanti, Francesco Susca, Margherita Fanelli, Mattia Gentile, Marilena Carmela Di Giacomo, Gabriella Serio, Nicoletta Resta, F Cassano, Antonio Capurso and Andrea Ballini and has published in prestigious journals such as International Journal of Molecular Sciences, Gene and Journal of Cellular Physiology.

In The Last Decade

Nenad Bukvić

37 papers receiving 492 citations

Peers

Nenad Bukvić

GENET

HTM

Bruna Tedeschi Italy

Chencheng Yao China

Rolf‐Dieter Wegner Germany

R.‐D. Wegner Germany

Anahita Mohseni Meybodi Iran

Jinhua Lu China

Christiane Massicotte United States

Junhao Yan China

Mehrdad Noruzinia Iran

Feikun Yang United States

Bruna Tedeschi Italy

Nenad Bukvić

287 ×1.3

209 ×1.2

GENET

135 ×0.9

64 ×0.7

15 ×0.2

HTM

Citations per year, relative to Nenad Bukvić Nenad Bukvić (= 1×) peers Bruna Tedeschi

Countries citing papers authored by Nenad Bukvić

Since Specialization

Citations

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

Fields of papers citing papers by Nenad Bukvić

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nenad Bukvić

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

Chetta, Massimiliano, et al.. (2024). A Copernican revolution of multigenic analysis: A retrospective study on clinical exome sequencing in unclear genetic disorders. Computational and Structural Biotechnology Journal. 23. 2615–2622. 1 indexed citations

Chetta, Massimiliano, Anna Basile, Marina Tarsitano, et al.. (2024). The Target Therapy Hyperbole: “KRAS (p.G12C)”—The Simplification of a Complex Biological Problem. Cancers. 16(13). 2389–2389. 1 indexed citations

Bukvić, Nenad, Massimiliano Chetta, Rosanna Bagnulo, et al.. (2023). What Have We Learned from Patients Who Have Arboleda-Tham Syndrome Due to a De Novo KAT6A Pathogenic Variant with Impaired Histone Acetyltransferase Function? A Precise Clinical Description May Be Critical for Genetic Testing Approach and Final Diagnosis. Genes. 14(1). 165–165. 3 indexed citations

Palumbo, Pietro, Orazio Palumbo, Massimiliano Chetta, et al.. (2020). The recurrent SETBP1 c.2608G > A, p.(Gly870Ser) variant in a patient with Schinzel-Giedion syndrome: an illustrative case of the utility of whole exome sequencing in a critically ill neonate. The Italian Journal of Pediatrics/Italian journal of pediatrics. 46(1). 74–74. 7 indexed citations

Lattanzi, Wanda, Nenad Bukvić, Marta Barba, et al.. (2012). Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications. Child s Nervous System. 28(9). 1301–1310. 36 indexed citations

Bukvić, Nenad, et al.. (2012). Characterization of the first adult de novo case of 46,X,der(Y)t(X;Y)(p22.3;q11.2). Gene. 513(1). 111–117. 3 indexed citations

Chetta, Massimiliano, et al.. (2011). McKusick-Kaufman or Bardet-Biedl syndrome? A new borderline case in an Italian nonconsanguineous healthy family. Indian journal of human genetics. 17(2). 94–94. 3 indexed citations

Vukov, Tanja, et al.. (2010). DETECTION OF PREMATURE SEGREGATION OF CENTROMERES IN PERSONS EXPOSED TO IONIZING RADIATION. Health Physics. 98(5). 717–727. 6 indexed citations

Bukvić, Nenad, Giuseppina Pustorino, Massimiliano Chetta, et al.. (2010). Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH. American Journal of Medical Genetics Part A. 152A(7). 1730–1734. 28 indexed citations

10.

Bukvić, Nenad, Piero Lovreglio, Margherita Fanelli, et al.. (2009). Influence of Some Detoxification Enzyme Polymorphisms on Cytogenetic Biomarkers Between Individuals Exposed to Very Low Doses of 1,3-Butadiene. Journal of Occupational and Environmental Medicine. 51(7). 811–821. 4 indexed citations

11.

Santacroce, Rosa, Valeria Bafunno, Francesco Sessa, et al.. (2009). Detection of New Deletions in a Group of Italian Patients with Hemophilia A by Multiplex Ligation–Dependent Probe Amplification. Genetic Testing and Molecular Biomarkers. 13(5). 573–576. 4 indexed citations

12.

Bukvić, Nenad, et al.. (2009). Coexistence of β-Thalassemia and Hereditary Hemochromatosis in Homozygosity: A Possible Synergic Effect?. Hemoglobin. 33(2). 155–157. 3 indexed citations

13.

Milić, Nataša, et al.. (2009). Chromosomal Aberrations in Subjects Exposed to Ionizing Radiation. Journal of Environmental Pathology Toxicology and Oncology. 28(1). 75–82. 5 indexed citations

14.

Bukvić, Nenad, et al.. (2009). Autism and Hypoplastic Corpus Callosum in a Case of Monocentric Marker Chromosome 15. Pediatric Neurology. 41(1). 65–67. 4 indexed citations

15.

Resta, Nicoletta, Francesco Susca, Marilena Carmela Di Giacomo, et al.. (2006). A homozygous frameshift mutation in the ESCO2 gene: Evidence of intertissue and interindividual variation in Nmd efficiency. Journal of Cellular Physiology. 209(1). 67–73. 45 indexed citations

16.

Giacomo, Marilena Carmela Di, et al.. (2004). Duplication of 9 p11.2‐p13.1: a benign cytogenetic variant. Prenatal Diagnosis. 24(8). 619–622. 19 indexed citations

17.

Bukvić, Nenad, Mattia Gentile, Francesco Susca, et al.. (2001). Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 498(1-2). 159–167. 73 indexed citations

18.

Bukvić, Nenad, Leonardo Soleo, Margherita Fanelli, et al.. (2000). Increment of sister chromatid exchange frequencies (SCE) due to epichlorohydrin (ECH) in vitro treatment in human lymphocytes. Teratogenesis Carcinogenesis and Mutagenesis. 20(5). 313–320. 2 indexed citations

19.

Bukvić, Nenad, et al.. (1998). Sister chromatid exchange (SCE) and micronucleus (MN) frequencies in lymphocytes of gasoline station attendants. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 415(1-2). 25–33. 60 indexed citations

20.

Soleo, Leonardo, Antonella Basso, Luigi Di Lorenzo, Nenad Bukvić, & N L'Abbate. (1996). Acute radiodermatitis from accidental overexposure to X-rays. American Journal of Industrial Medicine. 30(2). 207–211. 11 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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