Orazio Palumbo

4.3k total citations
125 papers, 2.5k citations indexed

About

Orazio Palumbo is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Orazio Palumbo has authored 125 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 78 papers in Molecular Biology, 61 papers in Genetics and 21 papers in Cancer Research. Recurrent topics in Orazio Palumbo's work include Genomic variations and chromosomal abnormalities (28 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Epigenetics and DNA Methylation (16 papers). Orazio Palumbo is often cited by papers focused on Genomic variations and chromosomal abnormalities (28 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Epigenetics and DNA Methylation (16 papers). Orazio Palumbo collaborates with scholars based in Italy, United States and Germany. Orazio Palumbo's co-authors include Massimo Carella, Pietro Palumbo, Ada Piepoli, Gianluigi Mazzoccoli, Angelo Andriulli, Tommaso Mazza, Anna Panza, Raffaella Stallone, Andrea Riccio and Leopoldo Zelante and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Orazio Palumbo

123 papers receiving 2.4k citations

Peers

Orazio Palumbo

GENET

PPCH

ONCOL

Giuseppe Merla Italy

Jean Charron Canada

Alexander Gow United States

Nicole Wagner France

Geri Méduri France

Marcelina Párrizas Spain

Bora Lee South Korea

Zoë Webster United Kingdom

Peter A. Cattini Canada

Alex Yick‐Lun So United States

Giuseppe Merla Italy

Orazio Palumbo

1.6k ×1.1

746 ×1.0

GENET

290 ×0.4

88 ×0.4

PPCH

242 ×1.2

ONCOL

Citations per year, relative to Orazio Palumbo Orazio Palumbo (= 1×) peers Giuseppe Merla

Countries citing papers authored by Orazio Palumbo

Since Specialization

Citations

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

Fields of papers citing papers by Orazio Palumbo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Orazio Palumbo

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

Conte, Elena, Orazio Palumbo, Pietro Palumbo, et al.. (2024). The Biallelic Inheritance of Two Novel SCN1A Variants Results in Developmental and Epileptic Encephalopathy Responsive to Levetiracetam. Biomedicines. 12(8). 1698–1698. 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

Visioli, Alberto, Fabrizio Giani, Massimiliano Copetti, et al.. (2023). Different states of stemness of glioblastoma stem cells sustain glioblastoma subtypes indicating novel clinical biomarkers and high-efficacy customized therapies. Journal of Experimental & Clinical Cancer Research. 42(1). 244–244. 5 indexed citations

Pignata, Laura, Bruno Hay Mele, Orazio Palumbo, et al.. (2023). Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer. Cancers. 15(7). 1944–1944. 3 indexed citations

Pignata, Laura, Fabio Acquaviva, Orazio Palumbo, et al.. (2023). Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?. Frontiers in Cell and Developmental Biology. 11. 1237629–1237629. 2 indexed citations

D’Orsi, G., Andrea Farolfi, Lorenzo Muccioli, et al.. (2023). Association of CSF and PET markers of neurodegeneration with electroclinical progression in Lafora disease. Frontiers in Neurology. 14. 1202971–1202971. 3 indexed citations

Colangelo, Tommaso, Annalucia Carbone, Roberto Cuttano, et al.. (2022). Loss of circadian gene Timeless induces EMT and tumor progression in colorectal cancer via Zeb1-dependent mechanism. Cell Death and Differentiation. 29(8). 1552–1568. 26 indexed citations

Palumbo, Orazio, Eleonora M. C. Trecca, Lucia Micale, et al.. (2021). Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family. SHILAP Revista de lepidopterología. 11(3). 443–451. 1 indexed citations

Pignata, Laura, Angela Sparago, Orazio Palumbo, et al.. (2021). Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome. Genes. 12(4). 581–581. 5 indexed citations

10.

Noguera, Nélida I., Tommaso Colangelo, Elisabetta De Marinis, et al.. (2020). Transcriptional and Metabolic Dissection of ATRA-Induced Granulocytic Differentiation in NB4 Acute Promyelocytic Leukemia Cells. Cells. 9(11). 2423–2423. 14 indexed citations

11.

Pignata, Laura, Orazio Palumbo, Flavia Cerrato, et al.. (2020). Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors. Cancers. 12(11). 3411–3411. 7 indexed citations

12.

Fusco, Carmela, Bartolomeo Augello, Francesca Boccafoschi, et al.. (2020). Pro-Fibrotic Phenotype in a Patient with Segmental Stiff Skin Syndrome via TGF-β Signaling Overactivation. International Journal of Molecular Sciences. 21(14). 5141–5141. 12 indexed citations

13.

Micale, Lucia, Vito Guarnieri, Bartolomeo Augello, et al.. (2019). Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome. Genes. 10(12). 967–967. 9 indexed citations

14.

Binda, Elena, Alberto Visioli, Fabrizio Giani, et al.. (2016). Wnt5a Drives an Invasive Phenotype in Human Glioblastoma Stem-like Cells. Cancer Research. 77(4). 996–1007. 76 indexed citations

15.

Nicoletti, Annalisa, Lucia Ziccardi, Paolo Enrico Maltese, et al.. (2016). Design and Validation of a New MLPA-Based Assay for the Detection of RS1 Gene Deletions and Application in a Large Family with X-Linked Juvenile Retinoschisis. Genetic Testing and Molecular Biomarkers. 21(2). 116–121. 1 indexed citations

16.

L’Abbate, Alberto, Doron Tolomeo, Angelo Lonoce, et al.. (2015). t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders. Molecular Cancer. 14(1). 211–211. 14 indexed citations

17.

Palumbo, Orazio, et al.. (2015). Report of a patient and further clinical and molecular characterization of interstitial 4p16.3 microduplication. Molecular Cytogenetics. 8(1). 15–15. 6 indexed citations

18.

Crescenzo, Agostina De, Angela Sparago, Flavia Cerrato, et al.. (2012). Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction. Journal of Medical Genetics. 50(2). 99–103. 33 indexed citations

19.

Palumbo, Orazio, Pietro Palumbo, Raffaella Stallone, et al.. (2012). 8q12.1q12.3 de novo microdeletion involving the CHD7 gene in a patient without the major features of CHARGE syndrome: Case report and critical review of the literature. Gene. 513(1). 209–213. 20 indexed citations

20.

Guastadisegni, Maria Corsignano, Roberta Roberto, Alberto L’Abbate, et al.. (2011). Thrombocytopenia-absent-radius syndrome in a child showing a larger 1q21.1 deletion than the one in his healthy mother, and a significant downregulation of the commonly deleted genes. European Journal of Medical Genetics. 55(2). 120–123. 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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