Pietro Palumbo

1.2k total citations
64 papers, 620 citations indexed

About

Pietro Palumbo is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Pietro Palumbo has authored 64 papers receiving a total of 620 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 31 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Pietro Palumbo's work include Genomic variations and chromosomal abnormalities (21 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Genomics and Rare Diseases (13 papers). Pietro Palumbo is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Genomics and Rare Diseases (13 papers). Pietro Palumbo collaborates with scholars based in Italy, United States and Spain. Pietro Palumbo's co-authors include Massimo Carella, Orazio Palumbo, Raffaella Stallone, Teresa Palladino, Leopoldo Zelante, Maurizio Delvecchio, Teresa Mattina, Tommaso Mazza, Stefano Castellana and Maria Accadia and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Medicine & Science in Sports & Exercise.

In The Last Decade

Pietro Palumbo

61 papers receiving 594 citations

Peers

Pietro Palumbo

GENET

SURGE

PPCH

Flavio Faletra Italy

Chantal Missirian France

Ninette Cohen United States

Elisa Tassano Italy

Pagon Ra United States

Pamela Magini Italy

Alex Magee United Kingdom

Dominique Martin‐Coignard France

Patricia Blanchet France

Joanna Wiszniewska United States

Flavio Faletra Italy

Pietro Palumbo

267 ×0.8

GENET

251 ×0.8

59 ×0.9

SURGE

50 ×0.8

PPCH

49 ×1.0

Citations per year, relative to Pietro Palumbo Pietro Palumbo (= 1×) peers Flavio Faletra

Countries citing papers authored by Pietro Palumbo

Since Specialization

Citations

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

Fields of papers citing papers by Pietro Palumbo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pietro Palumbo

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

Palumbo, Pietro, et al.. (2023). Identification of a Novel FOXP1 Variant in a Patient with Hypotonia, Intellectual Disability, and Severe Speech Impairment. Genes. 14(10). 1958–1958. 2 indexed citations

D’Orsi, G., Orazio Palumbo, Annarita Sabetta, et al.. (2020). The presenting symptoms of Lafora Disease: An electroclinical and genetic study in five Apulian (Southern Italy) families. Seizure. 83. 145–153. 5 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

10.

Palumbo, Pietro, Roberto Maggi, Tommaso Biagini, et al.. (2019). A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway. European Journal of Human Genetics. 27(7). 1113–1120. 11 indexed citations

11.

Castellana, Stefano, Sandra Mastroianno, Pietro Palumbo, et al.. (2019). Sudden death in mild hypertrophic cardiomyopathy with compound DSG2/DSC2/MYH6 mutations: Revisiting phenotype after genetic assessment in a master runner athlete. Journal of Electrocardiology. 53. 95–99. 10 indexed citations

12.

Palumbo, Orazio, Pietro Palumbo, Rosangela Ferese, et al.. (2017). Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter Deletion. Frontiers in Genetics. 8. 206–206. 5 indexed citations

13.

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

14.

Morgan, Anna, Ilaria Gandin, Pietro Palumbo, et al.. (2015). Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 781. 32–36. 9 indexed citations

15.

Palumbo, Pietro, Vincenzo Antona, Orazio Palumbo, et al.. (2014). Variable phenotype in 17q12 microdeletions: Clinical and molecular characterization of a new case. Gene. 538(2). 373–378. 26 indexed citations

16.

Mozzillo, Enza, Maurizio Delvecchio, Massimo Carella, et al.. (2014). A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2. BMC Medical Genetics. 15(1). 88–88. 59 indexed citations

17.

Palumbo, Orazio, Teresa Mattina, Pietro Palumbo, Massimo Carella, & Concetta Simona Perrotta. (2013). A de novo 11p13 Microduplication in a Patient with Some Features Invoking Silver-Russell Syndrome. Molecular Syndromology. 5(1). 11–18. 8 indexed citations

18.

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

19.

Palumbo, Orazio, Pietro Palumbo, Teresa Palladino, et al.. (2012). An emerging phenotype of interstitial 15q25.2 microdeletions: Clinical report and review. American Journal of Medical Genetics Part A. 158A(12). 3182–3189. 14 indexed citations

20.

Sommariva, D., et al.. (1986). Differential effects of benfluorex and two fibrate derivatives on serum lipoprotein patterns in hypertriglyceridemic type 2 diabetic patients. Current Therapeutic Research. 40(5). 859–870. 1 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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