Pietro Palumbo

1.2k citations

64 papers · 620 indexed · h-index 15

Co-authors: Massimo Carella Orazio Palumbo Raffaella Stallone Teresa Palladino Leopoldo Zelante Maurizio Delvecchio Teresa Mattina Tommaso Mazza
Topics: Genomic variations and chromosomal abnormalities (21 papers)Genetics and Neurodevelopmental Disorders (19 papers)Genomics and Rare Diseases (13 papers)
Cited by: Genetics Molecular Biology Sensory Systems
Journals: SHILAP Revista de lepidopterologíaInternational Journal of Molecular Sciences Medicine & Science in Sports & Exercise
Partner nations: Italy United States Spain

In The Last Decade

Pietro Palumbo

61 papers receiving 594 citations

Peers

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

#	Work	Indexed citations
1	The Biallelic Inheritance of Two Novel SCN1A Variants Results in Developmental and Epileptic Encephalopathy Responsive to Levetiracetam 2024 ·Biomedicines ·(unknown),Elena Conte,Orazio Palumbo,(unknown),(unknown),Pietro Palumbo,Patrizia Lastella,(unknown),(unknown),Marco Castori,Massimo Carella,Vittorio Sciruicchio,Marina de Tommaso,Antonella Liantonio,Annamaria De Luca,Angela La Neve,Paola Imbrici	1
2	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 2023 ·Genes ·Nenad Bukvić,Massimiliano Chetta,Rosanna Bagnulo,(unknown),(unknown),Orazio Palumbo,Pietro Palumbo,(unknown),(unknown),Nicola Laforgia,Marta De Rinaldis,Alessandra Rosati,Jennifer Kerkhof,Bekim Sadiković,Nicoletta Resta	3
3	Different states of stemness of glioblastoma stem cells sustain glioblastoma subtypes indicating novel clinical biomarkers and high-efficacy customized therapies 2023 ·Journal of Experimental & Clinical Cancer Research ·Alberto Visioli,(unknown),(unknown),Fabrizio Giani,Massimiliano Copetti,Orazio Palumbo,(unknown),(unknown),(unknown),(unknown),(unknown),Pietro Palumbo,Federico Legnani,Francesco DiMeco,(unknown),Graziano Pesole,Angelo L. Vescovi,Elena Binda	5
4	Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 2023 ·Cancers ·(unknown),Laura Pignata,Bruno Hay Mele,(unknown),(unknown),Orazio Palumbo,Pietro Palumbo,Massimo Carella,Gioacchino Scarano,Giovanni Battista Rossi,Claudia Angelini,Angela Sparago,Flavia Cerrato,Andrea Riccio	3
5	Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 2023 ·Frontiers in Cell and Developmental Biology ·Laura Pignata,(unknown),Fabio Acquaviva,(unknown),(unknown),(unknown),Orazio Palumbo,Pietro Palumbo,Massimo Carella,Angela Sparago,Daniele De Brasi,Flavia Cerrato,Andrea Riccio	2
6	Association of CSF and PET markers of neurodegeneration with electroclinical progression in Lafora disease 2023 ·Frontiers in Neurology ·G. D’Orsi,Andrea Farolfi,Lorenzo Muccioli,Orazio Palumbo,Pietro Palumbo,Sergio Modoni,Vincenzo Allegri,Valentina Garibotto,(unknown),(unknown),(unknown),Francesca Bisulli,Massimo Carella	3
7	Identification of a Novel FOXP1 Variant in a Patient with Hypotonia, Intellectual Disability, and Severe Speech Impairment 2023 ·Genes ·(unknown),Pietro Palumbo,(unknown),Concetta Simona Perrotta,Tommaso Mazza,(unknown),Orazio Palumbo,Massimo Carella	2
8	The presenting symptoms of Lafora Disease: An electroclinical and genetic study in five Apulian (Southern Italy) families 2020 ·Seizure ·G. D’Orsi,(unknown),Orazio Palumbo,(unknown),(unknown),Annarita Sabetta,(unknown),(unknown),Pietro Palumbo,Massimiliano Copetti,Massimo Carella,Carlo Avolio	5
9	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 2020 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·(unknown),Pietro Palumbo,Orazio Palumbo,(unknown),Massimiliano Chetta,Nicola Laforgia,Nicoletta Resta,Alessandro Stella,Stefano Castellana,Tommaso Mazza,Marco Castori,Massimo Carella,Nenad Bukvić	7
10	A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway 2019 ·European Journal of Human Genetics ·Pietro Palumbo,(unknown),Roberto Maggi,Tommaso Biagini,(unknown),Michele Sacco,Elia Di Schiavi,Massimo Carella,Lucia Micale,Marco Castori	11
11	Sudden death in mild hypertrophic cardiomyopathy with compound DSG2/DSC2/MYH6 mutations: Revisiting phenotype after genetic assessment in a master runner athlete 2019 ·Journal of Electrocardiology ·Stefano Castellana,Sandra Mastroianno,Pietro Palumbo,Orazio Palumbo,Tommaso Biagini,(unknown),Giovanni De Luca,Domenico Potenza,(unknown),Tommaso Mazza,(unknown),Giuseppe Di Stolfo,Massimo Carella	10
12	Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter Deletion 2017 ·Frontiers in Genetics ·(unknown),Orazio Palumbo,(unknown),(unknown),Pietro Palumbo,(unknown),(unknown),Rosangela Ferese,Stefano Gambardella,Antonella Angiolillo,Massimo Carella,Silvio Garofalo	5
13	Report of a patient and further clinical and molecular characterization of interstitial 4p16.3 microduplication 2015 ·Molecular Cytogenetics ·Orazio Palumbo,Pietro Palumbo,(unknown),(unknown),(unknown),Massimo Carella,Marilena Carmela Di Giacomo	6
14	Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability 2015 ·Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Anna Morgan,Ilaria Gandin,(unknown),Pietro Palumbo,Orazio Palumbo,Elisa Biamino,Valentina Dal Col,Erik Laurini,Sabrina Pricl,Paolo Bosco,Massimo Carella,Giovanni Battista Ferrero,Corrado Romano,Pio D’Adamo,Flavio Faletra,Diego Vozzi	9
15	Variable phenotype in 17q12 microdeletions: Clinical and molecular characterization of a new case 2014 ·Gene ·Pietro Palumbo,Vincenzo Antona,Orazio Palumbo,Maria Piccione,Rosaria Nardello,(unknown),Massimo Carella,Giovanni Corsello	26
16	A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2 2014 ·BMC Medical Genetics ·Enza Mozzillo,Maurizio Delvecchio,Massimo Carella,Elvira Grandone,Pietro Palumbo,Alessandro Salina,Concetta Aloi,Pietro Buono,Antonella Izzo,Giuseppe d’Annunzio,Gennaro Vecchione,Ada Orrico,Rita Genesio,Francesca Simonelli,Adriana Franzese	59
17	A de novo 11p13 Microduplication in a Patient with Some Features Invoking Silver-Russell Syndrome 2013 ·Molecular Syndromology ·Orazio Palumbo,Teresa Mattina,Pietro Palumbo,Massimo Carella,Concetta Simona Perrotta	8
18	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 2012 ·Gene ·Orazio Palumbo,Pietro Palumbo,Raffaella Stallone,Teresa Palladino,Leopoldo Zelante,Massimo Carella	20
19	An emerging phenotype of interstitial 15q25.2 microdeletions: Clinical report and review 2012 ·American Journal of Medical Genetics Part A ·Orazio Palumbo,Pietro Palumbo,Teresa Palladino,Raffaella Stallone,Mattia Miroballo,Maria Rosaria Piemontese,Leopoldo Zelante,Massimo Carella	14
20	Differential effects of benfluorex and two fibrate derivatives on serum lipoprotein patterns in hypertriglyceridemic type 2 diabetic patients 1986 ·Current Therapeutic Research ·D. Sommariva,Adriana Branchi,(unknown),Pietro Palumbo,(unknown),(unknown),U. Raggi	1

About Pietro Palumbo

Pietro Palumbo is a scholar working on Genetics, Genetics and Developmental Biology, having authored 64 papers that have together received 620 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Genomics and Rare Diseases (13 papers). The work is most often cited by research in Genetics (325 citations), Molecular Biology (314 citations) and Sensory Systems (16 citations). Pietro Palumbo has collaborated with scholars based in Italy, United States and Spain. Frequent co-authors include Massimo Carella, Orazio Palumbo, Raffaella Stallone, Teresa Palladino, Leopoldo Zelante, Maurizio Delvecchio, Teresa Mattina, Tommaso Mazza, Stefano Castellana and Maria Accadia. Their work appears in journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Medicine & Science in Sports & Exercise.

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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