Marco Seri

12.6k total citations · 1 hit paper
193 papers, 5.3k citations indexed

About

Marco Seri is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Marco Seri has authored 193 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Molecular Biology, 77 papers in Genetics and 28 papers in Surgery. Recurrent topics in Marco Seri's work include Platelet Disorders and Treatments (21 papers), Genomics and Rare Diseases (18 papers) and Genomic variations and chromosomal abnormalities (16 papers). Marco Seri is often cited by papers focused on Platelet Disorders and Treatments (21 papers), Genomics and Rare Diseases (18 papers) and Genomic variations and chromosomal abnormalities (16 papers). Marco Seri collaborates with scholars based in Italy, United States and United Kingdom. Marco Seri's co-authors include Isabella Ceccherini, Yin Luo, Renata Bocciardi, Margherita Lerone, Virginia Barone, Barbara Pasini, Giuseppe Martucciello, Giovanni Romeo, Tommaso Pippucci and Anna Savoia and has published in prestigious journals such as Nature, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Marco Seri

187 papers receiving 5.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

1994 532 citations Giovanni Romeo, Marco Seri et al. profile →

Peers

Countries citing papers authored by Marco Seri

Since Specialization

Citations

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

Fields of papers citing papers by Marco Seri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Seri

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Seri. A scholar is included among the top collaborators of Marco Seri 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 Marco Seri. Marco Seri is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	The CONVERSION Study: Open Conversion Risk in Robotic vs Laparoscopic Surgery—A 20-Year Meta-analysis 2025 ·Annals of Surgery ·Antonio Gangemi, (unknown), (unknown), Lisa Argnani, M. Negri, Matteo Cescon, Riccardo Casadei, Marco Seri, Gilberto Poggioli	0
2	Detection of somatic and germline pathogenic variants in adult cohort of drug-resistant focal epilepsies 2024 ·Epilepsy & Behavior ·Lorenzo Ferri, (unknown), Laura Licchetta, (unknown), Raffaella Minardi, (unknown), Lidia Di Vito, (unknown), Corrado Zenesini, Francesca Gozzo, Veronica Pelliccia, Valeria Mariani, (unknown), Stefano Gustincich, Marco Seri, Laura Tassi, Tommaso Pippucci, Francesca Bisulli	2
3	miRNA–221 and miRNA–483–3p Dysregulation in Esophageal Adenocarcinoma 2024 ·Cancers ·(unknown), (unknown), (unknown), Luca Mastracci, Deborah Malvi, Marialuisa Lugaresi, Silvia Fittipaldi, (unknown), Annalisa Astolfi, Jari Räsänen, Antonia D’Errico, Riccardo Rosati, Roberto Fiocca, Marco Seri, Kausilia K. Krishnadath, Elena Bonora, Sandro Mattioli	2
4	Behavioral profiling in children and adolescents with Malan syndrome 2023 ·PubMed ·Paolo Alfieri, (unknown), Marina Macchiaiolo, (unknown), (unknown), (unknown), (unknown), (unknown), Marcella Zollino, Marcello Chinali, (unknown), Marco Seri, (unknown), (unknown), Marco Tartaglia, Stefano Vicari, Manuela Priolo	2
5	A Male Child with Infantile Epilepsy due to a Mosaic Missense Variant of PCDH19 2023 ·Molecular Syndromology ·(unknown), Raffaella Minardi, Antonella Boni, Jacopo Pruccoli, Antonella Pini, Laura Licchetta, Francesca Bisulli, Claudio Graziano, Marco Seri	1
6	La morte improvvisa giovanile e in età adulta: cause e concause. L’esperienza della rete multidisciplinare in Emilia-Romagna 2022 ·Giornale italiano di cardiologia ·Ornella Leone, Valentina Agostini, Maddalena Graziosi, Cesare Rossi, Guido Pelletti, Alberto Foà, (unknown), Mattia Riefolo, Matteo Ziacchi, Paolo Fais, Susi Pelotti, Claudio Rapezzi, Marco Seri	4
7	Exploration of Tools for the Interpretation of Human Non-Coding Variants 2022 ·International Journal of Molecular Sciences ·(unknown), (unknown), Paolo Uva, (unknown), Tommaso Pippucci, Marco Seri, Andrea Cavalli, Isabella Ceccherini, Marta Rusmini, Federica Viti	11
8	Prenatal genetic counselling: issues and perspectives for pre-conceptional health care in Emilia Romagna (Northern Italy) 2022 ·SHILAP Revista de lepidopterología ·(unknown), Gianni Astolfi, Stefania Bigoni, Anna Baroncini, Olga Calabrese, Alessandra Ferlini, (unknown), (unknown), Marco Seri, Elisa Calzolari	0
9	Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype 2021 ·American Journal of Medical Genetics Part A ·(unknown), Fortunato Lonardo, (unknown), (unknown), M. Cristina Digilio, (unknown), Daniela Rogaia, Amedea Mencarelli, Chiara Leoni, Carmelo Piscopo, (unknown), Mariateresa Falco, Paolo Fontana, Anna Maria Nardone, Antonio Novelli, (unknown), Marco Seri, Paolo Prontera	5
10	unCOVERApp: an interactive graphical application for clinical assessment of sequence coverage at the base-pair level 2020 ·Bioinformatics ·(unknown), Marco Seri, Tommaso Pippucci	0
11	Whole‐exome sequencing in adult patients with developmental and epileptic encephalopathy: It is never too late 2020 ·Clinical Genetics ·Raffaella Minardi, Laura Licchetta, (unknown), Tommaso Pippucci, Carlotta Stipa, Barbara Mostacci, (unknown), Francesco Toni, (unknown), Valério Carelli, Marco Seri, Paolo Tinuper, Francesca Bisulli	27
12	Cataplexy and ataxia: red flags for the diagnosis of DNA methyltransferase 1 mutation 2020 ·Journal of Clinical Sleep Medicine ·(unknown), Elena Antelmi, Fabio Pizza, Stefano Vandi, Chiara La Morgia, Valério Carelli, Stefania Alessandra Nassetti, Marco Seri, Giuseppe Plazzi	3
13	Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia 2018 ·Blood ·Caterina Marconi, Christian A. Di Buduo, (unknown), Serena Barozzi, Michela Faleschini, Valeria Bozzi, Flavia Palombo, Spencer U. McKinstry, Giuseppe Lassandro, Paola Giordano, Patrizia Noris, Carlo L. Balduini, Anna Savoia, Alessandra Balduini, Tommaso Pippucci, Marco Seri, Nicholas Katsanis, Alessandro Pecci	37
14	Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration 2015 ·Molecular Cytogenetics ·Pamela Magini, Monica Poscente, Simona Ferrari, Manuela Vargiolu, Elena Bacchelli, Claudio Graziano, Anita Wischmeijer, Daniela Turchetti, Elisabetta Malaspina, Valentina Marchiani, Duccio Maria Cordelli, Emilio Franzonı, G. Cara Romeo, Marco Seri	15
15	Apolipoprotein B is a new target of the GDNF/RET and ET‐3/EDNRB signalling pathways 2012 ·Neurogastroenterology & Motility ·Cecilia Evangelisti, Francesca Bianco, (unknown), Aldamaria Puliti, (unknown), Isabella Sbrana, Mario Rossi, Manuela Vargiolu, Marco Seri, Giovanni Romeo, Vincenzo Stanghellini, Roberto De Giorgio, Elena Bonora	8
16	Heavy chain myosin 9-related disease (MYH9-RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder 2010 ·Thrombosis and Haemostasis ·Daniela De Rocco, Emanuele Panza, Valeria Bozzi, Raffaella Scandellari, Giuseppe Loffredo, Andrew Mumford, Paula G. Heller, Patrizia Noris, Marco de Groot, Marisa Giani, (unknown), Francesca Scognamiglio, Silvia Riondino, Núria Pujol‐Moix, Fabrizio Fabris, Marco Seri, Carlo Balduini, Alessandro Pecci, Anna Savoia	66
17	Localization of a Gene for Nonsyndromic Renal Hypodysplasia to Chromosome 1p32-33 2007 ·The American Journal of Human Genetics ·Simone Sanna‐Cherchi, Gianluca Caridi, Patricia L. Weng, Monica Dagnino, Marco Seri, (unknown), Danio Somenzi, Alba Carrea, Claudia Izzi, D. Casu, Landino Allegri, Kai M. Schmidt‐Ott, Jonathan Barasch, Francesco Scolari, Roberto Ravazzolo, Gian Marco Ghiggeri, Ali G. Gharavi	23
18	New clinical findings in oculo-ecNew clinical findings in oculo-ectodermal syndrome. 2000 ·Clinical Dysmorphology ·Margherita Silengo, Margherita Lerone, Marco Seri, Manuela Priolo, Laura Jarre	3
19	Exclusion of the SCN2B gene as candidate for CMT4B 1998 ·European Journal of Human Genetics ·Alessandra Bolino, Marco Seri, Francesco Caroli, James H. Eubanks, Jayashree Srinivasan, Paola Mandich, Angelo Schenone, Aldo Quattrone, Giovanni Romeo, (unknown), Marcella Devoto	1
20	A rare G6490 → substitution at the last nucleotide of exon 10 of the glucocerebrosidase gene in two unrelated Italian Gaucher patients 1995 ·Clinical Genetics ·Marco Seri, Mirella Filocamo, Fabio Corsolini, Bruno Bembi, (unknown), Rosanna Gatti	9

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.

Explore authors with similar magnitude of impact