Marco Venturin

1.3k total citations
33 papers, 927 citations indexed

About

Marco Venturin is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Marco Venturin has authored 33 papers receiving a total of 927 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 11 papers in Genetics and 9 papers in Cancer Research. Recurrent topics in Marco Venturin's work include Congenital heart defects research (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Marco Venturin is often cited by papers focused on Congenital heart defects research (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Marco Venturin collaborates with scholars based in Italy, Spain and United Kingdom. Marco Venturin's co-authors include Paola Riva, Antonia Ratti, Silvia Moncini, Elena Battaglioli, Francesco Rusconi, Giuseppina De Petro, Sergio Barlati, Alessandro Salvi, Lidia Larizza and Nazario Portolani and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Marco Venturin

31 papers receiving 920 citations

Peers

Countries citing papers authored by Marco Venturin

Since Specialization

Citations

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

Fields of papers citing papers by Marco Venturin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Venturin

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Venturin. A scholar is included among the top collaborators of Marco Venturin 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 Venturin. Marco Venturin 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	Exploring the Impact of Genetics in a Large Cohort of Moebius Patients by Trio Whole Exome Sequencing 2024 ·Genes ·(unknown), Maria Francesca Bedeschi, Marco Venturin, Roberta Villa, Jole Costanza, (unknown), (unknown), Odoardo Picciolini, (unknown), Fabio Triulzi, Monica Miozzo, (unknown), Laura Fontana	1
2	Divergent regulation of long non-coding RNAs H19 and PURPL affects cell senescence in human dermal fibroblasts 2024 ·GeroScience ·(unknown), (unknown), Jessica Ruzzolini, (unknown), (unknown), Anna Laurenzana, Anastasia Chillà, (unknown), Gabriella Fibbi, Mario Del Rosso, Alessandra Mocali, Marco Venturin, Cristina Battaglia, Lisa Giovannelli, Francesca Margheri	4
3	Modeling of TDP-43 proteinopathy by chronic oxidative stress identifies rapamycin as beneficial in ALS patient-derived 2D and 3D iPSC models 2024 ·Experimental Neurology ·(unknown), (unknown), (unknown), (unknown), Patrizia Bossolasco, (unknown), Cristina Battaglia, Marco Venturin, Vincenzo Silani, Claudia Colombrita, (unknown)	3
4	PURPL and NEAT1 Long Non-Coding RNAs Are Modulated in Vascular Smooth Muscle Cell Replicative Senescence 2023 ·Biomedicines ·(unknown), Marco Venturin, (unknown), Angelisa Frasca, Alberto Corsini, Cristina Battaglia, Stefano Bellosta	6
5	Candidate Genes and MiRNAs Linked to the Inverse Relationship Between Cancer and Alzheimer’s Disease: Insights From Data Mining and Enrichment Analysis 2019 ·Frontiers in Genetics ·Cristina Battaglia, Marco Venturin, Aleksandra Šojić, Nithiya Jesuthasan, Alessandro Orro, Roberta Spinelli, Massimo Musicco, Gianluca De Bellis, Fulvio Adorni	15
6	The Long Non-Coding RNAs in Neurodegenerative Diseases: Novel Mechanisms of Pathogenesis 2016 ·Current Alzheimer Research ·Paola Riva, Antonia Ratti, Marco Venturin	252
7	Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability 2015 ·Journal of Human Genetics ·Silvia Moncini, Paola Castronovo, Alessandra Murgia, Silvia Russo, Maria Francesca Bedeschi, (unknown), Angelo Selicorni, Maria Teresa Bonati, Paola Riva, Marco Venturin	13
8	Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules 2012 ·PLoS ONE ·Paola Zuccotti, Daniele Cartelli, (unknown), V. Pandini, Marco Venturin, Alessandro Aliverti, Elena Battaglioli, Graziella Cappelletti, Paola Riva	16
9	The Role of miR-103 and miR-107 in Regulation of CDK5R1 Expression and in Cellular Migration 2011 ·PLoS ONE ·Silvia Moncini, Alessandro Salvi, Paola Zuccotti, Gabriella Viero, Alessandro Quattrone, Sergio Barlati, Giuseppina De Petro, Marco Venturin, Paola Riva	83
10	Noonan syndrome associated with both a new Jnk‐activating familial SOS1 and a de novo RAF1 mutations 2010 ·American Journal of Medical Genetics Part A ·(unknown), Silvia Moncini, Mariangela Cisternino, Ilaria Morella, (unknown), Silvia Russo, Savina Mannarino, Valeria Brazzelli, (unknown), Renata Zippel, Marco Venturin, Paola Riva	14
11	MicroRNA‐23b mediates urokinase and c‐met downmodulation and a decreased migration of human hepatocellular carcinoma cells 2009 ·FEBS Journal ·Alessandro Salvi, Cristiano Sabelli, Silvia Moncini, Marco Venturin, Bruna Arici, Paola Riva, Nazario Portolani, Stefano Maria Giulini, Giuseppina De Petro, Sergio Barlati	127
12	Breakpoint characterization of a novel NF1 multiexonic deletion: a case showing expression of the mutated allele 2008 ·Neurogenetics ·Francesca Orzan, (unknown), Marco Venturin, M. Carmen Valero, (unknown), Paola Riva	2
13	Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation 2006 ·Neurogenetics ·Marco Venturin, Silvia Moncini, Valentina Villa, Silvia Russo, Maria Teresa Bonati, Lidia Larizza, Paola Riva	27
14	Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams–Beuren syndrome region in chromosomal rearrangements 2005 ·Journal of Human Genetics ·(unknown), Marco Venturin, (unknown), (unknown), Paola Riva, Leda Dalprà	1
15	Evidence by Expression Analysis of Candidate Genes for Congenital Heart Defects in the NF1 Microdeletion Interval 2005 ·Annals of Human Genetics ·Marco Venturin, Angela Bentivegna, Ramona Frida Moroni, Lidia Larizza, Paola Riva	13
16	Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions 2004 ·Human Genetics ·Cristina Gervasini, Francesca Orzan, Angela Bentivegna, Patrizia Colapietro, (unknown), Romano Tenconi, Meena Upadhyaya, Lidia Larizza, Lucia Corrado, Marco Venturin, Paola Riva	31
17	Genotype-phenotype correlation in patients with NF1 microdeletion syndrome: identification of candidate genes for mental retardation 2002 ·The American Journal of Human Genetics ·Paola Riva, Marco Venturin, Paolo Guarnieri, Francesca Orzan, Federica Natacci, Cristina Gervasini, (unknown), Angela Bentivegna, M Stabile, Romano Tenconi, Meena Upadhyaya, Carmen Hernández, Lidia Larizza	0
18	Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region 2002 ·Human Genetics ·Cristina Gervasini, Angela Bentivegna, Marco Venturin, Lucia Corrado, Lidia Larizza, Paola Riva	11
19	Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fibers 2001 ·Human Genetics ·Angela Bentivegna, Marco Venturin, Cristina Gervasini, Lucia Corrado, Lidia Larizza, Paola Riva	6
20	FISH with locus-specific probes on stretched chromosomes: A useful tool for genome organization studies 2001 ·Chromosome Research ·Angela Bentivegna, Marco Venturin, Cristina Gervasini, Lucia Corrado, Lidia Larizza, Paola Riva	6

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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