Marco Baccarin

679 total citations
25 papers, 480 citations indexed

About

Marco Baccarin is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Marco Baccarin has authored 25 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 12 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Marco Baccarin's work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Autism Spectrum Disorder Research (5 papers). Marco Baccarin is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Autism Spectrum Disorder Research (5 papers). Marco Baccarin collaborates with scholars based in Italy, United States and Czechia. Marco Baccarin's co-authors include Silvana Guerneri, Donatella Milani, Paola Castronovo, Alessandra Rossini, Antonio M. Persico, Carlo Gaetano, Laura Porretti, Federico Colombo, Maurizio C. Capogrossi and Giulio Pompilio and has published in prestigious journals such as PLoS ONE, Scientific Reports and Cardiovascular Research.

In The Last Decade

Marco Baccarin

25 papers receiving 471 citations

Peers

Countries citing papers authored by Marco Baccarin

Since Specialization

Citations

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

Fields of papers citing papers by Marco Baccarin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Baccarin

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Baccarin. A scholar is included among the top collaborators of Marco Baccarin 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 Baccarin. Marco Baccarin 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	Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorder 2023 ·Molecular Genetics & Genomic Medicine ·Francesca Cucinotta, Carla Lintas, (unknown), Marco Baccarin, (unknown), Paola Castronovo, Roberto Sacco, Ignazio S. Piras, (unknown), Arianna Ricciardello, María Luisa Scattoni, Antonio M. Persico	3
2	RNA sequencing of blood from sex- and age-matched discordant siblings supports immune and transcriptional dysregulation in autism spectrum disorder 2023 ·Scientific Reports ·(unknown), Ignazio S. Piras, Simona Baghai Sain, (unknown), Marco Baccarin, Paola Castronovo, Marco J. Morelli, Dejan Lazarević, María Luisa Scattoni, Giovanni Tonon, Antonio M. Persico	4
3	Huntingtin geneCAGrepeat size affects autism risk: Family‐based and case–control association study 2020 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Ignazio S. Piras, (unknown), (unknown), Marco Baccarin, Paola Castronovo, (unknown), Francesca Cucinotta, Arianna Ricciardello, (unknown), Lorenzo Nanetti, Caterina Mariotti, Cinzia Gellera, Carla Lintas, Roberto Sacco, Chiara Zuccato, Elena Cattaneo, Antonio M. Persico	7
4	Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review 2019 ·Clinical Genetics ·Paola Castronovo, Marco Baccarin, Arianna Ricciardello, (unknown), (unknown), Francesca Cucinotta, (unknown), Carla Lintas, Roberto Sacco, Antonio M. Persico	38
5	New Insights into Kleefstra Syndrome: Report of Two Novel Cases with Previously Unreported Features and Literature Review 2018 ·Cytogenetic and Genome Research ·Claudia Ciaccio, Giulietta Scuvera, Arianna Tucci, Barbara Gentilin, Marco Baccarin, Paola Marchisio, Sabrina Avignone, Donatella Milani	21
6	An Interstitial 17q11.2 de novo Deletion Involving the CDK5R1 Gene in a High-Functioning Autistic Patient 2018 ·Molecular Syndromology ·Carla Lintas, Roberto Sacco, Claudio Tabolacci, Claudia Brogna, (unknown), (unknown), (unknown), Paola Castronovo, Marco Baccarin, Antonio M. Persico	3
7	Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1 2017 ·Cytogenetic and Genome Research ·Rosamaria Silipigni, Edoardo Monfrini, Marco Baccarin, (unknown), Faustina Lalatta, Silvana Guerneri, Maria Francesca Bedeschi	2
8	Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4 2017 ·European Journal of Medical Genetics ·Maria Francesca Bedeschi, Giuseppe Marangi, Mariarosaria Calvello, (unknown), (unknown), Marco Baccarin, Silvana Guerneri, Daniela Orteschi, Marina Murdolo, Serena Lattante, (unknown), Beth Keena, Margaret Harr, Elaine H. Zackai, Marcella Zollino	19
9	Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases 2017 ·BMC Medical Genetics ·(unknown), Mariarosaria Calvello, Leda Paganini, Lidia Pezzani, Marco Baccarin, Laura Fontana, Silvia Maria Sirchia, Silvana Guerneri, (unknown), Ernesto Leva, Lorenzo Colombo, Faustina Lalatta, Fabio Mosca, Silvia Tabano, Monica Miozzo	3
10	Angiogenic and anti-inflammatory properties of mesenchymal stem cells from cord blood: soluble factors and extracellular vesicles for cell regeneration 2016 ·European Journal of Cell Biology ·Tiziana Montemurro, Mariele Viganò, Enrico Ragni, Mario Barilani, Valentina Parazzi, Valentina Boldrin, Cristiana Lavazza, Elisa Montelatici, Federica Banfi, Eleonora Lauri, S. Giovanelli, Marco Baccarin, Silvana Guerneri, Rosaria Giordano, Lorenza Lazzari	40
11	Insights into 6q21‐q22: Refinement of the critical region for acro‐cardio‐facial syndrome 2016 ·Congenital Anomalies ·Donatella Milani, Giulia Cagnoli, Marco Baccarin, Enrico Alfei, Silvana Guerneri, Susanna Esposito	6
12	7p22.1 microduplication syndrome: Refinement of the critical region 2016 ·European Journal of Medical Genetics ·Luisa Ronzoni, (unknown), Lidia Pezzani, Arianna Tucci, Marco Baccarin, Susanna Esposito, Donatella Milani	8
13	Impaired Angiogenic Potential of Human Placental Mesenchymal Stromal Cells in Intrauterine Growth Restriction 2016 ·Stem Cells Translational Medicine ·Chiara Mandò, P. Razini, Chiara Novielli, Gaia Maria Anelli, M. Belicchi, Silvia Erratico, (unknown), Mirella Meregalli, Alessandro Tavelli, Marco Baccarin, Alessandro Rolfo, S. Motta, Yvan Torrente, Irene Cetin	21
14	HOXA genes cluster: clinical implications of the smallest deletion 2015 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·Lidia Pezzani, Donatella Milani, Francesca Manzoni, Marco Baccarin, Rosamaria Silipigni, Silvana Guerneri, Susanna Esposito	8
15	Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical features 2015 ·European Journal of Medical Genetics ·Rosamaria Silipigni, Elisa Cattaneo, Marco Baccarin, Monica Fumagalli, Maria Francesca Bedeschi	2
16	Molecular cytogenetic characterization of a 2q35‐q37 duplication and a 4q35.1‐q35.2 deletion in two cousins: A genotype–phenotype analysis 2015 ·American Journal of Medical Genetics Part A ·Luisa Ronzoni, Angela Peron, Vera Bianchi, Marco Baccarin, Silvana Guerneri, Rosamaria Silipigni, Faustina Lalatta, Maria Francesca Bedeschi	4
17	Role of water in chromosome spreading and swelling induced by acetic acid treatment: a FTIR spectroscopy study 2014 ·European Journal of Histochemistry ·Diletta Ami, Matteo Di Segni, Matilde Forcella, Viviana Meraviglia, Marco Baccarin, Silvia Maria Doglia, G. L. Terzoli	9
18	Human chorionic villus mesenchymal stromal cells reveal strong endothelial conversion properties 2012 ·Differentiation ·Viviana Meraviglia, Matteo Vecellio, Annalisa Grasselli, Marco Baccarin, Antonella Farsetti, Maurizio C. Capogrossi, Giulio Pompilio, Domenico Coviello, Carlo Gaetano, (unknown), Alessandra Rossini	23
19	Evidence of Distinct Tumour-Propagating Cell Populations with Different Properties in Primary Human Hepatocellular Carcinoma 2011 ·PLoS ONE ·Federico Colombo, (unknown), (unknown), Inés Martín-Padura, Paola Marighetti, Alessandra Cattaneo, Barbara Foglieni, Marta Spreafico, Silvana Guerneri, Marco Baccarin, Francesco Bertolini, G. Rossi, Vincenzo Mazzaferro, Massimiliano Cadamuro, Marco Maggioni, Luca Agnelli, Paolo Rebulla, Daniele Prati, Laura Porretti	46
20	Human cardiac and bone marrow stromal cells exhibit distinctive properties related to their origin 2010 ·Cardiovascular Research ·Alessandra Rossini, Caterina Frati, Costanza Annamaria Lagrasta, Gallia Graiani, Alessandro Scopece, Stefano Cavalli, Ezio Musso, Marco Baccarin, (unknown), Francesco Fagnoni, Antonia Germani, Eugenio Quaini, Manuel Mayr, Qingbo Xu, Andrea Barbuti, Dario DiFrancesco, Giulio Pompilio, Federico Quaini, Carlo Gaetano, Maurizio C. Capogrossi	97

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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