Francesca Novara

5.5k total citations · 1 hit paper
56 papers, 2.3k citations indexed

About

Francesca Novara is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Francesca Novara has authored 56 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 20 papers in Molecular Biology and 15 papers in Genetics. Recurrent topics in Francesca Novara's work include Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Mesenchymal stem cell research (8 papers). Francesca Novara is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Mesenchymal stem cell research (8 papers). Francesca Novara collaborates with scholars based in Italy, United States and United Kingdom. Francesca Novara's co-authors include Orsetta Zuffardi, Rita Maccario, Angela Cometa, Maria Antonietta Avanzini, Antonia Moretta, Maria Ester Bernardo, Franco Locatelli, Raffaella Villa, Nadia Zaffaroni and Maria Grazia Daidone and has published in prestigious journals such as Nature Communications, Blood and Neurology.

In The Last Decade

Francesca Novara

55 papers receiving 2.2k 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.

Human Bone Marrow–Derived Mesenchymal Stem Cells Do Not Undergo Transformation after Long-termIn vitroCulture and Do Not Exhibit Telomere Maintenance Mechanisms

2007 539 citations Maria Ester Bernardo, Nadia Zaffaroni et al. profile →

Peers

Countries citing papers authored by Francesca Novara

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Novara

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Novara

This figure shows the co-authorship network connecting the top 25 collaborators of Francesca Novara. A scholar is included among the top collaborators of Francesca Novara 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 Francesca Novara. Francesca Novara 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	Missense variants in the Arg206 residue of HNRNPH2: Further evidence of causality and expansion of the phenotype 2020 ·American Journal of Medical Genetics Part A ·Angela Peron, Francesca Novara, Francesca La Briola, (unknown), (unknown), (unknown), (unknown), Aglaia Vignoli, Roberto Ciccone, Maria Paola Canevini	11
2	The Search for Molecular Markers in a Gene-Orphan Case Study of a Pediatric Spinal Cord Pilocytic Astrocytoma 2020 ·Cancer Genomics & Proteomics ·(unknown), (unknown), Federico Manai, Roberto Ciccone, Francesca Novara, Elisabetta Sauta, Riccardo Bellazzi, Monica Patanè, Isabella Moroni, Rosina Paterra, Sergio Comincini	7
3	Developmental trends of communicative skills in children with chromosome 14 aberrations 2017 ·European Journal of Pediatrics ·Laura Zampini, (unknown), Berardo Rinaldi, Francesca Novara, Orsetta Zuffardi	3
4	Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature 2016 ·Molecular Cytogenetics ·Edoardo Errichiello, Francesca Novara, (unknown), Annapia Verri, Jessica Galli, Elisa Fazzi, Daniela Bellotti, (unknown), Mariangela Cisternino, Orsetta Zuffardi	18
5	MECP2 duplication phenotype in symptomatic females: report of three further cases 2014 ·Molecular Cytogenetics ·Francesca Novara, Alessandro Simonati, Federico Sicca, Roberta Battini, Simona Fiori, Annarita Contaldo, (unknown), Orsetta Zuffardi, Roberto Ciccone	19
6	Wolfram syndrome 2: a novel CISD2 mutation identified in Italian siblings 2014 ·Acta Diabetologica ·Maurizio Rondinelli, Francesca Novara, Valeria Calcaterra, Orsetta Zuffardi, Stefano Genovese	31
7	In vitro biosafety profile evaluation of multipotent mesenchymal stem cells derived from the bone marrow of sarcoma patients 2014 ·Journal of Translational Medicine ·Enrico Lucarelli, Chiara Bellotti, Melissa Mantelli, Maria Antonietta Avanzini, Rita Maccario, Francesca Novara, Giulia Arrigo, Orsetta Zuffardi, Monia Zuntini, (unknown), Luca Sangiorgi, Daniela Lisini, Davide María Donati, Serena Duchi	11
8	5p13 microduplication syndrome: A new case and better clinical definition of the syndrome 2012 ·European Journal of Medical Genetics ·Francesca Novara, Enrico Alfei, Stefano D’Arrigo, Chiara Pantaleoni, Silvana Beri, (unknown), Francesca L. Sciacca, Roberto Giorda, Orsetta Zuffardi, Roberto Ciccone	24
9	22q11.2 Microduplication syndrome and epilepsy with continuous spikes and waves during sleep (CSWS). A case report and review of the literature 2012 ·Epilepsy & Behavior ·Giulia Valvo, Francesca Novara, Paola Brovedani, Anna Rita Ferrari, Renzo Guerrini, Orsetta Zuffardi, Federico Sicca	11
10	A wide methodological approach to identify a large duplication in CFTR gene in a CF patient uncharacterised by sequencing analysis 2011 ·Journal of Cystic Fibrosis ·Lucy Costantino, (unknown), Laura Claut, Carla Colombo, Francesca Novara, Valentina Paracchini, Luigi Porcaro, (unknown), Orsetta Zuffardi, Manuela Seia	5
11	The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia 2011 ·Pediatric Blood & Cancer ·Paola De Filippi, Marco Zecca, Francesca Novara, Daniela Lisini, Emanuela Maserati, Francesco Pasquali, Vittorio Rosti, Carmelo Carlo‐Stella, (unknown), (unknown), Orsetta Zuffardi, Daria Pagliara, Cesare Danesino, Franco Locatelli	2
12	CD5− diffuse large B-cell lymphoma with peculiar cyclin D1+ phenotype. Pathologic and molecular characterization of a single case 2011 ·Human Pathology ·Marco Lucioni, Francesca Novara, Roberta Riboni, Giacomo Fiandrino, Marta Di Nicola, S. Kindl, Emanuela Boveri, V. Jemos, Luca Arcaini, Orsetta Zuffardi, Marco Paulli	11
13	Cell‐cycle phases and genetic profile of bone marrow‐derived mesenchymal stromal cells expanded in vitro from healthy donors 2011 ·Journal of Cellular Biochemistry ·(unknown), Melissa Mantelli, Giulia Arrigo, Francesca Novara, Maria Antonietta Avanzini, Maria Ester Bernardo, Orsetta Zuffardi, Giovanni Barosi, Marco Zecca, Rita Maccario	18
14	Refining the phenotype associated with MEF2C haploinsufficiency 2010 ·European Journal of Human Genetics ·Hilde Van Esch, Francesca Novara, Silvana Beri, Roberto Giorda, (unknown), Francesca Darra, Bernardo Dalla Bernardina, Orsetta Zuffardi	4
15	Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor 2010 ·The American Journal of Human Genetics ·Daniele Ghezzi, Irina F. Sevrioukova, Federica Invernizzi, Costanza Lamperti, Marina Mora, Pio D’Adamo, Francesca Novara, Orsetta Zuffardi, Graziella Uziel, Massimo Zeviani	171
16	Refining the phenotype associated with MEF2C haploinsufficiency 2010 ·Clinical Genetics ·Francesca Novara, Silvana Beri, Roberto Giorda, Els Ortibus, (unknown), Francesca Darra, Bernardo Dalla Bernardina, Orsetta Zuffardi, Hilde Van Esch	65
17	Generation of mesenchymal stromal cells in the presence of platelet lysate: a phenotypic and functional comparison of umbilical cord blood- and bone marrow-derived progenitors 2009 ·Haematologica ·Maria Antonietta Avanzini, Maria Ester Bernardo, Angela Cometa, Cesare Perotti, Nadia Zaffaroni, Francesca Novara, Livia Visai, Antonia Moretta, Claudia Del Fante, Raffaella Villa, L.M. Ball, W.E. Fibbe, Rita Maccario, Franco Locatelli	99
18	High-resolution genome-wide array comparative genomic hybridization in splenic marginal zone B-cell lymphoma 2009 ·Human Pathology ·Francesca Novara, Luca Arcaini, Michele Merli, Francesco Passamonti, Silvia Zibellini, Silvia Rizzi, Sara Rattotti, Elisa Rumi, Cristiana Pascutto, Annalisa Vetro, Cesare Astori, Emanuela Boveri, Marco Lucioni, Marco Paulli, Orsetta Zuffardi, Mario Lazzarino	12
19	Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion 2008 ·European Journal of Human Genetics ·Claudia Torniero, Bernardo Dalla Bernardina, Francesca Novara, R. Cerini, María Clara Bonaglia, Tiziano Pramparo, Roberto Ciccone, Renzo Guerrini, Orsetta Zuffardi	50
20	Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams–Beuren locus 2006 ·European Journal of Human Genetics ·Claudia Torniero, Bernardo Dalla Bernardina, Francesca Novara, Annalisa Vetro, Ivana Ricca, Francesca Darra, Tiziano Pramparo, Renzo Guerrini, Orsetta Zuffardi	34

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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