Francesca Mari

10.6k total citations
103 papers, 3.8k citations indexed

About

Francesca Mari is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Francesca Mari has authored 103 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Genetics, 61 papers in Molecular Biology and 19 papers in Cognitive Neuroscience. Recurrent topics in Francesca Mari's work include Genetics and Neurodevelopmental Disorders (41 papers), Genomic variations and chromosomal abnormalities (29 papers) and Autism Spectrum Disorder Research (19 papers). Francesca Mari is often cited by papers focused on Genetics and Neurodevelopmental Disorders (41 papers), Genomic variations and chromosomal abnormalities (29 papers) and Autism Spectrum Disorder Research (19 papers). Francesca Mari collaborates with scholars based in Italy, United States and Germany. Francesca Mari's co-authors include Alessandra Renieri, Francesca Ariani, Ilaria Longo, Ilaria Meloni, Maria Antonietta Mencarelli, Joussef Hayek, Chiara Pescucci, Michele Zappella, Mirella Bruttini and Rossella Caselli and has published in prestigious journals such as Science, PLoS ONE and Brain.

In The Last Decade

Francesca Mari

102 papers receiving 3.8k citations

Peers

Countries citing papers authored by Francesca Mari

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Mari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Mari

This figure shows the co-authorship network connecting the top 25 collaborators of Francesca Mari. A scholar is included among the top collaborators of Francesca Mari 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 Mari. Francesca Mari 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 Genetic Analysis and Clinical Therapy in Lung Cancer: Current Advances and Future Directions 2024 ·Cancers ·(unknown), (unknown), (unknown), (unknown), Maria Palmieri, (unknown), (unknown), Francesca Mari, Elisa Frullanti, Francesca Colombo	3
2	The Evidence Base for Circulating Tumor DNA-Methylation in Non-Small Cell Lung Cancer: A Systematic Review and Meta-Analysis 2024 ·Cancers ·(unknown), (unknown), (unknown), Athina Markou, Tomasz Powrózek, Vera Constâncio, Sandra P. Nunes, Cármen Jerónimo, Alfonso Calvo, Francesca Mari, Elisa Frullanti, (unknown), Maria Palmieri	4
3	An Example of Neuro-Glial Commitment and Differentiation of Muse Stem Cells Obtained from Patients with IQSEC2-Related Neural Disorder: A Possible New Cell-Based Disease Model 2023 ·Cells ·(unknown), Domenico Aprile, Ilaria Meloni, Nicola Alessio, Francesca Mari, (unknown), Caterina Lo Rizzo, Giovanni Di Bernardo, Gianfranco Peluso, Alessandra Renieri, Umberto Galderisi	4
4	Heterozygosity for neuronal ceroid lipofuscinosis predisposes to bipolar disorder 2022 ·Brazilian Journal of Psychiatry ·(unknown), (unknown), Floriana Valentino, Gabriella Doddato, Chiara Fallerini, (unknown), Romina D’Aurizio, Simone Furini, Arianna Goracci, Andrea Fagiolini, Francesca Mari, Alessandra Renieri, Francesca Ariani	1
5	The role of the Genetic Counsellor in the multidisciplinary team: the perception of geneticists in Europe 2022 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Alessandra Renieri, Francesca Mari, Michael A. Morris, Christophe Cordier	11
6	Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women 2021 ·Genes ·Maria Monticelli, Bruno Hay Mele, Elisa Benetti, Chiara Fallerini, Margherita Baldassarri, Simone Furini, Elisa Frullanti, Francesca Mari, Giuseppina Andreotti, Maria Vittoria Cubellis, Alessandra Renieri	40
7	Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory Distress 2016 ·International Journal of Molecular Sciences ·(unknown), Maria Antonietta Mencarelli, Chiara Fallerini, Laura Bianciardi, Francesca Ariani, Simone Furini, Alessandra Renieri, Francesca Mari, Elisa Frullanti	6
8	Evidence of digenic inheritance in Alport syndrome 2015 ·Journal of Medical Genetics ·Maria Antonietta Mencarelli, Laurence Heidet, Helen Storey, Michel van Geel, Bertrand Knebelmann, Chiara Fallerini, Nunzia Miglietti, (unknown), Francesco Cetta, John A. Sayer, Arthur van den Wijngaard, Shu Yau, Francesca Mari, Mirella Bruttini, Francesca Ariani, Karin Dahan, H.J.M. Smeets, Corinne Antignac, Frances Flinter, Alessandra Renieri	107
9	Redox Imbalance and Morphological Changes in Skin Fibroblasts in Typical Rett Syndrome 2014 ·Oxidative Medicine and Cellular Longevity ·Cinzia Signorini, Silvia Leoncini, Claudio De Felice, Alessandra Pecorelli, Ilaria Meloni, Francesca Ariani, Francesca Mari, Sonia Amabile, Eugenio Paccagnini, Mariangela Gentile, Giuseppe Belmonte, Gloria Zollo, Giuseppe Valacchi, Thierry Durand, Jean‐Marie Galano, Lucia Ciccoli, Alessandra Renieri, Joussef Hayek	46
10	Oligogenic germline mutations identified in early non-smokers lung adenocarcinoma patients 2014 ·Lung Cancer ·Alessandra Renieri, Maria Antonietta Mencarelli, Francesco Cetta, Margherita Baldassarri, Francesca Mari, Simone Furini, Pietro Piu, Francesca Ariani, Tommaso A. Dragani, Elisa Frullanti	26
11	Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin‐binding dynamics 2011 ·Clinical Genetics ·Roberta De Filippis, (unknown), Kathrine Bjørgo, (unknown), Tjitske Kleefstra, Elisabetta Grillo, (unknown), Francesco Cardarelli, Ilaria Meloni, Francesca Ariani, Maria Antonietta Mencarelli, Joussef Hayek, Alessandra Renieri, Mario Costa, Francesca Mari	19
12	Al‐Awadi–Raas‐Rothschild (limb/pelvis/uterus–hypoplasia/aplasia) syndrome and WNT7A mutations: Genetic homogeneity and nosological delineation 2010 ·American Journal of Medical Genetics Part A ·Livia Garavelli, Anita Wischmeijer, Simonetta Rosato, (unknown), (unknown), (unknown), Adriano Ferrari, Francesca Mari, Bernhard Zabel, Ekkehart Lausch, Sheila Unger, Andrea Superti‐Furga	15
13	Disruption of the IQSEC2 transcript in a female with X;autosome translocation t(X;20)(p11.2;q11.2) and a phenotype resembling X-linked infantile spasms (ISSX) syndrome 2008 ·Molecular Medicine Reports ·Francesca Mari, Brunella Franco, Alessandra Renieri, R. Marzella, Ivana Peluso, Daniela Iaconis, David Chitayat, Manuela Morleo	18
14	Delineation of the phenotype associated with 7q36.1q36.2 deletion: Long QT syndrome, renal hypoplasia and mental retardation 2008 ·American Journal of Medical Genetics Part A ·Rossella Caselli, Maria Antonietta Mencarelli, Filomena Tiziana Papa, Francesca Ariani, Ilaria Longo, Ilaria Meloni, (unknown), Maurizio Acampa, A. Auteri, Stefano Vicari, A Orsi, Joussef Hayek, Alessandra Renieri, Francesca Mari	19
15	Genomic differences between retinoma and retinoblastoma 2008 ·Acta Oncologica ·Katia Sampieri, Maria Antonietta Mencarelli, Maria Carmela Epistolato, Paolo Toti, Stefano Lazzi, Mirella Bruttini, Sonia De Francesco, Ilaria Longo, Ilaria Meloni, Francesca Mari, Antonio Acquaviva, Theodora Hadjistilianou, Alessandra Renieri, Francesca Ariani	36
16	2q24–q31 Deletion: Report of a case and review of the literature 2006 ·European Journal of Medical Genetics ·Chiara Pescucci, Rossella Caselli, Salvatore Grosso, Maria Antonietta Mencarelli, Francesca Mari, (unknown), Barbara Piccini, Rosangela Artuso, Mirella Bruttini, Manuela Priolo, Orsetta Zuffardi, Stefania Gimelli, Paolo Balestri, Alessandra Renieri	61
17	Germline mosaicism in Rett syndrome identified by prenatal diagnosis 2005 ·Clinical Genetics ·Francesca Mari, Rossella Caselli, Silvia Russo, Francesca Cogliati, Francesca Ariani, Ilaria Longo, Mirella Bruttini, Ilaria Meloni, Chiara Pescucci, (unknown), Paolo Toti, Maria Tassini, Lidia Larizza, Joussef Hayek, Michele Zappella, Alessandra Renieri	21
18	Dyskeratosis Congenita and Cancer in Mice Deficient in Ribosomal RNA Modification 2003 ·Science ·Davide Ruggero, Silvia Grisendi, Francesco Piazza, Eduardo Magalhães Rego, Francesca Mari, Pulivarthi H. Rao, Carlos Cordon‐Cardo, Pier Paolo Pandolfi	345
19	Type-IV collagen related diseases 2003 ·Journal of Nephrology ·Chiara Pescucci, Ilaria Longo, Mirella Bruttini, Francesca Mari, Alessandra Renieri	18
20	Rett syndrome: the complex nature of a monogenic disease 2003 ·Journal of Molecular Medicine ·Alessandra Renieri, Ilaria Meloni, Ilaria Longo, Francesca Ariani, Francesca Mari, Chiara Pescucci, Franca Cambi	64

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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