Annalisa Botta

3.3k total citations
98 papers, 2.4k citations indexed

About

Annalisa Botta is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Annalisa Botta has authored 98 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 51 papers in Cellular and Molecular Neuroscience and 13 papers in Genetics. Recurrent topics in Annalisa Botta's work include Genetic Neurodegenerative Diseases (50 papers), Mitochondrial Function and Pathology (26 papers) and Muscle Physiology and Disorders (20 papers). Annalisa Botta is often cited by papers focused on Genetic Neurodegenerative Diseases (50 papers), Mitochondrial Function and Pathology (26 papers) and Muscle Physiology and Disorders (20 papers). Annalisa Botta collaborates with scholars based in Italy, United States and France. Annalisa Botta's co-authors include Giuseppe Novelli, Antonio Baldini, Elizabeth A. Lindsay, Vesna Jurecic, Allan Bradley, Howard M. Rosenblatt, Yin-Chai Cheah, Fabrizio Rinaldi, Bruno Dallapiccola and Lodovica Vergani and has published in prestigious journals such as Nature, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Annalisa Botta

98 papers receiving 2.3k citations

Peers

Countries citing papers authored by Annalisa Botta

Since Specialization

Citations

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

Fields of papers citing papers by Annalisa Botta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annalisa Botta

This figure shows the co-authorship network connecting the top 25 collaborators of Annalisa Botta. A scholar is included among the top collaborators of Annalisa Botta 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 Annalisa Botta. Annalisa Botta 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	Methylation of the Vitamin D Receptor Gene in Human Disorders 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), Eleonora Piccirilli, Umberto Tarantino, Annalisa Botta, (unknown)	4
2	Plasma heavy metal levels correlate with deregulated gene expression of detoxifying enzymes in osteoporotic patients 2023 ·Scientific Reports ·(unknown), (unknown), Chiara Greggi, (unknown), Antonio Messina, (unknown), (unknown), Riccardo Iundusi, Annalisa Botta, Leonardo Palombi, Umberto Tarantino	10
3	In Cis Effect of DMPK Expanded Alleles in Myotonic Dystrophy Type 1 Patients Carrying Variant Repeats at 5′ and 3′ Ends of the CTG Array 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), Maria Rosaria D’Apice, Federica Centofanti, Roberto Massa, Giuseppe Novelli, Annalisa Botta	1
4	Role of the Vitamin D Receptor (VDR) in the Pathogenesis of Osteoporosis: A Genetic, Epigenetic and Molecular Pilot Study 2023 ·Genes ·(unknown), (unknown), Cinzia Ciccacci, (unknown), Elena Gasbarra, Riccardo Iundusi, Maria Luisa Brandi, Annalisa Botta, Umberto Tarantino	13
5	Two Different Therapeutic Approaches for SARS-CoV-2 in hiPSCs-Derived Lung Organoids 2022 ·Cells ·Paola Spitalieri, Federica Centofanti, Michela Murdocca, Maria Giovanna Scioli, Andrea Latini, Silvia Di Cesare, Gennaro Citro, Antonio Rossi, Augusto Orlandi, Shane Miersch, Sachdev S. Sidhu, Pier Paolo Pandolfi, Annalisa Botta, Federica Sangiuolo, Giuseppe Novelli	24
6	Characterization of full-length CNBP expanded alleles in myotonic dystrophy type 2 patients by Cas9-mediated enrichment and nanopore sequencing 2022 ·eLife ·Massimiliano Alfano, (unknown), Federica Centofanti, (unknown), Simone Maestri, C. Degli Esposti, Roberto Massa, Maria Rosaria D’Apice, Giuseppe Novelli, Massimo Delledonne, Annalisa Botta, Marzia Rossato	12
7	DNA Methylation Signatures of Bone Metabolism in Osteoporosis and Osteoarthritis Aging-Related Diseases: An Updated Review 2021 ·International Journal of Molecular Sciences ·(unknown), Ida Cariati, Simona Fittipaldi, Riccardo Iundusi, Elena Gasbarra, Umberto Tarantino, Annalisa Botta	39
8	Epigenetics of Myotonic Dystrophies: A Minireview 2021 ·International Journal of Molecular Sciences ·(unknown), Federica Centofanti, Simona Fittipaldi, (unknown), Giuseppe Novelli, Annalisa Botta	10
9	Carrier frequency of CFTR variants in the non‐Caucasian populations by genome aggregation database (gnomAD)‐based analysis 2020 ·Annals of Human Genetics ·(unknown), L. Mannucci, Giuseppe Novelli, Federica Sangiuolo, Maria Rosaria D’Apice, Annalisa Botta	8
10	Circulating Long Non-Coding RNA GAS5 Is Overexpressed in Serum from Osteoporotic Patients and Is Associated with Increased Risk of Bone Fragility 2020 ·International Journal of Molecular Sciences ·(unknown), Simona Fittipaldi, Simone Ciuffi, Francesca Marini, Giancarlo Isaia, Patrizia D’Amelio, Silvia Migliaccio, Claudio Marcocci, Salvatore Minisola, Ranuccio Nuti, Giuseppe Novelli, Maria Luisa Brandi, Annalisa Botta, Umberto Tarantino	13
11	Genetic Variability in Noncoding RNAs: Involvement of miRNAs and Long Noncoding RNAs in Osteoporosis Pathogenesis 2020 ·Epigenomics ·Simona Fittipaldi, (unknown), Umberto Tarantino, Giuseppe Novelli, Annalisa Botta	6
12	TNNT2 Missplicing in Skeletal Muscle as a Cardiac Biomarker in Myotonic Dystrophy Type 1 but Not in Myotonic Dystrophy Type 2 2019 ·Frontiers in Neurology ·Francesca Bosè, Laura Valentina Renna, Barbara Fossati, Giovanni Arpa, Valentina Labate, Valentina Milani, Annalisa Botta, Emanuele Micaglio, G. Meola, Rosanna Cardani	11
13	SCN4A as modifier gene in patients with myotonic dystrophy type 2 2018 ·Scientific Reports ·Anna Binda, Laura Valentina Renna, Francesca Bosè, (unknown), Annalisa Botta, Rea Valaperta, Barbara Fossati, Ilaria Rivolta, G. Meola, Rosanna Cardani	14
14	An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy 2016 ·Neuroepidemiology ·Nicola Vanacore, Emanuele Rastelli, Giovanni Antonini, Maria Laura Ester Bianchi, Annalisa Botta, Elisabetta Bucci, Carlo Casali, (unknown), Manlio Giacanelli, (unknown), Anna Modoni, Giuseppe Novelli, E. Pennisi, Antonio Petrucci, (unknown), Gabriella Silvestri, Chiara Terracciano, Roberto Massa	32
15	Generation of Human Induced Pluripotent Stem Cells from Extraembryonic Tissues of Fetuses Affected by Monogenic Diseases 2015 ·Cellular Reprogramming ·Paola Spitalieri, (unknown), Annalisa Botta, Michela Murdocca, Maria Rosaria D’Apice, Augusto Orlandi, Emiliano Giardina, Massimo Santoro, Francesco Brancati, Giuseppe Novelli, Federica Sangiuolo	18
16	Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1) 2015 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Massimo Santoro, (unknown), Marcella Masciullo, Maria Laura Ester Bianchi, Salvatore Rossi, Emanuele Leoncini, Giuseppe Novelli, Annalisa Botta, Gabriella Silvestri	25
17	Prenatal Diagnosis of Cockayne Syndrome Type A Based on the Identification of Two Novel Mutations in the ERCC8 Gene 2009 ·Genetic Testing and Molecular Biomarkers ·Chiara Conte, Maria Rosaria D’Apice, Annalisa Botta, Federica Sangiuolo, Giuseppe Novelli	9
18	Risk Prediction for Clinical Phenotype in Myotonic Dystrophy Type 1: Data from 2,650 Patients 2007 ·Genetic Testing ·Leila Salehi, E. Bonifazi, Enrico Di Stasio, Massimo Gennarelli, Annalisa Botta, (unknown), (unknown), Roberto Massa, Giovanni Antonini, C. Angelini, Giuseppe Novelli	46
19	Localization of Azospirillum brasilense Cd in inoculated tomato (Lycopersicon esculentum Mill.) roots 2004 ·Annals of Microbiology ·M. Grilli Caiola, Antonella Canini, Annalisa Botta, Maddalena Del Gallo	9
20	Cloning and molecular characterization of three Ubiquitin Fusion Degradation 1 (Ufd1) ortholog genes from <i>Xenopus laevis, Gallus gallus</i> and<i>Drosophila melanogaster</i> 2001 ·Cytogenetic and Genome Research ·Antonia Ratti, Francesca Amati, Maura Bozzali, Eugenia Conti, Federica Sangiuolo, Maria Berloco, G. Palumbo, Annalisa Botta, Antonio Pizzuti, Giuseppe Novelli, Bruno Dallapiccola	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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