Daniela Toniolo

30.6k total citations · 3 hit papers
139 papers, 8.6k citations indexed

About

Daniela Toniolo is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Daniela Toniolo has authored 139 papers receiving a total of 8.6k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Molecular Biology, 47 papers in Genetics and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Daniela Toniolo's work include Genetics and Neurodevelopmental Disorders (24 papers), RNA Research and Splicing (24 papers) and Nuclear Structure and Function (23 papers). Daniela Toniolo is often cited by papers focused on Genetics and Neurodevelopmental Disorders (24 papers), RNA Research and Splicing (24 papers) and Nuclear Structure and Function (23 papers). Daniela Toniolo collaborates with scholars based in Italy, United States and France. Daniela Toniolo's co-authors include Silvia Bione, Elena Maestrini, Patrizia D’Adamo, Luciano Merlini, Ági K. Gedeon, Stefano Rivella, Cinzia Sala, Pieter A. Bolhuis, Mita Mancini and Gisèle Bonne and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Daniela Toniolo

137 papers receiving 8.4k 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.

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

1999 1.0k citations Gisèle Bonne, Marina Raffaele di Barletta et al. Nature Genetics profile →
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

1994 686 citations Silvia Bione, Elena Maestrini et al. Nature Genetics profile →
A novel X-linked gene, G4.5. is responsible for Barth syndrome

1996 565 citations Silvia Bione, Patrizia D’Adamo et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Daniela Toniolo Italy	47	5.6k	2.4k	844	828	772	139	8.6k
P. Pearson Netherlands	55	6.3k 1.1×	4.7k 1.9×	527 0.6×	412 0.5×	843 1.1×	209	10.7k
Niklas Dahl Sweden	50	5.9k 1.1×	2.9k 1.2×	360 0.4×	1.3k 1.6×	469 0.6×	245	9.8k
Jeanne Amiel France	60	6.5k 1.1×	3.2k 1.3×	202 0.2×	882 1.1×	1.1k 1.5×	324	14.2k
André Reis Germany	60	7.7k 1.4×	4.4k 1.8×	470 0.6×	1.8k 2.1×	451 0.6×	320	13.6k
Orsetta Zuffardi Italy	56	6.8k 1.2×	7.3k 3.0×	463 0.5×	513 0.6×	1.1k 1.4×	324	12.2k
Lisbeth Tranebjærg Denmark	43	3.6k 0.6×	2.3k 1.0×	407 0.5×	612 0.7×	349 0.5×	163	6.7k
G.A.P. Bruns United States	50	6.0k 1.1×	1.9k 0.8×	453 0.5×	761 0.9×	554 0.7×	108	9.7k
Robert S. Sparkes United States	47	4.0k 0.7×	2.7k 1.1×	208 0.2×	517 0.6×	901 1.2×	205	9.8k
Marco Tartaglia Italy	49	8.5k 1.5×	1.8k 0.8×	486 0.6×	535 0.6×	647 0.8×	322	10.8k
James F. Reynolds United States	48	4.7k 0.8×	3.3k 1.4×	263 0.3×	630 0.8×	622 0.8×	294	9.1k

Countries citing papers authored by Daniela Toniolo

Since Specialization

Citations

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

Fields of papers citing papers by Daniela Toniolo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Toniolo

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Toniolo. A scholar is included among the top collaborators of Daniela Toniolo 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 Daniela Toniolo. Daniela Toniolo 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

Cocca, Massimiliano, Caterina Barbieri, Maria Pina Concas, et al.. (2019). A bird’s-eye view of Italian genomic variation through whole-genome sequencing. European Journal of Human Genetics. 28(4). 435–444. 25 indexed citations

Concas, Maria Pina, Eulalia Catamo, Ginevra Biino, et al.. (2019). Factors associated with food liking and their relationship with metabolic traits in Italian cohorts. Food Quality and Preference. 75. 64–70. 13 indexed citations

Pirastu, Nicola, Maarten Kooyman, Michela Traglia, et al.. (2016). A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings. Reviews in Endocrine and Metabolic Disorders. 17(2). 209–219. 17 indexed citations

Milani, Giuseppe, Corrado Masciullo, Cinzia Sala, et al.. (2011). Computer-based genealogy reconstruction in founder populations. Journal of Biomedical Informatics. 44(6). 997–1003. 2 indexed citations

Traglia, Michela, Domenico Girelli, Ginevra Biino, et al.. (2011). Association of HFE and TMPRSS6 genetic variants with iron and erythrocyte parameters is only in part dependent on serum hepcidin concentrations. Journal of Medical Genetics. 48(9). 629–634. 79 indexed citations

Corre, Tanguy, J. Schuettler, Silvia Bione, et al.. (2009). A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. Human Reproduction. 24(8). 2023–2028. 28 indexed citations

Bianchi, Veronica, Mattia Pelizzola, Manuel Mayhaus, et al.. (2009). Temporal gene expression profile of the hippocampus following trace fear conditioning. Brain Research. 1308. 14–23. 12 indexed citations

Bianchi, Veronica, Pasqualina Farisello, Pietro Baldelli, et al.. (2008). Cognitive impairment in Gdi1-deficient mice is associated with altered synaptic vesicle pools and short-term synaptic plasticity, and can be corrected by appropriate learning training. Human Molecular Genetics. 18(1). 105–117. 41 indexed citations

Rossi, Elena, Anna Verri, Maria Grazia Patricelli, et al.. (2008). A 12 Mb deletion at 7q33–q35 associated with autism spectrum disorders and primary amenorrhea. European Journal of Medical Genetics. 51(6). 631–638. 59 indexed citations

10.

Toniolo, Daniela & Flavio Rizzolio. (2007). X Chromosome and Ovarian Failure. Seminars in Reproductive Medicine. 25(4). 264–271. 41 indexed citations

11.

Bodega, Beatrice, Silvia Bione, Leda Dalprà, et al.. (2005). Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation. Human Reproduction. 21(4). 952–957. 143 indexed citations

12.

Vytopil, Michal, Sara Benedetti, Enzo Ricci, et al.. (2003). Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes. Journal of Medical Genetics. 40(12). e132–e132. 87 indexed citations

13.

Bonne, Gisèle, Marina Raffaele di Barletta, Shaïda Varnous, et al.. (1999). Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nature Genetics. 21(3). 285–288. 1032 indexed citations breakdown →

14.

Ørstavik, Karen Helene, Ragnhild Ørstavik, Anna K. Naumova, et al.. (1998). X Chromosome Inactivation in Carriers of Barth Syndrome. The American Journal of Human Genetics. 63(5). 1457–1463. 58 indexed citations

15.

Squarzoni, Stefano, Patrizia Sabatelli, Andrea Ognibene, et al.. (1998). Immunocytochemical detection of emerin within the nuclear matrix. Neuromuscular Disorders. 8(5). 338–344. 41 indexed citations

16.

Mancini, Mita, Cinzia Sala, Stefano Rivella, & Daniela Toniolo. (1996). Selection and Fine Mapping of Chromosome-Specific cDNAs: Application to Human Chromosome 1. Genomics. 38(2). 149–154. 2 indexed citations

17.

Gariboldi, Manuela, Elena Maestrini, Federico Canzian, et al.. (1994). Comparative Mapping of the Actin-Binding Protein 280 Genes in Human and Mouse. Genomics. 21(2). 428–430. 16 indexed citations

18.

Maestrini, Elena, Mita Mancini, Stefano Rivella, et al.. (1993). Mapping of two genes encoding isoforms of the actin binding protein ABP-280, a dystrophin like protein, to Xq28 and to chromosome 7. Human Molecular Genetics. 2(6). 761–766. 64 indexed citations

19.

Heitz, Dominique, François Rousseau, Didier Devys, et al.. (1991). Isolation of Sequences that Span the Fragile X and Identification of a Fragile X-Related CpG Island. Science. 251(4998). 1236–1239. 153 indexed citations

20.

Toniolo, Daniela, G. Martini, Barbara R. Migeon, & Rosanna Dono. (1988). Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA.. The EMBO Journal. 7(2). 401–406. 108 indexed citations

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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