Antonio Pizzuti

17.9k total citations · 2 hit papers
217 papers, 10.0k citations indexed

About

Antonio Pizzuti is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Antonio Pizzuti has authored 217 papers receiving a total of 10.0k indexed citations (citations by other indexed papers that have themselves been cited), including 111 papers in Molecular Biology, 60 papers in Genetics and 36 papers in Cellular and Molecular Neuroscience. Recurrent topics in Antonio Pizzuti's work include Genetics and Neurodevelopmental Disorders (23 papers), Genetic Neurodegenerative Diseases (17 papers) and Congenital heart defects research (17 papers). Antonio Pizzuti is often cited by papers focused on Genetics and Neurodevelopmental Disorders (23 papers), Genetic Neurodegenerative Diseases (17 papers) and Congenital heart defects research (17 papers). Antonio Pizzuti collaborates with scholars based in Italy, United States and United Kingdom. Antonio Pizzuti's co-authors include C. Thomas Caskey, Raymond G. Fenwick, Bruno Dallapiccola, David L. Nelson, Francesca Megiorni, Ying‐Hui Fu, Stephen Richards, Ying‐Hui Fu, Maura Pieretti and Ben A. Oostra and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Antonio Pizzuti

212 papers receiving 9.8k 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.

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1991 1.6k citations Antonio Pizzuti et al. profile →
An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy

1992 1.2k citations Antonio Pizzuti et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Antonio Pizzuti Italy	44	6.5k	3.3k	2.5k	1.2k	935	217	10.0k
Vania Broccoli Italy	55	8.1k 1.2×	2.9k 0.9×	2.7k 1.1×	655 0.6×	292 0.3×	143	11.2k
Naomichi Matsumoto Japan	52	6.6k 1.0×	5.0k 1.5×	1.4k 0.6×	561 0.5×	622 0.7×	589	11.5k
André Reis Germany	60	7.7k 1.2×	4.4k 1.3×	1.4k 0.5×	462 0.4×	1.6k 1.7×	320	13.6k
C. Geoffrey Woods United Kingdom	48	6.8k 1.0×	3.4k 1.0×	1.6k 0.6×	898 0.8×	271 0.3×	97	11.0k
Brian K. Kaspar United States	54	7.3k 1.1×	3.3k 1.0×	2.6k 1.0×	2.9k 2.5×	395 0.4×	122	12.4k
Samuel J. Pleasure United States	52	4.7k 0.7×	1.4k 0.4×	3.7k 1.5×	617 0.5×	526 0.6×	131	9.0k
Hiroaki Mizukami Japan	44	3.2k 0.5×	2.2k 0.7×	1.2k 0.5×	448 0.4×	486 0.5×	196	6.4k
Alan H. Beggs United States	67	11.2k 1.7×	3.3k 1.0×	2.3k 0.9×	372 0.3×	465 0.5×	274	16.5k
Wendy H. Raskind United States	50	3.2k 0.5×	1.6k 0.5×	1.1k 0.5×	532 0.5×	526 0.6×	144	8.4k
Nigel Whittle Austria	34	4.2k 0.6×	854 0.3×	1.1k 0.4×	635 0.5×	898 1.0×	51	8.3k

Countries citing papers authored by Antonio Pizzuti

Since Specialization

Citations

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

Fields of papers citing papers by Antonio Pizzuti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonio Pizzuti

This figure shows the co-authorship network connecting the top 25 collaborators of Antonio Pizzuti. A scholar is included among the top collaborators of Antonio Pizzuti 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 Antonio Pizzuti. Antonio Pizzuti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Fabiani, Marco, Antonio Pizzuti, Aldo Germani, et al.. (2024). Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review. Preprints.org. 3 indexed citations

Fabiani, Marco, Giacomo Tini, Beatrice Musumeci, et al.. (2024). Reanalysis of Next-generation Sequencing Data in Patients With Hypertrophic Cardiomyopathy: Contribution of Spliceogenic MYBPC3 Variants in an Italian Cohort. Annals of Laboratory Medicine. 45(1). 96–100.

Fabiani, Marco, Antonio Pizzuti, Aldo Germani, et al.. (2024). Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review. International Journal of Molecular Sciences. 25(18). 9787–9787. 1 indexed citations

Germani, Aldo, et al.. (2023). Heterozygous Pathogenic Nonsense Variant in the ATM Gene in a Family with Unusually High Gastric Cancer Susceptibility. Biomedicines. 11(7). 2062–2062. 3 indexed citations

Fabiani, Marco, Erika Pagannone, Beatrice Musumeci, et al.. (2023). A Novel Nonsense Pathogenic TTN Variant Identified in a Patient with Severe Dilated Cardiomyopathy. Current Issues in Molecular Biology. 45(3). 2422–2430. 2 indexed citations

Piane, Maria, Aldo Germani, Marco Fabiani, et al.. (2022). A New SMAD4 Splice Site Variant in a Three-Generation Italian Family with Juvenile Polyposis Syndrome. Diagnostics. 12(11). 2684–2684. 4 indexed citations

Nebbioso, Marcella, et al.. (2021). X-linked dominant RPGR gene mutation in a familial Coats angiomatosis. BMC Ophthalmology. 21(1). 37–37. 2 indexed citations

Salehi, Leila, et al.. (2020). An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene. SHILAP Revista de lepidopterología. 8(8). 1445–1451. 2 indexed citations

Germani, Aldo, Simona Petrucci, Laura De Marchis, et al.. (2020). Beyond BRCA1 and BRCA2: Deleterious Variants in DNA Repair Pathway Genes in Italian Families with Breast/Ovarian and Pancreatic Cancers. Journal of Clinical Medicine. 9(9). 3003–3003. 7 indexed citations

10.

D’Ambrosio, Valentina, Flaminia Vena, Daniele Di Mascio, et al.. (2020). Obstetrical and perinatal outcomes in fetuses with early versus late sonographic diagnosis of short femur length: A single-center, prospective, cohort study. European Journal of Obstetrics & Gynecology and Reproductive Biology. 254. 170–174. 3 indexed citations

11.

Fanella, Martina, Marianna Frascarelli, Alessandra Morano, et al.. (2019). Myoclonic epilepsy, parkinsonism, schizophrenia and left-handedness as common neuropsychiatric features in 22q11.2 deletion syndrome. Journal of Medical Genetics. 57(3). 151–159. 9 indexed citations

12.

Nicita, Francesco, Fabrizia Stregapede, Alessandra Tessa, et al.. (2019). Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants. Journal of Neurology. 266(11). 2657–2664. 13 indexed citations

13.

Falasca, Francesca, Cinzia Dello Russo, Barbara Mora, et al.. (2016). Comparative Analysis of Real-Time Polymerase Chain Reaction Methods to Typing HLA-B*57:01 in HIV-1-Positive Patients. AIDS Research and Human Retroviruses. 32(7). 654–657. 7 indexed citations

14.

Colombrita, Claudia, Elisa Onesto, Francesca Megiorni, et al.. (2012). TDP-43 and FUS RNA-binding Proteins Bind Distinct Sets of Cytoplasmic Messenger RNAs and Differently Regulate Their Post-transcriptional Fate in Motoneuron-like Cells. Journal of Biological Chemistry. 287(19). 15635–15647. 227 indexed citations

15.

Luigetti, Marco, Antonio Pizzuti, Stefano Bartoletti, et al.. (2010). Triple A syndrome: A novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency. Journal of the Neurological Sciences. 290(1-2). 150–152. 11 indexed citations

16.

Giovannetti, Antonello, Marina Pierdominici, Francesca Mazzetta, et al.. (2007). Unravelling the Complexity of T Cell Abnormalities in Common Variable Immunodeficiency. The Journal of Immunology. 178(6). 3932–3943. 205 indexed citations

17.

Bottillo, Irene, Alessandro De Luca, Annalisa Schirinzi, et al.. (2007). Functional analysis of splicing mutations in exon 7 of NF1gene. BMC Medical Genetics. 8(1). 4–4. 27 indexed citations

18.

Bertolino, Alessandro, Giuseppe Blasi, Valeria Latorre, et al.. (2006). Additive Effects of Genetic Variation in Dopamine Regulating Genes on Working Memory Cortical Activity in Human Brain. Journal of Neuroscience. 26(15). 3918–3922. 172 indexed citations

19.

Sárközy, Anna, Emanuela Conti, M. Cristina Digilio, et al.. (2005). ZFPM2/FOG2 andHEY2 genes analysis in nonsyndromic tricuspid atresia. American Journal of Medical Genetics Part A. 133A(1). 68–70. 11 indexed citations

20.

Pizzuti, Antonio, Giuseppe Novelli, & Bruno Dallapiccola. (1996). Molecular genetics of myotonic dystrophy. 6(3). 1 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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