Simone Pizzi

2.0k total citations
31 papers, 313 citations indexed

About

Simone Pizzi is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Simone Pizzi has authored 31 papers receiving a total of 313 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 15 papers in Genetics and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Simone Pizzi's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Simone Pizzi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Simone Pizzi collaborates with scholars based in Italy, Canada and Netherlands. Simone Pizzi's co-authors include Marco Tartaglia, Sabina Barresi, Andrea Ciolfi, Alessandro Bruselles, Bruno Dallapiccola, Marcello Niceta, Maria Lisa Dentici, M. Cristina Digilio, Emilia Stellacci and Enrico Bertini and has published in prestigious journals such as International Journal of Cancer, Cellular and Molecular Life Sciences and Movement Disorders.

In The Last Decade

Simone Pizzi

31 papers receiving 305 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Simone Pizzi Italy	11	185	123	53	45	28	31	313
Tahir Naeem Khan Pakistan	11	118 0.6×	59 0.5×	40 0.8×	47 1.0×	30 1.1×	32	308
Robea Ballo South Africa	7	137 0.7×	79 0.6×	45 0.8×	39 0.9×	21 0.8×	19	281
Kemal O. Yariz United States	8	212 1.1×	90 0.7×	20 0.4×	78 1.7×	12 0.4×	9	346
Aziza Sbiti Morocco	9	211 1.1×	133 1.1×	34 0.6×	69 1.5×	7 0.3×	19	387
Rosamaria Silipigni Italy	10	144 0.8×	79 0.6×	16 0.3×	50 1.1×	9 0.3×	35	264
Florence Renaldo France	11	205 1.1×	47 0.4×	36 0.7×	13 0.3×	23 0.8×	19	339
Rachel Gillespie United Kingdom	10	341 1.8×	159 1.3×	12 0.2×	30 0.7×	22 0.8×	13	468
Christin Collins United States	8	210 1.1×	164 1.3×	24 0.5×	56 1.2×	8 0.3×	13	425
Sergio A. Cuevas‐Covarrubias Mexico	11	280 1.5×	167 1.4×	18 0.3×	15 0.3×	10 0.4×	41	418
Kristin McDonald Gibson United States	8	272 1.5×	118 1.0×	63 1.2×	36 0.8×	8 0.3×	9	424

Countries citing papers authored by Simone Pizzi

Since Specialization

Citations

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

Fields of papers citing papers by Simone Pizzi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simone Pizzi

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

Galosi, Serena, Cecilia Mancini, Paolo Calligari, et al.. (2024). Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome. Movement Disorders. 39(7). 1225–1231. 2 indexed citations

Niceta, Marcello, Simone Pizzi, Francesca Clementina Radio, et al.. (2023). Case report: Novel compound heterozygosity for pathogenic variants in MED23 in a syndromic patient with postnatal microcephaly. Frontiers in Neurology. 14. 1090082–1090082. 1 indexed citations

Pollazzon, Marzia, Cecilia Mancini, Simone Pizzi, et al.. (2023). Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures. Frontiers in Neurology. 14. 1207176–1207176. 3 indexed citations

Zuntini, Roberta, Lucia Pedace, Evelina Miele, et al.. (2023). Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation. Frontiers in Genetics. 14. 1231434–1231434. 1 indexed citations

Fragale, Alessandra, Emilia Stellacci, Giulia Romagnoli, et al.. (2023). Reversing vemurafenib‐resistance in primary melanoma cells by combined romidepsin and type I IFN treatment through blocking of tumorigenic signals and induction of immunogenic effects. International Journal of Cancer. 153(5). 1080–1095. 4 indexed citations

Tognon, Costanza, et al.. (2022). Lung Ultrasound to Assess One Lung Ventilation: A Pediatric Case Series. Journal of Laparoendoscopic & Advanced Surgical Techniques. 32(5). 566–570. 3 indexed citations

Zanni, Ginevra, Matthias Eckenweiler, Markus Storbeck, et al.. (2022). CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia. Cellular and Molecular Life Sciences. 79(10). 526–526. 9 indexed citations

Giannubilo, Stefano Raffaele, et al.. (2022). Maternal hemodynamics and computerized cardiotocography during labor with epidural analgesia. Archives of Gynecology and Obstetrics. 307(6). 1789–1794. 4 indexed citations

Castiglia, Daniele, Paola Fortugno, Angelo Giuseppe Condorelli, et al.. (2021). A Novel Phenotype of Junctional Epidermolysis Bullosa with Transient Skin Fragility and Predominant Ocular Involvement Responsive to Human Amniotic Membrane Eyedrops. Genes. 12(5). 716–716. 7 indexed citations

10.

Flex, Elisabetta, Giovanna Carpentieri, Alessandro Bruselles, et al.. (2021). A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3. Genes. 12(9). 1406–1406. 3 indexed citations

11.

Caraffi, Stefano Giuseppe, Francesca Clementina Radio, Sabina Barresi, et al.. (2021). Adducted Thumb and Peripheral Polyneuropathy: Diagnostic Supports in Suspecting White–Sutton Syndrome: Case Report and Review of the Literature. Genes. 12(7). 950–950. 3 indexed citations

12.

Ciolfi, Andrea, Erfan Aref‐Eshghi, Simone Pizzi, et al.. (2020). Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature. Clinical Epigenetics. 12(1). 7–7. 28 indexed citations

13.

D’Amico, Adele, Fabiana Fattori, Francesco Nicita, et al.. (2020). A Recurrent Pathogenic Variant of INPP5K Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern Italy. Frontiers in Genetics. 11. 565868–565868. 6 indexed citations

14.

Stellacci, Emilia, Gian Marco Moneta, Alessandro Bruselles, et al.. (2019). The activating p.Ser466Arg change in STAT1 causes a peculiar phenotype with features of interferonopathies. Clinical Genetics. 96(6). 585–589. 10 indexed citations

15.

Barresi, Sabina, Maria Lisa Dentici, Francesca Manzoni, et al.. (2019). Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations. Pediatric Neurology. 104. 40–45. 20 indexed citations

16.

Niceta, Marcello, Sabina Barresi, Francesca Pantaleoni, et al.. (2018). TARP syndrome: Long-term survival, anatomic patterns of congenital heart defects, differential diagnosis and pathogenetic considerations. European Journal of Medical Genetics. 62(6). 103534–103534. 16 indexed citations

17.

Manti, Filippo, Francesca Nardecchia, Sabina Barresi, et al.. (2018). Neurotransmitter trafficking defect in a patient with clathrin (CLTC) variation presenting with intellectual disability and early-onset parkinsonism. Parkinsonism & Related Disorders. 61. 207–210. 14 indexed citations

18.

Stellacci, Emilia, Roberta Onesimo, Alessandro Bruselles, et al.. (2016). Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A. American Journal of Medical Genetics Part A. 170(9). 2389–2393. 23 indexed citations

19.

Giorgio, Elisa, Alessandro Brussino, Elisa Biamino, et al.. (2016). Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes. European Journal of Paediatric Neurology. 21(3). 475–484. 11 indexed citations

20.

Torino, Giovanni, et al.. (2010). Epidural analgesia during labor and incidence of cesarian section: prospective study. The Journal of Maternal-Fetal & Neonatal Medicine. 24(2). 250–252. 5 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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