Matteo Cassina

6.2k total citations
60 papers, 1.4k citations indexed

About

Matteo Cassina is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Matteo Cassina has authored 60 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Genetics and 12 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Matteo Cassina's work include Pregnancy and Medication Impact (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Neurofibromatosis and Schwannoma Cases (7 papers). Matteo Cassina is often cited by papers focused on Pregnancy and Medication Impact (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Neurofibromatosis and Schwannoma Cases (7 papers). Matteo Cassina collaborates with scholars based in Italy, United States and France. Matteo Cassina's co-authors include Maurizio Clementi, Elena Di Gianantonio, Leonardo Salviati, Eva Trevisson, Mara Doimo, María Andrea Desbats, Cristina Cerqua, Pietro Litta, Pierpaolo Mastroiacovo and Lorenzo D. Botto and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Matteo Cassina

56 papers receiving 1.3k citations

Peers

Matteo Cassina
Daniel L. Keene Canada
Anja Harder Germany
Miklós Koppán Hungary
Nils Conradi Sweden
István Takács Hungary
Andreea Nissenkorn Israel
Karol Estrada United States
Maria Chang United States
Thomas Opladen Germany
Sonir Roberto Rauber Antonini Brazil
Daniel L. Keene Canada
Matteo Cassina
Citations per year, relative to Matteo Cassina Matteo Cassina (= 1×) peers Daniel L. Keene

Countries citing papers authored by Matteo Cassina

Since Specialization
Citations

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

Fields of papers citing papers by Matteo Cassina

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matteo Cassina

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

All Works

20 of 20 papers shown
1.
2.
Desbats, María Andrea, et al.. (2024). Characterization of Two Novel PNKP Splice‐Site Variants in a Proband With Microcephaly, Intellectual Disability, and Multiple Malformations. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 198(2). e33013–e33013.
3.
Rigon, Chiara, et al.. (2023). Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature. Genes. 14(3). 748–748. 9 indexed citations
4.
5.
Anglani, Franca, et al.. (2021). Genotype–phenotype correlation in Gordon’s syndrome: report of two cases carrying novel heterozygous mutations. Journal of Nephrology. 35(3). 859–862. 5 indexed citations
6.
Cassina, Matteo, Luisa Frizziero, Enrico Opocher, et al.. (2019). Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment Recommendations. Cancers. 11(11). 1790–1790. 32 indexed citations
7.
Cassina, Matteo, et al.. (2017). Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive cases. European Journal of Obstetrics & Gynecology and Reproductive Biology. 221. 23–27. 12 indexed citations
8.
Cassina, Matteo, Cristina Cerqua, Leonardo Salviati, et al.. (2016). A synonymous splicing mutation in the SF3B4 gene segregates in a family with highly variable Nager syndrome. European Journal of Human Genetics. 25(3). 371–375. 18 indexed citations
9.
Desbats, María Andrea, Valeria Morbidoni, Micol Silic‐Benussi, et al.. (2016). TheCOQ2genotype predicts the severity of coenzyme Q10deficiency. Human Molecular Genetics. 25(19). 4256–4265. 45 indexed citations
10.
Cao, Michelangelo, Maria Lucia Valentino, Claudio Semplicini, et al.. (2015). Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations. Neurogenetics. 17(1). 65–70. 21 indexed citations
11.
Collantoni, Enrico, Elena Tenconi, Daniela Degortes, et al.. (2015). Functional connectivity correlates of response inhibition impairment in anorexia nervosa. Psychiatry Research Neuroimaging. 247. 9–16. 40 indexed citations
12.
Cassina, Matteo, et al.. (2014). First-trimester exposure to metformin and risk of birth defects: a systematic review and meta-analysis. Human Reproduction Update. 20(5). 656–669. 107 indexed citations
13.
Doimo, Mara, María Andrea Desbats, Cristina Cerqua, et al.. (2014). Genetics of Coenzyme Q10 Deficiency. Molecular Syndromology. 5(3-4). 156–162. 94 indexed citations
14.
Cassina, Matteo, Elena Di Gianantonio, Elena Cesari, et al.. (2013). Pregnancy outcome in women exposed to antiepileptic drugs: Teratogenic role of maternal epilepsy and its pharmacologic treatment. Reproductive Toxicology. 39. 50–57. 20 indexed citations
15.
Salviati, Leonardo, Eva Trevisson, María Hernández, et al.. (2012). Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency. Journal of Medical Genetics. 49(3). 187–191. 85 indexed citations
16.
Cassina, Matteo, Diana L. Johnson, Luther K. Robinson, et al.. (2012). Pregnancy outcome in women exposed to leflunomide before or during pregnancy. Arthritis & Rheumatism. 64(7). 2085–2094. 81 indexed citations
17.
Pizzi, Marco, Matteo Fassan, Kathrin Ludwig, et al.. (2012). Congenital Pulmonary Airway Malformation (CPAM) [Congenital Cystic Adenomatoid Malformation] Associated with Tracheoesophageal Fistula and Agensesis of the Corpus Callosum. Fetal and Pediatric Pathology. 31(3). 169–175. 3 indexed citations
18.
Cassina, Matteo, et al.. (2012). Pharmacologic treatment of hyperthyroidism during pregnancy. Birth Defects Research Part A Clinical and Molecular Teratology. 94(8). 612–619. 14 indexed citations
19.
Vecchi, Marilena, Matteo Cassina, Alberto Casarin, et al.. (2011). Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A. Seizure. 20(10). 813–816. 18 indexed citations
20.
Cassina, Matteo, Marco De Santis, Elena Cesari, et al.. (2010). First trimester diclofenac exposure and pregnancy outcome. Reproductive Toxicology. 30(3). 401–404. 20 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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