Silvia Maitz

2.2k total citations
40 papers, 617 citations indexed

About

Silvia Maitz is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Silvia Maitz has authored 40 papers receiving a total of 617 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 21 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Silvia Maitz's work include Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (8 papers) and Prenatal Screening and Diagnostics (6 papers). Silvia Maitz is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (8 papers) and Prenatal Screening and Diagnostics (6 papers). Silvia Maitz collaborates with scholars based in Italy, United States and United Kingdom. Silvia Maitz's co-authors include Angelo Selicorni, Lidia Larizza, Anna Cereda, Monica Miozzo, Silvia Tabano, Faustina Lalatta, Donatella Milani, Patrizia Colapietro, Silvia Maria Sirchia and Barbara Gentilin and has published in prestigious journals such as Hepatology, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Silvia Maitz

38 papers receiving 612 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Silvia Maitz Italy 17 330 319 123 65 47 40 617
Jodi D. Hoffman United States 18 215 0.7× 365 1.1× 119 1.0× 52 0.8× 67 1.4× 33 654
Nicole L. Hoppman United States 14 279 0.8× 279 0.9× 115 0.9× 58 0.9× 31 0.7× 62 704
Anita Wischmeijer Italy 16 260 0.8× 333 1.0× 96 0.8× 71 1.1× 34 0.7× 29 622
Nicolas Richard France 16 446 1.4× 353 1.1× 74 0.6× 49 0.8× 39 0.8× 44 901
Sarah L. Withington Australia 9 399 1.2× 122 0.4× 90 0.7× 52 0.8× 64 1.4× 10 535
Kristen Deak United States 13 222 0.7× 194 0.6× 173 1.4× 70 1.1× 18 0.4× 24 531
Giuseppe Calabrese Italy 14 257 0.8× 173 0.5× 154 1.3× 31 0.5× 49 1.0× 45 711
Saghira Malik Sharif United Kingdom 10 343 1.0× 339 1.1× 79 0.6× 48 0.7× 43 0.9× 12 672
Periklis Makrythanasis Switzerland 18 402 1.2× 278 0.9× 59 0.5× 99 1.5× 54 1.1× 58 798
M. Mannens Netherlands 15 595 1.8× 314 1.0× 197 1.6× 40 0.6× 78 1.7× 30 836

Countries citing papers authored by Silvia Maitz

Since Specialization
Citations

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

Fields of papers citing papers by Silvia Maitz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvia Maitz

This figure shows the co-authorship network connecting the top 25 collaborators of Silvia Maitz. A scholar is included among the top collaborators of Silvia Maitz 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 Silvia Maitz. Silvia Maitz 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.
Maitz, Silvia, et al.. (2025). The gender-sensitive spectrum of neurodevelopmental disorders: a case report on a ZMYM3 variant in a 19-year-old female. Frontiers in Psychiatry. 16. 1604523–1604523.
2.
Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2023). Comparison of first‐tier whole‐exome sequencing with a multi‐step traditional approach for diagnosing paediatric outpatients: An Italian prospective study. Molecular Genetics & Genomic Medicine. 12(1). e2316–e2316. 4 indexed citations
3.
Pasquali, Daniela, Annalaura Torella, Anna Grandone, et al.. (2022). Patients with DeSanto–Shinawi syndrome: Further extension of phenotype from Italy. American Journal of Medical Genetics Part A. 191(3). 823–830. 1 indexed citations
4.
Maitz, Silvia, Mariasavina Severino, Gerarda Cappuccio, et al.. (2021). Epilepsy in KAT6A syndrome: Description of two individuals and revision of the literature. European Journal of Medical Genetics. 65(1). 104380–104380. 4 indexed citations
5.
Kerkhof, Jennifer, Gabriella Maria Squeo, Haley McConkey, et al.. (2021). DNA methylation episignature testing improves molecular diagnosis of Mendelian chromatinopathies. Genetics in Medicine. 24(1). 51–60. 22 indexed citations
6.
Li, Rachel, Scott A. Turner, Richard H. van Jaarsveld, et al.. (2020). HNRNPH1 ‐related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndrome. Clinical Genetics. 98(1). 91–98. 18 indexed citations
7.
Cristofoli, Francesca, Koenraad Devriendt, Heather Flanagan‐Steet, et al.. (2020). De Novo Variants in LMNB1 Cause Pronounced Syndromic Microcephaly and Disruption of Nuclear Envelope Integrity. The American Journal of Human Genetics. 107(4). 753–762. 24 indexed citations
8.
Fontana, Laura, Silvia Maitz, Silvia Tabano, et al.. (2020). Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients. Scientific Reports. 10(1). 8275–8275. 12 indexed citations
9.
Redaelli, Serena, Silvia Maitz, Francesca Crosti, et al.. (2019). Refining the Phenotype of Recurrent Rearrangements of Chromosome 16. International Journal of Molecular Sciences. 20(5). 1095–1095. 28 indexed citations
10.
Conconi, Donatella, Nicoletta Villa, Serena Redaelli, et al.. (2018). Familiar unbalanced complex rearrangements involving 13 p-arm: description of two cases. Molecular Cytogenetics. 11(1). 52–52. 1 indexed citations
11.
Mariani, Milena, Laura Rachele Bettini, Silvia Maitz, et al.. (2016). Adolescents and adults affected by Cornelia de Lange syndrome: A report of 73 Italian patients. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 172(2). 206–213. 18 indexed citations
12.
Villa, Nicoletta, Serena Redaelli, Donatella Conconi, et al.. (2016). 14q32.3-qter trisomic segment: a case report and literature review. Molecular Cytogenetics. 9(1). 60–60. 4 indexed citations
13.
Fazio, Grazia, Silvia Maitz, Marta Galbiati, et al.. (2016). Williams syndrome and mature B-Leukemia: A random association?. European Journal of Medical Genetics. 59(12). 634–640. 8 indexed citations
14.
Calvello, Mariarosaria, Silvia Tabano, Patrizia Colapietro, et al.. (2013). Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome. Epigenetics. 8(10). 1053–1060. 31 indexed citations
15.
Bedeschi, Maria Francesca, Vera Bianchi, Federica Natacci, et al.. (2011). Clinical follow‐up of young adults affected by Williams syndrome: Experience of 45 Italian patients. American Journal of Medical Genetics Part A. 155(2). 353–359. 22 indexed citations
16.
Ballarati, Lucia, Anna Cereda, Rossella Caselli, et al.. (2011). Deletion of the AP1S2 gene in a child with psychomotor delay and hypotonia. European Journal of Medical Genetics. 55(2). 124–127. 8 indexed citations
17.
Gervasini, Cristina, Francesca Romana Grati, Faustina Lalatta, et al.. (2010). SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome. Genetics in Medicine. 12(10). 634–640. 55 indexed citations
18.
Ballarati, Lucia, Anna Cereda, Rossella Caselli, et al.. (2010). Genotype–phenotype correlations in a new case of 8p23.1 deletion and review of the literature. European Journal of Medical Genetics. 54(1). 55–59. 38 indexed citations
19.
Milani, Donatella, Anna Cereda, Marta Cerutti, et al.. (2009). Clinical problems and everyday abilities of a group of Italian adolescent and young adults with Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 149A(11). 2532–2537. 6 indexed citations
20.
Maitz, Silvia, Barbara Gentilin, Tommaso Rizzuti, et al.. (2008). Expanding the phenotype of 22q13.3 deletion: report of a case detected prenatally. Prenatal Diagnosis. 28(10). 978–980. 6 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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