Pamela Magini

2.8k total citations
38 papers, 717 citations indexed

About

Pamela Magini is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Pamela Magini has authored 38 papers receiving a total of 717 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 18 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Pamela Magini's work include Genomic variations and chromosomal abnormalities (17 papers), Genomics and Rare Diseases (10 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Pamela Magini is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Genomics and Rare Diseases (10 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Pamela Magini collaborates with scholars based in Italy, United Kingdom and Russia. Pamela Magini's co-authors include Marco Seri, Tommaso Pippucci, G. Cara Romeo, Claudio Graziano, Matteo Benelli, Alberto Magi, Lorenzo Tattini, Gianluca De Bellis, Betti Giusti and Ingrid Cifola and has published in prestigious journals such as Blood, International Journal of Molecular Sciences and Genome Research.

In The Last Decade

Pamela Magini

37 papers receiving 697 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pamela Magini Italy 16 349 347 119 58 53 38 717
Thomas Schwarzbraun Austria 14 252 0.7× 517 1.5× 125 1.1× 36 0.6× 38 0.7× 26 852
Greg B. Peters Australia 14 385 1.1× 382 1.1× 84 0.7× 32 0.6× 101 1.9× 22 785
Bryn D. Webb United States 13 212 0.6× 588 1.7× 60 0.5× 58 1.0× 25 0.5× 35 896
Nisha Patel Saudi Arabia 17 267 0.8× 428 1.2× 60 0.5× 22 0.4× 37 0.7× 39 727
Shehla Mohammed United Kingdom 12 248 0.7× 497 1.4× 92 0.8× 18 0.3× 54 1.0× 25 680
Elisa Tassano Italy 15 272 0.8× 310 0.9× 58 0.5× 16 0.3× 46 0.9× 54 596
Sumita Danda India 16 269 0.8× 489 1.4× 45 0.4× 49 0.8× 38 0.7× 122 1.0k
Dominique Martin‐Coignard France 14 424 1.2× 522 1.5× 41 0.3× 36 0.6× 78 1.5× 22 817
Chiharu Torii Japan 16 243 0.7× 313 0.9× 43 0.4× 54 0.9× 106 2.0× 42 721
Jiong Yan United States 15 487 1.4× 650 1.9× 56 0.5× 42 0.7× 35 0.7× 27 1.0k

Countries citing papers authored by Pamela Magini

Since Specialization
Citations

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

Fields of papers citing papers by Pamela Magini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pamela Magini

This figure shows the co-authorship network connecting the top 25 collaborators of Pamela Magini. A scholar is included among the top collaborators of Pamela Magini 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 Pamela Magini. Pamela Magini 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.
Turchetti, Daniela, et al.. (2024). Long read sequencing on its way to the routine diagnostics of genetic diseases. Frontiers in Genetics. 15. 1374860–1374860. 17 indexed citations
2.
Monti, Luigi, et al.. (2024). Familial DMRT1-related non-obstructive azoospermia: a case report. Journal of Assisted Reproduction and Genetics. 41(11). 3173–3177.
3.
Dahan, Idit, Sarah Vergult, Marta Vidal‐García, et al.. (2022). HDAC9structural variants disruptingTWIST1transcriptional regulation lead to craniofacial and limb malformations. Genome Research. 32(7). 1242–1253. 11 indexed citations
4.
Magini, Pamela, Roberto Semeraro, Davide Bolognini, et al.. (2022). Third-Generation Cytogenetic Analysis. Journal of Molecular Diagnostics. 24(7). 711–718. 4 indexed citations
5.
Marconi, Caterina, Alessandro Pecci, Flavia Palombo, et al.. (2022). Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup. Haematologica. 108(7). 1909–1919. 1 indexed citations
6.
Bertulli, Cristina, Antonio Marzollo, Margherita Doria, et al.. (2020). Expanding Phenotype of Schimke Immuno-Osseous Dysplasia: Congenital Anomalies of the Kidneys and of the Urinary Tract and Alteration of NK Cells. International Journal of Molecular Sciences. 21(22). 8604–8604. 33 indexed citations
7.
Magini, Pamela, Emanuela Scarano, Alberto Sensi, et al.. (2019). Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disorders. Gene. 706. 162–171. 8 indexed citations
8.
Magini, Pamela, Monica Poscente, Simona Ferrari, et al.. (2015). Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration. Molecular Cytogenetics. 8(1). 58–58. 15 indexed citations
9.
Bartoletti‐Stella, Anna, Laura Gasparini, Caterina Giacomini, et al.. (2015). Messenger RNA processing is altered in autosomal dominant leukodystrophy. Human Molecular Genetics. 24(10). 2746–2756. 25 indexed citations
10.
Stanghellini, Ilaria, et al.. (2014). Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 40(1). 39–39. 12 indexed citations
11.
Bisulli, Francesca, Ilaria Naldi, Sara Baldassari, et al.. (2014). Autosomal dominant partial epilepsy with auditory features: A new locus on chromosome 19q13.11–q13.31. Epilepsia. 55(6). 841–848. 6 indexed citations
12.
Magini, Pamela, Francesca Bisulli, Sara Baldassari, et al.. (2014). LGI1 microdeletions are not a frequent cause of partial epilepsy with auditory features (PEAF). Epilepsy Research. 108(5). 972–977. 4 indexed citations
13.
Magi, Alberto, Lorenzo Tattini, Ingrid Cifola, et al.. (2013). EXCAVATOR: detecting copy number variants from whole-exome sequencing data. Genome biology. 14(10). R120–R120. 159 indexed citations
14.
Pittalis, Maria Carla, Michela Malacarne, Antonio Farina, et al.. (2013). Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangements. American Journal of Medical Genetics Part A. 161(10). 2559–2563. 2 indexed citations
15.
Magini, Pamela, Matteo Della Monica, Maria Luisa Giovannucci Uzielli, et al.. (2012). Two novel patients with Bohring–Opitz syndrome caused by de novo ASXL1 mutations. American Journal of Medical Genetics Part A. 158A(4). 917–921. 32 indexed citations
16.
Pippucci, Tommaso, Matteo Benelli, Alberto Magi, et al.. (2011). EX-HOM (EXome HOMozygosity): A Proof of Principle. Human Heredity. 72(1). 45–53. 23 indexed citations
17.
Zuntini, Roberta, Pamela Magini, Claudio Ceccarelli, et al.. (2011). Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion. Journal of Medical Genetics. 48(11). 779–782. 13 indexed citations
18.
Guerra, Flora, Ivana Kurelac, Pamela Magini, et al.. (2011). Mitochondrial DNA genotyping reveals synchronous nature of simultaneously detected endometrial and ovarian cancers. Gynecologic Oncology. 122(2). 457–458. 9 indexed citations
19.
Wischmeijer, Anita, Pamela Magini, Roberto Giorda, et al.. (2010). Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype. Molecular Syndromology. 1(4). 176–184. 23 indexed citations
20.
Graziano, Claudio, Simona Carone, Emanuele Panza, et al.. (2009). Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation. Blood. 114(8). 1655–1657. 16 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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