Matteo Della Monica

4.7k total citations
46 papers, 664 citations indexed

About

Matteo Della Monica is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Matteo Della Monica has authored 46 papers receiving a total of 664 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 16 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Matteo Della Monica's work include Genomic variations and chromosomal abnormalities (15 papers), Congenital limb and hand anomalies (6 papers) and Prenatal Screening and Diagnostics (5 papers). Matteo Della Monica is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Congenital limb and hand anomalies (6 papers) and Prenatal Screening and Diagnostics (5 papers). Matteo Della Monica collaborates with scholars based in Italy, United States and Canada. Matteo Della Monica's co-authors include Gioacchino Scarano, Fortunato Lonardo, Giovanni Neri, Nancy Govea, Fabio Acquaviva, Palma Finelli, Saul Surrey, Lodewijk A. Sandkuijl, Paolo Fortina and Lidia Larizza and has published in prestigious journals such as Ultrasound in Obstetrics and Gynecology, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Matteo Della Monica

44 papers receiving 621 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matteo Della Monica Italy 17 378 291 87 69 62 46 664
Gabriele Gillessen‐Kaesbach Germany 15 471 1.2× 337 1.2× 152 1.7× 43 0.6× 26 0.4× 23 753
Bruno Delobel France 19 481 1.3× 366 1.3× 91 1.0× 15 0.2× 47 0.8× 37 804
Ewa Obersztyn Poland 19 711 1.9× 692 2.4× 130 1.5× 17 0.2× 61 1.0× 78 1.2k
Judith P. Willner United States 14 527 1.4× 631 2.2× 191 2.2× 12 0.2× 55 0.9× 33 1.2k
Seher Başaran Türkiye 17 305 0.8× 278 1.0× 215 2.5× 20 0.3× 31 0.5× 73 814
Maria Francesca Bedeschi Italy 16 353 0.9× 264 0.9× 212 2.4× 55 0.8× 4 0.1× 64 811
Zöe Powis United States 15 562 1.5× 387 1.3× 115 1.3× 5 0.1× 47 0.8× 34 873
Maria Grigoriadou Greece 18 191 0.5× 329 1.1× 95 1.1× 6 0.1× 190 3.1× 48 723
Maria Teresa Bonati Italy 14 330 0.9× 327 1.1× 54 0.6× 24 0.3× 6 0.1× 44 756
Barbara Käsmann‐Kellner Germany 20 105 0.3× 417 1.4× 32 0.4× 7 0.1× 36 0.6× 100 1.3k

Countries citing papers authored by Matteo Della Monica

Since Specialization
Citations

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

Fields of papers citing papers by Matteo Della Monica

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matteo Della Monica

This figure shows the co-authorship network connecting the top 25 collaborators of Matteo Della Monica. A scholar is included among the top collaborators of Matteo Della Monica 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 Della Monica. Matteo Della Monica 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.
Terracciano, Antonio, Achille Iolascon, Matteo Della Monica, et al.. (2023). A New de novo Mosaic Mutation of PHEX Gene: A Case Report of a Boywith Hypophosphatemic Rickets. Endocrine Metabolic & Immune Disorders - Drug Targets. 23(9). 1235–1239. 2 indexed citations
2.
Siano, Maria, Ilaria Maggio, Roberta Petillo, et al.. (2022). De Novo Mutation in KMT2C Manifesting as Kleefstra Syndrome 2: Case Report and Literature Review. Pediatric Reports. 14(1). 131–139. 16 indexed citations
3.
Nistri, Stefano, Elena Sticchi, Gaia Spaziani, et al.. (2021). Differential Diagnosis between Marfan Syndrome and Loeys–Dietz Syndrome Type 4: A Novel Chromosomal Deletion Covering TGFB2. Genes. 12(10). 1462–1462. 3 indexed citations
4.
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
5.
Monica, Matteo Della, et al.. (2021). Roles and Interplay of SARS-CoV-2 Serology With Clinical Stages of Disease in COVID-19. Cureus. 13(6). e15953–e15953. 1 indexed citations
6.
Cellini, Elena, Annalisa Vetro, Valerio Conti, et al.. (2019). Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity. European Journal of Human Genetics. 27(6). 909–918. 21 indexed citations
7.
Monica, Matteo Della, Elena Andreucci, Giovanna Traficante, et al.. (2019). Michelangelo’s David: triumph of perfection or perfect combination of variation and disproportions? A human perspective.. UNICA IRIS Institutional Research Information System (University of Cagliari). 2019(2). 201–211.
8.
Ferrari, Daniela, Bárbara Torres, Marina Goldoni, et al.. (2018). Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7. Stem Cell Research. 32. 73–77. 2 indexed citations
9.
Torres, Bárbara, Daniela Ferrari, Antonella De Jaco, et al.. (2018). Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith–Magenis syndrome. Stem Cell Research. 28. 153–156. 1 indexed citations
10.
Lionetti, Paolo, et al.. (2018). An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 138–138. 7 indexed citations
11.
12.
Monica, Matteo Della, Domenico Galzerano, Fabio Acquaviva, et al.. (2013). Science, art, and mistery in the statues and in the anatomical machines of the prince of sansevero: The masterpieces of the “Sansevero Chapel”. American Journal of Medical Genetics Part A. 161(11). 2920–2929. 3 indexed citations
13.
Monica, Matteo Della, et al.. (2013). The Salernitan school of medicine: Women, men, and children. A syndromological review of the oldest medical school in the western world. American Journal of Medical Genetics Part A. 161(4). 809–816. 1 indexed citations
14.
Bachetti, Tiziana, et al.. (2013). Recurrence of CCHS associated PHOX2B poly‐alanine expansion mutation due to maternal mosaicism. Pediatric Pulmonology. 49(3). E45–7. 10 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.
Piane, Maria, Matteo Della Monica, Gianluca Piatelli, et al.. (2009). Majewski osteodysplastic primordial dwarfism type II (MOPD II) syndrome previously diagnosed as Seckel syndrome: Report of a novel mutation of the PCNT gene. American Journal of Medical Genetics Part A. 149A(11). 2452–2456. 29 indexed citations
17.
Rendina, Domenico, Gianpaolo De Filippo, Ernesto Soscia, et al.. (2008). Interleukin (IL)‐6 and receptor activator of nuclear factor (NF)‐κB ligand (RANKL) are increased in the serum of a patient with primary pachydermoperiostosis. Scandinavian Journal of Rheumatology. 37(3). 225–229. 16 indexed citations
18.
Lonardo, Fortunato, et al.. (2007). Al‐Awadi/Raas‐Rothschild syndrome: Two new cases and review. American Journal of Medical Genetics Part A. 143A(24). 3169–3174. 4 indexed citations
19.
Scarano, Gioacchino, Matteo Della Monica, Fortunato Lonardo, & Giovanni Neri. (1996). Novel findings in a patient with Weaver or a Weaver-like syndrome. American Journal of Medical Genetics. 63(2). 378–381. 5 indexed citations
20.
Scarano, Gioacchino, et al.. (1996). A case of short-rib syndrome without polydactyly in a stillborn: a new type?. PubMed. 30(1). 95–101. 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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