Daniela Orteschi

1.9k total citations
37 papers, 917 citations indexed

About

Daniela Orteschi is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Daniela Orteschi has authored 37 papers receiving a total of 917 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 21 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Daniela Orteschi's work include Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomics and Rare Diseases (9 papers). Daniela Orteschi is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomics and Rare Diseases (9 papers). Daniela Orteschi collaborates with scholars based in Italy, United States and Spain. Daniela Orteschi's co-authors include Marcella Zollino, Giovanni Neri, Giuseppe Marangi, Domenica Battaglia, Serena Lattante, Fiorella Gurrieri, Vincenzo Leuzzi, Marina Murdolo, Eugenio Mercuri and Vanna Pecile and has published in prestigious journals such as Nature Genetics, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Daniela Orteschi

36 papers receiving 866 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daniela Orteschi Italy	19	597	467	155	101	73	37	917
Chiara Pescucci Italy	19	745 1.2×	692 1.5×	224 1.4×	65 0.6×	40 0.5×	37	1.3k
Dorien Lugtenberg Netherlands	18	920 1.5×	1.0k 2.2×	209 1.3×	97 1.0×	70 1.0×	34	1.6k
Marisol del Rosario Netherlands	6	1.3k 2.2×	887 1.9×	138 0.9×	86 0.9×	127 1.7×	6	1.8k
Silvestre Oltra Spain	20	478 0.8×	626 1.3×	39 0.3×	109 1.1×	41 0.6×	69	1.1k
Alice Goldenberg France	20	565 0.9×	678 1.5×	50 0.3×	91 0.9×	124 1.7×	49	1.1k
Emilia K. Bijlsma Netherlands	16	696 1.2×	645 1.4×	170 1.1×	64 0.6×	101 1.4×	25	1.2k
Katherine Lachlan United Kingdom	19	659 1.1×	869 1.9×	122 0.8×	82 0.8×	58 0.8×	45	1.4k
Ewa Obersztyn Poland	19	711 1.2×	692 1.5×	86 0.6×	130 1.3×	49 0.7×	78	1.2k
Güney Bademci United States	19	331 0.6×	582 1.2×	91 0.6×	34 0.3×	91 1.2×	63	1.1k
Karen M. Lower Australia	15	400 0.7×	625 1.3×	37 0.2×	53 0.5×	91 1.2×	34	927

Countries citing papers authored by Daniela Orteschi

Since Specialization

Citations

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

Fields of papers citing papers by Daniela Orteschi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Orteschi

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

Marangi, Giuseppe, Daniela Orteschi, Domenica Battaglia, et al.. (2023). Linear Diagnostic Procedure Elicited by Clinical Genetics and Validated by mRNA Analysis in Neuronal Ceroid Lipofuscinosis 7 Associated with a Novel Non-Canonical Splice Site Variant in MFSD8. Genes. 14(2). 245–245. 3 indexed citations

Marangi, Giuseppe, Pietro Chiurazzi, Daniela Orteschi, et al.. (2023). Pathogenic variants in SOX11 mimicking Pitt‐Hopkins syndrome phenotype. Clinical Genetics. 105(1). 81–86. 2 indexed citations

Rossi, Salvatore, Daniela Orteschi, Paola Concolino, et al.. (2023). Triple Genetic Diagnosis in a Patient with Late-Onset Leukodystrophy and Mild Intellectual Disability. International Journal of Molecular Sciences. 25(1). 495–495. 1 indexed citations

Rossi, Ernesto, Monica Maria Pagliara, Daniela Orteschi, et al.. (2019). Pembrolizumab as first-line treatment for metastatic uveal melanoma. Cancer Immunology Immunotherapy. 68(7). 1179–1185. 63 indexed citations

Marangi, Giuseppe, Simone Garcovich, Gabriele Di Sante, et al.. (2019). Complex Muco-cutaneous Manifestations of CARMIL2-associated Combined Immunodeficiency: A Novel Presentation of Dysfunctional Epithelial Barriers. Acta Dermato Venereologica. 100(1). 1–2. 8 indexed citations

D’Ippolito, Silvia, Nicoletta Di Simone, Daniela Orteschi, et al.. (2017). The chromosome analysis of the miscarriage tissue. Miscarried embryo/fetal crown rump length (CRL) measurement: A practical use. PLoS ONE. 12(6). e0178113–e0178113. 3 indexed citations

Zollino, Marcella, Serena Lattante, Daniela Orteschi, et al.. (2017). Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples. Frontiers in Neuroscience. 11. 587–587. 19 indexed citations

Bedeschi, Maria Francesca, Giuseppe Marangi, Mariarosaria Calvello, et al.. (2017). Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4. European Journal of Medical Genetics. 60(11). 565–571. 19 indexed citations

Cafiero, Concetta, Giuseppe Marangi, Daniela Orteschi, et al.. (2015). Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome. European Journal of Human Genetics. 23(11). 1499–1504. 30 indexed citations

10.

Marangi, Giuseppe, et al.. (2013). Interstitial deletion of 3p22.3p22.2 encompassing ARPP21 and CLASP2 is a potential pathogenic factor for a syndromic form of intellectual disability: A co‐morbidity model with additional copy number variations in a large family. American Journal of Medical Genetics Part A. 161(11). 2890–2893. 20 indexed citations

11.

Mangiola, Annunziato, N. Saulnier, Pasquale De Bonis, et al.. (2013). Gene Expression Profile of Glioblastoma Peritumoral Tissue: An Ex Vivo Study. PLoS ONE. 8(3). e57145–e57145. 53 indexed citations

12.

Gurrieri, Fiorella, Marcella Zollino, Antonio Oliva, et al.. (2013). Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p. European Journal of Human Genetics. 21(9). 965–969. 32 indexed citations

13.

Boccuto, Luigi, Sara M. Sarasua, Cindy Skinner, et al.. (2012). Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. European Journal of Human Genetics. 21(3). 310–316. 176 indexed citations

14.

Marangi, Giuseppe, Vincenzo Leuzzi, Filippo Manti, et al.. (2012). TRAPPC9-related autosomal recessive intellectual disability: report of a new mutation and clinical phenotype. European Journal of Human Genetics. 21(2). 229–232. 54 indexed citations

15.

Marangi, Giuseppe, Daniela Orteschi, Federico Vigevano, et al.. (2012). Expanding the spectrum of rearrangements involving chromosome 19: A mild phenotype associated with a 19p13.12–p13.13 deletion. American Journal of Medical Genetics Part A. 158A(4). 888–893. 6 indexed citations

16.

Onesimo, Roberta, Daniela Orteschi, Maria Scalzone, et al.. (2012). Chromosome 9p deletion syndrome and sex reversal: Novel findings and redefinition of the critically deleted regions. American Journal of Medical Genetics Part A. 158A(9). 2266–2271. 37 indexed citations

17.

Savarese, Marco, Giulio Piluso, Daniela Orteschi, et al.. (2012). Enhancer Chip: Detecting Human Copy Number Variations in Regulatory Elements. PLoS ONE. 7(12). e52264–e52264. 4 indexed citations

18.

Zollino, Marcella, Daniela Orteschi, Giuseppe Marangi, et al.. (2009). A case of Beckwith–Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus. Journal of Medical Genetics. 47(6). 429–432. 39 indexed citations

19.

Veredice, Chiara, Flaviana Bianco, Ilaria Contaldo, et al.. (2009). Early onset myoclonic epilepsy and 15q26 microdeletion: Observation of the first case. Epilepsia. 50(7). 1810–1815. 26 indexed citations

20.

Marangi, Giuseppe, Vincenzo Leuzzi, Daniela Orteschi, et al.. (2008). Duplication of the Rubinstein–Taybi region on 16p13.3 is associated with a distinctive phenotype. American Journal of Medical Genetics Part A. 146A(18). 2313–2317. 26 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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