Daniela Rogaia

4.0k total citations · 1 hit paper
26 papers, 3.0k citations indexed

About

Daniela Rogaia is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Daniela Rogaia has authored 26 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Genetics and 5 papers in Surgery. Recurrent topics in Daniela Rogaia's work include Genomic variations and chromosomal abnormalities (6 papers), Retinoids in leukemia and cellular processes (6 papers) and Acute Myeloid Leukemia Research (3 papers). Daniela Rogaia is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Retinoids in leukemia and cellular processes (6 papers) and Acute Myeloid Leukemia Research (3 papers). Daniela Rogaia collaborates with scholars based in Italy, United States and Canada. Daniela Rogaia's co-authors include Francesco Frassoni, Maria Paola Martelli, Andrea Velardi, Franco Aversa, Antonellá Tosti, Elena Urbani, Warren D. Shlomchik, Loredana Ruggeri, Marusca Capanni and Katia Perruccio and has published in prestigious journals such as Science, The EMBO Journal and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Daniela Rogaia

26 papers receiving 3.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Effectiveness of Donor Natural Killer Cell Alloreactivity in Mismatched Hematopoietic Transplants

2002 2.6k citations Daniela Rogaia et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daniela Rogaia Italy	14	2.3k	1.5k	989	481	299	26	3.0k
Paul W. Wu United States	14	1.2k 0.5×	382 0.3×	447 0.5×	594 1.2×	267 0.9×	19	2.2k
Krzysztof Giannopoulos Poland	25	1.4k 0.6×	623 0.4×	935 0.9×	735 1.5×	97 0.3×	143	2.4k
Kyoko Masuda Japan	20	1.1k 0.5×	277 0.2×	617 0.6×	855 1.8×	152 0.5×	47	1.9k
Elwin Rombouts Netherlands	14	912 0.4×	773 0.5×	438 0.4×	520 1.1×	89 0.3×	17	1.8k
Agnieszka Czechowicz United States	16	661 0.3×	579 0.4×	480 0.5×	543 1.1×	243 0.8×	48	1.5k
Daniel Pietryga United States	14	518 0.2×	759 0.5×	305 0.3×	817 1.7×	178 0.6×	22	2.1k
Dengli Hong China	17	457 0.2×	516 0.3×	303 0.3×	684 1.4×	71 0.2×	30	1.5k
Francesca Ficara Italy	16	422 0.2×	316 0.2×	633 0.6×	1.2k 2.5×	786 2.6×	43	1.9k
Patricia Hermand France	25	408 0.2×	740 0.5×	208 0.2×	313 0.7×	155 0.5×	37	1.5k
Marina Scheller Germany	15	531 0.2×	555 0.4×	256 0.3×	1.2k 2.5×	122 0.4×	26	1.8k

Countries citing papers authored by Daniela Rogaia

Since Specialization

Citations

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

Fields of papers citing papers by Daniela Rogaia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Rogaia

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

Rooney, Kathleen, Michael A. Levy, Sadegheh Haghshenas, et al.. (2021). Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome. International Journal of Molecular Sciences. 22(16). 8611–8611. 13 indexed citations

Lonardo, Fortunato, M. Cristina Digilio, Daniela Rogaia, et al.. (2021). Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. American Journal of Medical Genetics Part A. 185(4). 1204–1210. 5 indexed citations

Flex, Elisabetta, Giovanna Carpentieri, Alessandro Bruselles, et al.. (2021). A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3. Genes. 12(9). 1406–1406. 3 indexed citations

Bedetti, Chiara, Amedea Mencarelli, Daniela Rogaia, et al.. (2020). A patient with novel MBOAT7 variant: The cerebellar atrophy is progressive and displays a peculiar neurometabolic profile. American Journal of Medical Genetics Part A. 182(10). 2377–2383. 9 indexed citations

Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2019). Schilbach–Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene. European Journal of Human Genetics. 27(8). 1260–1266. 1 indexed citations

Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2017). Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature. International Journal of Molecular Sciences. 18(9). 1998–1998. 8 indexed citations

Sparaneo, Angelo, Laura Penta, Amedea Mencarelli, et al.. (2017). Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism. The Journal of Clinical Endocrinology & Metabolism. 102(11). 3961–3969. 20 indexed citations

Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2016). A novel MED12 mutation: Evidence for a fourth phenotype. American Journal of Medical Genetics Part A. 170(9). 2377–2382. 23 indexed citations

Prontera, Paolo, Valerio Napolioni, Daniela Rogaia, et al.. (2014). DPP6 gene disruption in a family with Gilles de la Tourette syndrome. Neurogenetics. 15(4). 237–242. 22 indexed citations

10.

Prontera, Paolo, et al.. (2014). Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly. American Journal of Medical Genetics Part A. 164(12). 3137–3141. 27 indexed citations

11.

Prontera, Paolo, et al.. (2013). Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression?. Molecular Syndromology. 4(4). 197–202. 8 indexed citations

12.

Prontera, Paolo, Daniela Rogaia, Cristina Sobacchi, et al.. (2011). Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21‐22.1 locus. American Journal of Medical Genetics Part A. 155(5). 1106–1108. 6 indexed citations

13.

Prontera, Paolo, et al.. (2011). Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. American Journal of Medical Genetics Part A. 155(4). 928–930. 20 indexed citations

14.

Prontera, Paolo, Laura Bernardini, Gabriela Stangoni, et al.. (2011). Deletion 2p15–16.1 syndrome: Case report and review. American Journal of Medical Genetics Part A. 155(10). 2473–2478. 26 indexed citations

15.

Prontera, Paolo, Barbara Ferrando, Virginia Giuliani, et al.. (2008). A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implications.. PubMed. 19(4). 413–8. 1 indexed citations

16.

Grignani, F, Vania Gelmetti, Mirco Fanelli, et al.. (1999). Formation of PML/RARα high molecular weight nuclear complexes through the PML coiled-coil region is essential for the PML/RARα-mediated retinoic acid response. Oncogene. 18(46). 6313–6321. 37 indexed citations

17.

Testa, Ugo, F Grignani, H. J. Hassan, et al.. (1998). Terminal megakaryocytic differentiation of TF-1 cells is induced by phorbol esters and thrombopoietin and is blocked by expression of PML/RARα fusion protein. Leukemia. 12(4). 563–570. 18 indexed citations

18.

Grignani, F, Ugo Testa, Daniela Rogaia, et al.. (1996). Effects on differentiation by the promyelocytic leukemia PML/RARalpha protein depend on the fusion of the PML protein dimerization and RARalpha DNA binding domains.. The EMBO Journal. 15(18). 4949–4958. 120 indexed citations

19.

Dermime, Said, et al.. (1995). Acute Promyelocytic Leukaemia Cells Resistant to Retinoic Acid Show Further Perturbation of the RARα Signal Transduction System. Leukemia & lymphoma. 16(3-4). 289–295. 18 indexed citations

20.

Grignani, F, M Fagioli, Myriam Alcalay, et al.. (1994). Pathogenetic Relevance Of The Acute Promyelocytic Leukemia-Specific PML/RARa Fusion Protein. 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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