Daniela D’Agostino

2.4k total citations
27 papers, 1.1k citations indexed

About

Daniela D’Agostino is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Daniela D’Agostino has authored 27 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Oncology. Recurrent topics in Daniela D’Agostino's work include Epilepsy research and treatment (6 papers), RNA modifications and cancer (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Daniela D’Agostino is often cited by papers focused on Epilepsy research and treatment (6 papers), RNA modifications and cancer (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Daniela D’Agostino collaborates with scholars based in Canada, Italy and United States. Daniela D’Agostino's co-authors include Nancy Braverman, Frédérick Andermann, Vincenzo De Laurenzi, E. Andermann, Silvia Volpe, Antonella De Cola, Giorgio Stassi, Matilde Todaro, C. Di Ilio and Daniela Barcaroli and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Daniela D’Agostino

26 papers receiving 1.1k citations

Peers

Countries citing papers authored by Daniela D’Agostino

Since Specialization

Citations

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

Fields of papers citing papers by Daniela D’Agostino

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela D’Agostino

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

#	Work	Indexed citations
1	Using the ancestral recombination graph to study the history of rare variants in founder populations 2025 ·The American Journal of Human Genetics ·(unknown), Alex Diaz-Papkovich, Guillaume Sillon, Daniela D’Agostino, (unknown), George Chong, Ken Sin Lo, (unknown), Nancy Hamel, (unknown), William D. Foulkes, Daniel Taliun, Adam J. Shapiro, Guillaume Lettre, Simon Gravel	0
2	Genotype–Phenotype Correlation in Neurofibromatosis Type 1: Evidence for a Mild Phenotype Associated with Splicing Variants Leading to In-Frame Skipping of NF1 Exon 24 [19a] 2024 ·Cancers ·Yunjia Chen, Yulong Fu, Magdalena Koczkowska, Tom Callens, Alicia Gomes, Jian Liu, William E. Bradley, (unknown), (unknown), Daniela D’Agostino, Chuanhua Fu, Deeann Wallis	2
3	An adult patient with Tatton–Brown–Rahman syndrome caused by a novel DNMT3A variant and axonal polyneuropathy 2023 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Rami Massie, (unknown), Philippe M. Campeau, Serge McGraw, Daniela D’Agostino	1
4	Spectrum of white matter abnormalities associated with FOXC1‐related disorders in two unrelated cases 2023 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·(unknown), Daniela D’Agostino, Roberta La Piana	1
5	EV20‑sss‑vc/MMAF, an HER‑3 targeting antibody‑drug conjugate displays antitumor activity in liver cancer 2020 ·Oncology Reports ·Daniela D’Agostino, Roberta Gentile, (unknown), (unknown), Francesco Dituri, Gianluigi Giannelli, Cosmo Rossi, Liberato Marzullo, Francesco Giansanti, Vincenzo De Laurenzi, Stefano Iacobelli, Rodolfo Ippoliti, Emily Capone, Gianluca Sala	11
6	EV20-mediated delivery of cytotoxic auristatin MMAF exhibits potent therapeutic efficacy in cutaneous melanoma 2018 ·Journal of Controlled Release ·Emily Capone, Alessia Lamolinara, Daniela D’Agostino, Cosmo Rossi, Vincenzo De Laurenzi, Manuela Iezzi, Stefano Iacobelli, Gianluca Sala	28
7	Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease 2018 ·Journal of Child Neurology ·Andrea Accogli, Kether Guerrero, Daniela D’Agostino, Luan T. Tran, Cécile Cieuta‐Walti, Isabelle Thiffault, Sébastien Chénier, Jeremy Schwartzentruber, Jacek Majewski, Geneviève Bernard	8
8	Glucocorticoid resistance syndrome caused by a novel <i>NR3C1</i> point mutation 2018 ·Endocrine Journal ·(unknown), Avi Saskin, (unknown), Daniela D’Agostino, Juan Rivera	20
9	Atypical tuberous sclerosis complex presenting as familial renal cell carcinoma with leiomyomatous stroma 2018 ·The Journal of Pathology Clinical Research ·(unknown), Somayyeh Fahiminiya, Louis R. Bégin, Nancy Hamel, Daniela D’Agostino, Simon Tanguay, William D. Foulkes	10
10	miR-205-5p-mediated downregulation of ErbB/HER receptors in breast cancer stem cells results in targeted therapy resistance 2015 ·Cell Death and Disease ·Antonella De Cola, Silvia Volpe, Maria Cristina Budani, Manuela Ferracin, Rossano Lattanzio, Alice Turdo, Daniela D’Agostino, Emily Capone, Giorgio Stassi, Matilde Todaro, C. Di Ilio, Gianluca Sala, Mauro Piantelli, Massimo Negrini, Angelo Veronese, Vincenzo De Laurenzi	73
11	Breast cancer stem cells rely on fermentative glycolysis and are sensitive to 2-deoxyglucose treatment 2014 ·Cell Death and Disease ·Domenico Ciavardelli, Cláudia Rossi, Daniela Barcaroli, Silvia Volpe, Ada Consalvo, Mirco Zucchelli, Antonella De Cola, Emanuela Scavo, (unknown), Daniela D’Agostino, (unknown), Simona D’Aguanno, Matilde Todaro, Giorgio Stassi, C. Di Ilio, Vincenzo De Laurenzi, Andrea Urbani	214
12	Peroxisome biogenesis disorders: Biological, clinical and pathophysiological perspectives 2013 ·PubMed ·Nancy Braverman, Daniela D’Agostino, (unknown)	114
13	Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3 2007 ·Neurology ·Peter Hedera, Marcia Blair, E. Andermann, Frédérick Andermann, Daniela D’Agostino, (unknown), Lana M. Chahine, Massimo Pandolfo, Yvonne M. Bradford, Jonathan L. Haines, B. Abou‐Khalil	45
14	Mild Epilepsy Phenotype in TSC2 Patients with Codon 905 Mutations 2005 ·Epilepsia ·Anna Jansen, Őzgür Sancak, Daniela D’Agostino, AmanPreet Badhwar, Penelope Roberts, G. Gobbi, (unknown), Denis Melanson, (unknown), Madeleine Gans, A M van den Ouweland, Mark Nellist, Massimo Pandolfo, Katherine B. Sims, Elizabeth A. Thiele, Frédérick Andermann, François Dubeau, David J. Kwiatkowski, Dicky Halley, E. Andermann	2
15	Posterior quadrantic dysplasia or hemi-hemimegalencephaly 2004 ·Neurology ·Daniela D’Agostino, Alexandre Bastos, Cláudio Piras, Andrea Bernasconi, Thierry Grisar, (unknown), (unknown), Csaba Juhász, Harry T. Chugani, Renzo Guerrini, J. Helen Cross, E. Andermann, François Dubeau, J. Montes, André Olivier, Frédérick Andermann	68
16	Outcome of Surgical Treatment in Familial Mesial Temporal Lobe Epilepsy 2003 ·Epilepsia ·Eliane Kobayashi, Daniela D’Agostino, Íscia Lopes‐Cendes, Eva Andermann, François Dubeau, Carlos A.M. Guerreiro, André Almeida Schenka, Luciano S. Queiroz, André Olivier, Fernando Cendes, Frédérick Andermann	31
17	Nonsyndromic mental retardation and cryptogenic epilepsy in women with Doublecortin gene mutations 2003 ·Annals of Neurology ·Renzo Guerrini, Francesca Moro, Eva Andermann, Elaine Hughes, Daniela D’Agostino, Romeo Carrozzo, Andrea Bernasconi, Frances Flinter, Lucio Parmeggiani, Anna Volzone, Elena Parrini, Davide Mei, Józef Jarosz, Robin G. Morris, (unknown), Gaetano Tortorella, François Dubeau, Frédérick Andermann, William B. Dobyns, Soma Das	43
18	Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsy 2003 ·Neurology ·Eliane Kobayashi, Daniela D’Agostino, Íscia Lopes‐Cendes, Samuel F. Berkovic, (unknown), E. Andermann, Frédérick Andermann, Fernando Cendes	81
19	Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females 2002 ·Brain ·Daniela D’Agostino	80
20	Long-term Efficacy and Safety of Piracetam in the Treatment of Progressive Myoclonus Epilepsy 2001 ·Archives of Neurology ·Marco Fedi, David C. Reutens, F. Dubeau, Eva Andermann, Daniela D’Agostino, Frédérick Andermann	52

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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