Maja Di Rocco

1.5k total citations
20 papers, 459 citations indexed

About

Maja Di Rocco is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Maja Di Rocco has authored 20 papers receiving a total of 459 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 5 papers in Genetics. Recurrent topics in Maja Di Rocco's work include Metabolism and Genetic Disorders (8 papers), Amino Acid Enzymes and Metabolism (3 papers) and Lysosomal Storage Disorders Research (3 papers). Maja Di Rocco is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Amino Acid Enzymes and Metabolism (3 papers) and Lysosomal Storage Disorders Research (3 papers). Maja Di Rocco collaborates with scholars based in Italy, United States and Germany. Maja Di Rocco's co-authors include Ubaldo Caruso, Marta Romanengo, Paolo Tortori‐Donati, Gerd Scherer, E. Natt, Kaichi Kida, M Odièvre, Antonella Bellocchio, Livia Pisciotta and Alfredo Cantàfora and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Annals of Neurology.

In The Last Decade

Maja Di Rocco

20 papers receiving 450 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maja Di Rocco Italy 12 212 131 124 122 71 20 459
Teresa Pàmpols Spain 12 459 2.2× 267 2.0× 45 0.4× 206 1.7× 151 2.1× 27 640
Nina Aula Finland 8 258 1.2× 353 2.7× 50 0.4× 33 0.3× 208 2.9× 10 616
Jutta Gärtner Germany 14 366 1.7× 60 0.5× 29 0.2× 56 0.5× 29 0.4× 19 650
Merel S. Ebberink Netherlands 14 786 3.7× 142 1.1× 39 0.3× 227 1.9× 26 0.4× 22 872
Noora Shahbeck Qatar 11 193 0.9× 38 0.3× 47 0.4× 104 0.9× 41 0.6× 14 426
M. DiRocco Italy 8 353 1.7× 78 0.6× 50 0.4× 244 2.0× 48 0.7× 11 497
Laura Pollard United States 12 240 1.1× 137 1.0× 21 0.2× 79 0.6× 46 0.6× 43 391
Nobue Shinnoh Japan 14 407 1.9× 275 2.1× 46 0.4× 122 1.0× 68 1.0× 25 519
Dawn Peck United States 13 329 1.6× 320 2.4× 18 0.1× 287 2.4× 33 0.5× 32 607
K Takki Finland 12 378 1.8× 79 0.6× 161 1.3× 148 1.2× 45 0.6× 16 615

Countries citing papers authored by Maja Di Rocco

Since Specialization
Citations

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

Fields of papers citing papers by Maja Di Rocco

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maja Di Rocco. 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 Maja Di Rocco. The network helps show where Maja Di Rocco may publish in the future.

Co-authorship network of co-authors of Maja Di Rocco

This figure shows the co-authorship network connecting the top 25 collaborators of Maja Di Rocco. A scholar is included among the top collaborators of Maja Di Rocco 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 Maja Di Rocco. Maja Di Rocco 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.
Giacomini, Thea, Maria Stella Vari, Giulia Prato, et al.. (2019). Epileptic Encephalopathy, Myoclonus–Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene. Neuropediatrics. 50(5). 327–331. 6 indexed citations
2.
Stagnaro, Michela, Livia Pisciotta, Maja Di Rocco, et al.. (2018). ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases. European Journal of Paediatric Neurology. 22(2). 264–271. 10 indexed citations
3.
Chiabrando, Deborah, Marco Castori, Maja Di Rocco, et al.. (2016). Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception. PLoS Genetics. 12(12). e1006461–e1006461. 41 indexed citations
4.
Morana, Giovanni, Claudio Bruno, Maja Di Rocco, et al.. (2015). Inferior Olivary Nucleus Involvement in Pediatric Neurodegenerative Disorders: Does It Play a Role in Neuroimaging Pattern-Recognition Approach?. Neuropediatrics. 46(2). 104–109. 5 indexed citations
5.
Carulli, Giovanni, A Azzarà, Sara Grassi, et al.. (2013). Simultaneous presentation of Waldenström macroglobulinemia and multiple myeloma: multidisciplinary diagnosis, treatment and 30-month follow-up.sinensis leaf extract.. Journal of Clinical and Experimental Hematopathology. 53(1). 29–36. 5 indexed citations
6.
Gimelli, Stefania, Maja Di Rocco, Gianluca Caridi, et al.. (2013). A rare 3q13.31 microdeletion including GAP43 and LSAMP genes. Molecular Cytogenetics. 6(1). 52–52. 7 indexed citations
7.
Russo, Silvia, Maura Masciadri, Cristina Gervasini, et al.. (2012). Intragenic and large NIPBL rearrangements revealed by MLPA in Cornelia de Lange patients. European Journal of Human Genetics. 20(7). 734–741. 16 indexed citations
8.
Cangemi, Giuliana, Sebastiano Barco, Maja Di Rocco, et al.. (2011). Erythrocyte Galactose-1-phosphate measurement by GC-MS in the monitoring of classical galactosemia. Scandinavian Journal of Clinical and Laboratory Investigation. 72(1). 29–33. 5 indexed citations
9.
Siri, Laura, Francesca Battaglia, Alessandra Tessa, et al.. (2010). Cognitive Profile in Spastic Paraplegia with Thin Corpus Callosum and Mutations inSPG11. Neuropediatrics. 41(1). 35–38. 14 indexed citations
10.
Pisciotta, Livia, Raffaele Fresa, Antonella Bellocchio, et al.. (2009). Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene. Molecular Genetics and Metabolism. 97(2). 143–148. 53 indexed citations
11.
12.
Bruno, Claudio, Enrico Bertini, Maja Di Rocco, et al.. (2008). Clinical and genetic characterization of Chanarin–Dorfman syndrome. Biochemical and Biophysical Research Communications. 369(4). 1125–1128. 49 indexed citations
13.
Grossi, Serena, Stefano Regis, Camillo Rosano, et al.. (2008). Molecular analysis ofARSAandPSAPgenes in twenty-one Italian patients with metachromatic leukodystrophy: identification and functional characterization of 11 novelARSAalleles. Human Mutation. 29(11). E220–E230. 24 indexed citations
14.
Rocco, Maja Di, Ubaldo Caruso, Egill Briem, et al.. (2006). A case of ethylmalonic encephalopathy with atypical clinical and biochemical presentation. Molecular Genetics and Metabolism. 89(4). 395–397. 20 indexed citations
15.
Gattorno, Marco, Maja Di Rocco, Antonella Buoncompagni, et al.. (2004). Neonatal lupus and a seronegative mother. The Lancet. 363(9414). 1038–1038. 4 indexed citations
16.
Rocco, Maja Di, et al.. (2001). Monozygotic twins with X‐linked adrenoleukodystrophy and different phenotypes. Annals of Neurology. 50(3). 424–424. 29 indexed citations
17.
Sperandeo, Maria Pia, Maria Teresa Bassi, Mirko Riboni, et al.. (2000). Structure of the SLC7A7 Gene and Mutational Analysis of Patients Affected by Lysinuric Protein Intolerance. The American Journal of Human Genetics. 66(1). 92–99. 56 indexed citations
18.
Romanengo, Marta, Paolo Tortori‐Donati, & Maja Di Rocco. (1997). Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: a case report. Clinical Genetics. 52(3). 184–186. 32 indexed citations
19.
Natt, E., Kaichi Kida, M Odièvre, Maja Di Rocco, & Gerd Scherer. (1992). Point mutations in the tyrosine aminotransferase gene in tyrosinemia type II.. Proceedings of the National Academy of Sciences. 89(19). 9297–9301. 50 indexed citations
20.
Rocco, Maja Di, et al.. (1984). Phenotypic variability in biotinidasedeficiency. The Journal of Pediatrics. 104(6). 964–965. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Teresa Pàmpols Breakdown of academic impact, for papers by Nina Aula Breakdown of academic impact, for papers by Jutta Gärtner Breakdown of academic impact, for papers by Merel S. Ebberink Breakdown of academic impact, for papers by Noora Shahbeck Breakdown of academic impact, for papers by M. DiRocco Breakdown of academic impact, for papers by Laura Pollard Breakdown of academic impact, for papers by Nobue Shinnoh Breakdown of academic impact, for papers by Dawn Peck Breakdown of academic impact, for papers by K Takki
Rankless by CCL
2026