Patrizia D’Adamo

4.6k total citations · 1 hit paper
46 papers, 2.9k citations indexed

About

Patrizia D’Adamo is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Patrizia D’Adamo has authored 46 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 23 papers in Cellular and Molecular Neuroscience and 16 papers in Genetics. Recurrent topics in Patrizia D’Adamo's work include Neuroscience and Neuropharmacology Research (16 papers), Genetics and Neurodevelopmental Disorders (15 papers) and Cellular transport and secretion (13 papers). Patrizia D’Adamo is often cited by papers focused on Neuroscience and Neuropharmacology Research (16 papers), Genetics and Neurodevelopmental Disorders (15 papers) and Cellular transport and secretion (13 papers). Patrizia D’Adamo collaborates with scholars based in Italy, Switzerland and United States. Patrizia D’Adamo's co-authors include Daniela Toniolo, Ági K. Gedeon, Pieter A. Bolhuis, Silvia Bione, Elena Maestrini, Hans Welzl, Hans-Peter Lipp, Veronica Bianchi, Maria Lidia Mignogna and Roger M. Nitsch and has published in prestigious journals such as Nature Communications, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Patrizia D’Adamo

46 papers receiving 2.9k citations

Hit Papers

align trajectories sort by overperformance

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.

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1996 565 citations Patrizia D’Adamo, Ági K. Gedeon et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Patrizia D’Adamo Italy	28	1.8k	837	693	443	369	46	2.9k
Patrick Cossette Canada	30	1.4k 0.8×	1.1k 1.3×	1.3k 1.8×	335 0.8×	489 1.3×	68	3.2k
Toshikuni Sasaoka Japan	28	1.6k 0.9×	379 0.5×	1.0k 1.5×	329 0.7×	219 0.6×	77	2.5k
Nael Nadif Kasri Netherlands	37	2.3k 1.3×	837 1.0×	959 1.4×	516 1.2×	436 1.2×	103	3.5k
Tomoko Toyota Japan	31	1.5k 0.8×	850 1.0×	818 1.2×	192 0.4×	398 1.1×	87	2.8k
Steven J. Clapcote United Kingdom	25	1.5k 0.9×	574 0.7×	806 1.2×	109 0.2×	331 0.9×	49	2.5k
Rami Abou Jamra Germany	29	1.4k 0.8×	1.1k 1.3×	544 0.8×	317 0.7×	244 0.7×	99	2.8k
Philippe Ravassard France	36	2.8k 1.6×	1.8k 2.2×	1.6k 2.3×	411 0.9×	463 1.3×	100	5.9k
Robyn H. Wallace Australia	26	2.6k 1.5×	1.6k 2.0×	2.4k 3.4×	170 0.4×	316 0.9×	50	4.9k
Koko Ishizuka United States	21	1.4k 0.8×	431 0.5×	714 1.0×	144 0.3×	247 0.7×	59	2.5k
Oleg S. Gorbatyuk United States	24	1.4k 0.8×	559 0.7×	892 1.3×	576 1.3×	139 0.4×	41	2.6k

Countries citing papers authored by Patrizia D’Adamo

Since Specialization

Citations

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

Fields of papers citing papers by Patrizia D’Adamo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrizia D’Adamo

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

Brusco, Simone, Alessia Salamone, Mirko Luoni, et al.. (2022). Scn1a gene reactivation after symptom onset rescues pathological phenotypes in a mouse model of Dravet syndrome. Nature Communications. 13(1). 161–161. 36 indexed citations

Mignogna, Maria Lidia, Romina Ficarella, Lucia Marzulli, et al.. (2021). Clinical characterization of a novel RAB39B nonstop mutation in a family with ASD and severe ID causing RAB39B downregulation and study of a Rab39b knock down mouse model. Human Molecular Genetics. 31(9). 1389–1406. 4 indexed citations

Fratta, Pietro, Francesca Ornaghi, Gabriele Dati, et al.. (2018). A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function. Human Molecular Genetics. 28(1). 124–132. 18 indexed citations

Guarnieri, Fabrizia Claudia, Davide Pozzi, Andrea Raimondi, et al.. (2017). A novel SYN1 missense mutation in non-syndromic X-linked intellectual disability affects synaptic vesicle life cycle, clustering and mobility. Human Molecular Genetics. 26(23). 4699–4714. 32 indexed citations

Ciammola, Andrea, Paola Carrera, Alessio Di Fonzo, et al.. (2017). X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene. Parkinsonism & Related Disorders. 44. 142–146. 26 indexed citations

Morè, Lorenzo, Basil Künnecke, Latefa Yekhlef, et al.. (2017). Altered fronto-striatal functions in the Gdi1-null mouse model of X-linked Intellectual Disability. Neuroscience. 344. 346–359. 9 indexed citations

Potokar, Maja, Jernej Jorgačevski, Marko Kreft, et al.. (2016). Impaired αGDI Function in the X-Linked Intellectual Disability: The Impact on Astroglia Vesicle Dynamics. Molecular Neurobiology. 54(4). 2458–2468. 6 indexed citations

Ceglia, Roberta De, Linda Chaabane, Emilia Biffi, et al.. (2014). Down-sizing of neuronal network activity and density of presynaptic terminals by pathological acidosis are efficiently prevented by Diminazene Aceturate. Brain Behavior and Immunity. 45. 263–276. 28 indexed citations

Butti, Erica, Marco Bacigaluppi, Silvia Rossi, et al.. (2012). Subventricular zone neural progenitors protect striatal neurons from glutamatergic excitotoxicity. Brain. 135(11). 3320–3335. 54 indexed citations

10.

Bianchi, Veronica, Frédéric Gambino, Luca Muzio, et al.. (2012). Forebrain Deletion of αGDI in Adult Mice Worsens the Pre-Synaptic Deficit at Cortico-Lateral Amygdala Synaptic Connections. PLoS ONE. 7(1). e29763–e29763. 14 indexed citations

11.

Muzio, Luca, Alessandro Bertolo, Veronica Bianchi, et al.. (2012). Growth Defects and Impaired Cognitive–Behavioral Abilities in Mice with Knockout for Eif4h, a Gene Located in the Mouse Homolog of the Williams-Beuren Syndrome Critical Region. American Journal Of Pathology. 180(3). 1121–1135. 27 indexed citations

12.

Bianchi, Veronica, Mattia Pelizzola, Manuel Mayhaus, et al.. (2009). Temporal gene expression profile of the hippocampus following trace fear conditioning. Brain Research. 1308. 14–23. 12 indexed citations

13.

Triolo, Daniela, Carla Taveggia, Alessandra Bolino, et al.. (2009). ABNORMAL SCHWANN CELL-AXON UNITS AND MYELINATION IN VIMENTIN-DEFICIENT MICE. 14. 145–146. 1 indexed citations

14.

Bianchi, Veronica, Pasqualina Farisello, Pietro Baldelli, et al.. (2008). Cognitive impairment in Gdi1-deficient mice is associated with altered synaptic vesicle pools and short-term synaptic plasticity, and can be corrected by appropriate learning training. Human Molecular Genetics. 18(1). 105–117. 41 indexed citations

15.

Laforenza, Umberto, Emanuela Cova, Giulia Gastaldi, et al.. (2005). Aquaporin-8 Is Involved in Water Transport in Isolated Superficial Colonocytes from Rat Proximal Colon. Journal of Nutrition. 135(10). 2329–2336. 44 indexed citations

16.

Pennanen, Luis, Hans Welzl, Patrizia D’Adamo, Roger M. Nitsch, & Jürgen Götz. (2004). Accelerated extinction of conditioned taste aversion in P301L tau transgenic mice. Neurobiology of Disease. 15(3). 500–509. 67 indexed citations

17.

D’Adamo, Patrizia. (2002). Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in mice. Human Molecular Genetics. 11(21). 2567–2580. 85 indexed citations

18.

Ørstavik, Karen Helene, Ragnhild Ørstavik, Anna K. Naumova, et al.. (1998). X Chromosome Inactivation in Carriers of Barth Syndrome. The American Journal of Human Genetics. 63(5). 1457–1463. 58 indexed citations

19.

D’Adamo, Patrizia, Andrea Menegon, Cristiana Lo Nigro, et al.. (1998). Mutations in GDI1 are responsible for X-linked non-specific mental retardation. Nature Genetics. 19(2). 134–139. 264 indexed citations

20.

Malacrida, Anna R., et al.. (1996). Allozyme divergence and phylogenetic relationships among species of tephritid flies. Heredity. 76(6). 592–602. 20 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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