Diego Lopergolo

3.8k total citations
18 papers, 142 citations indexed

About

Diego Lopergolo is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Diego Lopergolo has authored 18 papers receiving a total of 142 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Diego Lopergolo's work include Genomics and Rare Diseases (3 papers), Hereditary Neurological Disorders (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Diego Lopergolo is often cited by papers focused on Genomics and Rare Diseases (3 papers), Hereditary Neurological Disorders (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Diego Lopergolo collaborates with scholars based in Italy, United States and United Kingdom. Diego Lopergolo's co-authors include Maurizio Inghilleri, Emanuela Onesti, Eleonora Palma, Pierangelo Cifelli, Gabriele Ruffolo, Cristina Bertollini, Cristina Roseti, Jorge Mauricio Reyes‐Ruiz, Ricardo Miledi and Cristina Limatola and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Brain and Clinical Neurophysiology.

In The Last Decade

Diego Lopergolo

15 papers receiving 139 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Diego Lopergolo Italy	6	57	55	27	23	22	18	142
Natalie Wen United States	4	67 1.2×	63 1.1×	19 0.7×	22 1.0×	11 0.5×	7	209
Yasuyoshi Kimura Japan	9	123 2.2×	65 1.2×	27 1.0×	17 0.7×	14 0.6×	27	227
Beata Kaźmierczak Poland	9	90 1.6×	74 1.3×	26 1.0×	9 0.4×	47 2.1×	19	186
Guo-Jun Tan China	8	65 1.1×	28 0.5×	24 0.9×	9 0.4×	27 1.2×	13	149
Marc Gistelinck Belgium	5	70 1.2×	66 1.2×	36 1.3×	12 0.5×	35 1.6×	5	152
Ricardo Romero‐Guevara Italy	9	145 2.5×	61 1.1×	14 0.5×	13 0.6×	51 2.3×	10	229
Eric Tamrazian United States	6	120 2.1×	54 1.0×	70 2.6×	11 0.5×	27 1.2×	10	206
Maria D. Purice United States	4	109 1.9×	51 0.9×	74 2.7×	10 0.4×	30 1.4×	7	224
Samiha S. Shaikh United Kingdom	7	69 1.2×	50 0.9×	67 2.5×	15 0.7×	6 0.3×	7	170
Jennifer Parker Canada	8	146 2.6×	75 1.4×	65 2.4×	9 0.4×	26 1.2×	10	249

Countries citing papers authored by Diego Lopergolo

Since Specialization

Citations

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

Fields of papers citing papers by Diego Lopergolo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diego Lopergolo

This figure shows the co-authorship network connecting the top 25 collaborators of Diego Lopergolo. A scholar is included among the top collaborators of Diego Lopergolo 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 Diego Lopergolo. Diego Lopergolo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

18 of 18 papers shown

Pagano, Stefano, Diego Lopergolo, Alessandro De Falco, et al.. (2025). Expanding the Clinical Spectrum Associated with the Recurrent Arg203Trp Variant in PACS1: An Italian Cohort Study. Genes. 16(2). 227–227.

Lopergolo, Diego, Gian Nicola Gallus, Giuseppe Pieraccini, et al.. (2024). CCDC78: Unveiling the Function of a Novel Gene Associated with Hereditary Myopathy. Cells. 13(17). 1504–1504. 1 indexed citations

Gallus, Gian Nicola, Silvia Bianchi, Simona Salvatore, et al.. (2024). Novel Biomarkers for Limb Girdle Muscular Dystrophy (LGMD). Cells. 13(4). 329–329. 2 indexed citations

Lopergolo, Diego, et al.. (2024). Autosomal recessive cerebellar ataxias: a diagnostic classification approach according to ocular features. Frontiers in Integrative Neuroscience. 17. 1275794–1275794.

Leoncini, Silvia, Diego Lopergolo, Roberto Canitano, et al.. (2023). Natural Course of IQSEC2-Related Encephalopathy: An Italian National Structured Survey. Children. 10(9). 1442–1442. 2 indexed citations

Lopergolo, Diego, Simona Salvatore, Vincenzo Sorrentino, et al.. (2023). Early-onset motor polyneuropathy associated with a novel dominant NAGLU mutation. Neurological Sciences. 44(4). 1415–1418. 1 indexed citations

Lopergolo, Diego, Silvia Bianchi, Gian Nicola Gallus, et al.. (2023). Familial Alzheimer’s disease associated with heterozygous NPC1 mutation. Journal of Medical Genetics. 61(4). 332–339. 7 indexed citations

Lopergolo, Diego, Gianna Berti, Francesca Mari, et al.. (2022). A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis. Neurological Sciences. 43(4). 2849–2852.

Lopergolo, Diego, et al.. (2022). CUL4B-associated epilepsy: Report of a novel truncating variant promoting drug-resistant seizures and systematic review of the literature.. Seizure. 104. 32–37. 4 indexed citations

10.

Ferrari, Anna Rita, et al.. (2022). Different epilepsy course of a novel AHDC1 mutation in a female monozygotic twin pair. Seizure. 99. 127–130. 2 indexed citations

11.

Lopergolo, Diego, Anna Maria Pinto, Floriana Valentino, et al.. (2021). A new mutation in DNM2 gene in a large Italian family. Neurological Sciences. 42(6). 2509–2513. 1 indexed citations

12.

Croci, Susanna, Miriam Lucia Carriero, Katia Capitani, et al.. (2020). AAV-mediated FOXG1 gene editing in human Rett primary cells. European Journal of Human Genetics. 28(10). 1446–1458. 13 indexed citations

13.

McNeill, Alisdair, Christel Vaché, David Baux, et al.. (2020). SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect. Brain. 143(8). 2380–2387. 34 indexed citations

14.

Lopergolo, Diego, et al.. (2018). La misura delle catene leggere libere nel liquor nella diagnosi della sclerosi multipla. 42(2). 1 indexed citations

15.

Palma, Eleonora, Jorge Mauricio Reyes‐Ruiz, Diego Lopergolo, et al.. (2016). Acetylcholine receptors from human muscle as pharmacological targets for ALS therapy. Proceedings of the National Academy of Sciences. 113(11). 3060–3065. 52 indexed citations

16.

Lopergolo, Diego, Maria Gabriele, Emanuela Onesti, et al.. (2014). Cutaneous silent period recordings in demyelinating and axonal polyneuropathies. Clinical Neurophysiology. 126(9). 1780–1789. 14 indexed citations

17.

Tomassini, Valentina, Emanuela Onesti, Emanuele Tinelli, et al.. (2014). Assessing the Neurophysiological Effects of Cannabinoids on Spasticity in Multiple Sclerosis. IRIS Research product catalog (Sapienza University of Rome). 1(2). 7 indexed citations

18.

Ceccanti, Marco, M. Gabriele, Chiara Cambieri, et al.. (2013). 74. Predictive role of neurophysiological features on Bell’s palsy. Clinical Neurophysiology. 124(11). e205–e206. 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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