Mario Loi

430 total citations
8 papers, 275 citations indexed

About

Mario Loi is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Neurology. According to data from OpenAlex, Mario Loi has authored 8 papers receiving a total of 275 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Pathology and Forensic Medicine and 2 papers in Neurology. Recurrent topics in Mario Loi's work include Genetics and Neurodevelopmental Disorders (2 papers), Cellular transport and secretion (2 papers) and Protein Kinase Regulation and GTPase Signaling (1 paper). Mario Loi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Cellular transport and secretion (2 papers) and Protein Kinase Regulation and GTPase Signaling (1 paper). Mario Loi collaborates with scholars based in Italy. Mario Loi's co-authors include Maria Addis, Maria Antonietta Melis, Milena Cau, Antonio Cao, Alberto Albanese, Aldo Quattrone, Rita Congiu, Pietro Tonali, Orsetta Zuffardi and Enza Maria Valente and has published in prestigious journals such as Movement Disorders, Human Mutation and Orphanet Journal of Rare Diseases.

In The Last Decade

Mario Loi

8 papers receiving 251 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mario Loi Italy	8	101	100	77	60	38	8	275
Gill Adams United Kingdom	10	58 0.6×	52 0.5×	42 0.5×	80 1.3×	33 0.9×	23	320
Susan L. Lightman United Kingdom	11	107 1.1×	85 0.8×	41 0.5×	44 0.7×	19 0.5×	11	376
Maria Papadopoulos United Kingdom	15	147 1.5×	21 0.2×	34 0.4×	61 1.0×	66 1.7×	32	867
Tim Vanderhasselt Belgium	10	52 0.5×	36 0.4×	44 0.6×	19 0.3×	27 0.7×	23	272
Luigina Spaccini Italy	13	208 2.1×	43 0.4×	159 2.1×	27 0.5×	43 1.1×	47	455
P Grimes United States	11	157 1.6×	44 0.4×	35 0.5×	18 0.3×	48 1.3×	18	283
Margriet van Kogelenberg New Zealand	7	87 0.9×	58 0.6×	76 1.0×	8 0.1×	18 0.5×	9	221
Karthik Muthusamy India	10	118 1.2×	15 0.1×	42 0.5×	30 0.5×	50 1.3×	43	268
Maria Varela United States	12	170 1.7×	22 0.2×	112 1.5×	15 0.3×	21 0.6×	19	421
Mutluay Arslan Türkiye	10	106 1.0×	25 0.3×	78 1.0×	10 0.2×	47 1.2×	29	245

Countries citing papers authored by Mario Loi

Since Specialization

Citations

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

Fields of papers citing papers by Mario Loi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mario Loi

This figure shows the co-authorship network connecting the top 25 collaborators of Mario Loi. A scholar is included among the top collaborators of Mario Loi 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 Mario Loi. Mario Loi 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:

8 of 8 papers shown

1.

Cau, Milena, Mario Loi, Maurizio Melis, et al.. (2009). C329X in KRIT1 is a founder mutation among CCM patients in Sardinia. European Journal of Medical Genetics. 52(5). 344–348. 10 indexed citations

2.

Pisano, Tiziana, Paola Melis, Elena Rossi, et al.. (2008). Familial translocation t(3;10) (p26.3;p12.31) leading to trisomy 10p12.31 → pter and monosomy 3p26.3 → pter in seven members. American Journal of Medical Genetics Part A. 146A(24). 3242–3245. 13 indexed citations

3.

Cau, Milena, Maria Addis, Rita Congiu, et al.. (2006). A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome. Journal of Human Genetics. 51(11). 1030–1036. 22 indexed citations

4.

Loi, Mario. (2006). Lowe syndrome. Orphanet Journal of Rare Diseases. 1(1). 16–16. 146 indexed citations

5.

Labate, Angelo, et al.. (2006). Reflex periodic spasms induced by eating. Brain and Development. 28(3). 170–174. 22 indexed citations

6.

Addis, Maria, et al.. (2004). OCRLMutation analysis in Italian patients with Lowe syndrome. Human Mutation. 23(5). 524–525. 33 indexed citations

7.

Bentivoglio, Anna Rita, Mario Loi, Enza Maria Valente, et al.. (2002). Phenotypic variability of DYT1‐PTD: Does the clinical spectrum include psychogenic dystonia?. Movement Disorders. 17(5). 1058–1063. 19 indexed citations

8.

Cianchetti, Carlo, Maria Giovanna Marrosu, Paolo Emilio Manconi, Mario Loi, & Antonio Cao. (1983). Subacute Sclerosing Panencephalitis in Only One of Identical Twins. European Neurology. 22(6). 428–432. 10 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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