Georgios Loudianos

2.5k total citations · 1 hit paper
59 papers, 1.8k citations indexed

About

Georgios Loudianos is a scholar working on Nutrition and Dietetics, Hematology and Health, Toxicology and Mutagenesis. According to data from OpenAlex, Georgios Loudianos has authored 59 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Nutrition and Dietetics, 31 papers in Hematology and 25 papers in Health, Toxicology and Mutagenesis. Recurrent topics in Georgios Loudianos's work include Trace Elements in Health (34 papers), Iron Metabolism and Disorders (28 papers) and Heavy Metal Exposure and Toxicity (25 papers). Georgios Loudianos is often cited by papers focused on Trace Elements in Health (34 papers), Iron Metabolism and Disorders (28 papers) and Heavy Metal Exposure and Toxicity (25 papers). Georgios Loudianos collaborates with scholars based in Italy, Greece and Türkiye. Georgios Loudianos's co-authors include Péter Ferenci, Michael L. Schilsky, Diane W. Cox, Giorgina Mieli‐Vergani, Irmin Sternlieb, Stuart Tanner, Karel Caca, Frieder Berr, Antonio Cao and Mario Pirastu and has published in prestigious journals such as Blood, Annals of the New York Academy of Sciences and Journal of Hepatology.

In The Last Decade

Georgios Loudianos

59 papers receiving 1.7k citations

Hit Papers

align trajectories

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.

Diagnosis and phenotypic classification of Wilson disease¹

2003 631 citations Péter Ferenci, Georgios Loudianos et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Georgios Loudianos Italy	22	1.3k	985	762	403	301	59	1.8k
Therese L. Murphy Australia	13	811 0.6×	147 0.1×	942 1.2×	79 0.2×	551 1.8×	21	1.4k
Małgorzata Lenartowicz Poland	18	416 0.3×	219 0.2×	265 0.3×	54 0.1×	99 0.3×	54	813
Majid Shayeghi United Kingdom	7	296 0.2×	74 0.1×	389 0.5×	34 0.1×	216 0.7×	13	695
Brie K. Fuqua United States	14	366 0.3×	81 0.1×	391 0.5×	52 0.1×	196 0.7×	18	797
Erdal Kurtoğlu Türkiye	13	134 0.1×	58 0.1×	249 0.3×	23 0.1×	190 0.6×	64	558
Meir Djaldetti Israel	11	139 0.1×	53 0.1×	104 0.1×	22 0.1×	54 0.2×	40	552
C. B. Modell United Kingdom	11	100 0.1×	28 0.0×	279 0.4×	29 0.1×	391 1.3×	17	686
Janine Büttner Germany	15	177 0.1×	42 0.0×	75 0.1×	25 0.1×	45 0.1×	27	738
Rachel M. Helston United States	8	108 0.1×	87 0.1×	45 0.1×	40 0.1×	13 0.0×	9	553
Nathalie Pilard France	10	235 0.2×	11 0.0×	443 0.6×	18 0.0×	343 1.1×	10	674

Countries citing papers authored by Georgios Loudianos

Since Specialization

Citations

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

Fields of papers citing papers by Georgios Loudianos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Georgios Loudianos

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

20 of 20 papers shown

Ferenci, Péter, Rajko Ostojić, Irena Hrstić, et al.. (2016). ATP7B Gene Mutations in Croatian Patients with Wilson Disease. Genetic Testing and Molecular Biomarkers. 20(3). 112–117. 7 indexed citations

Loudianos, Georgios, et al.. (2012). Wilson's disease in two consecutive generations: The detection of three mutated alleles in the ATP7B gene in two Sardinian families. Digestive and Liver Disease. 45(4). 342–345. 9 indexed citations

Cau, Milena, Loredana Boccone, Anna Mateddu, et al.. (2012). A new deletion in 5′-end of dystrophin gene removing M and P promoters and dystrophin muscle enhancers. Gene. 511(2). 437–440. 1 indexed citations

Zappu, Antonietta, Franco Lilliu, Rosa Anna Podda, & Georgios Loudianos. (2010). Molecular Analysis of Glycogen Storage Disease Type Ib in Sardinian Population: Evidence for a Founder Effect. Genetic Testing and Molecular Biomarkers. 14(3). 399–403. 3 indexed citations

Boccone, Loredana, et al.. (2010). Allan–Herndon–Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH. European Journal of Medical Genetics. 53(6). 392–395. 33 indexed citations

Lovicu, Mario, Antonietta Zappu, Raffaele Iorio, et al.. (2009). RNA Analysis of Consensus Sequence Splicing Mutations: Implications for the Diagnosis of Wilson Disease. Genetic Testing and Molecular Biomarkers. 13(2). 185–191. 10 indexed citations

Lovicu, Mario, Antonietta Zappu, Lucia Zancan, et al.. (2007). Twenty-Four Novel Mutations in Wilson Disease Patients of Predominantly Italian Origin. Genetic Testing. 11(3). 328–332. 26 indexed citations

Boccone, Loredana, et al.. (2007). Bannayan–Riley–Ruvalcaba syndrome with posterior subcapsular congenital cataract and a consensus sequence splicing PTEN mutation. American Journal of Medical Genetics Part A. 146A(2). 257–260. 4 indexed citations

Loudianos, Georgios, et al.. (2006). Direct Diagnosis of Wilson Disease by Molecular Genetics. The Journal of Pediatrics. 148(1). 138–140. 17 indexed citations

10.

Loudianos, Georgios, Vladimir Kostić, Paola Solinas, et al.. (2003). Characterization of the Molecular Defect in the ATP7B Gene in Wilson Disease Patients from Yugoslavia. Genetic Testing. 7(2). 107–112. 26 indexed citations

11.

Loudianos, Georgios, Mario Lovicu, Paola Solinas, et al.. (2000). Delineation of the Spectrum of Wilson Disease Mutations in the Greek Population and the Identification of Six Novel Mutations. Genetic Testing. 4(4). 399–402. 25 indexed citations

12.

Battisti, Carla, Georgios Loudianos, Alessandra Rufa, et al.. (1999). Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency. American Journal of Medical Genetics. 85(2). 175–178. 2 indexed citations

13.

Loudianos, Georgios, Valeria Dessì, Mario Lovicu, et al.. (1998). Further delineation of the molecular pathology of Wilson disease in the Mediterranean population. Human Mutation. 12(2). 89–94. 4 indexed citations

14.

Loudianos, Georgios, Valeria Dessì, Mario Lovicu, et al.. (1998). Haplotype and mutation analysis in Greek patients with Wilson disease. European Journal of Human Genetics. 6(5). 487–491. 35 indexed citations

15.

Loudianos, Georgios, Valeria Dessì, Andrea Angius, et al.. (1996). Wilson disease mutations associated with uncommon haplotypes in mediterranean patients. Human Genetics. 98(6). 640–642. 40 indexed citations

16.

Murru, S, Georgios Loudianos, Susanna Porcu, et al.. (1992). A β‐thalassaemia phenotype not linked to the β‐globin cluster in an Italian family. British Journal of Haematology. 81(2). 283–287. 31 indexed citations

17.

Moi, Paolo, Georgios Loudianos, João Lavinha, et al.. (1992). Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene. Blood. 79(2). 512–516. 28 indexed citations

18.

Murru, S, Georgios Loudianos, Manila Deiana, et al.. (1991). Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations. Blood. 77(6). 1342–1347. 52 indexed citations

19.

Ristaldi, Maria Serafina, S Murru, Georgios Loudianos, et al.. (1990). The C–T substitution in the distal CACCC box of the β‐globin gene promoter is a common cause of silent β thalassaemia in the Italian population. British Journal of Haematology. 74(4). 480–486. 31 indexed citations

20.

Pirastu, Mario, Maria Serafina Ristaldi, Georgios Loudianos, et al.. (1990). Molecular Analysis of Atypical β‐Thalassemia Heterozygotes^a. Annals of the New York Academy of Sciences. 612(1). 90–97. 19 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