Georgios Loudianos - Concepedia

Author

Georgios Loudianos

Ospedale Microcitemico ORCID

Also Known As

G Loudianos, G. LOUDIANOS, G. Loudianos, Georgios Loudianos, J. Loudianos, Loudianos Georgios

Publications

2.5K

Citations

H-Index

Concepts

All Affiliations

Ospedale Microcitemico University of Cagliari Institute of Genetic and Biomedical Research Institute of History of Mediterranean Europe University of Padua

About

Georgios Loudianos is an author at Ospedale Microcitemico specializing in genetics, medicine, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	30	958
2	Natural Sciences	4	4	101
3	Public Health	4	4	325
4	Health Sciences	3	3	55
5	Biochemistry	1	1	16

Georgios Loudianos

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Molecular characterization of Wilson disease in the Sardinian population?Evidence of a founder effect Georgios Loudianos, Valeria Dessì, Mario Lovicu, Human Mutation Mendelian DisorderDisease MechanismGenetic DisorderGeneticsPathogenesis	1999	167
Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations. A Figus, Andrea Angius, Georgios Loudianos, PubMed	1995	141
Further delineation of the molecular pathology of Wilson disease in the Mediterranean population Georgios Loudianos, Valeria Dessì, Mario Lovicu, Human Mutation GeneticsGenetic EpidemiologyPathologyDisease Gene IdentificationGenomics	1998	80
Genotype–phenotype correlation in Italian children with Wilson’s disease Emanuele Nicastro, Georgios Loudianos, Lucia Zancan, Journal of Hepatology Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyGenotype–phenotype Correlation	2008	69
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations S Murru, Georgios Loudianos, Manila Deiana, Blood	1991	67
Wilson disease mutations associated with uncommon haplotypes in mediterranean patients Georgios Loudianos, Valeria Dessì, Andrea Angius, Human Genetics Mendelian DisorderWilson Disease MutationsGenetic DisorderGeneticsPathology	1996	49
High Incidence and Allelic Homogeneity of Wilson Disease in 2 Isolated Populations: A Prerequisite for Efficient Disease Prevention Programs Antonietta Zappu, Magli Olympia, Maria Barbara Lepori, Journal of Pediatric Gastroenterology and Nutrition	2008	47
The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population Alessandro Gialluisi, Simona Incollu, Tommaso Pippucci, European Journal of Human Genetics Allelic VariantHaplotype DeterminationGenotype-phenotype AssociationMolecular EcologyMedicine	2013	47
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene Paolo Moi, Georgios Loudianos, João Lavinha, Blood	1992	45
Allan–Herndon–Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH Loredana Boccone, Stefano Mariotti, Valentina Dessì, European Journal of Medical Genetics Neurodegenerative DiseasesSevere Neurologic FeaturesMendelian DisorderNeurological DisorderMedicine	2010	41

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