Gianmauro Cuccuru - Concepedia

Author

Gianmauro Cuccuru

Institute of Genetic and Biomedical Research ORCID

Also Known As

Cuccuru, Gianmauro, G Cuccuru, G. Cuccuru, Gareth R Price, Gianmauro Cuccuru, Nate Coraor, Whalen, Michael B

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Institute of Genetic and Biomedical Research Center for Advanced Studies Research and Development in Sardinia University of Sassari National Research Council University of Cagliari

About

Gianmauro Cuccuru is an author at Institute of Genetic and Biomedical Research specializing in medicine, genetics, and geometric modeling.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	215
2	Engineering	1	1	17
3	Natural Sciences	1	1	17
4	Cell Biology	1	1	36
5	Computer Science	1	1	17

Gianmauro Cuccuru

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Overexpression of the Cytokine BAFF and Autoimmunity Risk Maristella Steri, Valeria Orrù, Maria Laura Idda, New England Journal of Medicine	2017	383
Orione, a web-based framework for NGS analysis in microbiology Gianmauro Cuccuru, Massimiliano Orsini, Andréa Pinna, Bioinformatics	2014	181
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis Serena Sanna, Maristella Pitzalis, Magdalena Żołędziewska, Nature Genetics ImmunogeneticsAutoimmune DiseaseImmunoregulatory Cblb GeneMedicineGenetics	2010	179
Tools and data services registry: a community effort to document bioinformatics resources Jon Ison, Kristoffer Rapacki, Hervé Ménager, Nucleic Acids Research	2015	156
Buried in the Middle but Guilty: Intronic Mutations in the <i>TCIRG1</i> Gene Cause Human Autosomal Recessive Osteopetrosis Eleonora Palagano, Harry C. Blair, Alessandra Pangrazio, Journal of Bone and Mineral Research	2015	40
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa Andrea Angius, Paolo Uva, Insa Buers, The American Journal of Human Genetics Bi-allelic MutationsEarly-onset Retinitis PigmentosaAllelic VariantGenetic DisorderGenetics	2016	36
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report Rita Maria Alves, Paolo Uva, Marielza Veiga, BMC Medical Genetics	2019	18
Fast low-memory streaming MLS reconstruction of point-sampled surfaces Gianmauro Cuccuru, Enrico Gobbetti, Fabio Marton, Graphics Interface Geometry CompressionEngineeringMls ProjectorComputer-aided DesignPoint Sample Datasets	2009	17
Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of <i>CREBBP</i> Andrea Angius, Paolo Uva, Manuela Oppo, American Journal of Medical Genetics Part A	2019	17
Genome-wide association study of susceptibility loci for breast cancer in Sardinian population Grazia Palomba, Angela Loi, Eleonora Porcu, BMC Cancer	2015	15

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