Rita Congiu - Concepedia

Author

Rita Congiu

University of Cagliari

Also Known As

Congiu, Rita, R Congiu, R. Congiu, Rita Congiu

Publications

832

Citations

H-Index

Concepts

All Affiliations

University of Cagliari Institute of Genetic and Biomedical Research Ospedale Microcitemico Policlinico San Matteo Fondazione University of Pavia

About

Rita Congiu is an author at University of Cagliari specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	505
2	Molecular Genetics	2	2	46
3	Public Health	1	1	415
4	Cell Biology	1	1	32
5	Molecular Medicine	1	1	12

Rita Congiu

Publications

739

Citations

H-Index

Page 1

	Year	Citations
Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy Francesco Muntoni, Milena Cau, Antonello Ganau, New England Journal of Medicine Skeletal Myopathy5Cardiac MuscleHeart FailureGeneticsGenetic Epidemiology	1993	415
A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron Maria Antonietta Melis, M. Cau, Rita Congiu, Haematologica	2008	185
Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophy. Francesco Muntoni, Anna Mateddu, Carlo Cianchetti, Journal of Neurology Neurosurgery & Psychiatry Muscle PathologyUrologyRare DiseasesSkeletal MuscleDuchenne Muscular Dystrophy	1993	32
A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome Milena Cau, Maria Addis, Rita Congiu, Journal of Human Genetics CytogeneticsGenetic DisorderGeneticsClinical GeneticsMolecular Genetics	2006	30
Thalassaemia and Glucose-6-Phosphate Dehydrogenase Screening in 13- to 14-Year-Old Students of the Sardinian Population: Preliminary Findings Antonio Cao, Rita Congiu, Mc Sollaino, Public Health Genomics	2008	29
Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrier Francesco Muntoni, Anna Mateddu, Maria Giovanna Marrosu, Clinical Genetics	1992	20
C329X in KRIT1 is a founder mutation among CCM patients in Sardinia Milena Cau, Mario Loi, Maurizio Melis, European Journal of Medical Genetics Founder MutationCcm PatientsAutoimmune DiseaseGenetic DisorderMedicine	2009	16
A novel interstitial deletion in Xq25, identified by array-CGH in a patient with Lowe syndrome Maria Addis, C. Meloni, Rita Congiu, European Journal of Medical Genetics Mendelian DisorderNovel Interstitial DeletionGenetic DisorderGeneticsHematology	2006	12

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