Rita Congiu

832 total citations
14 papers, 567 citations indexed

About

Rita Congiu is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Rita Congiu has authored 14 papers receiving a total of 567 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Hematology. Recurrent topics in Rita Congiu's work include Muscle Physiology and Disorders (6 papers), Hemoglobinopathies and Related Disorders (4 papers) and Iron Metabolism and Disorders (4 papers). Rita Congiu is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Hemoglobinopathies and Related Disorders (4 papers) and Iron Metabolism and Disorders (4 papers). Rita Congiu collaborates with scholars based in Italy. Rita Congiu's co-authors include Antonio Cao, Maria Antonietta Melis, Milena Cau, Anna Mateddu, Maria Giovanna Marrosu, Carlo Cianchetti, Francesco Muntoni, G. Realdi, Antonello Ganau and M. Cau and has published in prestigious journals such as New England Journal of Medicine, Journal of Neurology Neurosurgery & Psychiatry and Developmental Medicine & Child Neurology.

In The Last Decade

Rita Congiu

14 papers receiving 547 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rita Congiu Italy	9	284	270	175	162	64	14	567
Milena Cau Italy	10	313 1.1×	256 0.9×	122 0.7×	89 0.5×	57 0.9×	19	533
Xue Jun Fu Japan	16	434 1.5×	21 0.1×	45 0.3×	128 0.8×	59 0.9×	22	661
Oronzo Scarciolla Italy	10	222 0.8×	50 0.2×	123 0.7×	56 0.3×	3 0.0×	12	386
John C. Winkelmann United States	11	186 0.7×	21 0.1×	51 0.3×	76 0.5×	5 0.1×	13	390
Brian K. Buckley United States	9	312 1.1×	40 0.1×	42 0.2×	7 0.0×	22 0.3×	10	460
Omar El-Mounayri Canada	10	243 0.9×	56 0.2×	30 0.2×	14 0.1×	6 0.1×	12	415
Jie‐Yuan Jin China	11	170 0.6×	98 0.4×	27 0.2×	10 0.1×	8 0.1×	56	324
Stéphanie Michineau France	11	175 0.6×	68 0.3×	41 0.2×	7 0.0×	11 0.2×	14	429
Sarina Meinen Switzerland	10	338 1.2×	47 0.2×	57 0.3×	8 0.0×	4 0.1×	13	466
R. Hanke Germany	10	256 0.9×	66 0.2×	38 0.2×	9 0.1×	3 0.0×	19	356

Countries citing papers authored by Rita Congiu

Since Specialization

Citations

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

Fields of papers citing papers by Rita Congiu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rita Congiu

This figure shows the co-authorship network connecting the top 25 collaborators of Rita Congiu. A scholar is included among the top collaborators of Rita Congiu 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 Rita Congiu. Rita Congiu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Perseu, Lucia, et al.. (2010). Red cell pyruvate kinase deficiency in Southern Sardinia. Blood Cells Molecules and Diseases. 45(4). 280–283. 4 indexed citations

Cau, Milena, Maria Antonietta Melis, Rita Congiu, & Renzo Galanello. (2010). Iron-deficiency anemia secondary to mutations in genes controlling hepcidin. Expert Review of Hematology. 3(2). 205–216. 13 indexed citations

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

Cao, Antonio, et al.. (2008). Thalassaemia and Glucose-6-Phosphate Dehydrogenase Screening in 13- to 14-Year-Old Students of the Sardinian Population: Preliminary Findings. Public Health Genomics. 11(3). 121–128. 20 indexed citations

Melis, Maria Antonietta, M. Cau, Rita Congiu, et al.. (2008). A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron. Haematologica. 93(10). 1473–1479. 138 indexed citations

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

Addis, Maria, Rita Congiu, Francesco Emma, et al.. (2006). A novel interstitial deletion in Xq25, identified by array-CGH in a patient with Lowe syndrome. European Journal of Medical Genetics. 50(1). 79–84. 10 indexed citations

Melis, Maria Antonietta, et al.. (2002). Frequency of Hemochromatosis C282Y and H63D Mutations in Sardinia. Genetic Testing. 6(4). 327–329. 4 indexed citations

Muntoni, Francesco, Milena Cau, Antonello Ganau, et al.. (1993). Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy. New England Journal of Medicine. 329(13). 921–925. 300 indexed citations

10.

Muntoni, Francesco, M. Cau, Rita Congiu, et al.. (1993). Identification of a novel T-insertion polymorphism at the DMD locus. Human Genetics. 92(1). 103–103. 6 indexed citations

11.

Muntoni, Francesco, Anna Mateddu, M. Cau, et al.. (1993). Diagnosis of DMD Carrier Status in a Family with No Known Affected Males. Developmental Medicine & Child Neurology. 35(1). 70–73. 1 indexed citations

12.

Melis, Maria Antonietta, Milena Cau, Rita Congiu, et al.. (1993). Germinal mosaicism in a Duchenne muscular dystrophy family: implications for genetic counselling. Clinical Genetics. 43(5). 247–249. 5 indexed citations

13.

Muntoni, Francesco, Anna Mateddu, Carlo Cianchetti, et al.. (1993). Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophy.. Journal of Neurology Neurosurgery & Psychiatry. 56(1). 26–31. 23 indexed citations

14.

Muntoni, Francesco, Anna Mateddu, Maria Giovanna Marrosu, et al.. (1992). Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrier. Clinical Genetics. 42(1). 35–38. 11 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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