S Murru

707 citations

41 papers · 514 · h-index 16

Impact in

Genetics top 5%
- Hemoglobinopathies and Related Disorders
- Neurogenetic and Muscular Disorders Research
Hematology top 5%
- Iron Metabolism and Disorders
- Blood groups and transfusion

Papers in

Genetics 20
- Hemoglobinopathies and Related Disorders 17
- Neurogenetic and Muscular Disorders Research 3
Hematology 14
- Iron Metabolism and Disorders 10
- Hemophilia Treatment and Research 3

Co-authors: Mario Pirastu (19 shared papers)Antonio Cao (15 shared papers)Georgios Loudianos (11 shared papers)Steven J. Agosti (9 shared papers)G. V. Sciarratta (6 shared papers)Maria Serafina Ristaldi (6 shared papers)Bruno Dallapiccola (2 shared papers)Letizia Casula (4 shared papers)
Journals: Blood (9 papers)British Journal of Haematology (3 papers)Genomics (3 papers)Human Mutation (2 papers)Frontiers in Genetics (1 paper)
Partner nations: Italy United States United Kingdom

In The Last Decade

S Murru

37 papers receiving 495 citations

Peers

Countries citing papers authored by S Murru

Since Specialization

Citations

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

Fields of papers citing papers by S Murru

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside S Murru, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with S Murru Line = papers co-authored together S Murru links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification Neurogenetics ·Oronzo Scarciolla, Liborio Stuppia, Maria Vittoria De Angelis, S Murru, Chiara Palka, Rossella Giuliani, Marta Pace, Antonio Di Muzio, Isabella Torrente, Annunziata Morella, Paola Grammatico, Manlio Giacanelli, Maria Cristina Rosatelli, Antonino Uncini, Bruno Dallapiccola	2006	60
2	Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations Blood ·S Murru, Georgios Loudianos, Manila Deiana, Clara Camaschella, GV Sciarratta, Steven J. Agosti, MI Parodi, P Cerruti, Antonio Cao, Mario Pirastu	1991	55
3	Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene Blood ·Paolo Moi, Georgios Loudianos, João Lavinha, S Murru, P Cossu, Rosanne E. Casu, L Oggiano, Maurizio Longinotti, Antonio Cao, Mario Pirastu	1992	39
4	Plasma Leptin Levels in Newborns from Normal and Diabetic Mothers Hormone and Metabolic Research ·Margherita Maffei, Laura Volpe, Graziano Di Cianni, A. Bertacca, M Ferdeghini, S Murru, Giuseppe Teti, I Casadidio, P Cecchetti, Renzo Navalesi, Luca Benzi	1998	33
5	A β‐thalassaemia phenotype not linked to the β‐globin cluster in an Italian family British Journal of Haematology ·S Murru, Georgios Loudianos, Susanna Porcu, G. V. Sciarratta, Steven J. Agosti, MI Parodi, Antonio Cao, Mario Pirastu	1992	32
6	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 ·Maria Serafina Ristaldi, S Murru, Georgios Loudianos, Letizia Casula, Susanna Porcu, D. Pigheddu, B. Fanni, G. V. Sciarratta, Steven J. Agosti, M. I. Parodi, Daniela Leone, Clara Camaschella, Anna Serra, Mario Pirastu, Antonio Cao	1990	31
7	Illegitimate recombination produced a duplication within the FVIII gene in a patient with mild hemophilia A Genomics ·S Murru, Letizia Casula, M. Pecorara, Piergiorgio Mori, Antonio Cao, Mario Pirastu	1990	28
8	Promoter mutations producing mild β‐thalassaemia in the Italian population British Journal of Haematology ·Alessandra Meloni, Maria Cristina Rosatelli, V. Faà, R Sardu, L. Saba, S Murru, G. V. Sciarratta, Maurizia Baldi, N Tannoia, A. Vitucci, Antonio Cao	1992	27
9	Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia A patients of Italian descent Blood ·Letizia Casula, S Murru, M. Pecorara, Maria Serafina Ristaldi, Gabriella Restagno, Giuseppe Mancuso, Massimo Morfini, R. De Biasi, F. Baudo, A. O. Carbonara	1990	22
10	A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype [letter] Blood ·Maria Serafina Ristaldi, Mario Pirastu, S Murru, Laura Casula, Georgios Loudianos, Aili Cao, GV Sciarratta, Steven J. Agosti, MI Parodi, Daniela Leone	1990	22
11	A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis Genomics ·Federica Sangiuolo, Giuseppe Novelli, S Murru, Bruno Dallapiccola	1991	20
12	Molecular Analysis of Atypical β‐Thalassemia Heterozygotes^a Annals of the New York Academy of Sciences ·Mario Pirastu, Maria Serafina Ristaldi, Georgios Loudianos, S Murru, G. V. Sciarratta, M. I. Parodi, Daniela Leone, Steven J. Agosti, Antonio Cao	1990	20
13	Neonatal outcome and obstetric complications in women with gestational diabetes: effects of maternal body mass index. PubMed ·Graziano Di Cianni, Luca Benzi, P Bottone, Laura Volpe, Paolo Orsini, S Murru, I Casadidio, Filipe Manuel Clemente, Renzo Navalesi	1996	17
14	A beta-thalassemia carrier with normal sequence within the beta-globin gene [letter] Blood ·S Murru, Georgios Loudianos, Aili Cao, Simona Vaccargiu, Mario Pirastu, GV Sciarratta, Steven J. Agosti, MI Parodi	1990	16
15	A beta-thalassemia carrier with normal sequence within the beta-globin gene [letter] Blood ·S Murru, Georgios Loudianos, Antonio Cao, S Vaccargiu, Mario Pirastu, GV Sciarratta, Steven J. Agosti, MI Parodi	1990	16
16	A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype [letter] Blood ·Maria Serafina Ristaldi, Mario Pirastu, S Murru, L Casula, Georgios Loudianos, Antonio Cao, GV Sciarratta, Steven J. Agosti, MI Parodi, Daniela Leone	1990	16
17	Leukoencephalopathy in 21-β hydroxylase deficiency: Report of a family Brain and Development ·Carmen Gaudiano, Alessandro Malandrini, Marzia Pollazzon, S Murru, Francesca Mari, Alessandra Renieri, Antonio Federico	2009	9
18	A novel β-globin structural mutant, Hb Brescia (β114 Leu-Pro), causing a severe β-thalassemia intermedia phenotype Human Mutation ·S Murru, Daniela Poddie, G. V. Sciarratta, Steven J. Agosti, Maria Baffico, C Melevendi, Mario Pirastu, Antonio Cao	1992	8
19	A promoter mutation of the beta-globin gene (-101 C-->T) has an age- related expression pattern [letter] Blood ·S Murru, MC Pischedda, Aili Cao, MC Rosatelli, Mario Pirastu, GV Sciarratta, Laura Manca, D. Gallisai, C. Toffoli	1993	8
20	A genetic epidemiology study of congenital adrenal hyperplasia in Italy Clinical Genetics ·Alessandro Gialluisi, Soara Menabò, Lilia Baldazzi, Letizia Casula, Antonella Meloni, M. Farci, Stefano Mariotti, Luisa Balestrino, R. Ortolano, S Murru, Carlo Carcassi, S. Loche, Antonio Balsamo, G. Romeo	2017	7

About S Murru

S Murru is a scholar working on Genetics, Hematology, Molecular Biology, Physiology and Archeology, having authored 41 papers that have together received 514 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (17 papers), Iron Metabolism and Disorders (10 papers), Erythrocyte Function and Pathophysiology (6 papers), Medieval Architecture and Archaeology (4 papers), Hemophilia Treatment and Research (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), DNA and Nucleic Acid Chemistry (3 papers) and Maritime and Coastal Archaeology (3 papers). The work is most often cited by research in Genetics (319 citations), Hematology (235 citations), Pediatrics, Perinatology and Child Health (63 citations), Endocrine and Autonomic Systems (21 citations) and Obstetrics and Gynecology (22 citations). S Murru has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Mario Pirastu, Antonio Cao, Georgios Loudianos, Steven J. Agosti, G. V. Sciarratta, Maria Serafina Ristaldi, Bruno Dallapiccola, Letizia Casula, Clara Camaschella and Daniela Leone. Their work appears in journals such as Blood, British Journal of Haematology, Genomics, Human Mutation and Frontiers in Genetics.

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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S Murru

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