Sandro Orrù

3.1k total citations
84 papers, 1.8k citations indexed

About

Sandro Orrù is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Sandro Orrù has authored 84 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 23 papers in Immunology and 22 papers in Genetics. Recurrent topics in Sandro Orrù's work include Genomic variations and chromosomal abnormalities (15 papers), T-cell and B-cell Immunology (12 papers) and Prenatal Screening and Diagnostics (7 papers). Sandro Orrù is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), T-cell and B-cell Immunology (12 papers) and Prenatal Screening and Diagnostics (7 papers). Sandro Orrù collaborates with scholars based in Italy, Greece and Germany. Sandro Orrù's co-authors include Carlo Carcassi, Angelo Vacca, Maria Grazia Ennas, Doménico Ribatti, Fabio Ferreli, P. Sirigu, Beatrice Nico, Annalisa Loizedda, Emmanouil Manolakos and Giorgio La Nasa and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Sandro Orrù

82 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandro Orrù Italy	23	725	515	310	226	196	84	1.8k
Matthew F. Starost United States	28	1.3k 1.7×	392 0.8×	335 1.1×	260 1.2×	81 0.4×	97	2.4k
Tomoko Kobayashi Japan	23	833 1.1×	608 1.2×	221 0.7×	181 0.8×	153 0.8×	123	2.1k
David L. Ennist United States	18	917 1.3×	755 1.5×	520 1.7×	595 2.6×	111 0.6×	37	2.2k
Kevin S. Smith United States	27	1.8k 2.5×	415 0.8×	543 1.8×	266 1.2×	127 0.6×	61	3.1k
Takashi Imai Japan	32	1.7k 2.3×	801 1.6×	303 1.0×	360 1.6×	212 1.1×	134	3.3k
Rivkah Gonsky United States	22	837 1.2×	583 1.1×	583 1.9×	293 1.3×	169 0.9×	39	2.3k
Naoko Watanabe Japan	29	1.6k 2.2×	470 0.9×	247 0.8×	452 2.0×	101 0.5×	88	2.9k
Xin Geng China	26	1.3k 1.8×	982 1.9×	325 1.0×	217 1.0×	82 0.4×	87	3.1k
SJ Lee South Korea	26	778 1.1×	512 1.0×	142 0.5×	268 1.2×	62 0.3×	67	2.1k
Phong T. Le United States	28	474 0.7×	926 1.8×	141 0.5×	306 1.4×	126 0.6×	61	2.1k

Countries citing papers authored by Sandro Orrù

Since Specialization

Citations

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

Fields of papers citing papers by Sandro Orrù

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandro Orrù

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

All Works

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20 of 20 papers shown

Cocco, Pierluigi, et al.. (2024). The role of MicroRNAs as early biomarkers of asbestos-related lung cancer: A systematic review and meta-analysis. Pulmonology. 31(1). 2416792–2416792. 10 indexed citations

Castellano, Isabella, Tatiana Lopatina, Cristina Grange, et al.. (2022). Interleukin-3-Receptor-α in Triple-Negative Breast Cancer (TNBC): An Additional Novel Biomarker of TNBC Aggressiveness and a Therapeutic Target. Cancers. 14(16). 3918–3918. 8 indexed citations

Vega-Benedetti, Ana Florencia, Eleonora Loi, Loredana Moi, et al.. (2021). Colorectal cancer promoter methylation alteration affects the expression of glutamate ionotropic receptor AMPA type subunit 4 alternative isoforms potentially relevant in colon tissue. Human Cell. 35(1). 310–319. 9 indexed citations

Vega-Benedetti, Ana Florencia, Eleonora Loi, Loredana Moi, et al.. (2020). Colorectal Cancer Early Detection in Stool Samples Tracing CpG Islands Methylation Alterations Affecting Gene Expression. International Journal of Molecular Sciences. 21(12). 4494–4494. 25 indexed citations

Luo, Jia, Jacqueline A. Frank, Jennifer Zhou, et al.. (2019). Star-related lipid transfer protein 10 (STARD10): a novel key player in alcohol-induced breast cancer progression. Journal of Experimental & Clinical Cancer Research. 38(1). 4–4. 10 indexed citations

Greco, Marianna, Giovanni Caocci, Sonia Nemolato, et al.. (2019). Systemic Mastocytosis with Associated Primary Myelofibrosis. Indian Journal of Hematology and Blood Transfusion. 36(2). 442–443. 3 indexed citations

Caocci, Giovanni, Marianna Greco, Marcella Arras, et al.. (2017). HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia. Leukemia Research. 61. 1–5. 13 indexed citations

Santoru, Maria Laura, Cristina Piras, Antonio Murgia, et al.. (2017). Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients. Scientific Reports. 7(1). 9523–9523. 301 indexed citations

Brancia, Carla, Barbara Noli, Marina Boido, et al.. (2016). VGF Protein and Its C-Terminal Derived Peptides in Amyotrophic Lateral Sclerosis: Human and Animal Model Studies. PLoS ONE. 11(10). e0164689–e0164689. 26 indexed citations

10.

Leblond, Claire S., Ziv Gan‐Or, Dan Spiegelman, et al.. (2015). Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 37. 209.e17–209.e21. 58 indexed citations

11.

Papoulidis, Ioannis, Sandro Orrù, Stavros Sifakis, et al.. (2015). Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male. Molecular Cytogenetics. 8(1). 71–71. 4 indexed citations

12.

Papoulidis, Ioannis, Alexandros Sotiriadis, Makarios Eleftheriades, et al.. (2015). Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases. Prenatal Diagnosis. 35(13). 1269–1277. 25 indexed citations

13.

Manolakos, Emmanouil, Stavros Sifakis, Sotirios Sotiriou, et al.. (2011). Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature. Clinical Dysmorphology. 21(2). 101–105. 1 indexed citations

14.

Littera, Roberto, Alessandra Vacca, Alice Bertaina, et al.. (2010). The role of killer immunoglobulin-like receptor haplotypes on the outcome of unrelated donor haematopoietic SCT for thalassaemia. Bone Marrow Transplantation. 45(11). 1618–1624. 14 indexed citations

15.

Manolakos, Emmanouil, Annalisa Vetro, Antonios Garas, et al.. (2010). The use of array-CGH in a cohort of Greek children with developmental delay. Molecular Cytogenetics. 3(1). 22–22. 20 indexed citations

16.

Manolakos, Emmanouil, Panagiotis Peitsidis, Makarios Eleftheriades, et al.. (2010). Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature. Journal of obstetrics and gynaecology research. 36(2). 435–440. 13 indexed citations

17.

Manolakos, Emmanouil, Sandro Orrù, Ioannis Papoulidis, et al.. (2009). Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome). Molecular Cytogenetics. 2(1). 26–26. 10 indexed citations

18.

Moreau, Philippe, Licinio Contu, F. Alba, et al.. (2008). HLA-G Gene Polymorphism in Human Placentas: Possible Association of G*0106 Allele with Preeclampsia and Miscarriage. Biology of Reproduction. 79(3). 459–467. 82 indexed citations

19.

Orrù, Sandro, et al.. (2004). Mapping of the Major Psoriasis-Susceptibility Locus (PSORS1) in a 70-Kb Interval around the Corneodesmosin Gene (CDSN). The American Journal of Human Genetics. 76(1). 164–171. 43 indexed citations

20.

Orrù, Sandro, Gordon R. Thomas, Annalisa Loizedda, Cox Dw, & L. Contu. (1997). 24 bp deletion and Ala1278 to val mutation of the ATP7B gene in a Sardinian family with Wilson disease. Human Mutation. 10(1). 84–85. 9 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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