Antonella Minelli

1.7k total citations · 1 hit paper
46 papers, 1.2k citations indexed

About

Antonella Minelli is a scholar working on Genetics, Immunology and Hematology. According to data from OpenAlex, Antonella Minelli has authored 46 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 20 papers in Immunology and 12 papers in Hematology. Recurrent topics in Antonella Minelli's work include Blood disorders and treatments (19 papers), Immunodeficiency and Autoimmune Disorders (16 papers) and Acute Myeloid Leukemia Research (11 papers). Antonella Minelli is often cited by papers focused on Blood disorders and treatments (19 papers), Immunodeficiency and Autoimmune Disorders (16 papers) and Acute Myeloid Leukemia Research (11 papers). Antonella Minelli collaborates with scholars based in Italy, United Kingdom and Canada. Antonella Minelli's co-authors include Cesare Danesino, Franco Locatelli, Maria Ester Bernardo, Francesco Pasquali, Rita Maccario, C Alvisi, Emanuela Maserati, Alessandro Vanoli, Adele Sgarella and Gino Roberto Corazza and has published in prestigious journals such as Gut, British Journal of Haematology and Leukemia.

In The Last Decade

Antonella Minelli

44 papers receiving 1.2k citations

Hit Papers

Autologous bone marrow-derived mesenchymal stromal cells ... 2011 2026 2016 2021 2011 100 200 300 400

Peers

Antonella Minelli
Denise Batista United States
B. A. Bradley United Kingdom
Rod Monroy United States
DM Bodine United States
Cesare Campagnoli United Kingdom
Robert Emmons United States
AW Flake United States
Denise Batista United States
Antonella Minelli
Citations per year, relative to Antonella Minelli Antonella Minelli (= 1×) peers Denise Batista

Countries citing papers authored by Antonella Minelli

Since Specialization
Citations

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

Fields of papers citing papers by Antonella Minelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonella Minelli

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

All Works

20 of 20 papers shown
1.
Bezzerri, Valentino, et al.. (2023). The pathogenic variant c.258+533_459+403del in SBDS gene is the commonest rare variant in Italy and shows a founder effect. Gene Reports. 31. 101775–101775. 1 indexed citations
3.
Khan, Abdul Waheed, Alyssa L. Kennedy, Elissa Furutani, et al.. (2021). The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations. Molecular Cytogenetics. 14(1). 54–54. 11 indexed citations
4.
Khan, Abdul Waheed, Antonella Minelli, Annalisa Frattini, et al.. (2020). Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype. Molecular Cytogenetics. 13(1). 1–1. 2 indexed citations
5.
Valli, Roberto, Luciana Vinti, Annalisa Frattini, et al.. (2018). Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene. Molecular Cytogenetics. 11(1). 2–2. 3 indexed citations
6.
Radi, Orietta, Elisabetta Buscarini, Antonella Minelli, et al.. (2013). Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion in ACVRL1 Suggests the Causing Mechanism. Molecular Syndromology. 4(3). 119–124. 1 indexed citations
7.
Necchi, Vittorio, Antonella Minelli, Patrizia Sommi, et al.. (2012). Ubiquitin-proteasome-rich cytoplasmic structures in neutrophils of patients with Shwachman-Diamond syndrome. Haematologica. 97(7). 1057–1063. 10 indexed citations
8.
Minelli, Antonella, Andrea Guala, Gabriella Restagno, et al.. (2011). Mechanism of origin in two cases of chimerism. Open Journal of Pediatrics. 1(4). 79–86. 6 indexed citations
9.
Ciccocioppo, Rachele, Maria Ester Bernardo, Adele Sgarella, et al.. (2011). Autologous bone marrow-derived mesenchymal stromal cells in the treatment of fistulising Crohn's disease. Gut. 60(6). 788–798. 421 indexed citations breakdown →
10.
Gana, Simone, Laura Sainati, F. Poli, et al.. (2011). Shwachman-Diamond Syndrome and Type 1 Diabetes Mellitus: More Than a Chance Association?. Experimental and Clinical Endocrinology & Diabetes. 119(10). 610–612. 16 indexed citations
11.
Maserati, Emanuela, Roberto Valli, Antonella Minelli, et al.. (2009). The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman‐Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies. British Journal of Haematology. 145(2). 190–197. 42 indexed citations
12.
Minelli, Antonella, Emanuela Maserati, Elena Nicolis, et al.. (2009). The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome. Leukemia. 23(4). 708–711. 42 indexed citations
13.
Minelli, Antonella, Emanuela Maserati, Gabriele Rossi, et al.. (2004). Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies. Genes Chromosomes and Cancer. 40(3). 165–171. 18 indexed citations
14.
Dellavecchia, Claudia, Andrea Guala, Carla Olivieri, et al.. (1999). Early Onset of Gastric Carcinoma and Constitutional Deletion of 18p. Cancer Genetics and Cytogenetics. 113(1). 96–99. 12 indexed citations
15.
Minelli, Antonella, Giovanna Floridia, Elena Rossi, et al.. (1993). D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p). Human Genetics. 92(4). 391–396. 25 indexed citations
16.
Minelli, Antonella, M. Piantanida, Giuseppe Simoni, et al.. (1992). Prenatal diagnosis of metabolic diseases on chorionic villi obtained before the ninth week of pregnancy. Prenatal Diagnosis. 12(11). 959–963. 1 indexed citations
17.
Caufin, Daniele, et al.. (1991). Inv dup (8) (p21.1 → 22.1): further case report and a new hypothesis on the origin of the chromosome abnormality. Clinical Genetics. 39(1). 55–59. 26 indexed citations
18.
Sozzi, Gabriella, Monica Miozzo, Antonella Minelli, et al.. (1990). Involvement of the region 13q14 in a patient with adamantinoma of the long bones. Human Genetics. 85(5). 513–515. 14 indexed citations
19.
Minelli, Antonella, et al.. (1990). Gene dosage effect in acquired monosomy 7: Distinct behaviour of β‐glucuronidase and phosphoserine phosphatase. Genes Chromosomes and Cancer. 1(3). 216–220. 3 indexed citations
20.
Minelli, Antonella, Cesare Danesino, Francesco Lo Curto, et al.. (1988). First trimester prenatal diagnosis of Sanfilippo disease (MPSIII) type B. Prenatal Diagnosis. 8(1). 47–52. 5 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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