M. Piantanida

593 total citations
21 papers, 432 citations indexed

About

M. Piantanida is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, M. Piantanida has authored 21 papers receiving a total of 432 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in M. Piantanida's work include Genomic variations and chromosomal abnormalities (4 papers), Vascular Anomalies and Treatments (3 papers) and Acute Lymphoblastic Leukemia research (3 papers). M. Piantanida is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Vascular Anomalies and Treatments (3 papers) and Acute Lymphoblastic Leukemia research (3 papers). M. Piantanida collaborates with scholars based in Italy, Croatia and Argentina. M. Piantanida's co-authors include Elisabetta Buscarini, Cesare Danesino, L Buscarini, Giuseppe Civardi, Antonella Minelli, Claudia Dellavecchia, Orsetta Zuffardi, Antonio Rossi, M. Stasi and Giovanna Floridia and has published in prestigious journals such as The Journal of Immunology, Journal of Hepatology and Archives of Biochemistry and Biophysics.

In The Last Decade

M. Piantanida

21 papers receiving 418 citations

Peers

M. Piantanida

GENET

PRM

SURGE

J. Ganesan Malaysia

Olga Haus Poland

Н. П. Кулешов Russia

KA High United States

Tammy L. Edwards United States

EUGENE GOLDWASSER United States

W Liu United States

Jean Chiésa France

Gloria Lim Canada

Dustin L. Gable United States

J. Ganesan Malaysia

M. Piantanida

349 ×1.7

GENET

48 ×0.3

GENET

20 ×0.1

PRM

110 ×1.1

44 ×0.5

SURGE

Citations per year, relative to M. Piantanida M. Piantanida (= 1×) peers J. Ganesan

Countries citing papers authored by M. Piantanida

Since Specialization

Citations

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

Fields of papers citing papers by M. Piantanida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Piantanida

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Aricò, Maurizio, Claudia Dellavecchia, M. Piantanida, et al.. (1999). The breakpoints of a constitutional inversion of chromosome 9 associated with haemophagocytic lymphohistiocytosis are not linked to the disease gene. British Journal of Haematology. 104(1). 108–110. 2 indexed citations

Piantanida, M., Claudia Dellavecchia, Giovanna Floridia, et al.. (1997). Ataxic gait and mental retardation with absence of the paternal chromosome 8 and an idic(8)(p23.3): imprinting effect or nullisomy for distal 8p genes?. Human Genetics. 99(6). 766–771. 18 indexed citations

Buscarini, Elisabetta, Luigi Buscarini, Cesare Danesino, et al.. (1997). Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: Doppler sonographic screening in a large family. Journal of Hepatology. 26(1). 111–118. 70 indexed citations

Floridia, Giovanna, M. Piantanida, Antonella Minelli, et al.. (1996). The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.. PubMed. 58(4). 785–96. 95 indexed citations

Piantanida, M., Elisabetta Buscarini, Claudia Dellavecchia, et al.. (1996). Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.. Journal of Medical Genetics. 33(6). 441–443. 69 indexed citations

Piantanida, M., et al.. (1995). Effect of spirulina platensis on glucose, uric acid and cholesterol levels in the blood of rodents. 57(1). 93–96. 10 indexed citations

Buscarini, Elisabetta, et al.. (1994). Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: imaging findings.. American Journal of Roentgenology. 163(5). 1105–1110. 78 indexed citations

Piantanida, M., Alessandra Tiberti, Alessandro Plebani, Paola Martelli, & Cesare Danesino. (1993). Cerebro‐reno‐digital syndrome in two sibs. American Journal of Medical Genetics. 47(3). 420–422. 3 indexed citations

Andreis, C., et al.. (1993). Frequency of chromosomal aberrations after exposure to γ-radiation of human chorionic villi. Mutation Research/Environmental Mutagenesis and Related Subjects. 291(3). 213–216. 2 indexed citations

10.

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

11.

Buscaglia, M, et al.. (1992). Cyclophosphamide increases the frequency of sister chromatid exchange in direct preparations of human chorionic villi in the absence of supplementary enzymatic activation systems.. Journal of Medical Genetics. 29(2). 109–111. 7 indexed citations

12.

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

13.

Maraschio, P, et al.. (1990). Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivation. Human Genetics. 85(5). 491–4. 21 indexed citations

14.

Bardoni, Barbara, Giovanna Camerino, Silvana Guioli, et al.. (1989). Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl. Human Genetics. 84(1). 51–54. 14 indexed citations

15.

Pinelli, G, et al.. (1981). [Grisel's syndrome in childhood].. PubMed. 33(1). 39–41. 1 indexed citations

16.

Piantanida, M., et al.. (1955). A contribution to paper-strip chromatography of proteins. Archives of Biochemistry and Biophysics. 57(2). 334–339. 3 indexed citations

17.

Piantanida, M., et al.. (1955). Zur Kenntnis des Sandottergiftes: Elektrophoretische und chemische Charakterisierung der Hauptfraktionen. Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 299(Jahresband). 6–14. 10 indexed citations

18.

Piantanida, M., et al.. (1954). The Antigenic Composition of Ammodytes Viper Venom. The Journal of Immunology. 73(2). 115–119. 3 indexed citations

19.

Piantanida, M., et al.. (1953). Paper-strip chromatography of the proteinic components of ammodytes viper venom. Archives of Biochemistry and Biophysics. 46(1). 110–118. 5 indexed citations

20.

Piantanida, M., et al.. (1953). [The properties of Vipera ammodytes venom].. PubMed. 3. 207–20. 1 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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