Maria Luisa Tenchini

2.1k total citations
74 papers, 1.6k citations indexed

About

Maria Luisa Tenchini is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Hematology. According to data from OpenAlex, Maria Luisa Tenchini has authored 74 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 18 papers in Pulmonary and Respiratory Medicine and 17 papers in Hematology. Recurrent topics in Maria Luisa Tenchini's work include Blood properties and coagulation (18 papers), Blood Coagulation and Thrombosis Mechanisms (11 papers) and Neuroscience and Neuropharmacology Research (11 papers). Maria Luisa Tenchini is often cited by papers focused on Blood properties and coagulation (18 papers), Blood Coagulation and Thrombosis Mechanisms (11 papers) and Neuroscience and Neuropharmacology Research (11 papers). Maria Luisa Tenchini collaborates with scholars based in Italy, United Kingdom and Germany. Maria Luisa Tenchini's co-authors include Stefano Duga, Rosanna Asselta, Massimo Malcovati, Luigi Ferini‐Strambi, Romina Combi, Flora Peyvandi, Pier Mannuccio Mannucci, Silvia Spena, L. Dalpr� and Elena Santagostino and has published in prestigious journals such as Nucleic Acids Research, Blood and Annals of Neurology.

In The Last Decade

Maria Luisa Tenchini

74 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maria Luisa Tenchini Italy 24 555 407 354 252 209 74 1.6k
J F Bach France 18 795 1.4× 122 0.3× 148 0.4× 193 0.8× 143 0.7× 38 3.0k
Ayumi Kitano United States 18 842 1.5× 353 0.9× 62 0.2× 86 0.3× 167 0.8× 30 1.6k
John G. Gartner Canada 19 262 0.5× 293 0.7× 78 0.2× 401 1.6× 97 0.5× 52 1.5k
Irene E. Zohn United States 22 1.3k 2.4× 267 0.7× 128 0.4× 110 0.4× 117 0.6× 42 2.0k
Mihoko Yamamoto Brazil 24 493 0.9× 371 0.9× 140 0.4× 78 0.3× 140 0.7× 104 1.8k
Asbjørg Stray‐Pedersen Norway 22 516 0.9× 146 0.4× 118 0.3× 229 0.9× 69 0.3× 55 1.9k
C. Panzeri Italy 16 1.1k 2.0× 113 0.3× 66 0.2× 277 1.1× 151 0.7× 20 2.0k
Anthony J. Bakker Australia 22 778 1.4× 256 0.6× 144 0.4× 252 1.0× 447 2.1× 50 1.8k
Tanya Lehky United States 21 566 1.0× 211 0.5× 115 0.3× 336 1.3× 259 1.2× 57 2.2k
Ann Rearden United States 18 440 0.8× 204 0.5× 53 0.1× 71 0.3× 215 1.0× 47 1.1k

Countries citing papers authored by Maria Luisa Tenchini

Since Specialization
Citations

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

Fields of papers citing papers by Maria Luisa Tenchini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Luisa Tenchini. 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 Maria Luisa Tenchini. The network helps show where Maria Luisa Tenchini may publish in the future.

Co-authorship network of co-authors of Maria Luisa Tenchini

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Luisa Tenchini. A scholar is included among the top collaborators of Maria Luisa Tenchini 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 Maria Luisa Tenchini. Maria Luisa Tenchini 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.
Combi, Romina, Daniele Grioni, Serena Redaelli, et al.. (2009). Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy. Brain Research Bulletin. 79(2). 89–96. 13 indexed citations
2.
Combi, Romina, Luigi Ferini‐Strambi, & Maria Luisa Tenchini. (2008). CHRNA2 mutations are rare in the NFLE population: Evaluation of a large cohort of Italian patients. Sleep Medicine. 10(1). 139–142. 16 indexed citations
3.
Platé, Manuela, Rosanna Asselta, Silvia Spena, et al.. (2008). Congenital hypofibrinogenemia: Characterization of two missense mutations affecting fibrinogen assembly and secretion. Blood Cells Molecules and Diseases. 41(3). 292–297. 12 indexed citations
4.
Asselta, Rosanna, Stefano Duga, Flora Peyvandi, et al.. (2006). Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain gene.. PubMed. 91(5). 628–33. 15 indexed citations
5.
Spena, Silvia, Maria Luisa Tenchini, & Emanuele Buratti. (2006). Cryptic splice site usage in exon 7 of the human fibrinogen Bβ-chain gene is regulated by a naturally silent SF2/ASF binding site within this exon. RNA. 12(6). 948–958. 17 indexed citations
6.
Combi, Romina, Leda Dalprà, Luigi Ferini‐Strambi, & Maria Luisa Tenchini. (2005). Frontal lobe epilepsy and mutations of the corticotropin‐releasing hormone gene. Annals of Neurology. 58(6). 899–904. 36 indexed citations
7.
Soldà, Giulia, Stefano Duga, Diego Fornasari, et al.. (2005). In vivo RNA–RNA duplexes from human α3 and α5 nicotinic receptor subunit mRNAs. Gene. 345(2). 155–164. 21 indexed citations
8.
Asselta, Rosanna, Maria Luisa Tenchini, & Stefano Duga. (2005). Inherited defects of coagulation factor V: the hemorrhagic side. Journal of Thrombosis and Haemostasis. 4(1). 26–34. 58 indexed citations
9.
Spena, Silvia, Stefano Duga, Rosanna Asselta, et al.. (2004). Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aα-chain gene. European Journal of Human Genetics. 12(11). 891–898. 43 indexed citations
10.
Combi, Romina, L. Dalpr�, Maria Luisa Tenchini, & Luigi Ferini‐Strambi. (2004). Autosomal dominant nocturnal frontal lobe epilepsy. Journal of Neurology. 251(8). 923–34. 169 indexed citations
11.
Combi, Romina, Leda Dalprà, Massimo Malcovati, et al.. (2004). Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy. Brain Research Bulletin. 63(5). 353–359. 11 indexed citations
12.
Asselta, Rosanna, Stefano Duga, Massimo Malcovati, et al.. (2003). Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain. Journal of Thrombosis and Haemostasis. 1(6). 1237–1244. 18 indexed citations
13.
Duga, Stefano, Rosanna Asselta, & Maria Luisa Tenchini. (2003). Coagulation factor V. The International Journal of Biochemistry & Cell Biology. 36(8). 1393–1399. 43 indexed citations
14.
Bonati, Maria Teresa, Romina Combi, Rosanna Asselta, et al.. (2002). Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families. Journal of Neurology. 249(8). 967–974. 22 indexed citations
15.
Duga, Stefano, Giulia Soldà, Rosanna Asselta, et al.. (2001). Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms. Journal of Human Genetics. 46(11). 640–648. 23 indexed citations
16.
Asselta, Rosanna, Stefano Duga, Silvia Spena, et al.. (2001). Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen Aα-chain gene are not associated with the decay of the mutant mRNAs. Blood. 98(13). 3685–3692. 63 indexed citations
17.
Ferini‐Strambi, Luigi, A. Oldani, Marco Zucconi, et al.. (2000). Nocturnal frontal lobe epilepsy: Sporadic versus familial cases. 2(1). 22–25. 1 indexed citations
18.
Bonati, Maria Teresa, Rosanna Asselta, Stefano Duga, et al.. (2000). Refined mapping of CHRNA3/A5/B4 gene cluster and its implications in ADNFLE. Neuroreport. 11(10). 2097–2101. 9 indexed citations
19.
Malcovati, Massimo & Maria Luisa Tenchini. (1991). Cell density affects spreading and clustering, but not attachment, of human keratinocytes in serum-free medium. Journal of Cell Science. 99(2). 387–395. 10 indexed citations
20.
Valle, Giuliano Della, et al.. (1981). Comparison between a specific rRNA inhibitor (MPB) and X-ray effects on satellite associations in human chromosomes. Mutation Research/Environmental Mutagenesis and Related Subjects. 85(4). 253–253. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by J F Bach Breakdown of academic impact, for papers by Ayumi Kitano Breakdown of academic impact, for papers by John G. Gartner Breakdown of academic impact, for papers by Irene E. Zohn Breakdown of academic impact, for papers by Mihoko Yamamoto Breakdown of academic impact, for papers by Asbjørg Stray‐Pedersen Breakdown of academic impact, for papers by C. Panzeri Breakdown of academic impact, for papers by Anthony J. Bakker Breakdown of academic impact, for papers by Tanya Lehky Breakdown of academic impact, for papers by Ann Rearden
Rankless by CCL
2026