Elisa Tassano

1.2k total citations
54 papers, 596 citations indexed

About

Elisa Tassano is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Elisa Tassano has authored 54 papers receiving a total of 596 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 32 papers in Molecular Biology and 6 papers in Hematology. Recurrent topics in Elisa Tassano's work include Genomic variations and chromosomal abnormalities (29 papers), Genetics and Neurodevelopmental Disorders (15 papers) and Congenital heart defects research (13 papers). Elisa Tassano is often cited by papers focused on Genomic variations and chromosomal abnormalities (29 papers), Genetics and Neurodevelopmental Disorders (15 papers) and Congenital heart defects research (13 papers). Elisa Tassano collaborates with scholars based in Italy, Switzerland and Russia. Elisa Tassano's co-authors include Giorgio Gimelli, Cristina Cuoco, Stefania Gimelli, Cristina Morerio, Patrizia Ronchetto, Claudio Panarello, Valeria Capra, Margherita Lerone, Maja Di Rocco and Mariasavina Severino and has published in prestigious journals such as PLoS ONE, Gene and Bone.

In The Last Decade

Elisa Tassano

51 papers receiving 554 citations

Peers

Countries citing papers authored by Elisa Tassano

Since Specialization

Citations

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

Fields of papers citing papers by Elisa Tassano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Tassano

This figure shows the co-authorship network connecting the top 25 collaborators of Elisa Tassano. A scholar is included among the top collaborators of Elisa Tassano 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 Elisa Tassano. Elisa Tassano 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

#	Work	Indexed citations
1	Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness 2022 ·Cytogenetic and Genome Research ·Elisa Tassano, Sarà Uccella, Patrizia Ronchetto, (unknown), Silvia Viaggi, Maria Margherita Mancardi, Luca A. Ramenghi, Alessandra Murri, (unknown), Giorgio Gimelli, Cristina Morerio, Michela Malacarne, Domenico Coviello	0
2	17q23.3 de novo microdeletion involving only TANC2 gene: A new case 2020 ·European Journal of Medical Genetics ·Elisa Tassano, Andrea Accogli, Patrizia Ronchetto, Domenico Tortora, (unknown), Giorgio Gimelli, Maria Margherita Mancardi, Michela Malacarne, Domenico Coviello	5
3	Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability 2018 ·European Journal of Medical Genetics ·(unknown), Elisa Tassano, (unknown), Maria Teresa Divizia, Patrizia Ronchetto, (unknown), Margherita Lerone, Livia Pisciotta, Maria Margherita Mancardi, E. Veneselli, Aldamaria Puliti	13
4	Intragenic Microdeletion of <b><i>ULK4</i></b> and Partial Microduplication of <b><i>BRWD3</i></b> in Siblings with Neuropsychiatric Features and Obesity 2018 ·Cytogenetic and Genome Research ·Elisa Tassano, Sarà Uccella, Thea Giacomini, Pasquale Striano, Mariasavina Severino, (unknown), Giorgio Gimelli, Patrizia Ronchetto	10
5	Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number Variations 2018 ·Cytogenetic and Genome Research ·Elisa Tassano, Sarà Uccella, Thea Giacomini, Mariasavina Severino, (unknown), Giorgio Gimelli, Patrizia Ronchetto	6
6	Interstitial 11q24 deletion: a new case and review of the literature 2016 ·Journal of Applied Genetics ·Elisa Tassano, (unknown), Alberto Cánepa, (unknown), (unknown), Giorgio Gimelli, Cristina Cuoco	6
7	Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion 2015 ·American Journal of Medical Genetics Part A ·Elisa Tassano, Vidhya Jagannathan, Cord Drögemüller, (unknown), Marjo K. Hytönen, Mariasavina Severino, Stefania Gimelli, Cristina Cuoco, Maja Di Rocco, (unknown), Andrew K. Groves, Tosso Leeb, Giorgio Gimelli	26
8	Concomitant deletion of chromosome 16p13.11 and triplication of chromosome 19p13.3 in a child with developmental disorders, intellectual disability, and epilepsy 2015 ·Molecular Cytogenetics ·Elisa Tassano, Lucia De Santis, (unknown), Stefano Parmigiani, (unknown), (unknown), Giorgio Gimelli, Cristina Cuoco	4
9	Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a low-frequency noncoding RBM8A SNP: a new familial case 2015 ·Molecular Cytogenetics ·Elisa Tassano, Stefania Gimelli, Maria Teresa Divizia, Margherita Lerone, (unknown), Aldamaria Puliti, Giorgio Gimelli	13
10	Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion 2015 ·Molecular Cytogenetics ·Elisa Tassano, Marisol Mirabelli-Badenier, Edvige Veneselli, Aldamaria Puliti, Margherita Lerone, (unknown), Giovanni Morana, (unknown), Giorgio Gimelli, Cristina Cuoco	14
11	Clinical and molecular delineation of a 16p13.2p13.13 microduplication 2015 ·European Journal of Medical Genetics ·Elisa Tassano, M. G. Alpigiani, Andrea Calcagno, (unknown), (unknown), (unknown), Cristina Cuoco, Giorgio Gimelli	5
12	Constitutional chromosomal events at 22q11 and 15q26 in a child with a pilocytic astrocytoma of the spinal cord 2014 ·Molecular Cytogenetics ·Samantha Mascelli, Mariasavina Severino, Alessandro Raso, Paolo Nozza, Elisa Tassano, Giovanni Morana, Patrizia De Marco, Elisa Merello, Claudia Milanaccio, Marco Pavanello, Andrea Rossi, Armando Cama, Maria Luisa Garrè, Valeria Capra	2
13	Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1 2013 ·American Journal of Medical Genetics Part A ·Valeria Capra, Mariasavina Severino, Andrea Rossi, Paolo Nozza, Chiara Doneda, (unknown), Marco Pavanello, (unknown), Giorgio Gimelli, Elisa Tassano, E. Di Battista	9
14	Parental Imbalances Involving Chromosomes 15q and 22q May Predispose to the Formation of De Novo Pathogenic Microdeletions and Microduplications in the Offspring 2013 ·PLoS ONE ·Valeria Capra, Samantha Mascelli, Maria Luisa Garrè, Paolo Nozza, (unknown), (unknown), Frédérique Sloan‐Béna, Stefania Gimelli, Cristina Cuoco, Giorgio Gimelli, Elisa Tassano	5
15	Interstitial 2q24.3 deletion including SCN2A and SCN3A genes in a patient with autistic features, psychomotor delay, microcephaly and no history of seizures 2013 ·Gene ·(unknown), Cristina Cuoco, (unknown), Giorgio Gimelli, Elisa Tassano	12
16	New recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of short arm of chromosome 6 2012 ·Leukemia & lymphoma ·Elisa Tassano, (unknown), Roberto Valli, Concetta Micalizzi, Cristina Cuoco, Emanuela Maserati, Francesco Pasquali, Cristina Morerio	1
17	Monosomal complex karyotype in pediatric mixed phenotype acute leukemia 2011 ·Cancer Genetics ·Elisa Tassano, (unknown), Concetta Micalizzi, Francesca Scuderi, Cristina Cuoco, Cristina Morerio	2
18	Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma 2010 ·Cancer Genetics and Cytogenetics ·Elisa Tassano, Angela Rita Sementa, (unknown), Alberto Garaventa, Claudio Panarello, Cristina Morerio	4
19	MLL–MLLT10 fusion gene in pediatric acute megakaryoblastic leukemia 2005 ·Leukemia Research ·Cristina Morerio, (unknown), Elisa Tassano, Cristina Rosanda, Claudio Panarello	10
20	t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia 2004 ·Leukemia Research ·Cristina Morerio, Maura Acquila, Cristina Rosanda, (unknown), Elisa Tassano, Concetta Micalizzi, Claudio Panarello	23

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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