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E. Tassano · SciRah

Researcher profile · Semantic Scholar

E. Tassano

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E. Tassano — researcher profile on SciRah

h-index: 19
Works: 65
Citations: 996

Most-cited papers

Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration
V. Shashi, M. Magiera, D. Klein, M. Zaki +56 more
2018EMBO Journal118 citations Open access
Semantic Scholar
PLAG1-HAS2 fusion in lipoblastoma with masked 8q intrachromosomal rearrangement.
C. Morerio, A. Rapella, C. Rosanda, E. Tassano +3 more
2005Cancer Genetics and Cytogenetics47 citations
Semantic Scholar
Identification of a rare 17p13.3 duplication including the BHLHA9 and YWHAE genes in a family with developmental delay and behavioural problems
V. Capra, M. Mirabelli-Badenier, M. Stagnaro, A. Rossi +3 more
2012BMC Medical Genetics38 citations Open access
Semantic Scholar
t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia.
C. Morerio, M. Acquila, C. Rosanda, A. Rapella +3 more
2005Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis38 citations
Semantic Scholar
Congenital Aural Atresia Associated With Agenesis of Internal Carotid Artery in a Girl With a FOXI3 Deletion
E. Tassano, V. Jagannathan, C. Drögemüller, Massimiliano Leoni +9 more
2015American Journal of Medical Genetics. Part A37 citations Open access
Semantic Scholar
De novo deletion of chromosome 11q12.3 in monozygotic twins affected by Poland Syndrome
C. Vaccari, M. Romanini, I. Musante, E. Tassano +7 more
2014BMC Medical Genetics36 citations Open access
Semantic Scholar
RORB gene and 9q21.13 microdeletion: report on a patient with epilepsy and mild intellectual disability.
M. G. Baglietto, G. Caridi, G. Gimelli, M. Mancardi +4 more
2014European Journal of Medical Genetics34 citations
Semantic Scholar
Genotype-Phenotype Correlation of 2q37 Deletions Including NPPC Gene Associated with Skeletal Malformations
E. Tassano, Jens Buttgereit, M. Bader, M. Lerone +7 more
2013PLoS ONE34 citations Open access
Semantic Scholar
MicroRNA‐125b‐1 and BLID upregulation resulting from a novel IGH translocation in childhood B‐Cell precursor acute lymphoblastic leukemia
E. Tassano, M. Acquila, E. Tavella, C. Micalizzi +2 more
2010Genes, Chromosomes and Cancer34 citations
Semantic Scholar
Differential diagnosis of lipoma‐like lipoblastoma
C. Morerio, P. Nozza, E. Tassano, C. Rosanda +3 more
2009Pediatric Blood & Cancer32 citations Open access
Semantic Scholar
Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders
S. Gimelli, V. Capra, M. Dirocco, Massimiliano Leoni +6 more
2014Molecular Cytogenetics31 citations Open access
Semantic Scholar
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)
E. Maserati, C. Panarello, C. Morerio, Roberto Valli +10 more
2008Haematologica27 citations Open access
Semantic Scholar
Assessment of copy number variations in 120 patients with Poland syndrome
C. Vaccari, E. Tassano, M. Torre, S. Gimelli +14 more
2016BMC Medical Genetics26 citations Open access
Semantic Scholar
Heterozygous deletion of CHL1 gene: detailed array-CGH and clinical characterization of a new case and review of the literature.
E. Tassano, R. Biancheri, L. Denegri, Simona Porta +4 more
2014European Journal of Medical Genetics24 citations
Semantic Scholar
Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs
Martina Servetti, L. Pisciotta, E. Tassano, M. Cerminara +7 more
2021Frontiers in Genetics23 citations Open access
Semantic Scholar
De novo 13q31.1–q32.1 interstitial deletion encompassing the miR‐17‐92 cluster in a patient with Feingold syndrome‐2
E. Tassano, M. Dirocco, S. Signa, G. Gimelli
2013American Journal of Medical Genetics. Part A23 citations
Semantic Scholar
Clinical and Molecular Cytogenetic Characterization of a de novo Interstitial 1p31.1p31.3 Deletion in a Boy with Moderate Intellectual Disability and Severe Language Impairment
E. Tassano, Alessandra Gamucci, M. E. Celle, P. Ronchetto +2 more
2015Cytogenetic and Genome Research21 citations
Semantic Scholar
Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion
E. Tassano, M. Mirabelli-Badenier, E. Veneselli, A. Puliti +6 more
2015Molecular Cytogenetics20 citations Open access
Semantic Scholar
Interstitial 9p24.3 deletion involving only DOCK8 and KANK1 genes in two patients with non-overlapping phenotypic traits.
E. Tassano, A. Accogli, M. Pavanello, C. Bruno +3 more
2016European Journal of Medical Genetics19 citations
Semantic Scholar
Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1
V. Capra, M. Severino, A. Rossi, P. Nozza +7 more
2014American Journal of Medical Genetics. Part A18 citations
Semantic Scholar
Cytogenetic characterization of a fibrous hamartoma of infancy with complex translocations.
E. Tassano, P. Nozza, E. Tavella, A. Garaventa +2 more
2010Cancer Genetics and Cytogenetics18 citations
Semantic Scholar
Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability.
G. Rosti, E. Tassano, Simone Bossi, M. T. Divizia +7 more
2019European Journal of Medical Genetics17 citations
Semantic Scholar
3q29 microduplication syndrome: Description of two new cases and delineation of the minimal critical region.
E. Tassano, S. Uccella, Thea Giacomini, M. Severino +6 more
2018European Journal of Medical Genetics17 citations
Semantic Scholar
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
E. Tassano, S. Gimelli, M. T. Divizia, M. Lerone +3 more
2015Molecular Cytogenetics17 citations Open access
Semantic Scholar
Inversion (11)(p15q22) with NUP98-DDX10 fusion gene in pediatric acute myeloid leukemia.
C. Morerio, M. Acquila, A. Rapella, E. Tassano +2 more
2006Cancer Genetics and Cytogenetics17 citations
Semantic Scholar
MLL-MLLT10 fusion gene in pediatric acute megakaryoblastic leukemia.
C. Morerio, A. Rapella, E. Tassano, C. Rosanda +1 more
2005Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis17 citations
Semantic Scholar
Association of achondroplasia with sagittal synostosis and scaphocephaly in two patients, an underestimated condition?
A. Accogli, M. Pacetti, P. Fiaschi, M. Pavanello +7 more
2015American Journal of Medical Genetics. Part A16 citations
Semantic Scholar
Familial ROBO1 deletion associated with ectopic posterior pituitary, duplication of the pituitary stalk and anterior pituitary hypoplasia
M. Scala, A. Accogli, A. Allegri, E. Tassano +4 more
2019Journal of Pediatric Endocrinology & Metabolism (JPEM)13 citations
Semantic Scholar
Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number Variations
E. Tassano, S. Uccella, Thea Giacomini, M. Severino +3 more
2018Cytogenetic and Genome Research13 citations
Semantic Scholar
Interstitial 2q24.3 deletion including SCN2A and SCN3A genes in a patient with autistic features, psychomotor delay, microcephaly and no history of seizures.
M. E. Celle, C. Cuoco, Simona Porta, G. Gimelli +1 more
2013Gene13 citations
Semantic Scholar
Identification of an Interstitial 18p11.32-p11.31 Duplication Including the EMILIN2 Gene in a Family with Porokeratosis of Mibelli
C. Occella, D. Bleidl, P. Nozza, S. Mascelli +4 more
2013PLoS ONE13 citations Open access
Semantic Scholar
Intragenic Microdeletion of ULK4 and Partial Microduplication of BRWD3 in Siblings with Neuropsychiatric Features and Obesity
E. Tassano, S. Uccella, Thea Giacomini, P. Striano +4 more
2018Cytogenetic and Genome Research12 citations
Semantic Scholar
Interstitial deletion 14q31.1q31.3 transmitted from a mother to her daughter, both with features of hemifacial microsomia
S. Gimelli, C. Cuoco, P. Ronchetto, G. Gimelli +1 more
2013Journal of Applied Genetics12 citations
Semantic Scholar
Interstitial de novo 18q22.3q23 deletion: clinical, neuroradiological and molecular characterization of a new case and review of the literature
E. Tassano, M. Severino, S. Rosina, R. Papa +4 more
2016Molecular Cytogenetics11 citations Open access
Semantic Scholar
A rare 3q13.31 microdeletion including GAP43 and LSAMP genes
S. Gimelli, Massimiliano Leoni, M. Dirocco, G. Caridi +4 more
2013Molecular Cytogenetics11 citations Open access
Semantic Scholar
Gain of 1q in pediatric myelodysplastic syndromes.
C. Morerio, A. Rapella, E. Tassano, E. Lanino +3 more
2006Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis9 citations
Semantic Scholar
‘Distal 16p12.2 microdeletion’ in a patient with autosomal recessive deafness-22
E. Tassano, P. Ronchetto, A. Calcagno, Patrizia Fiorio +3 more
2019Journal Genetika8 citations
Semantic Scholar
Recurrent microdeletion 2q21.1: Report on a new patient with neurological disorders
S. Gimelli, E. Stathaki, F. Béna, Massimiliano Leoni +3 more
2014American Journal of Medical Genetics. Part A8 citations
Semantic Scholar
1p31.1 microdeletion including only NEGR1 gene in two patients.
E. Tassano, S. Uccella, Thea Giacomini, Patrizia Fiorio +5 more
2020European Journal of Medical Genetics7 citations
Semantic Scholar
Concomitant deletion of chromosome 16p13.11 and triplication of chromosome 19p13.3 in a child with developmental disorders, intellectual disability, and epilepsy
E. Tassano, L. De Santis, M. F. Corona, S. Parmigiani +4 more
2015Molecular Cytogenetics7 citations Open access
Semantic Scholar
Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.
E. Tassano, A. Sementa, E. Tavella, A. Garaventa +2 more
2010Cancer Genetics and Cytogenetics7 citations
Semantic Scholar
Differential diagnosis of congenital fibrosarcoma.
C. Morerio, A. Rapella, C. Rosanda, E. Tassano +3 more
2004Cancer Genetics and Cytogenetics7 citations
Semantic Scholar
Interstitial 11q24 deletion: a new case and review of the literature
E. Tassano, Sara Janis, A. Canepa, E. Zanotto +3 more
2016Journal of Applied Genetics6 citations
Semantic Scholar
Parental Imbalances Involving Chromosomes 15q and 22q May Predispose to the Formation of De Novo Pathogenic Microdeletions and Microduplications in the Offspring
V. Capra, S. Mascelli, M. Garrè, P. Nozza +7 more
2013PLoS ONE6 citations Open access
Semantic Scholar
Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruption.
E. Tassano, P. Ronchetto, M. Severino, M. T. Divizia +7 more
2021Bone4 citations
Semantic Scholar
Clinico-radiological and molecular characterization of a child with ring chromosome 2 presenting growth failure, microcephaly, kidney and brain malformations
M. Severino, A. Accogli, G. Gimelli, A. Rossi +5 more
2015Molecular Cytogenetics4 citations Open access
Semantic Scholar
Constitutional chromosomal events at 22q11 and 15q26 in a child with a pilocytic astrocytoma of the spinal cord
S. Mascelli, M. Severino, A. Raso, P. Nozza +10 more
2014Molecular Cytogenetics4 citations Open access
Semantic Scholar
Phenotypic and genetic characterization of a patient with a de novo interstitial 14q24.1q24.3 deletion
E. Tassano, A. Accogli, S. Panigada, P. Ronchetto +2 more
2014Molecular Cytogenetics4 citations Open access
Semantic Scholar
New recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of short arm of chromosome 6
E. Tassano, E. Tavella, Roberto Valli, C. Micalizzi +4 more
2012Leukemia and Lymphoma4 citations Open access
Semantic Scholar
Expanding the phenotype associated with interstitial 6p25.1p24.3 microdeletion: a new case and review of the literature
E. Tassano, S. Uccella, M. Severino, Thea Giacomini +6 more
2021Journal Genetika3 citations
Semantic Scholar

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C. Cuoco×18
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P. Ronchetto×14
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C. Morerio×13
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S. Gimelli — researcher profile on SciRah

C. Panarello×11

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M. Severino×10

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M. Severino — researcher profile on SciRah

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V. Capra — researcher profile on SciRah

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M. Lerone — researcher profile on SciRah

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E. Tavella — researcher profile on SciRah