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M. Lanciotti · SciRah

Researcher profile · Semantic Scholar

M. Lanciotti

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M. Lanciotti — researcher profile on SciRah

h-index: 22
Works: 112
Citations: 1,319

Most-cited papers

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia
E. Virts, A. Jankowska, C. Mackay, M. Glaas +28 more
2015Human Molecular Genetics76 citations Open access
Semantic Scholar
Homozygosis for (12) CA repeats in the first intron of the human IFN‐γ gene is significantly associated with the risk of aplastic anaemia in Caucasian population
C. Dufour, M. Capasso, J. Svahn, Agnese Marrone +11 more
2004British Journal of Haematology70 citations
Semantic Scholar
Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP).
A. Barone, A. Lucarelli, D. Onofrillo, F. Verzegnassi +27 more
2015Blood Cells, Molecules & Diseases64 citations
Semantic Scholar
The combination of γ-interferon and tumor necrosis factor causes a rapid and extensive differentiation of human neuroblastoma cells
M. Ponzoni, A. Casalaro, M. Lanciotti, P. Montaldo +1 more
199264 citations
Semantic Scholar
Digenic mutations in severe congenital neutropenia
M. Germeshausen, C. Zeidler, M. Stuhrmann, M. Lanciotti +2 more
2010Haematologica58 citations Open access
Semantic Scholar
Congenital and acquired neutropenias consensus guidelines on therapy and follow‐up in childhood from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato‐Oncologia Pediatrica)
F. Fioredda, M. Calvillo, S. Bonanomi, T. Coliva +15 more
2012American journal of hematology/oncology52 citations
Semantic Scholar
Congenital and acquired neutropenia consensus guidelines on diagnosis from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato‐Oncologia Pediatrica)
F. Fioredda, M. Calvillo, S. Bonanomi, T. Coliva +11 more
2011Pediatric Blood & Cancer52 citations Open access
Semantic Scholar
Genetic polymorphism of NAD(P)H:quinone oxidoreductase is associated with an increased risk of infant acute lymphoblastic leukemia without MLL gene rearrangements
M. Lanciotti, Carlo Dufour, L. Corral, P. Di Michele +10 more
2005Leukemia48 citations Open access
Semantic Scholar
Proteomic analysis of erythrocyte membranes by soft Immobiline gels combined with differential protein extraction.
M. Bruschi, C. Seppi, S. Arena, L. Musante +6 more
2005Journal of Proteome Research45 citations
Semantic Scholar
Accumulation of m-iodobenzylguanidine by neuroblastoma cells results from independent uptake and storage mechanisms.
P. Montaldo, M. Lanciotti, Antonella Casalaro, Paolo Cornaglia-Ferraris +1 more
1991Cancer Research41 citations
Semantic Scholar
Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia
A. Sherborne, K. Hemminki, Rajiv Kumar, C. Bartram +32 more
2011Haematologica40 citations Open access
Semantic Scholar
Prospective molecular monitoring of BCR/ABL transcript in children with Ph+ acute lymphoblastic leukaemia unravels differences in treatment response
G. Cazzaniga, M. Lanciotti, V. Rossi, D. Di Martino +6 more
2002British Journal of Haematology38 citations
Semantic Scholar
Genetic polymorphisms of CYP3A4, GSTT1, GSTM1, GSTP1 and NQO1 and the risk of acquired idiopathic aplastic anemia in Caucasian patients.
C. Dufour, J. Svahn, A. Bacigalupo, D. Longoni +7 more
2005Haematologica36 citations
Semantic Scholar
Changes in cytokine profile pre- and post-immunosuppression in acquired aplastic anemia
C. Dufour, E. Ferretti, F. Bagnasco, O. Burlando +14 more
2009Haematologica35 citations Open access
Semantic Scholar
Late-onset and long-lasting autoimmune neutropenia: an analysis from the Italian Neutropenia Registry.
F. Fioredda, G. Rotulo, P. Farruggia, F. Dagliano +29 more
2020Blood Advances29 citations Open access
Semantic Scholar
FAS‐mediated apoptosis impairment in patients with ALPS/ALPS‐like phenotype carrying variants on CASP10 gene
M. Miano, E. Cappelli, Agnese Pezzulla, R. Venè +17 more
2019British Journal of Haematology28 citations
Semantic Scholar
Negative staining of proteins in polyacrylamide gels with methyl trichloroacetate.
G. Candiano, Matteo Porotto, M. Lanciotti, G. Ghiggeri
1996Analytical Biochemistry28 citations
Semantic Scholar
Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis.
M. Lanciotti, P. Perutelli, A. Valetto, D. Di Martino +1 more
1997Haematologica25 citations
Semantic Scholar
Etiology, clinical outcome, and laboratory features in children with neutropenia: Analysis of 104 cases
G. Angelino, R. Caruso, P. D'Argenio, F. Carducci +7 more
2014Pediatric Allergy and Immunology24 citations Open access
Semantic Scholar
Underlying Inborn Errors of Immunity in Patients With Evans Syndrome and Multilineage Cytopenias: A Single-Centre Analysis
M. Miano, D. Guardo, A. Grossi, E. Palmisani +11 more
2022Frontiers in Immunology22 citations Open access
Semantic Scholar
Poikiloderma With Neutropenia: A Case Report and Review of the Literature
P. Farruggia, Stefania Indaco, C. Dufour, T. Lanza +5 more
2014Journal of pediatric hematology/oncology19 citations
Semantic Scholar
Genetic screening of children with marrow failure. The role of primary Immunodeficiencies
M. Miano, A. Grossi, G. Dell'Orso, M. Lanciotti +13 more
2021American journal of hematology/oncology18 citations Open access
Semantic Scholar
The combination of gamma-interferon and tumor necrosis factor causes a rapid and extensive differentiation of human neuroblastoma cells.
M. Ponzoni, A. Casalaro, M. Lanciotti, P. Montaldo +1 more
1992Cancer Research17 citations
Semantic Scholar
Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia
M. Lanciotti, Stefania Indaco, S. Bonanomi, T. Coliva +4 more
2010Haematologica16 citations Open access
Semantic Scholar
Pegfilgrastim in children with severe congenital neutropenia
F. Fioredda, M. Calvillo, M. Lanciotti, T. Lanza +6 more
2010Pediatric Blood & Cancer16 citations Open access
Semantic Scholar
Targeted NGS Yields Plentiful Ultra-Rare Variants in Inborn Errors of Immunity Patients
A. Grossi, M. Miano, M. Lanciotti, F. Fioredda +10 more
2021Genes15 citations Open access
Semantic Scholar
Clinical features and therapeutic challenges of cytopenias belonging to alps and alps‐related (ARS) phenotype
E. Palmisani, M. Miano, C. Micalizzi, M. Calvillo +10 more
2019British Journal of Haematology12 citations
Semantic Scholar
Possible role of toll‐like receptor 9 polymorphism in chemotherapy‐related invasive mold infections in children with hematological malignancies
M. Lanciotti, S. Pigullo, T. Lanza, C. Dufour +2 more
2008Pediatric Blood & Cancer12 citations
Semantic Scholar
Human Fanconi A cells are susceptible to TRAIL‐induced apoptosis
S. Pigullo, E. Ferretti, M. Lanciotti, M. Bruschi +6 more
2007British Journal of Haematology12 citations
Semantic Scholar
The polymorphisms −318C>T in the promoter and 49A>G in exon 1 of CTLA4 and the risk of aplastic anemia in a Caucasian population
J. Svahn, M. Capasso, M. Lanciotti, Agnese Marrone +16 more
2005Bone Marrow Transplantation12 citations
Semantic Scholar
Genotypes of the glutathione S-transferase superfamily do not correlate with outcome of childhood acute lymphoblastic leukemia
A. Sala, M. Lanciotti, M. Valsecchi, Paola di Michele +5 more
2003Leukemia12 citations
Semantic Scholar
Compound heterozygosity for two new TERT mutations in a patient with aplastic anemia
A. Aspesi, Stefano Vallero, A. Rocci, E. Pavesi +3 more
2010Pediatric Blood & Cancer11 citations
Semantic Scholar
Are genotypes of glutathione S-transferase superfamily a risk factor for childhood acute lymphoblastic leukemia? Results of an Italian case–control study
Simona Pigullo, Riccardo Haupt, Carlo Dufour, P. Di Michele +5 more
2007Leukemia11 citations
Semantic Scholar
Association of cytogenetic abnormalities with detection of BCR‐ABL fusion transcripts in children with T‐lineage lymphoproliferative diseases (T‐ALL and T‐NHL)
L. Lo Nigro, L. Sainati, E. Mirabile, M. Lanciotti +3 more
2004Pediatric Blood & Cancer11 citations
Semantic Scholar
A combined evaluation of biochemical and morphological changes during human neuroblastoma cell differentiation
M. Lanciotti, P. Montaldo, S. Folghera, Enrico Lucarelli +2 more
1992Cellular and molecular neurobiology11 citations
Semantic Scholar
Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?
E. Palmisani, M. Miano, A. Grossi, M. Lanciotti +25 more
2022HemaSphere10 citations Open access
Semantic Scholar
Lethal sepsis and malignant transformation in severe congenital neutropenia: Report from the Italian Neutropenia Registry
F. Fioredda, M. Calvillo, M. Lanciotti, M. Cefalo +18 more
2015Pediatric Blood & Cancer10 citations
Semantic Scholar
Clinical heterogeneity in a family with DKC1 mutation, dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome in first cousins
C. Olivieri, A. Mondino, M. Chinello, A. Risso +3 more
2017Pediatric Reports9 citations Open access
Semantic Scholar
Long-term use of pegfilgrastim in children with severe congenital neutropenia: clinical and pharmacokinetic data.
F. Fioredda, T. Lanza, F. Gallicola, F. Riccardi +6 more
2016Blood9 citations
Semantic Scholar
NOLA1 gene mutations in acquired aplastic anemia
S. Pigullo, E. Pavesi, I. Dianzani, G. Santamaria +9 more
2009Pediatric Blood & Cancer9 citations
Semantic Scholar
Severe congenital neutropenia: a negative synergistic effect of multiple mutations of ELANE (ELA2) gene
M. Lanciotti, G. Caridi, C. Rosano, S. Pigullo +2 more
2009British Journal of Haematology9 citations Open access
Semantic Scholar
Infection risk in patients with autoimmune cytopenias and immune dysregulation treated with mycophenolate mofetil and sirolimus
Mattia Comella, E. Palmisani, M. Mariani, G. Dell'Orso +13 more
2024Frontiers in Immunology7 citations Open access
Semantic Scholar
Mutational analysis of ribosomal proteins in a cohort of pediatric patients with T-cell acute lymphoblastic leukemia reveals Q123R, a novel mutation in RPL10
Lorenza Bacci, V. Indio, G. Rambaldelli, C. Bugarin +10 more
2022Frontiers in Genetics7 citations Open access
Semantic Scholar
Non-identical twin sisters concordant for Langerhans cell histiocytosis and discordant for secondary acute promyelocytic leukemia.
C. Dufour, M. Lanciotti, C. Micalizzi, A. Valetto +1 more
2001Medical and Pediatric Oncology7 citations
Semantic Scholar
Glutathione S-transferase polymorphisms and susceptibility to neuroblastoma
M. Lanciotti, S. Coco, Paola Di Michele, R. Haupt +5 more
2005Pharmacogenetics & Genomics6 citations
Semantic Scholar
Late‐onset and long‐lasting neutropenias in the young: A new entity anticipating immune‐dysregulation disorders
F. Fioredda, A. Beccaria, P. Casartelli, E. Turrini +21 more
2024American journal of hematology/oncology5 citations
Semantic Scholar
γ-interferon, retinoic acid, and cytosine arabinoside induce neuroblastoma differentiation by different mechanisms
M. Ponzoni, M. Lanciotti, P. Montaldo, Paolo Cornaglia-Ferraris
1991Cellular and molecular neurobiology5 citations
Semantic Scholar
TACI variants as underlying condition in autoimmune neutropenia: Description of four cases
F. Fioredda, A. Beccaria, E. Turrini, P. Casartelli +9 more
2022American journal of hematology/oncology4 citations Open access
Semantic Scholar
Ser245Tyr TINF2 mutation in a long-term survivor after a second myeloablative SCT following late graft failure for Aplastic Anaemia.
M. Miano, M. Lanciotti, S. Giardino, C. Dufour
2015Blood Cells, Molecules & Diseases4 citations
Semantic Scholar
Chromosomal locus 19p13 as potential hotspot for aberrant gene expression in relapsed paediatric acute lymphoblastic leukaemia
M. Lanciotti, M. d'Apolito, P. Paolucci, C. Dufour
2006British Journal of Haematology3 citations Open access
Semantic Scholar

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F. Fioredda×16
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