Francesco Pasquali

Medicine · Health Sciences

31h-index2.8kcitations170works1.02yr avg
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Research Topics

Acute Myeloid Leukemia Research(50), Blood disorders and treatments(41), Chronic Myeloid Leukemia Treatments(28), Genomic variations and chromosomal abnormalities(26), Immunodeficiency and Autoimmune Disorders(24)

Publications169 total

A Portable and Low‐Cost Single Board Computer‐Based Spectrophotometric Platform for Optical Analysis in the UV and Visible Range
Advanced Sensor Research·2025· 1 citedOpen Access
Donor Cell Acute Myeloid Leukemia after Hematopoietic Stem Cell Transplantation for Chronic Granulomatous Disease: A Case Report and Literature Review
Genes·2023· 1 citedOpen Access
Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman–Diamond Syndrome
Frontiers in Genetics·2022· 2 citedOpen Access
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations
Molecular Cytogenetics·2021· 14 citedOpen Access
Publisher Correction: Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes
Nature Medicine·2021· 4 citedOpen Access
Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes
Nature Medicine·2021· 161 citedOpen Access
Association of unbalanced translocation der(1;7) with germline GATA2 mutations
Blood·2021· 20 citedOpen Access
Sensing Optimum in the Raw: Leveraging the Raw-Data Imaging Capabilities of Raspberry Pi for Diagnostics Applications
Sensors·2021· 9 citedOpen Access
A Prospective Study of Hematologic Complications and Long-Term Survival of Italian Patients Affected by Shwachman-Diamond Syndrome
The Journal of Pediatrics·2020· 30 cited
Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype
Molecular Cytogenetics·2020· 3 citedOpen Access
Boosting accessibility of diagnostics tools for 3D printing, consumer electronics, digital imaging and open source software conversion (Conference Presentation)
2019· 2 cited
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas
Journal of Visualized Experiments·2019· 4 cited
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas
Journal of Visualized Experiments·2019· 8 cited
Novel evidence of karyotype instability in Shwachman Diamond Syndrome
IrInSubria (University of Insubria)·2019
Shwachman‐Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability
British Journal of Haematology·2018· 30 citedOpen Access
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene
Molecular Cytogenetics·2018· 4 citedOpen Access
Genotossicologia di Nanomateriali Ingegnerizzati (ENMs): l’esperienza e i risultati di un confronto di analisi genome-wide in lievito e in pianta.
DSpaceUnipr (University of Parma)·2017Open Access
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas
European Journal of Histochemistry·2017· 21 citedOpen Access
Novel recurrent chromosome anomalies in Shwachman–Diamond syndrome
Pediatric Blood & Cancer·2017· 18 cited
Exposure of Cucurbita pepo to binary combinations of engineered nanomaterials: physiological and molecular response
Environmental Science Nano·2017· 54 cited
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Frequent Co-authors

Emanuela Maserati(25), Francesco Lo Curto(19), Roberto Valli(13), Antonella Minelli(11), Cesare Danesino(11), Franco Locatelli(9), Barbara Pressato(8), Giovanni Porta(7), Giuseppe Montalbano(6), Laura Sainati(6), Cristina Marletta(6), M. Fraccaro(5), Annalisa Frattini(5), Rosario Casalone(4), Marco Zecca(4), Giuseppe Menna(4), F. Poli(4), Marco Cipolli(4), Elia Mattarucchi(4), Cristina Cuoco(3)