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Giuseppe Calabrese

Genomic and expression profiling identifies the B‐cell associated tyrosine kinase Syk as a possible therapeutic target in mantle cell lymphoma
2005 · Andrea Rinaldi, Ivo Kwee, et al. · British Journal of Haematology · 205
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11
1998 · Liborio Stuppia, Valentina Gatta, et al. · Human Genetics · 142
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA)
2005 · Valentina Gatta, Oronzo Scarciolla, et al. · Human Genetics · 111
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy
2002 · Liborio Stuppia, Valentina Gatta, et al. · European Journal of Human Genetics · 69
Zinc sulfate supplementation improves thyroid function in hypozincemic down children
1999 · Ines Bucci, Giorgio Napolitano, et al. · Biological Trace Element Research · 69
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis
2004 · Paolo Guanciali‐Franchi, Giuseppe Calabrese, et al. · American Journal of Medical Genetics Part A · 60
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs
2005 · Liborio Stuppia, Ivana Antonucci, et al. · European Journal of Human Genetics · 55
p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis
1997 · Liborio Stuppia, Giuseppe Calabrese, et al. · Cancer Genetics and Cytogenetics · 50
Complex translocations of the Ph chromosome and Ph negative CML arise from similar mechanisms, as evidenced by FISH analysis
1994 · Giuseppe Calabrese, Liborio Stuppia, et al. · Cancer Genetics and Cytogenetics · 46
Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment
2011 · Chiara Palka, Melissa Alfonsi, et al. · PEDIATRICS · 43
Identification and characterization of different SHOX gene deletions in patients with Leri–Weill dyschondrosteosys by MLPA assay
2006 · Valentina Gatta, Ivana Antonucci, et al. · Journal of Human Genetics · 36
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient.
2002 · Antonio Pizzuti, Giuseppe Calabrese, et al. · PubMed · 34
Clinical usefulness of NGS multi-gene panel testing in hereditary cancer analysis
2023 · Federico Anaclerio, Lucrezia Pilenzi, et al. · Frontiers in Genetics · 33
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Molecular studies in three patients with isodicentric Y chromosome
1996 · Liborio Stuppia, Giuseppe Calabrese, et al. · Human Genetics · 24
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy
2008 · Elena di Vera, Marco Liberati, et al. · Journal of Assisted Reproduction and Genetics · 23
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Isolation and Enrichment of Circulating Fetal Cells for NIPD: An Overview
2021 · Giulia Sabbatinelli, Donatella Fantasia, et al. · Diagnostics · 20
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Long-term remission in BCR/ABL-positive AML-M6 patient treated with Imatinib Mesylate
2006 · Franca Pompetti, Antonio Spadano, et al. · Leukemia Research · 19
Genomic Organization, Physical Mapping, and Involvement in Yq Microdeletions of the VCY2 (BPY 2) Gene
2001 · Liborio Stuppia, Valentina Gatta, et al. · Genomics · 16
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures
2015 · Alberto Verrotti, Chiara Palka, et al. · Cytogenetic and Genome Research · 15
Fetal translocation between chromosomes 2, 18, and 21 resolved by fish
1995 · Isabella Delaroche, Margherita Sabani, et al. · Prenatal Diagnosis · 14
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
2017 · Paolo Guanciali Franchi, Chiara Palka, et al. · PLoS ONE · 12
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16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer
2012 · Chiara Palka Bayard de Volo, Melissa Alfonsi, et al. · Gene · 12
Effectiveness of crosstrimester test in selecting high‐risk pregnant women to undergo invasive prenatal diagnosis
2010 · Paolo Guanciali‐Franchi, Irene Iezzi, et al. · Prenatal Diagnosis · 12
Aneuploidy screening using circulating fetal cells in maternal blood by dual‐probe FISH protocol: a prospective feasibility study on a series of 172 pregnant women
2016 · Giuseppe Calabrese, Donatella Fantasia, et al. · Molecular Genetics & Genomic Medicine · 11
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Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation
2012 · Chiara Palka-Bayard-de-Volo, Stefania De Marco, et al. · Gene · 10
Works count: 51
Citation count: 1,251
H-index: 17
I10-index: 26
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