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Elisena Morizio

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
A woman with an apparent non‐mosaic 45,X delivered a 46,X,der(X) liveborn female
1994 · G. Palka, G. Calabrese, et al. · Clinical Genetics · 82
Assignment 1 of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization
2001 · G. Calabrese, C. Crescenzi, et al. · Cytogenetic and Genome Research · 72
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene
1998 · G Calabrese, L Stuppia, et al. · European Journal of Human Genetics · 71
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
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
Inositide-specific phospholipase c β1 gene deletion in the progression of myelodysplastic syndrome to acute myeloid leukemia
2004 · V R Lo Vasco, G Calabrese, et al. · Leukemia · 59
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Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol
2009 · Ivana Antonucci, Irene Iezzi, et al. · BMC Biotechnology · 58
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
A New Case of Pure Partial 7q Duplication
2011 · M. Alfonsi, C. Palka, et al. · Cytogenetic and Genome Research · 47
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 · 45
Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment
2011 · Chiara Palka, Melissa Alfonsi, et al. · PEDIATRICS · 42
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb
2000 · G Calabrese, L Telvi, et al. · European Journal of Human Genetics · 37
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
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene.
1997 · L Stuppia, V Gatta, et al. · Journal of Medical Genetics · 33
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FISH analysis in detecting 9p duplication (p22p24)
2000 · P. Guanciali Franchi, G. Calabrese, et al. · American Journal of Medical Genetics · 30
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male
1999 · L Stuppia, G Calabrese, et al. · Journal of Medical Genetics · 29
Complex chromosome translocations of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by fluorescence in situ hybridization analysis
1996 · G. Calabrese, T. Min, et al. · Cancer Genetics and Cytogenetics · 25
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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Molecular studies in three patients with isodicentric Y chromosome
1996 · Liborio Stuppia, Giuseppe Calabrese, et al. · Human Genetics · 23
FISH detection of mixed chimerism in 33 patients submitted to bone marrow transplantation.
1996 · G Palka, L Stuppia, et al. · PubMed · 23
Deletion of the SHOX gene in patients with short stature of unknown cause
2003 · E. Morizio, L. Stuppia, et al. · American Journal of Medical Genetics Part A · 21
Isolation and Enrichment of Circulating Fetal Cells for NIPD: An Overview
2021 · Giulia Sabbatinelli, Donatella Fantasia, et al. · Diagnostics · 20
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A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia.
1994 · G Calabrese, P G Franchi, et al. · Journal of Medical Genetics · 20
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Works count: 62
Citation count: 1,353
H-index: 22
I10-index: 34
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