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E. Morizio · SciRah

Researcher profile · Semantic Scholar

E. Morizio

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E. Morizio — researcher profile on SciRah

h-index: 18
Works: 49
Citations: 994

Most-cited papers

A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11
L. Stuppia, V. Gatta, G. Calabrese, P. Guanciali-Franchi +7 more
1998Human Genetics82 citations
Semantic Scholar
Assignment1 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
G. Calabrese, Carlo Crescenzi, E. Morizio, Giandomenico Palka +2 more
2001Cytogenetic and Genome Research77 citations
Semantic Scholar
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy
L. Stuppia, V. Gatta, A. Gaspari, I. Antonucci +3 more
2002European Journal of Human Genetics73 citations
Semantic Scholar
Inositide-specific phospholipase c β1 gene deletion in the progression of myelodysplastic syndrome to acute myeloid leukemia
V. R. Lo Vasco, G. Calabrese, L. Manzoli, G. Palka +5 more
2004Leukemia63 citations Open access
Semantic Scholar
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol
I. Antonucci, I. Iezzi, E. Morizio, F. Mastrangelo +8 more
2009BMC Biotechnology60 citations Open access
Semantic Scholar
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene
G. Calabrese, L. Stuppia, E. Morizio, P. Franchi +7 more
1998European Journal of Human Genetics59 citations
Semantic Scholar
p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis.
L. Stuppia, G. Calabrese, R. Peila, P. Guanciali-Franchi +3 more
1997Cancer Genetics and Cytogenetics55 citations
Semantic Scholar
Complex translocations of the Ph chromosome and Ph negative CML arise from similar mechanisms, as evidenced by FISH analysis.
G. Calabrese, L. Stuppia, Paolo Guanciali Franchi, R. Peila +7 more
1994Cancer Genetics and Cytogenetics51 citations
Semantic Scholar
Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment
C. Palka, M. Alfonsi, A. Mohn, R. Cerbo +8 more
2012Pediatrics44 citations
Semantic Scholar
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient.
A. Pizzuti, G. Calabrese, M. Bozzali, L. Telvi +7 more
2002Investigative Ophthalmology and Visual Science43 citations
Semantic Scholar
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb
G. Calabrese, L. Telvi, F. Capodiferro, E. Morizio +7 more
2000European Journal of Human Genetics39 citations
Semantic Scholar
Identification and characterization of different SHOX gene deletions in patients with Leri–Weill dyschondrosteosys by MLPA assay
V. Gatta, I. Antonucci, E. Morizio, C. Palka +5 more
2006Journal of Human Genetics35 citations
Semantic Scholar
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male
L. Stuppia, G. Calabrese, P. Borrelli, V. Gatta +7 more
1999Journal of Medical Genetics27 citations Open access
Semantic Scholar
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis
P. Guanciali-Franchi, G. Calabrese, E. Morizio, D. Fantasia +11 more
2004American Journal of Medical Genetics. Part A24 citations
Semantic Scholar
Molecular studies in three patients with isodicentric Y chromosome
L. Stuppia, G. Calabrese, P. G. Franchi, R. Mingarelli +3 more
1996Human Genetics23 citations
Semantic Scholar
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy
Elena di Vera, M. Liberati, C. Celentano, G. Calabrese +3 more
2008Journal of Assisted Reproduction and Genetics21 citations Open access
Semantic Scholar
FISH analysis in detecting 9p duplication (p22p24).
P. Franchi, G. Calabrese, E. Morizio, E. Modestini +3 more
2000American journal of medical genetics21 citations
Semantic Scholar
Isolation and Enrichment of Circulating Fetal Cells for NIPD: An Overview
Giulia Sabbatinelli, D. Fantasia, C. Palka, E. Morizio +2 more
2021Diagnostics18 citations Open access
Semantic Scholar
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene.
L. Stuppia, V. Gatta, I. Fogh, A. Gaspari +6 more
2001Genomics17 citations
Semantic Scholar
A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia.
G. Calabrese, P. G. Franchi, L. Stuppia, R. Mingarelli +6 more
1994Journal of Medical Genetics16 citations Open access
Semantic Scholar
The Role of Lifestyle Intervention in Female Fertility: A Modifiable Factor for Preconception Health
Marisa Donato, A. Capalbo, E. Morizio, Rosa Maria Fratini +6 more
2025Nutrients14 citations
Semantic Scholar
Assignment of the β-Arrestin 1 Gene (ARRB1) to Human Chromosome 11q13
G. Calabrese, M. Sallese, A. Stornaiuolo, E. Morizio +2 more
199413 citations
Semantic Scholar
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
P. Guanciali-Franchi, C. Palka, E. Morizio, Giulia Sabbatinelli +5 more
2017PLoS ONE11 citations Open access
Semantic Scholar
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high‐risk pregnant women
P. Guanciali-Franchi, I. Iezzi, C. Palka, B. Matarrelli +3 more
2011Prenatal Diagnosis11 citations
Semantic Scholar
Effectiveness of crosstrimester test in selecting high‐risk pregnant women to undergo invasive prenatal diagnosis
P. Guanciali-Franchi, I. Iezzi, B. Matarrelli, E. Morizio +2 more
2010Prenatal Diagnosis10 citations
Semantic Scholar
Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation
G. Calabrese, D. Fantasia, P. G. Franchi, E. Morizio +6 more
2000Bone Marrow Transplantation10 citations
Semantic Scholar
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
G. Calabrese, D. Fantasia, M. Alfonsi, E. Morizio +6 more
2016Molecular Genetics & Genomic Medicine9 citations Open access
Semantic Scholar
Retrospective investigation of hematopoietic chimerism after BMT by PCR amplification of hypervariable DNA regions.
L. Stuppia, G. Calabrese, P. Di Bartolomeo, R. Peila +3 more
1995Cancer Genetics and Cytogenetics9 citations
Semantic Scholar
Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report
D. Dell'Edera, A. Allegretti, M. Ventura, L. Mercuri +6 more
2021Journal of Medical Case Reports7 citations Open access
Semantic Scholar
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts (RAEB)
G. Calabrese, D. Fantasia, E. Morizio, P. M. Toro +5 more
2003British Journal of Haematology7 citations
Semantic Scholar
Prenatal diagnosis using the triple test.
G. Palka, P. Guanciali Franchi, M. Papponetti, J. Marcuccitti +4 more
1998Minerva Ginecologica7 citations
Semantic Scholar
Assignment of the beta-arrestin 1 gene (ARRB1) to human chromosome 11q13.
G. Calabrese, M. Sallese, A. Stornaiuolo, E. Morizio +2 more
1994Genomics6 citations
Semantic Scholar
Lack of correlation between elevated maternal serum hCG during second‐trimester biochemical screening and fetal congenital anomaly
C. Celentano, P. Guanciali-Franchi, M. Liberati, C. Palka +5 more
2005Prenatal Diagnosis5 citations
Semantic Scholar
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene.
L. Stuppia, V. Gatta, O. Scarciolla, I. Antonucci +3 more
2005Genomics5 citations
Semantic Scholar
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells.
G. Calabrese, E. Morizio, P. Franchi, L. Stuppia +2 more
1998American journal of medical genetics5 citations
Semantic Scholar
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus.
C. Palka, M. Alfonsi, E. Morizio, Alessandra Soranno +6 more
2011European Journal of Medical Genetics4 citations
Semantic Scholar
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence?
S. Tumini, M. Alfonsi, S. Carinci, E. Morizio +7 more
2019Cytogenetic and Genome Research3 citations
Semantic Scholar
Non-invasive prenatal screening: A 20-year experience in Italy
C. Palka, P. Guanciali-Franchi, E. Morizio, M. Alfonsi +5 more
2019European Journal of Obstetrics & Gynecology and Reproductive Biology: X2 citations Open access
Semantic Scholar
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects.
M. Alfonsi, C. Palka, E. Morizio, V. Gatta +6 more
2013Clinical Dysmorphology2 citations
Semantic Scholar
1q21.1 Duplication Syndrome and Anorectal Malformations: A Literature Review and a New Case
Maria Minelli, Chiara Palka Bayard de Volo, M. Alfonsi, Serena Capanna +5 more
2025Current Issues in Molecular Biology1 citations
Semantic Scholar
A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties.
C. Palka Bayard de Volo, M. Alfonsi, E. Morizio, P. Guaciali-Franchi +2 more
2021Journal of Intellectual Disability Research1 citations
Semantic Scholar
Discovering a familial Xp11.4 microduplication: Does the mother matter?
C. Palka, S. De Marco, M. Alfonsi, S. Matricardi +6 more
2018Meta Gene1 citations
Semantic Scholar
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability
C. Palka, M. Alfonsi, E. Morizio, P. Guanciali-Franchi +4 more
20161 citations
Semantic Scholar
A case of triploidy detected by crosstrimester test.
P. Guanciali-Franchi, I. Iezzi, B. Matarrelli, E. Morizio +2 more
2012Journal of Prenatal Medicine1 citations
Semantic Scholar
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man.
P. Guanciali-Franchi, G. Calabrese, E. Morizio, V. Gatta +3 more
2008European Journal of Medical Genetics1 citations
Semantic Scholar
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis.
G. Calabrese, L. Stuppia, R. Mingarelli, P. Guanciali Franchi +4 more
1994Annales de Genetique1 citations
Semantic Scholar
A Case of Pallister–Killian Syndrome in a Newborn
Giulia Di Donato, Chiara Cauzzo, P. Cicioni, Teresa Topazio +5 more
2026Case Reports in Genetics0 citations Open access
Semantic Scholar
First case of two supernumerary markers derived from chromosome 5 and chromosome 8
Roberta Giansante, Chiara Palka Bayard De Volo, M. Alfonsi, E. Morizio +1 more
2022Molecular Cytogenetics0 citations Open access
Semantic Scholar
P65: Complete imatinib-induced CML remission as evidenced by FISH predicts good outcome but it is not achieved in patients with der(9) deletion within 18-month follow up
D. Fantasia, Paolo Guanciali-Franch, R. Di Gianfilippo, E. Morizio +5 more
20050 citations
Semantic Scholar

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