Publications by authors named "Giuseppe Simoni"

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Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.
Francesca Romana Grati, Francesca Malvestiti, Gloria Gallazzi, Silvia Saragozza, Beatrice Grimi, Giuseppe Simoni

Prenat Diagn· May 2021

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Risk of Fetal Loss in Pregnancies Undergoing Midtrimester Amniocentesis after Inconclusive Chorionic Villus Sampling.
Ginevra Salsi, Francesca Romana Grati, Federica Bellussi, Eva Pompilii, Federico Maggi, Giuseppe Simoni

Fetal Diagn Ther· February 2020

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Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA.
Francesca Romana Grati, Jose Ferreira, Peter Benn, Claudia Izzi, Federica Verdi, Giuseppe Simoni

Genet Med· February 2020

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Response: how PGS/PGT-A laboratories succeeded in losing all credibility.
Francesca Romana Grati, Gloria Gallazzi, Lara Branca, Federico Maggi, Giuseppe Simoni

Reprod Biomed Online· August 2018

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Response: scoring of mosaic embryos after preimplantation genetic testing - the rollercoaster ride between fear, hope and embryo wastage.
Francesca Romana Grati, Gloria Gallazzi, Lara Branca, Federico Maggi, Giuseppe Simoni

Reprod Biomed Online· July 2018

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An evidence-based scoring system for prioritizing mosaic aneuploid embryos following preimplantation genetic screening.
Francesca Romana Grati, Gloria Gallazzi, Lara Branca, Federico Maggi, Giuseppe Simoni

Reprod Biomed Online· April 2018

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Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.
Francesca Romana Grati, Komal Bajaj, Valentina Zanatta, Francesca Malvestiti, Barbara Malvestiti, Giuseppe Simoni

Prenat Diagn· October 2017

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Chromosomal mosaicism in the fetoplacental unit.
Francesca Romana Grati, Francesca Malvestiti, Lara Branca, Cristina Agrati, Federico Maggi, Giuseppe Simoni

Best Pract Res Clin Obstet Gynaecol· July 2017

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Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications.
Jose Carlos P Ferreira, Francesca R Grati, Komal Bajaj, Francesca Malvestiti, Maria Beatrice Grimi, Giuseppe Simoni

Prenat Diagn· December 2016

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Internalization of nanopolymeric tracers does not alter characteristics of placental cells.
Paolo Bigini, Elisa R Zanier, Silvia Saragozza, Simona Maciotta, Pietro Romele, Maria Grazia De Simoni, Giuseppe Simoni

J Cell Mol Med· June 2016

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Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis.
Francesca Malvestiti, Cristina Agrati, Beatrice Grimi, Eva Pompilii, Claudia Izzi, Giuseppe Simoni

Prenat Diagn· November 2015

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The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure.
Francesca Romana Grati, Komal Bajaj, Francesca Malvestiti, Cristina Agrati, Beatrice Grimi, Giuseppe Simoni

Prenat Diagn· October 2015

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Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Giuseppe Simoni

Prenat Diagn· August 2015

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Increased risk after noninvasive prenatal screening on cell-free DNA circulating in maternal blood: does a new indication for invasive prenatal diagnosis require new criteria for confirmatory cytogenetic analysis?
Francesca Romana Grati, Francesca Malvestiti, Beatrice Grimi, Rosaria Liuti, Cristina Agrati, Giuseppe Simoni

Prenat Diagn· March 2015

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Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations.
Céline Dupont, Francesca Romana Grati, Kwong Wai Choy, Sylvie Jaillard, Jérôme Toutain, Giuseppe Simoni

Prenat Diagn· January 2015

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Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results.
Francesca R Grati, Francesca Malvestiti, Jose C P B Ferreira, Komal Bajaj, Elisa Gaetani, Giuseppe Simoni

Genet Med· August 2014

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De novo small supernumerary marker chromosomes detected on 143,000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches.
Francesca Malvestiti, Simona De Toffol, Beatrice Grimi, Sara Chinetti, Livia Marcato, Giuseppe Simoni

Prenat Diagn· May 2014

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Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome.
Livia Marcato, Licia Turolla, Eva Pompilii, Celine Dupont, Nicolas Gruchy, Giuseppe Simoni

Clin Case Rep· April 2014

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Fetal mesenchymal stromal cells from cryopreserved human chorionic villi: cytogenetic and molecular analysis of genome stability in long-term cultures.
Emanuela Anna Roselli, Silvia Lazzati, Federico Iseppon, Massimiliano Manganini, Livia Marcato, Giuseppe Simoni

Cytotherapy· November 2013

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Response to "QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44 727 first-trimester prenatal diagnoses".
Francesca R Grati, Francesca Malvestiti, Beatrice Grimi, Elisa Gaetani, Anna Maria Di Meco, Giuseppe Simoni

Prenat Diagn· November 2013

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Recombinant chromosome 4 from a familial pericentric inversion: prenatal and adulthood wolf-hirschhorn phenotypes.
Francesca Malvestiti, Francesco Benedicenti, Simona De Toffol, Sara Chinetti, Adelheid Höller, Giuseppe Simoni

Case Rep Genet· June 2013

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QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnoses.
Francesca R Grati, Francesca Malvestiti, Beatrice Grimi, Elisa Gaetani, Anna Maria Di Meco, Giuseppe Simoni

Prenat Diagn· May 2013

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Application of a new molecular technique for the genetic evaluation of products of conception.
Francesca R Grati, Denise Molina Gomes, Devika Ganesamoorthy, Livia Marcato, Simona De Toffol, Giuseppe Simoni

Prenat Diagn· January 2013

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Prenatal BACs-on-Beads™: the prospective experience of five prenatal diagnosis laboratories.
François Vialard, Giuseppe Simoni, Denise Molina Gomes, Azzedine Abourra, Simona De Toffol

Prenat Diagn· April 2012

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Chromosome abnormalities investigated by non-invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypes.
Francesca Romana Grati, Andrea Barlocco, Beatrice Grimi, Silvia Milani, Giuditta Frascoli, Giuseppe Simoni

Am J Med Genet A· June 2010

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