Works by Guerneri, Silvana

Results: 35

Tetrasomy 18p: The challenges of noninvasive prenatal testing and combined test.

Published in:

Journal of Obstetrics & Gynaecology Research, 2019, v. 45, n. 3, p. 705, doi. 10.1111/jog.13873

By:

Tolva, Gianluca;
Silipigni, Rosamaria;
Quarenghi, Aida;
Vergani, Patrizia;
Guerneri, Silvana;
Milani, Donatella

Publication type:

Article

Incidental finding of APC deletion in a child: double trouble or double chance? – a case report.

Published in:

Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-00969-x

By:

Rosina, Erica;
Rinaldi, Berardo;
Silipigni, Rosamaria;
Bergamaschi, Luca;
Gattuso, Giovanna;
Signoroni, Stefano;
Guerneri, Silvana;
Carnevali, Alessandra;
Marchisio, Paola Giovanna;
Milani, Donatella

Publication type:

Article

Correction to: Incidental finding of APC deletion in a child: double trouble or double chance? – a case report.

Published in:

2021

By:

Rosina, Erica;
Rinaldi, Berardo;
Silipigni, Rosamaria;
Bergamaschi, Luca;
Gattuso, Giovanna;
Signoroni, Stefano;
Guerneri, Silvana;
Carnevali, Alessandra;
Marchisio, Paola Giovanna;
Milani, Donatella

Publication type:

Correction Notice

Incidental finding of APC deletion in a child: double trouble or double chance? – a case report.

Published in:

Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-00969-x

By:

Rosina, Erica;
Rinaldi, Berardo;
Silipigni, Rosamaria;
Bergamaschi, Luca;
Gattuso, Giovanna;
Signoroni, Stefano;
Guerneri, Silvana;
Carnevali, Alessandra;
Marchisio, Paola Giovanna;
Milani, Donatella

Publication type:

Article

The Core Stem Genes SOX2 , POU5F1/OCT4 , and NANOG Are Expressed in Human Parathyroid Tumors and Modulated by MEN1 , YAP1 , and β-catenin Pathways Activation.

Published in:

Biomedicines, 2021, v. 9, n. 6, p. 637, doi. 10.3390/biomedicines9060637

By:

Verdelli, Chiara;
Morotti, Annamaria;
Tavanti, Giulia Stefania;
Silipigni, Rosamaria;
Guerneri, Silvana;
Ferrero, Stefano;
Vicentini, Leonardo;
Vaira, Valentina;
Corbetta, Sabrina

Publication type:

Article

Insights into 6q21-q22: Refinement of the critical region for acro-cardio-facial syndrome.

Published in:

Congenital Anomalies, 2016, v. 56, n. 4, p. 187, doi. 10.1111/cga.12164

By:

Milani, Donatella;
Cagnoli, Giulia Anna;
Baccarin, Marco;
Alfei, Enrico;
Guerneri, Silvana;
Esposito, Susanna

Publication type:

Article

Yes-Associated Protein 1 Is a Novel Calcium Sensing Receptor Target in Human Parathyroid Tumors.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 4, p. 2016, doi. 10.3390/ijms22042016

By:

Tavanti, Giulia Stefania;
Verdelli, Chiara;
Morotti, Annamaria;
Maroni, Paola;
Guarnieri, Vito;
Scillitani, Alfredo;
Silipigni, Rosamaria;
Guerneri, Silvana;
Maggiore, Riccardo;
Mari, Gilberto;
Vicentini, Leonardo;
Dalino Ciaramella, Paolo;
Vaira, Valentina;
Corbetta, Sabrina;
Lee, Sang Yeol

Publication type:

Article

Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1.

Published in:

2018

By:

Silipigni, Rosamaria;
Monfrini, Edoardo;
Baccarin, Marco;
Giangiobbe, Sara;
Lalatta, Faustina;
Guerneri, Silvana;
Bedeschi, Maria Francesca

Publication type:

Case Study

Comprehensive Molecular Analyses in a Case of Masked Philadelphia Chronic Myeloid Leukemia.

Published in:

Cytogenetic & Genome Research, 2016, v. 147, n. 1, p. 35, doi. 10.1159/000442039

By:

Cattaneo, Daniele;
Morotti, Denise;
Bucelli, Cristina;
Cannone, Marta;
Zappa, Manuela;
Guerneri, Silvana;
Iurlo, alessandra

Publication type:

Article

Discordant prenatal phenotype and karyotype of monozygotic twins characterized by the unequal distribution of two cell lines investigated by different methods: a review.

Published in:

2008

By:

Gentilin, Barbara;
Guerneri, Silvana;
Bianchi, Vera;
Natacci, Federica;
Colombo, Augusto;
Fogliani, Roberto;
Fortuna, Renato;
Coviello, Domenico A.;
Curcio, Cristina;
Lalatta, Faustina

Publication type:

journal article

Cytogenetic study in primary myelofibrosis at diagnosis: Clinical and histological association and impact on survival according to WHO 2017 classification in an Italian multicenter series.

Published in:

Hematological Oncology, 2021, v. 39, n. 1, p. 123, doi. 10.1002/hon.2808

By:

Iurlo, Alessandra;
Palandri, Francesca;
Maria Elli, Elena;
Cattaneo, Daniele;
Bucelli, Cristina;
Sciumè, Mariarita;
Vincelli, Donatella;
Brioschi, Filippo;
Auteri, Giuseppe;
Croci, Giorgio Alberto;
Guerneri, Silvana;
Isimbaldi, Giuseppe;
Sabattini, Elena;
Cortinovis, Ivan;
Bossi, Anna;
Rosti, Vittorio;
Martino, Bruno;
Baldini, Luca;
Gianelli, Umberto

Publication type:

Article

HOXA genes cluster: clinical implications of the smallest deletion.

Published in:

Italian Journal of Pediatrics, 2015, v. 41, n. 1, p. 1, doi. 10.1186/s13052-015-0137-3

By:

Pezzani, Lidia;
Milani, Donatella;
Manzoni, Francesca;
Baccarin, Marco;
Silipigni, Rosamaria;
Guerneri, Silvana;
Esposito, Susanna

Publication type:

Article

Delineating the Mosaic Trisomy 15 Phenotype Using a Serendipitous Mechanism as a Clue.

Published in:

Cytogenetic & Genome Research, 2015, v. 146, n. 1, p. 44, doi. 10.1159/000435796

By:

Natacci, Federica;
Melloni, Giulia;
Motta, Francesca;
Silipigni, Rosamaria;
Doniselli, Fabio;
Rizzuti, Tommaso;
Frigerio, Marcello;
Guerneri, Silvana

Publication type:

Article

Molecular and transcriptional characterization of the novel 17p11.2-p12 amplicon in multiple myeloma.

Published in:

Genes, Chromosomes & Cancer, 2007, v. 46, n. 12, p. 1109, doi. 10.1002/gcc.20494

By:

Fabris, Sonia;
Todoerti, Katia;
Mosca, Laura;
Agnelli, Luca;
Intini, Daniela;
Lionetti, Marta;
Guerneri, Silvana;
Lambertenghi-Deliliers, Giorgio;
Bertoni, Francesco;
Neri, Antonino

Publication type:

Article

Author's reply regarding 'Confined placental mosaicism at chorionic villous sampling: risk factors and pregnancy outcome'.

Published in:

Prenatal Diagnosis, 2013, v. 33, n. 3, p. 303, doi. 10.1002/pd.4046

By:

Baffero, Giulia Maria;
Somigliana, Edgardo;
Crovetto, Francesca;
Paffoni, Alessio;
Persico, Nicola;
Guerneri, Silvana;
Lalatta, Faustina;
Fogliani, Roberto;
Fedele, Luigi

Publication type:

Article

Confined placental mosaicism at chorionic villous sampling: risk factors and pregnancy outcome.

Published in:

Prenatal Diagnosis, 2012, v. 32, n. 11, p. 1102, doi. 10.1002/pd.3965

By:

Baffero, Giulia Maria;
Somigliana, Edgardo;
Crovetto, Francesca;
Paffoni, Alessio;
Persico, Nicola;
Guerneri, Silvana;
Lalatta, Faustina;
Fogliani, Roberto;
Fedele, Luigi

Publication type:

Article

De novo balanced chromosome rearrangements in prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 3, p. 257, doi. 10.1002/pd.2215

By:

Giardino, Daniela;
Corti, Cecilia;
Ballarati, Lucia;
Colombo, Daniela;
Sala, Elena;
Villa, Nicoletta;
Piombo, Giuseppe;
Pierluigi, Mauro;
Faravelli, Francesca;
Guerneri, Silvana;
Coviello, Domenico;
Lalatta, Faustina;
Cavallari, Ugo;
Bellotti, Daniela;
Barlati, Sergio;
Croci, Gianfranco;
Franchi, Fabrizia;
Savin, Elisa;
Nocera, Gianfranco;
Amico, Francesco Paolo

Publication type:

Article

Expanding the phenotype of 22q13.3 deletion: report of a case detected prenatally.

Published in:

Prenatal Diagnosis, 2008, v. 28, n. 10, p. 978, doi. 10.1002/pd.2110

By:

Maitz, Silvia;
Gentilin, Barbara;
Colli, Anna Maria;
Rizzuti, Tommaso;
Brandolisio, Emilia;
Vetro, Annalisa;
Zuffardi, Orsetta;
Guerneri, Silvana;
Lalatta, Faustina

Publication type:

Article

Limited value of echography to predict true fetal mosaicism for trisomy 12.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1186, doi. 10.1002/pd.1587

By:

Gentilin, Barbara;
Giardino, Daniela;
Boschetto, Chiara;
Guerneri, Silvana;
Fortuna, Renato;
Rizzuti, Tommaso;
Lalatta, Faustina

Publication type:

Article

Prevalence and distribution of chromosome abnormalities in a sample of first trimester internal abortions.

Published in:

Human Reproduction, 1987, v. 2, n. 8, p. 735

By:

Guerneri, Silvana;
Bettio, Daniela;
Simoni, G.;
Brambati, B.;
Lanzani, A.;
Fraccaro, M.

Publication type:

Article

Cytogenetic mapping of a novel locus for type II Waardenburg syndrome.

Published in:

Human Genetics, 2002, v. 110, n. 1, p. 64, doi. 10.1007/s00439-001-0643-9

By:

Selicorni, Angelo;
Guerneri, Silvana;
Ratti, Antonia;
Pizzuti, Antonio

Publication type:

Article

Autism spectrum disorder and intellectual disability in an inherited 2q14.3 micro‐deletion involving CNTNAP5.

Published in:

American Journal of Medical Genetics. Part A, 2020, v. 182, n. 12, p. 3071, doi. 10.1002/ajmg.a.61881

By:

Aleo, Sebastiano;
Milani, Donatella;
Pansa, Alessandra;
Marchisio, Paola;
Guerneri, Silvana;
Silipigni, Rosamaria

Publication type:

Article

STAR syndrome plus: The first description of a female patient with the lethal form.

Published in:

American Journal of Medical Genetics. Part A, 2017, v. 173, n. 12, p. 3226, doi. 10.1002/ajmg.a.38484

By:

Bedeschi, Maria F.;
Giangiobbe, Sara;
Paganini, Leda;
Tabano, Silvia;
Silipigni, Rosamaria;
Colombo, Lorenzo;
Crippa, Beatrice L.;
Lalatta, Faustina;
Guerneri, Silvana;
Miozzo, Monica

Publication type:

Article

Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: A genotype-phenotype analysis.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 7, p. 1551, doi. 10.1002/ajmg.a.37063

By:

Ronzoni, Luisa;
Peron, Angela;
Bianchi, Vera;
Baccarin, Marco;
Guerneri, Silvana;
Silipigni, Rosamaria;
Lalatta, Faustina;
Bedeschi, Maria Francesca

Publication type:

Article

The Oncosuppressors MEN1 and CDC73 Are Involved in lncRNA Deregulation in Human Parathyroid Tumors.

Published in:

Journal of Bone & Mineral Research, 2020, v. 35, n. 12, p. 2423, doi. 10.1002/jbmr.4154

By:

Morotti, Annamaria;
Forno, Irene;
Verdelli, Chiara;
Guarnieri, Vito;
Cetani, Filomena;
Terrasi, Andrea;
Silipigni, Rosamaria;
Guerneri, Silvana;
Andrè, Valentina;
Scillitani, Alfredo;
Vicentini, Leonardo;
Ferrero, Stefano;
Corbetta, Sabrina;
Vaira, Valentina

Publication type:

Article

Prenatal confirmation of trisomy 12 mosaicism by fetal skin biopsy.

Published in:

1993

By:

Cartolano, Rosa;
Guerneri, Silvana;
Fogliani, Roberto;
Galimberti, Andrea;
Nicolini, Umberto;
Cartolano, R;
Guerneri, S;
Fogliani, R;
Galimberti, A;
Nicolini, U

Publication type:

journal article

Evidence of Distinct Tumour-Propagating Cell Populations with Different Properties in Primary Human Hepatocellular Carcinoma.

Published in:

PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0021369

By:

Colombo, Federico;
Baldan, Francesca;
Mazzucchelli, Silvia;
Martin-Padura, Ines;
Marighetti, Paola;
Cattaneo, Alessandra;
Foglieni, Barbara;
Spreafico, Marta;
Guerneri, Silvana;
Baccarin, Marco;
Bertolini, Francesco;
Rossi, Giorgio;
Mazzaferro, Vincenzo;
Cadamuro, Massimiliano;
Maggioni, Marco;
Agnelli, Luca;
Rebulla, Paolo;
Prati, Daniele;
Porretti, Laura

Publication type:

Article

Positive predictive values and outcomes for uninformative cell‐free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study).

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1575, doi. 10.1002/pd.6271

By:

Grati, Francesca Romana;
Bestetti, Ilaria;
De Siero, Daria;
Malvestiti, Francesca;
Villa, Nicoletta;
Sala, Elena;
Crosti, Francesca;
Parisi, Valentina;
Nardone, Anna Maria;
Di Giacomo, Gianluca;
Pettinari, Antonella;
Tortora, Giada;
Montaldi, Annamaria;
Calò, Annapaola;
Saccilotto, Donatella;
Zanchetti, Sara;
Celli, Paola;
Guerneri, Silvana;
Silipigni, Rosamaria;
Cardarelli, Laura

Publication type:

Article

Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 927, doi. 10.1002/pd.6171

By:

Rinaldi, Berardo;
Cesaretti, Claudia;
Boito, Simona;
Villa, Roberta;
Guerneri, Silvana;
Borzani, Irene;
Rizzuti, Tommaso;
Marchetti, Daniela;
Conte, Giorgio;
Cinnante, Claudia;
Triulzi, Fabio;
Persico, Nicola;
Iascone, Maria;
Natacci, Federica

Publication type:

Article

Partial Trisomy of 7q: Case Report and Literature Review.

Published in:

Journal of Child Neurology, 2008, v. 23, n. 5, p. 572, doi. 10.1177/0883073807309776

By:

Scelsa, Barbara;
Bedeschi, Francesca Maria;
Guerneri, Silvana;
Lalatta, Faustina;
Introvini, Paola

Publication type:

Article

De Novo Duplication of Chromosome 13(q32-q34) in a Child With Developmental Delay.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 12, p. 1084, doi. 10.1177/7010.2006.00229

By:

Milani, Donatella;
D'Arrigo, Stefano;
Guerneri, Silvana;
Selicorni, Angelo;
Riva, Daria;
Pantaleoni, Chiara

Publication type:

Article

Small supernumerary marker chromosomes: A legacy of trisomy rescue?

Published in:

Human Mutation, 2019, v. 40, n. 2, p. 193, doi. 10.1002/humu.23683

By:

Kurtas, Nehir Edibe;
Xumerle, Luciano;
Leonardelli, Lorena;
Delledonne, Massimo;
Brusco, Alfredo;
Chrzanowska, Krystyna;
Schinzel, Albert;
Larizza, Daniela;
Guerneri, Silvana;
Natacci, Federica;
Bonaglia, Maria Clara;
Reho, Paolo;
Manolakos, Emmanouil;
Mattina, Teresa;
Soli, Fiorenza;
Provenzano, Aldesia;
Al‐Rikabi, Ahmed H.;
Errichiello, Edoardo;
Nazaryan‐Petersen, Lusine;
Giglio, Sabrina

Publication type:

Article

Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes.

Published in:

Molecular Cytogenetics (17558166), 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8166-6-45

By:

Castronovo, Chiara;
Valtorta, Emanuele;
Crippa, Milena;
Tedoldi, Sara;
Romitti, Lorenza;
Amione, Maria Cristina;
Guerneri, Silvana;
Rusconi, Daniela;
Ballarati, Lucia;
Milani, Donatella;
Grosso, Enrico;
Cavalli, Pietro;
Giardino, Daniela;
Bonati, Maria Teresa;
Larizza, Lidia;
Finelli, Palma

Publication type:

Article

Beckwith–Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi.

Published in:

Epigenetics, 2015, v. 10, n. 7, p. 643, doi. 10.1080/15592294.2015.1057383

By:

Paganini, Leda;
Carlessi, Nicole;
Fontana, Laura;
Silipigni, Rosamaria;
Motta, Silvia;
Fiori, Stefano;
Guerneri, Silvana;
Lalatta, Faustina;
Cereda, Anna;
Sirchia, Silvia;
Miozzo, Monica;
Tabano, Silvia

Publication type:

Article

Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.

Published in:

BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0470-z

By:

Bedeschi, Maria Francesca;
Calvello, Mariarosaria;
Paganini, Leda;
Pezzani, Lidia;
Baccarin, Marco;
Fontana, Laura;
Sirchia, Silvia M.;
Guerneri, Silvana;
Canazza, Lorena;
Leva, Ernesto;
Colombo, Lorenzo;
Lalatta, Faustina;
Mosca, Fabio;
Tabano, Silvia;
Miozzo, Monica

Publication type:

Article