Olga Calabrese - Medical Genetics Unit, Azienda Ospedaliera Universitaria di Modena

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论文共 26 篇作者统计合作学者相似作者

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The Approach to a Child with Dysmorphic Features: What the Pediatrician Should Know

Silvia Ciancia,Simona Filomena Madeo,Olga Calabrese,Lorenzo Iughetti

Childrenno. 5 (2024): 578

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Clinical Genetic Services in the Emilia-Romagna Region, Italy: Current Activity and Open Issues. A Mixed-Method Study

Lea Godino,Enrico Ambrosini,Valeria Barili,Claudio Graziano,Livia Garavelli,Olga Calabrese,Marcella Neri,Luca Sangiorgi,Benedetta Bertonazzi,Giovanni Innella, Daniela Turchetti,Antonio Percesepe

crossref（2024）

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Positive Predictive Values and Outcomes for Uninformative Cell-Free DNA Tests: an Italian Multicentric Cytogenetic and Cytogenomic Audit of DiagnOstic Testing (ICARO Study)

Francesca Romana Grati,Ilaria Bestetti,Daria de Siero,Francesca Malvestiti,Nicoletta Villa,Elena Sala,Francesca Crosti,Valentina Parisi,Anna Maria Nardone,Gianluca Di Giacomo,Antonella Pettinari,Giada Tortora,Annamaria Montaldi,Annapaola Calò,Donatella Saccilotto,Sara Zanchetti,Paola Celli,Silvana Guerneri,Rosamaria Silipigni,Laura Cardarelli,Elisabetta Lippi,Simona Cavani,Michela Malacarne,Rita Genesio,Nicola Beltrami,Maria Carla Pittalis,Laura Desiderio,Mattia Gentile,Romina Ficarella,Maria Paola Recalcati,Ilaria Catusi,Maria Garzo,Lorena Miele,Cecilia Corti,Sara Ghezzo,Veronica Bertini,Francesca Cambi,Angelo Valetto,Barbara Facchinetti,Laura Bernardini,Anna Capalbo,Federica Balducci,Elisabetta Pelo,Barbara Minuti,Chiara Pescucci,Costanza Giuliani,Alessandra Renieri,Ilaria Longo,Rossella Tita,Giuseppe Castello,Rosario Casalone,R. Righi,Barbara Raso,Alessandro Civolani,Maria Cristina Muzi,Manuela di Natale,Luigia Varriale,D. Gasperini,Maria Cristina Nuzzi,Angelo Cellamare,Paola Casieri,Rosa Busuito,Caterina Ceccarini,Carla Cesarano,O. Privitera,Daniela Melani,C Menozzi,Cristina Falcinelli,Olga Calabrese,Paola Battaglia,Antonella Tanzariello,Tamara Stampalija,Carmela Ardisia,Paolo Gasparini,Peter Benn,Antonio Novelli

Obstetrical & gynecological surveyno. 6 (2023): 318-320

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#2684 DIAGNOSTIC YIELD OF A TARGETED GENE PANEL FOR MONOGENIC KIDNEY DISEASES: A EUROPEAN STUDY

Silvia Giovanella,Antonio M. Poyatos Andujar,Almudena Avila-Fernandez,Ana Bustamante-Aragones,Antonio Percesepe,Davide Martorana,Alessandra Terracciano,Laura Massella,Giulia Ligabue,Francesca Testa,Camilla Ferri,Marco Marino,Enrico Tagliafico,Olga Calabrese,Donati Gabriele,Riccardo Magistroni

NEPHROLOGY DIALYSIS TRANSPLANTATION (2023): I5-I6

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Positive Predictive Values and Outcomes for Uninformative Cell-Free DNA Tests: an Italian Multicentric Cytogenetic and Cytogenomic Audit of Diagnostic Testing (ICARO Study)

Francesca Romana Grati,Ilaria Bestetti,Daria De Siero,Francesca Malvestiti,Nicoletta Villa,Elena Sala,Francesca Crosti,Valentina Parisi,Anna Maria Nardone,Gianluca Di Giacomo,Antonella Pettinari,Giada Tortora,Annamaria Montaldi,Annapaola Calo,Donatella Saccilotto,Sara Zanchetti,Paola Celli,Silvana Guerneri,Rosamaria Silipigni,Laura Cardarelli,Elisabetta Lippi,Simona Cavani,Michela Malacarne,Rita Genesio,Nicola Beltrami,Maria Carla Pittalis,Laura Desiderio,Mattia Gentile,Romina Ficarella,Maria Paola Recalcati,Ilaria Catusi,Maria Garzo,Lorena Miele,Cecilia Corti,Sara Ghezzo,Veronica Bertini,Francesca Cambi,Angelo Valetto,Barbara Facchinetti,Laura Bernardini,Anna Capalbo,Federica Balducci,Elisabetta Pelo,Barbara Minuti,Chiara Pescucci,Costanza Giuliani,Alessandra Renieri,Ilaria Longo,Rossella Tita,Giuseppe Castello,Rosario Casalone,Rossana Righi,Barbara Raso,Alessandro Civolani,Maria Cristina Muzi,Manuela di Natale,Luigia Varriale,Daniela Gasperini,Maria Cristina Nuzzi,Angelo Cellamare,Paola Casieri,Rosa Busuito,Caterina Ceccarini,Carla Cesarano,Orsola Privitera,Daniela Melani,Cristina Menozzi,Cristina Falcinelli,Olga Calabrese,Paola Battaglia,Antonella Tanzariello,Tamara Stampalija,Carmela Ardisia,Paolo Gasparini,Peter Benn,Antonio Novelli

Prenatal diagnosis（2022）

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Townes-Brocks Syndrome with Craniosynostosis in Two Siblings

Licia Lugli,Cecilia Rossi,Pier Luca Ceccarelli,Olga Calabrese,Luca Bedetti,Francesca Miselli,Maria Anastasia Bianchini,Lorenzo Iughetti,Alberto Berardi

European Journal of Medical Genetics（2022）

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Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed Patients

Erica Rosina,Lidia Pezzani,Laura Pezzoli,Daniela Marchetti,Matteo Bellini,Alba Pilotta,Olga Calabrese,Emanuele Nicastro,Francesco Cirillo,Anna Cereda,Agnese Scatigno,Donatella Milani,Maria Iascone

Genes（2022）

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Copy Number Variation Analysis Increases the Number of Candidate Loci Associated with Pediatric Obesity

Simona Filomena Madeo,Ilaria Stanghellini,Barbara Predieri,Silvia Ciancia,Francesco Leo,Patrizia Bruzzi,Olga Calabrese,Lorenzo Iughetti

Hormone research in paediatrics（2021）

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Correspondence on “disorder of Sex Development Associated with a Novel Homozygous Nonsense Mutation in COG6 Expands the Phenotypic Spectrum of COG6‐CDG”

Licia Lugli,Marzia Pollazzon,Stefania Bigoni,Stefano Giuseppe Caraffi,Alessandra Ferlini,Lorenzo Ferri,Amelia Morrone,Olga Calabrese,Lorenzo Iughetti,Livia Garavelli,Alberto Berardi

American journal of medical genetics Part A（2021）

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Correspondence on “clinical Spectrum of MTOR-related Hypomelanosis of Ito with Neurodevelopmental Abnormalities,” by Carmignac Et Al

Nicoletta Resta,Olga Calabrese,Valentina Grossi,Licia Lugli,Cristiano Simone,Carlotta Ranieri,Marilidia Piglionica,Martina Lepore Signorile,Katia Rossi,Diana Carli,Alessandro Mussa

Genetics in medicine official journal of the American College of Medical Genetics（2021）

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