Search Results - Anna Maria Di Blasio
- Showing 1 - 13 results of 13
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NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis. by Davide Gentilini, Antonino Oliveri, Teresa Fazia, Alessandro Pini, Susan Marelli, Luisa Bernardinelli, Anna Maria Di Blasio
Published 2019-01-01
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Differences in visceral fat and fat bacterial colonization between ulcerative colitis and Crohn's disease. An in vivo and in vitro study. by Alessandra Zulian, Raffaella Cancello, Chiara Ruocco, Davide Gentilini, Anna Maria Di Blasio, Piergiorgio Danelli, Giancarlo Micheletto, Elisabetta Cesana, Cecilia Invitti
Published 2013-01-01
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Epigenome Wide Association and Stochastic Epigenetic Mutation Analysis on Cord Blood of Preterm Birth by Elena Spada, Luciano Calzari, Luigi Corsaro, Teresa Fazia, Monica Mencarelli, Anna Maria Di Blasio, Luisa Bernardinelli, Giulia Zangheri, Michele Vignali, Davide Gentilini
Published 2020-07-01
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Role of epigenetics in the clinical evolution of COVID-19 disease. Epigenome-wide association study identifies markers of severe outcome by Luciano Calzari, Lucia Zanotti, Elvira Inglese, Francesco Scaglione, Rebecca Cavagnola, Francesco Ranucci, Anna Maria Di Blasio, Giulio Stefanini, Gaetano Carlo, Gianfranco Parati, Davide Gentilini
Published 2023-02-01
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The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report by Alessandro Cattoni, Alice Spano, Anna Tulone, Annalisa Boneschi, Nicoletta Masera, Silvia Maitz, Anna Maria Di Blasio, Luca Persani, Luca Persani, Fabiana Guizzardi, Fabiana Guizzardi, Raffaella Rossetti
Published 2020-09-01
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Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations by Elisa Adele Colombo, Hatice Mutlu-Albayrak, Yousef Shafeghati, Mine Balasar, Juliette Piard, Davide Gentilini, Davide Gentilini, Anna Maria Di Blasio, Cristina Gervasini, Lionel Van Maldergem, Lidia Larizza
Published 2019-05-01
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Biventricular Arrhythmogenic Cardiomyopathy: a paradigmatic case by camilla torlasco, Franco Cecchi, P. J. Schwartz, G. Parati, L. Crotti, federica dagradi, Barbara Bilo, G. Perego, M. Revera, Anna Maria Di Blasio, Maria-Christina Kotta, Alice Ghidoni, Giulia Girardengo, Margherita Calcagnino
Published 2015-01-01
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Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients by Melania Lippi, Mattia Chiesa, Ciro Ascione, Matteo Pedrazzini, Saima Mushtaq, Davide Rovina, Daniela Riggio, Anna Maria Di Blasio, Maria Luisa Biondi, Giulio Pompilio, Gualtiero I. Colombo, Michela Casella, Valeria Novelli, Elena Sommariva
Published 2022-07-01
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Genomic adaptations to cereal‐based diets contribute to mitigate metabolic risk in some human populations of East Asian ancestry by Arianna Landini, Shaobo Yu, Guido Alberto Gnecchi‐Ruscone, Paolo Abondio, Claudia Ojeda‐Granados, Stefania Sarno, Sara De Fanti, Davide Gentilini, Anna Maria Di Blasio, Hanjun Jin, Thanh Tin Nguyen, Giovanni Romeo, Cecilia Prata, Eugenio Bortolini, Donata Luiselli, Davide Pettener, Marco Sazzini
Published 2021-02-01
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An overview of the genetic structure within the Italian population from genome-wide data. by Cornelia Di Gaetano, Floriana Voglino, Simonetta Guarrera, Giovanni Fiorito, Fabio Rosa, Anna Maria Di Blasio, Paola Manzini, Irma Dianzani, Marta Betti, Marta Betti, Daniele Cusi, Francesca Frau, Cristina Barlassina, Dario Mirabelli, Corrado Magnani, Nicola Glorioso, Stefano Bonassi, Alberto Piazza, Giuseppe Matullo
Published 2012-01-01
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Genome-wide DNA promoter methylation and transcriptome analysis in human adipose tissue unravels novel candidate genes for obesity by Maria Keller, Lydia Hopp, Xuanshi Liu, Tobias Wohland, Kerstin Rohde, Raffaella Cancello, Matthias Klös, Karl Bacos, Matthias Kern, Fabian Eichelmann, Arne Dietrich, Michael R. Schön, Daniel Gärtner, Tobias Lohmann, Miriam Dreßler, Michael Stumvoll, Peter Kovacs, Anna-Maria DiBlasio, Charlotte Ling, Hans Binder, Matthias Blüher, Yvonne Böttcher
Published 2017-01-01
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Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. by Sandosh Padmanabhan, Olle Melander, Toby Johnson, Anna Maria Di Blasio, Wai K Lee, Davide Gentilini, Claire E Hastie, Cristina Menni, Maria Cristina Monti, Christian Delles, Stewart Laing, Barbara Corso, Gerjan Navis, Arjan J Kwakernaak, Pim van der Harst, Murielle Bochud, Marc Maillard, Michel Burnier, Thomas Hedner, Sverre Kjeldsen, Björn Wahlstrand, Marketa Sjögren, Cristiano Fava, Martina Montagnana, Elisa Danese, Ole Torffvit, Bo Hedblad, Harold Snieder, John M C Connell, Morris Brown, Nilesh J Samani, Martin Farrall, Giancarlo Cesana, Giuseppe Mancia, Stefano Signorini, Guido Grassi, Susana Eyheramendy, H Erich Wichmann, Maris Laan, David P Strachan, Peter Sever, Denis Colm Shields, Alice Stanton, Peter Vollenweider, Alexander Teumer, Henry Völzke, Rainer Rettig, Christopher Newton-Cheh, Pankaj Arora, Feng Zhang, Nicole Soranzo, Timothy D Spector, Gavin Lucas, Sekar Kathiresan, David S Siscovick, Jian'an Luan, Ruth J F Loos, Nicholas J Wareham, Brenda W Penninx, Ilja M Nolte, Martin McBride, William H Miller, Stuart A Nicklin, Andrew H Baker, Delyth Graham, Robert A McDonald, Jill P Pell, Naveed Sattar, Paul Welsh, Global BPgen Consortium, Patricia Munroe, Mark J Caulfield, Alberto Zanchetti, Anna F Dominiczak
Published 2010-10-01
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