Pyrosequencing Evaluation of Widely Available Bisulfite Conversion Methods: Considerations for Application

Por Izzi, Benedetta, Binder, Alexandra M., Michels, Karin B.
Publicado em 2014

Methylome analysis for spina bifida shows SOX18 hypomethylation as a risk factor with evidence for a complex (epi)genetic interplay to affect neural tube development

Por Rochtus, Anne, Winand, Raf, Laenen, Griet, Vangeel, Elise, Izzi, Benedetta, Wittevrongel, Christine, Moreau, Yves, Verpoorten, Carla, Jansen, Katrien, Van Geet, Chris, Freson, Kathleen
Publicado no Clin Epigenetics (2016)

Comparison of multiplexed reduced representation bisulfite sequencing (mRRBS) with the 450K Illumina Human BeadChip: from concordance to practical applications for methylomic profi...

Por Carmona, Juan J, Izzi, Benedetta, Just, Allan C, Barupal, Jitendra, Binder, Alexandra M, Hutchinson, John, Hofmann, Oliver, Schwartz, Joel, Baccarelli, Andrea, Michels, Karin B
Publicado em 2013

DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects

Por Rochtus, Anne, Izzi, Benedetta, Vangeel, Elise, Louwette, Sophie, Wittevrongel, Christine, Lambrechts, Diether, Moreau, Yves, Winand, Raf, Verpoorten, Carla, Jansen, Katrien, Van Geet, Chris, Freson, Kathleen
Publicado no Epigenetics (2015)

Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects

Por Rochtus, Anne, Martin-Trujillo, Alejandro, Izzi, Benedetta, Elli, Francesca, Garin, Intza, Linglart, Agnes, Mantovani, Giovanna, Perez de Nanclares, Guiomar, Thiele, Suzanne, Decallonne, Brigitte, Van Geet, Chris, Monk, David, Freson, Kathleen
Publicado no Clin Epigenetics (2016)

Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction

Por Izzi, Benedetta, Francois, Inge, Labarque, Veerle, Thys, Chantal, Wittevrongel, Christine, Devriendt, Koen, Legius, Eric, Van den Bruel, Annick, D'Hooghe, Marc, Lambrechts, Diether, de Zegher, Francis, Van Geet, Chris, Freson, Kathleen
Publicado em 2012

European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study

Por Garin, Intza, Mantovani, Giovanna, Aguirre, Urko, Barlier, Anne, Brix, Bettina, Elli, Francesca M, Freson, Kathleen, Grybek, Virginie, Izzi, Benedetta, Linglart, Agnès, Perez de Nanclares, Guiomar, Silve, Caroline, Thiele, Susanne, Werner, Ralf
Publicado no Eur J Hum Genet (2015)

European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study

Por Garin, Intza, Mantovani, Giovanna, Aguirre, Urko, Barlier, Anne, Brix, Bettina, Elli, Francesca M, Freson, Kathleen, Grybek, Virginie, Izzi, Benedetta, Linglart, Agne's, de Nanclares, Guiomar Perez, Silve, Caroline, Thiele, Susanne, Werner, Ralf
Publicado no Eur J Hum Genet (2015)