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Benedetta Izzi
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Anno
Recommendations for the design and analysis of epigenome-wide association studies
KB Michels, AM Binder, S Dedeurwaerder, CB Epstein, JM Greally, I Gut, ...
Nature methods 10 (10), 949-955, 2013
4182013
Investigating the influence of maternal cortisol and emotional state during pregnancy on the DNA methylation status of the glucocorticoid receptor gene (NR3C1) promoter region …
T Hompes, B Izzi, E Gellens, M Morreels, S Fieuws, A Pexsters, G Schops, ...
Journal of psychiatric research 47 (7), 880-891, 2013
3212013
Platelet-leukocyte interactions in thrombosis
C Cerletti, C Tamburrelli, B Izzi, F Gianfagna, G de Gaetano
Thrombosis research 129 (3), 263-266, 2012
2012012
From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network
S Thiele, G Mantovani, A Barlier, V Boldrin, P Bordogna, L De Sanctis, ...
European Journal of Endocrinology 175 (6), P1-P17, 2016
1442016
Regulators of platelet cAMP levels: clinical and therapeutic implications
L Noé, K Peeters, B Izzi, C Van Geet, K Freson
Current medicinal chemistry 17 (26), 2897-2905, 2010
742010
DNA methylation in imprinted genes IGF2 and GNASXL is associated with prenatal maternal stress
EB Vangeel, B Izzi, T Hompes, K Vansteelandt, D Lambrechts, K Freson, ...
Genes, Brain and Behavior 14 (8), 573-582, 2015
682015
Allele-specific DNA methylation reinforces PEAR1 enhancer activity
B Izzi, M Pistoni, K Cludts, P Akkor, D Lambrechts, C Verfaillie, ...
Blood, The Journal of the American Society of Hematology 128 (7), 1003-1012, 2016
572016
Chronic fatigue syndrome and DNA hypomethylation of the glucocorticoid receptor gene promoter 1F region: associations with HPA axis hypofunction and childhood trauma
E Vangeel, F Van Den Eede, T Hompes, B Izzi, J Del Favero, G Moorkens, ...
Psychosomatic medicine 77 (8), 853-862, 2015
522015
Precision medicine and public health: new challenges for effective and sustainable health
D Traversi, A Pulliero, A Izzotti, E Franchitti, L Iacoviello, F Gianfagna, ...
Journal of Personalized Medicine 11 (2), 135, 2021
472021
GNAS defects identified by stimulatory G protein α-subunit signalling studies in platelets
K Freson, B Izzi, V Labarque, M Van Helvoirt, C Thys, C Wittevrongel, ...
The Journal of Clinical Endocrinology & Metabolism 93 (12), 4851-4859, 2008
462008
Beyond haemostasis and thrombosis: platelets in depression and its co-morbidities
B Izzi, A Tirozzi, C Cerletti, MB Donati, G de Gaetano, MF Hoylaerts, ...
International Journal of Molecular Sciences 21 (22), 8817, 2020
442020
Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects
A Rochtus, A Martin-Trujillo, B Izzi, F Elli, I Garin, A Linglart, G Mantovani, ...
Clinical epigenetics 8, 1-12, 2016
442016
DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects
A Rochtus, B Izzi, E Vangeel, S Louwette, C Wittevrongel, D Lambrechts, ...
Epigenetics 10 (1), 92-101, 2015
412015
Pyrosequencing evaluation of widely available bisulfite conversion methods: considerations for application
B Izzi, AM Binder, KB Michels
Medical epigenetics 2 (1), 28-36, 2014
392014
Human platelet pathology related to defects in the G-protein signaling cascade
C Van Geet, B Izzi, V Labarque, K Freson
Journal of Thrombosis and Haemostasis 7, 282-286, 2009
392009
Determinants of platelet conjugate formation with polymorphonuclear leukocytes or monocytes in whole blood
B Izzi, A Pampuch, S Costanzo, B Vohnout, L Iacoviello, C Cerletti, ...
Thrombosis and haemostasis 98 (12), 1276-1284, 2007
382007
Newborn genome-wide DNA methylation in association with pregnancy anxiety reveals a potential role for GABBR1
EB Vangeel, E Pishva, T Hompes, D van den Hove, D Lambrechts, ...
Clinical epigenetics 9, 1-12, 2017
372017
Epoprostenol inhibits human platelet-leukocyte mixed conjugate and platelet microparticle formation in whole blood
C Tamburrelli, M Crescente, B Izzi, M Barisciano, MB Donati, ...
Thrombosis research 128 (5), 446-451, 2011
362011
European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study
I Garin, G Mantovani, U Aguirre, A Barlier, B Brix, FM Elli, K Freson, ...
European Journal of Human Genetics 23 (4), 438-444, 2015
352015
Variation of DNA methylation in candidate age-related targets on the mitochondrial-telomere axis in cord blood and placenta
BG Janssen, HM Byun, B Cox, W Gyselaers, B Izzi, AA Baccarelli, ...
Placenta 35 (9), 665-672, 2014
352014
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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