GUELLA, ILARIA
GUELLA, ILARIA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family
2009 J. Song, I. Guella, K.Y. Kwon, H. Cho, R. Park, R. Asselta, J.R. Choi
Analysis of miR-137 expression and rs1625579 in dorsolateral prefrontal cortex
2013 I. Guella, A. Sequeira, B. Rollins, L. Morgan, F. Torri, T.G.M. van Erp, R.M. Myers, J.D. Barchas, A.F. Schatzberg, S.J. Watson, H. Akil, W.E. Bunney, S.G. Potkin, F. Macciardi, M.P. Vawter
Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease
2012 I. Guella, G. Soldà, R. Cilia, G. Pezzoli, R. Asselta, S. Duga, S. Goldwurm
Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease
2009 I. Guella, V. Rimoldi, R. Asselta, D. Ardissino, M. Francolini, N. Martinelli, D. Girelli, F. Peyvandi, M. Tubaro, P.A. Merlini, P.M. Mannucci, S. Duga
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation FXI isoform
2008 V. Rimoldi, I. Guella, R. Asselta, R. De Cristofaro, F. Peyvandi, P.M. Mannucci, S. Duga
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform
2006 R. Asselta, I. Guella, V. Rimoldi, M. Malcovati, M.L. Tenchini, S. Duga
Characterization of the F11 alternative splicing pattern : identification of a novel coagulation FXI isoform
2007 I. Guella, R. Asselta, V. Rimoldi, M.L. Tenchini, S. Duga
Characterization of the genetic basis of FXI deficiency in fourteen unrelated patients
2009 V. Rimoldi, I. Guella, S. Spena, N. Ciavarella, F. Peyvandi, R. Asselta, P.M. Mannucci, S. Duga
Common variants in the haemostatic gene pathway contribute to risk of early-onset myocardial infarction in the Italian population
2011 I. Guella, S. Duga, D. Ardissino, P.A. Merlini, F. Peyvandi, P.M. Mannucci, R. Asselta
DNAJC12 and dopa-responsive nonprogressive parkinsonism
2017 L. Straniero, I. Guella, R. Cilia, L. Parkkinen, V. Rimoldi, A. Young, R. Asselta, G. Soldã , V. Sossi, A.J. Stoessl, A. Priori, K. Nishioka, N. Hattori, J. Follett, A. Rajput, N. Blau, G. Pezzoli, M.J. Farrer, S. Goldwurm, A.H. Rajput, S. Duga
Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population
2010 I. Guella, R. Asselta, D. Ardissino, P.A. Merlini, F. Peyvandi, S. Kathiresan, P.M. Mannucci, M. Tubaro, S. Duga
Factor XI deficiency in Southern Iran: identification of a novel missense mutation
2009 M. Karimi, H. Jafari, S. Lahsaeizadeh, A. Afrasiabi, A. Akbari, J. Dehbozorgian, R. Ardeshiri, I. Guella, R. Asselta, F. Peyvandi
Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction
2008 I. Guella, V. Rimoldi, P.A. Merlini, R. Asselta, E.M. Paraboschi, M. Francolini, F. Peyvandi, D. Ardissino, P.M. Mannucci, S. Duga
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency
2012 E.M. Paraboschi, S.M. Kayiran, N. Ozbek, B. Gürakan, F. Peyvandi, I. Guella, S. Duga, R. Asselta
Glucocerebrosidase mutations in primary parkinsonism
2014 R. Asselta, V. Rimoldi, C. Siri, R. Cilia, I. Guella, S. Tesei, G. Soldà, G. Pezzoli, S. Duga, S. Goldwurm
Identification and characterization of 6 novel genetic defects leading to factor V deficiency
2008 I. Guella, E.M. Paraboschi, S. Duga, R. Asselta
Identification of the first alu-mediated large deletion involving the f5 gene in a compound heterozygous patient with severe factor v deficiency
2011 I. Guella, E.M. Paraboschi, W.A. van Schalkwyk, R. Asselta, S. Duga
Identificazione e caratterizzazione del pattern di splicing alternativo del gene F11 e di una nuova isoforma FXI della coagulazione
2006 R. Asselta, V. Rimoldi, I. Guella, M. Malcovati, M.L. Tenchini, S. Duga
Molecular characterization of 9 genetic defects responsible for FV deficiency
2009 E.M. Paraboschi, I. Guella, S. Duga, F. Peyvandi, P.M. Mannucci, R. Asselta
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA
2010 R. Asselta, V. Rimoldi, I. Guella, G.Soldà, R. De Cristofaro, F. Peyvandi, S. Duga