Computational modelling of emboli travel trajectories in cerebral arteries: influence of microembolic particle size and density

por Fabbri, Dario, Long, Quan, Das, Saroj, Pinelli, Michele
Publicado 2014

Schizophrenia and vitamin D related genes could have been subject to latitude-driven adaptation

por Amato, Roberto, Pinelli, Michele, Monticelli, Antonella, Miele, Gennaro, Cocozza, Sergio
Publicado 2010

Simulating gene-gene and gene-environment interactions in complex diseases: Gene-Environment iNteraction Simulator 2

por Pinelli, Michele, Scala, Giovanni, Amato, Roberto, Cocozza, Sergio, Miele, Gennaro
Publicado 2012

Genome-Wide Scan for Signatures of Human Population Differentiation and Their Relationship with Natural Selection, Functional Pathways and Diseases

por Amato, Roberto, Pinelli, Michele, Monticelli, Antonella, Marino, Davide, Miele, Gennaro, Cocozza, Sergio
Publicado 2009

A novel approach to simulate gene-environment interactions in complex diseases

por Amato, Roberto, Pinelli, Michele, D'Andrea, Daniel, Miele, Gennaro, Nicodemi, Mario, Raiconi, Giancarlo, Cocozza, Sergio
Publicado 2010

The PPARγ2 Pro12Ala variant is protective against progression of nephropathy in people with type 2 diabetes

por Lapice, Emanuela, Monticelli, Antonella, Cocozza, Sergio, Pinelli, Michele, Cocozza, Sara, Bruzzese, Dario, Riccardi, Gabriele, Vaccaro, Olga
Publicado 2015

Sphingolipid Metabolism Perturbations in Rett Syndrome

por Cappuccio, Gerarda, Donti, Taraka, Pinelli, Michele, Bernardo, Pia, Bravaccio, Carmela, Elsea, Sarah H., Brunetti-Pierri, Nicola
Publicado 2019

Definition of the transcriptional units of inherited retinal disease genes by meta-analysis of human retinal transcriptome data

por Ruiz-Ceja, Karla Alejandra, Capasso, Dalila, Pinelli, Michele, Del Prete, Eugenio, Carrella, Diego, di Bernardo, Diego, Banfi, Sandro
Publicado 2023

β2-adrenergic receptor and UCP3 variants modulate the relationship between age and type 2 diabetes mellitus

por Pinelli, Michele, Giacchetti, Manuela, Acquaviva, Fabio, Cocozza, Sergio, Donnarumma, Giovanna, Lapice, Emanuela, Riccardi, Gabriele, Romano, Geremia, Vaccaro, Olga, Monticelli, Antonella
Publicado 2006

Uncoupling protein 2 G(-866)A polymorphism: a new gene polymorphism associated with C-reactive protein in type 2 diabetic patients C-reactive protein in type 2 diabetic patients

por Lapice, Emanuela, Pinelli, Michele, Pisu, Elisabetta, Monticelli, Antonella, Gambino, Roberto, Pagano, Gianfranco, Valsecchi, Silvia, Cocozza, Sergio, Riccardi, Gabriele, Vaccaro, Olga
Publicado 2010

Improving the Estimation of Celiac Disease Sibling Risk by Non-HLA Genes

por Izzo, Valentina, Pinelli, Michele, Tinto, Nadia, Esposito, Maria Valeria, Cola, Arturo, Sperandeo, Maria Pia, Tucci, Francesca, Cocozza, Sergio, Greco, Luigi, Sacchetti, Lucia
Publicado 2011

Allelic Expression Imbalance in the Human Retinal Transcriptome and Potential Impact on Inherited Retinal Diseases

por Llavona, Pablo, Pinelli, Michele, Mutarelli, Margherita, Singh Marwah, Veer, Schimpf-Linzenbold, Simone, Thaler, Sebastian, Yoeruek, Efdal, Vetter, Jan, Kohl, Susanne, Wissinger, Bernd
Publicado 2017

A child with Myhre syndrome presenting with corectopia and tetralogy of Fallot

por Alagia, Marianna, Cappuccio, Gerarda, Pinelli, Michele, Torella, Annalaura, Brunetti‐Pierri, Raffaella, Simonelli, Francesca, Limongelli, Giuseppe, Oppido, Guido, Nigro, Vincenzo, Brunetti‐Pierri, Nicola
Publicado 2017

Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4

por Cappuccio, Gerarda, Brunetti‐Pierri, Raffaella, Torella, Annalaura, Pinelli, Michele, Castello, Raffaele, Casari, Giorgio, Nigro, Vincenzo, Banfi, Sandro, Simonelli, Francesca, Brunetti‐Pierri, Nicola
Publicado 2019

Expansion of the phenotype of lateral meningocele syndrome

por Cappuccio, Gerarda, Apuzzo, Diletta, Alagia, Marianna, Torella, Annalaura, Pinelli, Michele, Franco, Brunella, Corrado, Bruno, del Giudice, Ennio, D'Amico, Alessandra, Nigro, Vincenzo, Brunetti‐Pierri, Nicola
Publicado 2020

Aldo-Keto Reductase 1C1 (AKR1C1) as the First Mutated Gene in a Family with Nonsyndromic Primary Lipedema

por Michelini, Sandro, Chiurazzi, Pietro, Marino, Valerio, Dell’Orco, Daniele, Manara, Elena, Baglivo, Mirko, Fiorentino, Alessandro, Maltese, Paolo Enrico, Pinelli, Michele, Herbst, Karen Louise, Dautaj, Astrit, Bertelli, Matteo
Publicado 2020

A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability

por Pinelli, Michele, Terrone, Gaetano, Troglio, Flavia, Squeo, Gabriella Maria, Cappuccio, Gerarda, Imperati, Floriana, Pignataro, Piero, Genesio, Rita, Nitch, Lucio, Del Giudice, Ennio, Merla, Giuseppe, Testa, Giuseppe, Brunetti‐Pierri, Nicola
Publicado 2020

Identification of Candidate Children for Maturity-Onset Diabetes of the Young Type 2 (MODY2) Gene Testing: A Seven-Item Clinical Flowchart (7-iF)

por Pinelli, Michele, Acquaviva, Fabio, Barbetti, Fabrizio, Caredda, Elisabetta, Cocozza, Sergio, Delvecchio, Maurizio, Mozzillo, Enza, Pirozzi, Daniele, Prisco, Francesco, Rabbone, Ivana, Sacchetti, Lucia, Tinto, Nadia, Toni, Sonia, Zucchini, Stefano, Iafusco, Dario
Publicado 2013

High-resolution analysis of the human retina miRNome reveals isomiR variations and novel microRNAs

por Karali, Marianthi, Persico, Maria, Mutarelli, Margherita, Carissimo, Annamaria, Pizzo, Mariateresa, Singh Marwah, Veer, Ambrosio, Concetta, Pinelli, Michele, Carrella, Diego, Ferrari, Stefano, Ponzin, Diego, Nigro, Vincenzo, di Bernardo, Diego, Banfi, Sandro
Publicado 2016

Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet

por Cappuccio, Gerarda, Pinelli, Michele, Alagia, Marianna, Donti, Taraka, Day-Salvatore, Debra-Lynn, Veggiotti, Pierangelo, De Giorgis, Valentina, Lunghi, Simona, Vari, Maria Stella, Striano, Pasquale, Brunetti-Pierri, Nicola, Kennedy, Adam D., Elsea, Sarah H.
Publicado 2017