Alpha-synuclein as a biomarker in Parkinson's disease: focus on neural derived extracelluar vesicles

por Agliardi, Cristina, Guerini, Franca R., Meloni, Mario, Clerici, Mario
Publicado 2021

The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease

por Guerini, Franca R., Ripamonti, Enrico, Costa, Andrea S., Zanzottera, Milena, Agliardi, Cristina, Bolognesi, Elisabetta, Clerici, Mario, Racca, Vittorio
Publicado 2019

A Possible Role for HSV-1-Specific Humoral Response and PILRA rs1859788 Polymorphism in the Pathogenesis of Parkinson’s Disease

por Agostini, Simone, Mancuso, Roberta, Costa, Andrea S., Citterio, Lorenzo A., Guerini, Franca R., Meloni, Mario, Navarro, Jorge, Clerici, Mario
Publicado 2021

Synaptosomal Protein of 25 kDa (Snap25) Polymorphisms Associated with Glycemic Parameters in Type 2 Diabetes Patients

por Al-Daghri, Nasser M., Costa, Andrea S., Alokail, Majed S., Zanzottera, Milena, Alenad, Amal M., Mohammed, Abdul Khader, Clerici, Mario, Guerini, Franca R.
Publicado 2016

The evolutionary history of genes involved in spoken and written language: beyond FOXP2

por Mozzi, Alessandra, Forni, Diego, Clerici, Mario, Pozzoli, Uberto, Mascheretti, Sara, Guerini, Franca R., Riva, Stefania, Bresolin, Nereo, Cagliani, Rachele, Sironi, Manuela
Publicado 2016

A role for activatory KIR/HLA complexes in HIV-associated Kaposi’s sarcoma development

por Agostini, Simone, Guerini, Franca R, Bandera, Alessandra, Mancuso, Roberta, Hernis, Ambra, Agliardi, Cristina, Sabbatici, Francesca, Beretta, Ilaria, Fusco, Caterina, Gori, Andrea, Clerici, Mario
Publicado 2011

Activating KIR/HLA complexes in classic Kaposi's Sarcoma

por Guerini, Franca R, Mancuso, Roberta, Agostini, Simone, Agliardi, Cristina, Zanzottera, Milena, Hernis, Ambra, Tourlaki, Athanasia, Calvo, Maria G, Bellinvia, Monica, Brambilla, Lucia, Clerici, Mario
Publicado 2012

Relationship between herpes simplex virus-1-specific antibody titers and cortical brain damage in Alzheimer’s disease and amnestic mild cognitive impairment

por Mancuso, Roberta, Baglio, Francesca, Agostini, Simone, Agostini, Monia Cabinio, Laganà, Maria M., Hernis, Ambra, Margaritella, Nicolò, Guerini, Franca R., Zanzottera, Milena, Nemni, Raffaello, Clerici, Mario
Publicado 2014

Genetic adaptation of the human circadian clock to day-length latitudinal variations and relevance for affective disorders

por Forni, Diego, Pozzoli, Uberto, Cagliani, Rachele, Tresoldi, Claudia, Menozzi, Giorgia, Riva, Stefania, Guerini, Franca R, Comi, Giacomo P, Bolognesi, Elisabetta, Bresolin, Nereo, Clerici, Mario, Sironi, Manuela
Publicado 2014

HLA alleles modulate EBV viral load in multiple sclerosis

por Agostini, Simone, Mancuso, Roberta, Guerini, Franca R., D’Alfonso, Sandra, Agliardi, Cristina, Hernis, Ambra, Zanzottera, Milena, Barizzone, Nadia, Leone, Maurizio A., Caputo, Domenico, Rovaris, Marco, Clerici, Mario
Publicado 2018

Ancient and Recent Selective Pressures Shaped Genetic Diversity at AIM2-Like Nucleic Acid Sensors

por Cagliani, Rachele, Forni, Diego, Biasin, Mara, Comabella, Manuel, Guerini, Franca R., Riva, Stefania, Pozzoli, Uberto, Agliardi, Cristina, Caputo, Domenico, Malhotra, Sunny, Montalban, Xavier, Bresolin, Nereo, Clerici, Mario, Sironi, Manuela
Publicado 2014

Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring

por Carta, Alessandra, Zarbo, Ignazio R, Scoppola, Chiara, Pisuttu, Giulia, Conti, Marta, Melis, Maria C, Martino, Federica De, Serra, Antonella, Biancu, Maria A, Guerini, Franca R, Bazzardi, Riccardo, Sotgiu, Stefano
Publicado 2021

Vitamin D Receptor Gene Polymorphisms Are Associated with Obesity and Inflammosome Activity

por Al-Daghri, Nasser M., Guerini, Franca R., Al-Attas, Omar S., Alokail, Majed S., Alkharfy, Khalid M., Draz, Hossam M., Agliardi, Cristina, Costa, Andrea S., Saulle, Irma, Mohammed, Abdul Khader, Biasin, Mara, Clerici, Mario
Publicado 2014

Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis

por Cagliani, Rachele, Fumagalli, Matteo, Guerini, Franca R., Riva, Stefania, Galimberti, Daniela, Comi, Giacomo P., Agliardi, Cristina, Scarpini, Elio, Pozzoli, Uberto, Forni, Diego, Caputo, Domenico, Asselta, Rosanna, Biasin, Mara, Paraboschi, Elvezia M., Bresolin, Nereo, Clerici, Mario, Sironi, Manuela
Publicado 2011

Association of Genetic Markers with CSF Oligoclonal Bands in Multiple Sclerosis Patients

por Leone, Maurizio A., Barizzone, Nadia, Esposito, Federica, Lucenti, Ausiliatrice, Harbo, Hanne F., Goris, An, Kockum, Ingrid, Oturai, Annette Bang, Celius, Elisabeth Gulowsen, Mero, Inger L., Dubois, Bénédicte, Olsson, Tomas, Søndergaard, Helle Bach, Cusi, Daniele, Lupoli, Sara, Andreassen, Bettina Kulle, Myhr, Kjell-Morten, Guerini, Franca R., Comi, Giancarlo, Martinelli-Boneschi, Filippo, D'Alfonso, Sandra
Publicado 2013

A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis

por Ban, Maria, McCauley, Jacob L., Zuvich, Rebecca, Baker, Amie, Bergamaschi, Laura, Cox, Mathew, Kemppinen, Anu, D’Alfonso, Sandra, Guerini, Franca R., Lechner-Scott, Jeannette, Dudbridge, Frank, Wason, James, Robertson, Neil P., De Jager, Philip L., Hafler, David A., Barcellos, Lisa F., Ivinson, Adrian J., Sexton, David, Oksenberg, Jorge R., Hauser, Stephen L., Pericak-Vance, Margaret A., Haines, Jonathan, Compston, Alastair, Sawcer, Stephen
Publicado 2010