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

par Guerini, Franca R., Ripamonti, Enrico, Costa, Andrea S., Zanzottera, Milena, Agliardi, Cristina, Bolognesi, Elisabetta, Clerici, Mario, Racca, Vittorio
Publié dans Medicine (Baltimore) (2019)

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

par Agostini, Simone, Mancuso, Roberta, Costa, Andrea S., Citterio, Lorenzo A., Guerini, Franca R., Meloni, Mario, Navarro, Jorge, Clerici, Mario
Publié dans Vaccines (Basel) (2021)

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

par Al-Daghri, Nasser M., Costa, Andrea S., Alokail, Majed S., Zanzottera, Milena, Alenad, Amal M., Mohammed, Abdul Khader, Clerici, Mario, Guerini, Franca R.
Publié dans J Diabetes Res (2016)

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

par Mozzi, Alessandra, Forni, Diego, Clerici, Mario, Pozzoli, Uberto, Mascheretti, Sara, Guerini, Franca R., Riva, Stefania, Bresolin, Nereo, Cagliani, Rachele, Sironi, Manuela
Publié dans Sci Rep (2016)

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

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

Activating KIR/HLA complexes in classic Kaposi's Sarcoma

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

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

par 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
Publié 2014

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

par 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
Publié dans Genome Biol (2014)

HLA alleles modulate EBV viral load in multiple sclerosis

par 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
Publié dans J Transl Med (2018)

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

par 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
Publié 2014

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

par 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
Publié dans Mult Scler J Exp Transl Clin (2021)

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

par 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
Publié 2014

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

par 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
Publié dans Hum Genet (2011)

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

par 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
Publié 2013

Epstein-Barr virus genetic variants are associated with multiple sclerosis

par Mechelli, Rosella, Manzari, Caterina, Policano, Claudia, Annese, Anita, Picardi, Ernesto, Umeton, Renato, Fornasiero, Arianna, D'Erchia, Anna Maria, Buscarinu, Maria Chiara, Agliardi, Cristina, Annibali, Viviana, Serafini, Barbara, Rosicarelli, Barbara, Romano, Silvia, Angelini, Daniela F., Ricigliano, Vito A.G., Buttari, Fabio, Battistini, Luca, Centonze, Diego, Guerini, Franca R., D'Alfonso, Sandra, Pesole, Graziano, Salvetti, Marco, Ristori, Giovanni
Publié dans Neurology (2015)

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

par 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
Publié 2010