FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans

gan Molokhia, Mariam, Fanciulli, Manuela, Petretto, Enrico, Patrick, Alan Leslie, McKeigue, Paul, Roberts, Amy L., Vyse, Tim J., Aitman, Tim J.
Cyhoeddwyd 2011

A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search

gan Angius, Andrea, Petretto, Enrico, Maestrale, Giovanni Battista, Forabosco, Paola, Casu, Giuseppina, Piras, Daniela, Fanciulli, Manuela, Falchi, Mario, Melis, Paola Maria, Palermo, Mario, Pirastu, Mario
Cyhoeddwyd 2002

Molecular changes induced by the curcumin analogue D6 in human melanoma cells

gan Rozzo, Carla, Fanciulli, Manuela, Fraumene, Cristina, Corrias, Antonio, Cubeddu, Tiziana, Sassu, Ilaria, Cossu, Sara, Nieddu, Valentina, Galleri, Grazia, Azara, Emanuela, Dettori, Maria Antonietta, Fabbri, Davide, Palmieri, Giuseppe, Pisano, Marina
Cyhoeddwyd 2013

Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations

gan Mocci, Evelina, Concas, Maria P, Fanciulli, Manuela, Pirastu, Nicola, Adamo, Mauro, Cabras, Valentina, Fraumene, Cristina, Persico, Ivana, Sassu, Alessandro, Picciau, Andrea, Prodi, Dionigio A, Serra, Donatella, Biino, Ginevra, Pirastu, Mario, Angius, Andrea
Cyhoeddwyd 2009

The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations

gan Michelucci, Roberto, Pulitano, Patrizia, Di Bonaventura, Carlo, Binelli, Simona, Luisi, Concetta, Pasini, Elena, Striano, Salvatore, Striano, Pasquale, Coppola, Giangennaro, La Neve, Angela, Giallonardo, Anna Teresa, Mecarelli, Oriano, Serioli, Elena, Dazzo, Emanuela, Fanciulli, Manuela, Nobile, Carlo
Cyhoeddwyd yn Epilepsy Behav (2017)

Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy

gan Li Mura, Ilena Egle Astrid, Bauce, Barbara, Nava, Andrea, Fanciulli, Manuela, Vazza, Giovanni, Mazzotti, Elisa, Rigato, Ilaria, De Bortoli, Marzia, Beffagna, Giorgia, Lorenzon, Alessandra, Calore, Martina, Dazzo, Emanuela, Nobile, Carlo, Luisa Mostacciuolo, Maria, Corrado, Domenico, Basso, Cristina, Daliento, Luciano, Thiene, Gaetano, Rampazzo, Alessandra
Cyhoeddwyd 2013

Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy

gan Dazzo, Emanuela, Fanciulli, Manuela, Serioli, Elena, Minervini, Giovanni, Pulitano, Patrizia, Binelli, Simona, Di Bonaventura, Carlo, Luisi, Concetta, Pasini, Elena, Striano, Salvatore, Striano, Pasquale, Coppola, Giangennaro, Chiavegato, Angela, Radovic, Slobodanka, Spadotto, Alessandro, Uzzau, Sergio, La Neve, Angela, Giallonardo, Anna Teresa, Mecarelli, Oriano, Tosatto, Silvio C.E., Ottman, Ruth, Michelucci, Roberto, Nobile, Carlo
Cyhoeddwyd yn Am J Hum Genet (2015)

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

gan Fanciulli, Manuela, Norsworthy, Penny J, Petretto, Enrico, Dong, Rong, Harper, Lorraine, Kamesh, Lavanya, Heward, Joanne M, Gough, Stephen C L, de Smith, Adam, Blakemore, Alexandra I F, Froguel, Philippe, Owen, Catherine J, Pearce, Simon H S, Teixeira, Luis, Guillevin, Loic, Graham, Deborah S Cunninghame, Pusey, Charles D, Cook, H Terence, Vyse, Timothy J, Aitman, Timothy J
Cyhoeddwyd 2007

Association of variation in Fcγ receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples

gan McKinney, Cushla, Fanciulli, Manuela, Merriman, Marilyn E, Phipps-Green, Amanda, Alizadeh, Behrooz Z, Koeleman, Bobby P C, Dalbeth, Nicola, Gow, Peter J, Harrison, Andrew A, Highton, John, Jones, Peter B, Stamp, Lisa K, Steer, Sophia, Barrera, Pilar, Coenen, Marieke J H, Franke, Barbara, van Riel, Piet L C M, Vyse, Tim J, Aitman, Tim J, Radstake, Timothy R D J, Merriman, Tony R
Cyhoeddwyd 2010