D'ALFONSO, Sandra
D'ALFONSO, Sandra
Dipartimento di Scienze della Salute
. Linkage disequilibrium between intra-locus variants in the Aminopeptidase N gene and test of their association with coeliac disease
1999-01-01 Giordano, Mara; Bolognesi, E.; S., Dalfonso; M., Lessi; P., Zavattari; G., Oderda; F., Clot; S., Percopo; G., Casari; L., Greco; R., Tosi; P., MOMIGLIANO RICHIARDI
[Viral genotype and HLA class II alleles influence on extra-hepatic manifestations of chronic HCV infection]
2008-01-01 Giannitti, C; Morozzi, G; D'Alfonso, Sandra; Bellisai, F; Galeazzi, M.
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis.
2013-01-01 R., Mechelli; R., Umeton; C., Policano; V., Annibali; G., Coarelli; V. A., G.; D., Vittori; A., Fornasiero; M. C., Buscarinu; I. M., Sclerosis; 2. W., Trust; Collaborators Sawcer, S; Hellenthal, G; Pirinen, M; Spencer, Cc; Patsopoulos, Na; Moutsianas, L; Dilthey, A; Su, Z; Freeman, C; Hunt, Se; Edkins, S; Gray, E; Booth, Dr; Potter, Sc; Goris, A; Band, G; Oturai, Ab; Strange, A; Saarela, J; Bellenguez, C; Fontaine, B; Gillman, M; Hemmer, B; Gwilliam, R; Zipp, F; Jayakumar, A; Martin, R; Leslie, S; Hawkins, S; Giannoulatou, E; D'Alfonso, Sandra; Blackburn, H; Boneschi, Fm; Liddle, J; Harbo, Hf; Perez, Ml; Spurkland, A; Waller, Mj; Mycko, Mp; Ricketts, M; Comabella, M; Hammond, N; Kockum, I; Mccann, Ot; Ban, M; Whittaker, P; Kemppinen, A; Weston, P; Hawkins, C; Widaa, S; Zajicek, J; Dronov, S; Robertson, N; Bumpstead, Sj; Barcellos, Lf; Ravindrarajah, R; Abraham, R; Alfredsson, L; Ardlie, K; Aubin, C; Baker, A; Baker, K; Baranzini, Se; Bergamaschi, L; Bergamaschi, R; Bernstein, A; Berthele, A; Boggild, M; Bradfield, Jp; Brassat, D; Broadley, Sa; Buck, D; Butzkueven, H; Capra, R; Carroll, Wm; Cavalla, P; Celius, Eg; Cepok, S; Chiavacci, R; Clerget Darpoux, F; Clysters, K; Comi, G; Cossburn, M; Cournu Rebeix, I; Cox, Mb; Cozen, W; Cree, Ba; Cross, Ah; Cusi, D; Daly, Mj; Davis, E; de Bakker, Pi; Debouverie, M; D'Hooghe, Mb; Dixon, K; Dobosi, R; Dubois, B; Ellinghaus, D; Elovaara, I; Esposito, F; Fontenille, C; Foote, S; Franke, A; Galimberti, D; Ghezzi, A; Glessner, J; Gomez, R; Gout, O; Graham, C; Grant, Sf; Guerini, Fr; Hakonarson, H; Hall, P; Hamsten, A; Hartung, Hp; Heard, Rn; Heath, S; Hobart, J; Hoshi, M; Infante Duarte, C; Ingram, G; Ingram, W; Islam, T; Jagodic, M; Kabesch, M; Kermode, Ag; Kilpatrick, Tj; Kim, C; Klopp, N; Koivisto, K; Larsson, M; Lathrop, M; Lechner Scott, Js; Leone, Ma; Leppä, V; Liljedahl, U; Lima Bomfim, I; Lincoln, Rr; Link, J; Liu, J; Lorentzen, År; Lupoli, S; Macciardi, F; Mack, T; Marriott, M; Martinelli, V; Mason, D; Mccauley, Jl; Mentch, F; Mero, Il; Mihalova, T; Montalban, X; Mottershead, J; Myhr, Km; Naldi, P; Ollier, W; Page, A; Palotie, A; Pelletier, J; Piccio, L; Pickersgill, T; Piehl, F; Pobywajlo, S; Quach, Hl; Ramsay, Pp; Reunanen, M; Reynolds, R; Rioux, Jd; Rodegher, M; Roesner, S; Rubio, Jp; Rückert, Im; Salvi, E; Santaniello, A; Schaefer, Ca; Schreiber, S; Schulze, C; Scott, Rj; Sellebjerg, F; Selmaj, Kw; Sexton, D; Shen, L; Simms Acuna, B; Skidmore, S; Sleiman, Pm; Smestad, C; Sørensen, Ps; Søndergaard, Hb; Stankovich, J; Strange, Rc; Sulonen, Am; Sundqvist, E; Syvänen, Ac; Taddeo, F; Taylor, B; Blackwell, Jm; Tienari, P; Bramon, E; Tourbah, A; Brown, Ma; Tronczynska, E; Casas, Jp; Tubridy, N; Corvin, A; Vickery, J; Jankowski, J; Villoslada, P; Markus, Hs; Wang, K; Mathew, Cg; Wason, J; Palmer, Cn; Wichmann, He; Plomin, R; Willoughby, E; Rautanen, A; Winkelmann, J; Wittig, M; Trembath, Rc; Yaouanq, J; Viswanathan, Ac; Zhang, H; Wood, Nw; Zuvich, R; Deloukas, P; Langford, C; Duncanson, A; Oksenberg, Jr; Pericak Vance, Ma; Haines, Jl; Olsson, T; Hillert, J; Ivinson, Aj; De Jager, Pl; Peltonen, L; Stewart, Gj; Hafler, Da; Hauser, Sl; Mcvean, G; Donnelly, P; Compston A. S., Romano; M., Salvetti; G., Ristori
A 3'-untranslated region variant is associated with impaired expression of CD226 in T and natural killer T cells and is associated with susceptibility to systemic lupus erythematosus
2010-01-01 Löfgren, Se; DELGADO VEGA, Am; Gallant, Cj; Sánchez, E; Frostegård, J; Truedsson, L; DE RAMÓN GARRIDO, E; Sabio, Jm; GONZÁLEZ ESCRIBANO, Mf; PONS ESTEL, Ba; D'Alfonso, Sandra; Witte, T; Lauwerys, Br; Endreffy, E; Kovács, L; Vasconcelos, C; MARTINS DA SILVA, B; Martín, J; ALARCÓN RIQUELME, Me; Kozyrev, Sv
A case of early-onset Parkinson's disease in a patient with KBG syndrome
2023-01-01 Magistrelli, Luca; Contaldi, Elena; Caushi, Fjorilda; Spano, Alice; Cantello, Roberto; D'Alfonso, Sandra; Corrado, Lucia
A case of late-onset OCD developing PLS and FTD
2018-01-01 Bersano, Enrica; Sarnelli, Maria Francesca; Solara, Valentina; De Marchi, Fabiola; Sacchetti, Gian Mauro; Stecco, Alessandro; Corrado, Lucia; D'Alfonso, Sandra; Cantello, Roberto; Mazzini, Letizia
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia
2018-01-01 De Marchi, F; Tondo, G; Sarnelli, M F; Corrado, L; Solara, V; D'Alfonso, S; Cantello, R; Mazzini, L
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies
2018-01-01 Genovese, Loredana M.; Geraci, Filippo; Corrado, Lucia; Mangano, Eleonora; D'Aurizio, Romina; Bordoni, Roberta; Severgnini, Marco; Manzini, Giovanni; De Bellis, Gianluca; D'Alfonso, Sandra; Pellegrini, Marco
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility.
2014-01-01 V., Damotte; L., Guillot Noel; N. A., Patsopoulos; L., Madireddy; M. E., Behi; I. M., Sclerosis; W. T., Case; P. L., collaborators: Barcellos L; Booth, D; Mccauley, Jl; Comabella, M; Compston, A; D'Alfonso, Sandra; De Jager, P; Fontaine, B; Goris, A; Hafler, D; Haines, J; Harbo, Hf; Hauser, Sl; Hawkins, C; Hemmer, B; Hillert, J; Ivinson, A; Kockum, I; Martin, R; Martinelli Boneschi, F; Oksenberg, J; Olsson, T; Oturai, A; Patsopoulos, N; Pericak Vance, M; Saarela, J; Sawcer, S; Spurkland, A; Stewart, G; Zipp, F; Scott, Rj; Lechner Scott, J; Moscato, P; Booth, Dr; Stewart, Gj; Heard, Rn; Mason, D; Griffiths, L; Broadley, S; Brown, Ma; Slee, M; Foote, Sj; Stankovich, J; Taylor, Bv; Wiley, J; Bahlo, M; Perreau, V; Field, J; Butzkueven, H; Kilpatrick, Tj; Rubio, J; Marriott, M; Carroll, Wm; Kermode A. G., De; S. E., Baranzini; I., Cournu Rebeix; B., Fontaine
A genome screen for multiple sclerosis in Italian families
2001-01-01 S., Broadley; S., Sawcer; D'Alfonso, Sandra; A., Hensiek; F., Coraddu; J., Gray; R., Roxburgh; D., Clayton; M., Salvetti; A., Quattrone; M., Trojano; L., Massacesi; GENES AND IMMUNITY, A. C. O. M. P. S. T. O. N.
A genome screen for multiple sclerosis in Sardinian multiplex families
2001-01-01 Coraddu, F; Sawcer, S; D'Alfonso, Sandra; Lai, M; Hensiek, A; Solla, E; Broadley, S; Mancosu, C; Pugliatti, M; Marrosu, Mg; Compston, A.
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
2014-01-01 Fogh, I; Ratti, A; Gellera, C; Lin, K; Tiloca, C; Moskvina, V; Corrado, Lucia; Sorarù, G; Cereda, C; Corti, S; Gentilini, D; Calini, D; Castellotti, B; Mazzini, L; Querin, G; Gagliardi, S; Del Bo, R; Conforti, Fl; Siciliano, G; Inghilleri, M; Saccà, F; Bongioanni, P; Penco, S; Corbo, M; Sorbi, S; Filosto, M; Ferlini, A; Di Blasio, Am; Signorini, S; Shatunov, A; Jones, A; Shaw, Pj; Morrison, Ke; Farmer, Ae; Van Damme, P; Robberecht, W; Chiò, A; Traynor, Bj; Sendtner, M; Melki, J; Meininger, V; Hardiman, O; Andersen, Pm; Leigh, Np; Glass, Jd; Overste, D; Diekstra, Fp; Veldink, Jh; van Es, Ma; Shaw, Ce; Weale, Me; Lewis, Cm; Williams, J; Brown, Rh; Landers, Je; Ticozzi, N; Ceroni, M; Pegoraro, E; Comi, Gp; D'Alfonso, Sandra; van den Berg, Lh; Taroni, F; Al Chalabi, A; Powell, J; Silani, V; the SLAGEN, Consortium; Collaborators,
A Large twins study in coeliac disease
2002-01-01 I., Coto; S., Percopo; Mg, Limongelli; V., Gasperi; M., Maglio; F., Paparo; N., Tinto; L., Sacchetti; D'Alfonso, Sandra; P., MOMIGLIANO RICHIARDI; R., Scoglio; G., Magazzu'; D., Renzi; A., Calabro'; F., Cataldo; L., Greco
A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus
2009-01-01 Orrú, V; Tsai, Sj; Rueda, B; Fiorillo, E; Stanford, Sm; Dasgupta, J; Hartiala, J; Zhao, L; ORTEGO CENTENO, N; D'Alfonso, Sandra; ITALIAN COLLABORATIVE, Group; Arnett, Fc; Wu, H; GONZALEZ GAY, Ma; Tsao, Bp; PONS ESTEL, B; ALARCON RIQUELME, Me; He, Y; Zhang, Zy; Allayee, H; Chen, Xs; Martin, J; Bottini, N.
A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility
2022-01-01 Sorosina, Melissa; Barizzone, Nadia; Clarelli, Ferdinando; Anand, Santosh; Lupoli, Sara; Salvi, Erika; Mangano, Eleonora; Bordoni, Roberta; Roostaei, Tina; Mascia, Elisabetta; Zuccalà, Miriam; Vecchio, Domizia; Cavalla, Paola; Santoro, Silvia; Ferrè, Laura; Zollo, Alen; Barlassina, Cristina; Cusi, Daniele; Martinelli, Vittorio; Comi, Giancarlo; Leone, Maurizio; Filippi, Massimo; Patsopoulos, Nikolaos A; De Jager, Philip L; De Bellis, Gianluca; Esposito, Federica; D'Alfonso, Sandra; Martinelli Boneschi, Filippo
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis
2010-01-01 Ban, M; Mccauley, Jl; Zuvich, R; Baker, A; Bergamaschi, L; Cox, M; Kemppinen, A; D'Alfonso, Sandra; Guerini, Fr; LECHNER SCOTT, J; Dudbridge, F; Wason, J; Robertson, Np; De, ; Jager, Pl; Hafler, Da; Barcellos, Lf; Ivinson, Aj; Sexton, D; Oksenberg, Jr; Hauser, Sl; PERICAK VANCE, Ma; Haines, J; Compston, A; Sawcer, S.
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient
2011-01-01 Corrado, Lucia; Caromagno, Y; Falasco, L; Mellone, S; Godi, M; Cova, E; Cereda, C; Testa, L; Mazzini, L; D'Alfonso, Sandra
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b
2016-01-01 Corrado, Lucia; Magri, S; Bagarotti, Alessandra; Carecchio, Miryam; Piscosquito, G; Pareyson, D; Varrasi, C; Vecchio, D; Zonta, Andrea; Cantello, Roberto; Taroni, F; D'Alfonso, Sandra
A polymorphic variation in a putative regulation box of the TNFA promoter region.
1994-01-01 D'Alfonso, Sandra; Immunogenetics, Richiardi P. M.
A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86.
1994-01-01 el Borai, Mh; D'Alfonso, Sandra; Mazzola, G; Fasano, M. E.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| . Linkage disequilibrium between intra-locus variants in the Aminopeptidase N gene and test of their association with coeliac disease | 1-gen-1999 | Giordano, Mara; Bolognesi, E.; S., Dalfonso; M., Lessi; P., Zavattari; G., Oderda; F., Clot; S., Percopo; G., Casari; L., Greco; R., Tosi; P., MOMIGLIANO RICHIARDI | |
| [Viral genotype and HLA class II alleles influence on extra-hepatic manifestations of chronic HCV infection] | 1-gen-2008 | Giannitti, C; Morozzi, G; D'Alfonso, Sandra; Bellisai, F; Galeazzi, M. | |
| A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. | 1-gen-2013 | R., Mechelli; R., Umeton; C., Policano; V., Annibali; G., Coarelli; V. A., G.; D., Vittori; A., Fornasiero; M. C., Buscarinu; I. M., Sclerosis; 2. W., Trust; Collaborators Sawcer, S; Hellenthal, G; Pirinen, M; Spencer, Cc; Patsopoulos, Na; Moutsianas, L; Dilthey, A; Su, Z; Freeman, C; Hunt, Se; Edkins, S; Gray, E; Booth, Dr; Potter, Sc; Goris, A; Band, G; Oturai, Ab; Strange, A; Saarela, J; Bellenguez, C; Fontaine, B; Gillman, M; Hemmer, B; Gwilliam, R; Zipp, F; Jayakumar, A; Martin, R; Leslie, S; Hawkins, S; Giannoulatou, E; D'Alfonso, Sandra; Blackburn, H; Boneschi, Fm; Liddle, J; Harbo, Hf; Perez, Ml; Spurkland, A; Waller, Mj; Mycko, Mp; Ricketts, M; Comabella, M; Hammond, N; Kockum, I; Mccann, Ot; Ban, M; Whittaker, P; Kemppinen, A; Weston, P; Hawkins, C; Widaa, S; Zajicek, J; Dronov, S; Robertson, N; Bumpstead, Sj; Barcellos, Lf; Ravindrarajah, R; Abraham, R; Alfredsson, L; Ardlie, K; Aubin, C; Baker, A; Baker, K; Baranzini, Se; Bergamaschi, L; Bergamaschi, R; Bernstein, A; Berthele, A; Boggild, M; Bradfield, Jp; Brassat, D; Broadley, Sa; Buck, D; Butzkueven, H; Capra, R; Carroll, Wm; Cavalla, P; Celius, Eg; Cepok, S; Chiavacci, R; Clerget Darpoux, F; Clysters, K; Comi, G; Cossburn, M; Cournu Rebeix, I; Cox, Mb; Cozen, W; Cree, Ba; Cross, Ah; Cusi, D; Daly, Mj; Davis, E; de Bakker, Pi; Debouverie, M; D'Hooghe, Mb; Dixon, K; Dobosi, R; Dubois, B; Ellinghaus, D; Elovaara, I; Esposito, F; Fontenille, C; Foote, S; Franke, A; Galimberti, D; Ghezzi, A; Glessner, J; Gomez, R; Gout, O; Graham, C; Grant, Sf; Guerini, Fr; Hakonarson, H; Hall, P; Hamsten, A; Hartung, Hp; Heard, Rn; Heath, S; Hobart, J; Hoshi, M; Infante Duarte, C; Ingram, G; Ingram, W; Islam, T; Jagodic, M; Kabesch, M; Kermode, Ag; Kilpatrick, Tj; Kim, C; Klopp, N; Koivisto, K; Larsson, M; Lathrop, M; Lechner Scott, Js; Leone, Ma; Leppä, V; Liljedahl, U; Lima Bomfim, I; Lincoln, Rr; Link, J; Liu, J; Lorentzen, År; Lupoli, S; Macciardi, F; Mack, T; Marriott, M; Martinelli, V; Mason, D; Mccauley, Jl; Mentch, F; Mero, Il; Mihalova, T; Montalban, X; Mottershead, J; Myhr, Km; Naldi, P; Ollier, W; Page, A; Palotie, A; Pelletier, J; Piccio, L; Pickersgill, T; Piehl, F; Pobywajlo, S; Quach, Hl; Ramsay, Pp; Reunanen, M; Reynolds, R; Rioux, Jd; Rodegher, M; Roesner, S; Rubio, Jp; Rückert, Im; Salvi, E; Santaniello, A; Schaefer, Ca; Schreiber, S; Schulze, C; Scott, Rj; Sellebjerg, F; Selmaj, Kw; Sexton, D; Shen, L; Simms Acuna, B; Skidmore, S; Sleiman, Pm; Smestad, C; Sørensen, Ps; Søndergaard, Hb; Stankovich, J; Strange, Rc; Sulonen, Am; Sundqvist, E; Syvänen, Ac; Taddeo, F; Taylor, B; Blackwell, Jm; Tienari, P; Bramon, E; Tourbah, A; Brown, Ma; Tronczynska, E; Casas, Jp; Tubridy, N; Corvin, A; Vickery, J; Jankowski, J; Villoslada, P; Markus, Hs; Wang, K; Mathew, Cg; Wason, J; Palmer, Cn; Wichmann, He; Plomin, R; Willoughby, E; Rautanen, A; Winkelmann, J; Wittig, M; Trembath, Rc; Yaouanq, J; Viswanathan, Ac; Zhang, H; Wood, Nw; Zuvich, R; Deloukas, P; Langford, C; Duncanson, A; Oksenberg, Jr; Pericak Vance, Ma; Haines, Jl; Olsson, T; Hillert, J; Ivinson, Aj; De Jager, Pl; Peltonen, L; Stewart, Gj; Hafler, Da; Hauser, Sl; Mcvean, G; Donnelly, P; Compston A. S., Romano; M., Salvetti; G., Ristori | |
| A 3'-untranslated region variant is associated with impaired expression of CD226 in T and natural killer T cells and is associated with susceptibility to systemic lupus erythematosus | 1-gen-2010 | Löfgren, Se; DELGADO VEGA, Am; Gallant, Cj; Sánchez, E; Frostegård, J; Truedsson, L; DE RAMÓN GARRIDO, E; Sabio, Jm; GONZÁLEZ ESCRIBANO, Mf; PONS ESTEL, Ba; D'Alfonso, Sandra; Witte, T; Lauwerys, Br; Endreffy, E; Kovács, L; Vasconcelos, C; MARTINS DA SILVA, B; Martín, J; ALARCÓN RIQUELME, Me; Kozyrev, Sv | |
| A case of early-onset Parkinson's disease in a patient with KBG syndrome | 1-gen-2023 | Magistrelli, Luca; Contaldi, Elena; Caushi, Fjorilda; Spano, Alice; Cantello, Roberto; D'Alfonso, Sandra; Corrado, Lucia | |
| A case of late-onset OCD developing PLS and FTD | 1-gen-2018 | Bersano, Enrica; Sarnelli, Maria Francesca; Solara, Valentina; De Marchi, Fabiola; Sacchetti, Gian Mauro; Stecco, Alessandro; Corrado, Lucia; D'Alfonso, Sandra; Cantello, Roberto; Mazzini, Letizia | |
| A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia | 1-gen-2018 | De Marchi, F; Tondo, G; Sarnelli, M F; Corrado, L; Solara, V; D'Alfonso, S; Cantello, R; Mazzini, L | |
| A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies | 1-gen-2018 | Genovese, Loredana M.; Geraci, Filippo; Corrado, Lucia; Mangano, Eleonora; D'Aurizio, Romina; Bordoni, Roberta; Severgnini, Marco; Manzini, Giovanni; De Bellis, Gianluca; D'Alfonso, Sandra; Pellegrini, Marco | |
| A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. | 1-gen-2014 | V., Damotte; L., Guillot Noel; N. A., Patsopoulos; L., Madireddy; M. E., Behi; I. M., Sclerosis; W. T., Case; P. L., collaborators: Barcellos L; Booth, D; Mccauley, Jl; Comabella, M; Compston, A; D'Alfonso, Sandra; De Jager, P; Fontaine, B; Goris, A; Hafler, D; Haines, J; Harbo, Hf; Hauser, Sl; Hawkins, C; Hemmer, B; Hillert, J; Ivinson, A; Kockum, I; Martin, R; Martinelli Boneschi, F; Oksenberg, J; Olsson, T; Oturai, A; Patsopoulos, N; Pericak Vance, M; Saarela, J; Sawcer, S; Spurkland, A; Stewart, G; Zipp, F; Scott, Rj; Lechner Scott, J; Moscato, P; Booth, Dr; Stewart, Gj; Heard, Rn; Mason, D; Griffiths, L; Broadley, S; Brown, Ma; Slee, M; Foote, Sj; Stankovich, J; Taylor, Bv; Wiley, J; Bahlo, M; Perreau, V; Field, J; Butzkueven, H; Kilpatrick, Tj; Rubio, J; Marriott, M; Carroll, Wm; Kermode A. G., De; S. E., Baranzini; I., Cournu Rebeix; B., Fontaine | |
| A genome screen for multiple sclerosis in Italian families | 1-gen-2001 | S., Broadley; S., Sawcer; D'Alfonso, Sandra; A., Hensiek; F., Coraddu; J., Gray; R., Roxburgh; D., Clayton; M., Salvetti; A., Quattrone; M., Trojano; L., Massacesi; GENES AND IMMUNITY, A. C. O. M. P. S. T. O. N. | |
| A genome screen for multiple sclerosis in Sardinian multiplex families | 1-gen-2001 | Coraddu, F; Sawcer, S; D'Alfonso, Sandra; Lai, M; Hensiek, A; Solla, E; Broadley, S; Mancosu, C; Pugliatti, M; Marrosu, Mg; Compston, A. | |
| A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis | 1-gen-2014 | Fogh, I; Ratti, A; Gellera, C; Lin, K; Tiloca, C; Moskvina, V; Corrado, Lucia; Sorarù, G; Cereda, C; Corti, S; Gentilini, D; Calini, D; Castellotti, B; Mazzini, L; Querin, G; Gagliardi, S; Del Bo, R; Conforti, Fl; Siciliano, G; Inghilleri, M; Saccà, F; Bongioanni, P; Penco, S; Corbo, M; Sorbi, S; Filosto, M; Ferlini, A; Di Blasio, Am; Signorini, S; Shatunov, A; Jones, A; Shaw, Pj; Morrison, Ke; Farmer, Ae; Van Damme, P; Robberecht, W; Chiò, A; Traynor, Bj; Sendtner, M; Melki, J; Meininger, V; Hardiman, O; Andersen, Pm; Leigh, Np; Glass, Jd; Overste, D; Diekstra, Fp; Veldink, Jh; van Es, Ma; Shaw, Ce; Weale, Me; Lewis, Cm; Williams, J; Brown, Rh; Landers, Je; Ticozzi, N; Ceroni, M; Pegoraro, E; Comi, Gp; D'Alfonso, Sandra; van den Berg, Lh; Taroni, F; Al Chalabi, A; Powell, J; Silani, V; the SLAGEN, Consortium; Collaborators, | |
| A Large twins study in coeliac disease | 1-gen-2002 | I., Coto; S., Percopo; Mg, Limongelli; V., Gasperi; M., Maglio; F., Paparo; N., Tinto; L., Sacchetti; D'Alfonso, Sandra; P., MOMIGLIANO RICHIARDI; R., Scoglio; G., Magazzu'; D., Renzi; A., Calabro'; F., Cataldo; L., Greco | |
| A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus | 1-gen-2009 | Orrú, V; Tsai, Sj; Rueda, B; Fiorillo, E; Stanford, Sm; Dasgupta, J; Hartiala, J; Zhao, L; ORTEGO CENTENO, N; D'Alfonso, Sandra; ITALIAN COLLABORATIVE, Group; Arnett, Fc; Wu, H; GONZALEZ GAY, Ma; Tsao, Bp; PONS ESTEL, B; ALARCON RIQUELME, Me; He, Y; Zhang, Zy; Allayee, H; Chen, Xs; Martin, J; Bottini, N. | |
| A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility | 1-gen-2022 | Sorosina, Melissa; Barizzone, Nadia; Clarelli, Ferdinando; Anand, Santosh; Lupoli, Sara; Salvi, Erika; Mangano, Eleonora; Bordoni, Roberta; Roostaei, Tina; Mascia, Elisabetta; Zuccalà, Miriam; Vecchio, Domizia; Cavalla, Paola; Santoro, Silvia; Ferrè, Laura; Zollo, Alen; Barlassina, Cristina; Cusi, Daniele; Martinelli, Vittorio; Comi, Giancarlo; Leone, Maurizio; Filippi, Massimo; Patsopoulos, Nikolaos A; De Jager, Philip L; De Bellis, Gianluca; Esposito, Federica; D'Alfonso, Sandra; Martinelli Boneschi, Filippo | |
| A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis | 1-gen-2010 | Ban, M; Mccauley, Jl; Zuvich, R; Baker, A; Bergamaschi, L; Cox, M; Kemppinen, A; D'Alfonso, Sandra; Guerini, Fr; LECHNER SCOTT, J; Dudbridge, F; Wason, J; Robertson, Np; De, ; Jager, Pl; Hafler, Da; Barcellos, Lf; Ivinson, Aj; Sexton, D; Oksenberg, Jr; Hauser, Sl; PERICAK VANCE, Ma; Haines, J; Compston, A; Sawcer, S. | |
| A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient | 1-gen-2011 | Corrado, Lucia; Caromagno, Y; Falasco, L; Mellone, S; Godi, M; Cova, E; Cereda, C; Testa, L; Mazzini, L; D'Alfonso, Sandra | |
| A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b | 1-gen-2016 | Corrado, Lucia; Magri, S; Bagarotti, Alessandra; Carecchio, Miryam; Piscosquito, G; Pareyson, D; Varrasi, C; Vecchio, D; Zonta, Andrea; Cantello, Roberto; Taroni, F; D'Alfonso, Sandra | |
| A polymorphic variation in a putative regulation box of the TNFA promoter region. | 1-gen-1994 | D'Alfonso, Sandra; Immunogenetics, Richiardi P. M. | |
| A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86. | 1-gen-1994 | el Borai, Mh; D'Alfonso, Sandra; Mazzola, G; Fasano, M. E. |