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Nicola Ticozzi

  • 4832 Citations
  • 30 h-Index
20082019
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Research Output 2008 2019

  • 4832 Citations
  • 30 h-Index
  • 105 Article
  • 3 Review article
  • 2 Chapter
  • 1 Letter
2019
1 Citation (Scopus)

Comparative analysis of C9Orf72 and sporadic disease in a large multicenter ALS population: The effect of Male sex on survival of C9Orf72 positive patients

Trojsi, F., Siciliano, M., Femiano, C., Santangelo, G., Lunetta, C., Calvo, A., Moglia, C., Marinou, K., Ticozzi, N., Ferro, C., Scialò, C., Sorarù, G., Conte, A., Falzone, Y. M., Tortelli, R., Russo, M., Sansone, V. A., Chiò, A., Mora, G., Silani, V. & 11 others, Volanti, P., Caponnetto, C., Querin, G., Sabatelli, M., Riva, N., Logroscino, G., Messina, S., Fasano, A., Monsurrò, M. R., Tedeschi, G. & Mandrioli, J., Jan 1 2019, In : Frontiers in Neuroscience. 13, MAY, 485.

Research output: Contribution to journal › Article

Open Access
Amyotrophic Lateral Sclerosis
Survival
Population
Mutation
Dementia

Response to the commentary "The effect of C9orf72 intermediate repeat expansions in neurodegenerative and autoimmune diseases" by Biasiotto G and Zanella I.✰

Tiloca, C., Sorosina, M., Esposito, F., Peroni, S., Colombrita, C., Ticozzi, N., Ratti, A., Martinelli-Boneschi, F. & Silani, V., Jan 2019, In : Multiple Sclerosis and Related Disorders. 27, p. 79-80 2 p.

Research output: Contribution to journal › Article

2018

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function

de Majo, M., Topp, S. D., Smith, B. N., Nishimura, A. L., Chen, H. J., Gkazi, A. S., Miller, J., Wong, C. H., Vance, C., Baas, F., ten Asbroek, A. L. M. A., Kenna, K. P., Ticozzi, N., Redondo, A. G., Esteban-Pérez, J., Tiloca, C., Verde, F., Duga, S., Morrison, K. E., Shaw, P. J. & 13 others, Kirby, J., Turner, M. R., Talbot, K., Hardiman, O., Glass, J. D., de Belleroche, J., Gellera, C., Ratti, A., Al-Chalabi, A., Brown, R. H., Silani, V., Landers, J. E. & Shaw, C. E., Nov 1 2018, In : Neurobiology of Aging. 71, p. 266.e1-266.e10

Research output: Contribution to journal › Article

Phosphotransferases
Mutation
Missense Mutation
Phosphorylation
Exome
7 Citations (Scopus)

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function

de Majo, M., Topp, S. D., Smith, B. N., Nishimura, A. L., Chen, H. J., Gkazi, A. S., Miller, J., Wong, C. H., Vance, C., Baas, F., ten Asbroek, A. L. M. A., Kenna, K. P., Ticozzi, N., Redondo, A. G., Esteban-Pérez, J., Tiloca, C., Verde, F., Duga, S., Morrison, K. E., Shaw, P. J. & 13 others, Kirby, J., Turner, M. R., Talbot, K., Hardiman, O., Glass, J. D., de Belleroche, J., Gellera, C., Ratti, A., Al-Chalabi, A., Brown, R. H., Silani, V., Landers, J. E. & Shaw, C. E., Nov 1 2018, In : Neurobiology of Aging. 71, p. 266.e1-266.e10

Research output: Contribution to journal › Article

Phosphotransferases
Mutation
Missense Mutation
Phosphorylation
Exome

Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

Mandrioli, J., Ferri, L., Fasano, A., Zucchi, E., Fini, N., Moglia, C., Lunetta, C., Marinou, K., Ticozzi, N., Drago Ferrante, G., Scialo, C., Sorarù, G., Trojsi, F., Conte, A., Falzone, Y. M., Tortelli, R., Russo, M., Sansone, V. A., Mora, G., Silani, V. & 10 others, Volanti, P., Caponnetto, C., Querin, G., Monsurrò, M. R., Sabatelli, M., Chiò, A., Riva, N., Logroscino, G., Messina, S. & Calvo, A., Jun 2018, In : European Journal of Neurology. 25, 6, p. 861-868 8 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Cardiovascular Diseases
Heart Diseases
Hematologic Diseases
Survival

Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

Mandrioli, J., Ferri, L., Fasano, A., Zucchi, E., Fini, N., Moglia, C., Lunetta, C., Marinou, K., Ticozzi, N., Drago Ferrante, G., Scialo, C., Sorarù, G., Trojsi, F., Conte, A., Falzone, Y. M., Tortelli, R., Russo, M., Sansone, V. A., Mora, G., Silani, V. & 10 others, Volanti, P., Caponnetto, C., Querin, G., Monsurrò, M. R., Sabatelli, M., Chiò, A., Riva, N., Logroscino, G., Messina, S. & Calvo, A., Jun 2018, In : European Journal of Neurology. 25, 6, p. 861-868 8 p.

Research output: Contribution to journal › Article

4 Citations (Scopus)

Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

Mandrioli, J., Ferri, L., Fasano, A., Zucchi, E., Fini, N., Moglia, C., Lunetta, C., Marinou, K., Ticozzi, N., Drago Ferrante, G., Scialo, C., Sorarù, G., Trojsi, F., Conte, A., Falzone, Y. M., Tortelli, R., Russo, M., Sansone, V. A., Mora, G., Silani, V. & 10 others, Volanti, P., Caponnetto, C., Querin, G., Monsurrò, M. R., Sabatelli, M., Chiò, A., Riva, N., Logroscino, G., Messina, S. & Calvo, A., Jan 1 2018, (Accepted/In press) In : European Journal of Neurology.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Cardiovascular Diseases
Heart Diseases
Hematologic Diseases
Survival
1 Citation (Scopus)

Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases

Corrado, L., Tiloca, C., Locci, C., Bagarotti, A., Hamzeiy, H., Colombrita, C., De marchi, F., Barizzone, N., Cotella, D., Ticozzi, N., Mazzini, L., Nazli Basak, A. Y. S. E., Ratti, A., Silani, V. & D’alfonso, S., Jul 3 2018, In : Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19, 5-6, p. 426-431 6 p.

Research output: Contribution to journal › Article

GC Rich Sequence
Amyotrophic Lateral Sclerosis
Genes
1 Citation (Scopus)

Cognitive-behavioral longitudinal assessment in ALS: the Italian Edinburgh Cognitive and Behavioral ALS screen (ECAS)

Poletti, B., Solca, F., Carelli, L., Faini, A., Madotto, F., Lafronza, A., Monti, A., Zago, S., Ciammola, A., Ratti, A., Ticozzi, N., Abrahams, S. & Silani, V., 2018, In : Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19, 5-6, p. 387-395 9 p.

Research output: Contribution to journal › Article

Behavioral Genetics
Apathy
Behavioral Symptoms
Neuropsychological Tests
Caregivers

Cognitive-behavioral longitudinal assessment in ALS: the Italian Edinburgh Cognitive and Behavioral ALS screen (ECAS)

Poletti, B., Solca, F., Carelli, L., Faini, A., Madotto, F., Lafronza, A., Monti, A., Zago, S., Ciammola, A., Ratti, A., Ticozzi, N., Abrahams, S. & Silani, V., Aug 2018, In : Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19, 5-6, p. 387-395 9 p.

Research output: Contribution to journal › Article

Behavioral Genetics
Apathy
Behavioral Symptoms
Neuropsychological Tests
Caregivers
7 Citations (Scopus)

Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2

Hamzeiy, H., Savaş, D., Tunca, C., Şen, N. E., Gündoǧdu Eken, A., Şahbaz, I., Calini, D., Tiloca, C., Ticozzi, N., Ratti, A., Silani, V. & Başak, A. N., Mar 1 2018, In : Neurodegenerative Diseases. 18, 1, p. 38-48 11 p.

Research output: Contribution to journal › Article

Spinocerebellar Ataxias
5-Methylcytosine
Amyotrophic Lateral Sclerosis
DNA Methylation
Epigenomics

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

ITALSGEN consortium, Mar 21 2018, In : Neuron. 97, 6, p. 1268-1283.e6

Research output: Contribution to journal › Article

Kinesin
Genome
Mutation
Genes
Hereditary Spastic Paraplegia

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

Nicolas, A., Kenna, K., Renton, A. E., Ticozzi, N., Faghri, F., Chia, R., Dominov, J. A., Kenna, B. J., Nalls, M. A., Keagle, P., Rivera, A. M., van Rheenen, W., Murphy, N. A., van Vugt, J., Geiger, J. T., Van der Spek, R. A., Pliner, H. A., [Unknown], S., Smith, B. N., Marangi, G. & 401 others, Topp, S. D., Abramzon, Y., Gkazi, A. S., Eicher, J. D., Kenna, A., Logullo, F. O., Simone, I. L., Logroscino, G., Salvi, F., Bartolomei, I., Borghero, G., Murru, M. R., Costantino, E., Pani, C., Puddu, R., Caredda, C., Piras, V., Tranquilli, S., Cuccu, S., Corongiu, D., Melis, M., Milia, A., Marrosu, F., Marrosu, M. G., Floris, G., Cannas, A., Capasso, M., Caponnetto, C., Mancardi, G., Origone, P., Mandich, P., Conforti, F. L., Cavallaro, S., Mora, G., Marinou, K., Sideri, R., Penco, S., Mosca, L., Lunetta, C., Pinter, G. L., Corbo, M., Riva, N., Carrera, P., Volanti, P., Mandrioli, J., Fini, N., Fasano, A., Tremolizzo, L., Arosio, A., Ferrarese, C., Trojsi, F., Tedeschi, G., Monsurrò, M. R., Piccirillo, G., Femiano, C., Ticca, A., Ortu, E., La Bella, V., Spataro, R., Colletti, T., Sabatelli, M., Zollino, M., Conte, A., Luigetti, M., Lattante, S., Santarelli, M., Petrucci, A., Pugliatti, M., Pirisi, A., Parish, L. D., Occhineri, P., Giannini, F., Battistini, S., Ricci, C., Benigni, M., Cau, T. B., Loi, D., Calvo, A., Moglia, C., Brunetti, M., Barberis, M., Restagno, G., Casale, F., Marrali, G., Fuda, G., Ossola, I., Cammarosano, S., Canosa, A., Ilardi, A., Manera, U., Grassano, M., Tanel, R., Pisano, F., Mazzini, L., Messina, S., D'Alfonso, S., Corrado, L., Ferrucci, L., Harms, M. B., Goldstein, D. B., Shneider, N. A., Goutman, S., Simmons, Z., Miller, T. M., Chandran, S., Pal, S., Manousakis, G., Appel, S. H., Simpson, E., Wang, L., Baloh, R. H., Gibson, S., Bedlack, R., Lacomis, D., Sareen, D., Sherman, A., Bruijn, L., Penny, M., Moreno, C. D. A. M., Kamalakaran, S., Allen, A. S., Boone, B. E., Brown, R., Carulli, J. P., Chesi, A., Chung, W. K., Cirulli, E. T., Cooper, G. M., Couthouis, J., Day-Williams, A. G., Dion, P. A., Gitler, A. D., Glass, J. D., Han, Y., Harris, T., Hayes, S. D., Jones, A. L., Keebler, J., Krueger, B. J., Lasseigne, B. N., Levy, S. E., Lu, Y-F., Maniatis, T., McKenna-Yasek, D., Myers, R. M., Petrovski, S., Pulst, S. M., Raphael, A. R., Ravits, J., Ren, Z., Rouleau, G. A., Sapp, P. C., Sims, K. B., Staropoli, J. F., Waite, L. L., Wang, Q., Wimbish, J. R., Xin, W. W., Phatnani, H., Kwan, J., Broach, J. R., Arcila-Londono, X., Lee, E. B., Van Deerlin, V. M., Fraenkel, E., Ostrow, L. W., Baas, F., Zaitlen, N., Berry, J. D., Malaspina, A., Fratta, P., Cox, G. A., Thompson, L. M., Finkbeiner, S., Dardiotis, E., Hornstein, E., MacGowan, D. J., Heiman-Patterson, T., Hammell, M. G., Patsopoulos, N. A., Dubnau, J., Nath, A., Musunuri, R. L., Evani, U. S., Abhyankar, A., Zody, M. C., Kaye, J., Wyman, S., LeNail, A., Lima, L., Rothstein, J. D., Svendsen, C. N., Van Eyk, J., Maragakis, N. J., Kolb, S. J., Cudkowicz, M., Baxi, E., Wyman, S. K., Van Eyk, J. E., Benatar, M., Taylor, J. P., Wu, G., Rampersaud, E., Wuu, J., Rademakers, R., Züchner, S., Schule, R., McCauley, J., Hussain, S., Cooley, A., Wallace, M., Clayman, C., Barohn, R., Statland, J., Ravits, J., Swenson, A., Jackson, C., Trivedi, J., Khan, S., Katz, J., Jenkins, L., Burns, T., Gwathmey, K., Caress, J., McMillan, C., Elman, L., Pioro, E., Heckmann, J., So, Y., Walk, D., Maiser, S., Zhang, J., Silani, V., Gellera, C., Ratti, A., Taroni, F., Lauria, G., Verde, F., Fogh, I., Tiloca, C., Comi, G. P., Sorarù, G., Cereda, C., De Marchi, F., Corti, S., Ceroni, M., Siciliano, G., Filosto, M., Inghilleri, M., Peverelli, S., Colombrita, C., Poletti, B., Maderna, L., Del Bo, R., Gagliardi, S., Querin, G., Bertolin, C., Pensato, V., Castellotti, B., Camu, W., Mouzat, K., Lumbroso, S., Corcia, P., Meininger, V., Besson, G., Lagrange, E., Clavelou, P., Guy, N., Couratier, P., Vourch, P., Danel, V., Bernard, E., Lemasson, G., Laaksovirta, H., Myllykangas, L., Jansson, L., Valori, M., Ealing, J., Hamdalla, H., Rollinson, S., Pickering-Brown, S., Orrell, R. W., Sidle, K. C., Hardy, J., Singleton, A. B., Johnson, J. O., Arepalli, S., Polak, M., Asress, S., Al-Sarraj, S., King, A., Troakes, C., Vance, C., de Belleroche, J., ten Asbroek, A. L. M. A., Muñoz-Blanco, J. L., Hernandez, D. G., Ding, J., Gibbs, J. R., Scholz, S. W., Floeter, M. K., Campbell, R. H., Landi, F., Bowser, R., MacGowan, D. J. L., Kirby, J., Pioro, E. P., Pamphlett, R., Broach, J., Gerhard, G., Dunckley, T. L., Brady, C. B., Kowall, N. W., Troncoso, J. C., Le Ber, I., Heiman-Patterson, T. D., Kamel, F., Van Den Bosch, L., Strom, T. M., Meitinger, T., Shatunov, A., Van Eijk, K. R., de Carvalho, M., Kooyman, M., Middelkoop, B., Moisse, M., McLaughlin, R. L., van Es, M., Weber, M., Boylan, K. B., Van Blitterswijk, M., Morrison, K., Basak, A. N., Mora, J. S., Drory, V., Shaw, P. J., Turner, M. R., Talbot, K., Hardiman, O., Williams, K. L., Fifita, J. A., Nicholson, G. A., Blair, I. P., Esteban-Pérez, J., García-Redondo, A., Al-Chalabi, A., Al Kheifat, A., Andersen, P., Chio, A., Cooper-Knock, J., Dekker, A., Drory, V., Redondo, A. G., Gotkine, M., Hide, W., Iacoangeli, A., Glass, J., Kenna, K., Kiernan, M., Landers, J., McLaughlin, R., Mill, J., Neto, M. M., Pardina, J. M., Morrison, K., Newhouse, S., Pinto, S., Pulit, S., Robberecht, W., Shaw, P., Shaw, C., Sproviero, W., Tazelaar, G., Van Damme, P., van den Berg, L., van Eijk, K., van Es, M., van Vugt, J., Veldink, J., Zatz, M., Bauer, D. C., Twine, N. A., Rogaeva, E., Zinman, L., Brice, A., Goutman, S. A., Feldman, E. L., Gibson, S. B., Ludolph, A. C., Andersen, P. M., Weishaupt, J. H., Trojanowski, J. Q., Brown R.H., J., van den Berg, L. H., Veldink, J. H., Stone, D. J., Tienari, P., Chiò, A., Shaw, C. E., Traynor, B. J. & Landers, J. E., 2018, In : Neuron. 97, 6, p. 1268-1283.e6

Research output: Contribution to journal › Article

67 Citations (Scopus)

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

Answer ALS Foundation, Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium, SLAGEN Consortium, French ALS Consortium, Project MinE ALS Sequencing Consortium, ITALSGEN consortium, Genomic Translation for ALS Care (GTAC) Consortium, ALS Sequencing Consortium, NYGC ALS Consortium & Caponnetto, C., Mar 21 2018, In : Neuron. 97, 6, p. 1268-1283.e6

Research output: Contribution to journal › Article

Kinesin
Genome
Mutation
Genes
Genome-Wide Association Study

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

consortium, ITALSGEN., Nicolas, A., Kenna, K. P., Renton, A. E., Ticozzi, N., Faghri, F., Chia, R., Dominov, J. A., Kenna, B. J., Nalls, M. A., Keagle, P., Rivera, A. M., van Rheenen, W., Murphy, N. A., van Vugt, J. J. F. A., Geiger, J. T., Van der Spek, R. A., Pliner, H. A., Shankaracharya, N., Smith, B. N. & 31 others, Marangi, G., Topp, S. D., Abramzon, Y., Gkazi, A. S., Eicher, J. D., Kenna, A., Mora, G., Calvo, A., Mazzini, L., Riva, N., Mandrioli, J., Caponnetto, C., Battistini, S., Volanti, P., La Bella, V., Conforti, F. L., Borghero, G., Messina, S., Simone, I. L., Trojsi, F., Salvi, F., Logullo, F. O., D'Alfonso, S., Lauria, G., Tiloca, C., Comi, G. P., Cereda, C., Taroni, F., Ratti, A., Gellera, C. & Silani, V., Mar 21 2018, In : Neuron. 97, 6, p. 1268-1283.e6

Research output: Contribution to journal › Article

4 Citations (Scopus)

No C9orf72 repeat expansion in patients with primary progressive multiple sclerosis

Tiloca, C., Sorosina, M., Esposito, F., Peroni, S., Colombrita, C., Ticozzi, N., Ratti, A., Boneschi, F. M. & Silani, V., Oct 1 2018, In : Multiple Sclerosis and Related Disorders. 25, p. 192-195 4 p.

Research output: Contribution to journal › Article

Chronic Progressive Multiple Sclerosis
Multiple Sclerosis
Alleles
Amyotrophic Lateral Sclerosis
Parkinson Disease

Sexuality and intimacy in ALS: systematic literature review and future perspectives

Poletti, B., Carelli, L., Solca, F., Pezzati, R., Faini, A., Ticozzi, N., Mitsumoto, H. & Silani, V., Dec 11 2018, In : Journal of neurology, neurosurgery, and psychiatry.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Sexuality
Sexual Behavior
Literature
PubMed

The Arrows and Colors Cognitive Test (ACCT): A new verbal-motor free cognitive measure for executive functions in ALS

Poletti, B., Carelli, L., Faini, A., Solca, F., Meriggi, P., Lafronza, A., Ciringione, L., Pedroli, E., Ticozzi, N., Ciammola, A., Cipresso, P., Riva, G. & Silani, V., 2018, In : PLoS One. 13, 8, p. e0200953

Research output: Contribution to journal › Article

Executive Function
Color
color
eyes
testing
3 Citations (Scopus)

The Arrows and Colors Cognitive Test (ACCT): A new verbal-motor free cognitive measure for executive functions in ALS

Poletti, B., Carelli, L., Faini, A., Solca, F., Meriggi, P., Lafronza, A., Ciringione, L., Pedroli, E., Ticozzi, N., Ciammola, A., Cipresso, P., Riva, G. & Silani, V., Aug 1 2018, In : PLoS One. 13, 8, e0200953.

Research output: Contribution to journal › Article

Executive Function
Color
color
eyes
testing
3 Citations (Scopus)

The complex interplay between depression/anxiety and executive functioning: Insights from the ECAS in a large ALS Population

Carelli, L., Solca, F., Faini, A., Madotto, F., Lafronza, A., Monti, A., Zago, S., Doretti, A., Ciammola, A., Ticozzi, N., Silani, V. & Poletti, B., Apr 5 2018, In : Frontiers in Psychology. 9, APR, 450.

Research output: Contribution to journal › Article

Anxiety
Depression
Amyotrophic Lateral Sclerosis
Population
Executive Function

The Complex Interplay Between Depression/Anxiety and Executive Functioning: Insights From the ECAS in a Large ALS Population

Carelli, L., Solca, F., Faini, A., Madotto, F., Lafronza, A., Monti, A., Zago, S., Doretti, A., Ciammola, A., Ticozzi, N., Silani, V. & Poletti, B., 2018, In : Frontiers in Psychology. 9, p. 450

Research output: Contribution to journal › Article

Anxiety
Depression
Amyotrophic Lateral Sclerosis
Population
Executive Function

The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1

Perez Carrion, M., Pischedda, F., Biosa, A., Russo, I., Straniero, L., Civiero, L., Guida, M., Gloeckner, C. J., Ticozzi, N., Tiloca, C., Mariani, C., Pezzoli, G., Duga, S., Pichler, I., Pan, L., Landers, J. E., Greggio, E., Hess, M. W., Goldwurm, S. & Piccoli, G., 2018, In : Frontiers in Molecular Neuroscience. 11, p. 64

Research output: Contribution to journal › Article

Mitochondrial Dynamics
Leucine
Phosphotransferases
Genes
1-Methyl-4-phenylpyridinium
2017
4 Citations (Scopus)

An eye-tracker controlled cognitive battery: overcoming verbal-motor limitations in ALS

Poletti, B., Carelli, L., Solca, F., Lafronza, A., Pedroli, E., Faini, A., Ticozzi, N., Ciammola, A., Meriggi, P., Cipresso, P., Lulé, D., Ludolph, A. C., Riva, G. & Silani, V., Jun 2017, In : Journal of Neurology. 264, 6, p. 1136-1145 10 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Equipment and Supplies
Cognition
Anxiety
Depression
4 Citations (Scopus)

An eye-tracker controlled cognitive battery: overcoming verbal-motor limitations in ALS

Poletti, B., Carelli, L., Solca, F., Lafronza, A., Pedroli, E., Faini, A., Ticozzi, N., Ciammola, A., Meriggi, P., Cipresso, P., Lulé, D., Ludolph, A. C., Riva, G. & Silani, V., Jun 2017, In : Journal of Neurology. p. 1-10 10 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Equipment and Supplies
Cognition
Anxiety
Depression
6 Citations (Scopus)

An eye-tracking controlled neuropsychological battery for cognitive assessment in neurological diseases

Poletti, B., Carelli, L., Solca, F., Lafronza, A., Pedroli, E., Faini, A., Zago, S., Ticozzi, N., Ciammola, A., Morelli, C., Meriggi, P., Cipresso, P., Lulé, D., Ludolph, A. C., Riva, G. & Silani, V., Apr 2017, In : Neurological Sciences. p. 1-9 9 p.

Research output: Contribution to journal › Article

Aptitude
Short-Term Memory
Cognition
Healthy Volunteers
Anxiety
6 Citations (Scopus)

An eye-tracking controlled neuropsychological battery for cognitive assessment in neurological diseases

Poletti, B., Carelli, L., Solca, F., Lafronza, A., Pedroli, E., Faini, A., Zago, S., Ticozzi, N., Ciammola, A., Morelli, C., Meriggi, P., Cipresso, P., Lulé, D., Ludolph, A. C., Riva, G. & Silani, V., 2017, In : Neurological Sciences. 38, 4, p. 595-603 9 p.

Research output: Contribution to journal › Article

Aptitude
Short-Term Memory
Cognition
Healthy Volunteers
Anxiety
6 Citations (Scopus)

An eye-tracking controlled neuropsychological battery for cognitive assessment in neurological diseases

Poletti, B., Carelli, L., Solca, F., Lafronza, A., Pedroli, E., Faini, A., Zago, S., Ticozzi, N., Ciammola, A., Morelli, C., Meriggi, P., Cipresso, P., Lulé, D., Ludolph, A. C., Riva, G. & Silani, V., Apr 2017, In : Neurological Sciences. 38, 4, p. 595-603 9 p.

Research output: Contribution to journal › Article

Aptitude
Short-Term Memory
Cognition
Healthy Volunteers
Anxiety
2 Citations (Scopus)

A novel nonsense ATP7A pathogenic variant in a family exhibiting a variable occipital horn syndrome phenotype

Bonati, M. T., Verde, F., Hladnik, U., Cattelan, P., Campana, L., Castronovo, C., Ticozzi, N., Maderna, L., Colombrita, C., Papa, S., Banfi, P. & Silani, V., Dec 2017, In : Molecular Genetics and Metabolism Reports. 13, p. 14-17 4 p.

Research output: Contribution to journal › Article

Menkes Kinky Hair Syndrome
Phenotype
Maintenance
Proteins
Occipital horn syndrome
2 Citations (Scopus)

A novel nonsense ATP7A pathogenic variant in a family exhibiting a variable occipital horn syndrome phenotype

Bonati, M. T., Verde, F., Hladnik, U., Cattelan, P., Campana, L., Castronovo, C., Ticozzi, N., Maderna, L., Colombrita, C., Papa, S., Banfi, P. & Silani, V., Dec 1 2017, In : Molecular Genetics and Metabolism Reports. 13, p. 14-17 4 p.

Research output: Contribution to journal › Article

Menkes Kinky Hair Syndrome
Phenotype
Maintenance
Proteins
Occipital horn syndrome
10 Citations (Scopus)

Brain-Computer Interface for Clinical Purposes: Cognitive Assessment and Rehabilitation

Carelli, L., Solca, F., Faini, A., Meriggi, P., Sangalli, D., Cipresso, P., Riva, G., Ticozzi, N., Ciammola, A., Silani, V. & Poletti, B., 2017, In : BioMed Research International. 2017, 1695290.

Research output: Contribution to journal › Review article

Brain-Computer Interfaces
Brain computer interface
Patient rehabilitation
Rehabilitation
Neurofeedback
10 Citations (Scopus)

Brain-Computer Interface for Clinical Purposes: Cognitive Assessment and Rehabilitation

Carelli, L., Solca, F., Faini, A., Meriggi, P., Sangalli, D., Cipresso, P., Riva, G., Ticozzi, N., Ciammola, A., Silani, V. & Poletti, B., 2017, In : BioMed Research International. 2017, p. 1695290

Research output: Contribution to journal › Review article

Brain-Computer Interfaces
Brain computer interface
Patient rehabilitation
Rehabilitation
Neurofeedback
4 Citations (Scopus)

Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort

Trojsi, F., Siciliano, M., Femiano, C., Santangelo, G., Lunetta, C., Calvo, A., Moglia, C., Marinou, K., Ticozzi, N., Drago Ferrante, G., Scialò, C., Sorarù, G., Conte, A., Falzone, Y. M., Tortelli, R., Russo, M., Sansone, V. A., Chiò, A., Mora, G., Poletti, B. & 11 others, Volanti, P., Caponnetto, C., Querin, G., Sabatelli, M., Riva, N., Logroscino, G., Messina, S., Fasano, A., Monsurrò, M. R., Tedeschi, G. & Mandrioli, J., Nov 2017, In : Journal of Neurology. 264, 11, p. 2224-2231 8 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Comorbidity
Dementia
Logistic Models
Phenotype
4 Citations (Scopus)

Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort

Trojsi, F., Siciliano, M., Femiano, C., Santangelo, G., Lunetta, C., Calvo, A., Moglia, C., Marinou, K., Ticozzi, N., Drago Ferrante, G., Scialò, C., Sorarù, G., Conte, A., Falzone, Y. M., Tortelli, R., Russo, M., Sansone, V. A., Chiò, A., Mora, G., Poletti, B. & 11 others, Volanti, P., Caponnetto, C., Querin, G., Sabatelli, M., Riva, N., Logroscino, G., Messina, S., Fasano, A., Monsurrò, M. R., Tedeschi, G. & Mandrioli, J., Nov 2017, In : Journal of Neurology. p. 1-8 8 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Comorbidity
Dementia
Logistic Models
Phenotype
4 Citations (Scopus)

Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort

Trojsi, F., Siciliano, M., Femiano, C., Santangelo, G., Lunetta, C., Calvo, A., Moglia, C., Marinou, K., Ticozzi, N., Drago Ferrante, G., Scialò, C., Sorarù, G., Conte, A., Falzone, YM., Tortelli, R., Russo, M., Sansone, VA., Chiò, A., Mora, G., Poletti, B. & 11 others, Volanti, P., Caponnetto, C., Querin, G., Sabatelli, M., Riva, N., Logroscino, G., Messina, S., Fasano, A., Monsurrò, MR., Tedeschi, G. & Mandrioli, J., 2017, In : Journal of Neurology. 264, 11, p. 2224-2231 8 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Comorbidity
Dementia
Logistic Models
Phenotype

Factors predicting survival in ALS: a multicenter Italian study

Calvo, A., Moglia, C., Lunetta, C., Marinou Aktipi, K., Ticozzi, N., Ferrante, G. D., Scialò, C., Soraru, G., Trojsi, F., Conte, A., Falzone, Y. M., Tortelli, R., Russo, M., Chiò, A., Sansone, V., Mora, G., Silani, V., Volanti, P., Caponnetto, C., Querin, G. & 7 others, Monsurrò, M. R., Sabatelli, M., Riva, N., Logroscino, G., Messina, S., Fini, N. & Mandrioli, J., Jan 2017, In : Journal of Neurology. 264, p. 54-63 10 p.

Research output: Contribution to journal › Article

Multicenter Studies
Survival
Tracheostomy
Age of Onset
Dementia
30 Citations (Scopus)

Factors predicting survival in ALS: a multicenter Italian study

Calvo, A., Moglia, C., Lunetta, C., Marinou, K., Ticozzi, N., Ferrante, G. D., Scialo, C., Sorarù, G., Trojsi, F., Conte, A., Falzone, Y. M., Tortelli, R., Russo, M., Chiò, A., Sansone, V. A., Mora, G., Silani, V., Volanti, P., Caponnetto, C., Querin, G. & 7 others, Monsurrò, M. R., Sabatelli, M., Riva, N., Logroscino, G., Messina, S., Fini, N. & Mandrioli, J., Jan 2017, In : Journal of Neurology. p. 54-63 10 p.

Research output: Contribution to journal › Article

Multicenter Studies
Survival
Tracheostomy
Age of Onset
Dementia
30 Citations (Scopus)

Factors predicting survival in ALS: a multicenter Italian study

Calvo, A., Moglia, C., Lunetta, C., Marinou, K., Ticozzi, N., Ferrante, GD., Scialo, C., Sorarù, G., Trojsi, F., Conte, A., Falzone, YM., Tortelli, R., Russo, M., Chiò, A., Sansone, VA., Mora, G., Silani, V., Volanti, P., Caponnetto, C., Querin, G. & 7 others, Monsurrò, MR., Sabatelli, M., Riva, N., Logroscino, G., Messina, S., Fini, N. & Mandrioli, J., 2017, In : Journal of Neurology. 264, 1, p. 54-63 10 p.

Research output: Contribution to journal › Article

Multicenter Studies
Survival
Tracheostomy
Age of Onset
Dementia
30 Citations (Scopus)

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

McLaughlin, R. L., Schijven, D., Van Rheenen, W., van Eijk, K. R., O'Brien, M., Kahn, R. S., Ophoff, R. A., Goris, A., Bradley, D. G., Al-Chalabi, A., Van Den Berg, L. H., Luykx, J. J., Hardiman, O., Veldink, J. H., Shatunov, A., Dekker, A. M., Diekstra, F. P., Pulit, S. L., van der Spek, R. A. A., van Doormaal, P. T. C. & 416 others, Sproviero, W., Jones, A. R., Nicholson, G. A., Rowe, D. B., Pamphlett, R., Kiernan, M. C., Bauer, D., Kahlke, T., Williams, K. L., Eftimov, F., Fogh, I., Ticozzi, N., Lin, K., Millecamps, S., Salachas, F., Meininger, V., de Carvalho, M., Pinto, S., Mora, J. S., Rojas-Garcyá, R., Polak, M., Chandran, S., Colville, S., Swingler, R., Morrison, K. E., Shaw, P. J., Hardy, J., Orrell, R. W., Pittman, A., Sidle, K., Fratta, P., Malaspina, A., Petri, S., Abdulla, S., Drepper, C., Sendtner, M., Meyer, T., Wiedau-Pazos, M., Lomen-Hoerth, C., Van Deerlin, V. M., Trojanowski, J. Q., Elman, L., McCluskey, L., Basak, A. N., Meitinger, T., Lichtner, P., Radivojkov-Blagojevic, M., Andres, C. R., Maurel, C., Bensimon, G., Landwehrmeyer, B., Brice, A., Payan, C. A. M., Saker-Delye, S., Durr, A., Wood, N., Tittmann, L., Lieb, W., Franke, A., Rietschel, M., Cichon, S., Nothen, M. M., Amouyel, P., Tzourio, C., Dartigues, J. F., Uitterlinden, A. G., Rivadeneira, F., Estrada, K., Hofman, A., Curtis, C., Derkooi, A. J. V., De Visser, M., Weber, M., Shaw, C. E., Smith, B. N., Pansarasa, O., Cereda, C., Bo, R. D., Comi, G. P., D'Alfonso, S., Bertolin, C., Soraru, G., Mazzini, L., Pensato, V., Gellera, C., Tiloca, C., Ratti, A., Calvo, A., Moglia, C., Brunetti, M., Arcuti, S., Capozzo, R., Zecca, C., Lunetta, C., Penco, S., Riva, N., Padovani, A., Filosto, M., Blair, I. P., Nigel Leigh, P., Casale, F., Chio, A., Beghi, E., Pupillo, E., Tortelli, R., Logroscino, G., Powell, J., Ludolph, A. C., Weishaupt, J. H., Robberecht, W., van Damme, P., Brown, R. H., Glass, J. D., Landers, J. E., Andersen, P. M., Corcia, P., Vourc'h, P., Silani, V., van Es, M. A., Pasterkamp, R. J., Lewis, C. M., Breen, G., Ripke, S., Neale, B. M., Corvin, A., Walters, J. T. R., Farh, K. H., Holmans, P. A., Lee, P. H., Bulik-Sullivan, B., Collier, D. A., Huang, H., Pers, T. H., Agartz, I., Agerbo, E., Albus, M., Alexander, M., Amin, F., Bacanu, S. A., Begemann, M., Belliveau, R. A., Bene, J., Bergen, S. E., Bevilacqua, E., Bigdeli, T. B., Black, D. W., Bruggeman, R., Buccola, N. G., Buckner, R. L., Byerley, W. F., Cahn, W., Cai, G., Campion, D., Cantor, R. M., Carr, V. J., Carrera, N., Catts, S. V., Chambert, K. D., Chan, R. C. K., Chan, R. Y. L., Chen, E. Y. H., Cheng, W., Cheung, E. F. C., Chong, S. A., Cloninger, C. R., Cohen, D. J., Cohen, N., Cormican, P., Craddock, N., Crowley, J. J., Curtis, D., Davidson, M., Davis, K. L., Degenhardt, F., Favero, J. D., Demontis, D., Dikeos, D., Dinan, T., Djurovic, S., Donohoe, G., Drapeau, E., Duan, J., Dudbridge, F., Durmishi, N., Eichhammer, P., Eriksson, J., Escott-Price, V., Essioux, L., Fanous, A. H., Farrell, M. S., Frank, J., Franke, L., Freedman, R., Freimer, N. B., Friedl, M., Friedman, J. I., Fromer, M., Genovese, G., Georgieva, L., Giegling, I., Giusti-Rodrýguez, P., Godard, S., Goldstein, J. I., Golimbet, V., Gopal, S., Gratten, J., De Haan, L., Hammer, C., Hamshere, M. L., Hansen, M. B., Hansen, T., Haroutunian, V., Hartmann, A. M., Henskens, F. A., Herms, S., Hirschhorn, J. N., Hoffmann, P., Hofman, A., Hollegaard, M. V., Hougaard, D. M., Ikeda, M., Joa, I., Julia, A., Kalaydjieva, L., Karachanak-Yankova, S., Karjalainen, J., Kavanagh, D., Keller, M. C., Kennedy, J. L., Khrunin, A., Kim, Y., Klovins, J., Knowles, J. A., Konte, B., Kucinskas, V., Kucinskiene, Z. A., Kuzelova-Ptackova, H., Kahler, A. K., Laurent, C., Lee, J., Hong Lee, S., Legge, S. E., Lerer, B., Li, M., Li, T., Liang, K. Y., Lieberman, J., Limborska, S., Loughland, C. M., Lubinski, J., Lonnqvist, J., Macek, M., Magnusson, P. K. E., Maher, B. S., Maier, W., Mallet, J., Marsal, S., Mattheisen, M., Mattingsdal, M., McCarley, R. W., McDonald, C., McIntosh, A. M., Meier, S., Meijer, C. J., Melegh, B., Melle, I., Mesholam-Gately, R. I., Metspalu, A., Michie, P. T., Milani, L., Milanova, V., Mokrab, Y., Morris, D. W., Mors, O., Murphy, K. C., Murray, R. M., Myin-Germeys, I., Muller-Myhsok, B., Nelis, M., Nenadic, I., Nertney, D. A., Nestadt, G., Nicodemus, K. K., Nikitina-Zake, L., Nisenbaum, L., Nordin, A., O'Callaghan, E., O'Dushlaine, C., Anthony O'Neill, F., Oh, S. Y., Olincy, A., Olsen, L., Vanos, J., Pantelis, C., Papadimitriou, G. N., Papiol, S., Parkhomenko, E., Pato, M. T., Paunio, T., Pejovic-Milovancevic, M., Perkins, D. O., Pietilainen, O., Pimm, J., Pocklington, A. J., Price, A., Pulver, A. E., Purcell, S. M., Quested, D., Rasmussen, H. B., Reichenberg, A., Reimers, M. A., Richards, A. L., Roffman, J. L., Roussos, P., Ruderfer, D. M., Salomaa, V., Sanders, A. R., Schall, U., Schubert, C. R., Schulze, T. G., Schwab, S. G., Scolnick, E. M., Scott, R. J., Seidman, L. J., Shi, J., Sigurdsson, E., Silagadze, T., Silverman, J. M., Sim, K., Slominsky, P., Smoller, J. W., So, H. C., Spencer, C. C. A., Stah, E. A., Stefansson, H., Steinberg, S., Stogmann, E., Straub, R. E., Strengman, E., Strohmaier, J., Scott Stroup, T., Subramaniam, M., Suvisaari, J., Svrakic, D. M., Szatkiewicz, J. P., Söderman, E., Thirumalai, S., Toncheva, D., Tosato, S., Veijola, J., Waddington, J., Walsh, D., Wang, D., Wang, Q., Webb, B. T., Weiser, M., Wildenauer, D. B., Williams, N. M., Williams, S., Witt, S. H., Wolen, A. R., Wong, E. H. M., Wormley, B. K., Xi, H. S., Zai, C. C., Zheng, X., Zimprich, F., Wray, N. R., Stefansson, K., Visscher, P. M., Adolfsson, R., Andreassen, O. A., Blackwood, D. H. R., Bramon, E., Buxbaum, J. D., Børglum, A. D., Darvasi, A., Domenici, E., Ehrenreich, H., Esko, T., Gejman, P. V., Gil, M., Gurling, H., Hultman, C. M., Iwata, N., Jablensky, A. V., Jonsson, E. G., Kendler, K. S., Kirov, G., Knight, J., Lencz, T., Levinson, D. F., Li, Q. S., Liu, J., Malhotra, A. K., McCarrol, S. A., McQuillin, A., Moran, J. L., Mortensen, P. B., Mowry, B. J., Owen, M. J., Palotie, A., Pato, C. N., Petryshen, T. L., Posthuma, D., Riley, B. P., Rujescu, D., Sham, P. C., Sklar, P., Clair, D. S., Weinberger, D. R., Wendland, J. R., Werge, T., Daly, M. J., Sullivan, P. F. & O'Donovan, M. C., Mar 21 2017, In : Nature Communications. 8, 14774.

Research output: Contribution to journal › Article

schizophrenia
Amyotrophic Lateral Sclerosis
Schizophrenia
Genes
genome
30 Citations (Scopus)

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

McLaughlin, R. L., Schijven, D., Van Rheenen, W., van Eijk, K. R., O'Brien, M., Kahn, R. S., Ophoff, R. A., Goris, A., Bradley, D. G., Al-Chalabi, A., Van Den Berg, L. H., Luykx, J. J., Hardiman, O., Veldink, J. H., Shatunov, A., Dekker, A. M., Diekstra, F. P., Pulit, S. L., van der Spek, R. A. A., van Doormaal, P. T. C. & 416 others, Sproviero, W., Jones, A. R., Nicholson, G. A., Rowe, D. B., Pamphlett, R., Kiernan, M. C., Bauer, D., Kahlke, T., Williams, K. L., Eftimov, F., Fogh, I., Ticozzi, N., Lin, K., Millecamps, S., Salachas, F., Meininger, V., de Carvalho, M., Pinto, S., Mora, J. S., Rojas-Garcyá, R., Polak, M., Chandran, S., Colville, S., Swingler, R., Morrison, K. E., Shaw, P. J., Hardy, J., Orrell, R. W., Pittman, A., Sidle, K., Fratta, P., Malaspina, A., Petri, S., Abdulla, S., Drepper, C., Sendtner, M., Meyer, T., Wiedau-Pazos, M., Lomen-Hoerth, C., Van Deerlin, V. M., Trojanowski, J. Q., Elman, L., McCluskey, L., Basak, A. N., Meitinger, T., Lichtner, P., Radivojkov-Blagojevic, M., Andres, C. R., Maurel, C., Bensimon, G., Landwehrmeyer, B., Brice, A., Payan, C. A. M., Saker-Delye, S., Durr, A., Wood, N., Tittmann, L., Lieb, W., Franke, A., Rietschel, M., Cichon, S., Nothen, M. M., Amouyel, P., Tzourio, C., Dartigues, J. F., Uitterlinden, A. G., Rivadeneira, F., Estrada, K., Hofman, A., Curtis, C., Derkooi, A. J. V., De Visser, M., Weber, M., Shaw, C. E., Smith, B. N., Pansarasa, O., Cereda, C., Bo, R. D., Comi, G. P., D'Alfonso, S., Bertolin, C., Soraru, G., Mazzini, L., Pensato, V., Gellera, C., Tiloca, C., Ratti, A., Calvo, A., Moglia, C., Brunetti, M., Arcuti, S., Capozzo, R., Zecca, C., Lunetta, C., Penco, S., Riva, N., Padovani, A., Filosto, M., Blair, I. P., Nigel Leigh, P., Casale, F., Chio, A., Beghi, E., Pupillo, E., Tortelli, R., Logroscino, G., Powell, J., Ludolph, A. C., Weishaupt, J. H., Robberecht, W., van Damme, P., Brown, R. H., Glass, J. D., Landers, J. E., Andersen, P. M., Corcia, P., Vourc'h, P., Silani, V., van Es, M. A., Pasterkamp, R. J., Lewis, C. M., Breen, G., Ripke, S., Neale, B. M., Corvin, A., Walters, J. T. R., Farh, K. H., Holmans, P. A., Lee, P. H., Bulik-Sullivan, B., Collier, D. A., Huang, H., Pers, T. H., Agartz, I., Agerbo, E., Albus, M., Alexander, M., Amin, F., Bacanu, S. A., Begemann, M., Belliveau, R. A., Bene, J., Bergen, S. E., Bevilacqua, E., Bigdeli, T. B., Black, D. W., Bruggeman, R., Buccola, N. G., Buckner, R. L., Byerley, W. F., Cahn, W., Cai, G., Campion, D., Cantor, R. M., Carr, V. J., Carrera, N., Catts, S. V., Chambert, K. D., Chan, R. C. K., Chan, R. Y. L., Chen, E. Y. H., Cheng, W., Cheung, E. F. C., Chong, S. A., Cloninger, C. R., Cohen, D. J., Cohen, N., Cormican, P., Craddock, N., Crowley, J. J., Curtis, D., Davidson, M., Davis, K. L., Degenhardt, F., Favero, J. D., Demontis, D., Dikeos, D., Dinan, T., Djurovic, S., Donohoe, G., Drapeau, E., Duan, J., Dudbridge, F., Durmishi, N., Eichhammer, P., Eriksson, J., Escott-Price, V., Essioux, L., Fanous, A. H., Farrell, M. S., Frank, J., Franke, L., Freedman, R., Freimer, N. B., Friedl, M., Friedman, J. I., Fromer, M., Genovese, G., Georgieva, L., Giegling, I., Giusti-Rodrýguez, P., Godard, S., Goldstein, J. I., Golimbet, V., Gopal, S., Gratten, J., De Haan, L., Hammer, C., Hamshere, M. L., Hansen, M. B., Hansen, T., Haroutunian, V., Hartmann, A. M., Henskens, F. A., Herms, S., Hirschhorn, J. N., Hoffmann, P., Hofman, A., Hollegaard, M. V., Hougaard, D. M., Ikeda, M., Joa, I., Julia, A., Kalaydjieva, L., Karachanak-Yankova, S., Karjalainen, J., Kavanagh, D., Keller, M. C., Kennedy, J. L., Khrunin, A., Kim, Y., Klovins, J., Knowles, J. A., Konte, B., Kucinskas, V., Kucinskiene, Z. A., Kuzelova-Ptackova, H., Kahler, A. K., Laurent, C., Lee, J., Hong Lee, S., Legge, S. E., Lerer, B., Li, M., Li, T., Liang, K. Y., Lieberman, J., Limborska, S., Loughland, C. M., Lubinski, J., Lonnqvist, J., Macek, M., Magnusson, P. K. E., Maher, B. S., Maier, W., Mallet, J., Marsal, S., Mattheisen, M., Mattingsdal, M., McCarley, R. W., McDonald, C., McIntosh, A. M., Meier, S., Meijer, C. J., Melegh, B., Melle, I., Mesholam-Gately, R. I., Metspalu, A., Michie, P. T., Milani, L., Milanova, V., Mokrab, Y., Morris, D. W., Mors, O., Murphy, K. C., Murray, R. M., Myin-Germeys, I., Muller-Myhsok, B., Nelis, M., Nenadic, I., Nertney, D. A., Nestadt, G., Nicodemus, K. K., Nikitina-Zake, L., Nisenbaum, L., Nordin, A., O'Callaghan, E., O'Dushlaine, C., Anthony O'Neill, F., Oh, S. Y., Olincy, A., Olsen, L., Vanos, J., Pantelis, C., Papadimitriou, G. N., Papiol, S., Parkhomenko, E., Pato, M. T., Paunio, T., Pejovic-Milovancevic, M., Perkins, D. O., Pietilainen, O., Pimm, J., Pocklington, A. J., Price, A., Pulver, A. E., Purcell, S. M., Quested, D., Rasmussen, H. B., Reichenberg, A., Reimers, M. A., Richards, A. L., Roffman, J. L., Roussos, P., Ruderfer, D. M., Salomaa, V., Sanders, A. R., Schall, U., Schubert, C. R., Schulze, T. G., Schwab, S. G., Scolnick, E. M., Scott, R. J., Seidman, L. J., Shi, J., Sigurdsson, E., Silagadze, T., Silverman, J. M., Sim, K., Slominsky, P., Smoller, J. W., So, H. C., Spencer, C. C. A., Stah, E. A., Stefansson, H., Steinberg, S., Stogmann, E., Straub, R. E., Strengman, E., Strohmaier, J., Scott Stroup, T., Subramaniam, M., Suvisaari, J., Svrakic, D. M., Szatkiewicz, J. P., Söderman, E., Thirumalai, S., Toncheva, D., Tosato, S., Veijola, J., Waddington, J., Walsh, D., Wang, D., Wang, Q., Webb, B. T., Weiser, M., Wildenauer, D. B., Williams, N. M., Williams, S., Witt, S. H., Wolen, A. R., Wong, E. H. M., Wormley, B. K., Xi, H. S., Zai, C. C., Zheng, X., Zimprich, F., Wray, N. R., Stefansson, K., Visscher, P. M., Adolfsson, R., Andreassen, O. A., Blackwood, D. H. R., Bramon, E., Buxbaum, J. D., Børglum, A. D., Darvasi, A., Domenici, E., Ehrenreich, H., Esko, T., Gejman, P. V., Gil, M., Gurling, H., Hultman, C. M., Iwata, N., Jablensky, A. V., Jonsson, E. G., Kendler, K. S., Kirov, G., Knight, J., Lencz, T., Levinson, D. F., Li, Q. S., Liu, J., Malhotra, A. K., McCarrol, S. A., McQuillin, A., Moran, J. L., Mortensen, P. B., Mowry, B. J., Owen, M. J., Palotie, A., Pato, C. N., Petryshen, T. L., Posthuma, D., Riley, B. P., Rujescu, D., Sham, P. C., Sklar, P., Clair, D. S., Weinberger, D. R., Wendland, J. R., Werge, T., Daly, M. J., Sullivan, P. F. & O'Donovan, M. C., Mar 21 2017, In : Nature Communications. 8, p. 14774

Research output: Contribution to journal › Article

30 Citations (Scopus)

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

McLaughlin, R. L., Schijven, D., Van Rheenen, W., Van Eijk, K. R., O'Brien, M., Kahn, R. S., Ophoff, R. A., Goris, A., Bradley, D. G., Al-Chalabi, A., Van Den Berg, L. H., Luykx, J. J., Hardiman, O., Veldink, J. H., Shatunov, A., Dekker, A. M., Diekstra, F. P., Pulit, S. L., Van Der Spek, R. A. A., Van Doormaal, P. T. C. & 416 others, Sproviero, W., Jones, A. R., Nicholson, G. A., Rowe, D. B., Pamphlett, R., Kiernan, M. C., Bauer, D., Kahlke, T., Williams, K., Eftimov, F., Fogh, I., Ticozzi, N., Lin, K., Millecamps, S., Salachas, F., Meininger, V., Carvalho, M. D., Pinto, S., Mora, J. S., Rojas-Garcyá, R., Polak, M., Chandran, S., Colville, S., Swingler, R., Morrison, K. E., Shaw, P. J., Hardy, J., Orrell, R. W., Pittman, A., Sidle, K., Fratta, P., Malaspina, A., Petri, S., Abdulla, S., Drepper, C., Sendtner, M., Meyer, T., Wiedau-Pazos, M., Lomen-Hoerth, C., Deerlin, V. M. V., Trojanowski, J. Q., Elman, L., McCluskey, L., Basak, N., Meitinger, T., Lichtner, P., Blagojevic-Radivojkov, M., Andres, C. R., Maurel, C., Bensimon, G., Landwehrmeyer, B., Brice, A., Payan, C. A. M., Saker-Delye, S., Durr, A., Wood, N., Tittmann, L., Lieb, W., Franke, A., Rietschel, M., Cichon, S., Nothen, M. M., Amouyel, P., Tzourio, C., Dartigues, J-F., Uitterlinden, A. G., Rivadeneira, F., Estrada, K., Hofman, A., Curtis, C., Derkooi, A. J. V., De Visser, M., Weber, M., Shaw, C. E., Smith, B. N., Pansarasa, O., Cereda, C., Bo, R. D., Comi, G. P., D'Alfonso, S., Bertolin, C., Soraru, G., Mazzini, L., Pensato, V., Gellera, C., Tiloca, C., Ratti, A., Calvo, A., Moglia, C., Brunetti, M., Arcuti, S., Capozzo, R., Zecca, C., Lunetta, C., Penco, S., Riva, N., Padovani, A., Filosto, M., Blair, I., Nigel Leigh, P., Casale, F., Chio, A., Beghi, E., Pupillo, E., Tortelli, R., Logroscino, G., Powell, J., Ludolph, A. C., Weishaupt, J. H., Robberecht, W., Damme, P. V., Brown, R. H., Glass, J., Landers, J. E., Andersen, P. M., Corcia, P., Vourc'H, P., Silani, V., Es, M. A. V., Pasterkamp, R. J., Lewis, C. M., Breen, G., Ripke, S., Neale, B. M., Corvin, A., Walters, J. T. R., Farh, K-H., Holmans, P. A., Lee, P., Bulik-Sullivan, B., Collier, D. A., Huang, H., Pers, T. H., Agartz, I., Agerbo, E., Albus, M., Alexander, M., Amin, F., Bacanu, S. A., Begemann, M., Belliveau, R. A., Bene, J., Bergen, S. E., Bevilacqua, E., Bigdeli, T. B., Black, D. W., Bruggeman, R., Buccola, N. G., Buckner, R. L., Byerley, W., Cahn, W., Cai, G., Campion, D., Cantor, R. M., Carr, V. J., Carrera, N., Catts, S. V., Chambert, K. D., Chan, R. C. K., Chan, R. Y. L., Chen, E. Y. H., Cheng, W., Cheung, E. F. C., Chong, S. A., Cloninger, C. R., Cohen, D., Cohen, N., Cormican, P., Craddock, N., Crowley, J. J., Curtis, D., Davidson, M., Davis, K. L., Degenhardt, F., Favero, J. D., Demontis, D., Dikeos, D., Dinan, T., Djurovic, S., Donohoe, G., Drapeau, E., Duan, J., Dudbridge, F., Durmishi, N., Eichhammer, P., Eriksson, J., Escott-Price, V., Essioux, L., Fanous, A. H., Farrell, M. S., Frank, J., Franke, L., Freedman, R., Freimer, N. B., Friedl, M., Friedman, J. I., Fromer, M., Genovese, G., Georgieva, L., Giegling, I., Giusti-Rodrýguez, P., Godard, S., Goldstein, J. I., Golimbet, V., Gopal, S., Gratten, J., De Haan, L., Hammer, C., Hamshere, M. L., Hansen, M., Hansen, T., Haroutunian, V., Hartmann, A. M., Henskens, F. A., Herms, S., Hirschhorn, J. N., Hoffmann, P., Hofman, A., Hollegaard, M. V., Hougaard, D. M., Ikeda, M., Joa, I., Julia, A., Kalaydjieva, L., Karachanak-Yankova, S., Karjalainen, J., Kavanagh, D., Keller, M. C., Kennedy, J. L., Khrunin, A., Kim, Y., Klovins, J., Knowles, J. A., Konte, B., Kucinskas, V., Kucinskiene, Z. A., Kuzelova-Ptackova, H., Kahler, A. K., Laurent, C., Lee, J., Hong Lee, S., Legge, S. E., Lerer, B., Li, M., Li, T., Liang, K-Y., Lieberman, J., Limborska, S., Loughland, C. M., Lubinski, J., Lonnqvist, J., MacEk, M., Magnusson, P. K. E., Maher, B. S., Maier, W., Mallet, J., Marsal, S., Mattheisen, M., Mattingsdal, M., McCarley, R. W., McDonald, C., McIntosh, A. M., Meier, S., Meijer, C. J., Melegh, B., Melle, I., Mesholam-Gately, R. I., Metspalu, A., Michie, P. T., Milani, L., Milanova, V., Mokrab, Y., Morris, D. W., Mors, O., Murphy, K. C., Murray, R. M., Myin-Germeys, I., Muller-Myhsok, B., Nelis, M., Nenadic, I., Nertney, D. A., Nestadt, G., Nicodemus, K. K., Nikitina-Zake, L., Nisenbaum, L., Nordin, A., O'Callaghan, E., O'Dushlaine, C., Anthony O'Neill, F., Oh, S-Y., Olincy, A., Olsen, L., Vanos, J., Pantelis, C., Papadimitriou, G. N., Papiol, S., Parkhomenko, E., Pato, M. T., Paunio, T., Pejovic-Milovancevic, M., Perkins, D. O., Pietilainen, O., Pimm, J., Pocklington, A. J., Price, A., Pulver, A. E., Purcell, S. M., Quested, D., Rasmussen, H. B., Reichenberg, A., Reimers, M. A., Richards, A. L., Roffman, J. L., Roussos, P., Ruderfer, D. M., Salomaa, V., Sanders, A. R., Schall, U., Schubert, C. R., Schulze, T. G., Schwab, S. G., Scolnick, E. M., Scott, R. J., Seidman, L. J., Shi, J., Sigurdsson, E., Silagadze, T., Silverman, J. M., Sim, K., Slominsky, P., Smoller, J. W., So, H-C., Spencer, C. C. A., Stah, E. A., Stefansson, H., Steinberg, S., Stogmann, E., Straub, R. E., Strengman, E., Strohmaier, J., Scott Stroup, T., Subramaniam, M., Suvisaari, J., Svrakic, D. M., Szatkiewicz, J. P., Söderman, E., Thirumalai, S., Toncheva, D., Tosato, S., Veijola, J., Waddington, J., Walsh, D., Wang, D., Wang, Q., Webb, B. T., Weiser, M., Wildenauer, D. B., Williams, N. M., Williams, S., Witt, S. H., Wolen, A. R., Wong, E. H. M., Wormley, B. K., Xi, H. S., Zai, C. C., Zheng, X., Zimprich, F., Wray, N. R., Stefansson, K., Visscher, P. M., Adolfsson, R., Andreassen, O. A., Blackwood, D. H. R., Bramon, E., Buxbaum, J. D., Børglum, A. D., Darvasi, A., Domenici, E., Ehrenreich, H., Esko, T., Gejman, P. V., Gil, M., Gurling, H., Hultman, C. M., Iwata, N., Jablensky, A. V., Jonsson, E. G., Kendler, K. S., Kirov, G., Knight, J., Lencz, T., Levinson, D. F., Li, Q. S., Liu, J., Malhotra, A. K., McCarrol, S. A., McQuillin, A., Moran, J. L., Mortensen, P. B., Mowry, B. J., Owen, M. J., Palotie, A., Pato, C. N., Petryshen, T. L., Posthuma, D., Riley, B. P., Rujescu, D., Sham, P. C., Sklar, P., Clair, D. S., Weinberger, D. R., Wendland, J. R., Werge, T., Daly, M. J., Sullivan, P. F. & O'Donovan, M. C., 2017, In : Nature Communications. 8

Research output: Contribution to journal › Article

Genetics of Amyotrophic Lateral Sclerosis

Kenna, K. P., Landers, J. E. & Ticozzi, N., Jan 19 2017, Molecular and Cellular Therapies for Motor Neuron Diseases. Elsevier Inc., p. 43-59 17 p.

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Amyotrophic Lateral Sclerosis
Genes
Mutation
Animal Models
Therapeutics
19 Citations (Scopus)

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis

Smith, B. N., Topp, S. D., Fallini, C., Shibata, H., Chen, H-J., Troakes, C., King, A., Ticozzi, N., Kenna, K. P., Soragia-Gkazi, A., Miller, J. W., Sato, A., Dias, D. M., Jeon, M., Vance, C., Wong, C. H., de Majo, M., Kattuah, W., Mitchell, J. C., Scotter, E. L. & 36 others, Parkin, N. W., Sapp, P. C., Nolan, M., Nestor, P. J., Simpson, M., Weale, M., Lek, M., Baas, F., Vianney de Jong, J. M., Ten Asbroek, A. L. M. A., Redondo, A. G., Esteban-Pérez, J., Tiloca, C., Verde, F., Duga, S., Leigh, N., Pall, H., Morrison, K. E., Al-Chalabi, A., Shaw, P. J., Kirby, J., Turner, M. R., Talbot, K., Hardiman, O., Glass, J. D., De Belleroche, J., Maki, M., Moss, S. E., Miller, C., Gellera, C., Ratti, A., Al-Sarraj, S., Brown, R. H., Silani, V., Landers, J. E. & Shaw, C. E., May 3 2017, In : Science Translational Medicine. 9, 388, eaad9157.

Research output: Contribution to journal › Article

Annexins
Amyotrophic Lateral Sclerosis
Protein Transport
Mutation
Exome
19 Citations (Scopus)

Mutations in the vesicular trafficking protein Annexin A11 are associated with amyotrophic lateral sclerosis Bradley N. Smith

Topp, S. D., Fallini, C., Shibata, H., Chen, H. J., Troakes, C., King, A., Ticozzi, N., Kenna, K. P., Soragia-Gkazi, A., Miller, J. W., Sato, A., Dias, D. M., Jeon, M., Vance, C., Wong, C. H., De Majo, M., Kattuah, W., Mitchell, J. C., Scotter, E. L., Parkin, N. W. & 35 others, Sapp, P. C., Nolan, M., Nestor, P. J., Simpson, M., Weale, M., Lek, M., Baas, F., De Jong, J. M. V., Ten Asbroek, A. L. M. A., Redondo, A. G., Esteban-Pérez, J., Tiloca, C., Verde, F., Duga, S., Leigh, N., Pall, H., Morrison, K. E., Al-Chalabi, A., Shaw, P. J., Kirby, J., Turner, M. R., Talbot, K., Hardiman, O., Glass, J. D., De Belleroche, J., Maki, M., Moss, S. E., Miller, C., Gellera, C., Ratti, A., Al-Sarraj, S., Brown, R. H., Silani, V., Landers, J. E. & Shaw, C. E., May 3 2017, In : Science Translational Medicine. 9, 388, aad9157.

Research output: Contribution to journal › Article

Annexins
Amyotrophic Lateral Sclerosis
Protein Transport
Mutation
Exome
3 Citations (Scopus)

The role of de novo mutations in the development of amyotrophic lateral sclerosis

van Doormaal, P. T. C., Ticozzi, N., Weishaupt, J. H., Kenna, K., Diekstra, F. P., Verde, F., Andersen, P. M., Dekker, A. M., Tiloca, C., Marroquin, N., Overste, D. J., Pensato, V., Nürnberg, P., Pulit, S. L., Schellevis, R. D., Calini, D., Altmüller, J., Francioli, L. C., Muller, B., Castellotti, B. & 11 others, Motameny, S., Ratti, A., Wolf, J., Gellera, C., Ludolph, A. C., van den Berg, L. H., Kubisch, C., Landers, J. E., Veldink, J. H., Silani, V. & Volk, A. E., Nov 1 2017, In : Human Mutation. 38, 11, p. 1534-1541 8 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Mutation
Genes
Exome
Parents
4 Citations (Scopus)

Use of Noninvasive Ventilation During Feeding Tube Placement

Banfi, P., Volpato, E., Valota, C., D'Ascenzo, S., Alunno, C. B., Lax, A., Nicolini, A., Ticozzi, N., Silani, V. & Bach, J. R., Nov 2017, In : Respiratory Care. 62, 11, p. 1474-1484 11 p.

Research output: Contribution to journal › Article

Noninvasive Ventilation
Enteral Nutrition
Gastrostomy
Randomized Controlled Trials
Amyotrophic Lateral Sclerosis
4 Citations (Scopus)

Use of Noninvasive Ventilation During Feeding Tube Placement

Banfi, P., Volpato, E., Valota, C., D'Ascenzo, S., Alunno, C. B., Lax, A., Nicolini, A., Ticozzi, N., Silani, V. & Bach, J. R., Nov 2017, In : Respiratory Care. 62, 11, p. 1474-1484 11 p.

Research output: Contribution to journal › Review article

Noninvasive Ventilation
Enteral Nutrition
Gastrostomy
Randomized Controlled Trials
Amyotrophic Lateral Sclerosis
2016

Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis

Fogh, I., Lin, K., Tiloca, C., Rooney, J., Gellera, C., Diekstra, F. P., Ratti, A., Shatunov, A., van Es, M. A., Proitsi, P., Jones, A., Sproviero, W., Chiò, A., McLaughlin, R. L., Soraru, G., Corrado, L., Stahl, D., Del Bo, R., Cereda, C., Castellotti, B. & 29 others, Glass, J. D., Newhouse, S., Dobson, R. J., Smith, B. N., Topp, S., Van Rheenen, W., Meininger, V., Melki, J., Morrison, K. E., Shaw, P. J., Leigh, P. N., Andersen, P. M., Comi, G. P., Ticozzi, N., Mazzini, L., D'Alfonso, S., Traynor, B. J., van Damme, P., Robberecht, W., Brown, R. H., Landers, J., Hardiman, O., Lewis, C. M., Van Den Berg, L. H., Shaw, C. E., Veldink, J., Silani, V., Al-Chalabi, A. & Powell, J., Jul 1 2016, In : JAMA Neurology. 73, 7, p. 812-820 9 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Survival
Genes
Genome-Wide Association Study
Genotype

Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis

Fogh, I., Lin, K., Tiloca, C., Rooney, J., Gellera, C., Diekstra, F. P., Ratti, A., Shatunov, A., van Es, M. A., Proitsi, P., Jones, A., Sproviero, W., Chiò, A., McLaughlin, R. L., Soraru, G., Corrado, L., Stahl, D., Del Bo, R., Cereda, C., Castellotti, B. & 29 others, Glass, J. D., Newhouse, S., Dobson, R. J., Smith, B. N., Topp, S., Van Rheenen, W., Meininger, V., Melki, J., Morrison, K. E., Shaw, P. J., Leigh, P. N., Andersen, P. M., Comi, G. P., Ticozzi, N., Mazzini, L., D'Alfonso, S., Traynor, B. J., van Damme, P., Robberecht, W., Brown, R. H., Landers, J., Hardiman, O., Lewis, C. M., Van Den Berg, L. H., Shaw, C. E., Veldink, J., Silani, V., Al-Chalabi, A. & Powell, J., Jul 1 2016, In : JAMA Neurology. 73, 7, p. 812-820 9 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Survival
Genes
Genome-Wide Association Study
Genotype

Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis

Fogh, I., Lin, K., Tiloca, C., Rooney, J., Gellera, C., Diekstra, F. P., Ratti, A., Shatunov, A., van Es, M. A., Proitsi, P., Jones, A., Sproviero, W., Chiò, A., McLaughlin, R. L., Soraru, G., Corrado, L., Stahl, D., Del Bo, R., Cereda, C., Castellotti, B. & 29 others, Glass, J. D., Newhouse, S., Dobson, R. J., Smith, B. N., Topp, S., Van Rheenen, W., Meininger, V., Melki, J., Morrison, K. E., Shaw, P. J., Leigh, P. N., Andersen, P. M., Comi, G. P., Ticozzi, N., Mazzini, L., D'Alfonso, S., Traynor, B. J., van Damme, P., Robberecht, W., Brown, R. H., Landers, J., Hardiman, O., Lewis, C. M., Van Den Berg, L. H., Shaw, C. E., Veldink, J., Silani, V., Al-Chalabi, A. & Powell, J., Jul 1 2016, In : JAMA Neurology. 73, 7, p. 812-820 9 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Survival
Genes
Genome-Wide Association Study
Genotype
28 Citations (Scopus)

Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis

Fogh, I., Lin, K., Tiloca, C., Rooney, J., Gellera, C., Diekstra, F. P., Ratti, A., Shatunov, A., Van Es, M. A., Proitsi, P., Jones, A., Sproviero, W., Chiò, A., McLaughlin, R. L., Sorarù, G., Corrado, L., Stahl, D., Del Bo, R., Cereda, C., Castellotti, B. & 29 others, Glass, J. D., Newhouse, S., Dobson, R., Smith, B. N., Topp, S., Van Rheenen, W., Meininger, V., Melki, J., Morrison, K. E., Shaw, P. J., Leigh, P. N., Andersen, P. M., Comi, G. P., Ticozzi, N., Mazzini, L., D'Alfonso, S., Traynor, B. J., Van Damme, P., Robberecht, W., Brown, R. H., Landers, J. E., Hardiman, O., Lewis, C. M., Van Den Berg, L. H., Shaw, C. E., Veldink, J. H., Silani, V., Al-Chalabi, A. & Powell, J., Jul 1 2016, In : JAMA Neurology. 73, 7, p. 812-820 9 p.

Research output: Contribution to journal › Article

Amyotrophic Lateral Sclerosis
Survival
Genes
Genome-Wide Association Study
Genotype