Reconsidering the causality of TIA1 mutations in ALS

Rick A. Van Der Spek; Wouter Van Rheenen; Sara L. Pulit; Kevin P. Kenna; Nicola Ticozzi; Maarten Kooyman; Russell L. McLaughlin; Matthieu Moisse; Kristel R. Van Eijk; Joke J.F.A. Van Vugt; Jens Peter Andersen; A. Nazli Basak; Ian Blair; Mamede de Carvalho; Adriano Chio; Philippe Corcia; Phillipe Couratier; Vivian E Drory; Jonathan D Glass; Orla Hardiman; Jesús S. Mora; Karen E Morrison; Miguel Mitne-Neto; Wim Robberecht; Pamela J Shaw; Monica P Panadés; Philip Van Damme; Vincenzo Silani; Marc Gotkine; Markus Weber; Michael A. Van Es; John E Landers; Ammar Al-Chalabi; Leonard H. Van Den Berg; Jan H. Veldink

doi:10.1080/21678421.2017.1413118

Reconsidering the causality of TIA1 mutations in ALS

Rick A. Van Der Spek
, Wouter Van Rheenen
, Sara L. Pulit
, Kevin P. Kenna
, Nicola Ticozzi
, Maarten Kooyman
, Russell L. McLaughlin
, Matthieu Moisse
, Kristel R. Van Eijk
, Joke J.F.A. Van Vugt
, Jens Peter Andersen
, A. Nazli Basak
, Ian Blair
, Mamede de Carvalho
, Adriano Chio
, Philippe Corcia
, Phillipe Couratier
, Vivian E Drory
, Jonathan D Glass
, Orla Hardiman

Jesús S. Mora, Karen E Morrison, Miguel Mitne-Neto, Wim Robberecht, Pamela J Shaw, Monica P Panadés, Philip Van Damme, Vincenzo Silani, Marc Gotkine, Markus Weber, Michael A. Van Es, John E Landers, Ammar Al-Chalabi, Leonard H. Van Den Berg, Jan H. Veldink^*,

^*Corresponding author for this work

Research output: Contribution to journal › Editorial › Academic › peer-review

Original language	English
Pages (from-to)	1-3
Number of pages	3
Journal	Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
Volume	19
Issue number	1-2
Early online date	13 Dec 2017
DOIs	https://doi.org/10.1080/21678421.2017.1413118
Publication status	Published - 2018

Keywords

Amyotrophic Lateral Sclerosis/genetics
Genetic Predisposition to Disease
Genetic Testing/methods
Humans
Mutation/genetics
T-Cell Intracellular Antigen-1/genetics

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10.1080/21678421.2017.1413118

Cite this

Van Der Spek, R. A., Van Rheenen, W., Pulit, S. L., Kenna, K. P., Ticozzi, N., Kooyman, M., McLaughlin, R. L., Moisse, M., Van Eijk, K. R., Van Vugt, J. J. F. A., Andersen, J. P., Nazli Basak, A., Blair, I., de Carvalho, M., Chio, A., Corcia, P., Couratier, P., Drory, V. E., Glass, J. D. (2018). Reconsidering the causality of TIA1 mutations in ALS. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 19(1-2), 1-3. https://doi.org/10.1080/21678421.2017.1413118

@article{3c22018e3ca743899471c7ba1a2c8461,

title = "Reconsidering the causality of TIA1 mutations in ALS",

keywords = "Amyotrophic Lateral Sclerosis/genetics, Genetic Predisposition to Disease, Genetic Testing/methods, Humans, Mutation/genetics, T-Cell Intracellular Antigen-1/genetics",

author = "\{Van Der Spek\}, \{Rick A.\} and \{Van Rheenen\}, Wouter and Pulit, \{Sara L.\} and Kenna, \{Kevin P.\} and Nicola Ticozzi and Maarten Kooyman and McLaughlin, \{Russell L.\} and Matthieu Moisse and \{Van Eijk\}, \{Kristel R.\} and \{Van Vugt\}, \{Joke J.F.A.\} and Andersen, \{Jens Peter\} and \{Nazli Basak\}, A. and Ian Blair and \{de Carvalho\}, Mamede and Adriano Chio and Philippe Corcia and Phillipe Couratier and Drory, \{Vivian E\} and Glass, \{Jonathan D\} and Orla Hardiman and Mora, \{Jes{\'u}s S.\} and Morrison, \{Karen E\} and Miguel Mitne-Neto and Wim Robberecht and Shaw, \{Pamela J\} and Panad{\'e}s, \{Monica P\} and \{Van Damme\}, Philip and Vincenzo Silani and Marc Gotkine and Markus Weber and \{Van Es\}, \{Michael A.\} and Landers, \{John E\} and Ammar Al-Chalabi and \{Van Den Berg\}, \{Leonard H.\} and Veldink, \{Jan H.\}",

year = "2018",

doi = "10.1080/21678421.2017.1413118",

language = "English",

volume = "19",

pages = "1--3",

journal = "Amyotrophic Lateral Sclerosis \& Frontotemporal Degeneration",

issn = "2167-8421",

publisher = "Taylor and Francis Ltd.",

number = "1-2",

}

Van Der Spek, RA, Van Rheenen, W, Pulit, SL, Kenna, KP, Ticozzi, N, Kooyman, M, McLaughlin, RL, Moisse, M, Van Eijk, KR, Van Vugt, JJFA, Andersen, JP, Nazli Basak, A, Blair, I, de Carvalho, M, Chio, A, Corcia, P, Couratier, P, Drory, VE, Glass, JD, Hardiman, O, Mora, JS, Morrison, KE, Mitne-Neto, M, Robberecht, W, Shaw, PJ, Panadés, MP, Van Damme, P, Silani, V, Gotkine, M, Weber, M, Van Es, MA, Landers, JE, Al-Chalabi, A, Van Den Berg, LH , Veldink, JH 2018, 'Reconsidering the causality of TIA1 mutations in ALS', Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, vol. 19, no. 1-2, pp. 1-3. https://doi.org/10.1080/21678421.2017.1413118

TY - JOUR

T1 - Reconsidering the causality of TIA1 mutations in ALS

AU - Van Der Spek, Rick A.

AU - Van Rheenen, Wouter

AU - Pulit, Sara L.

AU - Kenna, Kevin P.

AU - Ticozzi, Nicola

AU - Kooyman, Maarten

AU - McLaughlin, Russell L.

AU - Moisse, Matthieu

AU - Van Eijk, Kristel R.

AU - Van Vugt, Joke J.F.A.

AU - Andersen, Jens Peter

AU - Nazli Basak, A.

AU - Blair, Ian

AU - de Carvalho, Mamede

AU - Chio, Adriano

AU - Corcia, Philippe

AU - Couratier, Phillipe

AU - Drory, Vivian E

AU - Glass, Jonathan D

AU - Hardiman, Orla

AU - Mora, Jesús S.

AU - Morrison, Karen E

AU - Mitne-Neto, Miguel

AU - Robberecht, Wim

AU - Shaw, Pamela J

AU - Panadés, Monica P

AU - Van Damme, Philip

AU - Silani, Vincenzo

AU - Gotkine, Marc

AU - Weber, Markus

AU - Van Es, Michael A.

AU - Landers, John E

AU - Al-Chalabi, Ammar

AU - Van Den Berg, Leonard H.

AU - Veldink, Jan H.

PY - 2018

Y1 - 2018

KW - Amyotrophic Lateral Sclerosis/genetics

KW - Genetic Predisposition to Disease

KW - Genetic Testing/methods

KW - Humans

KW - Mutation/genetics

KW - T-Cell Intracellular Antigen-1/genetics

UR - https://www.scopus.com/pages/publications/85038017115

U2 - 10.1080/21678421.2017.1413118

DO - 10.1080/21678421.2017.1413118

M3 - Editorial

C2 - 29235362

SN - 2167-8421

VL - 19

SP - 1

EP - 3

JO - Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration

JF - Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration

IS - 1-2

ER -

Reconsidering the causality of TIA1 mutations in ALS

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