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TREM2 rare variant p.R47H is not associated with Parkinson's disease

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TREM2 rare variant p.R47H is not associated with Parkinson's disease. / Mengel, David; Thelen, Mathias; Balzer-Geldsetzer, Monika; Söling, Charlotte; Bach, Jan-Philipp; Schaeffer, Eva; Herold, Christine; Becker, Tim; Liepelt, Inga; Becker, Julian; Riedel-Heller, Steffi; Scherer, Martin; Jessen, Frank; Maier, Wolfgang; Dodel, Richard; Ramirez, Alfredo.

in: PARKINSONISM RELAT D, Jahrgang 23, 01.02.2016, S. 109-11.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › Andere (Vorworte u.ä.) › Forschung

Harvard

Mengel, D, Thelen, M, Balzer-Geldsetzer, M, Söling, C, Bach, J-P, Schaeffer, E, Herold, C, Becker, T, Liepelt, I, Becker, J, Riedel-Heller, S, Scherer, M, Jessen, F, Maier, W, Dodel, R & Ramirez, A 2016, 'TREM2 rare variant p.R47H is not associated with Parkinson's disease', PARKINSONISM RELAT D, Jg. 23, S. 109-11. https://doi.org/10.1016/j.parkreldis.2015.11.026

APA

Mengel, D., Thelen, M., Balzer-Geldsetzer, M., Söling, C., Bach, J-P., Schaeffer, E., Herold, C., Becker, T., Liepelt, I., Becker, J., Riedel-Heller, S., Scherer, M., Jessen, F., Maier, W., Dodel, R., & Ramirez, A. (2016). TREM2 rare variant p.R47H is not associated with Parkinson's disease. PARKINSONISM RELAT D, 23, 109-11. https://doi.org/10.1016/j.parkreldis.2015.11.026

Vancouver

Mengel D, Thelen M, Balzer-Geldsetzer M, Söling C, Bach J-P, Schaeffer E et al. TREM2 rare variant p.R47H is not associated with Parkinson's disease. PARKINSONISM RELAT D. 2016 Feb 1;23:109-11. https://doi.org/10.1016/j.parkreldis.2015.11.026

Bibtex

@article{7c652cd68cc545debc4616abecfecc67,
title = "TREM2 rare variant p.R47H is not associated with Parkinson's disease",
abstract = "Variant p.R47H of triggering receptor expressed on myeloid cells 2 (TREM2) has been associated with Parkinson's disease (PD). We screened this TREM2-variant in 821 PD patients including 261 demented PD patients (PDD) and in healthy controls (n = 919). Neither the entire PD nor the small PDD sample was associated with p.R47H.",
author = "David Mengel and Mathias Thelen and Monika Balzer-Geldsetzer and Charlotte S{\"o}ling and Jan-Philipp Bach and Eva Schaeffer and Christine Herold and Tim Becker and Inga Liepelt and Julian Becker and Steffi Riedel-Heller and Martin Scherer and Frank Jessen and Wolfgang Maier and Richard Dodel and Alfredo Ramirez",
note = "Copyright {\textcopyright} 2015 Elsevier Ltd. All rights reserved.",
year = "2016",
month = feb,
day = "1",
doi = "10.1016/j.parkreldis.2015.11.026",
language = "English",
volume = "23",
pages = "109--11",
journal = "PARKINSONISM RELAT D",
issn = "1353-8020",
publisher = "Elsevier BV",

}

RIS

TY - JOUR

T1 - TREM2 rare variant p.R47H is not associated with Parkinson's disease

AU - Mengel, David

AU - Thelen, Mathias

AU - Balzer-Geldsetzer, Monika

AU - Söling, Charlotte

AU - Bach, Jan-Philipp

AU - Schaeffer, Eva

AU - Herold, Christine

AU - Becker, Tim

AU - Liepelt, Inga

AU - Becker, Julian

AU - Riedel-Heller, Steffi

AU - Scherer, Martin

AU - Jessen, Frank

AU - Maier, Wolfgang

AU - Dodel, Richard

AU - Ramirez, Alfredo

N1 - Copyright © 2015 Elsevier Ltd. All rights reserved.

PY - 2016/2/1

Y1 - 2016/2/1

N2 - Variant p.R47H of triggering receptor expressed on myeloid cells 2 (TREM2) has been associated with Parkinson's disease (PD). We screened this TREM2-variant in 821 PD patients including 261 demented PD patients (PDD) and in healthy controls (n = 919). Neither the entire PD nor the small PDD sample was associated with p.R47H.

AB - Variant p.R47H of triggering receptor expressed on myeloid cells 2 (TREM2) has been associated with Parkinson's disease (PD). We screened this TREM2-variant in 821 PD patients including 261 demented PD patients (PDD) and in healthy controls (n = 919). Neither the entire PD nor the small PDD sample was associated with p.R47H.

U2 - 10.1016/j.parkreldis.2015.11.026

DO - 10.1016/j.parkreldis.2015.11.026

M3 - Other (editorial matter etc.)

C2 - 26651418

VL - 23

SP - 109

EP - 111

JO - PARKINSONISM RELAT D

JF - PARKINSONISM RELAT D

SN - 1353-8020

ER -