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Acta Neuropathologica Communications. 12(1)

Matt, Stephanie M.; Nolan, Rachel; Manikandan, Samyuktha; Agarwal, Yash; Channer, Breana; Oteju, Oluwatofunmi; Daniali, Marzieh; Canagarajah, Joanna A.; LuPone, Teresa; Mompho, Krisna; Runner, Kaitlyn; Nickoloff-Bybel, Emily; Li, Benjamin; Niu, Meng; Schlachetzki, Johannes C. M.; Fox, Howard S.; Gaskill, Peter J.

Journal of Neuroinflammation. 22(1)

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Nature Reviews Neurology. 19(11):668-687

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Acta Neuropathol
Acta Neuropathol . 2019 Aug;138(2):237-250.
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Acta Neuropathologica
van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernández, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Hulsman, M, Beker, N, Tesi, N, Collij, L E, van Berckel, B N M, Reinders, M J T, van Schoor, N M, Lemstra, A W, Pijnenburg, Y A L, Scheltens, P, Huisman, M A, Heutink, P, Posthuma, D, van der Flier, W M, Holstege, H, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB) & The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group 2019, 'A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250. https://doi.org/10.1007/s00401-019-02026-8
Acta neuropathologica 138(2), 237-250 (2019). doi:10.1007/s00401-019-02026-8
Acta neuropathologica 139(5), 959-962 (2020). doi:10.1007/s00401-019-02107-8
2019, 'A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250. https://doi.org/10.1007/s00401-019-02026-8
van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernandez, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleo, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illan-Gala, I, Wei, W, Jeune, B, Orellana, A, Bergh, F T, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, C M, Indakoetxea, B, Collij, L E, Scherer, M, Morenas-Rodriguez, E, Ironside, J W, van Berckel, B N M, Alcolea, D, Wiendl, H, Strickland, S L, Pastor, P, Rodriguez Rodriguez, E, Boeve, B F, Petersen, R C, Ferman, T J, van Gerpen, J A, Reinders, M J T, Uitti, R J, Tarraga, L, Maier, W, Dols-Icardo, O, Kawalia, A, Dalmasso, M C, Boada, M, Zettl, U K, van Schoor, N M, Beekman, M, Allen, M, Masliah, E, Lopez de Munain, A, Pantelyat, A, Wszolek, Z K, Ross, O A, Dickson, D W, Graff-Radford, N R, Knopman, D, Rademakers, R, Lemstra, A W, Pijnenburg, Y A L, Scheltens, P, Gasser, T, Chinnery, P F, Hemmer, B, Huisman, M A, Troncoso, J, Moreno, F, Nohr, E A, Sørensen, T I A, Heutink, P, Sanchez-Juan, P, Posthuma, D, Clarimon, J, Christensen, K, Ertekin-Taner, N, Scholz, S W, Ramirez, A, Ruiz, A, Slagboom, E, van der Flier, W M & Holstege, H 2019, ' A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250 . https://doi.org/10.1007/s00401-019-02026-8
van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernández, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, C M, Indakoetxea, B, Collij, L E, Scherer, M, Morenas-Rodríguez, E, Ironside, J W, van Berckel, B N M, Nohr, E A, Sørensen, T I A, Christensen, K & DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank) 2019, ' A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250 . https://doi.org/10.1007/s00401-019-02026-8
van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernández, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, C M, Indakoetxea, B, Collij, L E, Scherer, M, Morenas-Rodríguez, E, Ironside, J W, van Berckel, B N M, Alcolea, D & Wiendl, H 2019, ' Correction to : A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica . https://doi.org/10.1007/s00401-019-02107-8
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Acta Neuropathologica, vol 139, iss 5

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JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
The IFGC and IPDGC members 2017, 'Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases', Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, no. 2, pp. 152-164. https://doi.org/10.1136/jnnp-2016-314411
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Ging K; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.; Frick L; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.; Schlachetzki J; Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.; Armani A; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.; Zhu Y; Department of Chemistry, Simon Fraser University, Burnaby, BC, Canada.; Gilormini PA; Department of Chemistry, Simon Fraser University, Burnaby, BC, Canada.; Dhingra A; German Center for Neurodegenerative Diseases, Tübingen, Germany.; Böck D; Institute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland.; Marques A; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.; Deen M; Department of Chemistry, Simon Fraser University, Burnaby, BC, Canada.; Chen X; Department of Chemistry, Simon Fraser University, Burnaby, BC, Canada.; Serdiuk T; Department of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.; Trevisan C; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.; Sellitto S; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.; Pisano C; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.; Glass CK; Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.; Heutink P; German Center for Neurodegenerative Diseases, Tübingen, Germany.; Yin JA; Institute of Neuropathology, University of Zurich, Zurich, Switzerland. jiang-an.yin@usz.ch.; Vocadlo DJ; Department of Chemistry, Simon Fraser University, Burnaby, BC, Canada. dvocadlo@sfu.ca.; Aguzzi A; Institute of Neuropathology, University of Zurich, Zurich, Switzerland. adriano.aguzzi@uzh.ch.

Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 101675390 Publication Model: Electronic Cited Medium: Print ISSN: 2373-8057 (Print) Linking ISSN: 23738057 NLM ISO Abbreviation: NPJ Parkinsons Dis Subsets: PubMed not MEDLINE

Patrick Süβ; Addison J Lana; Johannes C. M. Schlachetzki

Neural Regeneration Research, Vol 16, Iss 9, Pp 1711-1714 (2021)

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Neurology: Genetics. Oct 01, 2018 4(5)

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Sci Rep
Scientific Reports
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
Bonham, L W, Steele, N Z R, Karch, C M, Broce, I, Geier, E G, Wen, N L, Momeni, P, Hardy, J, Miller, Z A, Gorno-Tempini, M L, Hess, C P, Lewis, P, Miller, B L, Seeley, W W, Manzoni, C, Desikan, R S, Baranzini, S E, Ferrari, R, Yokoyama, J S & International FTD-Genomics Consortium (IFGC) 2019, 'Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia', Scientific Reports, vol. 9, no. 1, 10854. https://doi.org/10.1038/s41598-019-46415-1
Scientific reports
Nielsen, J E & International FTD-Genomics Consortium (IFGC) 2019, ' Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia ', Scientific Reports, vol. 9, no. 1, 10854 . https://doi.org/10.1038/s41598-019-46415-1
2019, ' Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia ', Scientific Reports, vol. 9, no. 1, 10854 . https://doi.org/10.1038/s41598-019-46415-1
Scientific Reports, vol 9, iss 1

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