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Journal Article
by Kun-Rodrigues, Celia and Ross, Owen A and Orme, Tatiana and Shepherd, Claire and Parkkinen, Laura and Darwent, Lee and Hernandez, Dena and Ansorge, Olaf and Clark, Lorraine N and Honig, Lawrence S and Marder, Karen and Lemstra, Afina and Scheltens, Philippe and van der Flier, Wiesje and Louwersheimer, Eva and Holstege, Henne and Rogaeva, Ekaterina and St. George-Hyslop, Peter and Londos, Elisabet and Zetterberg, Henrik and Barber, Imelda and Braae, Anne and Brown, Kristelle and Morgan, Kevin and Maetzler, Walter and Berg, Daniela and Troakes, Claire and Al-Sarraj, Safa and Lashley, Tammaryn and Holton, Janice and Compta, Yaroslau and Van Deerlin, Vivianna and Trojanowski, John Q and Serrano, Geidy E and Beach, Thomas G and Clarimon, Jordi and Lleó, Alberto and Morenas-Rodríguez, Estrella and Lesage, Suzanne and Galasko, Douglas and Masliah, Eliezer and Santana, Isabel and Diez, Monica and Pastor, Pau and Tienari, Pentti J and Myllykangas, Liisa and Oinas, Minna and Revesz, Tamas and Lees, Andrew and Boeve, Brad F and Petersen, Ronald C and Ferman, Tanis J and Escott-Price, Valentina and Graff-Radford, Neill and Cairns, Nigel J and Morris, John C and Stone, David J and Pickering-Brown, Stuart and Mann, David and Dickson, Dennis W and Halliday, Glenda M and Singleton, Andrew and Guerreiro, Rita and Bras, Jose and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Neurobiology of Aging, ISSN 0197-4580, 2016, Volume 49, pp. 214.e13 - 214.e15
Abstract C9orf72 repeat expansions are a common cause of amyotrophic lateral sclerosis and frontotemporal dementia. To date, no large-scale study of dementia... 
Neurology | Internal Medicine | Dementia with Lewy bodies (DLB) | Genetic screen | C9orf72 | NEUROSCIENCES | GERIATRICS & GERONTOLOGY | C9orf72 Protein - genetics | Lewy Body Disease - genetics | Genetic Association Studies | DNA Repeat Expansion - genetics | Humans | Cohort Studies | Analysis | Dementia | Neurosciences | Neurovetenskaper
Journal Article
by Jones, Lesley and Jones, Nicola and Lambert, Jean-Charles and Wang, Li-San and Choi, Seung-Hoan and Harold, Denise and Vedernikov, Alexey and Escott-Price, Valentina and Stone, Timothy and Richards, Alexander and Bellenguez, Céline and Ibrahim-Verbaas, Carla A and Naj, Adam C and Sims, Rebecca and Gerrish, Amy and Jun, Gyungah and DeStefano, Anita L and Bis, Joshua C and Beecham, Gary W and Grenier-Boley, Benjamin and Russo, Giancarlo and Thornton-Wells, Tricia A and Smith, Albert V and Chouraki, Vincent and Thomas, Charlene and Ikram, M. Arfan and Zelenika, Diana and Vardarajan, Badri N and Kamatani, Yoichiro and Lin, Chiao-Feng and Schmidt, Reinhold and Schmidt, Helena and Kunkle, Brian W and Dunstan, Melanie L and Ruiz, Agustin and Bihoreau, Marie-Thérèse and Reitz, Christiane and Pasquier, Florence and Hollingworth, Paul and Hanon, Olivier and Fitzpatrick, Annette L and Buxbaum, Joseph D and Campion, Dominique and Crane, Paul K and Becker, Tim and Gudnason, Vilmundur and Cruchaga, Carlos and Craig, David and Amin, Najaf and Berr, Claudine and Lopez, Oscar L and De Jager, Philip L and Deramecourt, Vincent and Johnston, Janet A and Evans, Denis and Lovestone, Simon and Letteneur, Luc and Kornhuber, Johanes and Tárraga, Lluís and Rubinsztein, David C and Eiriksdottir, Gudny and Sleegers, Kristel and Goate, Alison M and Fiévet, Nathalie and Huentelman, Matthew J and Gill, Michael and Emilsson, Valur and Brown, Kristelle and Kamboh, M. Ilyas and Keller, Lina and Barberger-Gateau, Pascale and McGuinness, Bernadette and Larson, Eric B and Myers, Amanda J and Dufouil, Carole and Todd, Stephen and Wallon, David and Love, Seth and Kehoe, Pat and Rogaeva, Ekaterina and Gallacher, John and St George-Hyslop, Peter and Clarimon, Jordi and Lleò, Alberti and Bayer, Anthony and Tsuang, Debby W and Yu, Lei and Tsolaki, Magda and Bossù, Paola and Spalletta, Gianfranco and Proitsi, Petra and Collinge, John and Sorbi, Sandro and Sanchez Garcia, Florentino and Fox, Nick and Hardy, John and Deniz Naranjo, Maria Candida and Razquin, Cristina and Bosco, Paola and Clarke, Robert and ... and MRC CFAS and Int Genomics Alzheimer's Dis Conso and International Genomics of Alzheimer's Disease Consortium (IGAP) and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 2015, Volume 11, Issue 6, pp. 658 - 671
Journal Article
Annals of Neurology, ISSN 0364-5134, 07/1994, Volume 36, Issue 1, pp. 97 - 100
Allele frequencies for polymorphisms in the aplipoprotein E and the apolipoprotein CII genes were determined in subjects of Ashkenazi Jewish origin with... 
TYPE-4 ALLELE | DIAGNOSIS | CHROMOSOME-19 | MUTATION | EARLY-ONSET | RISK | EPSILON-4 | BINDING | LOCUS | NEUROSCIENCES | CLINICAL NEUROLOGY | Apolipoprotein C-II | Gene Frequency | Humans | Male | Jews - genetics | Linkage Disequilibrium | Polymorphism, Genetic | Apolipoproteins E - genetics | Alleles | Apolipoproteins C - genetics | Female | Aged | Alzheimer Disease - genetics
Journal Article
by Ferrari, R and Hernandez, D.G and Nalls, M.A and Rohrer, J.D and Ramasamy, A and Kwok, J.B.J and Dobson-Stone, C and Brooks, W.S and Schofield, P.R and Halliday, G.M and Hodges, J.R and Piguet, O and Bartley, L and Thompson, E and Haan, E and Hernandez, I and Ruiz, A and Boada, M and Borroni, B and Padovani, A and Cruchaga, C and Cairns, N.J and Benussi, L and Binetti, G and Ghidoni, R and Forloni, G and Galimberti, D and Fenoglio, C and Serpente, M and Scarpini, E and Clarimon, J and Lleo, A and Blesa, R and Waldo, M.L and Nilsson, K and Nilsson, C and Mackenzie, I.R.A and Hsiung, G.Y.R and Mann, D.M.A and Grafman, J and Morris, C.M and Attems, J and Griffiths, T.D and McKeith, I.G and Thomas, A. J and Pietrini, P and Huey, E.D and Wassermann, E.M and Baborie, A and Jaros, E and Tierney, M.C and Pastor, P and Razquin, C and Ortega-Cubero, S and Alonso, E and Perneczky, R and ehl-Schmid, J and Alexopoulos, P and Kurz, A and Rainero, I and Rubino, E and Pinessi, L and Rogaeva, E and St George-Hyslop, P and Rossi, G and Tagliavini, F and Giaccone, G and Rowe, J.B and Schlachetzki, J.C.M and Uphill, J and Collinge, J and Mead, S and Danek, A and Van Deerlin, V.M and Grossman, M and Trojanowski, J.Q and van der Zee, J and Deschamps, W and Van Langenhove, T and Cruts, M and Van Broeckhoven, C and Cappa, S.F and Le Ber, I and Hannequin, D and Golfier, V and Vercelletto, M and Brice, A and Nacmias, B and Sorbi, S and Bagnoli, S and Piaceri, I and Nielsen, J.E and Hjermind, L.E and Riemenschneider, M and Mayhaus, M and Ibach, B and Gasparoni, G and Pichler, S and Gu, W and van Swieten, J.C and ...
Lancet Neurology, ISSN 1474-4422, 2014, Volume 13, Issue 7, pp. 686 - 699
Background: Frontotemporal dementia (FTD) is a complex disorder characterised by a broad range of clinical manifestations, differential pathological... 
Journal Article
Movement Disorders, ISSN 0885-3185, 04/2017, Volume 32, Issue 4, pp. 610 - 614
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 06/2019, Volume 63, pp. 217 - 220
To confirm that there is a diagnostic delay in Parkin-related Parkinson Disease and to explore possible factors causing such a delay. We retrospectively... 
Atypical presentation | Parkin disease | PARK2 mutation | Delayed diagnosis | CLINICAL NEUROLOGY | Ubiquitin | Medical research | Parkinson's disease | Ligases | Analysis | Medicine, Experimental | Genetic aspects | Diagnosis
Journal Article
JAMA, ISSN 0098-7484, 11/2001, Volume 286, Issue 18, pp. 2257 - 2263
Journal Article
Neurology, ISSN 0028-3878, 10/2015, Volume 85, Issue 15, pp. 1283 - 1292
Journal Article