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by Majounie, Elisa, PhD and Renton, Alan E, PhD and Mok, Kin, MSc and Dopper, Elise GP and Waite, Adrian, PhD and Rollinson, Sara, PhD and Chiò, Adriano, MD and Restagno, Gabriella, MD and Nicolaou, Nayia, MSc and Simon-Sanchez, Javier, PhD and van Swieten, John C, Prof and Abramzon, Yevgeniya and Johnson, Janel O, PhD and Sendtner, Michael, Prof and Pamphlett, Roger, MD and Orrell, Richard W, MD and Mead, Simon, MD and Sidle, Katie C, MD and Houlden, Henry, Prof and Rohrer, Jonathan D, MD and Morrison, Karen E, Prof and Pall, Hardev, MD and Talbot, Kevin, Prof and Ansorge, Olaf, MD and Hernandez, Dena G, MSc and Arepalli, Sampath, MS and Sabatelli, Mario, MD and Mora, Gabriele, MD and Corbo, Massimo, MD and Giannini, Fabio, MD and Calvo, Andrea, MD and Englund, Elisabet, MD and Borghero, Giuseppe, MD and Floris, Gian Luca, MD and Remes, Anne M, Prof and Laaksovirta, Hannu, MD and McCluskey, Leo, MD and Trojanowski, John Q, Prof and Van Deerlin, Vivianna M, MD and Schellenberg, Gerard D, Prof and Nalls, Michael A, PhD and Drory, Vivian E, MD and Lu, Chin-Song, Prof and Yeh, Tu-Hsueh, MD and Ishiura, Hiroyuki, MD and Takahashi, Yuji, MD and Tsuji, Shoji, Prof and Le Ber, Isabelle, MD and Brice, Alexis, Prof and Drepper, Carsten, PhD and Williams, Nigel, PhD and Kirby, Janine, PhD and Shaw, Pamela, Prof and Hardy, John, Prof and Tienari, Pentti J, MD and Heutink, Peter, Prof and Morris, Huw R, MD and Pickering-Brown, Stuart, Prof and Traynor, Bryan J, Dr and Chromosome 9-ALS FTD Consortium and French Res Network FTLD FTLD ALS and ITALSGEN Consortium and French research network on FTLD/FTLD/ALS and Chromosome 9-ALS/FTD Consortium and Oncology and Pathology, Kamprad Lab and Lund University and Lunds universitet and Onkologi och Patologi, Kampradlab
Lancet Neurology, The, ISSN 1474-4422, 2012, Volume 11, Issue 4, pp. 323 - 330
Summary Background We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9orf72 that has been associated with a large... 
Neurology | PREVALENCE | MUTATIONS | LOBAR DEGENERATION | GENETICS | TDP-43 | CLINICAL NEUROLOGY | Frontotemporal Dementia - genetics | Cross-Sectional Studies | DNA Repeat Expansion - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Child, Preschool | Genotype | Male | Genetic Loci | Open Reading Frames - genetics | Young Adult | Chromosomes, Human, Pair 9 - genetics | Adolescent | Age of Onset | Aged, 80 and over | Adult | Female | Aged | Child | Cohort Studies | Medical research | Medical colleges | Care and treatment | Nervous system diseases | Neurosciences | Molecular genetics | Oncology, Experimental | Questions and answers | Amyotrophic lateral sclerosis | Research | Medicine, Experimental | Agriculture | Physicians (General practice) | Alzheimer's disease | Dementia | Cancer | Biomedical engineering | Haplotypes | Polymerase chain reaction | Neurodegenerative diseases | Ethnic groups | Data processing | Mutation | Frontotemporal dementia | Genetic counselling | Islands | Age | Toll-Like Receptor 4 | Open Reading Frames | Adaptor Proteins, Vesicular Transport | Lipopolysaccharides | Life Sciences | DNA Repeat Expansion | Interferon Regulatory Factor-3 | Transfection | Amyotrophic Lateral Sclerosis | RNA Interference | HEK293 Cells | Membrane Glycoproteins | Vesicular Transport Proteins | Protein Structure, Tertiary | Cell Line | Chemokine CCL5 | Frontotemporal Dementia | Signal Transduction | Myeloid Differentiation Factor 88 | Chromosomes, Human, Pair 9 | Protein Transport | Adaptor Proteins, Signal Transducing | Santé publique et épidémiologie | RNA, Small Interfering | Endosomes | Neurologi | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
by Chauhan, Ganesh and Adams, Hieab H.H and Satizabal, Claudia L and Bis, Joshua C and Teumer, Alexander and Sargurupremraj, Muralidharan and Hofer, Edith and Trompet, Stella and Hilal, Saima and Smith, Albert Vernon and Jian, Xueqiu and Malik, Rainer and Traylor, Matthew and Pulit, Sara L and Amouyel, Philippe and Mazoyer, Bernard and Zhu, Yi-Cheng and Kaffashian, Sara and Schilling, Sabrina and Beecham, Gary W and Montine, Thomas J and Schellenberg, Gerard D and Kjartansson, Olafur and Guðnason, Vilmundur and Knopman, David S and Griswold, Michael E and Windham, B Gwen and Gottesman, Rebecca F and Mosley, Thomas H and Schmidt, Reinhold and Saba, Yasaman and Schmidt, Helena and Takeuchi, Fumihiko and Yamaguchi, Shuhei and Nabika, Toru and Kato, Norihiro and Rajan, Kumar B and Aggarwal, Neelum T and De Jager, Philip L and Evans, Denis A and Psaty, Bruce M and Rotter, Jerome I and Rice, Kenneth and Lopez, Oscar L and Liao, Jiemin and Chen, Christopher and Cheng, Ching-Yu and Wong, Tien Y and Ikram, Mohammad K and van der Lee, Sven J and Amin, Najaf and Chouraki, Vincent and DeStefano, Anita L and Aparicio, Hugo J and Romero, Jose R and Maillard, Pauline and DeCarli, Charles and Wardlaw, Joanna M and Hernández, Maria del C Valdés and Luciano, Michelle and Liewald, David and Deary, Ian J and Starr, John M and Bastin, Mark E and Muñoz Maniega, Susana and Slagboom, P Eline and Beekman, Marian and Deelen, Joris and Uh, Hae-Won and Lemmens, Robin and Brodaty, Henry and Wright, Margaret J and Ames, David and Boncoraglio, Giorgio B and Hopewell, Jemma C and Beecham, Ashley H and Blanton, Susan H and Wright, Clinton B and Sacco, Ralph L and Wen, Wei and Thalamuthu, Anbupalam and Armstrong, Nicola J and Chong, Elizabeth and Schofield, Peter R and Kwok, John B and van der Grond, Jeroen and Stott, David J and Ford, Ian and Jukema, J Wouter and Vernooij, Meike W and Hofman, Albert and Uitterlinden, André G and van der Lugt, Aad and Wittfeld, Katharina and Grabe, Hans J and Hosten, Norbert and von Sarnowski, Bettina and Völker, Uwe and Levi, Christopher and Jimenez-Conde, Jordi and ... and Stroke Genetics Network SiGN and CHARGE Consortium and ISGC and METASTROKE and ADGC and Stroke Genetics Network (SiGN), the International Stroke Genetics Consortium (ISGC), METASTROKE, Alzheimer's Disease Genetics Consortium (ADGC), and the Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
Neurology, ISSN 0028-3878, 01/2019, Volume 92, Issue 5, pp. e486 - e503
OBJECTIVETo explore genetic and lifestyle risk factors of MRI-defined brain infarcts (BI) in large population-based cohorts. METHODSWe performed meta-analyses... 
SMALL VESSEL DISEASE | METAANALYSIS | POLYMORPHISMS | MENDELIAN RANDOMIZATION | MATTER HYPERINTENSITY VOLUME | ISCHEMIC-STROKE | BLOOD-PRESSURE | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | SILENT | INSIGHTS
Journal Article
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