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1. Full Text Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
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
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2. Full Text Frontotemporal dementia and its subtypes: a genome-wide association study
by Ferrari, Raffaele, PhD and Hernandez, Dena G, MSc and Nalls, Michael A, PhD and Rohrer, Jonathan D, PhD and Ramasamy, Adaikalavan, PhD and Kwok, John B J, PhD and Dobson-Stone, Carol, PhD and Brooks, William S, MBBS and Schofield, Peter R, Prof and Halliday, Glenda M, Prof and Hodges, John R, Prof and Piguet, Olivier, PhD and Bartley, Lauren, MSc and Thompson, Elizabeth, MD and Haan, Eric, Prof and Hernández, Isabel, MD and Ruiz, Agustín, MD and Boada, Mercè, MD and Borroni, Barbara, MD and Padovani, Alessandro, Prof and Cruchaga, Carlos, PhD and Cairns, Nigel J, Prof and Benussi, Luisa, PhD and Binetti, Giuliano, MD and Ghidoni, Roberta, PhD and Forloni, Gianluigi, PhD and Galimberti, Daniela, PhD and Fenoglio, Chiara, PhD and Serpente, Maria, PhD and Scarpini, Elio, MD and Clarimón, Jordi, PhD and Lleó, Alberto, MD and Blesa, Rafael, MD and Waldö, Maria Landqvist, MD and Nilsson, Karin, PhD and Nilsson, Christer, PhD and Mackenzie, Ian R A, Prof and Hsiung, Ging-Yuek R, MD and Mann, David M A, Prof and Grafman, Jordan, Prof and Morris, Christopher M, PhD and Attems, Johannes, Prof and Griffiths, Timothy D, Prof and McKeith, Ian G, Prof and Thomas, Alan J, Prof and Pietrini, P, Prof and Huey, Edward D, MD and Wassermann, Eric M, MD and Baborie, Atik, MD and Jaros, Evelyn, PhD and Tierney, Michael C, MSc and Pastor, Pau, MD and Razquin, Cristina, PhD and Ortega-Cubero, Sara, MD and Alonso, Elena, BSc and Perneczky, Robert, MD and Diehl-Schmid, Janine, MD and Alexopoulos, Panagiotis, MD and Kurz, Alexander, MD and Rainero, Innocenzo, MD and Rubino, Elisa, MD and Pinessi, Lorenzo, Prof and Rogaeva, Ekaterina, PhD and St George-Hyslop, Peter, MD and Rossi, Giacomina, PhD and Tagliavini, Fabrizio, MD and Giaccone, Giorgio, MD and Rowe, James B, PhD and Schlachetzki, Johannes C M, MD and Uphill, James, BSc and Collinge, John, Prof and Mead, Simon, Prof and Danek, Adrian, MD and Van Deerlin, Vivianna M, PhD and Grossman, Murray, Prof and Trojanowski, John Q, Prof and van der Zee, Julie, PhD and Deschamps, William, MSc and Van Langenhove, Tim, MD and Cruts, Marc, PhD and Van Broeckhoven, Christine, Prof and Cappa, Stefano F, Prof and Le Ber, Isabelle, MD and Hannequin, Didier, Prof and Golfier, Véronique, MD and Vercelletto, Martine, MD and Brice, Alexis, MD and Nacmias, Benedetta, PhD and Sorbi, Sandro, Prof and Bagnoli, Silvia, PhD and Piaceri, Irene, PhD and Nielsen, Jørgen E, MD and Hjermind, Lena E, MD and Riemenschneider, Matthias, Prof and Mayhaus, Manuel, PhD and Ibach, Bernd, PhD and Gasparoni, Gilles, PhD and Pichler, Sabrina, MSc and Gu, Wei, PhD and Rossor, Martin N, Prof and ... and Lund University and Psychiatry (Lund) and MultiPark: Multidisciplinary research focused on Parkinson´s disease and Psykiatri, Lund and Lunds universitet
Lancet Neurology, The, ISSN 1474-4422, 2014, Volume 13, Issue 7, pp. 686 - 699
Summary Background Frontotemporal dementia (FTD) is a complex disorder characterised by a broad range of clinical manifestations, differential pathological... 
Neurology | GENETIC-VARIATION | COMMON VARIANTS | PROTEIN | LOBAR DEGENERATION | DISEASE | SUSCEPTIBILITY LOCI | RISK | MUTATIONS | HEXANUCLEOTIDE REPEAT | BRAIN | CLINICAL NEUROLOGY | Frontotemporal Dementia - genetics | Humans | Middle Aged | Aged, 80 and over | Adult | Female | Genotype | Male | Aged | Frontotemporal Dementia - diagnosis | Genome-Wide Association Study - methods | Frontotemporal Dementia - classification | Genetic research | Genomics | Dementia | Genealogy | Principal components analysis | Genomes | Patients | Proteins | Studies | Pathology | Semantics | Consent | Quality control | Aging | Aphasia | DNA methylation | Mutation | Genetic testing | Chromosomes | Deoxyribonucleic acid--DNA | Neurologi | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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3. Full Text Tracking pathophysiological processes in Alzheimer's disease: an updated hypothetical model of dynamic biomarkers
by Jack, Clifford R, Prof Dr and Knopman, David S, Prof and Jagust, William J, Prof and Petersen, Ronald C, Prof and Weiner, Michael W, Prof and Aisen, Paul S, Prof and Shaw, Leslie M, Prof and Vemuri, Prashanthi, PhD and Wiste, Heather J and Weigand, Stephen D and Lesnick, Timothy G and Pankratz, Vernon S, PhD and Donohue, Michael C, PhD and Trojanowski, John Q, Prof
Lancet Neurology, The, ISSN 1474-4422, 2013, Volume 12, Issue 2, pp. 207 - 216
Summary In 2010, we put forward a hypothetical model of the major biomarkers of Alzheimer's disease (AD). The model was received with interest because we... 
Neurology | BRAIN ATROPHY | POSITRON-EMISSION-TOMOGRAPHY | AMYLOID DEPOSITION | IN-VIVO | A-BETA | CSF BIOMARKERS | CEREBROSPINAL-FLUID A-BETA | MILD COGNITIVE IMPAIRMENT | PITTSBURGH COMPOUND-B | CLINICAL NEUROLOGY | APOLIPOPROTEIN-E | Alzheimer Disease - physiopathology | Models, Biological | Cognition Disorders - etiology | Humans | Amyloid beta-Peptides - cerebrospinal fluid | tau Proteins - cerebrospinal fluid | Biomarkers - cerebrospinal fluid | Alzheimer Disease - cerebrospinal fluid | Nonlinear Dynamics | Alzheimer Disease - pathology
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4. Full Text Global surveillance of cancer survival 1995–2009: analysis of individual data for 25 676 887 patients from 279 population-based registries in 67 countries (CONCORD-2)
by Allemani, Claudia, PhD and Weir, Hannah K, PhD and Carreira, Helena, MPH and Harewood, Rhea, MSc and Spika, Devon, MSc and Wang, Xiao-Si, PhD and Bannon, Finian, PhD and Ahn, Jane V, MSc and Johnson, Christopher J, MPH and Bonaventure, Audrey, MD and Marcos-Gragera, Rafael, PhD and Stiller, Charles, MSc and Azevedo e Silva, Gulnar, Prof and Chen, Wan-Qing, PhD and Ogunbiyi, Olufemi J, Prof and Rachet, Bernard, FFPH and Soeberg, Matthew J, PhD and You, Hui, MAppStats and Matsuda, Tomohiro, PhD and Bielska-Lasota, Magdalena, Prof and Storm, Hans, MD and Tucker, Thomas C, Prof and Coleman, Michel P, Prof and CONCORD Working Grp and CONCORD Working Group
Lancet, The, ISSN 0140-6736, 2015, Volume 385, Issue 9972, pp. 977 - 1010
Summary Background Worldwide data for cancer survival are scarce. We aimed to initiate worldwide surveillance of cancer survival by central analysis of... 
Internal Medicine | BREAST-CANCER | MEDICINE, GENERAL & INTERNAL | RECTAL-CANCER | CHILDHOOD-CANCER | BENCHMARKING PARTNERSHIP | EUROPE 1999-2007 | HIGH-RESOLUTION | NORDIC COUNTRIES | OVARIAN-CANCER | NET SURVIVAL | HIGH-INCOME COUNTRIES | Age Distribution | Global Health | Humans | Middle Aged | Child, Preschool | Neoplasms - mortality | Infant | Male | Young Adult | Adolescent | Survival Analysis | Aged, 80 and over | Sex Distribution | Adult | Female | Registries | Aged | Child | Infant, Newborn | Prevention | Patient outcomes | Analysis | Cancer | Medical research | Global health | Survival analysis | Surveillance | Mortality | Population
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5. Full Text TDP-43 Depletion in Microglia Promotes Amyloid Clearance but Also Induces Synapse Loss
by Paolicelli, Rosa C and Jawaid, Ali and Henstridge, Christopher M and Valeri, Andrea and Merlini, Mario and Robinson, John L and Lee, Virginia M.-Y and Lee, Edward B and Rose, Jamie and Appel, Stanley and Trojanowski, John Q and Spires-Jones, Tara and Schulz, Paul E and Rajendran, Lawrence
Neuron, ISSN 0896-6273, 07/2017, Volume 95, Issue 2, pp. 297 - 308.e6
Microglia coordinate various functions in the central nervous system ranging from removing synaptic connections, to maintaining brain homeostasis by monitoring... 
Alzheimer’s Disease | Amyotrophic Lateral Sclerosis | Synapse Loss | TDP-43 | Frontotemporal Lobar Degeneration | Synaptic Pruning | Amyloid | Clearance | Tardbp | Phagocytosis | Microglia | Alzheimer's Disease | PROTEIN | ALZHEIMERS-DISEASE | IN-VIVO | A-BETA | NEURODEGENERATION | PHENOTYPES | AMYOTROPHIC-LATERAL-SCLEROSIS | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | BRAIN | TRANSGENIC MICE | Nervous system diseases | Alzheimer's disease | Analysis | Cells | Protein binding | Neurophysiology | Brain | Disease | Peptides | Pathogenesis | Genes | Central nervous system | Disorders | Cognitive ability | Homeostasis | Nervous system | Proteins | Phagocytes | Neurodegeneration | Coding | Transgenic animals | Rodents | Deoxyribonucleic acid--DNA | Clearing | Neurodegenerative diseases | Amyotrophic lateral sclerosis | Ribonucleic acid--RNA | Pathology | RNA-binding protein | Life span | Aggregates | β-Amyloid | Mice | Synapses
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6. Full Text Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
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
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