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Nature Genetics, ISSN 1061-4036, 09/2017, Volume 49, Issue 9, pp. 1373 - 1384
Journal Article
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 02/2017, Volume 62, Issue 2, pp. 321 - 324
Hexanucleotide expansion mutations in the chromosome 9 open reading frame 72 (C9orf72) gene is the most common genetic cause for frontotemporal dementia (FTD)... 
ALS | HEXANUCLEOTIDE REPEAT | FTD | GENETICS & HEREDITY | Frontotemporal Dementia - genetics | DNA Repeat Expansion - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Male | Proteins - genetics | Haplotypes - genetics | Sweden | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | C9orf72 Protein
Journal Article
Nature Neuroscience, ISSN 1097-6256, 09/2001, Volume 4, Issue 9, pp. 887 - 893
Several pathogenic Alzheimer's disease (AD) mutations have been described, all of which cause increased amyloid beta -protein (A beta) levels. Here we present... 
FIBRIL FORMATION | IN-VITRO | A-BETA(1-42) | PRESENILINS | PEPTIDES | PLASMA | CEREBRAL-HEMORRHAGE | GENE | AMYLOID PRECURSOR PROTEIN | FIBRILLOGENESIS | NEUROSCIENCES
Journal Article
Journal Article
Neurobiology of aging, ISSN 0197-4580, 03/2019
Frontotemporal dementia (FTD) is the second most common early-onset dementia. Up to half of the cases are familial, and several mutations have been identified... 
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 2014, Volume 10, Issue 4, pp. P480 - P480
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 06/2018, Volume 22, Issue 6, p. 3016
Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a familial fatal progressive degenerative disorder. One... 
Viral antibodies | Analysis | Genetic research | Antibodies | Smooth muscle | Bone morphogenetic proteins | Transforming growth factors | Gene expression
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 11/2013, Volume 21, Issue 11, pp. 1260 - 1265
Journal Article
by van der Zee, Julie and Gijselinck, Ilse and Dillen, Lubina and Van Langenhove, Tim and Theuns, Jessie and Engelborghs, Sebastiaan and Philtjens, Stéphanie and Vandenbulcke, Mathieu and Sleegers, Kristel and Sieben, Anne and Bäumer, Veerle and Maes, Githa and Corsmit, Ellen and Borroni, Barbara and Padovani, Alessandro and Archetti, Silvana and Perneczky, Robert and Diehl‐Schmid, Janine and de Mendonça, Alexandre and Miltenberger‐Miltenyi, Gabriel and Pereira, Sónia and Pimentel, José and Nacmias, Benedetta and Bagnoli, Silvia and Sorbi, Sandro and Graff, Caroline and Chiang, Huei‐Hsin and Westerlund, Marie and Sanchez‐Valle, Raquel and Llado, Albert and Gelpi, Ellen and Santana, Isabel and Almeida, Maria Rosário and Santiago, Beatriz and Frisoni, Giovanni and Zanetti, Orazio and Bonvicini, Cristian and Synofzik, Matthis and Maetzler, Walter and vom Hagen, Jennifer Müller and Schöls, Ludger and Heneka, Michael T and Jessen, Frank and Matej, Radoslav and Parobkova, Eva and Kovacs, Gabor G and Ströbel, Thomas and Sarafov, Stayko and Tournev, Ivailo and Jordanova, Albena and Danek, Adrian and Arzberger, Thomas and Fabrizi, Gian Maria and Testi, Silvia and Salmon, Eric and Santens, Patrick and Martin, Jean‐Jacques and Cras, Patrick and Vandenberghe, Rik and De Deyn, Peter Paul and Cruts, Marc and Van Broeckhoven, Christine and van der Zee, Julie and Gijselinck, Ilse and Dillen, Lubina and Van Langenhove, Tim and Theuns, Jessie and Philtjens, Stéphanie and Sleegers, Kristel and Bäumer, Veerle and Maes, Githa and Corsmit, Ellen and Cruts, Marc and Van Broeckhoven, Christine and van der Zee, Julie and Gijselinck, Ilse and Dillen, Lubina and Van Langenhove, Tim and Philtjens, Stéphanie and Theuns, Jessie and Sleegers, Kristel and Bäumer, Veerle and Maes, Githa and Cruts, Marc and Van Broeckhoven, Christine and Engelborghs, Sebastiaan and De Deyn, Peter P and Cras, Patrick and Engelborghs, Sebastiaan and De Deyn, Peter P and Vandenbulcke, Mathieu and Vandenbulcke, Mathieu and Borroni, Barbara and Padovani, Alessandro and Archetti, Silvana and Perneczky, Robert and Diehl‐Schmid, Janine and Synofzik, Matthis and Maetzler, Walter and Müller vom Hagen, Jennifer and ... and European Early-Onset Dementia EOD and European Early-Onset Dementia Consortium
Human Mutation, ISSN 1059-7794, 02/2013, Volume 34, Issue 2, pp. 363 - 373
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2005, Volume 102, Issue 41, pp. 14854 - 14859
Journal Article
Dementia and Geriatric Cognitive Disorders, ISSN 1420-8008, 03/2011, Volume 31, Issue 2, pp. 109 - 118
Background/Aims: We have previously reported the results of an extended genome-wide scan of Swedish Alzheimer disease (AD)-affected families; in this paper, we... 
Original Research Article | Association study | Genome scan | Alzheimer disease | Chromosome 8 | Linkage analysis | SENSORY NEUROPATHY-LOM | PSYCHIATRY | CANDIDATE GENES | APOLIPOPROTEIN-E GENOTYPE | NEURODEGENERATIVE DISEASES | CLINICAL NEUROLOGY | GERIATRICS & GERONTOLOGY | IDENTIFIES VARIANTS | HEREDITARY MOTOR | EARLY-ONSET | DIAGNOSTIC-CRITERIA | GENOME-WIDE ASSOCIATION | ENDOTHELIAL GROWTH-FACTOR | Chromosomes, Human, Pair 8 - genetics | Genome-Wide Association Study | Humans | Middle Aged | Genotype | Male | Chromosome Mapping | Reverse Transcriptase Polymerase Chain Reaction | Sweden - epidemiology | Lod Score | Alzheimer Disease - pathology | DNA - genetics | Autopsy | Aged, 80 and over | Brain - pathology | Adult | Alzheimer Disease - epidemiology | Female | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Microsatellite Repeats | Genetic Linkage | Medical and Health Sciences | Medicin och hälsovetenskap | Geriatrics and medical gerontology | Biology | Klinisk medicin | MEDICINE | Geriatrik och medicinsk gerontologi | Genetics | Biologi | Natural Sciences | Invärtesmedicin | Dermatologi och venerologi, klinisk genetik, invärtesmedicin | Biological Sciences | Internal medicine | Dermatology and venerology,clinical genetics, internal medicine | Genetik | Clinical Medicine | Naturvetenskap | MEDICIN | Biologiska vetenskaper | Cell and molecular biology | Cell- och molekylärbiologi | Geriatrik | Geriatrics
Journal Article