X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (68) 68
female (46) 46
male (46) 46
middle aged (46) 46
aged (42) 42
index medicus (42) 42
neurosciences (37) 37
adult (36) 36
dementia (35) 35
frontotemporal lobar degeneration (29) 29
genotype (26) 26
clinical neurology (24) 24
amyotrophic-lateral-sclerosis (23) 23
mutations (21) 21
aged, 80 and over (19) 19
mutation (18) 18
neurology (18) 18
amyotrophic lateral sclerosis (16) 16
c9orf72 (16) 16
frontotemporal dementia (16) 16
frontotemporal lobar degeneration - genetics (16) 16
physiological aspects (16) 16
risk factors (16) 16
tau (16) 16
hexanucleotide repeat (15) 15
pathology (14) 14
polymorphism, genetic (13) 13
research (13) 13
c9orf72 protein (12) 12
frontotemporal dementia - genetics (12) 12
genetic predisposition to disease (12) 12
genetic research (12) 12
haplotypes (12) 12
internal medicine (12) 12
mental disorders (12) 12
nervous system diseases (12) 12
proteins - genetics (12) 12
alleles (11) 11
als (11) 11
amyotrophic lateral sclerosis - genetics (11) 11
case-control studies (11) 11
cohort studies (11) 11
disease (11) 11
geriatrics & gerontology (11) 11
hematology (11) 11
oncology (11) 11
brain - pathology (10) 10
tdp-43 (10) 10
adolescent (9) 9
analysis (9) 9
brain - metabolism (9) 9
frontotemporal lobar degeneration - pathology (9) 9
genetic aspects (9) 9
polymorphism, single nucleotide (9) 9
progranulin (9) 9
proteins (9) 9
risk (9) 9
acute disease (8) 8
alzheimer's disease (8) 8
cancer (8) 8
genomics (8) 8
intercellular signaling peptides and proteins - genetics (8) 8
motor neuron disease - genetics (8) 8
mutation - genetics (8) 8
nutritional and metabolic diseases (8) 8
brain (7) 7
diagnostic-criteria (7) 7
dna repeat expansion - genetics (7) 7
gene (7) 7
gene frequency (7) 7
genetics (7) 7
alzheimers-disease (6) 6
association (6) 6
base sequence (6) 6
criteria (6) 6
dna-binding proteins - genetics (6) 6
dna-binding proteins - metabolism (6) 6
frontotemporal lobar degeneration - metabolism (6) 6
ftd (6) 6
genetic predisposition to disease - genetics (6) 6
inclusion bodies - metabolism (6) 6
inclusion bodies - pathology (6) 6
linkage disequilibrium (6) 6
medical colleges (6) 6
neurodegeneration (6) 6
neurons (6) 6
neurons - metabolism (6) 6
tau proteins - genetics (6) 6
universities and colleges (6) 6
article (5) 5
consensus (5) 5
degeneration (5) 5
dementia - genetics (5) 5
dipeptide repeat proteins (5) 5
dna repeat expansion (5) 5
expression (5) 5
frontotemporal lobar degeneration - epidemiology (5) 5
gene expression (5) 5
genes (5) 5
genetics & heredity (5) 5
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


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
Journal Article
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 Nicolas, Aude and Kenna, Kevin P and Kenna, Aoife and Kenna, Kevin and Kenna, Brendan J and Renton, Alan E and Ticozzi, Nicola and Faghri, Faraz and Chia, Ruth and Dominov, Janice A and Nalls, Mike A and Keagle, Pamela and Rivera, Alberto M and van Rheenen, Wouter and Murphy, Natalie A and van Vugt, Joke and van Vugt, Joke J.F.A and Geiger, Joshua T and Van der Spek, Rick A and Pliner, Hannah A and Shankaracharya and Smith, Bradley N and Marangi, Giuseppe and Topp, Simon D and Abramzon, Yevgeniya and Gkazi, Athina Soragia and Eicher, John D and Logullo, Francesco O and Simone, Isabella and Simone, Isabella L and Logroscino, Giancarlo and Salvi, Fabrizio and Bartolomei, Ilaria and Borghero, Giuseppe and Murru, Maria Rita and Costantino, Emanuela and Pani, Carla and Puddu, Roberta and Caredda, Carla and Piras, Valeria and Tranquilli, Stefania and Cuccu, Stefania and Corongiu, Daniela and Melis, Maurizio and Milia, Antonio and Marrosu, Francesco and Marrosu, Maria Giovanna and Floris, Gianluca and Cannas, Antonino and Capasso, Margherita and Caponnetto, Claudia and Mancardi, Gianluigi and Origone, Paola and Mandich, Paola and Conforti, Francesca L and Cavallaro, Sebastiano and Mora, Gabriele and Mora, Jesús S and Marinou, Kalliopi and Sideri, Riccardo and Penco, Silvana and Mosca, Lorena and Lunetta, Christian and Pinter, Giuseppe Lauria and Corbo, Massimo and Riva, Nilo and Carrera, Paola and Volanti, Paolo and Mandrioli, Jessica and Fini, Nicola and Fasano, Antonio and Tremolizzo, Lucio and Arosio, Alessandro and Ferrarese, Carlo and Trojsi, Francesca and Tedeschi, Gioacchino and Monsurrò, Maria Rosaria and Piccirillo, Giovanni and Femiano, Cinzia and Ticca, Anna and Ortu, Enzo and La Bella, Vincenzo and Spataro, Rossella and Colletti, Tiziana and Sabatelli, Mario and Zollino, Marcella and Conte, Amelia and Luigetti, Marco and Lattante, Serena and Santarelli, Marialuisa and Petrucci, Antonio and Pugliatti, Maura and Pirisi, Angelo and Parish, Leslie D and Occhineri, Patrizia and Giannini, Fabio and Battistini, Stefania and Ricci, Claudia and Benigni, Michele and Cau, Tea B and ... and Genomic Translation ALS Care GTAC and ALS Sequencing Consortium and Clinical Res ALS Related Disorders and NYGC ALS Consortium and ITALSGEN Consortium and SLAGEN Consortium and French ALS Consortium and Project MinE ALS Sequencing Consor and Answer ALS Fdn and Project MinE ALS Sequencing Consortium and Genomic Translation for ALS Care (GTAC) Consortium and Answer ALS Foundation and Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk neurovetenskap and Umeå universitet
Neuron, ISSN 0896-6273, 03/2018, Volume 97, Issue 6, pp. 1268 - 1283.e6
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 07/2016, Volume 87, Issue 7, pp. 793 - 795
  Introduction The commonest genetic cause of frontotemporal dementia (FTD) is a hexanucleotide repeat expansion in the chromosome 9 open reading frame 72 gene... 
SURGERY | PSYCHIATRY | EXPANSIONS | FTD | ALS | HEXANUCLEOTIDE REPEAT | CLINICAL NEUROLOGY | Psychosis | Mutation | Alzheimers disease | Patients | Dementia
Journal Article
by Bandres‐Ciga, Sara and Noyce, Alastair J and Hemani, Gibran and Nicolas, Aude and Calvo, Andrea and Mora, Gabriele and Arosio, Alessandro and Barberis, Marco and Bartolomei, Ilaria and Battistini, Stefania and Benigni, Michele and Borghero, Giuseppe and Brunetti, Maura and Calvo, Andrea and Cammarosano, Stefania and Cannas, Antonino and Canosa, Antonio and Capasso, Margherita and Caponnetto, Claudia and Caredda, Carla and Carrera, Paola and Casale, Federico and Cavallaro, Sebastiano and Chiò, Adriano and Colletti, Tiziana and Conforti, Francesca L and Conte, Amelia and Corrado, Lucia and Costantino, Emanuela and D'Alfonso, Sandra and Fasano, Antonio and Femiano, Cinzia and Ferrarese, Carlo and Fini, Nicola and Floris, Gianluca and Fuda, Giuseppe and Giannini, Fabio and Grassano, Maurizio and Ilardi, Antonio and La Bella, Vincenzo and Lattante, Serena and Logroscino, Giancarlo and Logullo, Francesco O and Loi, Daniela and Lunetta, Christian and Mancardi, Gianluigi and Mandich, Paola and Mandrioli, Jessica and Manera, Umberto and Marangi, Giuseppe and Marinou, Kalliopi and Marrali, Giuseppe and Marrosu, Maria Giovanna and Mazzini, Letizia and Melis, Maurizio and Messina, Sonia and Moglia, Cristina and Monsurro, Maria Rosaria and Mora, Gabriele and Mosca, Lorena and Occhineri, Patrizia and Origone, Paola and Pani, Carla and Penco, Silvana and Petrucci, Antonio and Piccirillo, Giovanni and Pirisi, Angelo and Pisano, Fabrizio and Pugliatti, Maura and Restagno, Gabriella and Ricci, Claudia and Rita Murru, Maria and Riva, Nilo and Sabatelli, Mario and Salvi, Fabrizio and Santarelli, Marialuisa and Sideri, Riccardo and Simone, Isabella and Spataro, Rossella and Tanel, Raffaella and Tedeschi, Gioacchino and Tranquilli, Stefania and Tremolizzo, Lucio and Trojsi, Francesca and Volanti, Paolo and Zollino, Marcella and Abramzon, Yevgeniya and Arepalli, Sampath and Baloh, Robert H and Bowser, Robert and Brady, Christopher B and Brice, Alexis and Broach, James and Campbell, Roy H and Camu, William and Chia, Ruth and Chiò, Adriano and Cooper‐Knock, John and Cusi, Daniele and Ding, Jinhui and ... and Int ALS Genomics Consortium and ITALSGEN Consortium and International ALS Genomics Consortium and The ITALSGEN Consortium and The International ALS Genomics Consortium
Annals of Neurology, ISSN 0364-5134, 04/2019, Volume 85, Issue 4, pp. 470 - 481
Journal Article
by Swarup, Vivek and Hinz, Flora I and Rexach, Jessica E and Noguchi, Ken-ichi and Toyoshiba, Hiroyoshi and Oda, Akira and Hirai, Keisuke and Sarkar, Arjun and Seyfried, Nicholas T and Cheng, Chialin and Haggarty, Stephen J and Ferrari, Raffaele and Rohrer, Jonathan D and Ramasamy, Adaikalavan and Hardy, John and Hernandez, Dena G and Nalls, Michael A and Singleton, Andrew B and Kwok, John B. J and Dobson-Stone, Carol and Brooks, William S and Schofield, Peter R and Halliday, Glenda M and Hodges, John R and Piguet, Olivier and Bartley, Lauren and Thompson, Elizabeth and Haan, Eric and Hernández, Isabel and Ruiz, Agustín and Boada, Mercè and Borroni, Barbara and Padovani, Alessandro and Cairns, Nigel J and Cruchaga, Carlos and Binetti, Giuliano and Ghidoni, Roberta and Benussi, Luisa and Forloni, Gianluigi and Albani, Diego and Galimberti, Daniela and Fenoglio, Chiara and Serpente, Maria and Scarpini, Elio and Clarimón, Jordi and Lleó, Alberto and Blesa, Rafael and Waldö, Maria Landqvist and Nilsson, Karin and Nilsson, Christer and Mackenzie, Ian R. A and Hsiung, Ging-Yuek R and Mann, David M. A and Grafman, Jordan and Morris, Christopher M and Attems, Johannes and Griffiths, Timothy D and McKeith, Ian G and Thomas, Alan J and Jaros, Evelyn and Pietrini, Pietro and Huey, Edward D and Wassermann, Eric M and Tierney, Michael C and Baborie, Atik and Pastor, Pau and Ortega-Cubero, Sara and Razquin, Cristina and Alonso, Elena and Perneczky, Robert and Diehl-Schmid, Janine and Alexopoulos, Panagiotis and Kurz, Alexander and Rainero, Innocenzo and Rubino, Elisa and Pinessi, Lorenzo and Rogaeva, Ekaterina and George-Hyslop, Peter St and Rossi, Giacomina and Tagliavini, Fabrizio and Giaccone, Giorgio and Rowe, James B and Schlachetzki, Johannes C. M and Uphill, James and Collinge, John and Mead, Simon and Danek, Adrian and Van Deerlin, Vivianna M and Grossman, Murray and Trojanowski, John Q and Pickering-Brown, Stuart and Momeni, Parastoo and van der Zee, Julie and Cruts, Marc and Van Broeckhoven, Christine and Cappa, Stefano F and Leber, Isabelle and Brice, Alexis and Hannequin, Didier and Golfier, Véronique and ... and Int Frontotemporal Dementia Gen and International Frontotemporal Dementia Genomics Consortium
Nature Medicine, ISSN 1078-8956, 01/2019, Volume 25, Issue 1, pp. 152 - 164
Journal Article
Nature, ISSN 0028-0836, 08/2006, Volume 442, Issue 7105, pp. 916 - 919
Journal Article