X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (25) 25
index medicus (24) 24
alzheimer's disease (19) 19
alzheimer disease - genetics (17) 17
clinical neurology (16) 16
aged (15) 15
neurosciences (14) 14
female (13) 13
male (13) 13
neurology (13) 13
dementia (11) 11
genome-wide association study (11) 11
aged, 80 and over (9) 9
alzheimers disease (8) 8
common variants (8) 8
genetics (8) 8
genotype (8) 8
middle aged (8) 8
polymorphism, single nucleotide (8) 8
research (8) 8
aging (7) 7
genetic aspects (7) 7
genetic predisposition to disease (7) 7
neurodegenerative diseases (7) 7
gene (6) 6
genome-wide association (6) 6
genomes (6) 6
genomics (6) 6
risk (6) 6
tau (6) 6
adult (5) 5
alzheimer disease (5) 5
analysis (5) 5
apoe (5) 5
apolipoproteins (5) 5
association (5) 5
brain - pathology (5) 5
case-control studies (5) 5
genetics & heredity (5) 5
high energy physics - experiment (5) 5
medical research (5) 5
metaanalysis (5) 5
mutation (5) 5
neuropathology (5) 5
susceptibility loci (5) 5
tau proteins - genetics (5) 5
age (4) 4
age of onset (4) 4
amyloid precursor protein (4) 4
apolipoprotein-e genotype (4) 4
article (4) 4
brain - metabolism (4) 4
disease (4) 4
ex (4) 4
experiment (4) 4
expression (4) 4
frontotemporal lobar degeneration (4) 4
genes (4) 4
genetic loci (4) 4
genetic predisposition to disease - genetics (4) 4
genome-wide association studies (4) 4
hep (4) 4
mutation - genetics (4) 4
neurovetenskaper (4) 4
particle physics (4) 4
pathology (4) 4
physics (4) 4
physics - high energy physics - experiment (4) 4
prevalence (4) 4
protein (4) 4
public health (4) 4
quantitative trait loci (4) 4
risk factors (4) 4
[phys.hexp]physics [physics]/high energy physics - experiment [hep-ex] (3) 3
abridged index medicus (3) 3
adolescent (3) 3
advertising executives (3) 3
aggregation (3) 3
alzheimer disease - diagnosis (3) 3
alzheimer disease - pathology (3) 3
alzheimers-disease (3) 3
animals (3) 3
apolipoprotein e (3) 3
apolipoproteins e - genetics (3) 3
brain research (3) 3
cern lhc coll (3) 3
child (3) 3
chromosome mapping (3) 3
clinical medicine (3) 3
cognitive decline (3) 3
cohort studies (3) 3
colleges & universities (3) 3
dementia - genetics (3) 3
disease susceptibility (3) 3
epidemiology (3) 3
experimental results (3) 3
family health (3) 3
frontotemporal dementia (3) 3
gene expression (3) 3
gene frequency (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Lancet Neurology, The, ISSN 1474-4422, 2008, Volume 7, Issue 5, pp. 409 - 416
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2007, Volume 6, Issue 10, pp. 857 - 868
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
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2017
Hypogammaglobulinemia (total IgG levels < 7.0 g/L) is present in 1 in 4 patients with moderate to severe COPD and is associated with 50% to 100% increase in... 
Allergy and Immunology
Journal Article
Journal Article
by Escott-Price, Valentina and Bellenguez, Céline and Wang, L.-S and Choi, Seung-Hoan and Harold, Denise and Jones, Louisa and Holmans, Peter and Gerrish, Amy and Vedernikov, Alexey and Richards, Alex and DeStefano, Anita and Lambert, J and Ibrahim-Verbaas, Carla and Naj, Adam and Sims, Rebecca and Jun, Yang and Bis, Joshua and Beecham, Gary and Grenier-Boley, Benjamin and Russo, Giancarlo and Thornton-Wells, Tricia and Denning, Nicola and Smith, G.D and Chouraki, Vincent and Thomas, Charlene and Ikram, Arfan and Zelenika, Diana and Vardarajan, Bai and Kamatani, Yoichiro and Lin, Chiao-Feng and Schmidt, Reinhold and Kunkle, Brian and Dunstan, Melanie and Vronskaya, Maria and Johnson, Anew and Ruiz, Agustin and Bihoreau, Marie-Thérèse and Reitz, Christiane and Pasquier, Florence and Hollingworth, Paul and Hanon, Olivier and Fitzpatrick, Annette and Buxbaum, Joseph D and Campion, Dominique and Crane, L.M.A and Becker, Clinton and Gudnason, Vilmundur and Cruchaga, Carlos and Craig, David and Amin, Najaf and Berr, Claudine and Lopez, Oscar and Jager, Philip and Deramecourt, Vincent and Johnston, Janet and Evans, Denis and Lovestone, Simon and Letenneur, L and Hernández, Isabel and Rubinsztein, David and Eiriksdottir, Gudny and Sleegers, Kristel and Goate, Alison and Fiévet, Nathalie and Huentelman, Matthew and Gill, Michael and Brown, Kristelle and Kamboh, M. Ilyas and Keller, Lina and Barberger-Gateau, Pascale and McGuinness, Bernadette and Larson, Eric and Myers, Amanda and Dufouil, Carole and Todd, Stephen and Wallon, David and Love, Seth and Rogaeva, Ekaterina and Gallacher, John and St George-Hyslop, Peter and Clarimon, Jordi and Lleo, Alberto and Bayer, T and Tsuang, Debby and Yu, Lei and Tsolaki, Magda and Bossù, Paola and Spalletta, Gianfranco and Proitsi, Petroula and Collinge, John and Sorbi, Sano and Sanchez Garcia, Florentino and Fox, Nick and Hardy, John and Naranjo, Antonio and Bosco, Paolo and Clarke, Robert and Brayne, Carol and Galimberti, Daniela and Scarpini, Elio and ... and United Kingdom Brain Expression and United Kingdom Brain Expression Consortium and Cardiovascular Health Study (CHS) and the United Kingdom Brain Expression Consortium and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
PLoS ONE, ISSN 1932-6203, 06/2014, Volume 9, Issue 6, p. e94661
Journal Article
PLoS Genetics, ISSN 1553-7390, 09/2014, Volume 10, Issue 9, p. e1004606
Journal Article
by De Rubeis, Silvia and He, Xin and Goldberg, Arthur P and Poultney, Christopher S and Samocha, Kaitlin and Cicek, A. Ercument and Kou, Yan and Liu, Li and Fromer, Menachem and Walker, Susan and Singh, Tarjinder and Klei, Lambertus and Kosmicki, Jack and Fu, Shih-Chen and Aleksic, Branko and Biscaldi, Monica and Bolton, Patrick F and Brownfeld, Jessica M and Cai, Jinlu and Campbell, Nicholas G and Carracedo, Angel and Chahrour, Maria H and Chiocchetti, Andreas G and Coon, Hilary and Crawford, Emily L and Crooks, Lucy and Curran, Sarah R and Dawson, Geraldine and Duketis, Eftichia and Fernandez, Bridget A and Gallagher, Louise and Geller, Evan and Guter, Stephen J and Hill, R. Sean and Ionita-Laza, Iuliana and Gonzalez, Patricia Jimenez and Kilpinen, Helena and Klauck, Sabine M and Kolevzon, Alexander and Lee, Irene and Lei, Jing and Lehtimäki, Terho and Lin, Chiao-Feng and Ma'ayan, Avi and Marshall, Christian R and McInnes, Alison L and Neale, Benjamin and Owen, Michael J and Ozaki, Norio and Parellada, Mara and Parr, Jeremy R and Purcell, Shaun and Puura, Kaija and Rajagopalan, Deepthi and Rehnström, Karola and Reichenberg, Abraham and Sabo, Aniko and Sachse, Michael and Sanders, Stephan J and Schafer, Chad and Schulte-Rüther, Martin and Skuse, David and Stevens, Christine and Szatmari, Peter and Tammimies, Kristiina and Valladares, Otto and Voran, Annette and Wang, Li-San and Weiss, Lauren A and Willsey, A. Jeremy and Yu, Timothy W and Yuen, Ryan K. C and Cook, Edwin H and Freitag, Christine M and Gill, Michael and Hultman, Christina M and Lehner, Thomas and Palotie, Aarno and Schellenberg, Gerard D and Sklar, Pamela and State, Matthew W and Sutcliffe, James S and Walsh, Christopher A and Scherer, Stephen W and Zwick, Michael E and Barrett, Jeffrey C and Cutler, David J and Roeder, Kathryn and Devlin, Bernie and Daly, Mark J and Buxbaum, Joseph D and Homozygosity Mapping Collaborative and DDD Study and Autism Sequencing Consortium and UK10K Consortium and Homozygosity Mapping Collaborative for Autism and The Autism Sequencing Consortium and The DDD Study
Nature, ISSN 0028-0836, 11/2014, Volume 515, Issue 7526, pp. 209 - 215
Journal Article
PLoS Genetics, ISSN 1553-7390, 06/2012, Volume 8, Issue 6, p. e1002707
Journal Article