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1. Full Text GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment
by Cornelius A. Rietveld and Sarah E. Medland and Jaime Derringer and Jian Yang and Tõnu Esko and Nicolas W. Martin and Harm-Jan Westra and Konstantin Shakhbazov and Abdel Abdellaoui and Arpana Agrawal and Eva Albrecht and Behrooz Z. Alizadeh and Najaf Amin and John Barnard and Sebastian E. Baumeister and Kelly S. Benke and Lawrence F. Bielak and Jeffrey A. Boatman and Patricia A. Boyle and Gail Davies and Christiaan de Leeuw and Niina Eklund and Daniel S. Evans and Rudolf Ferhmann and Krista Fischer and Christian Gieger and Håkon K. Gjessing and Sara Hägg and Jennifer R. Harris and Caroline Hayward and Christina Holzapfel and Carla A. Ibrahim-Verbaas and Erik Ingelsson and Bo Jacobsson and Peter K. Joshi and Astanand Jugessur and Marika Kaakinen and Stavroula Kanoni and Juha Karjalainen and Ivana Kolcic and Kati Kristiansson and Zoltán Kutalik and Jari Lahti and Sang H. Lee and Peng Lin and Penelope A. Lind and Yongmei Liu and Kurt Lohman and Marisa Loitfelder and George McMahon and Pedro Marques Vidal and Osorio Meirelles and Lili Milani and Ronny Myhre and Marja-Liisa Nuotio and Christopher J. Oldmeadow and Katja E. Petrovic and Wouter J. Peyrot and Ozren Polašek and Lydia Quaye and Eva Reinmaa and John P. Rice and Thais S. Rizzi and Helena Schmidt and Reinhold Schmidt and Albert V. Smith and Jennifer A. Smith and Toshiko Tanaka and Antonio Terracciano and Matthijs J. H. M. van der Loos and Veronique Vitart and Henry Völzke and Jürgen Wellmann and Lei Yu and Wei Zhao and Jüri Allik and John R. Attia and Stefania Bandinelli and François Bastardot and Jonathan Beauchamp and David A. Bennett and Klaus Berger and Laura J. Bierut and Dorret I. Boomsma and Ute Bültmann and Harry Campbell and Christopher F. Chabris and Lynn Cherkas and Mina K. Chung and Francesco Cueca and Mariza de Andrade and Philip L. De Jager and Jan-Emmanuel De Neve and Ian J. Deary and George V. Dedoussis and Panos Deloukas and Maria Dimitriou and Guðný Eiríksdóttir and Martin F. Elderson and Johan G. Eriksson and ... and LifeLines Cohort Study and The LifeLines Cohort Study and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för medicinska vetenskaper
Science, ISSN 0036-8075, 6/2013, Volume 340, Issue 6139, pp. 1467 - 1471
A genome-wide association study (GWAS) of educational attainment was conducted in a discovery sample of 101,069 individuals and a replication sample of 25,490.... 
Medical research | Phenotypes | Psychology | REPORTS | Personality traits | Genetic research | Research facilities | Genetics | Epidemiology | Research universities | Educational attainment | MULTIDISCIPLINARY SCIENCES | LOCI | ENVIRONMENT | Genome-Wide Association Study | Endophenotypes | Humans | Female | Male | Cognition | Educational Status | Polymorphism, Single Nucleotide | Genetic Loci | Multifactorial Inheritance | Academic achievement | Genetic aspects | Research | Single nucleotide polymorphisms | Genetic variation | Genomics | Science education | Medical and Health Sciences | Medicin och hälsovetenskap
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2. Full Text Variant of TREM2 Associated with the Risk of Alzheimer's Disease
by Jonsson, Thorlakur and Jonsson, Palmi V and Stefansson, Hreinn and Stefansson, Kari and Steinberg, Stacy and Jonsdottir, Ingileif and Snaedal, Jon and Bjornsson, Sigurbjorn and Huttenlocher, Johanna and Levey, Allan I and Lah, James J and Rujescu, Dan and Hampel, Harald and Giegling, Ina and Andreassen, Ole A and Engedal, Knut and Ulstein, Ingun and Djurovic, Srdjan and Ibrahim-Verbaas, Carla and Hofman, Albert and Ikram, M. Arfan and van Duijn, Cornelia M and Thorsteinsdottir, Unnur and Kong, Augustine
The New England Journal of Medicine, ISSN 0028-4793, 01/2013, Volume 368, Issue 2, pp. 107 - 116
This study shows that a variant of TREM2 , which encodes a protein that suppresses inflammation, causes susceptibility to Alzheimer's disease. Although the... 
RESPONSES | MEDICINE, GENERAL & INTERNAL | IMMUNE-SYSTEM | DEMENTIA | DENDRITIC CELLS | RECEPTOR | MUTATIONS | GENOME-WIDE ASSOCIATION | APOLIPOPROTEIN-E | SENILE PLAQUES | CUTTING EDGE | Apolipoprotein E4 - genetics | Humans | Risk Factors | Cognition | Mutation, Missense | Genotyping Techniques | Sequence Analysis, DNA | Case-Control Studies | Iceland | Membrane Glycoproteins - genetics | Genetic Variation | Aged, 80 and over | Heterozygote | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Receptors, Immunologic - genetics | Genetic variation | Causes of | Genetic aspects | Research | Apolipoproteins | Alzheimer's disease | Health aspects | Genomes | Alzheimers disease | Older people | Age | Cognitive ability
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3. Full Text APOE-stratified genome-wide association analysis reveals differential effects by APOE status and potential new risk loci for Alzheimer's disease
by Ibrahim-Verbaas, Carla
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 2013, Volume 9, Issue 4, pp. P123 - P123
Neurology | Apolipoproteins | Alzheimer's disease | Genomics | Risk factors
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4. Full Text Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
by Lambert, Jean-Charles and Ibrahim-Verbaas, Carla A and Harold, Denise and Naj, Adam C and Sims, Rebecca and Bellenguez, Céline and Jun, Gyungah and DeStefano, Anita L and Bis, Joshua C and Beecham, Gary W and Grenier-Boley, Benjamin and Russo, Giancarlo and Thornton-Wells, Tricia A and Jones, Nicola and Smith, Albert V and Chouraki, Vincent and Thomas, Charlene and Ikram, M. Arfan and Zelenika, Diana and Vardarajan, Badri N and Kamatani, Yoichiro and Lin, Chiao-Feng and Gerrish, Amy and Schmidt, Helena and Kunkle, Brian and Fiévet, Nathalie and Amouyel, Philippe and Pasquier, Florence and Deramecourt, Vincent and De Bruijn, Renee F.A.G and Amin, Najaf and Hofman, Albert and Van Duijn, Cornelia M and Dunstan, Melanie L and Hollingworth, Paul and Owen, Michael J and O'Donovan, Michael C and Jones, Lesley and Holmans, Peter A and Moskvina, Valentina and Williams, Julie and Baldwin, Clinton and Farrer, Lindsay A and Choi, Seung-Hoan and Lunetta, Kathryn L and Fitzpatrick, Annette L and Harris, Tamara B and Psaty, Bruce M and Gilbert, John R and Hamilton-Nelson, Kara L and Martin, Eden R and Kunkle, Brian and Haines, Jonathan L and Gudnason, Vilmundur and Jonsson, Palmi V and Eiriksdottir, Gudny and Bihoreau, Marie-Thérèse and Lathrop, Mark and Valladares, Otto and Cantwell, Laura B and Wang, Li-San and Schellenberg, Gerard D and Ruiz, Agustin and Boada, Mercè and Reitz, Christiane and Mayeux, Richard and Ramirez, Alfredo and Maier, Wolfgang and Hanon, Olivier and Kukull, Walter A and Buxbaum, Joseph D and Campion, Dominique and Wallon, David and Hannequin, Didier and Crane, Paul K and Larson, Eric B and Becker, Tim and Cruchaga, Carlos and Goate, Alison M and Craig, David and Johnston, Janet A and Mc-Guinness, Bernadette and Todd, Stephen and Passmore, Peter and Berr, Claudine and Ritchie, Karen and Lopez, Oscar L and De Jager, Philip L and Evans, Denis and Lovestone, Simon and Proitsi, Petroula and Powell, John F and Letenneur, Luc and Barberger-Gateau, Pascale and Dufouil, Carole and Dartigues, Jean-François and Morón, Francisco J and Rubinsztein, David C and St. George-Hyslop, Peter and Sleegers, Kristel and ... and EADI and CHARGE and ADGC and GERAD and Cohorts for Heart and Aging Research in Genomic Epidemiology and Genetic and Environmental Risk in Alzheimer's Disease and Alzheimer's Disease Genetic Consortium and European Alzheimer's Disease Initiative (EADI) and Alzheimer's Disease Genetic Consortium (ADGC) and Genetic and Environmental Risk in Alzheimer's Disease (GERAD) and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 12/2013, Volume 45, Issue 12, pp. 1452 - 1458
Eleven susceptibility loci for late-onset Alzheimer's disease (LOAD) were identified by previous studies; however, a large portion of the genetic risk for this... 
GENOTYPES | COMMON VARIANTS | IMPUTATION | GENETIC RISK | SEQUENCE | GENETICS & HEREDITY | NEURONS | RECEPTOR | MUTATIONS | CD33 | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Humans | Middle Aged | Male | Genetic Loci | Genome-Wide Association Study - statistics & numerical data | Case-Control Studies | Age of Onset | Aged, 80 and over | Alzheimer Disease - epidemiology | Female | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Cohort Studies | Quantitative trait loci | Genetic aspects | Research | Genetic susceptibility | Alzheimer's disease | Identification and classification | Genealogy | Genomics | Genes | Quality control | Aging | Genomes | Alzheimers disease | Health risk assessment | Meta-analysis | Genetik | Biological Sciences | Genetics | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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5. Full Text Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease
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
Background: Alzheimer's disease is a common debilitating dementia with known heritability, for which 20 late onset susceptibility loci have been identified,... 
TARGET | COMMON VARIANTS | IDENTIFIES VARIANTS | MULTIDISCIPLINARY SCIENCES | TP53INP1 | GENOME SCAN METAANALYSIS | SCHIZOPHRENIA | LOCI | BIPOLAR DISORDER | ASSOCIATION | CLU | Carrier Proteins - genetics | Heat-Shock Proteins - genetics | Genome-Wide Association Study | Humans | Receptors, Antigen, B-Cell - genetics | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Case-Control Studies | Analysis | Genes | Genomics | Disease susceptibility | Genetic aspects | Genomes | Alzheimer's disease | Energy metabolism | Neurosciences | Laboratories | Physicians | Epidemiology | Protein turnover | Consortia | Cell cycle | Dementia disorders | Aging | Genetics | Chromosomes | Genotypes | Public health | Immune system | Obesity | Neurodegenerative diseases | Metabolism | Loci | Medicine | Neurology | Brain research | Heritability | Diabetes | Alzheimers disease | Basic Medicine | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin | Geriatrik | Neurovetenskaper | Geriatrics
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6. Full Text Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
by Cornelius A. Rietveld and Tõnu Esko and Gail Davies and Tune H. Pers and Patrick Turley and Beben Benyamin and Christopher F. Chabris and Valur Emilsson and Andrew D. Johnson and James J. Lee and Christiaan de Leeuw and Riccardo E. Marioni and Sarah E. Medland and Michael B. Miller and Olga Rostapshova and Sven J. van der Lee and Anna A. E. Vinkhuyzen and Najaf Amin and Dalton Conley and Jaime Derringer and Cornelia M. van Duijn and Rudolf Fehrmann and Lude Franke and Edward L. Glaeser and Narelle K. Hansell and Caroline Hayward and William G. Iacono and Carla Ibrahim-Verbaas and Vincent Jaddoe and Juha Karjalainen and David Laibson and Paul Lichtenstein and David C. Liewald and Patrik K. E. Magnusson and Nicholas G. Martin and Matt McGue and George McMahon and Nancy L. Pedersen and Steven Pinker and David J. Porteous and Danielle Posthuma and Fernando Rivadeneira and Blair H. Smith and John M. Starr and Henning Tiemeier and Nicholas J. Timpson and Maciej Trzaskowski and André G. Uitterlinden and Frank C. Verhulst and Mary E. Ward and Margaret J. Wright and George Davey Smith and Ian J. Deary and Magnus Johannesson and Robert Plomin and Peter M. Visscher and Daniel J. Benjamin and David Cesarini and Philipp D. Koellinger
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 09/2014, Volume 111, Issue 38, pp. 13790 - 13794
We identify common genetic variants associated with cognitive performance using a two-stage approach, which we call the proxy-phenotype method. First, we... 
Quantitative genetics | Medical research | Phenotypes | Medical genetics | Genetic research | Population genetics | Human genetics | Research universities | Educational attainment | Universities | ACADEMIC-ACHIEVEMENT | INTELLIGENCE | GWAS | MULTIDISCIPLINARY SCIENCES | COMPONENTS | LOCI | GENOME-WIDE ASSOCIATION | Synaptic Transmission - genetics | Humans | Male | Nerve Tissue Proteins - genetics | Cell Adhesion Molecules, Neuronal - genetics | Multifactorial Inheritance - physiology | Learning - physiology | Neuronal Plasticity - genetics | Octamer Transcription Factors - genetics | Cognition - physiology | Female | Polymorphism, Single Nucleotide | Memory - physiology | Phenotype | Cognition | Genetic aspects | Research | Genetic variation | Biological Sciences | Social Sciences
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7. Full Text Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
by Jakobsdottir, Margret and Lee, Sven and Bis, Joshua and Chouraki, Vincent and Li-Kroeger, D and Yamamoto, S and Grove, Megan and Naj, Adam and Vronskaya, M and Salazar, J.L and DeStefano, Anita and Brody, Jennifer and Smith, Albert Vernon and Amin, Najaf and Sims, Rebecca and Ibrahim-Verbaas, Carla and Choi, Seung-Hoan and Satizabal, Claudia L and Lopez, Oscar L and Beiser, Alexa and Ikram, Kamran and Garcia, M and Hayward, Caroline and Varga, Tibor V and Ripatti, Samuli and Franks, Paul and Hallmans, Göran and Rolandsson, Olov and Jansson, J.-H and Porteous, David J and Salomaa, Veikko and Eiriksdottir, Gudny and Rice, Kenneth and Bellen, H.J and Levy, Daniel and Uitterlinden, Ané and Emilsson, Valur and Rotter, J.I and Aspelund, Thor and Ódonnell, Christopher and Fitzpatrick, Annette and Launer, Lenore and Hofman, Albert and Wang, Liang and Williams, Julie and Schellenberg, Gerard D and Boerwinkle, Eric and Psaty, Bruce and Seshai, Sudha and Shulman, Lee and Gudnason, Vilmundur and Duijn, Cornelia and Cohorts Heart Aging Res Genomic Ep and Genetic Environm Risk Alzheimer's and Cohorts for Heart and Aging Research in Genomic Epidemiology consortium and Alzheimer’s Disease Genetic Consortium and Genetic and Environmental Risk in Alzheimer’s Disease consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet
PL o S Genetics (Online), ISSN 1553-7390, 10/2016, Volume 12, Issue 10, p. e1006327
textabstractWe performed an exome-wide association analysis in 1393 late-onset Alzheimer’s disease (LOAD) cases and 8141 controls from the CHARGE consortium.... 
UNITED-STATES | HAPLOTYPE RECONSTRUCTION | COMMON VARIANTS | IDENTIFIES VARIANTS | PROTEIN | EARLY NEUROGENESIS | GENETICS & HEREDITY | MUTATIONS | DROSOPHILA-MELANOGASTER DEVELOPMENT | GENOME-WIDE ASSOCIATION | APOLIPOPROTEIN-E | Tropomyosin - genetics | Genome-Wide Association Study | Membrane Proteins - genetics | Genomics | Humans | European Continental Ancestry Group | Male | Receptors, Notch - genetics | Drosophila melanogaster - genetics | Iceland | Alzheimer Disease - pathology | Exome - genetics | Phenotype | Amyloid beta-Protein Precursor - genetics | Animals | Apolipoproteins E - genetics | Age of Onset | Alleles | Female | Aged | Drosophila Proteins - genetics | Mutation | Alzheimer Disease - genetics | Intracellular Signaling Peptides and Proteins - genetics | Genetic aspects | Genetic variation | Health aspects | Alzheimer's disease | Consortia | Amino acids | Analysis | Drosophila | Heart | Medical research | Neurosciences | Physicians | Colleges & universities | Epidemiology | Medicine | Neurology | Hospitals | Genetics | Clinical medicine | Alzheimers disease | Public health | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
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8. Full Text Common variants at 12q14 and 12q24 are associated with hippocampal volume
by Bis, Joshua C and Decarli, Charles and Smith, Albert Vernon and van der Lijn, Fedde and Crivello, Fabrice and Fornage, Myriam and Debette, Stephanie and Shulman, Joshua M and Schmidt, Helena and Srikanth, Velandai and Schuur, Maaike and Yu, Lei and Choi, Seung-Hoan and Sigurdsson, Sigurdur and Verhaaren, Benjamin F. J and DeStefano, Anita L and Lambert, Jean-Charles and Jack, Clifford R and Struchalin, Maksim and Stankovich, Jim and Ibrahim-Verbaas, Carla A and Fleischman, Debra and Zijdenbos, Alex and den Heijer, Tom and Mazoyer, Bernard and Coker, Laura H and Enzinger, Christian and Danoy, Patrick and Amin, Najaf and Arfanakis, Konstantinos and van Buchem, Mark A and de Bruijn, Renée F. A. G and Beiser, Alexa and Dufouil, Carole and Huang, Juebin and Cavalieri, Margherita and Thomson, Russell and Niessen, Wiro J and Chibnik, Lori B and Gislason, Gauti K and Hofman, Albert and Pikula, Aleksana and Amouyel, Philippe and Freeman, Kevin B and Phan, Thanh G and Oostra, Ben A and Stein, Jason L and Medland, Sarah E and Vasquez, Alejano Arias and Hibar, Derrek P and Wright, Margaret J and Franke, Barbara and Martin, Nicholas G and Thompson, Paul M and Nalls, Michael A and Uitterlinden, Ane G and Au, Rhoda and Elbaz, Alexis and Beare, Richard J and van Swieten, John C and Lopez, Oscar L and Harris, Tamara B and Chouraki, Vincent and Breteler, Monique M. B and de Jager, Philip L and Becker, James T and Vernooij, Meike W and Knopman, David and Fazekas, Franz and Wolf, Philip A and van der Lugt, Aad and Gudnason, Vilmundur and Longstreth, W. T and Brown, Matthew A and Bennett, David A and van Duijn, Cornelia M and Mosley, Thomas H and Schmidt, Reinhold and Tzourio, Christophe and Launer, Lenore J and Ikram, M. Arfan and Seshai, Sudha and Arias Vasquez, Alejano and Senstad, Rudy E and Winkler, Anderson M and Toro, Roberto and Appel, Katja and Bartecek, Richard and Bergmann, Ørjan and Bernard, Manon and Brown, Anew A and Cannon, Dara M and Chakravarty, Mallar and Christoforou, Anea and Domin, Martin and Grimm, Oliver and Hollinshead, Marisa and Holmes, Avram J and Homuth, Georg and Hottenga, Jouke-Jan and ... and Cohorts Heart Aging Res Genomic Ep and Enhancing Neuro Imaging Genetics M and Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium and Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium and Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium and the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 5, pp. 545 - 551
Aging is associated with reductions in hippocampal volume that are accelerated by Alzheimer's disease and vascular risk factors. Our genome-wide association... 
IDENTIFIES VARIANTS | PROTEIN | GLUCAGON-LIKE PEPTIDE-1 | ATROPHY | ALZHEIMERS-DISEASE | GENETICS & HEREDITY | TOTAL HOMOCYSTEINE | CLU | EXPRESSION | GENOME-WIDE ASSOCIATION | CELL-DEATH | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Polymorphism, Single Nucleotide - genetics | Cognition Disorders - genetics | Genetic Loci | Genetic Markers | Alzheimer Disease - genetics | Dementia - genetics | Chromosomes, Human, Pair 12 - genetics | Hippocampus - physiopathology | Proteins | Neurology | Medical research | Genotype & phenotype | Ischemia | Education | Religious orders | Aging | Genetics | Genomes | Alzheimers disease | Neuroscience | Cognitive science
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