Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (431) 431
index medicus (314) 314
female (302) 302
male (281) 281
article (196) 196
genetics (173) 173
adult (155) 155
middle aged (142) 142
genotype (139) 139
genetics & heredity (124) 124
aged (123) 123
genetic aspects (120) 120
genome-wide association study (117) 117
genetic predisposition to disease (108) 108
neurosciences (108) 108
polymorphism, single nucleotide (106) 106
risk factors (106) 106
phenotype (105) 105
clinical neurology (103) 103
neurology (103) 103
alzheimer's disease (98) 98
alcoholism (93) 93
genome-wide association (89) 89
genomics (87) 87
research (87) 87
genes (83) 83
psychiatry (83) 83
alcoholism - genetics (81) 81
risk (79) 79
linkage (73) 73
genetic linkage (71) 71
linkage disequilibrium (71) 71
alzheimer disease - genetics (68) 68
analysis (68) 68
quantitative trait loci (68) 68
aged, 80 and over (66) 66
adolescent (65) 65
association (65) 65
genetic research (64) 64
genomes (64) 64
substance abuse (64) 64
animals (63) 63
polymorphism, single nucleotide - genetics (63) 63
pedigree (57) 57
dementia (56) 56
alleles (54) 54
case-control studies (54) 54
chromosome mapping (51) 51
genetic predisposition to disease - genetics (50) 50
mutation (49) 49
bipolar disorder (47) 47
lod score (47) 47
alcohol use (46) 46
studies (45) 45
bipolar disorder - genetics (42) 42
endocrinology & metabolism (41) 41
parkinson's disease (41) 41
abridged index medicus (40) 40
medical research (40) 40
parkinson disease - genetics (40) 40
schizophrenia (40) 40
young adult (40) 40
cohort studies (39) 39
metaanalysis (38) 38
diagnosis (37) 37
genetic variation (37) 37
alcohol dependence (36) 36
child (36) 36
alzheimers disease (35) 35
alzheimers-disease (35) 35
brain (35) 35
family (35) 35
linkage analysis (35) 35
loci (35) 35
magnetic resonance imaging (35) 35
mice (35) 35
gene expression (34) 34
multidisciplinary sciences (34) 34
rats (34) 34
medical colleges (33) 33
neuroimaging (33) 33
age of onset (32) 32
biochemistry & molecular biology (32) 32
gene (32) 32
human genetics (32) 32
osteoporosis (32) 32
single nucleotide polymorphisms (32) 32
age (31) 31
alcohol drinking - genetics (31) 31
biomarkers (31) 31
variants (31) 31
common variants (30) 30
european continental ancestry group - genetics (30) 30
medicine (29) 29
memory (29) 29
genetic markers (28) 28
health aspects (28) 28
medicin och hälsovetenskap (28) 28
physiological aspects (28) 28
research article (28) 28
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text A novel Alzheimer disease locus located near the gene encoding tau protein
by Jun, Yang and Ibrahim-Verbaas, Carla and Vronskaya, M and Lambert, J.-C and Chung, J and Naj, Adam and Kunkle, Brian and Wang, L.-S and Bis, Joshua and Bellenguez, Céline and Harold, Denise and Lunetta, Kathryn and DeStefano, Anita L and Grenier-Boley, Benjamin and Sims, Rebecca and Beecham, G.W and Smith, A.V and Chouraki, Vincent and Hamilton-Nelson, Kara and Ikram, Arfan and Fiévet, Nathalie and Denning, Nicola and Martin, E.R and Schmidt, H and Kamatani, Y and Dunstan, M.L and Valladares, Otto and Laza, A.R and Zelenika, Diana and Ramirez, Alfredo and Foroud, Tatiana and Choi, Seung-Hoan and Boland, A and Becker, T and Kukull, W.A and Lee, Sven and Pasquier, Florence and Cruchaga, Carlos and Beekly, Duane and Fitzpatrick, Annette and Hanon, Olivier and Gill, M and Barber, Rachel and Gudnason, Vilmundur and Campion, D and Love, S and Bennett, David A and Amin, Najaf and Berr, Claudine and Tsolaki, Magda and Buxbaum, J.D and Lopez, O.L and Deramecourt, Vincent and Fox, N.C and Cantwell, Laura B and Tárraga, L and Dufouil, Carole and Hardy, J and Crane, L.M.A and Eiriksdottir, Gudny and Hannequin, Didier and Clarke, Robert and Evans, D and Mosley, Thomas H and Letenneur, L and Brayne, Carol and Maier, W and De Jager, P and Emilsson, Valur and Dartigues, Jean-François and Hampel, H and Kamboh, M. Ilyas and Bruijn, Renée and Tzourio, Christophe and Pastor, Pau and Larson, Eric B and Rotter, J.I and O'donovan, Michael and Montine, Thomas J and Nalls, Michael and Mead, Simon and Reiman, Eric and Jonsson, P.V and Holmes, C and St George-Hyslop, P.H and Boada, Mercè and Passmore, Peter and Wendland, Annika and Schmidt, R and Morgan, Kevin and Winslow, A.R and Powell, J.F and Carasquillo, M and Younkin, S and Jakobsdottir, Margret and Kauwe, J.S.K and Wilhelmsen, K.C and Rujescu, Dan and Nöthen, Markus M and Hofman, Albert and ... and IGAP Consortium
Molecular Psychiatry, ISSN 1359-4184, 01/2016, Volume 21, Issue 1, pp. 108 - 117
textabstractAPOE ε4, the most significant genetic risk factor for Alzheimer disease (AD), may mask effects of other loci. We re-analyzed genome-wide... 
COMMON VARIANTS | ASSOCIATION ANALYSIS | PSYCHIATRY | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUSCEPTIBILITY LOCI | KANSL1 CAUSE | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | RISK-FACTOR | MAPT LOCUS | TMEM106B | HAPLOTYPE | EXPRESSION | Genome-Wide Association Study | Apolipoprotein E4 - genetics | tau Proteins - genetics | Chromosomes, Human, Pair 17 | Humans | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Complications and side effects | Care and treatment | Usage | Influence | Research | Single nucleotide polymorphisms | Apolipoproteins | Alzheimer's disease
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text APOE and BCHE as modulators of cerebral amyloid deposition: A florbetapir PET genome-wide association study
by Ramanan, V.K and Risacher, S.L and Nho, K and Kim, S and Swaminathan, S and Shen, L and Foroud, T.M and Hakonarson, H and Huentelman, M.J and Aisen, P.S and Petersen, R.C and Green, R.C and Jack, C.R and Koeppe, R.A and Jagust, W.J and Weiner, M.W and Saykin, A.J and Alzheimer's Dis Neuroimaging Initi and Alzheimer’s Disease Neuroimaging Initiative and for the Alzheimer’s Disease Neuroimaging Initiative
Molecular Psychiatry, ISSN 1359-4184, 03/2014, Volume 19, Issue 3, pp. 351 - 357
Deposition of amyloid-beta (A beta) in the cerebral cortex is thought to be a pivotal event in Alzheimer's disease (AD) pathogenesis with a significant genetic... 
Alzheimer's disease (AD) | Apolipoprotein E (APOE) | Amyloid | Butyrylcholinesterase (BCHE) | Florbetapir (AV-45) | Genomewide association study (GWAS) | APOLIPOPROTEIN-E EPSILON-4 | COMMON VARIANTS | florbetapir (AV-45) | butyrylcholinesterase (BCHE) | PSYCHIATRY | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLAQUES | MILD COGNITIVE IMPAIRMENT | IDENTIFICATION | NEUROSCIENCES | BETA | amyloid | apolipoprotein E (APOE) | PROGRESS | genome-wide association study (GWAS) | NEUROPATHOLOGY | BUTYRYLCHOLINESTERASE-K-VARIANT | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Butyrylcholinesterase - genetics | Aniline Compounds | Humans | Middle Aged | Male | Positron-Emission Tomography | Cerebral Cortex - diagnostic imaging | Cerebral Cortex - metabolism | Plaque, Amyloid - diagnostic imaging | Functional Neuroimaging | Ethylene Glycols | Apolipoproteins E - genetics | Aged, 80 and over | Cognitive Dysfunction - genetics | Female | Plaque, Amyloid - metabolism | Aged | Alzheimer Disease - genetics | Physiological aspects | Research | Alzheimer's disease | Psychiatric research | Amyloid beta-protein | Alzheimer’s disease (AD)
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Whole exome sequencing of intracranial aneurysm
by Foroud, Tatiana and FIA Study Investigators and for the FIA Study Investigators
Stroke, ISSN 0039-2499, 01/2013, Volume 44, Issue 1, pp. S26 - S28
Whole exome sequencing | Rare variant | Intracranial aneurysm | intracranial aneurysm | RISK | PERIPHERAL VASCULAR DISEASE | LOCI | rare variant | whole exome sequencing | CLINICAL NEUROLOGY | DNA - genetics | Exome - genetics | Genome-Wide Association Study | Animals | Intracranial Aneurysm - genetics | Pedigree | Humans | Exons - genetics | Intracranial Aneurysm - epidemiology | Genome, Human | Sequence Analysis, DNA
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Identification of common variants associated with human hippocampal and intracranial volumes
by Stein, J.L and Medland, S.E and Arias Vasquez, A and Hibar, D.P and Senstad, R.E and Winkler, A.M and Toro, R and Appel, K and Bartecek, R and Bergmann, O and Bernard, M and Brown, A.A and Cannon, D.M and Chakravarty, M.M and Christoforou, A and Domin, M and Grimm, O and Hollinshead, M and Holmes, A.J and Homuth, G and Hottenga, J.J and Langan, C and Lopez, L.M and Hansell, N.K and Hwang, K.S and Kim, S and Laje, G and Lee, P.H and Liu, X and Loth, E and Lourdusamy, A and Mattingsdal, M and Mohnke, S and Maniega, S.M and Nho, K and Nugent, A.C and O'Brien, C and Papmeyer, M and Putz, B and Ramasamy, A and Rasmussen, J and Rijpkema, M.J.P and Risacher, S.L and Roddey, J.C and Rose, E.J and Ryten, M and Shen, L and Sprooten, E and Strengman, E and Teumer, A and Trabzuni, D and Turner, J and Eijk, K. van and Erp, T.G. van and Tol, M.J. van and Wittfeld, K and Wolf, C. de and Woudstra, S and Aleman, A and Alhusaini, S and Almasy, L and Binder, E.B and Brohawn, D.G and Cantor, R.M and Carless, M.A and Corvin, A and Czisch, M and Curran, J.E and Davies, G and Almeida, M.A. de and Delanty, N and Depondt, C and Duggirala, R and Dyer, T.D and Erk, S and Fagerness, J and Fox, P.T and Freimer, N.B and Gill, M and Goring, H.H and Hagler, D.J and Hoehn, D and Holsboer, F and Hoogman, M and Hosten, N and Jahanshad, N and Johnson, M.P and Kasperaviciute, D and Kent Jr., J.W and Kochunov, P and Lancaster, J.L and Lawrie, S.M and Liewald, D.C and Mandl, R.C.W and Matarin, M and Mattheisen, M and Meisenzahl, E and Melle, I and Moses, E.K and Muhleisen, T.W and ... and Cohorts Heart Aging Res Genomic Ep and EPIGEN Consortium and ADNI and Saguenay Youth Study Grp SYS and IMAGEN Consortium and Enhancing Neuro Imaging Genetics M and Alzheimer's Disease Neuroimaging Initiative and Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium and Saguenay Youth Study Group and Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium and the Alzheimer's Disease Neuroimaging Initiative (ADNI) and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and Saguenay Youth Study Group (SYS) and for the Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium
Nature Genetics, ISSN 1061-4036, 2012, Volume 44, Issue 5, pp. 552 - 561
Identifying genetic variants influencing human brain structures may reveal new biological mechanisms underlying cognition and neuropsychiatric illness. The... 
AUTOMATED SEGMENTATION | HUMAN HEIGHT | FUNCTIONAL IMPLICATIONS | TEMPORAL-LOBE EPILEPSY | UNIFIED APPROACH | GENOTYPE IMPUTATION | ALZHEIMERS-DISEASE | GENETICS & HEREDITY | BRAIN VOLUME | NA+/H+ EXCHANGER | GENOME-WIDE ASSOCIATION | Neuroimaging | Genome-Wide Association Study | Meta-Analysis as Topic | Brain - physiopathology | Humans | Polymorphism, Single Nucleotide - genetics | Genetic Loci | Genetic Markers | Chromosomes, Human, Pair 12 - genetics | Hippocampus - physiopathology | Head | Genetic aspects | Hippocampus (Brain) | Genetic variation | Identification and classification | Body size | Studies | Haplotypes | Neurology | Brain | Genealogy | Statistical analysis | Quality control | Genetics | Genomes | Meta-analysis | Life Sciences | Neurons and Cognition
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. 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
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Genetics and alcoholism
by Edenberg, Howard J and Foroud, Tatiana
Nature Reviews Gastroenterology and Hepatology, ISSN 1759-5045, 08/2013, Volume 10, Issue 8, pp. 487 - 494
Alcohol is widely consumed; however, excessive use creates serious physical, psychological and social problems and contributes to the pathogenesis of many... 
DRUG-DEPENDENCE | GABRA2 | DSM-IV | LINKAGE DISEQUILIBRIUM | RISK | CROSS-FOSTERING ANALYSIS | ENVIRONMENTAL CONTRIBUTIONS | GASTROENTEROLOGY & HEPATOLOGY | CHRM2 GENE | DEHYDROGENASE | GENOME-WIDE ASSOCIATION | Receptor, Muscarinic M2 - genetics | Aldehyde Dehydrogenase, Mitochondrial | Humans | Risk Factors | Aldehyde Dehydrogenase - genetics | G Protein-Coupled Inwardly-Rectifying Potassium Channels - genetics | Alcoholism - epidemiology | Proteins - genetics | Receptors, GABA-A - genetics | Alcohol Dehydrogenase - genetics | Liver - physiology | Alcoholism - genetics | Alcoholism - physiopathology | Complications and side effects | Genetic variation | Alcoholism | Causes of | Physiological aspects | Genetic aspects | Research
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights