X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (24) 24
index medicus (24) 24
female (17) 17
male (17) 17
genetics & heredity (14) 14
genetic aspects (10) 10
research (10) 10
aged (9) 9
genome-wide association study (9) 9
alzheimer disease - genetics (8) 8
genetic predisposition to disease (8) 8
alzheimer's disease (7) 7
genetics (7) 7
identifies variants (7) 7
population (7) 7
aged, 80 and over (6) 6
article (6) 6
middle aged (6) 6
mutation (6) 6
psychiatry (6) 6
susceptibility loci (6) 6
apoe (5) 5
association (5) 5
biochemistry & molecular biology (5) 5
case-control studies (5) 5
chromosome mapping (5) 5
common variants (5) 5
engineering, electrical & electronic (5) 5
genes (5) 5
genetic linkage (5) 5
genetic predisposition to disease - genetics (5) 5
genomics (5) 5
pedigree (5) 5
phenotype (5) 5
polymorphism, single nucleotide (5) 5
polymorphism, single nucleotide - genetics (5) 5
age of onset (4) 4
colitis, ulcerative - genetics (4) 4
crohn disease - genetics (4) 4
gastroenterology & hepatology (4) 4
genetic disorders (4) 4
genetic markers - genetics (4) 4
genome-wide search (4) 4
genotype (4) 4
inflammatory-bowel-disease (4) 4
lod score (4) 4
meta-analysis (4) 4
neurosciences (4) 4
physiological aspects (4) 4
provides evidence (4) 4
replication (4) 4
risk (4) 4
susceptibility (4) 4
abridged index medicus (3) 3
adolescent (3) 3
adult (3) 3
age-at-onset (3) 3
analysis (3) 3
apolipoprotein e (3) 3
child, preschool (3) 3
chronic disease (3) 3
crohn's disease (3) 3
crohns-disease (3) 3
diagnosis (3) 3
dna mutational analysis (3) 3
gene (3) 3
genetic markers (3) 3
genome-wide association study - methods (3) 3
human genetics (3) 3
identification (3) 3
inflammatory bowel diseases - genetics (3) 3
loci (3) 3
metaanalysis (3) 3
neurodegenerative diseases (3) 3
original (3) 3
original article (3) 3
pancreatitis (3) 3
pancreatitis - genetics (3) 3
risk factors (3) 3
single-nucleotide polymorphism (3) 3
trypsin inhibitor, kazal pancreatic - genetics (3) 3
type 2 diabetes (3) 3
ulcerative colitis (3) 3
alcohol (2) 2
alleles (2) 2
alzheimer disease - psychology (2) 2
apolipoprotein e4 - genetics (2) 2
apolipoproteins e - genetics (2) 2
association analysis (2) 2
ataxia (2) 2
bipolar disorder (2) 2
bit rate (2) 2
channel coding (2) 2
child (2) 2
chromosome 4 (2) 2
chromosome-16 (2) 2
chromosomes (2) 2
chromosomes, human, pair 1 (2) 2
chromosomes, human, pair 12 - genetics (2) 2
chromosomes, human, pair 17 (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Molecular Psychiatry, ISSN 1359-4184, 12/2012, Volume 17, Issue 12, pp. 1340 - 1346
Journal Article
IEEE Signal Processing Letters, ISSN 1070-9908, 08/2005, Volume 12, Issue 8, pp. 577 - 580
In this letter, hierarchical quadrature amplitude modulation (HQAM) is used to provide unequal error protection (UEP) for layered (data partitioned) H.264... 
Quadrature amplitude modulation | Source coding | Bit error rate | Hierarchical constellation | Decoding | Channel coding | Degradation | unequal error protection (UEP) | layered video transmission | Bit rate | Bandwidth | Video compression | Error correction codes | Unequal error protection (UEP) | Layered video transmission
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 2012, Volume 17, Issue 12, pp. 1316 - 1327
Psychotic symptoms occur in similar to 40% of subjects with Alzheimer's disease (AD) and are associated with more rapid cognitive decline and increased... 
genetic | behavioural symptoms | genome-wide associationstudy | Alzheimer's disease | psychosis | COMMON VARIANTS | PSYCHIATRY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CEREBROSPINAL-FLUID | BIPOLAR DISORDER | NEUROSCIENCES | INCREASED FAMILIAL RISK | NEUROPSYCHIATRIC INVENTORY | IDENTIFIES VARIANTS | NATIONAL INSTITUTE | genome-wide association study | COMPLEMENT RECEPTOR 1 | URIC-ACID | ONSET | Psychiatric Status Rating Scales - statistics & numerical data | Psychotic Disorders - diagnosis | Genetic Predisposition to Disease - genetics | Alzheimer Disease - complications | Psychotic Disorders - complications | Humans | Middle Aged | Male | Genome-Wide Association Study - statistics & numerical data | Chromosomes, Human, Pair 4 - genetics | DNA, Intergenic - genetics | Case-Control Studies | Psychotic Disorders - genetics | Apolipoproteins E - genetics | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Female | Aged | Glucose Transport Proteins, Facilitative - genetics | Neurocalcin - genetics | Alzheimer Disease - genetics | Genome-Wide Association Study - methods | Alzheimer Disease - psychology | Psychoses | Genomics | Physiological aspects | Development and progression | Genetic aspects | Research | Psychosis | chromosome 4 | Neurodegenerative diseases | Apolipoprotein E | Cognitive ability | Aging | Family studies | Data processing | Heritability | Single-nucleotide polymorphism | Gene mapping | Index Medicus | Life Sciences | Human health and pathology | Psychiatrics and mental health
Journal Article
Journal Article
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
Journal Article
by van Heel, David A and Fisher, Sheila A and Kirby, Andrew and Daly, Mark J and Rioux, John D and Lewis, Cathryn M and Silverberg, M.S and Steinhart, A.H and McLeod, R.S and Griffiths, A.M and Green, T and Brettin, T.S and Stone, V and Bull, S.B and Bitton, A and Williams, C.N and Greenberg, G.R and Cohen, Z and Lander, E.S and Hudson, T.J and Siminovitch, K.A and Cho, J.H and Nicolae, D.L and Karaliukas, R and Swanson, E and Bayless, T.M and Brant, S.R and Paavola-Sakki, P and Ollikainen, V and Helio, T and Halme, L and Turunen, U and Lahermo, P and Lappalainen, M and Farkkila, M and Kontula, K and Hugot, J.P and Laurent Puig, P and Gower Rousseau, C and Olson, J.M and Lee, J.C and Beaugerie, L and Naom, I and Dupas, J.L and van Gossum, A and Orholm, M and Bonaiti-Pellie, C and Weissenbach, J and Mathew, C.G and Lennard-Jones, J.E and Cortot, A and Colombel, J.F and Thomas, G and Hampe, J and Mathew, C.G and Schreiber, S and Curran, M.E and Ma, Y and Ohmen, J.D and Li, Z and Bentley, L.G and McElree, C and Pressman, S and Targan, S.R and Fischel-Ghodsian, N and Rotter, J.I and Yang, H and Williams, C.N and Kocher, K and Miller, K and Farwell, L and Lander, E.S and Dechairo, B.M and Dawson, G and McGovern, D.P.B and Negoro, K and Carey, A.H and Cardon, L.R and MacKay, I and Jewell, D.P and Lench, N.J and Duerr, R.H and Barmada, M.M and Zhang, L and Pfutzer, R and Weeks, D.E and Brant, S.R and Nicolae, D.L and Achkar, J.P and Panhuysen, C and Bayless, T.M and Cho, J.H and Duerr, R.H and Genome Scan Meta Anal Grp IBD Int and Genome Scan Meta-Analysis Group of the IBD International Genetics Consortium
Human Molecular Genetics, ISSN 0964-6906, 04/2004, Volume 13, Issue 7, pp. 763 - 770
Journal Article