X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (822) 822
Publication (162) 162
Patent (34) 34
Book Chapter (7) 7
Book / eBook (5) 5
Book Review (2) 2
Conference Proceeding (2) 2
Web Resource (2) 2
Report (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (440) 440
female (255) 255
male (249) 249
index medicus (235) 235
genetics & heredity (201) 201
genetics (167) 167
aged (165) 165
genotype (150) 150
middle aged (137) 137
genetic predisposition to disease (136) 136
article (135) 135
risk factors (134) 134
genetic aspects (133) 133
polymorphism, single nucleotide (132) 132
genome-wide association study (111) 111
association (100) 100
case-control studies (97) 97
alzheimer disease - genetics (95) 95
adult (94) 94
genes (91) 91
research (90) 90
genetic linkage (89) 89
risk (87) 87
alzheimer's disease (86) 86
aged, 80 and over (85) 85
genome-wide association (85) 85
genomics (82) 82
alleles (79) 79
genomes (79) 79
pedigree (79) 79
neurosciences (76) 76
chromosome mapping (74) 74
linkage (73) 73
clinical neurology (72) 72
neurology (72) 72
gene (63) 63
ophthalmology (63) 63
analysis (60) 60
phenotype (59) 59
polymorphism, single nucleotide - genetics (59) 59
eye diseases (57) 57
gene frequency (55) 55
macular degeneration - genetics (55) 55
biochemistry & molecular biology (53) 53
haplotypes (53) 53
disease (52) 52
genetic variation (52) 52
linkage disequilibrium (50) 50
research article (48) 48
genetic markers (47) 47
lod score (47) 47
common variants (44) 44
medical research (43) 43
multiple sclerosis - genetics (43) 43
mutation (43) 43
studies (43) 43
susceptibility (43) 43
polymorphism (42) 42
age of onset (41) 41
genetic research (41) 41
physiological aspects (41) 41
alzheimers disease (39) 39
genetic predisposition to disease - genetics (39) 39
genetic structures (39) 39
population (38) 38
variants (38) 38
autism (37) 37
glaucoma, open-angle - genetics (37) 37
multiple sclerosis (37) 37
child (36) 36
chromosomes (36) 36
dementia (36) 36
medicine (36) 36
mutations (36) 36
single nucleotide polymorphisms (36) 36
macular degeneration (35) 35
metaanalysis (35) 35
multidisciplinary sciences (35) 35
sense organs (35) 35
locus (34) 34
prevalence (34) 34
alzheimer disease (33) 33
epidemiology (33) 33
expression (33) 33
susceptibility loci (33) 33
apolipoproteins e - genetics (32) 32
gene expression (32) 32
human genetics (32) 32
loci (32) 32
base sequence (30) 30
biochemistry (30) 30
health aspects (30) 30
proteins (30) 30
adolescent (29) 29
age (29) 29
aging (28) 28
european continental ancestry group - genetics (27) 27
genome, human (27) 27
molecular sequence data (27) 27
polymerase chain reaction (27) 27
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


ISSN 2055-6756, 4/2016, Volume 1, Issue 3, pp. 22 - 226
We discuss the use of carbon nanodots (CNDs) as sensitizers in mesoscopic solar cells. The CNDs are synthesized using a one-step, bottom-up microwave approach... 
Journal Article
2003, 2nd ed., ISBN 0471089524, 512
Second Edition features the latest tools for uncovering the genetic basis of human disease The Second Edition of this landmark publication brings together a... 
Medical genetics | Genetic disorders | Molecular diagnosis | Technique | Gene mapping
Book
The Journal of Law, Medicine & Ethics, ISSN 1073-1105, 9/2018, Volume 46, Issue 3, pp. 694 - 698
Alzheimer disease (AD) is a huge and growing societal problem with upwards of 35% of the population over the age of 80 developing the disease. AD results in a... 
UNITED-STATES | ALLELE | DEMENTIA | LAW | VARIANTS | MEDICINE, LEGAL | RISK | MEDICAL ETHICS | LOCI | HERITABILITY | LINKAGE ANALYSES | FAMILIES IDENTIFY | ONSET | ETHICS
Journal Article
Current protocols in human genetics, 04/2016, Volume 89, pp. 1.0.1 - 7
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 08/2017, Volume 26, Issue 1, pp. R1 - R1
Journal Article
Journal Article
Nature, ISSN 0028-0836, 09/2011, Volume 477, Issue 7363, pp. 211 - 215
Journal Article
Neurology, ISSN 0028-3878, 03/2013, Volume 80, Issue 11, pp. 974 - 975
Neurology has been one of the leaders in applying the developing tools of genetics to understand the etiology of disease. This extends as far back as the early... 
VPS35 | MUTATIONS | CLINICAL NEUROLOGY | PARKINSON DISEASE | Exome - genetics | Humans | Vesicular Transport Proteins - genetics | Female | Male | Eukaryotic Initiation Factor-4G - genetics | Genetic Variation - genetics | Parkinson Disease - genetics
Journal Article
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
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 2010, Volume 6, Issue 4, pp. S60 - S60
Journal Article