X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (258) 258
Publication (39) 39
Book Review (17) 17
Patent (12) 12
Book / eBook (5) 5
Book Chapter (2) 2
Conference Proceeding (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (182) 182
humans (166) 166
genetics & heredity (103) 103
genetics (68) 68
research (68) 68
female (57) 57
male (55) 55
genotype (51) 51
genetic aspects (50) 50
polymorphism, single nucleotide (44) 44
linkage disequilibrium (42) 42
genetic predisposition to disease (41) 41
chromosome mapping (39) 39
models, genetic (37) 37
association (36) 36
genomics (35) 35
risk factors (32) 32
genome, human (31) 31
alleles (30) 30
haplotypes (29) 29
adult (27) 27
case-control studies (27) 27
gene frequency (27) 27
genetic linkage (27) 27
phenotype (27) 27
article (26) 26
middle aged (26) 26
genes (25) 25
genetic markers (25) 25
genetic variation (25) 25
linkage (25) 25
polymorphism, single nucleotide - genetics (25) 25
polymorphism (24) 24
risk (24) 24
single nucleotide polymorphisms (23) 23
biochemistry & molecular biology (22) 22
disease (22) 22
human genome (22) 22
multidisciplinary sciences (22) 22
gene (21) 21
genome-wide association (21) 21
haplotypes - genetics (21) 21
genetic research (20) 20
human genetics (20) 20
analysis (19) 19
genetics, population (19) 19
genomes (19) 19
physiological aspects (19) 19
susceptibility (19) 19
quantitative trait loci (18) 18
pedigree (17) 17
population (17) 17
united kingdom (17) 17
usage (17) 17
aged (16) 16
chromosome mapping - methods (16) 16
computer simulation (16) 16
genome-wide association study (16) 16
genotype & phenotype (16) 16
lod score (16) 16
quantitative trait, heritable (16) 16
animals (15) 15
chromosomes (15) 15
single-nucleotide polymorphisms (15) 15
studies (15) 15
crohns-disease (14) 14
linkage disequilibrium - genetics (14) 14
population genetics (14) 14
biochemistry (13) 13
biotechnology & applied microbiology (13) 13
child (13) 13
crohn disease - genetics (13) 13
european continental ancestry group - genetics (13) 13
genetic predisposition to disease - genetics (13) 13
linkage analysis (13) 13
map (13) 13
methods (13) 13
power (13) 13
twins (13) 13
chemistry (12) 12
cohort studies (12) 12
expression (12) 12
metallurgy (12) 12
microbiology (12) 12
abridged index medicus (11) 11
beer (11) 11
complex traits (11) 11
compositions or test papers therefor (11) 11
condition-responsive control in microbiological orenzymological processes (11) 11
diseases (11) 11
dyslexia - genetics (11) 11
enzymology (11) 11
epidemiology (11) 11
human necessities (11) 11
loci (11) 11
measuring or testing processes involving enzymes, nucleicacids or microorganisms (11) 11
medical research (11) 11
mutation or genetic engineering (11) 11
processes of preparing such compositions (11) 11
public, environmental & occupational health (11) 11
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


eBook
LANCET, ISSN 0140-6736, 10/2005, Volume 366, Issue 9492, pp. 1223 - 1234
Much effort and expense are being spent internationally to detect genetic polymorphisms contributing to susceptibility to complex human disease. Concomitantly,... 
BREAST-CANCER | MEDICINE, GENERAL & INTERNAL | ASSOCIATION STUDIES | QUANTITATIVE TRAITS | PUBLIC-HEALTH | POPULATION STRATIFICATION | HAPLOTYPE BLOCKS | STRUCTURED POPULATIONS | HUMAN-GENOME | SINGLE-NUCLEOTIDE POLYMORPHISMS | COMMON DISEASE | Chromosome mapping | Genetic aspects | Epidemiology | Epidemiologic methods | Methods | Genetic research | Genotype & phenotype | Genomics
Journal Article
Nature Reviews Drug Discovery, ISSN 1474-1776, 09/2016
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 10/2016, Volume 25, Issue R2, pp. R166 - R172
Journal Article
Science, ISSN 0036-8075, 12/2006, Volume 314, Issue 5804, pp. 1403 - 1405
Complex diseases represent an extraordinary challenge to geneticists, but recent results are revealing some successful strategies. 
Macular degeneration | Crohn disease | Phenotypes | Medical genetics | Disease risk | Genetic loci | Genomes | Perspectives | Genetic diseases | Human genetics | CROHNS-DISEASE | CFH | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | MACULAR DEGENERATION | POLYMORPHISM | ASSOCIATION | VARIANT | Genetics | Genes | Crohns disease
Journal Article
Nature Genetics, ISSN 1061-4036, 06/2006, Volume 38, Issue 6, pp. 659 - 662
Journal Article
by Burton, Paul R and Clayton, David G and Cardon, Lon R and Craddock, Nick and Deloukas, Panos and Duncanson, Audrey and Kwiatkowski, Dominic P and McCarthy, Mark I and Ouwehand, Willem H and Samani, Nilesh J and Todd, John A and Donnelly, Peter and Barrett, Jeffrey C and Davison, Dan and Easton, Doug and Evans, David and Leung, Hin-Tak and Marchini, Jonathan L and Morris, Andrew P and Spencer, Chris C. A and Tobin, Martin D and Attwood, Antony P and Boorman, James P and Cant, Barbara and Everson, Ursula and Hussey, Judith M and Jolley, Jennifer D and Knight, Alexandra S and Koch, Kerstin and Meech, Elizabeth and Nutland, Sarah and Prowse, Christopher V and Stevens, Helen E and Taylor, Niall C and Walters, Graham R and Walker, Neil M and Watkins, Nicholas A and Winzer, Thilo and Jones, Richard W and McArdle, Wendy L and Ring, Susan M and Strachan, David P and Pembrey, Marcus and Breen, Gerome and St. Clair, David and Caesar, Sian and Gordon-Smith, Katherine and Jones, Lisa and Fraser, Christine and Green, Elaine K and Grozeva, Detelina and Hamshere, Marian L and Holmans, Peter A and Jones, Ian R and Kirov, George and Moskvina, Valentina and Nikolov, Ivan and O'Donovan, Michael C and Owen, Michael J and Collier, David A and Elkin, Amanda and Farmer, Anne and Williamson, Richard and McGuffin, Peter and Young, Allan H and Ferrier, I. Nicol and Ball, Stephen G and Balmforth, Anthony J and Barrett, Jennifer H and Bishop, D. Timothy and Iles, Mark M and Maqbool, Azhar and Yuldasheva, Nadira and Hall, Alistair S and Braund, Peter S and Dixon, Richard J and Mangino, Massimo and Stevens, Suzanne and Thompson, John R and Bredin, Francesca and Tremelling, Mark and Parkes, Miles and Drummond, Hazel and Lees, Charles W and Nimmo, Elaine R and Satsangi, Jack and Fisher, Sheila A and Forbes, Alastair and Lewis, Cathryn M and Onnie, Clive M and Prescott, Natalie J and Sanderson, Jeremy and Mathew, Christopher G and Barbour, Jamie and Mohiuddin, M. Khalid and Todhunter, Catherine E and Mansfield, John C and Ahmad, Tariq and Cummings, Fraser R and Jewell, Derek P and ... and Breast Canc Susceptib Collaborat and Wellcome Trust Case Control Cons and Biol RA Genet & Genom Study and Wellcome Trust Case Control Consortium and The Wellcome Trust Case Control Consortium
Nature, ISSN 0028-0836, 06/2007, Volume 447, Issue 7145, pp. 661 - 678
Journal Article
Nature Genetics, ISSN 1061-4036, 04/2005, Volume 37, Issue 4, pp. 413 - 417
Journal Article
Nature Protocols, ISSN 1754-2189, 09/2010, Volume 5, Issue 9, pp. 1564 - 1573
This protocol details the steps for data quality assessment and control that are typically carried out during case-control association studies. The steps... 
POPULATION | RISK LOCI | STRATIFICATION | BIOCHEMICAL RESEARCH METHODS | GENOME-WIDE ASSOCIATION | Computational Biology - methods | Animals | Humans | Female | Male | Genetic Techniques | Genome-Wide Association Study - methods | Case-Control Studies | Quality Control | Usage | Quality control | Genetic research | Management | Methods | Applications software | Quality management | DNA | Index Medicus
Journal Article