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
index medicus (49) 49
humans (47) 47
genome-wide association study (33) 33
genetics & heredity (26) 26
genetic aspects (23) 23
research (23) 23
genetic predisposition to disease (22) 22
polymorphism, single nucleotide (22) 22
genetics (21) 21
genomes (20) 20
male (20) 20
risk factors (20) 20
article (19) 19
female (19) 19
case-control studies (18) 18
studies (17) 17
disease (16) 16
genome-wide association (15) 15
genomics (14) 14
genotype (14) 14
middle aged (14) 14
multidisciplinary sciences (14) 14
medical research (13) 13
polymorphism, single nucleotide - genetics (13) 13
adult (12) 12
aged (12) 12
gene expression (12) 12
physiological aspects (11) 11
risk (11) 11
single nucleotide polymorphisms (10) 10
common variants (9) 9
european continental ancestry group - genetics (9) 9
genes (9) 9
genetic research (9) 9
metaanalysis (9) 9
association (8) 8
diabetes (8) 8
gene frequency (8) 8
genetic variation (8) 8
health aspects (8) 8
loci (8) 8
meta-analysis (8) 8
susceptibility (8) 8
susceptibility loci (8) 8
gene (7) 7
gene loci (7) 7
genetic loci (7) 7
genetic predisposition to disease - genetics (7) 7
heritability (7) 7
medicin och hälsovetenskap (7) 7
methods (7) 7
population (7) 7
schizophrenia - genetics (7) 7
variants (7) 7
autoimmune diseases (6) 6
disease susceptibility (6) 6
eye diseases (6) 6
medical and health sciences (6) 6
medicine (6) 6
phenotype (6) 6
polymorphism (6) 6
psychiatry (6) 6
schizophrenia (6) 6
aged, 80 and over (5) 5
alleles (5) 5
bayes theorem (5) 5
biochemistry & molecular biology (5) 5
biology (5) 5
biomedical research (5) 5
bipolar disorder (5) 5
chromosomes (5) 5
clinical medicine (5) 5
crohn disease - genetics (5) 5
epidemiology (5) 5
expression (5) 5
gene-expression (5) 5
genome-wide association studies (5) 5
haplotypes (5) 5
klinisk medicin (5) 5
linkage disequilibrium (5) 5
mutations (5) 5
oligonucleotide array sequence analysis (5) 5
parkinson disease - genetics (5) 5
quantitative trait loci (5) 5
statistical analysis (5) 5
united kingdom (5) 5
usage (5) 5
association studies (4) 4
cardiovascular disease (4) 4
chromosome mapping (4) 4
cohort studies (4) 4
diagnosis (4) 4
genetic association studies (4) 4
genetic structures (4) 4
genetics, population (4) 4
glaucoma, open-angle - genetics (4) 4
haplotypes - genetics (4) 4
health risk assessment (4) 4
histocompatibility antigens (4) 4
hla histocompatibility antigens (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
by Giambartolomei, Claudia and Vukcevic, Damjan and Schadt, Eric E and Franke, Lude and Hingorani, Aroon D and Wallace, Chris and Plagnol, Vincent
PLOS Genetics, ISSN 1553-7390, 05/2014, Volume 10, Issue 5, pp. e1004383 - e1004383
Genetic association studies, in particular the genome-wide association study (GWAS) design, have provided a wealth of novel insights into the aetiology of a... 
NETWORK | MULTIPLE COMMON | PROTEIN | CHOLESTEROL | GENOTYPE IMPUTATION | GENETICS & HEREDITY | SIGNALS | RISK VARIANTS | TRAITS | EXPRESSION | GENOME-WIDE ASSOCIATION | Genome-Wide Association Study | Sample Size | Humans | Bayes Theorem | Bayesian statistical decision theory | Usage | Genome-wide association studies | Statistical methods | Methods | Index Medicus | Quantitative Biology - Genomics | Medical research | Statistical analysis | Biomedical research | Disease | Probability | Lipids | Genomes | Gene expression | Statistics | Meta-analysis | Studies | Biomarkers | Gene loci
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text The UK Biobank resource with deep phenotyping and genomic data
by Bycroft, Clare and Freeman, Colin and Petkova, Desislava and Band, Gavin and Elliott, Lloyd T and Sharp, Kevin and Motyer, Allan and Vukcevic, Damjan and Delaneau, Olivier and O’Connell, Jared and Cortes, Adrian and Welsh, Samantha and Young, Alan and Effingham, Mark and McVean, Gil and Leslie, Stephen and Allen, Naomi and Donnelly, Peter and Marchini, Jonathan
Nature, ISSN 0028-0836, 10/2018, Volume 562, Issue 7726, pp. 203 - 209
The UK Biobank project is a prospective cohort study with deep genetic and phenotypic data collected on approximately 500,000 individuals from across the... 
CRYPTIC RELATEDNESS | GENETIC ASSOCIATION | MULTIPLE-SCLEROSIS | GENOTYPE IMPUTATION | MULTIDISCIPLINARY SCIENCES | DISEASE | ARCHITECTURE | PROTOCOL | HUMAN BLOOD | COHORT | WIDE ASSOCIATION | Brain - diagnostic imaging | Life Style | Biomarkers - urine | Genomics | Humans | Middle Aged | Databases, Genetic | Male | Haplotypes - genetics | Adult | Female | Databases, Factual | Quality Control | Genome-Wide Association Study | Major Histocompatibility Complex - genetics | United Kingdom | Biomarkers - blood | Continental Population Groups - genetics | Body Height - genetics | Phenotype | Alleles | Family | Aged | Electronic Health Records | Cohort Studies | Human genome | Genetic research | Genotype | Research | Genetic screening | Methods | Data entry | Haplotypes | Neuroimaging | Brain | Multiple sclerosis | Nuclear magnetic resonance--NMR | Laboratories | Medical records | Cardiovascular disease | Genomes | Datasets | Consortia | Genotype & phenotype | Genetic analysis | Population | Bioindicators | Genotypes | Deoxyribonucleic acid--DNA | Urine | Antigens | Population structure | White blood cells | Phenotyping | Biomarkers | Histocompatibility antigen HLA | Diabetes | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Young Writers Competition: GUESTimation: Breaking the deadlock on wedding guest lists
by Vukcevic, Damjan
Significance, ISSN 1740-9705, 08/2013, Volume 10, Issue 4, pp. 45 - 48
Earlier this year, together with the Young Statisticians Group of the RSS, Significance ran its second Young Writers Competition. A selection of runners‐up... 
Weddings | Analysis | Studies | Competition
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Bayesian refinement of association signals for 14 loci in 3 common diseases
by Maller, Julian B and McVean, Gilean and Byrnes, Jake and Vukcevic, Damjan and Palin, Kimmo and Su, Zhan and Howson, Joanna M. M and Auton, Adam and Myers, Simon and Morris, Andrew and Pirinen, Matti and Brown, Matthew A and Burton, Paul R and Caulfield, Mark J and Compston, Alastair and Farrall, Martin and Hall, Alistair S and Hattersley, Andrew T and Hill, Adrian V. S and Mathew, Christopher G and Pembrey, Marcus and Satsangi, Jack and Stratton, Michael R and Worthington, Jane and Craddock, Nick and Hurles, Matthew and Ouwehand, Willem and Parkes, Miles and Rahman, Nazneen and Duncanson, Audrey and Todd, John A and Kwiatkowski, Dominic P and Samani, Nilesh J and Gough, Stephen C. L and McCarthy, Mark I and Deloukas, Panagiotis and Donnelly, Peter and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and The Wellcome Trust Case Control Consortium
Nature Genetics, ISSN 1061-4036, 12/2012, Volume 44, Issue 12, pp. 1294 - 1301
To further investigate susceptibility loci identified by genome-wide association studies, we genotyped 5,500 SNPs across 14 associated regions in 8,000 samples... 
GENOME | GENETICS & HEREDITY | Genetic Predisposition to Disease | Genome-Wide Association Study | Transcription Factor 7-Like 2 Protein - genetics | Diabetes Mellitus, Type 2 - genetics | Humans | Alpha-Ketoglutarate-Dependent Dioxygenase FTO | CTLA-4 Antigen - genetics | Genetic Loci | Transcription Factors - genetics | Genes, p16 | Homeodomain Proteins - genetics | Cyclin-Dependent Kinase 5 - genetics | Graves Disease - genetics | Proteins - genetics | Cyclin-Dependent Kinase Inhibitor p15 - genetics | tRNA Methyltransferases | Bayes Theorem | Coronary Artery Disease - genetics | Polymorphism, Single Nucleotide | Statistical analysis | Biomedical research | Disease | Thyroid diseases | Probability | Genomes | Gene expression | Experiments | Studies | Confidence intervals | Genetics | Diabetes | Methods | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Quantifying the underestimation of relative risks from genome-wide association studies
by Spencer, Chris and Hechter, Eliana and Vukcevic, Damjan and Donnelly, Peter
PLoS Genetics, ISSN 1553-7390, 03/2011, Volume 7, Issue 3, pp. e1001337 - e1001337
Genome-wide association studies (GWAS) have identified hundreds of associated loci across many common diseases. Most risk variants identified by GWAS will... 
BREAST-CANCER | PROJECT | METAANALYSIS | HAPLOTYPE MAP | DISEASE | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | RATIO | Crohn Disease - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Algorithms | Breast Neoplasms - genetics | Diabetes Mellitus, Type 2 - genetics | Gene Frequency | Humans | Risk | Polymorphism, Single Nucleotide | Linkage Disequilibrium | Heritability | Disease susceptibility | Genetic aspects | Single nucleotide polymorphisms | Research | Index Medicus | Studies | Genomes | Disease | Health risk assessment | Experiments
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Bayesian analysis of genetic association across tree-structured routine healthcare data in the UK Biobank
by Cortes, Adrian and Dendrou, Calliope A and Motyer, Allan and Jostins, Luke and Vukcevic, Damjan and Dilthey, Alexander and Donnelly, Peter and Leslie, Stephen and Fugger, Lars and McVean, Gil
Nature Genetics, ISSN 1061-4036, 09/2017, Volume 49, Issue 9, pp. 1311 - 1318
Genetic discovery from the multitude of phenotypes extractable from routine healthcare data can transform understanding of the human phenome and accelerate... 
SYSTEMIC-LUPUS-ERYTHEMATOSUS | INFLAMMATORY-BOWEL-DISEASE | POLYMYALGIA-RHEUMATICA | ULCERATIVE-COLITIS | RECORD DATA | GENETICS & HEREDITY | PHENOME-WIDE ASSOCIATION | SUSCEPTIBILITY LOCI | RISK | PSORIASIS | CELIAC-DISEASE | Health Information Systems - statistics & numerical data | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Logistic Models | Male | United Kingdom | Genome-Wide Association Study - statistics & numerical data | HLA Antigens - genetics | International Classification of Diseases - classification | Genetic Association Studies - statistics & numerical data | Alleles | Bayes Theorem | Adult | Female | Aged | Polymorphism, Single Nucleotide | Delivery of Health Care - classification | Delivery of Health Care - statistics & numerical data | International Classification of Diseases - statistics & numerical data | Cluster Analysis | Bayesian statistical decision theory | Genetic research | Usage | Information management | Research | Health care | Lupus | Haplotypes | Multiple sclerosis | Statistical analysis | Probability | Structural hierarchy | Studies | Inflammatory bowel disease | Genetic effects | Dimensional analysis | Classification | Genetics | Histocompatibility antigen HLA | Diabetes | Dynamic programming | Random variables | Diagnosis | Bayesian analysis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Identification and Stoichiometry of Glycosylphosphatidylinositol-anchored Membrane Proteins of the Human Malaria Parasite Plasmodium falciparum
by Paul R. Gilson and Thomas Nebl and Damjan Vukcevic and Robert L. Moritz and Tobias Sargeant and Terence P. Speed and Louis Schofield and Brendan S. Crabb
Molecular & Cellular Proteomics, ISSN 1535-9476, 07/2006, Volume 5, Issue 7, pp. 1286 - 1299
Most proteins that coat the surface of the extracellular forms of the human malaria parasite Plasmodium falciparum are attached to the plasma membrane via... 
COMPLETE GENOMES | LIFE-CYCLE | IMMUNODOMINANT SURFACE-ANTIGEN | DOMAIN-CONTAINING PROTEIN | CIRCUMSPOROZOITE PROTEIN | GENES | BIOCHEMICAL RESEARCH METHODS | 2-DIMENSIONAL ELECTROPHORESIS | HOST ERYTHROCYTE | INTRAERYTHROCYTIC STAGE | ERYTHROCYTIC STAGES | Protein Structure, Tertiary | Blood-Borne Pathogens | Markov Chains | Membrane Proteins - isolation & purification | Reproducibility of Results | Protein Structure, Secondary | Humans | Gene Expression Profiling | Proteome - analysis | Life Cycle Stages | Animals | Glycosylphosphatidylinositols - metabolism | Membrane Proteins - chemistry | Databases, Protein | Protein Array Analysis | Plasmodium falciparum - metabolism | Membrane Proteins - metabolism | Antigens, Surface - analysis | Cluster Analysis | Plasmodium falciparum - chemistry | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Lack of transparency in software used to analyze multiple breath washout data
by Mahar, Robert K and Vukcevic, Damjan and King, Louise and Carlin, John B and Ranganathan, Sarath
Pediatric Pulmonology, ISSN 8755-6863, 11/2016, Volume 51, Issue 11, pp. 1108 - 1110
PEDIATRICS | LUNG CLEARANCE INDEX | CYSTIC-FIBROSIS | RESPIRATORY SYSTEM
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Bayesian modelling of lung function data from multiple‐breath washout tests
by Mahar, Robert K and Carlin, John B and Ranganathan, Sarath and Ponsonby, Anne‐Louise and Vuillermin, Peter and Vukcevic, Damjan
Statistics in Medicine, ISSN 0277-6715, 05/2018, Volume 37, Issue 12, pp. 2016 - 2033
Paediatric respiratory researchers have widely adopted the multiple‐breath washout (MBW) test because it allows assessment of lung function in unsedated... 
variance components | Stan | multiple‐breath washout | incomplete data | lung clearance index | multiple-breath washout | STATEMENT | MEDICINE, RESEARCH & EXPERIMENTAL | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | MEDICAL INFORMATICS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | STATISTICS & PROBABILITY | Medicine, Experimental | Medical research | Usage | Models | Analysis | Babies | Medical tests | Lungs | Health risk assessment | Respiration | Bayesian analysis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Imputation of KIR Types from SNP Variation Data
by Vukcevic, Damjan and Traherne, James A and Næss, Sigrid and Ellinghaus, Eva and Kamatani, Yoichiro and Dilthey, Alexander and Lathrop, Mark and Karlsen, Tom H and Franke, Andre and Moffatt, Miriam and Cookson, William and Trowsdale, John and McVean, Gil and Sawcer, Stephen and Leslie, Stephen
The American Journal of Human Genetics, ISSN 0002-9297, 10/2015, Volume 97, Issue 4, pp. 593 - 607
Large population studies of immune system genes are essential for characterizing their role in diseases, including autoimmune conditions. Of key interest are a... 
CLASSICAL HLA ALLELES | LIGANDS | DISEASE | SUSCEPTIBILITY | ERAP1 | GENETICS & HEREDITY | RISK | LOCI | NK CELL RECEPTORS | Dermatitis, Atopic - genetics | Genetic Predisposition to Disease | Receptors, KIR - genetics | Receptors, KIR - classification | Europe | Humans | Genotype | Male | DNA Copy Number Variations - genetics | Sequence Analysis, DNA | Asthma - genetics | Case-Control Studies | Polymorphism, Single Nucleotide - genetics | Family | Female | High-Throughput Nucleotide Sequencing | Cohort Studies | Genetic aspects | Single nucleotide polymorphisms | Observations | Autoimmune diseases | Genetic variation | Antigens | Immunoglobulins | T cell receptors | Genes | Immune system | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
by Fakiola, Michaela and Strange, Amy and Cordell, Heather J and Miller, E Nancy and Pirinen, Matti and Su, Zhan and Mishra, Anshuman and Mehrotra, Sanjana and Monteiro, Gloria R and Band, Gavin and Bellenguez, Céline and Dronov, Serge and Edkins, Sarah and Freeman, Colin and Giannoulatou, Eleni and Gray, Emma and Hunt, Sarah E and Lacerda, Henio G and Langford, Cordelia and Pearson, Richard and Pontes, Núbia N and Rai, Madhukar and Singh, Shri P and Smith, Linda and Sousa, Olivia and Vukcevic, Damjan and Bramon, Elvira and Brown, Matthew A and Casas, Juan P and Corvin, Aiden and Duncanson, Audrey and Jankowski, Janusz and Markus, Hugh S and Mathew, Christopher G and Palmer, Colin N. A and Plomin, Robert and Rautanen, Anna and Sawcer, Stephen J and Trembath, Richard C and Viswanathan, Ananth C and Wood, Nicholas W and Wilson, Mary E and Deloukas, Panos and Peltonen, Leena and Christiansen, Frank and Witt, Campbell and Jeronimo, Selma M. B and Sundar, Shyam and Spencer, Chris C. A and Blackwell, Jenefer M and Donnelly, Peter and Wellcome Trust Case Control and LeishGEN Consortium and Wellcome Trust Case Control Consortium 2
Nature Genetics, ISSN 1061-4036, 02/2013, Volume 45, Issue 2, pp. 208 - 213
To identify susceptibility loci for visceral leishmaniasis, we undertook genome-wide association studies in two populations: 989 cases and 1,089 controls from... 
INFECTIOUS-DISEASES | SUDAN | GENES | GENETICS & HEREDITY | NORTHEASTERN BRAZIL | POLYMORPHISM | MODEL | SCAN | GENOME-WIDE ASSOCIATION | CHAGASI | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | HLA-DRB1 Chains - genetics | Oligonucleotide Array Sequence Analysis | Gene Frequency | Humans | Genotype | Linear Models | HLA-DQ alpha-Chains - genetics | India | Haplotypes - genetics | Electrophoresis, Agar Gel | Leishmaniasis, Visceral - genetics | Brazil | Polymorphism, Single Nucleotide - genetics | Odds Ratio | Quantitative trait loci | Kala-azar | Disease susceptibility | Genetic aspects | Research | Health aspects | Identification and classification | Risk factors | Studies | Disease | Parasitic diseases | Quality control | Genetics | Tropical diseases | Methods | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text The correlation between reading and mathematics ability at age twelve has a substantial genetic component
by Davis, Oliver S. P and Band, Gavin and Pirinen, Matti and Haworth, Claire M. A and Meaburn, Emma L and Kovas, Yulia and Harlaar, Nicole and Docherty, Sophia J and Hanscombe, Ken B and Trzaskowski, MacIej and Curtis, Charles J. C and Strange, Amy and Freeman, Colin and Bellenguez, Céline and Su, Zhan and Pearson, Richard and Vukcevic, Damjan and Langford, Cordelia and Deloukas, Panos and Hunt, Sarah and Gray, Emma and Dronov, Serge and Potter, Simon C and Tashakkori-Ghanbaria, Avazeh and Edkins, Sarah and Bumpstead, Suzannah J and Blackwell, Jenefer M and Bramon, Elvira and Brown, Matthew A and Casas, Juan P and Corvin, Aiden and Duncanson, Audrey and Jankowski, Janusz A. Z and Markus, Hugh S and Mathew, Christopher G and Palmer, Colin N. A and Rautanen, Anna and Sawcer, Stephen J and Trembath, Richard C and Viswanathan, Ananth C and Wood, Nicholas W and Barroso, Ines and Peltonen, Leena and Dale, Philip S and Petrill, Stephen A and Schalkwyk, Leonard S and Craig, Ian W and Lewis, Cathryn M and Price, Thomas S and Donnelly, Peter and Plomin, Robert and Spencer, Chris C. A and Wellcome Trust Case Control and Wellcome Trust Case Control Consortium 2 and The Wellcome Trust Case Control Consortium
Nature Communications, ISSN 2041-1723, 07/2014, Volume 5, Issue 1, pp. 4204 - 4204
Dissecting how genetic and environmental influences impact on learning is helpful for maximizing numeracy and literacy. Here we show, using twin and... 
INTELLIGENCE | LEARNING-DISABILITIES | VARIANTS | DYSLEXIA | MULTIDISCIPLINARY SCIENCES | QUANTITATIVE TRAIT LOCUS | DCDC2 | CHILDHOOD | HERITABILITY | GENOME-WIDE ASSOCIATION | TWIN | Genetics, Population | Twins - genetics | Genome-Wide Association Study | Quantitative Trait, Heritable | Humans | Male | United Kingdom | Mathematics | Dyslexia - genetics | Learning | Twins - psychology | Reading | Dyslexia - psychology | Female | Polymorphism, Single Nucleotide | Child | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text Temporal clustering of rotational glitches in the Crab pulsar
by Carlin, JB and Melatos, A and Vukcevic, D
MONTHLY NOTICES OF THE ROYAL ASTRONOMICAL SOCIETY, ISSN 0035-8711, 01/2019, Volume 482, Issue 3, pp. 3736 - 3743
It is an open question whether glitch activity in individual pulsars varies on decadal time-scales. The Crab pulsar has experienced 23 spin-up glitches in the... 
methods: statistical | PATTERN | PINE | pulsars: general | ASTRONOMY & ASTROPHYSICS | stars: neutron | Physics - High Energy Astrophysical Phenomena
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights