Articles

UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

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
science & technology (392) 392
humans (317) 317
life sciences & biomedicine (315) 315
female (165) 165
genetics & heredity (153) 153
genome-wide association study (152) 152
polymorphism, single nucleotide (143) 143
male (138) 138
genomes (119) 119
genetics (118) 118
research (100) 100
genetic predisposition to disease (97) 97
genetic aspects (95) 95
risk factors (92) 92
genomics (90) 90
genotype (82) 82
middle aged (81) 81
medicin och hälsovetenskap (75) 75
aged (74) 74
studies (70) 70
science & technology - other topics (68) 68
multidisciplinary sciences (66) 66
adult (64) 64
biological and medical sciences (63) 63
polymorphism, single nucleotide - genetics (61) 61
case-control studies (57) 57
genes (52) 52
analysis (51) 51
genetic variation (51) 51
neurosciences & neurology (51) 51
alleles (49) 49
genetic research (45) 45
research article (45) 45
gene expression (44) 44
haplotypes (44) 44
fundamental and applied biological sciences. psychology (43) 43
neurosciences (42) 42
quantitative trait loci (40) 40
medical sciences (39) 39
biochemistry & molecular biology (37) 37
genome-wide association studies (37) 37
single-nucleotide polymorphism (37) 37
cohort studies (36) 36
genetics of eukaryotes. biological and molecular evolution (36) 36
physiological aspects (36) 36
aged, 80 and over (35) 35
gene frequency (35) 35
genome, human (35) 35
models, genetic (35) 35
single nucleotide polymorphisms (35) 35
medicine (34) 34
phenotype (34) 34
animals (33) 33
medical research (33) 33
genetic predisposition to disease - genetics (32) 32
psychiatry (32) 32
genetic loci (31) 31
genotype & phenotype (31) 31
health aspects (31) 31
methods (31) 31
medical genetics (30) 30
neurology (30) 30
european continental ancestry group - genetics (29) 29
chromosomes (28) 28
epidemiology (28) 28
consortia (27) 27
meta-analysis (27) 27
population genetics (27) 27
adolescent (26) 26
genome-wide association study - methods (26) 26
linkage disequilibrium (26) 26
chromosome mapping (25) 25
medical and health sciences (25) 25
mutation (25) 25
population (25) 25
science (25) 25
child (24) 24
disease (24) 24
genetic association studies (24) 24
physical sciences (24) 24
clinical neurology (23) 23
polymorphism (23) 23
young adult (23) 23
cell biology (22) 22
genetic markers (22) 22
klinisk medicin (22) 22
algorithms (21) 21
gwas (21) 21
identification and classification (21) 21
schizophrenia (21) 21
usage (21) 21
cancer (20) 20
deoxyribonucleic acid--dna (20) 20
mice (20) 20
biology (19) 19
clinical medicine (19) 19
computational biology (19) 19
genetics, population (19) 19
genotypes (19) 19
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Genotype imputation for genome-wide association studies
by Marchini, Jonathan and Howie, Bryan
Nature reviews. Genetics, ISSN 1471-0056, 06/2010, Volume 11, Issue 7, pp. 499 - 511
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Genotype | Genome-Wide Association Study | Models, Genetic | Polymorphism, Single Nucleotide | Biostatistics - methods | Physiological aspects | Usage | Statistical methods | Single nucleotide polymorphisms | Analysis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Genome-wide association studies of brain imaging phenotypes in UK Biobank
by Elliott, Lloyd T and Sharp, Kevin and Alfaro-Almagro, Fidel and Shi, Sinan and Miller, Karla L and Douaud, Gwenaëlle and Marchini, Jonathan and Smith, Stephen M
Nature (London), ISSN 0028-0836, 10/2018, Volume 562, Issue 7726, pp. 210 - 216
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Neuroimaging | Brain - diagnostic imaging | Brain - anatomy & histology | White Matter - anatomy & histology | White Matter - metabolism | Humans | Male | Brain - growth & development | Neuronal Plasticity - genetics | Putamen - anatomy & histology | Aging - genetics | Female | Genome-Wide Association Study | Datasets as Topic | Extracellular Matrix | Epidermal Growth Factor - genetics | United Kingdom | Heredity | Signal Transduction - genetics | Iron - metabolism | White Matter - pathology | Phenotype | Biological Specimen Banks | Brain - pathology | Polymorphism, Single Nucleotide - genetics | Putamen - metabolism | Brain | Brain research | Genetic aspects | Research | Single nucleotide polymorphisms | Structure | Nuclear magnetic resonance--NMR | Mental disorders | Genes | Genomics | Developmental plasticity | Schizophrenia | Genomes | Iron | Single-nucleotide polymorphism | Neurodevelopmental disorders | Magnetic susceptibility | Consortia | Signal transduction | Epidermal growth factor | Functional anatomy | Imaging | Aging | Extracellular matrix | Lesions | Growth factors | Phenotypes | Automation | Brain architecture | Medical imaging | Architecture | Axonogenesis | Iron transport | Behavior disorders | Substantia alba | Neurological diseases | Studies | Magnetic permeability | Gene loci | Alzheimers disease | Structure-function relationships | Index Medicus | Genetics of the nervous system | Quantitative trait | Genome-wide association studies
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Genome-wide strategies for detecting multiple loci that influence complex diseases
by Marchini, Jonathan and Donnelly, Peter and Cardon, Lon R
Nature genetics, ISSN 1061-4036, 04/2005, Volume 37, Issue 4, pp. 413 - 417
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Genetics, Population | Genetic Predisposition to Disease | Humans | Alleles | Genetic Diseases, Inborn - genetics | Models, Genetic | Genetic Markers | Genome, Human | Genetic Linkage | Quantitative trait loci | Physiological aspects | United Kingdom | Genetic aspects | Research | Gene expression | Risk factors | Diseases | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text The effects of human population structure on large genetic association studies
by Phillips, Michael S and Donnelly, Peter and Cardon, Lon R and Marchini, Jonathan
Nature genetics, ISSN 1061-4036, 05/2004, Volume 36, Issue 5, pp. 512 - 517
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Human | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Genetic Variation | Genetics, Population | Genetic Predisposition to Disease | Quantitative Trait, Heritable | Humans | Polymorphism, Single Nucleotide - genetics | Models, Genetic | Genetic Markers | Linkage Disequilibrium | Usage | Research | Single nucleotide polymorphisms | Population genetics | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
by Howie, Bryan and Fuchsberger, Christian and Stephens, Matthew and Marchini, Jonathan and Abecasis, Gonçalo R
Nature genetics, ISSN 1061-4036, 08/2012, Volume 44, Issue 8, pp. 955 - 959
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Haplotypes | Humans | Computational Biology | Databases, Genetic | Genotype | Genome-Wide Association Study - statistics & numerical data | Genome-Wide Association Study - methods | Human Genome Project | Physiological aspects | Nucleotide sequencing | Research | Methods | DNA sequencing | Studies | Accuracy | Genomes | Algorithms | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. 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 (London), ISSN 0028-0836, 10/2018, Volume 562, Issue 7726, pp. 203 - 209
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | 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 | Genome-wide association studies | Genome | Population genetics
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold
by Menelaou, Androniki and Marchini, Jonathan
Bioinformatics, ISSN 1367-4803, 01/2013, Volume 29, Issue 1, pp. 84 - 91
Statistics & Probability | Biochemistry & Molecular Biology | Physical Sciences | Computer Science, Interdisciplinary Applications | Life Sciences & Biomedicine | Technology | Biochemical Research Methods | Computer Science | Mathematics | Biotechnology & Applied Microbiology | Science & Technology | Mathematical & Computational Biology | Haplotypes | Algorithms | Gene Frequency | Humans | Alleles | Genotype | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 20 | Genotyping Techniques | Linkage Disequilibrium | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Accurate, scalable and integrative haplotype estimation
by Delaneau, Olivier and Zagury, Jean-François and Robinson, Matthew R and Marchini, Jonathan L and Dermitzakis, Emmanouil T
Nature communications, ISSN 2041-1723, 12/2019, Volume 10, Issue 1, pp. 5436 - 10
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Haplotypes | Data Interpretation, Statistical | Sample Size | Datasets as Topic | Biological Specimen Banks | Humans | Genotype | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | Software | Sequence Analysis, DNA | Data collection | Genomes | Data sets | Genotypes | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Identification of loci associated with schizophrenia by genome-wide association and follow-up
by O'Donovan, Michael C and Craddock, Nicholas and Norton, Nadine and Williams, Hywel and Peirce, Timothy and Moskvina, Valentina and Nikolov, Ivan and Hamshere, Marian and Carroll, Liam and Georgieva, Lyudmila and Dwyer, Sarah and Holmans, Peter and Marchini, Jonathan L and Spencer, Chris C. A and Howie, Bryan and Leung, Hin-Tak and Hartmann, Annette M and Möller, Hans-Jürgen and Morris, Derek W and Shi, YongYong and Feng, GuoYin and Hoffmann, Per and Propping, Peter and Vasilescu, Catalina and Maier, Wolfgang and Rietschel, Marcella and Zammit, Stanley and Schumacher, Johannes and Quinn, Emma M and Schulze, Thomas G and Williams, Nigel M and Giegling, Ina and Iwata, Nakao and Ikeda, Masashi and Darvasi, Ariel and Shifman, Sagiv and He, Lin and Duan, Jubao and Sanders, Alan R and Levinson, Douglas F and Gejman, Pablo V and Buccola, Nancy G and Mowry, Bryan J and Freedman, Robert and Amin, Farooq and Black, Donald W and Silverman, Jeremy M and Byerley, William F and Cloninger, C Robert and Cichon, Sven and Nöthen, Markus M and Gill, Michael and Corvin, Aiden and Rujescu, Dan and Kirov, George and Owen, Michael J and Mol Genetics Of Schizophrenia Coll and Molecular Genetics of Schizophrenia Collaboration
Nature genetics, ISSN 1061-4036, 09/2008, Volume 40, Issue 9, pp. 1053 - 1055
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Psychology. Psychoanalysis. Psychiatry | Psychoses | Adult and adolescent clinical studies | Psychopathology. Psychiatry | Schizophrenia | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Genetic Predisposition to Disease | Genome-Wide Association Study | Schizophrenia - genetics | Follow-Up Studies | Humans | Chromosome Mapping | Polymorphism, Single Nucleotide | Bipolar Disorder - genetics | Kruppel-Like Transcription Factors - genetics | Case-Control Studies | Genetic aspects | Research | Genetic susceptibility | Genetic variation | Risk factors | Medical research | Genetics | Quality control | Meta-analysis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text A New Statistical Approach to Detecting Significant Activation in Functional MRI
by Marchini, Jonathan L and Ripley, Brian D
NeuroImage (Orlando, Fla.), ISSN 1053-8119, 10/2000, Volume 12, Issue 4, pp. 366 - 380
Neuroimaging | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Radiology, Nuclear Medicine & Medical Imaging | Science & Technology | Magnetic Resonance Imaging | Acoustic Stimulation | Humans | Linear Models | Models, Neurological | Photic Stimulation | Brain - physiology | Magnetic resonance imaging | Statistical analysis | Nuclear magnetic resonance--NMR | Time series | Brain mapping | Functional magnetic resonance imaging | Artefacts | Trends | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights