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1. Full Text Characterizing the Causal Pathway for Genetic Variants Associated with Neurological Phenotypes Using Human Brain-Derived Proteome Data
by Kibinge, Nelson K and Relton, Caroline L and Gaunt, Tom R and Richardson, Tom G
American journal of human genetics, ISSN 0002-9297, 06/2020, Volume 106, Issue 6, pp. 885 - 892
cognitive | brain-derived proteins | protein quantitative trait loci | genetic colocalization | Mendelian randomization | phenome-wide association study | neurological | psychaitric | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Brain | Medical research | Genes | Genomics | Schizophrenia | Epidemiology | Proteins | Quantitative genetics | Phenotype | Anopheles | Genetic research | Medicine, Experimental | Genetic aspects | Alzheimer's disease | Index Medicus
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2. Full Text Prioritizing putative influential genes in cardiovascular disease susceptibility by applying tissue-specific Mendelian randomization
by Taylor, Kurt and Davey Smith, George and Relton, Caroline L and Gaunt, Tom R and Richardson, Tom G
Genome medicine, ISSN 1756-994X, 01/2019, Volume 11, Issue 1, pp. 6 - 6
Quantitative trait loci | DNA methylation | Tissue specificity | Cardiovascular disease | ALSPAC | Mendelian randomization | ARIES | Gene expression | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genome-wide association studies | Usage | Genetic susceptibility | Genetic variation | Analysis | Genetic aspects | Research | Cardiovascular diseases | Statistical analysis | Liver | Cholesterol | Studies | Genetic variance | Body mass index | Gene loci | Gene mapping | Bayesian analysis | Index Medicus
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3. Full Text A transcriptome-wide Mendelian randomization study to uncover tissue-dependent regulatory mechanisms across the human phenome
by Richardson, Tom G and Hemani, Gibran and Gaunt, Tom R and Relton, Caroline L and Davey Smith, George
Nature communications, ISSN 2041-1723, 12/2020, Volume 11, Issue 1, pp. 185 - 185
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetic Predisposition to Disease | Genetic Association Studies | Ribosomal Proteins - genetics | Humans | Gene Expression Regulation | Transcriptome | Fibrillin-2 - genetics | Phenomics | Multifactorial Inheritance | Genetic Variation | Aromatase - genetics | Phenotype | Mendelian Randomization Analysis | Thyroid Diseases - genetics | Thyroid Diseases - metabolism | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Hydroxymethylglutaryl CoA Reductases - genetics | Genetic variance | Randomization | Phenotypes | Transcription | Regulatory mechanisms (biology) | Gene expression | Tissues | Index Medicus | Genetic association study | Medical research | Quantitative trait
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4. Full Text FATHMM-XF: accurate prediction of pathogenic point mutations via extended features
by Rogers, Mark F and Shihab, Hashem A and Mort, Matthew and Cooper, David N and Gaunt, Tom R and Campbell, Colin
Bioinformatics, ISSN 1367-4803, 02/2018, Volume 34, Issue 3, pp. 511 - 513
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 | Point Mutation | Software | Genome, Human | Genomics - methods | Sequence Analysis, DNA - methods | Humans | Index Medicus | Applications Notes
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5. Full Text Neonatal DNA methylation and early-onset conduct problems: A genome-wide, prospective study
by Cecil, Charlotte A. M and Walton, Esther and Jaffee, Sara R and O'Connor, Tom and Maughan, Barbara and Relton, Caroline L and Smith, Rebecca G and McArdle, Wendy and Gaunt, Tom R and Ouellet-Morin, Isabelle and Barker, Edward D
Development and psychopathology, ISSN 0954-5794, 05/2018, Volume 30, Issue 2, pp. 383 - 397
Regular Articles | Psychology, Developmental | Psychology | Social Sciences | Genome-Wide Association Study | Humans | Child, Preschool | Male | DNA Methylation - genetics | Fetal Blood - metabolism | Conduct Disorder - genetics | Epigenesis, Genetic - genetics | Adolescent | Age of Onset | Female | Child | Longitudinal Studies | Infant, Newborn | Neonates | Pain perception | Mental disorders | Criminality | Genomes | Behavior disorders | Lipase | Amine oxidase (flavin-containing) | Quantitative trait loci | Studies | Cannabinoids | Brain-derived neurotrophic factor | Tacrolimus-binding protein | Tacrolimus | Cord blood | Child development | DNA methylation | Epigenetics | Children | Prenatal experience | Age | Aggressiveness | Index Medicus
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6. Full Text MELODI Presto: A fast and agile tool to explore semantic triples derived from biomedical literature
by Elsworth, Benjamin and Gaunt, Tom R
Bioinformatics, ISSN 1367-4803, 08/2020
Index Medicus
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7. Full Text Hardy-Weinberg Equilibrium Testing of Biological Ascertainment for Mendelian Randomization Studies
by Rodriguez, Santiago and Gaunt, Tom R and Day, Ian N. M
American journal of epidemiology, ISSN 0002-9262, 2/2009, Volume 169, Issue 4, pp. 505 - 514
Genetics | Random allocation | Research design | Epidemiologic methods | Hardy-Weinberg equilibrium | Life Sciences & Biomedicine | Public, Environmental & Occupational Health | Science & Technology | Public health. Hygiene-occupational medicine | Public health. Hygiene | General aspects | Prevention and actions | Analysis. Health state | Biological and medical sciences | Medical sciences | Epidemiology | Genetics, Population | Gene Frequency | Humans | Genotype | Molecular Epidemiology - methods | Randomized Controlled Trials as Topic | Genetic Variation | Confounding Factors (Epidemiology) | Epidemiologic Methods | Alleles | Models, Genetic | Software | Internet | Causality | Hardy-Weinberg formula | Research | Clinical trials | Medical research | Genotype & phenotype | Index Medicus | Practice of Epidemiology | epidemiologic methods | genetics | research design | random allocation
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8. Full Text A pathway-centric approach to rare variant association analysis
by Richardson, Tom G and Timpson, Nicholas J and Campbell, Colin and Gaunt, Tom R
European journal of human genetics : EJHG, ISSN 1018-4813, 01/2016, Volume 25, Issue 1, pp. 123 - 129
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Phenotype | Biosynthetic Pathways - genetics | Genetic Association Studies | Humans | Molecular Sequence Annotation | Polymorphism, Single Nucleotide - genetics | Genetic Diseases, Inborn | Genotype | High-Throughput Nucleotide Sequencing | Genome, Human | Hypertension | Disease | Genomics | Genes | Licenses | Association analysis | Proline | Genomes | Epidemiology | Studies | Consortia | Arginine | Genetics | Blood pressure | Random variables | Children | Power | Index Medicus
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9. Full Text Leveraging brain cortex-derived molecular data to elucidate epigenetic and transcriptomic drivers of complex traits and disease
by Hatcher, Charlie and Relton, Caroline L and Gaunt, Tom R and Richardson, Tom G
Translational psychiatry, ISSN 2158-3188, 12/2019, Volume 9, Issue 1, pp. 105 - 105
Life Sciences & Biomedicine | Psychiatry | Science & Technology | DNA methylation | Schizophrenia | Epigenetics | Genomes | Gene expression | Deoxyribonucleic acid--DNA | Index Medicus
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10. Full Text Cubic exact solutions for the estimation of pairwise haplotype frequencies: Implications for linkage disequilibrium analyses and a web tool 'CubeX'
by Gaunt, Tom R and Rodríguez, Santiago and Day, Ian N.M
BMC bioinformatics, ISSN 1471-2105, 11/2007, Volume 8, Issue 1, pp. 428 - 428
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Biochemical Research Methods | Science & Technology | Mathematical & Computational Biology | Haplotypes | Models, Theoretical | Genetics, Population | Computational Biology - methods | Genetic Predisposition to Disease | Gene Frequency | Humans | Models, Statistical | Linkage Disequilibrium | Algorithms | Animals | Alleles | Models, Genetic | Software | Internet | Genetic Linkage | Usage | Analysis | Methods | Genetic algorithms | Index Medicus
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