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Nature genetics, ISSN 1061-4036, 2007, Volume 39, Issue 12, pp. 1443 - 1452
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | European Continental Ancestry Group - genetics | Hair Color - genetics | Humans | Receptor, Melanocortin, Type 1 - genetics | Male | Eye Color - genetics | Stem Cell Factor - genetics | Iceland | Skin Pigmentation - genetics | Netherlands | Membrane Transport Proteins - genetics | Antiporters - genetics | Female | Monophenol Monooxygenase - genetics | Polymorphism, Single Nucleotide | Physiological aspects | Europeans | Genetic aspects | Single nucleotide polymorphisms | Research | Skin color | Hair | Pigments | Genetic research | Genetics | Skin | Eyes & eyesight | Index Medicus
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Leukemia, ISSN 0887-6924, 2014, Volume 28, Issue 6, pp. 1371 - 1374
Genetic Predisposition to Disease | Prognosis | Telomerase - genetics | Germ-Line Mutation - genetics | Myeloproliferative Disorders - genetics | Humans | Cell proliferation | Gene mutations | Genetic variation | Physiological aspects | Genetic aspects | Research | Blood diseases | Myeloproliferative disorders | Index Medicus | Letter to the Editor
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Nature genetics, ISSN 1061-4036, 2008, Volume 40, Issue 7, pp. 835 - 837
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 | Genetics, Population | Gene Frequency | Humans | Eye Color - genetics | Iceland | Netherlands | Pigmentation - genetics | Solar System | Agouti Signaling Protein - genetics | Hair - physiology | Polymorphism, Single Nucleotide | Odds Ratio | Calcium Channels - genetics | Genetic Linkage | Melanosis - genetics | Physiological aspects | Genetic aspects | Research | Genetic variation | Skin color | Identification and classification | Proteins | Genetics | Skin | Sample size | Genes | Color | Index Medicus
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Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density
Nature genetics, ISSN 1061-4036, 2009, Volume 41, Issue 8, pp. 926 - 930
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Nephrology. Urinary tract diseases | Biological and medical sciences | Urinary lithiasis | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Genetic Predisposition to Disease | Calcium - metabolism | Membrane Proteins - genetics | Humans | Middle Aged | Molecular Sequence Data | Bone Density - genetics | Chromosomes, Human, Pair 21 - genetics | Mutation - genetics | Claudins | Base Sequence | Aged, 80 and over | Adult | Female | Aged | Kidney Calculi - genetics | Genetic variation | Physiological aspects | Bones | Genetic aspects | Research | Density | Risk factors | Kidney stones | Proteins | Diet | Bone density | Females | Stone | Index Medicus
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Nature genetics, ISSN 1061-4036, 2009, Volume 41, Issue 6, pp. 734 - 738
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Methods, theories and miscellaneous | Body Mass Index | Genome-Wide Association Study | Menarche - genetics | Humans | Chromosome Mapping | Body Height - genetics | Chromosomes, Human, Pair 6 - genetics | Iceland | Genetic Variation | Netherlands | Aging - physiology | Base Sequence | Denmark | Polymorphism, Single Nucleotide - genetics | Adult | Anthropometry - methods | Female | Transcription, Genetic | Adipose Tissue - anatomy & histology | Adipose tissues | Physiological aspects | Menarche | Genetic aspects | Research | Genetic variation | Menstruation | Industrialized nations | Genes | Genomics | Risk factors | Index Medicus
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Nature communications, ISSN 2041-1723, 01/2020, Volume 11, Issue 1, pp. 163 - 163
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genome-Wide Association Study | Humans | Risk Factors | Ventricular Function, Left - genetics | Cardiomyopathies - pathology | Heart Failure - genetics | Heart Failure - pathology | Atrial Fibrillation - genetics | Case-Control Studies | Muscle Proteins - genetics | Cardiomyopathies - genetics | Carrier Proteins - genetics | Cyclin-Dependent Kinase Inhibitor p21 - genetics | Adaptor Proteins, Signal Transducing - genetics | Coronary Artery Disease - genetics | Mendelian Randomization Analysis | Apoptosis Regulatory Proteins - genetics | Microfilament Proteins - genetics | Cardiac arrhythmia | Senescence | Pathogenesis | Cardiovascular disease | Genomes | Risk factors | Body mass index | Randomization | Fibrillation | Failure analysis | Genetic analysis | Heart diseases | Heart failure | Hypertension | Coronary artery | Functional analysis | Risk analysis | Coronary artery disease | Loci | Morbidity | Body mass | Body size | Gene loci | Heritability | Ventricle | Index Medicus | Life Sciences | Human health and pathology | Cardiology and cardiovascular system | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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Nature communications, ISSN 2041-1723, 2013, Volume 4, Issue 1, pp. 2776 - 2776
Iceland - epidemiology | Genetic Predisposition to Disease | Kidney Neoplasms - genetics | Kidney Neoplasms - epidemiology | Humans | Risk Factors | Computational Biology | Gene Expression Regulation, Neoplastic | Carcinoma, Renal Cell - genetics | Genotype | Carcinoma, Renal Cell - epidemiology | Aged | Polymorphism, Single Nucleotide | Genome, Human | Odds Ratio | Index Medicus
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Human molecular genetics, ISSN 0964-6906, 2011, Volume 20, Issue 10, pp. 2071 - 2077
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Cytochrome P-450 CYP1A1 - genetics | Genome-Wide Association Study | Humans | Middle Aged | Receptors, Aryl Hydrocarbon - genetics | Male | Coffee - metabolism | Promoter Regions, Genetic - genetics | Genetic Variation | Models, Biological | Chromosomes, Human, Pair 15 | Cytochrome P-450 CYP1A2 - genetics | Alleles | Sex Factors | Adult | Female | Aged | Polymorphism, Single Nucleotide | Drinking Behavior - physiology | Index Medicus | Association Studies
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Human molecular genetics, ISSN 0964-6906, 2017, Volume 26, Issue 12, pp. 2364 - 2376
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Gene Frequency - genetics | Lipids - genetics | RNA Splice Sites - genetics | Lipoproteins - genetics | Coronary Artery Disease - metabolism | Humans | Risk Factors | Genetic Association Studies - methods | Haptoglobins - genetics | Male | DNA Copy Number Variations - genetics | Haptoglobins - metabolism | Iceland | Genetic Variation | Base Sequence | Lipids - blood | Alleles | Coronary Artery Disease - genetics | Adult | Female | Mutation | Odds Ratio | Index Medicus
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Translational psychiatry, ISSN 2158-3188, 2017, Volume 7, Issue 4, pp. e1109 - e1109
Life Sciences & Biomedicine | Psychiatry | Science & Technology | Iceland - epidemiology | Humans | Middle Aged | Magnetic Resonance Imaging - methods | Male | Temporal Lobe - anatomy & histology | Developmental Disabilities - genetics | Functional Neuroimaging - methods | Functional Neuroimaging - standards | Temporal Lobe - diagnostic imaging | Intellectual Disability - genetics | Young Adult | Dyscalculia - genetics | Cognition - physiology | Adult | Female | Chromosome Deletion | Neuropsychological Tests - standards | DNA Copy Number Variations - genetics | Chromosomes, Human, Pair 15 - genetics | Dyslexia - genetics | Phenotype | Adolescent | Chromosome Aberrations | Heterozygote | Aged | Index Medicus | Original
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