Suchergebnisse - "Genome-Wide Association Study (mesh)"
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1
Autoren: et al.
Quelle: The Plant Journal. 124(3)
Schlagwörter: 31 Biological Sciences (for-2020), 3105 Genetics (for-2020), Zea mays (mesh), Cytochrome P-450 Enzyme System (mesh), Alkyl and Aryl Transferases (mesh), Sesquiterpenes (mesh), Terpenes (mesh), Plant Proteins (mesh), Genome-Wide Association Study (mesh), Gene Expression Regulation, Plant (mesh), maize specialized metabolism, sesquiterpenoids, terpene synthase, alpha-santalenoic acid, cytochrome P450, defense network, Zea mays (mesh), Terpenes (mesh), Sesquiterpenes (mesh), Cytochrome P-450 Enzyme System (mesh), Alkyl and Aryl Transferases (mesh), Plant Proteins (mesh), Gene Expression Regulation, Plant (mesh), Genome-Wide Association Study (mesh), cytochrome P450, defense network, maize specialized metabolism, sesquiterpenoids, terpene synthase, α‐santalenoic acid, Zea mays (mesh), Cytochrome P-450 Enzyme System (mesh), Alkyl and Aryl Transferases (mesh), Sesquiterpenes (mesh), Terpenes (mesh), Plant Proteins (mesh), Genome-Wide Association Study (mesh), Gene Expression Regulation, Plant (mesh), 0601 Biochemistry and Cell Biology (for), 0607 Plant Biology (for), Plant Biology & Botany (science-metrix), 3101 Biochemistry and cell biology (for-2020), 3108 Plant biology (for-2020)
Dateibeschreibung: application/pdf
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2
Autoren: et al.
Quelle: Arteriosclerosis Thrombosis and Vascular Biology. 45(9)
Schlagwörter: 32 Biomedical and Clinical Sciences (for-2020), 3201 Cardiovascular Medicine and Haematology (for-2020), 3202 Clinical Sciences (for-2020), Clinical Research (rcdc), Genetics (rcdc), Rare Diseases (rcdc), Human Genome (rcdc), Biotechnology (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Cardiovascular (hrcs-hc), Humans (mesh), Aortic Aneurysm, Abdominal (mesh), Mendelian Randomization Analysis (mesh), Genome-Wide Association Study (mesh), Smoking (mesh), Risk Factors (mesh), Genetic Predisposition to Disease (mesh), Proteomics (mesh), Male (mesh), Female (mesh), Blood Proteins (mesh), Risk Assessment (mesh), Middle Aged (mesh), Phenotype (mesh), Aged (mesh), Case-Control Studies (mesh), Biomarkers (mesh), Polymorphism, Single Nucleotide (mesh), Humans (mesh), Aortic Aneurysm, Abdominal (mesh), Genetic Predisposition to Disease (mesh), Blood Proteins (mesh), Risk Assessment (mesh), Risk Factors (mesh), Case-Control Studies (mesh), Smoking (mesh), Proteomics (mesh), Phenotype (mesh), Polymorphism, Single Nucleotide (mesh), Aged (mesh), Middle Aged (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Mendelian Randomization Analysis (mesh), Biomarkers (mesh), aortic aneurysm, abdominal, blood proteins, genetics, smoking, Humans (mesh), Aortic Aneurysm, Abdominal (mesh), Mendelian Randomization Analysis (mesh), Genome-Wide Association Study (mesh), Smoking (mesh), Risk Factors (mesh), Genetic Predisposition to Disease (mesh), Proteomics (mesh), Male (mesh), Female (mesh), Blood Proteins (mesh), Risk Assessment (mesh), Middle Aged (mesh), Phenotype (mesh), Aged (mesh), Case-Control Studies (mesh), Biomarkers (mesh), Polymorphism, Single Nucleotide (mesh), 1102 Cardiorespiratory Medicine and Haematology (for), 1103 Clinical Sciences (for), Cardiovascular System & Hematology (science-metrix), 3201 Cardiovascular medicine and haematology (for-2020), 3202 Clinical sciences (for-2020)
Zugangs-URL: https://escholarship.org/uc/item/05g7x9hj
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3
Autoren: et al.
Quelle: Mammalian Genome. 36(3)
Schlagwörter: 31 Biological Sciences (for-2020), 3105 Genetics (for-2020), Genetics (rcdc), Human Genome (rcdc), Biotechnology (rcdc), Clinical Research (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Animals (mesh), Thrombospondins (mesh), Dogs (mesh), Ectromelia (mesh), Male (mesh), Polymorphism, Single Nucleotide (mesh), Female (mesh), Genome-Wide Association Study (mesh), Homozygote (mesh), Humans (mesh), Dog Diseases (mesh), Animals (mesh), Dogs (mesh), Humans (mesh), Ectromelia (mesh), Dog Diseases (mesh), Thrombospondins (mesh), Homozygote (mesh), Polymorphism, Single Nucleotide (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Animals (mesh), Thrombospondins (mesh), Dogs (mesh), Ectromelia (mesh), Male (mesh), Polymorphism, Single Nucleotide (mesh), Female (mesh), Genome-Wide Association Study (mesh), Homozygote (mesh), Humans (mesh), Dog Diseases (mesh), 0604 Genetics (for), Genetics & Heredity (science-metrix), 3105 Genetics (for-2020)
Dateibeschreibung: application/pdf
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4
Autoren: et al.
Quelle: Alzheimer's & Dementia. 21(7)
Schlagwörter: 32 Biomedical and Clinical Sciences (for-2020), 5202 Biological Psychology (for-2020), 3202 Clinical Sciences (for-2020), 3209 Neurosciences (for-2020), 52 Psychology (for-2020), Neurosciences (rcdc), Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) (rcdc), Dementia (rcdc), Human Genome (rcdc), Prevention (rcdc), Neurodegenerative (rcdc), Biomedical Imaging (rcdc), Intellectual and Developmental Disabilities (IDD) (rcdc), Acquired Cognitive Impairment (rcdc), Genetics (rcdc), Down Syndrome (rcdc), Alzheimer's Disease (rcdc), Aging (rcdc), Brain Disorders (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), 4.2 Evaluation of markers and technologies (hrcs-rac), Neurological (hrcs-hc), Congenital (hrcs-hc), Humans (mesh), Down Syndrome (mesh), Genome-Wide Association Study (mesh), Amyloid beta-Peptides (mesh), Biomarkers (mesh), Male (mesh), Positron-Emission Tomography (mesh), Female (mesh), Adult (mesh), Brain (mesh), Peptide Fragments (mesh), Middle Aged (mesh), Polymorphism, Single Nucleotide (mesh), Cohort Studies (mesh), AD biomarker, amyloid-PET, Centiloid, plasma A beta, trisomy 21, Alzheimer's Biomarker Consortium – Down Syndrome (ABC‐DS), Brain (mesh), Humans (mesh), Down Syndrome (mesh), Peptide Fragments (mesh), Positron-Emission Tomography (mesh), Cohort Studies (mesh), Polymorphism, Single Nucleotide (mesh), Adult (mesh), Middle Aged (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Amyloid beta-Peptides (mesh), Biomarkers (mesh), AD biomarker, Centiloid, amyloid‐PET, plasma Aβ, trisomy 21, Humans (mesh), Down Syndrome (mesh), Genome-Wide Association Study (mesh), Amyloid beta-Peptides (mesh), Biomarkers (mesh), Male (mesh), Positron-Emission Tomography (mesh), Female (mesh), Adult (mesh), Brain (mesh), Peptide Fragments (mesh), Middle Aged (mesh), Polymorphism, Single Nucleotide (mesh), Cohort Studies (mesh), 1103 Clinical Sciences (for), 1109 Neurosciences (for), Geriatrics (science-metrix), 3202 Clinical sciences (for-2020), 3209 Neurosciences (for-2020), 5202 Biological psychology (for-2020)
Dateibeschreibung: application/pdf
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5
Autoren: et al.
Quelle: Nature. 639(8054)
Schlagwörter: 31 Biological Sciences (for-2020), 42 Health Sciences (for-2020), 3105 Genetics (for-2020), Genetics (rcdc), Human Genome (rcdc), Health Disparities (rcdc), Generic health relevance (hrcs-hc), Greenland (mesh), Humans (mesh), Inuit (mesh), Selection, Genetic (mesh), Multifactorial Inheritance (mesh), Genome-Wide Association Study (mesh), White People (mesh), Genome, Human (mesh), Arctic Regions (mesh), Genetic Drift (mesh), Phenotype (mesh), Male (mesh), Demography (mesh), Female (mesh), Europe (mesh), White (mesh), Humans (mesh), Demography (mesh), Genetic Drift (mesh), Multifactorial Inheritance (mesh), Phenotype (mesh), Genome, Human (mesh), Greenland (mesh), Arctic Regions (mesh), Europe (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Selection, Genetic (mesh), White People (mesh), White (mesh), Inuit (mesh), Greenland (mesh), Humans (mesh), Inuit (mesh), Selection, Genetic (mesh), Multifactorial Inheritance (mesh), Genome-Wide Association Study (mesh), White People (mesh), Genome, Human (mesh), Arctic Regions (mesh), Genetic Drift (mesh), Phenotype (mesh), Male (mesh), Demography (mesh), Female (mesh), Europe (mesh), White (mesh), General Science & Technology (science-metrix)
Dateibeschreibung: application/pdf
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6
Autoren: et al.
Quelle: G3: Genes, Genomes, Genetics. 15(2)
Schlagwörter: 31 Biological Sciences (for-2020), 3105 Genetics (for-2020), Human Genome (rcdc), Genetics (rcdc), Biotechnology (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Animals (mesh), Genotyping Techniques (mesh), Rats (mesh), Polymorphism, Single Nucleotide (mesh), Cost-Benefit Analysis (mesh), High-Throughput Nucleotide Sequencing (mesh), Genotype (mesh), Genome-Wide Association Study (mesh), Whole Genome Sequencing (mesh), low-coverage, whole-genome sequencing, genotyping, heterogeneous stock rat, Animals (mesh), Rats (mesh), Genotype (mesh), Polymorphism, Single Nucleotide (mesh), Cost-Benefit Analysis (mesh), Genome-Wide Association Study (mesh), High-Throughput Nucleotide Sequencing (mesh), Genotyping Techniques (mesh), Whole Genome Sequencing (mesh), genotyping, heterogeneous stock rat, low-coverage, whole-genome sequencing, Animals (mesh), Genotyping Techniques (mesh), Rats (mesh), Polymorphism, Single Nucleotide (mesh), Cost-Benefit Analysis (mesh), High-Throughput Nucleotide Sequencing (mesh), Genotype (mesh), Genome-Wide Association Study (mesh), Whole Genome Sequencing (mesh), 0604 Genetics (for), 3101 Biochemistry and cell biology (for-2020), 3105 Genetics (for-2020), 4905 Statistics (for-2020)
Dateibeschreibung: application/pdf
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7
Autoren: et al.
Quelle: Nature Aging. 5(2)
Schlagwörter: 3214 Pharmacology and Pharmaceutical Sciences (for-2020), 32 Biomedical and Clinical Sciences (for-2020), Schizophrenia (rcdc), Genetics (rcdc), Neurosciences (rcdc), Biotechnology (rcdc), Mental Illness (rcdc), Mental Health (rcdc), Serious Mental Illness (rcdc), Human Genome (rcdc), Brain Disorders (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), 1.1 Normal biological development and functioning (hrcs-rac), Neurological (hrcs-hc), Mental health (hrcs-hc), Humans (mesh), MicroRNAs (mesh), Aged (mesh), Quantitative Trait Loci (mesh), Genome-Wide Association Study (mesh), Brain (mesh), Male (mesh), Female (mesh), Mental Disorders (mesh), Middle Aged (mesh), Aging (mesh), Gene Expression Regulation (mesh), Aged, 80 and over (mesh), Brain (mesh), Humans (mesh), MicroRNAs (mesh), Mental Disorders (mesh), Gene Expression Regulation (mesh), Aging (mesh), Quantitative Trait Loci (mesh), Aged (mesh), Aged, 80 and over (mesh), Middle Aged (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Humans (mesh), MicroRNAs (mesh), Aged (mesh), Quantitative Trait Loci (mesh), Genome-Wide Association Study (mesh), Brain (mesh), Male (mesh), Female (mesh), Mental Disorders (mesh), Middle Aged (mesh), Aging (mesh), Gene Expression Regulation (mesh), Aged, 80 and over (mesh), 3202 Clinical sciences (for-2020)
Dateibeschreibung: application/pdf
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8
Autoren: et al.
Quelle: Genome Medicine. 17(1)
Schlagwörter: 31 Biological Sciences (for-2020), 3105 Genetics (for-2020), Genetics (rcdc), Clinical Research (rcdc), Alzheimer's Disease (rcdc), Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) (rcdc), Neurosciences (rcdc), Dementia (rcdc), Brain Disorders (rcdc), Prevention (rcdc), Aging (rcdc), Neurodegenerative (rcdc), Acquired Cognitive Impairment (rcdc), Biotechnology (rcdc), Human Genome (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Neurological (hrcs-hc), Humans (mesh), Alzheimer Disease (mesh), Genome-Wide Association Study (mesh), Male (mesh), Female (mesh), Aged (mesh), Genetic Predisposition to Disease (mesh), Phenotype (mesh), Linkage Disequilibrium (mesh), Genomic Structural Variation (mesh), Aged, 80 and over (mesh), Nerve Tissue Proteins (mesh), Membrane Proteins (mesh), Aging (mesh), Polymorphism, Single Nucleotide (mesh), Whole Genome Sequencing (mesh), Alzheimer's disease, Structural variants, GWAS, WGS, Cognitive decline, Humans (mesh), Alzheimer Disease (mesh), Genetic Predisposition to Disease (mesh), Membrane Proteins (mesh), Nerve Tissue Proteins (mesh), Aging (mesh), Linkage Disequilibrium (mesh), Phenotype (mesh), Polymorphism, Single Nucleotide (mesh), Aged (mesh), Aged, 80 and over (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Genomic Structural Variation (mesh), Whole Genome Sequencing (mesh), Alzheimer’s disease, Cognitive decline, GWAS, Structural variants, WGS, Humans (mesh), Alzheimer Disease (mesh), Genome-Wide Association Study (mesh), Male (mesh), Female (mesh), Aged (mesh), Genetic Predisposition to Disease (mesh), Phenotype (mesh), Linkage Disequilibrium (mesh), Genomic Structural Variation (mesh), Aged, 80 and over (mesh), Nerve Tissue Proteins (mesh), Membrane Proteins (mesh), Aging (mesh), Polymorphism, Single Nucleotide (mesh), Whole Genome Sequencing (mesh), 0604 Genetics (for), 1103 Clinical Sciences (for), 3105 Genetics (for-2020)
Dateibeschreibung: application/pdf
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9
Autoren: et al.
Quelle: Communications Biology. 8(1)
Schlagwörter: 31 Biological Sciences (for-2020), 3105 Genetics (for-2020), Basic Behavioral and Social Science (rcdc), Human Genome (rcdc), Behavioral and Social Science (rcdc), Genetics (rcdc), Neurosciences (rcdc), Prevention (rcdc), Sleep Research (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Generic health relevance (hrcs-hc), 3 Good Health and Well Being (sdg), Humans (mesh), Genome-Wide Association Study (mesh), Sleep (mesh), Male (mesh), Female (mesh), Middle Aged (mesh), Adult (mesh), Polymorphism, Single Nucleotide (mesh), Sleep Initiation and Maintenance Disorders (mesh), Humans (mesh), Sleep Initiation and Maintenance Disorders (mesh), Sleep (mesh), Polymorphism, Single Nucleotide (mesh), Adult (mesh), Middle Aged (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Humans (mesh), Genome-Wide Association Study (mesh), Sleep (mesh), Male (mesh), Female (mesh), Middle Aged (mesh), Adult (mesh), Polymorphism, Single Nucleotide (mesh), Sleep Initiation and Maintenance Disorders (mesh), 31 Biological sciences (for-2020), 32 Biomedical and clinical sciences (for-2020)
Dateibeschreibung: application/pdf
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10
Autoren: et al.
Quelle: Nature Communications. 16(1)
Schlagwörter: 31 Biological Sciences (for-2020), 3105 Genetics (for-2020), Inflammatory Bowel Disease (rcdc), Prevention (rcdc), Human Genome (rcdc), Digestive Diseases (rcdc), Genetics (rcdc), Autoimmune Disease (rcdc), Clinical Research (rcdc), Crohn's Disease (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Humans (mesh), Crohn Disease (mesh), CD4-Positive T-Lymphocytes (mesh), Promoter Regions, Genetic (mesh), Genome-Wide Association Study (mesh), Gene Expression Regulation (mesh), Polymorphism, Single Nucleotide (mesh), Laccase (mesh), Genetic Predisposition to Disease (mesh), T-Lymphocytes, Regulatory (mesh), Cell Differentiation (mesh), Alleles (mesh), CD4-Positive T-Lymphocytes (mesh), Humans (mesh), Crohn Disease (mesh), Genetic Predisposition to Disease (mesh), Laccase (mesh), Cell Differentiation (mesh), Gene Expression Regulation (mesh), Polymorphism, Single Nucleotide (mesh), Alleles (mesh), T-Lymphocytes, Regulatory (mesh), Promoter Regions, Genetic (mesh), Genome-Wide Association Study (mesh), Humans (mesh), Crohn Disease (mesh), CD4-Positive T-Lymphocytes (mesh), Promoter Regions, Genetic (mesh), Genome-Wide Association Study (mesh), Gene Expression Regulation (mesh), Polymorphism, Single Nucleotide (mesh), Laccase (mesh), Genetic Predisposition to Disease (mesh), T-Lymphocytes, Regulatory (mesh), Cell Differentiation (mesh), Alleles (mesh)
Dateibeschreibung: application/pdf
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11
Autoren: et al.
Quelle: Psychiatry and Clinical Neurosciences. 78(12)
Schlagwörter: 5202 Biological Psychology (for-2020), 32 Biomedical and Clinical Sciences (for-2020), 52 Psychology (for-2020), Brain Disorders (rcdc), Human Genome (rcdc), Mental Illness (rcdc), Pediatric (rcdc), Behavioral and Social Science (rcdc), Schizophrenia (rcdc), Genetics (rcdc), Biotechnology (rcdc), Serious Mental Illness (rcdc), Mental Health (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Mental health (hrcs-hc), 3 Good Health and Well Being (sdg), Humans (mesh), Genome-Wide Association Study (mesh), Bipolar Disorder (mesh), Autism Spectrum Disorder (mesh), Depressive Disorder, Major (mesh), Attention Deficit Disorder with Hyperactivity (mesh), Female (mesh), Anxiety Disorders (mesh), Male (mesh), Schizophrenia (mesh), Multifactorial Inheritance (mesh), Adult (mesh), Genetic Loci (mesh), Anxiety (mesh), Comorbidity (mesh), Middle Aged (mesh), Mental Disorders (mesh), anxiety, genetic loci, genetic overlap, psychiatric disorder, Humans (mesh), Anxiety (mesh), Mental Disorders (mesh), Anxiety Disorders (mesh), Attention Deficit Disorder with Hyperactivity (mesh), Bipolar Disorder (mesh), Depressive Disorder, Major (mesh), Schizophrenia (mesh), Comorbidity (mesh), Multifactorial Inheritance (mesh), Adult (mesh), Middle Aged (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Genetic Loci (mesh), Autism Spectrum Disorder (mesh), anxiety, genetic loci, genetic overlap, psychiatric disorder, Humans (mesh), Genome-Wide Association Study (mesh), Bipolar Disorder (mesh), Autism Spectrum Disorder (mesh), Depressive Disorder, Major (mesh), Attention Deficit Disorder with Hyperactivity (mesh), Female (mesh), Anxiety Disorders (mesh), Male (mesh), Schizophrenia (mesh), Multifactorial Inheritance (mesh), Adult (mesh), Genetic Loci (mesh), Anxiety (mesh), Comorbidity (mesh), Middle Aged (mesh), Mental Disorders (mesh), 1103 Clinical Sciences (for), 1109 Neurosciences (for), 1702 Cognitive Sciences (for), 3202 Clinical sciences (for-2020), 3209 Neurosciences (for-2020), 5202 Biological psychology (for-2020)
Dateibeschreibung: application/pdf
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12
Autoren: et al.
Quelle: Nature Communications. 15(1)
Schlagwörter: 31 Biological Sciences (for-2020), 32 Biomedical and Clinical Sciences (for-2020), 3105 Genetics (for-2020), 3203 Dentistry (for-2020), Minority Health (rcdc), Human Genome (rcdc), Clinical Research (rcdc), Genetics (rcdc), Dental/Oral and Craniofacial Disease (rcdc), Health Disparities (rcdc), Pediatric (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), 1.1 Normal biological development and functioning (hrcs-rac), Oral and gastrointestinal (hrcs-hc), Humans (mesh), Finland (mesh), Interferon Regulatory Factors (mesh), Cleft Palate (mesh), Polymorphism, Single Nucleotide (mesh), Genome-Wide Association Study (mesh), Genetic Predisposition to Disease (mesh), Incidence (mesh), Gene Frequency (mesh), Cleft Lip (mesh), Female (mesh), Male (mesh), Estonia (mesh), Alleles (mesh), FinnGen, Estonian Biobank Research Team, Humans (mesh), Cleft Palate (mesh), Cleft Lip (mesh), Genetic Predisposition to Disease (mesh), Incidence (mesh), Gene Frequency (mesh), Polymorphism, Single Nucleotide (mesh), Alleles (mesh), Estonia (mesh), Finland (mesh), Female (mesh), Male (mesh), Interferon Regulatory Factors (mesh), Genome-Wide Association Study (mesh), Humans (mesh), Finland (mesh), Interferon Regulatory Factors (mesh), Cleft Palate (mesh), Polymorphism, Single Nucleotide (mesh), Genome-Wide Association Study (mesh), Genetic Predisposition to Disease (mesh), Incidence (mesh), Gene Frequency (mesh), Cleft Lip (mesh), Female (mesh), Male (mesh), Estonia (mesh), Alleles (mesh)
Dateibeschreibung: application/pdf
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13
Autoren: et al.
Quelle: G3: Genes, Genomes, Genetics. 14(11)
Schlagwörter: 31 Biological Sciences (for-2020), 3105 Genetics (for-2020), Human Genome (rcdc), Substance Misuse (rcdc), Genetics (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Animals (mesh), Rats (mesh), Y Chromosome (mesh), Mitochondria (mesh), Male (mesh), Genome-Wide Association Study (mesh), Female (mesh), Genotype (mesh), heterogeneous stock, rat, Y Chromosome, mitochondria, haplotype, low-coverage, PheWAS, RNA-seq, Y Chromosome (mesh), Mitochondria (mesh), Animals (mesh), Rats (mesh), Genotype (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), PheWAS, RNA-seq, Y Chromosome, haplotype, heterogeneous stock, low-coverage, mitochondria, rat, Animals (mesh), Rats (mesh), Y Chromosome (mesh), Mitochondria (mesh), Male (mesh), Genome-Wide Association Study (mesh), Female (mesh), Genotype (mesh), 0604 Genetics (for), 3101 Biochemistry and cell biology (for-2020), 3105 Genetics (for-2020), 4905 Statistics (for-2020)
Dateibeschreibung: application/pdf
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14
Autoren: et al.
Quelle: Seizure. 122
Schlagwörter: 32 Biomedical and Clinical Sciences (for-2020), 5202 Biological Psychology (for-2020), 3202 Clinical Sciences (for-2020), 3209 Neurosciences (for-2020), 52 Psychology (for-2020), Neurosciences (rcdc), Epilepsy (rcdc), Genetics (rcdc), Pediatric (rcdc), Neurodegenerative (rcdc), Brain Disorders (rcdc), Human Genome (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Neurological (hrcs-hc), Humans (mesh), Genome-Wide Association Study (mesh), Epilepsy (mesh), Cognition (mesh), Cognitive Dysfunction (mesh), Female (mesh), Male (mesh), Linkage Disequilibrium (mesh), Polymorphism, Single Nucleotide (mesh), Phenotype (mesh), Epilepsy, Cognition, Polygenic overlap, Linkage disequilibrium score regression, LDSC, Gaussian causal mixture models, MiXeR, Conjunctional False Discovery Rate, ConjFDR, Humans (mesh), Epilepsy (mesh), Cognition (mesh), Linkage Disequilibrium (mesh), Phenotype (mesh), Polymorphism, Single Nucleotide (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Cognitive Dysfunction (mesh), Cognition, ConjFDR, Conjunctional False Discovery Rate, Epilepsy, Gaussian causal mixture models, LDSC, Linkage disequilibrium score regression, MiXeR, Polygenic overlap, Humans (mesh), Genome-Wide Association Study (mesh), Epilepsy (mesh), Cognition (mesh), Cognitive Dysfunction (mesh), Female (mesh), Male (mesh), Linkage Disequilibrium (mesh), Polymorphism, Single Nucleotide (mesh), Phenotype (mesh), 1103 Clinical Sciences (for), 1109 Neurosciences (for), 1701 Psychology (for), Neurology & Neurosurgery (science-metrix), 3202 Clinical sciences (for-2020), 3209 Neurosciences (for-2020), 5202 Biological psychology (for-2020)
Dateibeschreibung: application/pdf
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15
Autoren: et al.
Quelle: Nature Human Behaviour. 8(11)
Schlagwörter: 5202 Biological Psychology (for-2020), 5205 Social and Personality Psychology (for-2020), 52 Psychology (for-2020), Mental Illness (rcdc), Mental Health (rcdc), Genetics (rcdc), Behavioral and Social Science (rcdc), Brain Disorders (rcdc), Human Genome (rcdc), Depression (rcdc), Mental health (hrcs-hc), 3 Good Health and Well Being (sdg), Female (mesh), Humans (mesh), Male (mesh), Genome-Wide Association Study (mesh), Mental Disorders (mesh), Multifactorial Inheritance (mesh), Neuroticism (mesh), Personality (mesh), White People (mesh), Black People (mesh), VA Million Veteran Program, Humans (mesh), Personality (mesh), Mental Disorders (mesh), Multifactorial Inheritance (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Neuroticism (mesh), White People (mesh), Black People (mesh), Female (mesh), Humans (mesh), Male (mesh), Genome-Wide Association Study (mesh), Mental Disorders (mesh), Multifactorial Inheritance (mesh), Neuroticism (mesh), Personality (mesh), White People (mesh), Black People (mesh), 32 Biomedical and clinical sciences (for-2020), 42 Health sciences (for-2020), 52 Psychology (for-2020)
Dateibeschreibung: application/pdf
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16
Autoren: et al.
Quelle: Cancer Epidemiology Biomarkers & Prevention. 33(9)
Schlagwörter: 4202 Epidemiology (for-2020), 42 Health Sciences (for-2020), Cancer (rcdc), Health Disparities (rcdc), Minority Health (rcdc), Clinical Research (rcdc), Childhood Leukemia (rcdc), Hematology (rcdc), Pediatric Cancer (rcdc), Genetics (rcdc), Rare Diseases (rcdc), Pediatric (rcdc), Human Genome (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Cancer (hrcs-hc), Humans (mesh), Precursor Cell Lymphoblastic Leukemia-Lymphoma (mesh), Folic Acid (mesh), Polymorphism, Single Nucleotide (mesh), Child (mesh), Case-Control Studies (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Risk Factors (mesh), Genetic Predisposition to Disease (mesh), Child, Preschool (mesh), Humans (mesh), Genetic Predisposition to Disease (mesh), Folic Acid (mesh), Risk Factors (mesh), Case-Control Studies (mesh), Polymorphism, Single Nucleotide (mesh), Child (mesh), Child, Preschool (mesh), Female (mesh), Male (mesh), Precursor Cell Lymphoblastic Leukemia-Lymphoma (mesh), Genome-Wide Association Study (mesh), Humans (mesh), Precursor Cell Lymphoblastic Leukemia-Lymphoma (mesh), Folic Acid (mesh), Polymorphism, Single Nucleotide (mesh), Child (mesh), Case-Control Studies (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Risk Factors (mesh), Genetic Predisposition to Disease (mesh), Child, Preschool (mesh), 11 Medical and Health Sciences (for), Epidemiology (science-metrix), 32 Biomedical and clinical sciences (for-2020), 42 Health sciences (for-2020)
Dateibeschreibung: application/pdf
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17
Autoren: et al.
Quelle: Bioinformatics. 40(8)
Schlagwörter: 31 Biological Sciences (for-2020), 3105 Genetics (for-2020), Networking and Information Technology R&D (NITRD) (rcdc), Human Genome (rcdc), Genetics (rcdc), Polymorphism, Single Nucleotide (mesh), Software (mesh), Genotype (mesh), Genome-Wide Association Study (mesh), Humans (mesh), Databases, Genetic (mesh), Alleles (mesh), Humans (mesh), Genotype (mesh), Polymorphism, Single Nucleotide (mesh), Alleles (mesh), Software (mesh), Databases, Genetic (mesh), Genome-Wide Association Study (mesh), Polymorphism, Single Nucleotide (mesh), Software (mesh), Genotype (mesh), Genome-Wide Association Study (mesh), Humans (mesh), Databases, Genetic (mesh), Alleles (mesh), 01 Mathematical Sciences (for), 06 Biological Sciences (for), 08 Information and Computing Sciences (for), Bioinformatics (science-metrix), 31 Biological sciences (for-2020), 46 Information and computing sciences (for-2020), 49 Mathematical sciences (for-2020)
Dateibeschreibung: application/pdf
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18
Autoren: et al.
Quelle: EBioMedicine. 106
Schlagwörter: 32 Biomedical and Clinical Sciences (for-2020), 3211 Oncology and Carcinogenesis (for-2020), Cancer (rcdc), Lung (rcdc), Human Genome (rcdc), Genetics (rcdc), Breast Cancer (rcdc), Women's Health (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Cancer (hrcs-hc), Animals (mesh), Female (mesh), Humans (mesh), Mice (mesh), Biomarkers, Tumor (mesh), Breast Neoplasms (mesh), Collaborative Cross Mice (mesh), Disease Models, Animal (mesh), Gene Expression Profiling (mesh), Gene Expression Regulation, Neoplastic (mesh), Genetic Predisposition to Disease (mesh), Genome-Wide Association Study (mesh), Neoplasm Metastasis (mesh), Polymorphism, Single Nucleotide (mesh), Receptor, ErbB-2 (mesh), Transcriptome (mesh), Breast cancer, Collaborative cross mice, Tumour susceptibility, Gene signature, Prognosis, Treatment response prediction, Animals (mesh), Humans (mesh), Mice (mesh), Breast Neoplasms (mesh), Neoplasm Metastasis (mesh), Disease Models, Animal (mesh), Genetic Predisposition to Disease (mesh), Receptor, erbB-2 (mesh), Gene Expression Profiling (mesh), Gene Expression Regulation, Neoplastic (mesh), Polymorphism, Single Nucleotide (mesh), Female (mesh), Genome-Wide Association Study (mesh), Transcriptome (mesh), Biomarkers, Tumor (mesh), Collaborative Cross Mice (mesh), Breast cancer, Collaborative cross mice, Gene signature, Prognosis, Treatment response prediction, Tumour susceptibility, Animals (mesh), Female (mesh), Humans (mesh), Mice (mesh), Biomarkers, Tumor (mesh), Breast Neoplasms (mesh), Collaborative Cross Mice (mesh), Disease Models, Animal (mesh), Gene Expression Profiling (mesh), Gene Expression Regulation, Neoplastic (mesh), Genetic Predisposition to Disease (mesh), Genome-Wide Association Study (mesh), Neoplasm Metastasis (mesh), Polymorphism, Single Nucleotide (mesh), Receptor, ErbB-2 (mesh), Transcriptome (mesh), 1103 Clinical Sciences (for), 1117 Public Health and Health Services (for), 3202 Clinical sciences (for-2020), 4202 Epidemiology (for-2020)
Dateibeschreibung: application/pdf
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19
Autoren: et al.
Quelle: American Journal of Human Genetics. 111(7)
Schlagwörter: 31 Biological Sciences (for-2020), 42 Health Sciences (for-2020), 3105 Genetics (for-2020), Aging (rcdc), Alzheimer's Disease Related Dementias (ADRD) (rcdc), Human Genome (rcdc), Genetics (rcdc), Brain Disorders (rcdc), Neurosciences (rcdc), Neurodegenerative (rcdc), Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) (rcdc), Rare Diseases (rcdc), Parkinson's Disease (rcdc), Dementia (rcdc), Acquired Cognitive Impairment (rcdc), Alzheimer's Disease (rcdc), Frontotemporal Dementia (FTD) (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), Neurological (hrcs-hc), Humans (mesh), Frontotemporal Dementia (mesh), tau Proteins (mesh), Genome-Wide Association Study (mesh), Apolipoproteins E (mesh), Male (mesh), Female (mesh), Genetic Predisposition to Disease (mesh), Aged (mesh), Polymorphism, Single Nucleotide (mesh), Genetic Loci (mesh), Middle Aged (mesh), Case-Control Studies (mesh), Myelin Proteins (mesh), Humans (mesh), Genetic Predisposition to Disease (mesh), Apolipoproteins E (mesh), tau Proteins (mesh), Myelin Proteins (mesh), Case-Control Studies (mesh), Polymorphism, Single Nucleotide (mesh), Aged (mesh), Middle Aged (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Genetic Loci (mesh), Frontotemporal Dementia (mesh), Humans (mesh), Frontotemporal Dementia (mesh), tau Proteins (mesh), Genome-Wide Association Study (mesh), Apolipoproteins E (mesh), Male (mesh), Female (mesh), Genetic Predisposition to Disease (mesh), Aged (mesh), Polymorphism, Single Nucleotide (mesh), Genetic Loci (mesh), Middle Aged (mesh), Case-Control Studies (mesh), Myelin Proteins (mesh), 06 Biological Sciences (for), 11 Medical and Health Sciences (for), Genetics & Heredity (science-metrix), 31 Biological sciences (for-2020), 32 Biomedical and clinical sciences (for-2020), 42 Health sciences (for-2020)
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Autoren: et al.
Quelle: Journal of Alzheimer’s Disease. 99(4)
Schlagwörter: 32 Biomedical and Clinical Sciences (for-2020), 5202 Biological Psychology (for-2020), 3202 Clinical Sciences (for-2020), 3209 Neurosciences (for-2020), 52 Psychology (for-2020), Aging (rcdc), Alzheimer's Disease (rcdc), Neurodegenerative (rcdc), Neurosciences (rcdc), Acquired Cognitive Impairment (rcdc), Genetics (rcdc), Dementia (rcdc), Brain Disorders (rcdc), Bioengineering (rcdc), Prevention (rcdc), Machine Learning and Artificial Intelligence (rcdc), Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), 3 Good Health and Well Being (sdg), Humans (mesh), Alzheimer Disease (mesh), Machine Learning (mesh), Multifactorial Inheritance (mesh), Epistasis, Genetic (mesh), Genetic Predisposition to Disease (mesh), Female (mesh), Male (mesh), Polymorphism, Single Nucleotide (mesh), Aged (mesh), Genome-Wide Association Study (mesh), Apolipoproteins E (mesh), Models, Genetic (mesh), Genetic Risk Score (mesh), the Alzheimer’s Disease Neuroimaging Initiative, Humans (mesh), Alzheimer Disease (mesh), Genetic Predisposition to Disease (mesh), Apolipoproteins E (mesh), Epistasis, Genetic (mesh), Multifactorial Inheritance (mesh), Polymorphism, Single Nucleotide (mesh), Models, Genetic (mesh), Aged (mesh), Female (mesh), Male (mesh), Genome-Wide Association Study (mesh), Machine Learning (mesh), Genetic Risk Score (mesh), Alzheimer’s disease, data mining, deep learning, epistasis, machine learning, predictive genetic testing, Humans (mesh), Alzheimer Disease (mesh), Machine Learning (mesh), Multifactorial Inheritance (mesh), Epistasis, Genetic (mesh), Genetic Predisposition to Disease (mesh), Female (mesh), Male (mesh), Polymorphism, Single Nucleotide (mesh), Aged (mesh), Genome-Wide Association Study (mesh), Apolipoproteins E (mesh), Models, Genetic (mesh), Genetic Risk Score (mesh), 1103 Clinical Sciences (for), 1109 Neurosciences (for), 1702 Cognitive Sciences (for), Neurology & Neurosurgery (science-metrix), 3202 Clinical sciences (for-2020), 3209 Neurosciences (for-2020), 5202 Biological psychology (for-2020)
Dateibeschreibung: application/pdf