Genetic Association Studies

SLC6A4 gene variants and temporal lobe epilepsy susceptibility: a meta-analysis

Humans / Genetic Association Studies / Temporal Lobe Epilepsy / Odds ratio / Biochemistry and cell biology / Case Control Studies / Molecular Biology Reports / Case Control Studies / Molecular Biology Reports

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No association of PGRN 3′UTR rs5848 in frontotemporal lobar degeneration

Humans / Genetic Association Studies / Risk factors / Clinical Sciences / Genotype / Neurodegenerative Disease / Risk Factors / Neurobiology of Aging / Neurosciences / Neurodegenerative Disease / Risk Factors / Neurobiology of Aging / Neurosciences

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KD4v: comprehensible knowledge discovery system for missense variant

Biological Sciences / Software / Environmental Sciences / Humans / Disease / Genetic Association Studies / Nucleic Acids / Proteins / Phenotype / Knowledge Bases / Internet / Genetic Association Studies / Nucleic Acids / Proteins / Phenotype / Knowledge Bases / Internet

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Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Syndrome: Time to Review Diagnostic Criteria?

Endocrinology / Immunology / Autoimmunity / Adolescent / Transcription Factors / Innate immunity / Multidisciplinary / Disease susceptibility / Signal Transduction / Visual acuity / Italy / Mental Retardation / Clinical immunology / Gene Mapping / Humans / Child / Mutation / Sicily / Female / Male / Genetic Association Studies / Young Adult / Zinc / Clinical Sciences / Eye / IL / Electrocardiogram / Adult / Hormone / Prognosis / Interleukins / Antifungal Agents / CHRONIC MUCOCUTANEOUS CANDIDIASIS / Genetic Analysis / Autosomal Recessive / Case History / Autoantibodies / Interleukin / Thyroid Function / Diagnostic Criteria / Innate immunity / Multidisciplinary / Disease susceptibility / Signal Transduction / Visual acuity / Italy / Mental Retardation / Clinical immunology / Gene Mapping / Humans / Child / Mutation / Sicily / Female / Male / Genetic Association Studies / Young Adult / Zinc / Clinical Sciences / Eye / IL / Electrocardiogram / Adult / Hormone / Prognosis / Interleukins / Antifungal Agents / CHRONIC MUCOCUTANEOUS CANDIDIASIS / Genetic Analysis / Autosomal Recessive / Case History / Autoantibodies / Interleukin / Thyroid Function / Diagnostic Criteria

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Estimativas de parâmetros genéticos para características de desempenho de suínos em fase de crescimento e terminação

Genetics / Breeding / China / Aquaculture / Animal Production / Female / Animals / Male / Genetic Association Studies / Fisheries Sciences / Floresta / Veterinary Sciences / Oncorhynchus Mykiss / Female / Animals / Male / Genetic Association Studies / Fisheries Sciences / Floresta / Veterinary Sciences / Oncorhynchus Mykiss

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Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer

Genetic Epidemiology / Breast Cancer / Genetic Association Studies / Parent of origin effect

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GABRG2 rs211037 polymorphism and epilepsy: A systematic review and meta-analysis

Psychology / Epilepsy / Seizure / Humans / Genetic Association Studies / Clinical Sciences / Neurosciences / Clinical Sciences / Neurosciences

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Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood

Adolescent / Movement disorders / Brain / Humans / Child / Female / Male / Polymerase Chain Reaction / Genetic Association Studies / Young Adult / Infant / Pedigree / Phenotype / Adult / Juvenile / Age of Onset / Immunoblotting / Female / Male / Polymerase Chain Reaction / Genetic Association Studies / Young Adult / Infant / Pedigree / Phenotype / Adult / Juvenile / Age of Onset / Immunoblotting

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RUNX2 analysis of Danish cleidocranial dysplasia families

Genetics / Denmark / Humans / Mutation / Female / Clinical Genetics / Male / Genetic Association Studies / Gene Order / Pedigree / Phenotype / Clinical Sciences / Genotype / Adult / Amino Acid Substitution Rates / Cohort Studies / Clinical Genetics / Male / Genetic Association Studies / Gene Order / Pedigree / Phenotype / Clinical Sciences / Genotype / Adult / Amino Acid Substitution Rates / Cohort Studies

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RUNX2 analysis of Danish cleidocranial dysplasia families

Genetics / Denmark / Humans / Mutation / Female / Clinical Genetics / Male / Genetic Association Studies / Gene Order / Pedigree / Phenotype / Clinical Sciences / Genotype / Adult / Amino Acid Substitution Rates / Cohort Studies / Clinical Genetics / Male / Genetic Association Studies / Gene Order / Pedigree / Phenotype / Clinical Sciences / Genotype / Adult / Amino Acid Substitution Rates / Cohort Studies

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Racial and tissue-specific cancer risk associated with PARP1 (ADPRT) Val762Ala polymorphism: a meta-analysis

China / Humans / Genetic Association Studies / Meta Analysis / Publication Bias / Neoplasms / European Continental Ancestry Group / Asian Continental Ancestry Group / Amino Acid Substitution Rates / Biochemistry and cell biology / Molecular Biology Reports / Neoplasms / European Continental Ancestry Group / Asian Continental Ancestry Group / Amino Acid Substitution Rates / Biochemistry and cell biology / Molecular Biology Reports

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Racial and tissue-specific cancer risk associated with PARP1 (ADPRT) Val762Ala polymorphism: a meta-analysis

China / Humans / Genetic Association Studies / Meta Analysis / Publication Bias / Neoplasms / European Continental Ancestry Group / Asian Continental Ancestry Group / Amino Acid Substitution Rates / Biochemistry and cell biology / Molecular Biology Reports / Neoplasms / European Continental Ancestry Group / Asian Continental Ancestry Group / Amino Acid Substitution Rates / Biochemistry and cell biology / Molecular Biology Reports

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