Genetic markers of human evolution are enriched in schizophrenia
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Genetic modifiers of cancer risk in Lynch syndrome: a review
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Genetic mutation of Cep76 results in male infertility due to abnormal sperm tail composition
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Genetic overlap between diagnostic subtypes of ischemic stroke
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Genetic overlap between endometriosis and endometrial cancer: Evidence from cross-disease genetic correlation and GWAS meta-analyses
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Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE)
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Genetic polymorphisms in xenobiotic clearance genes and their influence on disease expression in hereditary nonpolyposis colorectal cancer patients
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Genetic regulation of embryo development and formation of seed storage products in the legume model Medicago truncatula
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Genetic reprogramming of plant cells in vitro via dedifferentiation or pre-existing stem cells
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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
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Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies
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Genetic risk score mendelian randomization shows that obesity measured as body mass index, but not waist:hip ratio, is causal for endometrial cancer
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Genetic schizophrenia risk variants jointly modulate total brain and white matter volume
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Genetic signatures for a rodent model of Parkinson's disease using combinatorial optimization methods
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The genetic status of Garrwan
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Genetic studies of body mass index yield new insights for obesity biology
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Genetic susceptibility, dietary antioxidants, and long-term incidence of age-related macular degeneration in two populations
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Genetic testing in sport: considerations for young athletes
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A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants
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Genetic variants are major determinants of CSF antibody levels in multiple sclerosis
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Genetic Variants Associated with Long-Terminal Repeats Can Diagnostically Classify Cannabis Varieties
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Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
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Genetic variants for head size share genes and pathways with cancer
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Genetic variants in MUTYH are not associated with endometrial cancer risk
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Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome
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Genetic variation and its role in malignancy
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Genetic variation and risk of endometrial cancer
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Genetic variation at 16q24.2 is associated with small vessel stroke
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Genetic variation at the IGF1 locus shows association with post-stroke outcome and to circulating IGF1
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Genetic variation in glutamate carboxypeptidase II and interaction with dietary natural vitamin C may predict risk for adenomatous polyp occurrence
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Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade
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Genetic variation in the bitter receptors responsible for epicatechin detection are associated with BMI in an elderly cohort
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Genetically determined risk of depression and functional outcome after Ischemic Stroke: mendelian randomization study
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Genetically engineered people: autonomy and moral virtue
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Genetics and other risk factors for past concussions in active-duty soldiers
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Genetics of early-life head circumference and genetic correlations with neurological, psychiatric and cognitive outcomes
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Genetics of hand grip strength in mid to late life
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The genetics of overgrowth syndromes
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Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke
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Genetics, mucosal inflammation, and the environment in post-infectious chronic gut syndromes
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Genetics-informed precision treatment formulation in schizophrenia and bipolar disorder
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Genetics-related service and information needs of childhood cancer survivors and parents: a mixed-methods study
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The Genitive And Dative Cases Of Voldu
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Genitourinary Quality-of-Life Comparison Between Urethral Sparing Prostate Stereotactic Body Radiation Therapy Monotherapy and Virtual High-Dose-Rate Brachytherapy Boost
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Genocide
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Genocide by any other name
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Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders
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Genome analysis of the platypus reveals unique signatures of evolution
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Genome mining and evolutionary analysis reveal diverse Type III polyketide synthase pathways in cyanobacteria
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Genome mining of a fungal endophyte of Taxus yunnanensis (Chinese yew) leads to the discovery of a novel azaphilone polyketide, lijiquinone
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Genome variation in nine co-occurring toxic Cylindrospermopsis raciborskii strains
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Genome-based evolutionary history of Pseudomonas spp
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Genome-scale oscillations in DNA methylation during exit from pluripotency
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Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
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Genome-wide analyses of vocabulary size in infancy and toddlerhood: Associations with Attention-Deficit/Hyperactivity Disorder, literacy, and cognition-related traits
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Genome-wide analysis identifies 12 loci influencing human reproductive behavior
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Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
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Genome-wide analysis of blood pressure variability and ischemic stroke
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Genome-wide analysis of DNA methylation in single cells using a post-bisulfite adapter tagging approach
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Genome-wide analysis of long noncoding RNA stability
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Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3
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Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
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Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH
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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
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Genome-wide association analysis identifies six new loci associated with forced vital capacity
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Genome-wide association analysis of young-onset stroke identifies a locus on chromosome 10q25 near HABP2
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Genome-wide association and functional follow-up reveals new loci for kidney function
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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
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Genome-wide association meta-analysis identifies new endometriosis risk loci
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Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms
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Genome-wide association meta-analysis of functional outcome after ischemic stroke
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Genome-wide association studies suggest limited immune gene enrichment in schizophrenia compared to 5 autoimmune diseases
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Genome-wide association study identifies 74 loci associated with educational attainment
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Genome-wide association study identifies a common variant associated with risk of endometrial cancer
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Genome-wide association study identifies a possible susceptibility locus for endometrial cancer
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Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
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Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease
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Genome-wide association study identifies five new schizophrenia loci
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Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
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Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero
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Genome-wide association study identifies novel breast cancer susceptibility loci
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Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome
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Genome-wide association study of endometrial cancer in E2C2
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Genome-wide association study of germline variants and breast cancer-specific mortality
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Genome-wide association study of kidney function decline in individuals of European descent.
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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
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Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
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Genome-wide association study of retinopathy in individuals without diabetes
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A Genome-Wide Association Study of Total Child Psychiatric Problems Scores
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Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness
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Genome-wide base-resolution mapping of DNA methylation in single cells using single-cell bisulfite sequencing (scBS-seq)
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Genome-wide DNA methylation changes in CD19⁺ B cells from relapsing-remitting multiple sclerosis patients
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Genome-wide DNA methylation profiling of CD8+T cells shows a distinct epigenetic signature to CD4+T cells in multiple sclerosis patients
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Genome-Wide Interaction Analysis With DASH Diet Score Identified Novel Loci for Systolic Blood Pressure
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Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
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Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci
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Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke
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