Web-based, participant-driven studies yield novel genetic associations for common traits - Test2 - elhamkhani - TriplyDB

Web-based, participant-driven studies yield novel genetic associations for common traits

Web-based, participant-driven studies yield novel genetic associations for common traits

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Common variants in left/right asymmetry genes and pathways are associated with relative hand skill Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations Replicability and robustness of genome-wide-association studies for behavioral traits PCSK6 is associated with handedness in individuals with dyslexia Genetic analysis of chemosensory traits in human twins Excretion and perception of a characteristic odor in urine after asparagus ingestion: a psychophysical and genetic study Neurogenethics: An emerging discipline at the intersection of ethics, neuroscience, and genomics Evidence for archaic adaptive introgression in humans Human pigmentation genes under environmental selection Translational bioinformatics: linking the molecular world to the clinical world From patients to partners: participant-centric initiatives in biomedical research Use of contemporary genetics in cardiovascular diagnosis Genetic variants associated with breast size also influence breast cancer risk Research Conducted Using Data Obtained through Online Communities: Ethical Implications of Methodological Limitations A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features Mammalian odorant receptors: functional evolution and variation A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway Exposome informatics: considerations for the design of future biomedical research information systems PER1 rs3027172 Genotype Interacts with Early Life Stress to Predict Problematic Alcohol Use, but Not Reward-Related Ventral Striatum Activity Sensitivity of genome-wide-association signals to phenotyping strategy: the PROP-TAS2R38 taste association as a benchmark Crowdsourced health research studies: an important emerging complement to clinical trials in the public health research ecosystem Sniffing out significant "Pee values": genome wide association study of asparagus anosmia openSNP--a crowdsourced web resource for personal genomics Disentangling public participation in science and biomedicine Left brain, right brain: facts and fantasies Novel associations for hypothyroidism include known autoimmune risk loci Efficient replication of over 180 genetic associations with self-reported medical data A genome-wide association study of brain lesion distribution in multiple sclerosis Nucleic acid detection with CRISPR-Cas13a/C2c2 Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis Convergent effects of mouse Pet-1 deletion and human PET-1 variation on amygdala fear and threat processing Genetic variation in the odorant receptor OR2J3 is associated with the ability to detect the "grassy" smelling odor, cis-3-hexen-1-ol.Effectiveness of a web-based protocol for the screening and phenotyping of individuals with Tourette syndrome for genetic studies Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies.Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.FRAS1-related extracellular matrix 3 (FREM3) single-nucleotide polymorphism effects on gene expression, amygdala reactivity and perceptual processing speed: An accelerated aging pathway of depression risk Gradient Boosting as a SNP Filter: an Evaluation Using Simulated and Hair Morphology Data.Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response

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Web-based, participant-driven studies yield novel genetic associations for common traits

http://www.wikidata.org/entity/Q21092440

description

2010 nî lūn-bûn

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2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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Web-based, participant-driven studies yield novel genetic associations for common traits

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Web-based, participant-driven studies yield novel genetic associations for common traits

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Web-based, participant-driven studies yield novel genetic associations for common traits

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Web-based, participant-driven studies yield novel genetic associations for common traits

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Web-based, participant-driven studies yield novel genetic associations for common traits

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Web-based, participant-driven studies yield novel genetic associations for common traits

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Web-based, participant-driven studies yield novel genetic associations for common traits

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J Michael Macpherson

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Joanna Mountain

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Joyce Y Tung

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Lawrence S Hon

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Serge Saxonov

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Why Most Discovered True Associations Are Inflated

Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia

The structure of human trichohyalin. Potential multiple roles as a functional EF-hand-like calcium-binding protein, a cornified cell envelope precursor, and an intermediate filament-associated (cross-linking) protein

The human olfactory receptor gene family

Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

A note on exact tests of Hardy-Weinberg equilibrium

ACTN3 genotype is associated with human elite athletic performance

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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