Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis

Human Molecular Genetics

Volumn 24, Issue 9, 2015, Pages 2700-2708

  Hromatka, Bethann S ^a   Tung, Joyce Y ^a   Kiefer, Amy K ^a   Do, Chuong B ^a   Hinds, David A ^a   Eriksson, Nicholas ^a  

^a 23andMe Inc ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

G PROTEIN COUPLED RECEPTOR; GLUCOSE; GLYCEROL; GLYCEROL 3 PHOSPHATE DEHYDROGENASE; INSULIN; PROTEASOME; RGS PROTEIN; UBIQUITIN;

ADULT; ALTITUDE DISEASE; ARTICLE; BODY EQUILIBRIUM; COMORBIDITY; DISEASE ASSOCIATION; EAR; EYE; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC CORRELATION; GENETIC RISK; GENETIC VARIABILITY; GLUCOSE HOMEOSTASIS; GLYCEROL BLOOD LEVEL; HERITABILITY; HUMAN; HYPOXIA; INNER EAR; INNER EAR DEVELOPMENT; MAJOR CLINICAL STUDY; MALE; MIDDLE AGED; MIGRAINE; MOLECULAR PATHOLOGY; MORNING SICKNESS; MOTION SICKNESS; MOUSE; NAUSEA AND VOMITING; NERVOUS SYSTEM FUNCTION; NONHUMAN; ORGANOGENESIS; PHENOTYPE; POSTOPERATIVE NAUSEA AND VOMITING; PRIORITY JOURNAL; SEX DIFFERENCE; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SKULL DEVELOPMENT; VERTIGO; AGED; ALLELE; EMBRYOLOGY; GENETIC ASSOCIATION STUDY; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HOMEOSTASIS; METABOLISM; PATHOPHYSIOLOGY; YOUNG ADULT;

ADULT; AGED; ALLELES; EAR, INNER; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; GLUCOSE; HOMEOSTASIS; HUMANS; MALE; MIDDLE AGED; MOTION SICKNESS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEX FACTORS; YOUNG ADULT;

EID: 84941979085     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddv028     Document Type: Article

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