about
The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligenceRecently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or languageGWAS of 126,559 individuals identifies genetic variants associated with educational attainmentDyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sampleAssociations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysisA meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hipDyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutationA haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling abilityDirectional dominance on stature and cognition in diverse human populationsA quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implicationsGenetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Genome-wide analysis identifies 12 loci influencing human reproductive behavior.A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations.Association between single nucleotide polymorphisms in the mu opioid receptor gene (OPRM1) and self-reported responses to alcohol in American Indians.Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression.Genome-wide association study identifies 74 loci associated with educational attainment.Interaction of chronic stress with serotonin transporter and catechol-O-methyltransferase polymorphisms in predicting youth depressionInteractions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes.No association between Cholinergic Muscarinic Receptor 2 (CHRM2) genetic variation and cognitive abilities in three independent samples.Can we identify genes for alcohol consumption in samples ascertained for heterogeneous purposes?GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factorsLinkage analysis of alcohol dependence symptoms in the community.Coaction of stress and serotonin transporter genotype in predicting aggression at the transition to adulthood.Genome-wide association study of a quantitative disordered gambling traitThe Genetic and Environmental Contributions to Internet Use and Associations With Psychopathology: A Twin Study.Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.Genetic variation in female BMI increases with number of children born but failure to replicate association between GNbeta3 variants and increased BMI in parous femalesThe role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sampleIdentification of heart rate-associated loci and their effects on cardiac conduction and rhythm disordersAssociation between in vivo alcohol metabolism and genetic variation in pathways that metabolize the carbon skeleton of ethanol and NADH reoxidation in the alcohol challenge twin study.Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smokingCohort Profile: Nausea and vomiting during pregnancy genetics consortium (NVP Genetics Consortium).Nausea and Vomiting During Pregnancy is Highly Heritable.Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.Personality Polygenes, Positive Affect, and Life Satisfaction.International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents.Association between single nucleotide polymorphisms in the cannabinoid receptor gene (CNR1) and impulsivity in southwest California Indians.Long-term stability and heritability of telephone interview measures of alcohol consumption and dependence.Effects of GABRA2 variation on physiological, psychomotor and subjective responses in the alcohol challenge twin study.Vitamin D receptor gene polymorphisms have negligible effect on human height.
P50
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Penelope A. Lind
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Penelope A. Lind
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Penelope A. Lind
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Penelope A. Lind
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Penelope A. Lind
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type
label
Penelope A. Lind
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Penelope A. Lind
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Penelope A. Lind
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Penelope A. Lind
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Penelope A. Lind
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Penelope A Lind
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Penelope Lind
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prefLabel
Penelope A. Lind
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Penelope A. Lind
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Penelope A. Lind
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Penelope A. Lind
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Penelope A. Lind
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P1053
B-2553-2009
P106
P1153
23019149500
P21
P2798
P31
P3829
P496
0000-0002-3887-2598