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Tim D Spector

Datos Biográficos

ID1728232
NOMBRETim D Spector
NOMBRESTim D
APELLIDOSpector
FIRMASPECTOR T D
AFILIACIONESKing's College London
ORCID0000-0002-9795-0365
VERIFICADOSí
TOTAL DE OBRAS16
TOTAL DE CITAS6
TOTAL COMO AUTOR16
TOTAL COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN1991
AÑO MÁS RECIENTE DE PUBLICACIÓN2022
ÍNDICE H2
  • Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

    Open Access•Aysu Okbay, Yeda Wu et al.•ARTICLE•Nature Genetics•2022

    We conduct a genome-wide association study (GWAS) of educational attainment (EA) in a sample of ~3 million individuals and identify 3,952 approximately uncorrelated genome-wide-significant single-nucleotide polymorphisms (SNPs). A genome-wide polygenic predictor, or polygenic index (PGI), explains 12–16% of EA variance and contributes to risk prediction for ten diseases. Direct effects (i.e., controlling for parental PGIs) explain roughly half th…

  • Knowledge barriers in a national symptomatic-Covid-19 testing programme

    Open Access•Mark S Graham, Anna May et al.•ARTICLE•PLOS Global Public Health•2022

    Symptomatic testing programmes are crucial to the COVID-19 pandemic response. We sought to examine United Kingdom (UK) testing rates amongst individuals with test-qualifying symptoms, and factors associated with not testing. We analysed a cohort of untested symptomatic app users (N = 1,237), nested in the Zoe COVID Symptom Study (Zoe, N = 4,394,948); and symptomatic respondents who wanted, but did not have a test (N = 1,956), drawn from a Univers…

  • Attributes and predictors of long Covid

    Open Access•Carole H Sudre, Benjamin Murray et al.•ARTICLE•Nature Medicine•2021

  • Real-time tracking of self-reported symptoms to predict potential Covid-19

    Open Access•Cristina Menni, Ana M Valdes et al.•ARTICLE•Nature Medicine•2020

  • Risk of Covid-19 among front-line health-care workers and the general community

    Open Access•Long H Nguyen, David A Drew et al.•ARTICLE•The Lancet Public Health•2020

    BACKGROUND: Data for front-line health-care workers and risk of COVID-19 are limited. We sought to assess risk of COVID-19 among front-line health-care workers compared with the general community and the effect of personal protective equipment (PPE) on risk. METHODS: We did a prospective, observational cohort study in the UK and the USA of the general community, including front-line health-care workers, using self-reported data from the COVID Sym…

  • Genome-wide association study identifies 48 common genetic variants associated with handedness

    Open Access•Gabriel Cuellar-Partida, Joyce Y Tung et al.•ARTICLE•Nature Human Behaviour•2020•Citada por: 2•Referencias: 68

    Handedness has been extensively studied because of its relationship with language and the over-representation of left-handers in some neurodevelopmental disorders. Using data from the UK Biobank, 23andMe and the International Handedness Consortium, we conducted a genome-wide association meta-analysis of handedness (N = 1,766,671). We found 41 loci associated (P < 5 × 10−8) with left-handedness and 7 associated with ambidexterity. Tissue-enrichmen…

  • New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

    Open Access•E Evangelou, He Gao et al.•ARTICLE•Nature Human Behaviour•2019•Referencias: 85

    Excessive alcohol consumption is one of the main causes of death and disability worldwide. Alcohol consumption is a heritable complex trait. We conducted a meta-analysis of genome-wide association studies (GWAS) of gram/day (g/d) alcohol consumption in UK-Biobank, AlcGen and CHARGE+ consortia accumulating 480,842 people of European descent to decipher the genetic architecture of alcohol intake. We identified 46 novel, common loci, and investigate…

  • Does education attenuate the genetic risk of obesity? Evidence from U.K. Twins

    Open Access•Vikesh Amin, Paul Dunn et al.•ARTICLE•Economics & Human Biology•2018

  • Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

    Open Access•Lifelines Cohort Study, Aysu Okbay et al.•ARTICLE•Nature Genetics•2016

  • Genome-wide association study identifies 74 loci associated with educational attainment

    Open Access•Aysu Okbay, Jonathan P Beauchamp et al.•ARTICLE•Nature•2016

  • Genetic studies of body mass index yield new insights for obesity biology

    Open Access•The Lifelines Cohort Study, Adam E Locke et al.•ARTICLE•Nature•2015

  • Beyond the gene roundtable discussion

    Mandy Bloomfield, Peter J Garratt et al.•ARTICLE•Textual Practice•2015

    This virtual discussion between biomedical researchers and academics in the literary humanities took place in June–July 2013, through the medium of blog and email. The participants are Tim Spector (Genetic Epidemiology), Karen Temple (Medical Genetics), Angelique Richardson (Literary Studies), Deborah J.G. Mackay (Human Genetics) and Peter Garratt (Literary Studies). The conversation was initiated and convened by Mandy Bloomfield (Literary Studie…

  • Twins

    Open Access•Barbara Prainsack, Tim D Spector•ARTICLE•Social Science & Medicine•2006•Citada por: 2•Referencias: 27

  • Epigenetic differences arise during the lifetime of monozygotic twins

    Open Access•Mario F Fraga, Esteban Ballestar et al.•ARTICLE•Proceedings of the National…•2005

    Monozygous twins share a common genotype. However, most monozygotic twin pairs are not identical; several types of phenotypic discordance may be observed, such as differences in susceptibilities to disease and a wide range of anthropomorphic features. There are several possible explanations for these observations, but one is the existence of epigenetic differences. To address this issue, we examined the global and locus-specific differences in DN…

  • Heritability of Adult Body Height

    Karri Silventoinen, Sampo Sammalisto et al.•ARTICLE•The Marketing Review•2003

    A major component of variation in body height is due to genetic differences, but environmental factors have a substantial contributory effect. In this study we aimed to analyse whether the genetic architecture of body height varies between affluent western societies. We analysed twin data from eight countries comprising 30,111 complete twin pairs by using the univariate genetic model of the Mx statistical package. Body height and zygosity were se…

  • The potential and limitations of meta-analysis

    Tim D Spector, Simon G Thompson•ARTICLE•Journal of Epidemiology and…•1991•Citada por: 2•Referencias: 34

    We are currently wimessing an "epidemic" of meta-analyses and overviews in the scientific literature. This is a relatively new phenomenon and this article addresses some of the important issues raised by their increasing use. In particular the differing applications and limitations of meta- analysis are discussed, with a review of the analytic methods used and the problems and biases encountered

  • Genome-wide association study identifies 48 common genetic variants associated with handedness

    Open Access•Gabriel Cuellar-Partida, Joyce Y Tung et al.•ARTICLE•Nature Human Behaviour•2020•Citada por: 2•Referencias: 68

    Handedness has been extensively studied because of its relationship with language and the over-representation of left-handers in some neurodevelopmental disorders. Using data from the UK Biobank, 23andMe and the International Handedness Consortium, we conducted a genome-wide association meta-analysis of handedness (N = 1,766,671). We found 41 loci associated (P < 5 × 10−8) with left-handedness and 7 associated with ambidexterity. Tissue-enrichmen…

  • Twins

    Open Access•Barbara Prainsack, Tim D Spector•ARTICLE•Social Science & Medicine•2006•Citada por: 2•Referencias: 27

  • The potential and limitations of meta-analysis

    Tim D Spector, Simon G Thompson•ARTICLE•Journal of Epidemiology and…•1991•Citada por: 2•Referencias: 34

    We are currently wimessing an "epidemic" of meta-analyses and overviews in the scientific literature. This is a relatively new phenomenon and this article addresses some of the important issues raised by their increasing use. In particular the differing applications and limitations of meta- analysis are discussed, with a review of the analytic methods used and the problems and biases encountered

  • The potential and limitations of meta-analysis

    Tim D Spector, Simon G Thompson•ARTICLE•Journal of Epidemiology and…•1991•Citada por: 2•Referencias: 34

    We are currently wimessing an "epidemic" of meta-analyses and overviews in the scientific literature. This is a relatively new phenomenon and this article addresses some of the important issues raised by their increasing use. In particular the differing applications and limitations of meta- analysis are discussed, with a review of the analytic methods used and the problems and biases encountered

  • Heritability of Adult Body Height

    Karri Silventoinen, Sampo Sammalisto et al.•ARTICLE•The Marketing Review•2003

    A major component of variation in body height is due to genetic differences, but environmental factors have a substantial contributory effect. In this study we aimed to analyse whether the genetic architecture of body height varies between affluent western societies. We analysed twin data from eight countries comprising 30,111 complete twin pairs by using the univariate genetic model of the Mx statistical package. Body height and zygosity were se…

  • Epigenetic differences arise during the lifetime of monozygotic twins

    Open Access•Mario F Fraga, Esteban Ballestar et al.•ARTICLE•Proceedings of the National…•2005

    Monozygous twins share a common genotype. However, most monozygotic twin pairs are not identical; several types of phenotypic discordance may be observed, such as differences in susceptibilities to disease and a wide range of anthropomorphic features. There are several possible explanations for these observations, but one is the existence of epigenetic differences. To address this issue, we examined the global and locus-specific differences in DN…

  • Twins

    Open Access•Barbara Prainsack, Tim D Spector•ARTICLE•Social Science & Medicine•2006•Citada por: 2•Referencias: 27

  • Genetic studies of body mass index yield new insights for obesity biology

    Open Access•The Lifelines Cohort Study, Adam E Locke et al.•ARTICLE•Nature•2015

  • Beyond the gene roundtable discussion

    Mandy Bloomfield, Peter J Garratt et al.•ARTICLE•Textual Practice•2015

    This virtual discussion between biomedical researchers and academics in the literary humanities took place in June–July 2013, through the medium of blog and email. The participants are Tim Spector (Genetic Epidemiology), Karen Temple (Medical Genetics), Angelique Richardson (Literary Studies), Deborah J.G. Mackay (Human Genetics) and Peter Garratt (Literary Studies). The conversation was initiated and convened by Mandy Bloomfield (Literary Studie…

  • Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

    Open Access•Lifelines Cohort Study, Aysu Okbay et al.•ARTICLE•Nature Genetics•2016

  • Genome-wide association study identifies 74 loci associated with educational attainment

    Open Access•Aysu Okbay, Jonathan P Beauchamp et al.•ARTICLE•Nature•2016

  • Does education attenuate the genetic risk of obesity? Evidence from U.K. Twins

    Open Access•Vikesh Amin, Paul Dunn et al.•ARTICLE•Economics & Human Biology•2018

  • New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

    Open Access•E Evangelou, He Gao et al.•ARTICLE•Nature Human Behaviour•2019•Referencias: 85

    Excessive alcohol consumption is one of the main causes of death and disability worldwide. Alcohol consumption is a heritable complex trait. We conducted a meta-analysis of genome-wide association studies (GWAS) of gram/day (g/d) alcohol consumption in UK-Biobank, AlcGen and CHARGE+ consortia accumulating 480,842 people of European descent to decipher the genetic architecture of alcohol intake. We identified 46 novel, common loci, and investigate…

  • Real-time tracking of self-reported symptoms to predict potential Covid-19

    Open Access•Cristina Menni, Ana M Valdes et al.•ARTICLE•Nature Medicine•2020

  • Risk of Covid-19 among front-line health-care workers and the general community

    Open Access•Long H Nguyen, David A Drew et al.•ARTICLE•The Lancet Public Health•2020

    BACKGROUND: Data for front-line health-care workers and risk of COVID-19 are limited. We sought to assess risk of COVID-19 among front-line health-care workers compared with the general community and the effect of personal protective equipment (PPE) on risk. METHODS: We did a prospective, observational cohort study in the UK and the USA of the general community, including front-line health-care workers, using self-reported data from the COVID Sym…

  • Genome-wide association study identifies 48 common genetic variants associated with handedness

    Open Access•Gabriel Cuellar-Partida, Joyce Y Tung et al.•ARTICLE•Nature Human Behaviour•2020•Citada por: 2•Referencias: 68

    Handedness has been extensively studied because of its relationship with language and the over-representation of left-handers in some neurodevelopmental disorders. Using data from the UK Biobank, 23andMe and the International Handedness Consortium, we conducted a genome-wide association meta-analysis of handedness (N = 1,766,671). We found 41 loci associated (P < 5 × 10−8) with left-handedness and 7 associated with ambidexterity. Tissue-enrichmen…

  • Attributes and predictors of long Covid

    Open Access•Carole H Sudre, Benjamin Murray et al.•ARTICLE•Nature Medicine•2021

  • Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

    Open Access•Aysu Okbay, Yeda Wu et al.•ARTICLE•Nature Genetics•2022

    We conduct a genome-wide association study (GWAS) of educational attainment (EA) in a sample of ~3 million individuals and identify 3,952 approximately uncorrelated genome-wide-significant single-nucleotide polymorphisms (SNPs). A genome-wide polygenic predictor, or polygenic index (PGI), explains 12–16% of EA variance and contributes to risk prediction for ten diseases. Direct effects (i.e., controlling for parental PGIs) explain roughly half th…

  • Knowledge barriers in a national symptomatic-Covid-19 testing programme

    Open Access•Mark S Graham, Anna May et al.•ARTICLE•PLOS Global Public Health•2022

    Symptomatic testing programmes are crucial to the COVID-19 pandemic response. We sought to examine United Kingdom (UK) testing rates amongst individuals with test-qualifying symptoms, and factors associated with not testing. We analysed a cohort of untested symptomatic app users (N = 1,237), nested in the Zoe COVID Symptom Study (Zoe, N = 4,394,948); and symptomatic respondents who wanted, but did not have a test (N = 1,956), drawn from a Univers…

Biology (10 obras) · Genetic Associations and Epidemiology (7 obras) · Medicine (7 obras) · Gene (6 obras) · Genotype (6 obras) · Genetics (5 obras) · Genome-wide association study (5 obras) · Single-nucleotide polymorphism (5 obras) · Birth, Development, and Health (4 obras) · Demography (4 obras)

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