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Lon R Cardon

Biographic Data

ID5757740
NAMELon R Cardon
GIVEN NAMESLon R
FAMILY NAMECardon
SIGNATURECARDON L R
AFFILIATIONSGenetics of Complex Traits, Institute of Biomedical and Clinical Science, Peninsula Medical School, Magdalen Road, Exeter, UK.
VERIFIEDNo
TOTAL WORKS5
TOTAL CITATIONS6
AUTHOR COUNT5
EDITOR COUNT0
FIRST PUBLICATION YEAR1992
LATEST PUBLICATION YEAR2009
H-INDEX1
  • Finding the missing heritability of complex diseases

    Open Access•Teri A Manolio, Francis S Collins et al.•ARTICLE•Nature•2009

  • A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity

    Open Access•Timothy M Frayling, Nicholas John Timpson et al.•ARTICLE•Science•2007

    Obesity is a serious international health problem that increases the risk of several common diseases. The genetic factors predisposing to obesity are poorly understood. A genome-wide search for type 2 diabetesâ susceptibility genes identified a common variant in the FTO (fat mass and obesity associated) gene that predisposes to diabetes through an effect on body mass index (BMI). An additive association of the variant with BMI was replicated in 1…

  • The International HapMap Project

    Open Access•Richard A Gibbs, John W Belmont et al.•ARTICLE•Nature•2003

    The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. An international consortium is developing a map of these patterns across the genome by determining the genotypes of one million or more sequence variants, their frequencies and the degree of association between them, in DNA samples from populations with a…

  • Methodology for Genetic Studies of Twins and Families

    Open Access•Michael C Neale, Lon R Cardon et al.•BOOK•Methodology for Genetic Studies…•1992

  • Continuity and change in general cognitive ability from 1 to 7 years of age

    Lon R Cardon, David W Fulker et al.•ARTICLE•Developmental Psychology•1992•Cited by: 6•References: 1

    Observed and latent sources of individual differences in cognitive development were explored in data from adopted and nonadopted siblings measured from 12 months to 7 years and identical and nonidentical twins measured from 12 to 36 months. Longitudinal path models, designed to examine the structure of observed stability and assess the genetic and environmental sources of age-to-age change and continuity, suggest that observed continuity arises f…

  • Continuity and change in general cognitive ability from 1 to 7 years of age

    Lon R Cardon, David W Fulker et al.•ARTICLE•Developmental Psychology•1992•Cited by: 6•References: 1

    Observed and latent sources of individual differences in cognitive development were explored in data from adopted and nonadopted siblings measured from 12 months to 7 years and identical and nonidentical twins measured from 12 to 36 months. Longitudinal path models, designed to examine the structure of observed stability and assess the genetic and environmental sources of age-to-age change and continuity, suggest that observed continuity arises f…

  • Methodology for Genetic Studies of Twins and Families

    Open Access•Michael C Neale, Lon R Cardon et al.•BOOK•Methodology for Genetic Studies…•1992

  • Continuity and change in general cognitive ability from 1 to 7 years of age

    Lon R Cardon, David W Fulker et al.•ARTICLE•Developmental Psychology•1992•Cited by: 6•References: 1

    Observed and latent sources of individual differences in cognitive development were explored in data from adopted and nonadopted siblings measured from 12 months to 7 years and identical and nonidentical twins measured from 12 to 36 months. Longitudinal path models, designed to examine the structure of observed stability and assess the genetic and environmental sources of age-to-age change and continuity, suggest that observed continuity arises f…

  • The International HapMap Project

    Open Access•Richard A Gibbs, John W Belmont et al.•ARTICLE•Nature•2003

    The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. An international consortium is developing a map of these patterns across the genome by determining the genotypes of one million or more sequence variants, their frequencies and the degree of association between them, in DNA samples from populations with a…

  • A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity

    Open Access•Timothy M Frayling, Nicholas John Timpson et al.•ARTICLE•Science•2007

    Obesity is a serious international health problem that increases the risk of several common diseases. The genetic factors predisposing to obesity are poorly understood. A genome-wide search for type 2 diabetesâ susceptibility genes identified a common variant in the FTO (fat mass and obesity associated) gene that predisposes to diabetes through an effect on body mass index (BMI). An additive association of the variant with BMI was replicated in 1…

  • Finding the missing heritability of complex diseases

    Open Access•Teri A Manolio, Francis S Collins et al.•ARTICLE•Nature•2009

Biology (4 works) · Evolutionary biology (4 works) · Genetic Associations and Epidemiology (4 works) · Gene (3 works) · Genetics (3 works) · Genotype (3 works) · Cognitive Abilities and Testing (2 works) · Computational biology (2 works) · Computer Science (2 works) · Genome-wide association study (2 works)

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