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Family-based association study of IGF1 microsatellites and height, weight, and body mass index
by
Ozcelik, Hilmi
, Knight, Julia A
, Dite, Gillian S
, Boyd, Norman F
, Fehringer, Gordon
, Southey, Melissa C
, Hopper, John L
, Paterson, Andrew D
, Giles, Graham G
, Andrulis, Irene L
in
631/208/205
/ 631/208/726/649
/ Adult
/ Alleles
/ Biomedical and Life Sciences
/ Biomedicine
/ Body Height
/ Body Mass Index
/ Body Size
/ Body Weight
/ Chronic illnesses
/ Dinucleotide Repeats - genetics
/ Family Health
/ Female
/ Gene Expression
/ Gene Frequency
/ Gene Function
/ Gene Therapy
/ Genetic diversity
/ Genome-Wide Association Study
/ Genotype
/ Haplotypes
/ Human Genetics
/ Humans
/ Insulin
/ Insulin-like growth factor I
/ Insulin-Like Growth Factor I - genetics
/ Insulin-like growth factors
/ Male
/ Microsatellites
/ Middle Aged
/ Molecular Medicine
/ Physical growth
/ Polymorphism, Single Nucleotide
/ Premenopause
/ short-communication
2010
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Family-based association study of IGF1 microsatellites and height, weight, and body mass index
by
Ozcelik, Hilmi
, Knight, Julia A
, Dite, Gillian S
, Boyd, Norman F
, Fehringer, Gordon
, Southey, Melissa C
, Hopper, John L
, Paterson, Andrew D
, Giles, Graham G
, Andrulis, Irene L
in
631/208/205
/ 631/208/726/649
/ Adult
/ Alleles
/ Biomedical and Life Sciences
/ Biomedicine
/ Body Height
/ Body Mass Index
/ Body Size
/ Body Weight
/ Chronic illnesses
/ Dinucleotide Repeats - genetics
/ Family Health
/ Female
/ Gene Expression
/ Gene Frequency
/ Gene Function
/ Gene Therapy
/ Genetic diversity
/ Genome-Wide Association Study
/ Genotype
/ Haplotypes
/ Human Genetics
/ Humans
/ Insulin
/ Insulin-like growth factor I
/ Insulin-Like Growth Factor I - genetics
/ Insulin-like growth factors
/ Male
/ Microsatellites
/ Middle Aged
/ Molecular Medicine
/ Physical growth
/ Polymorphism, Single Nucleotide
/ Premenopause
/ short-communication
2010
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Do you wish to request the book?
Family-based association study of IGF1 microsatellites and height, weight, and body mass index
by
Ozcelik, Hilmi
, Knight, Julia A
, Dite, Gillian S
, Boyd, Norman F
, Fehringer, Gordon
, Southey, Melissa C
, Hopper, John L
, Paterson, Andrew D
, Giles, Graham G
, Andrulis, Irene L
in
631/208/205
/ 631/208/726/649
/ Adult
/ Alleles
/ Biomedical and Life Sciences
/ Biomedicine
/ Body Height
/ Body Mass Index
/ Body Size
/ Body Weight
/ Chronic illnesses
/ Dinucleotide Repeats - genetics
/ Family Health
/ Female
/ Gene Expression
/ Gene Frequency
/ Gene Function
/ Gene Therapy
/ Genetic diversity
/ Genome-Wide Association Study
/ Genotype
/ Haplotypes
/ Human Genetics
/ Humans
/ Insulin
/ Insulin-like growth factor I
/ Insulin-Like Growth Factor I - genetics
/ Insulin-like growth factors
/ Male
/ Microsatellites
/ Middle Aged
/ Molecular Medicine
/ Physical growth
/ Polymorphism, Single Nucleotide
/ Premenopause
/ short-communication
2010
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Family-based association study of IGF1 microsatellites and height, weight, and body mass index
Journal Article
Family-based association study of IGF1 microsatellites and height, weight, and body mass index
2010
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Overview
Height, weight, and body mass index (BMI) are partly heritable, known to be associated with chronic diseases, and are linked to circulating insulin-like growth factor I (IGF-I) concentrations. IGF-I concentrations are also partly heritable and thus genetic variation at
IGF1
could influence height, weight, BMI and the risk of developing chronic diseases. Our objective was to examine the association of genetic variation at
IGF1
with height, weight and BMI using a sample of premenopausal women. A family-based study design was used to investigate the association of three
IGF1
CA repeat variants at 5′ (5′CA), intron 2 (In2CA) and 3′ (3′CA) with these anthropometric measures. We analyzed the data for 827 families of different sizes and configurations, which included 1520 premenopausal women. Nominally significant associations (
P
⩽0.05) were found for a rare 3′ variant allele (3′CA-193) and BMI (
P
=0.05), and for the more common 3′CA-187 allele and weight (
P
=0.04). These associations did not remain significant when adjusted for multiple comparisons. Haplotype analysis did not support an association between these variants and anthropometric measures. This study does not support an association between
IGF1
and these anthropometric measures. Study limitations, including sample size and capturing genetic variation at
IGF1
with these markers, could mean associations were missed.
Publisher
Nature Publishing Group UK,Nature Publishing Group
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