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Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland
by
Rydzewska, Kamila
, Posiadło, Konrad
, van de Wetering, Thierry
, Marciniak, Błażej
, Clark, Jeremy S. C.
, Strapagiel, Dominik
, Ciechanowicz, Andrzej
, Kaczmarczyk, Mariusz
, Żądzińska, Elżbieta
, Boroń, Agnieszka
in
631/208/721
/ 692/308/53
/ 692/53
/ Artificial chromosomes
/ Case-Control Studies
/ Child
/ Children
/ Chromosome 17
/ Environmental protection
/ Female
/ Fertility
/ Genetic Predisposition to Disease
/ Genomes
/ Genotype
/ Genotype & phenotype
/ Heterozygotes
/ Homozygotes
/ Humanities and Social Sciences
/ Humans
/ Inversion
/ Male
/ Mathematical models
/ multidisciplinary
/ Phenotype
/ Poland
/ Polymorphism, Single Nucleotide
/ Population
/ Science
/ Science (multidisciplinary)
/ Sexes
/ Single-nucleotide polymorphism
/ Statistical analysis
/ Statistical models
2022
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Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland
by
Rydzewska, Kamila
, Posiadło, Konrad
, van de Wetering, Thierry
, Marciniak, Błażej
, Clark, Jeremy S. C.
, Strapagiel, Dominik
, Ciechanowicz, Andrzej
, Kaczmarczyk, Mariusz
, Żądzińska, Elżbieta
, Boroń, Agnieszka
in
631/208/721
/ 692/308/53
/ 692/53
/ Artificial chromosomes
/ Case-Control Studies
/ Child
/ Children
/ Chromosome 17
/ Environmental protection
/ Female
/ Fertility
/ Genetic Predisposition to Disease
/ Genomes
/ Genotype
/ Genotype & phenotype
/ Heterozygotes
/ Homozygotes
/ Humanities and Social Sciences
/ Humans
/ Inversion
/ Male
/ Mathematical models
/ multidisciplinary
/ Phenotype
/ Poland
/ Polymorphism, Single Nucleotide
/ Population
/ Science
/ Science (multidisciplinary)
/ Sexes
/ Single-nucleotide polymorphism
/ Statistical analysis
/ Statistical models
2022
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Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland
by
Rydzewska, Kamila
, Posiadło, Konrad
, van de Wetering, Thierry
, Marciniak, Błażej
, Clark, Jeremy S. C.
, Strapagiel, Dominik
, Ciechanowicz, Andrzej
, Kaczmarczyk, Mariusz
, Żądzińska, Elżbieta
, Boroń, Agnieszka
in
631/208/721
/ 692/308/53
/ 692/53
/ Artificial chromosomes
/ Case-Control Studies
/ Child
/ Children
/ Chromosome 17
/ Environmental protection
/ Female
/ Fertility
/ Genetic Predisposition to Disease
/ Genomes
/ Genotype
/ Genotype & phenotype
/ Heterozygotes
/ Homozygotes
/ Humanities and Social Sciences
/ Humans
/ Inversion
/ Male
/ Mathematical models
/ multidisciplinary
/ Phenotype
/ Poland
/ Polymorphism, Single Nucleotide
/ Population
/ Science
/ Science (multidisciplinary)
/ Sexes
/ Single-nucleotide polymorphism
/ Statistical analysis
/ Statistical models
2022
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Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland
Journal Article
Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland
2022
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Overview
Number of children is an important human trait and studies have indicated associations with single-nucleotide polymorphisms (SNPs). Aim: to give further evidence for four associations using a large sample of Polish subjects. Data from the POPULOUS genetic database was provided from anonymous, healthy, unrelated, Polish volunteers of both sexes (N = 5760). SNPs (n = 173) studied: (a) 69 from the chromosome 17 H1/H2 inversion; (b) six from 1q21.3, 5q21.3 and 14q21.2; and (c) 98 random negative controls. Zero-inflated negative-binomial regression (z.i.) was performed (0–3 numbers of children per individual (NCI) set as non-events; adjustors: year of birth, sex). Significance level
p
= 0.05 with Bonferroni correction. Statistically-significant differences (with data from both sexes combined) were obtained from highly-linked inversion SNPs: representative rs12373123 gave means: homozygotes TT: 2.31 NCI (n = 1418); heterozygotes CT: 2.35 NCI (n = 554); homozygotes CC: 2.44 NCI (n = 43) (genotype
p
= 0.01; TTvs.CC
p
= 0.004; CTvs.CC
p
= 0.009). (Male data alone gave similar results.) Recessive modeling indicated that H2-homozygotes had 0.118 more children than H1-homozygotes + heterozygotes (z.i.-count estimates ± standard errors: CT, − 0.508 ± 0.194; TT, − 0.557 ± 0.191). The non-over-dispersed count model detected no interactions: of importance there was no significant interaction with age. No positive results were obtained from negative-control SNPs or (b). Conclusions: association between the H1/H2 inversion and numbers of children (previously reported in Iceland) has been confirmed, albeit using a different statistical model. One limitation is the small amount of data, despite initially ~ 6000 subjects. Causal studies require further investigation.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
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