Prenatal famine and genetic variation are independently and additively associated with DNA methylation at regulatory loci within IGF2/H19.

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Prenatal famine and genetic variation are independently and additively associated with DNA methylation at regulatory loci within IGF2/H19. is …
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scholarly articleQ13442814

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P819ADS bibcode2012PLoSO...737933T
P356DOI10.1371/JOURNAL.PONE.0037933
P932PMC publication ID3364289
P698PubMed publication ID22666415
P5875ResearchGate publication ID225187305

P50authorEline SlagboomQ5361119
Aryeh D. SteinQ39184297
Elmar W TobiQ49706135
Hein PutterQ53547246
Jenny van DongenQ55426346
Bastiaan T HeijmansQ87686234
Dennis KremerQ114300760
P2093author name stringL H Lumey
P2860cites workIntegrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locusQ21136048
Periconceptional maternal folic acid use of 400 microg per day is related to increased methylation of the IGF2 gene in the very young childQ21142704
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DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specificQ24656230
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Associations of IGF2 ApaI RFLP and INS VNTR class I allele size with obesityQ47253004
Paternal allele of IGF2 gene haplotype CTG is associated with fetal and placental growth in JapaneseQ47951370
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human.Q48096674
The insulin gene variable number of tandem repeat: associations and interactions with childhood body fat mass and insulin secretion in normal children.Q51500201
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Epigenetics as a unifying principle in the aetiology of complex traits and diseases.Q51849916
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The culture of zygotes to the blastocyst stage changes the postnatal expression of an epigentically labile allele, agouti viable yellow, in mice.Q51953924
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INS VNTR class genotype and the function of isolated human islets.Q54400663
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Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locusQ58201304
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Loss of IGF2 imprinting: a potential marker of colorectal cancer riskQ73128690
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Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2Q78532732
Heritable rather than age-related environmental and stochastic factors dominate variation in DNA methylation of the human IGF2/H19 locusQ79879933
Association between paternally inherited haplotypes upstream of the insulin gene and umbilical cord IGF-II levelsQ80714979
Hypermethylation of the IGF2 differentially methylated region 2 is a specific event in insulinomas leading to loss-of-imprinting and overexpressionQ84013932
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue5
P407language of work or nameEnglishQ1860
P921main subjectgenetic variationQ349856
DNA methylationQ874745
P304page(s)e37933
P577publication date2012-05-30
P1433published inPLOS OneQ564954
P1476titlePrenatal famine and genetic variation are independently and additively associated with DNA methylation at regulatory loci within IGF2/H19
P478volume7

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