{{Rsnum
|rsid=12325817
|Gene=PEMT
|Chromosome=17
|position=17583205
|Orientation=plus
|GMAF=0.2883
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=PEMT
}}{{PMID Auto
|PMID=20662904
|Title=Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts
}}
{{PMID Auto
|PMID=21059658
|Title=Aberrant estrogen regulation of PEMT results in choline deficiency-associated liver dysfunction
|OA=1
}}
{{PMID Auto
|PMID=21411618
|Title=Docosahexaenoic acid in plasma phosphatidylcholine may be a potential marker for in vivo phosphatidylethanolamine N-methyltransferase activity in humans
|OA=1
}}{{PMID Auto
|PMID=16816108
|Title=Common genetic polymorphisms affect the human requirement for the nutrient choline.
|OA=1
}}

{{PMID Auto
|PMID=17613168
|Title=Gene response elements, genetic polymorphisms and epigenetics influence the human dietary requirement for choline.
|OA=1
}}

{{PMID Auto
|PMID=17616785
|Title=Lymphocyte gene expression in subjects fed a low-choline diet differs between those who develop organ dysfunction and those who do not.
|OA=1
}}

{{PMID Auto
|PMID=18230680
|Title=Choline metabolism and risk of breast cancer in a population-based study.
|OA=1
}}

{{PMID Auto
|PMID=18789905
|Title=Genetic polymorphisms in methyl-group metabolism and epigenetics: lessons from humans and mouse models.
|OA=1
}}

{{PMID Auto
|PMID=19116320
|Title=Importance of methyl donors during reproduction.
|OA=1
}}

{{PMID Auto
|PMID=19167960
|Title=Genetic variants in phosphatidylethanolamine N-methyltransferase and methylenetetrahydrofolate dehydrogenase influence biomarkers of choline metabolism when folate intake is restricted.
|OA=1
}}

{{PMID Auto
|PMID=19261726
|Title=Epigenetic mechanisms for nutrition determinants of later health outcomes.
|OA=1
}}

{{PMID Auto
|PMID=20861172
|Title=Dietary choline requirements of women: effects of estrogen and genetic variation.
|OA=1
}}{{PMID Auto
|PMID=23794489
|Title=Higher homocysteine and lower betaine increase the risk of microangiopathy in patients with diabetes mellitus carrying the GG genotype of PEMT G774C.
}}