[PMID 19841875] Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the DESIR prospective study

[PMID 15637659] Linkage disequilibrium patterns and tagSNP transferability among European populations.

[PMID 16262891] Aging syndrome genes and premature coronary artery disease.

[PMID 17327437] Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population: studies of 7,495 Danish whites.

[PMID 17327460] Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects.

[PMID 17327461] Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome: case-control and quantitative trait studies.

[PMID 17994215] Evaluating the association of common LMNA variants with type 2 diabetes and quantitative metabolic phenotypes in French Europids.

[PMID 20501691] LMNA rs4641 and the muscle lamin A and C isoforms in twins--metabolic implications and transcriptional regulation.

[PMID 24831476] [Association between LMNA mutation and familial and idiopathic dilated cardiomyopathy patients in Xinjiang]

[PMID 26634508] Association of the LMNA gene single nucleotide polymorphism rs4641 with bdilated cardiomyopathy.


Parent Gene: LMNA

Importance: 1
Less common allele: T = 22%
More common allele: C = 78%
My Genotype: Log In