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The obesity associated FTO gene variant and the risk of adverse pregnancy outcomes: Evidence from the SCOPE study
MMP-2 gene polymorphisms are associated with type A aortic dissection and aortic diameters in patients
Methylome analysis for spina bifida shows SOX18 hypomethylation as a risk factor with evidence for a complex (epi)genetic interplay to affect neural tube development
Hypermethylation of AKT2 gene is associated with neural-tube defects in fetus
New evidence for involvement of ESR1 gene in susceptibility to Chinese migraine
Variants in the CNR1 gene predispose to headache with nausea in the presence of life stress
Age at menarche and age at natural menopause in East Asian women: a genome-wide association study
The impact of ERBB-family germline single nucleotide polymorphisms on survival response to adjuvant trastuzumab treatment in HER2-positive breast cancer
Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples
Genomic Characterisation and Response to Trastuzumab and Paclitaxel in Advanced or Recurrent HER2-positive Endometrial Carcinoma