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Single Nucleotide Polymorphisms in Thyroid Hormone Transporter Genes MCT8, MCT10 and Deiodinase DIO2 Contribute to Inter-Individual Variance of Executive Functions and Personality Traits
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene
Insights into malaria susceptibility using genome-wide data on 17,000 individuals from Africa, Asia and Oceania
TRPM8 genetic variant is associated with chronic migraine and allodynia
PCSK9 E670G polymorphism increases risk of coronary artery disease in a Chinese Han population
Evaluation of the relationships of the WBP1L gene with schizophrenia and the general psychopathology scale based on a case–control study
Transcription Factor Enrichment Analysis in Enhancers Identifies EZH2 as A Susceptibility Gene for Osteoporosis
Single nucleotide polymorphisms associated with susceptibility for development of colorectal cancer: Case-control study in a Basque population
A novel multi‐locus genetic risk score identifies patients with higher risk of generalized aggressive periodontitis
Imprinting aberrations of SNRPN, ZAC1 and INPP5F genes involved in the pathogenesis of congenital heart disease with extracardiac malformations