Contemporary management of TMJ involvement in JIA patients and its orofacial consequencesGenetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control studySusceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients.Genome-wide association and functional follow-up reveals new loci for kidney functionDe novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disorders.Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta.Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.Common variants in Mendelian kidney disease genes and their association with renal function.Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays.MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.ROS1 Asp2213Asn polymorphism is not associated with coronary artery disease in a Greek case-control study.Analysis of allele and haplotype diversity across 25 genomic regions in three Eastern European populations.Association study of 90 candidate gene polymorphisms in panic disorder.Exome analysis in an Estonian multiplex family with neural tube defects-a case report.De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion.Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.Evaluation of the 124-plex SNP typing microarray for forensic testing.Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients
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