List of works - Tiit Nikopensius

Analysis of allele and haplotype diversity across 25 genomic regions in three Eastern European populations

scientific article published in April 2009

Association study of 90 candidate gene polymorphisms in panic disorder

scientific article

Common variants in Mendelian kidney disease genes and their association with renal function

scientific article published on 12 September 2013

Contemporary management of TMJ involvement in JIA patients and its orofacial consequences

scientific article

De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disorders

scientific article

De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion

scientific article published on 3 December 2015

Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays

scientific article published on 5 June 2008

Evaluation of the 124-plex SNP typing microarray for forensic testing

scientific article

Exome analysis in an Estonian multiplex family with neural tube defects-a case report

scientific article

Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study

scientific article

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

scientific article

Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate

scientific article published in September 2010

Genome-wide association and functional follow-up reveals new loci for kidney function

scientific article

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

scientific article published on 8 September 2012

MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate

scientific article published on June 2010

ROS1 Asp2213Asn polymorphism is not associated with coronary artery disease in a Greek case-control study

scientific article published in January 2009

Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients

article published in 2009

Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients

scientific article

Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta

scientific article published on 10 May 2015

List of works by Tiit Nikopensius

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

Common variants in Mendelian kidney disease genes and their association with renal function

Contemporary management of TMJ involvement in JIA patients and its orofacial consequences

De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disorders

De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion

Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays

Evaluation of the 124-plex SNP typing microarray for forensic testing

Exome analysis in an Estonian multiplex family with neural tube defects-a case report

Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate

Genome-wide association and functional follow-up reveals new loci for kidney function

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

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

Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients

Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients

Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta