about
Genome-wide meta-analysis identifies new susceptibility loci for migraine.Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraineDetection of tmRNA molecules on microarrays at low temperatures using helper oligonucleotidesDetection of NASBA amplified bacterial tmRNA molecules on SLICSel designed microarray probesDistribution and medical impact of loss-of-function variants in the Finnish founder population.A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(®) for methylome profiling.De novo mutations in schizophrenia implicate synaptic networksStructural genomic variation as risk factor for idiopathic recurrent miscarriage.The GENCODE exome: sequencing the complete human exomeHaplotype phasing and inheritance of copy number variants in nuclear families.Genetic analysis for a shared biological basis between migraine and coronary artery disease.Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications.Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United KingdomEnrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations.Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study.Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel.Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type-specific hypomethylated regions.Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia.Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies.Evaluation of the 124-plex SNP typing microarray for forensic testing.Comparison of DNA extraction methods for multiplex polymerase chain reaction.Analysis of shared heritability in common disorders of the brainCommon Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesErratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraineCommon Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesApplication of two different microarray-based copy-number detection methodologies – array-comparative genomic hybridization and array-multiplex amplifiable probe hybridization – with identical amplifiable target sequencesArray-MAPH: a methodology for the detection of locus copy-number changes in complex genomesDetection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridizationTAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule countingA molecular tool for menstrual cycle phase dating of endometrial samples in endometriosis transcriptome studies†Genetic architecture of human plasma lipidome and its link to cardiovascular diseaseCreating basis for introducing non-invasive prenatal testing in the Estonian public health settingComputational framework for targeted high-coverage sequencing based NIPT
P50
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P50
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hulumtues
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Priit Palta
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P106
P21
P31
P496
0000-0001-9320-7008
P569
2000-01-01T00:00:00Z