about
Large-scale inference of the point mutational spectrum in human segmental duplicationsBRAF V600E mutation in early-stage multiple myeloma: good response to broad acting drugs and no relation to prognosisAutomated amplicon design suitable for analysis of DNA variants by melting techniques.A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes.GSuite HyperBrowser: integrative analysis of dataset collections across the genome and epigenomeCellLineMiner: a knowledge portal for human cell lines.Unstable DNA repair genes shaped by their own sequence modifying phenotypes.Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses.Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database.Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database.Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome databaseColorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report.The disruptive positions in human G-quadruplex motifs are less polymorphic and more conserved than their neutral counterparts.Personal Cancer Genome Reporter: variant interpretation report for precision oncology.Sequencing of FTO and ALKBH5 in men undergoing infertility work-up identifies an infertility-associated variant and two missense mutations.Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families.Identification of genetic variants for clinical management of familial colorectal tumors.Sample-Index Misassignment Impacts Tumour Exome Sequencing.Implementing precision cancer medicine in the public health services of Norway: the diagnostic infrastructure and a cost estimate.Patterns of genomic evolution in advanced melanoma.Impact of DNA physical properties on local sequence bias of human mutationLack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database reportIntegrative genomic analysis of peritoneal malignant mesothelioma: understanding a case with extraordinary chemotherapy responseResults of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testingCancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMutational dynamics and immune evasion in diffuse large B-cell lymphoma explored in a relapse-enriched patient series
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Sigve Nakken
@ast
Sigve Nakken
@en
Sigve Nakken
@es
Sigve Nakken
@nl
Sigve Nakken
@sl
type
label
Sigve Nakken
@ast
Sigve Nakken
@en
Sigve Nakken
@es
Sigve Nakken
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Sigve Nakken
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prefLabel
Sigve Nakken
@ast
Sigve Nakken
@en
Sigve Nakken
@es
Sigve Nakken
@nl
Sigve Nakken
@sl
P106
P31
P496
0000-0001-8468-2050