Sigve Nakken
Sigve Nakken
Scientist, Institute for Cancer Research, Oslo University Hospital, Norway
Verified email at
Cited by
Cited by
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
P Møller, T Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 66 (3), 464-472, 2017
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
P Møller, TT Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 67 (7), 1306-1316, 2018
A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing
TS Alioto, I Buchhalter, S Derdak, B Hutter, MD Eldridge, E Hovig, ...
Nature Communications 6, 2015
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
M Dominguez-Valentin, JR Sampson, TT Seppälä, SW Ten Broeke, ...
Genetics in Medicine 22 (1), 15-25, 2020
Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen
MP Menden, D Wang, MJ Mason, B Szalai, KC Bulusu, Y Guan, T Yu, ...
Nature communications 10 (1), 1-17, 2019
Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database
P Møller, T Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 66 (9), 1657-1664, 2017
Variants of the genes encoding AQP4 and Kir4. 1 are associated with subgroups of patients with temporal lobe epilepsy
K Heuser, EA Nagelhus, E Taubøll, U Indahl, PR Berg, S Lien, S Nakken, ...
Epilepsy Research 88 (1), 55-64, 2010
Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report
T Seppälä, K Pylvänäinen, DG Evans, H Järvinen, L Renkonen-Sinisalo, ...
Hereditary cancer in clinical practice 15 (1), 1-10, 2017
The disruptive positions in human G-quadruplex motifs are less polymorphic and more conserved than their neutral counterparts
S Nakken, T Rognes, E Hovig
Nucleic Acids Research, gkp590, 2009
Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes
S Nakken, I Alseth, T Rognes
Neuroscience 145 (4), 1273-1279, 2007
Patterns of genomic evolution in advanced melanoma
E Birkeland, S Zhang, D Poduval, J Geisler, S Nakken, D Vodak, ...
Nature communications 9 (1), 1-12, 2018
Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses
ØL Holla, S Nakken, M Mattingsdal, T Ranheim, KE Berge, JC Defesche, ...
Molecular Genetics and Metabolism 96 (4), 245-252, 2009
Sequencing of FTO and ALKBH5 in men undergoing infertility work-up identifies an infertility-associated variant and two missense mutations
M Landfors, S Nakken, M Fusser, JA Dahl, A Klungland, P Fedorcsak
Fertility and Sterility 105 (5), 1170-1179. e5, 2016
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
TT Seppälä, A Ahadova, M Dominguez-Valentin, F Macrae, DG Evans, ...
Hereditary cancer in clinical practice 17 (1), 1-8, 2019
ABCB4 sequence variations in young adults with cholesterol gallstone disease
KE Nakken, KJ Labori, OK Rødningen, S Nakken, KE Berge, K Eiklid, ...
Liver International 29 (5), 743-747, 2009
BRAF V600E mutation in early-stage multiple myeloma: good response to broad acting drugs and no relation to prognosis
EH Rustad, HY Dai, H Hov, E Coward, V Beisvag, O Myklebost, E Hovig, ...
Blood Cancer Journal 5 (3), e299, 2015
Is the brain water channel aquaporin‐4 a pathogenetic factor in idiopathic intracranial hypertension? Results from a combined clinical and genetic study in a Norwegian cohort
E Kerty, K Heuser, UG Indahl, PR Berg, S Nakken, S Lien, SW Omholt, ...
Acta ophthalmologica 91 (1), 88-91, 2013
A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions
KK Selmer, GD Gilfillan, P Strømme, R Lyle, T Hughes, HS Hjorthaug, ...
European journal of human genetics 20 (1), 58-63, 2012
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
M Dominguez-Valentin, TT Seppälä, JR Sampson, F Macrae, I Winship, ...
Hereditary cancer in clinical practice 17 (1), 1-6, 2019
GSuite HyperBrowser: integrative analysis of dataset collections across the genome and epigenome
B Simovski, D Vodák, S Gundersen, D Domanska, A Azab, L Holden, ...
Gigascience 6 (7), gix032, 2017
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