Sigve Nakken
Sigve Nakken
Scientist, Institute for Cancer Research, Oslo University Hospital, Norway
Geverifieerd e-mailadres voor ifi.uio.no
Titel
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Jaar
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
2722017
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
2242015
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
2102018
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
892010
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
782017
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
652019
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), 2020
642020
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
492007
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
452009
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
382009
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), 18, 2017
342017
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
332009
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
292013
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
252012
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
222016
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
212019
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
212015
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
202018
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
142017
Personal Cancer Genome Reporter: variant interpretation report for precision oncology
S Nakken, G Fournous, D Vodàk, LB Aasheim, O Myklebost, E Hovig
Bioinformatics, 2017
132017
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