Sigve Nakken
Førsteamanuensis
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Senter for bioinformatikk
English version of this page
E-post
sigven@ifi.uio.no
Mobiltelefon
+47 95753022
Brukernavn
Besøksadresse
Gaustadalleen 23 B
Ole Johan Dahls hus
0373 Oslo
Postadresse
Postboks 1080, Blindern
0316 Oslo
Publikasjoner
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Møller, Pål; Seppälä, Toni T.; Ahadova, Aysel; Crosbie, Emma J.; Holinski-Feder, Elke & Scott, Rodney [Vis alle 49 forfattere av denne artikkelen] (2023). Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement. Hereditary Cancer in Clinical Practice. ISSN 1731-2302. 21(1), s. 1–12. doi: 10.1186/s13053-023-00263-3. Fulltekst i vitenarkiv
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Namløs, Heidi Maria; Khelik, Ksenia; Nakken, Sigve; Vodak, Daniel; Hovig, Eivind & Myklebost, Ola [Vis alle 8 forfattere av denne artikkelen] (2023). Chromosomal instability and a deregulated cell cycle are intrinsic features of high-risk gastrointestinal stromal tumours with a metastatic potential. Molecular Oncology. ISSN 1574-7891. 17(11), s. 2432–2450. doi: 10.1002/1878-0261.13514. Fulltekst i vitenarkiv
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Nakken, Sigve; Gundersen, Sveinung; Bernal, Fabian Leonardo Martinez; Polychronopoulos, Dimitris; Hovig, Eivind & Wesche, Jørgen (2023). Comprehensive interrogation of gene lists from genome-scale cancer screens with oncoEnrichR. International Journal of Cancer. ISSN 0020-7136. 153(10), s. 1819–1828. doi: 10.1002/ijc.34666. Fulltekst i vitenarkiv
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Dominguez-Valentin, Mev; Haupt, Saskia; Seppälä, Toni T.; Sampson, Julian R.; Sunde, Lone & Bernstein, Inge [Vis alle 116 forfattere av denne artikkelen] (2023). Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database. EClinicalMedicine. ISSN 2589-5370. 58. doi: 10.1016/j.eclinm.2023.101909.
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Hanes, Robert; Ayuda-Duran, Maria del Pilar; Rønneberg, Leiv; Nakken, Sigve; Hovig, Eivind & Zucknick, Manuela [Vis alle 7 forfattere av denne artikkelen] (2022). screenwerk: a modular tool for the design and analysis of drug combination screens. Bioinformatics. ISSN 1367-4803. 39(1). doi: 10.1093/bioinformatics/btac840. Fulltekst i vitenarkiv
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Giliberto, Mariaserena; Miranda Santana, Leonardo; Holien, Toril; Misund, Kristine; Nakken, Sigve & Vodak, Daniel [Vis alle 12 forfattere av denne artikkelen] (2022). Mutational analysis and protein profiling predict drug sensitivity in multiple myeloma cell lines. Frontiers in Oncology. ISSN 2234-943X. 12:1040730, s. 1–14. doi: 10.3389/fonc.2022.1040730. Fulltekst i vitenarkiv
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Zavaleta, Elizabeth; Solis, Nelly; Palacios, Maria Isabel; Zevallos-Escobar, Liz Elva; Corales, Edison Vasquez & Bazo-Alvarez, Juan Carlos [Vis alle 17 forfattere av denne artikkelen] (2022). Genetic Characterization in High-Risk Individuals from a Low-Resource City of Peru. Cancers. ISSN 2072-6694. 14(22), s. 1–13. doi: 10.3390/cancers14225603. Fulltekst i vitenarkiv
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Ng, Matthew; Charsou, Chara; Da Silva Lapao, Ana Sofia; Singh, Sakshi; Trachsel Moncho, Laura Cristina & Schultz, Sebastian Wolfgang [Vis alle 9 forfattere av denne artikkelen] (2022). The cholesterol transport protein GRAMD1C regulates autophagy initiation and mitochondrial bioenergetics. Nature Communications. ISSN 2041-1723. 13(1). doi: 10.1038/s41467-022-33933-2. Fulltekst i vitenarkiv
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Møller, Pål; Seppälä, Toni; Dowty, James G.; Haupt, Saskia; Dominguez-Valentin, Mev & Sunde, Lone [Vis alle 157 forfattere av denne artikkelen] (2022). Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium. Hereditary Cancer in Clinical Practice. ISSN 1731-2302. 20(1). doi: 10.1186/s13053-022-00241-1.
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Fiorito, Elisa; Szybowska, Patrycja Maria; Haugsten, Ellen Margrethe; Kostas, Michal Janusz; Øy, Geir Frode & Wiedlocha, Antoni [Vis alle 12 forfattere av denne artikkelen] (2022). Strategies to inhibit FGFR4 V550L-driven rhabdomyosarcoma. British Journal of Cancer. ISSN 0007-0920. 127, s. 1939–1953. doi: 10.1038/s41416-022-01973-6. Fulltekst i vitenarkiv
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Venizelos, Andreas; Engebrethsen, Christina; Deng, Wei; Geisler, Jürgen; Geisler, Stephanie & Iversen, Gjertrud Titlestad [Vis alle 18 forfattere av denne artikkelen] (2022). Clonal evolution in primary breast cancers under sequential epirubicin and docetaxel monotherapy. Genome Medicine. ISSN 1756-994X. 14, s. 1–18. doi: 10.1186/s13073-022-01090-2. Fulltekst i vitenarkiv
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Dominguez-Valentin, Mev; Plazzer, John-Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan & Jenkins, Mark A. [Vis alle 89 forfattere av denne artikkelen] (2021). No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in mlh1 and msh2: A prospective lynch syndrome database study. Journal of Clinical Medicine. ISSN 2077-0383. 10(13), s. 1–12. doi: 10.3390/jcm10132856. Fulltekst i vitenarkiv
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Nakken, Sigve; Saveliev, Vladislav; Hofmann, Oliver; Møller, Pål; Myklebost, Ola & Hovig, Eivind (2021). Cancer Predisposition Sequencing Reporter (CPSR): A flexible variant report engine for high-throughput germline screening in cancer. International Journal of Cancer. ISSN 0020-7136. s. 1–6. doi: 10.1002/ijc.33749. Fulltekst i vitenarkiv Vis sammendrag
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Nakken, Sigve; Lilleby, Wolfgang; Switlyk, Marta Daniela; Knudsen, Karen E.; Lilleby, Oscar & Zhao, Sen [Vis alle 10 forfattere av denne artikkelen] (2021). The quandary of dna-based treatment assessment in de novo metastatic prostate cancer in the era of precision oncology. Journal of Personalized Medicine. 11(5), s. 1–18. doi: 10.3390/jpm11050330. Fulltekst i vitenarkiv
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Aamdal, Elin; Inderberg, Else Marit ; Ellingsen, Espen Basmo; Rasch, Wenche; Brunsvig, Paal Fr. & Aamdal, Steinar [Vis alle 13 forfattere av denne artikkelen] (2021). Combining a universal telomerase based cancer vaccine with ipilimumab in patients with metastatic melanoma - Five-year follow up of a phase I/IIa trial. Frontiers in Immunology. ISSN 1664-3224. 12, s. 1–10. doi: 10.3389/fimmu.2021.663865. Fulltekst i vitenarkiv
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Wise, Jillian; Nakken, Sigve; Steen, Chloe Beate; Vodak, Daniel; Trøen, Gunhild & Johannessen, Bjarne [Vis alle 24 forfattere av denne artikkelen] (2020). Mutational dynamics and immune evasion in diffuse large B-cell lymphoma explored in a relapse-enriched patient series. Blood Advances. ISSN 2473-9529. 4(9), s. 1859–1866. doi: 10.1182/bloodadvances.2019001325. Vis sammendrag
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Dominguez-Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; MacRae, Finlay & Winship, Ingrid [Vis alle 88 forfattere av denne artikkelen] (2020). Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report. Genetics in Medicine. ISSN 1098-3600. s. 1–8. doi: 10.1038/s41436-020-01029-1. Fulltekst i vitenarkiv
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Lavelle, Timothy J; Alver, Tine Norman; Heintz, Karen Marie; Wernhoff, Patrik; Nygaard, Vegard & Nakken, Sigve [Vis alle 10 forfattere av denne artikkelen] (2020). Dysregulation of MITF Leads to Transformation in MC1R-Defective Melanocytes. Cancers. ISSN 2072-6694. 12(7), s. 1–20. doi: 10.3390/cancers12071719. Fulltekst i vitenarkiv
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Ree, Anne Hansen; Nygaard, Vigdis; Pedersen, Kjetil Boye; Heinrich, Daniel; Dueland, Svein & Bergheim, Inger Riise [Vis alle 25 forfattere av denne artikkelen] (2020). Molecularly matched therapy in the context of sensitivity, resistance, and safety; patient outcomes in end-stage cancer?the MetAction study. Acta Oncologica. ISSN 0284-186X. s. 1–10. doi: 10.1080/0284186X.2020.1742377. Fulltekst i vitenarkiv
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Lund-Andersen, Christin; Nakken, Sigve; Nygård, Ståle; Fromm, Bastian; Aasheim, Lars Birger & Davidson, Ben [Vis alle 13 forfattere av denne artikkelen] (2019). Integrative genomic analysis of peritoneal malignant mesothelioma: Understanding a case with extraordinary chemotherapy response. Cold Spring Harbor Molecular Case Studies. ISSN 2373-2873. 5:a003566(2), s. 1–15. doi: 10.1101/mcs.a003566. Fulltekst i vitenarkiv
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Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Hélène; Vodák, Daniel; Ekstrøm, Per Olaf & Nissen, Anke M. [Vis alle 15 forfattere av denne artikkelen] (2019). Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing. Scientific Reports. ISSN 2045-2322. 9:18555, s. 1–9. doi: 10.1038/s41598-019-54517-z. Fulltekst i vitenarkiv
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Dominguez-Valentin, Mev; Sampson, Julian R.; Seppälä, Toni T.; ten Broeke, Sanne W.; Plazzer, John-Paul & Nakken, Sigve [Vis alle 88 forfattere av denne artikkelen] (2019). Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database. Genetics in Medicine. ISSN 1098-3600. 22, s. 15–25. doi: 10.1038/s41436-019-0596-9. Fulltekst i vitenarkiv
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Dominguez-Valentin, Mev; Seppälä, Toni T.; Sampson, Julian R.; MacRae, Finlay; Winship, Ingrid & Evans, D. Gareth [Vis alle 43 forfattere av denne artikkelen] (2019). Survival by colon cancer stage and screening interval in Lynch syndrome: A prospective Lynch syndrome database report. Hereditary Cancer in Clinical Practice. ISSN 1731-2302. 17:28, s. 1–6. doi: 10.1186/s13053-019-0127-3.
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Seppälä, Toni T.; Ahadova, Aysel; Dominguez-Valentin, Mev; Macrae, Finlay; Evans, D. Gareth & Therkildsen, Christina [Vis alle 57 forfattere av denne artikkelen] (2019). 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. Hereditary Cancer in Clinical Practice. ISSN 1731-2302. 17:8, s. 1–8. doi: 10.1186/s13053-019-0106-8.
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Møller, Pål; Seppälä, Toni T.; Bernstein, Inge; Holinski-Feder, Elke; Sala, Paulo & Evans, D. Gareth [Vis alle 39 forfattere av denne artikkelen] (2018). 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. Gut. ISSN 0017-5749. 67(7), s. 1306–1316. doi: 10.1136/gutjnl-2017-314057. Fulltekst i vitenarkiv
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Dominguez Valentin, Mev; Evans, D. Gareth R.; Nakken, Sigve; Tubeuf, Hélène; Vodak, Daniel & Ekstrøm, Per Olaf [Vis alle 12 forfattere av denne artikkelen] (2018). Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds. Hereditary Cancer in Clinical Practice. ISSN 1731-2302. 16:4, s. 1–14. doi: 10.1186/s13053-018-0086-0. Fulltekst i vitenarkiv
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Dominguez Valentin, Mev; Nakken, Sigve; Tubeuf, Hélène; Vodak, Daniel; Ekstrøm, Per Olaf & Nissen, Anke M. [Vis alle 11 forfattere av denne artikkelen] (2018). Identification of genetic variants for clinical management of familial colorectal tumors. BMC Medical Genetics. ISSN 1471-2350. 19(1). doi: 10.1186/s12881-018-0533-9. Fulltekst i vitenarkiv
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Vodak, Daniel; Lorenz, Susanne; Nakken, Sigve; Aasheim, Lars Birger; Holte, Harald & Bai, Baoyan [Vis alle 9 forfattere av denne artikkelen] (2018). Sample-Index Misassignment Impacts Tumour Exome Sequencing. Scientific Reports. ISSN 2045-2322. 8:5307, s. 1–6. doi: 10.1038/s41598-018-23563-4. Fulltekst i vitenarkiv
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Birkeland, Einar Elvbakken; Zhang, Shan; Poduval, Deepak; Geisler, Jürgen; Nakken, Sigve & Vodak, Daniel [Vis alle 11 forfattere av denne artikkelen] (2018). Patterns of genomic evolution in advanced melanoma. Nature Communications. ISSN 2041-1723. 9:2665, s. 1–12. doi: 10.1038/s41467-018-05063-1. Fulltekst i vitenarkiv
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Seppälä, Toni; Pylvänäinen, Kirsi; Evans, Dafydd Gareth; Järvinen, Heikki; Renkonen-Sinisalo, Laura & Bernstein, Inge [Vis alle 39 forfattere av denne artikkelen] (2017). Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: A Prospective Lynch Syndrome Database report. Hereditary Cancer in Clinical Practice. ISSN 1731-2302. 15:18, s. 1–10. doi: 10.1186/s13053-017-0078-5. Fulltekst i vitenarkiv
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Møller, Pål; Seppälä, Toni; Bernstein, Inge; Holinski-Feder, Elke; Sala, Paola & Evans, D. Gareth [Vis alle 38 forfattere av denne artikkelen] (2017). Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: A report from the prospective Lynch syndrome database. Gut. ISSN 0017-5749. 66(9), s. 1657–1664. doi: 10.1136/gutjnl-2016-311403. Fulltekst i vitenarkiv
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Dominguez Valentin, Mev; Nakken, Sigve; Tubeuf, Hélène; Vodak, Daniel; Ekstrøm, Per Olaf & Nissen, Anke M. [Vis alle 11 forfattere av denne artikkelen] (2017). Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families. Familial Cancer. ISSN 1389-9600. 17(1), s. 141–153. doi: 10.1007/s10689-017-0011-0.
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Helland, Åslaug; Brustugun, Odd Terje; Nakken, Sigve; Halvorsen, Ann Rita; Dønnem, Tom & Bremnes, Roy M. [Vis alle 15 forfattere av denne artikkelen] (2017). High number of kinome-mutations in non-small cell lung cancer is associated with reduced immune response and poor relapse-free survival. International Journal of Cancer. ISSN 0020-7136. 141(1), s. 184–190. doi: 10.1002/ijc.30726. Fulltekst i vitenarkiv
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Ree, Anne Hansen; Russnes, Hege Elisabeth Giercksky; Heinrich, Daniel; Dueland, Svein; Pedersen, Kjetil Boye & Nygaard, Vigdis [Vis alle 34 forfattere av denne artikkelen] (2017). Implementing precision cancer medicine in the public health services of Norway: the diagnostic infrastructure and a cost estimate. ESMO Open. ISSN 2059-7029. 2(2), s. 1–10. doi: 10.1136/esmoopen-2017-000158. Fulltekst i vitenarkiv
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Simovski, Boris; Vodak, Daniel; Gundersen, Sveinung; Domanska, Diana Ewa; Azab, Abdulrahman & Holden, Lars [Vis alle 25 forfattere av denne artikkelen] (2017). GSuite HyperBrowser: integrative analysis of dataset collections across the genome and epigenome. GigaScience. ISSN 2047-217X. 6(7), s. 1–12. doi: 10.1093/gigascience/gix032. Fulltekst i vitenarkiv Vis sammendrag
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Landfors, Miriam; Nakken, Sigve; Fusser, Markus; Dahl, John Arne; Klungland, Arne & Fedorcsák, Péter (2016). Sequencing of FTO and ALKBH5 in men undergoing infertility work-up identifies an infertility-associated variant and two missense mutations. Fertility and Sterility. ISSN 0015-0282. 105(5), s. 1170–1179e5. doi: 10.1016/j.fertnstert.2016.01.002.
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Wise, Jillian Frances; Nakken, Sigve; Vodak, Daniel; Trøen, Gunhild; Lingjærde, Ole Christian & Meza-Zepeda, Leonardo A [Vis alle 12 forfattere av denne artikkelen] (2015). Discovery of recurrent mutations associated with chemo-immunotherapy relapse in diffuse large B-cell lymphoma. Blood. ISSN 0006-4971. 126(23), s. 110–110. doi: 10.1182/blood.v126.23.110.110.
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Møller, Pål; Seppälä, Toni; Bernstein, Inge; Holinski-Feder, Elke; Sala, Paola & Evans, D Gareth [Vis alle 36 forfattere av denne artikkelen] (2015). Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database. Gut. ISSN 0017-5749. 66(3), s. 464–472. doi: 10.1136/gutjnl-2015-309675.
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Alioto, Tyler S.; Buchhalter, Ivo; Derdak, Sophia; Hutter, Barbara; Eldridge, Matthew D. & Hovig, Johannes Eivind [Vis alle 83 forfattere av denne artikkelen] (2015). A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing. Nature Communications. ISSN 2041-1723. 6:10001. doi: 10.1038/ncomms10001.
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Ekstrøm, Per Olaf; Nakken, Sigve; Johansen, Morten & Hovig, Johannes Eivind (2015). Automated amplicon design suitable for analysis of DNA variants by melting techniques. BMC Research Notes. ISSN 1756-0500. 8(1). doi: 10.1186/s13104-015-1624-8.
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Rustad, Even Holth; Dai, Hong Yan; Hov, Håkon; Coward, Eivind; Beisvag, Vidar & Myklebost, Ola [Vis alle 16 forfattere av denne artikkelen] (2015). BRAF V600E mutation in early-stage multiple myeloma: good response to broad acting drugs and no relation to prognosis. Blood Cancer Journal. ISSN 2044-5385. 5:e299(3), s. 1–7. doi: 10.1038/bcj.2015.24. Fulltekst i vitenarkiv
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Kerty, Emilia; Heuser, Kjell; Indahl, Ulf Geir; Berg, Paul Ragnar; Nakken, Sigve & Lien, Sigbjørn [Vis alle 9 forfattere av denne artikkelen] (2013). 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. Acta Ophthalmologica. ISSN 1755-375X. 91(1), s. 88–91. doi: 10.1111/j.1755-3768.2011.02231.x.
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Selmer, Kaja Kristine; Gilfillan, Gregor Duncan; Strømme, Petter; Lyle, Robert; Hughes, Timothy & Hjorthaug, Hanne Sagsveen [Vis alle 13 forfattere av denne artikkelen] (2012). A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions. European Journal of Human Genetics. ISSN 1018-4813. 20(1), s. 58–63. doi: 10.1038/ejhg.2011.126.
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Nakken, Sigve; Johansen, Morten; Fillebeen, Julien; Berge, Ole Petter; Kirkerød, Harald & Jenssen, Tor-Kristian [Vis alle 7 forfattere av denne artikkelen] (2012). CellLineMiner: a knowledge portal for human cell lines. Bioinformation. ISSN 0973-8894. 8(22), s. 1119–1122. doi: 10.6026/97320630081119.
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Nakken, Sigve; Rødland, Einar Andreas & Hovig, Eivind (2010). Impact of DNA Physical Properties on Local Sequence Bias of Human Mutation. Human Mutation. ISSN 1059-7794. 31(12), s. 1316–1325. doi: 10.1002/humu.21371.
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Heuser, Kjell; Nagelhus, Erlend Arnulf; Taubøll, Erik; Indahl, Ulf Geir; Berg, Paul Ragnar & Lien, Sigbjørn [Vis alle 9 forfattere av denne artikkelen] (2010). Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy. Epilepsy Research. ISSN 0920-1211. 88(1), s. 55–64. doi: 10.1016/j.eplepsyres.2009.09.023.
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Falster, DS; Nakken, S; Bergem-Ohr, M; Rødland, Einar Andreas & Breivik, J (2010). Unstable DNA Repair Genes Shaped by Their Own Sequence Modifying Phenotypes. Journal of Molecular Evolution. ISSN 0022-2844. 70(3), s. 266–274. doi: 10.1007/s00239-010-9328-0.
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Nakken, Karl Esten; Labori, Knut Jørgen; Rødningen, Olaug Kristin; Nakken, Sigve; Berge, Knut Erik & Eiklid, Kristin Louise [Vis alle 7 forfattere av denne artikkelen] (2009). ABCB4 sequence variations in young adults with cholesterol gallstone disease. Liver international (Print). ISSN 1478-3223. 29(5), s. 743–747. doi: 10.1111/j.1478-3231.2008.01914.x.
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Nakken, Sigve; Rødland, Einar Andreas; Rognes, Torbjørn & Hovig, Eivind (2009). Large-scale inference of the point mutational spectrum in human segmental duplications. BMC Genomics. ISSN 1471-2164. 10. doi: 10.1186/1471-2164-10-43. Fulltekst i vitenarkiv
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Nakken, Sigve; Aussedat, Ophelie; Kristoffersen, Anja Bråthen; Holst-Jensen, Arne & Tengs, Torstein (2009). UniquePrimer - a web utility for design of specific PCR primers and probes. Annales de microbiologie. ISSN 0300-5410. 59(2), s. 391–393.
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Nakken, Sigve; Rognes, Torbjørn & Hovig, Eivind (2009). The disruptive positions in human G-quadruplex motifs are less polymorphic and more conserved than their neutral counterparts. Nucleic Acids Research (NAR). ISSN 0305-1048. 37(17), s. 5749–5756. doi: 10.1093/nar/gkp590. Fulltekst i vitenarkiv
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Holla, Øystein Lunde; Nakken, Sigve; Mattingsdal, Morten; Ranheim, Trine; Berge, Knut Erik & Defesche, JC [Vis alle 7 forfattere av denne artikkelen] (2009). Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses. Molecular Genetics and Metabolism. ISSN 1096-7192. 96(4), s. 245–252. doi: 10.1016/j.ymgme.2008.12.014.
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Nakken, Karl Esten; Labori, Knut Jørgen; Rødningen, Olaug Kristin; Nakken, Sigve; Berge, Knut & Eiklid, Kristin Louise [Vis alle 7 forfattere av denne artikkelen] (2008). ABCB4 sequence variations in young adults with cholesterol gallstone disease. Liver international (Print). ISSN 1478-3223.
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Nakken, Sigve; Alseth, Ingrun & Rognes, Torbjørn (2007). Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes. Neuroscience. ISSN 0306-4522. 145. doi: 10.1016/j.neuroscience.2006.09.004.
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Dominguez-Valentin, Mev; Sampson, Julian R.; Møller, Pål; Seppälä, Toni T.; Plazzer, John-Paul & Nakken, Sigve [Vis alle 88 forfattere av denne artikkelen] (2021). Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum. International Journal of Cancer. ISSN 0020-7136. 148(2), s. 512–513. doi: 10.1002/ijc.33214.
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Dominguez-Valentin, Mev; Sampson, Julian R.; Seppälä, Toni T.; ten Broeke, Sanne W.; Plazzer, John-Paul & Nakken, Sigve [Vis alle 88 forfattere av denne artikkelen] (2020). Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (Genetics in Medicine, (2020), 22, 1, (15-25), 10.1038/s41436-019-0596-9). Genetics in Medicine. ISSN 1098-3600. 22(9). doi: 10.1038/s41436-020-0892-4.
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Bai, Baoyan; Vodák, Daniel; Nakken, Sigve; Wise, Jillian; Blaker, Yngvild Nuvin & Lingjærde, Ole Christian [Vis alle 18 forfattere av denne artikkelen] (2019). Deep profiling of genetic aberrations and clonal evolution in follicular lymphoma. Blood. ISSN 0006-4971. 134(1), s. 20–20. doi: 10.1182/blood-2019-128403.
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Nakken, Sigve; Fournous, Ghislain; Vodak, Daniel; Aasheim, Lars Birger; Myklebost, Ola & Hovig, Eivind (2018). Personal Cancer Genome Reporter: Variant interpretation report for precision oncology. Bioinformatics. ISSN 1367-4803. 34(10), s. 1778–1780. doi: 10.1093/bioinformatics/btx817. Fulltekst i vitenarkiv
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Nakken, Sigve; Vodák, Daniel; Fournous, Ghislain; Thomassen, Gard O Sundby & Hovig, Johannes Eivind (2013). Big challenges in personalized cancer medicine. META. ISSN 1890-1956. s. 8–12. Vis sammendrag
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Nakken, Karl Esten; Labori, Knut Jørgen; Rødningen, Olaug K.; Nakken, Sigve; Eiklid, Kristin Louise & Ræder, Morten (2007). Variability of the ABCB4 gene in young adult cholecystectomized patients.
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Nakken, Sigve & Rognes, Torbjørn (2010). Inference of molecular mechanisms from sequence patterns in human DNA variation. Unipub forlag.
Publisert
21. apr. 2022 14:13
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21. apr. 2022 14:13