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Page 1
Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease.
Steinberg S, Stefansson H, Jonsson T, Johannsdottir H, Ingason A, Helgason H, Sulem P, Magnusson OT, Gudjonsson SA, Unnsteinsdottir U, Kong A, Helisalmi S, Soininen H, Lah JJ; DemGene; Aarsland D, Fladby T, Ulstein ID, Djurovic S, Sando SB, White LR, Knudsen GP, Westlye LT, Selbæk G, Giegling I, Hampel H, Hiltunen M, Levey AI, Andreassen OA, Rujescu D, Jonsson PV, Bjornsson S, Snaedal J, Stefansson K. Steinberg S, et al. Among authors: knudsen gp. Nat Genet. 2015 May;47(5):445-7. doi: 10.1038/ng.3246. Epub 2015 Mar 25. Nat Genet. 2015. PMID: 25807283 Free article.
Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents.
Smajlagić D, Lavrichenko K, Berland S, Helgeland Ø, Knudsen GP, Vaudel M, Haavik J, Knappskog PM, Njølstad PR, Houge G, Johansson S. Smajlagić D, et al. Among authors: knudsen gp. Eur J Hum Genet. 2021 Jan;29(1):205-215. doi: 10.1038/s41431-020-00707-7. Epub 2020 Aug 10. Eur J Hum Genet. 2021. PMID: 32778765 Free PMC article.
Roadmap for a precision-medicine initiative in the Nordic region.
Njølstad PR, Andreassen OA, Brunak S, Børglum AD, Dillner J, Esko T, Franks PW, Freimer N, Groop L, Heimer H, Hougaard DM, Hovig E, Hveem K, Jalanko A, Kaprio J, Knudsen GP, Melbye M, Metspalu A, Mortensen PB, Palmgren J, Palotie A, Reed W, Stefánsson H, Stitziel NO, Sullivan PF, Thorsteinsdóttir U, Vaudel M, Vuorio E, Werge T, Stoltenberg C, Stefánsson K. Njølstad PR, et al. Among authors: knudsen gp. Nat Genet. 2019 Jun;51(6):924-930. doi: 10.1038/s41588-019-0391-1. Nat Genet. 2019. PMID: 30988515 No abstract available.
Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations.
Olafsson S, Stridh P, Bos SD, Ingason A, Euesden J, Sulem P, Thorleifsson G, Gustafsson O, Johannesson A, Geirsson AJ, Thorsson AV, Sigurgeirsson B, Ludviksson BR, Olafsson E, Kristjansdottir H, Jonasson JG, Olafsson JH, Orvar KB, Benediktsson R, Bjarnason R, Kristjansdottir S, Gislason T, Valdimarsson T, Mikaelsdottir E, Sigurdsson S, Jonsson S, Rafnar T, Aarsland D, Djurovic S, Fladby T, Knudsen GP, Celius EG, Myhr KM, Grondal G, Steinsson K, Valdimarsson H, Bjornsson S, Bjornsdottir US, Bjornsson ES, Nilsson B, Andreassen OA, Alfredsson L, Hillert J, Kockum IS, Masson G, Thorsteinsdottir U, Gudbjartsson DF, Stefansson H, Hjaltason H, Harbo HF, Olsson T, Jonsdottir I, Stefansson K. Olafsson S, et al. Among authors: knudsen gp. NPJ Genom Med. 2017 Aug 8;2:24. doi: 10.1038/s41525-017-0027-2. eCollection 2017. NPJ Genom Med. 2017. PMID: 29263835 Free PMC article.
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.
Helgeland Ø, Vaudel M, Juliusson PB, Lingaas Holmen O, Juodakis J, Bacelis J, Jacobsson B, Lindekleiv H, Hveem K, Lie RT, Knudsen GP, Stoltenberg C, Magnus P, Sagen JV, Molven A, Johansson S, Njølstad PR. Helgeland Ø, et al. Among authors: knudsen gp. Nat Commun. 2019 Oct 1;10(1):4448. doi: 10.1038/s41467-019-12308-0. Nat Commun. 2019. PMID: 31575865 Free PMC article.
A Twin Study of Normative Personality and DSM-IV Personality Disorder Criterion Counts: Evidence for Separate Genetic Influences.
Czajkowski N, Aggen SH, Krueger RF, Kendler KS, Neale MC, Knudsen GP, Gillespie NA, Røysamb E, Tambs K, Reichborn-Kjennerud T. Czajkowski N, et al. Among authors: knudsen gp. Am J Psychiatry. 2018 Jul 1;175(7):649-656. doi: 10.1176/appi.ajp.2017.17050493. Epub 2018 Mar 21. Am J Psychiatry. 2018. PMID: 29558815 Free PMC article.
The Norwegian Twin Registry from a public health perspective: a research update.
Nilsen TS, Knudsen GP, Gervin K, Brandt I, Røysamb E, Tambs K, Orstavik R, Lyle R, Reichborn-Kjennerud T, Magnus P, Harris JR. Nilsen TS, et al. Among authors: knudsen gp. Twin Res Hum Genet. 2013 Feb;16(1):285-95. doi: 10.1017/thg.2012.117. Epub 2012 Nov 28. Twin Res Hum Genet. 2013. PMID: 23186607
120 results