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Association of NFE2L2 and KEAP1 haplotypes with amyotrophic lateral sclerosis.
Bergström P, von Otter M, Nilsson S, Nilsson AC, Nilsson M, Andersen PM, Hammarsten O, Zetterberg H. Bergström P, et al. Among authors: nilsson ac, nilsson m, nilsson s. Amyotroph Lateral Scler Frontotemporal Degener. 2014 Mar;15(1-2):130-7. doi: 10.3109/21678421.2013.839708. Epub 2013 Oct 8. Amyotroph Lateral Scler Frontotemporal Degener. 2014. PMID: 24102512
Association of nAChR gene haplotypes with heavy alcohol use and body mass.
Landgren S, Engel JA, Andersson ME, Gonzalez-Quintela A, Campos J, Nilsson S, Zetterberg H, Blennow K, Jerlhag E. Landgren S, et al. Among authors: nilsson s. Brain Res. 2009 Dec 11;1305 Suppl:S72-9. doi: 10.1016/j.brainres.2009.08.026. Epub 2009 Aug 19. Brain Res. 2009. PMID: 19698703
Kinesin light chain 1 gene haplotypes in three conformational diseases.
von Otter M, Landgren S, Nilsson S, Lundvall C, Minthon L, Bogdanovic N, Andreasen N, Gustafson DR, Skoog I, Wallin A, Håkansson A, Nissbrandt H, Zetterberg M, Tasa G, Blennow K, Zetterberg H. von Otter M, et al. Among authors: nilsson s. Neuromolecular Med. 2010 Sep;12(3):229-36. doi: 10.1007/s12017-009-8103-0. Epub 2009 Nov 13. Neuromolecular Med. 2010. PMID: 19911314
Nrf2-encoding NFE2L2 haplotypes influence disease progression but not risk in Alzheimer's disease and age-related cataract.
von Otter M, Landgren S, Nilsson S, Zetterberg M, Celojevic D, Bergström P, Minthon L, Bogdanovic N, Andreasen N, Gustafson DR, Skoog I, Wallin A, Tasa G, Blennow K, Nilsson M, Hammarsten O, Zetterberg H. von Otter M, et al. Among authors: nilsson m, nilsson s. Mech Ageing Dev. 2010 Feb;131(2):105-10. doi: 10.1016/j.mad.2009.12.007. Epub 2010 Jan 12. Mech Ageing Dev. 2010. PMID: 20064547
Association of Nrf2-encoding NFE2L2 haplotypes with Parkinson's disease.
von Otter M, Landgren S, Nilsson S, Celojevic D, Bergström P, Håkansson A, Nissbrandt H, Drozdzik M, Bialecka M, Kurzawski M, Blennow K, Nilsson M, Hammarsten O, Zetterberg H. von Otter M, et al. Among authors: nilsson m, nilsson s. BMC Med Genet. 2010 Mar 2;11:36. doi: 10.1186/1471-2350-11-36. BMC Med Genet. 2010. PMID: 20196834 Free PMC article.
Association of the RAGE G82S polymorphism with Alzheimer's disease.
Daborg J, von Otter M, Sjölander A, Nilsson S, Minthon L, Gustafson DR, Skoog I, Blennow K, Zetterberg H. Daborg J, et al. Among authors: nilsson s. J Neural Transm (Vienna). 2010 Jul;117(7):861-7. doi: 10.1007/s00702-010-0437-0. Epub 2010 Jun 22. J Neural Transm (Vienna). 2010. PMID: 20567859 Free PMC article.
A novel ARC gene polymorphism is associated with reduced risk of Alzheimer's disease.
Landgren S, von Otter M, Palmér MS, Zetterström C, Nilsson S, Skoog I, Gustafson DR, Minthon L, Wallin A, Andreasen N, Bogdanovic N, Marcusson J, Blennow K, Zetterberg H, Kettunen P. Landgren S, et al. Among authors: nilsson s. J Neural Transm (Vienna). 2012 Jul;119(7):833-42. doi: 10.1007/s00702-012-0823-x. Epub 2012 May 25. J Neural Transm (Vienna). 2012. PMID: 22622366
Superoxide dismutase gene polymorphisms in patients with age-related cataract.
Celojevic D, Nilsson S, Behndig A, Tasa G, Juronen E, Karlsson JO, Zetterberg H, Petersen A, Zetterberg M. Celojevic D, et al. Among authors: nilsson s. Ophthalmic Genet. 2013 Sep;34(3):140-5. doi: 10.3109/13816810.2012.746377. Epub 2013 Jan 4. Ophthalmic Genet. 2013. PMID: 23289810
1,908 results