Sillén A - Search Results

1

Brain-derived neurotrophic factor gene (BDNF) variants and schizophrenia: an association study.

Jönsson EG, Edman-Ahlbom B, Sillén A, Gunnar A, Kulle B, Frigessi A, Vares M, Ekholm B, Wode-Helgodt B, Schumacher J, Cichon S, Agartz I, Sedvall GC, Hall H, Terenius L. Jönsson EG, et al. Among authors: sillen a. Prog Neuropsychopharmacol Biol Psychiatry. 2006 Jul;30(5):924-33. doi: 10.1016/j.pnpbp.2006.02.008. Epub 2006 Apr 3. Prog Neuropsychopharmacol Biol Psychiatry. 2006. PMID: 16581172

2

Dopamine D2 receptor gene Ser311Cys variant and schizophrenia: association study and meta-analysis.

Jönsson EG, Sillén A, Vares M, Ekholm B, Terenius L, Sedvall GC. Jönsson EG, et al. Among authors: sillen a. Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):28-34. doi: 10.1002/ajmg.b.20004. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12707934

3

Potential genetic variants in schizophrenia: a Bayesian analysis.

Hall H, Lawyer G, Sillén A, Jönsson EG, Agartz I, Terenius L, Arnborg S. Hall H, et al. Among authors: sillen a. World J Biol Psychiatry. 2007;8(1):12-22. doi: 10.1080/15622970600892004. World J Biol Psychiatry. 2007. PMID: 17366345

4

Brain-derived neurotrophic factor gene variation influences cerebrospinal fluid 3-methoxy-4-hydroxyphenylglycol concentrations in healthy volunteers.

Jönsson EG, Saetre P, Edman-Ahlbom B, Sillén A, Gunnar A, Andreou D, Agartz I, Sedvall G, Hall H, Terenius L. Jönsson EG, et al. Among authors: sillen a. J Neural Transm (Vienna). 2008 Dec;115(12):1695-9. doi: 10.1007/s00702-008-0113-9. Epub 2008 Sep 10. J Neural Transm (Vienna). 2008. PMID: 18781277

5

Linkage analysis of autopsy-confirmed familial Alzheimer disease supports an Alzheimer disease locus in 8q24.

Sillén A, Brohede J, Forsell C, Lilius L, Andrade J, Odeberg J, Kimura T, Winblad B, Graff C. Sillén A, et al. Dement Geriatr Cogn Disord. 2011;31(2):109-18. doi: 10.1159/000323808. Epub 2011 Jan 27. Dement Geriatr Cogn Disord. 2011. PMID: 21273770

6

Genome scan on Swedish Alzheimer's disease families.

Sillén A, Forsell C, Lilius L, Axelman K, Björk BF, Onkamo P, Kere J, Winblad B, Graff C. Sillén A, et al. Mol Psychiatry. 2006 Feb;11(2):182-6. doi: 10.1038/sj.mp.4001772. Mol Psychiatry. 2006. PMID: 16288313 Clinical Trial.

7

Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome.

Sillén A, Anton-Lamprecht I, Braun-Quentin C, Kraus CS, Sayli BS, Ayuso C, Jagell S, Küster W, Wadelius C. Sillén A, et al. Hum Mutat. 1998;12(6):377-84. doi: 10.1002/(SICI)1098-1004(1998)12:6<377::AID-HUMU3>3.0.CO;2-I. Hum Mutat. 1998. PMID: 9829906

8

The Sjögren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic association.

Pigg M, Jagell S, Sillén A, Weissenbach J, Gustavson KH, Wadelius C. Pigg M, et al. Among authors: sillen a. Nat Genet. 1994 Dec;8(4):361-4. doi: 10.1038/ng1294-361. Nat Genet. 1994. PMID: 7894487

9

The use of grid computing to drive data-intensive genetic research.

Andrade J, Andersen M, Sillén A, Graff C, Odeberg J. Andrade J, et al. Among authors: sillen a. Eur J Hum Genet. 2007 Jun;15(6):694-702. doi: 10.1038/sj.ejhg.5201815. Epub 2007 Mar 21. Eur J Hum Genet. 2007. PMID: 17377522

10

Hyperkalemic periodic paralysis caused by recurring mutation in the adult muscle sodium channel alpha-subunit gene.

Sillén A, Wadelius C, Sundvall M, Ahlsten G, Gustavson KH. Sillén A, et al. Genet Couns. 1996;7(4):267-75. Genet Couns. 1996. PMID: 8985730

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