Gulcher J - Search Results

1

Genome-wide TDT analysis in a localized population with a high prevalence of multiple sclerosis indicates the importance of a region on chromosome 14q.

Giedraitis V, Modin H, Callander M, Landtblom AM, Fossdal R, Stefansson K, Hillert J, Gulcher J. Giedraitis V, et al. Among authors: gulcher j. Genes Immun. 2003 Dec;4(8):559-63. doi: 10.1038/sj.gene.6364024. Genes Immun. 2003. PMID: 14647195

2

Genome-wide linkage screen of a consanguineous multiple sclerosis kinship.

Modin H, Masterman T, Thorlacius T, Stefánsson M, Jónasdóttir A, Stefánsson K, Hillert J, Gulcher J. Modin H, et al. Among authors: gulcher j. Mult Scler. 2003 Mar;9(2):128-34. doi: 10.1191/1352458503ms894oa. Mult Scler. 2003. PMID: 12708807

3

The hexabrachion gene as a candidate for a tuberous sclerosis gene.

Gulcher J, Stefansson K. Gulcher J, et al. Ann N Y Acad Sci. 1991;615:220-7. doi: 10.1111/j.1749-6632.1991.tb37763.x. Ann N Y Acad Sci. 1991. PMID: 1710095 Review. No abstract available.

4

Is multiple sclerosis an autoimmune disease?

Gulcher JR, Vartanian T, Stefansson K. Gulcher JR, et al. Clin Neurosci. 1994;2(3-4):246-52. Clin Neurosci. 1994. PMID: 7749894 Review.

5

Positional cloning: complex cardiovascular traits.

Gulcher J, Stefansson K. Gulcher J, et al. Methods Mol Med. 2006;128:137-52. doi: 10.1385/1-59745-159-2:137. Methods Mol Med. 2006. PMID: 17071994

6

A whole genome association study in Icelandic multiple sclerosis patients with 4804 markers.

Jonasdottir A, Thorlacius T, Fossdal R, Jonasdottir A, Benediktsson K, Benedikz J, Jonsson HH, Sainz J, Einarsdottir H, Sigurdardottir S, Kristjansdottir G, Sawcer S, Compston A, Stefansson K, Gulcher J. Jonasdottir A, et al. Among authors: gulcher j. J Neuroimmunol. 2003 Oct;143(1-2):88-92. doi: 10.1016/j.jneuroim.2003.08.018. J Neuroimmunol. 2003. PMID: 14575921

7

PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in Sweden.

Kostulas K, Gretarsdottir S, Kostulas V, Manolescu A, Helgadottir A, Thorleifsson G, Gudmundsson LJ, Thorsteinsdottir U, Gulcher JR, Stefansson K, Hillert J. Kostulas K, et al. Among authors: gulcher jr. J Neurol Sci. 2007 Dec 15;263(1-2):113-7. doi: 10.1016/j.jns.2007.06.042. Epub 2007 Jul 25. J Neurol Sci. 2007. PMID: 17655870

8

A genome wide linkage disequilibrium screen in Parkinson's disease.

Foltynie T, Hicks A, Sawcer S, Jonasdottir A, Setakis E, Maranian M, Yeo T, Lewis S, Brayne C, Stefansson K, Compston A, Gulcher J, Barker RA. Foltynie T, et al. Among authors: gulcher j. J Neurol. 2005 May;252(5):597-602. doi: 10.1007/s00415-005-0686-2. Epub 2005 Feb 23. J Neurol. 2005. PMID: 15726250

9

The genealogic approach to human genetics of disease.

Gulcher J, Kong A, Stefansson K. Gulcher J, et al. Cancer J. 2001 Jan-Feb;7(1):61-8. Cancer J. 2001. PMID: 11269649 Review.

10

A whole genome association study in Finnish multiple sclerosis patients with 3669 markers.

Laaksonen M, Jonasdottir A, Fossdal R, Ruutiainen J, Sawcer S, Compston A, Benediktsson K, Thorlacius T, Gulcher J, Ilonen J. Laaksonen M, et al. Among authors: gulcher j. J Neuroimmunol. 2003 Oct;143(1-2):70-3. doi: 10.1016/j.jneuroim.2003.08.014. J Neuroimmunol. 2003. PMID: 14575917

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