R Fossdal
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Explore the profile of R Fossdal including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
239
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Recent Articles
1.
Steinberg S, Mors O, Borglum A, Gustafsson O, Werge T, Mortensen P, et al.
Mol Psychiatry
. 2010 Jan;
16(1):59-66.
PMID: 20048749
A trio of genome-wide association studies recently reported sequence variants at three loci to be significantly associated with schizophrenia. No sequence polymorphism had been unequivocally (P<5 × 10(-8)) associated with...
2.
Fossdal R, Bodvarsson M, Asmundsson P, Ragnarsson J, Palsson R
Laeknabladid
. 2009 Mar;
85(1):33-42.
PMID: 19321914
Objective: Autosomal dominand polycystic kidney disease (ADPKD) is one of the most common genetic diseases in humans and accounts for 8-10% of end-stage renal failure. The disease is caused by...
3.
Giedraitis V, Modin H, Callander M, Landtblom A, Fossdal R, Stefansson K, et al.
Genes Immun
. 2003 Dec;
4(8):559-63.
PMID: 14647195
Epidemiological studies show that susceptibility to multiple sclerosis (MS) has a strong genetic component, but apart from the HLA gene complex, additional genetic factors have proven difficult to map in...
4.
Laaksonen M, Jonasdottir A, Fossdal R, Ruutiainen J, Sawcer S, Compston A, et al.
J Neuroimmunol
. 2003 Oct;
143(1-2):70-3.
PMID: 14575917
Multiple sclerosis (MS) is a demyelinating disease of the central nervous system with complex genetic background. In the present study, based in the Finnish population, we typed a large number...
5.
Reynolds D, Hayashi T, Cai Y, Veldhuisen B, Watnick T, Lens X, et al.
J Am Soc Nephrol
. 1999 Nov;
10(11):2342-51.
PMID: 10541293
It is estimated that approximately 15% of families with autosomal dominant polycystic kidney disease (ADPKD) have mutations in PKD2. Identification of these mutations is central to identifying functionally important regions...
6.
Steinsson K, Jonsdottir S, Arason G, Kristjansdottir H, Fossdal R, Skaftadottir I, et al.
Ann Rheum Dis
. 1998 Nov;
57(8):503-5.
PMID: 9797559
Objective: To perform an exploratory analysis of the relative contribution of single MHC genes to the pathogenesis of systemic lupus erythematosus (SLE) in a homogenous white population. Methods: MHC class...
7.
Veldhuisen B, Saris J, de Haij S, Hayashi T, Reynolds D, Mochizuki T, et al.
Am J Hum Genet
. 1997 Oct;
61(3):547-55.
PMID: 9326320
Recently the second gene for autosomal dominant polycystic kidney disease (ADPKD), located on chromosome 4q21-q22, has been cloned and characterized. The gene encodes an integral membrane protein, polycystin-2, that shows...
8.
Steinsson K, Arnason A, Erlendsson K, Fossdal R, Skaftadottir I, Jonsdottir S, et al.
J Rheumatol
. 1995 Oct;
22(10):1862-6.
PMID: 8991982
Objective: In an epidemiological survey of systemic lupus erythematosus (SLE) in Iceland several families with multiple cases were identified. In one family, 35 individuals (family members and spouses) in 3...
9.
Fossdal R, Magnusson L, Weber J, Jensson O
Hum Mol Genet
. 1995 Mar;
4(3):479-83.
PMID: 7795606
Atrophia areata (AA) is an early onset autosomal dominant helicoid peripapillary chorioretinal degeneration, which was first demonstrated to be hereditary in an Icelandic family. It is characterized by bilateral wing-shaped...
10.
Peters D, Spruit L, Saris J, Ravine D, Sandkuijl L, Fossdal R, et al.
Nat Genet
. 1993 Dec;
5(4):359-62.
PMID: 8298643
Autosomal dominant polycystic kidney disease (ADPKD) is a genetically heterogeneous disorder. A gene defect located on the short arm of chromosome 16 is responsible for the disease in roughly 86%...