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2006
Mark Comprehensive association testing of common mitochondrial DNA variation in metabolic disease
Saxena, R ; de Bakker, PIW ; Singer, K ; Mootha, V ; Burtt, N ; Hirschhorn, JN ; Gaudet, D ; Isomaa, B ; Daly, MJ and Groop, Leif ^LU , et al. (2006) In American Journal of Human Genetics 79(1). p.54-61
- Contribution to journal › Article
Mark Genetic mapping at 3-kilobase resolution reveals inositol 1,4,5-triphosphate receptor 3 as a risk factor for type 1 diabetes in Sweden.
Roach, J C ; Deutsch, K ; Li, S ; Siegel, A F ; Bekris, L M ; Einhaus, D C ; Janer, M ; Sheridan, C M ; Glusman, G and Lernmark, Åke ^LU , et al. (2006) In American Journal of Human Genetics 79(4). p.614-627
- Contribution to journal › Article
2005
Mark Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus
Sigurdsson, S ; Nordmark, G ; Goring, HHH ; Lindroos, K ; Wiman, AC ; Sturfelt, Gunnar ^LU ; Jönsen, Andreas ^LU ; Rantapaa-Dahlqvist, S ; Moller, B and Kere, J , et al. (2005) In American Journal of Human Genetics 76(3). p.528-537
- Contribution to journal › Article
2004
Mark The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.
Barbouti, Aikaterini ; Stankiewicz, Pawel ; Nusbaum, Chad ; Cuomo, Christina ; Cook, April ; Höglund, Mattias ^LU ; Johansson, Bertil ^LU ; Hagemeijer, Anne ; Park, Sung-Sup and Mitelman, Felix ^LU , et al. (2004) In American Journal of Human Genetics 74(1). p.1-10
- Contribution to journal › Article
Mark Deficiency of GDP-Man:GlcNAc₂-PP-Dolichol Mannosyltransferase Causes Congenital Disorder of Glycosylation Type Ik
Schwarz, Markus ; Thiel, Christian ; Lübbehusen, Jürgen ; Dorland, Bert ; De Koning, Tom ^LU ; Von Figura, Kurt ; Lehle, Ludwig and Körner, Christian (2004) In American Journal of Human Genetics 74(3). p.472-481
- Contribution to journal › Article
2003
Mark Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies
Antoniou, A ; Pharoah, PDP ; Narod, S ; Risch, HA ; Eyfjord, JE ; Hopper, JL ; Loman, Niklas ^LU ; Olsson, H ^LU ; Johannsson, O and Borg, Åke ^LU , et al. (2003) In American Journal of Human Genetics 72(5). p.1117-1130
- Contribution to journal › Article
Mark A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1
Storlazzi, C. ; Anelli, L. ; Albano, F. ; Zagaria, A. ; Ventura, M. ; Rocchi, M. ; Panagopoulos, Ioannis ^LU ; Pannunzio, A. ; Ottaviani, E. and Liso, V. , et al. (2003) In American Journal of Human Genetics 73(5). p.223-223
- Contribution to journal › Published meeting abstract
Mark Localization of a novel melanoma susceptibility locus to 1p22
Gillanders, E ; Juo, SHH ; Holland, EA ; Jones, M ; Nancarrow, D ; Freas-Lutz, D ; Sood, R ; Park, N ; Faruque, M and Markey, Christopher ^LU , et al. (2003) In American Journal of Human Genetics 73(2). p.301-313
- Contribution to journal › Article
2002
Mark A variation in 3 ' UTR of hPTP1B increases specific gene expression and associates with insulin resistance
Di Paola, R ; Frittitta, L ; Miscio, G ; Bozzali, M ; Baratta, R ; Centra, M ; Spampinato, D ; Santagati, MG ; Ercolino, T and Cisternino, C , et al. (2002) In American Journal of Human Genetics 70(3). p.806-812
- Contribution to journal › Article
Mark GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L
Visapaa, Ilona ; Fellman, Vineta ^LU ; Vesa, Jouni ; Dasvarma, Ayan ; Hutton, Jenna L ; Kumar, Vijay ; Payne, Gregory S ; Makarow, Marja ; Van Coster, Rudy and Taylor, Robert W , et al. (2002) In American Journal of Human Genetics 71(4). p.863-876
- Contribution to journal › Article

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