Hubner N - Search Results

1

PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.

Decker E, Stellzig-Eisenhauer A, Fiebig BS, Rau C, Kress W, Saar K, Rüschendorf F, Hubner N, Grimm T, Weber BH. Decker E, et al. Among authors: hubner n. Am J Hum Genet. 2008 Dec;83(6):781-6. doi: 10.1016/j.ajhg.2008.11.006. Am J Hum Genet. 2008. PMID: 19061984 Free PMC article.

2

Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p.

Lee-Kirsch MA, Gong M, Schulz H, Rüschendorf F, Stein A, Pfeiffer C, Ballarini A, Gahr M, Hubner N, Linné M. Lee-Kirsch MA, et al. Among authors: hubner n. Am J Hum Genet. 2006 Oct;79(4):731-7. doi: 10.1086/507848. Epub 2006 Aug 17. Am J Hum Genet. 2006. PMID: 16960810 Free PMC article.

3

Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis.

Söderhäll C, Marenholz I, Kerscher T, Rüschendorf F, Esparza-Gordillo J, Worm M, Gruber C, Mayr G, Albrecht M, Rohde K, Schulz H, Wahn U, Hubner N, Lee YA. Söderhäll C, et al. Among authors: hubner n. PLoS Biol. 2007 Sep;5(9):e242. doi: 10.1371/journal.pbio.0050242. PLoS Biol. 2007. PMID: 17850181 Free PMC article.

4

A common haplotype of the IL-31 gene influencing gene expression is associated with nonatopic eczema.

Schulz F, Marenholz I, Fölster-Holst R, Chen C, Sternjak A, Baumgrass R, Esparza-Gordillo J, Grüber C, Nickel R, Schreiber S, Stoll M, Kurek M, Rüschendorf F, Hubner N, Wahn U, Lee YA. Schulz F, et al. Among authors: hubner n. J Allergy Clin Immunol. 2007 Nov;120(5):1097-102. doi: 10.1016/j.jaci.2007.07.065. Epub 2007 Sep 27. J Allergy Clin Immunol. 2007. PMID: 17900679

5

Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease.

Monti J, Fischer J, Paskas S, Heinig M, Schulz H, Gösele C, Heuser A, Fischer R, Schmidt C, Schirdewan A, Gross V, Hummel O, Maatz H, Patone G, Saar K, Vingron M, Weldon SM, Lindpaintner K, Hammock BD, Rohde K, Dietz R, Cook SA, Schunck WH, Luft FC, Hubner N. Monti J, et al. Among authors: hubner n. Nat Genet. 2008 May;40(5):529-37. doi: 10.1038/ng.129. Nat Genet. 2008. PMID: 18443590 Free PMC article.

6

Distribution and functional impact of DNA copy number variation in the rat.

Guryev V, Saar K, Adamovic T, Verheul M, van Heesch SA, Cook S, Pravenec M, Aitman T, Jacob H, Shull JD, Hubner N, Cuppen E. Guryev V, et al. Among authors: hubner n. Nat Genet. 2008 May;40(5):538-45. doi: 10.1038/ng.141. Nat Genet. 2008. PMID: 18443591

7

SNP and haplotype mapping for genetic analysis in the rat.

STAR Consortium; Saar K, Beck A, Bihoreau MT, Birney E, Brocklebank D, Chen Y, Cuppen E, Demonchy S, Dopazo J, Flicek P, Foglio M, Fujiyama A, Gut IG, Gauguier D, Guigo R, Guryev V, Heinig M, Hummel O, Jahn N, Klages S, Kren V, Kube M, Kuhl H, Kuramoto T, Kuroki Y, Lechner D, Lee YA, Lopez-Bigas N, Lathrop GM, Mashimo T, Medina I, Mott R, Patone G, Perrier-Cornet JA, Platzer M, Pravenec M, Reinhardt R, Sakaki Y, Schilhabel M, Schulz H, Serikawa T, Shikhagaie M, Tatsumoto S, Taudien S, Toyoda A, Voigt B, Zelenika D, Zimdahl H, Hubner N. STAR Consortium, et al. Among authors: hubner n. Nat Genet. 2008 May;40(5):560-6. doi: 10.1038/ng.124. Nat Genet. 2008. PMID: 18443594 Free PMC article.

8

Genome-wide linkage scan for bladder exstrophy-epispadias complex.

Ludwig M, Rüschendorf F, Saar K, Hübner N, Siekmann L, Boyadjiev SA, Reutter H. Ludwig M, et al. Among authors: hubner n. Birth Defects Res A Clin Mol Teratol. 2009 Feb;85(2):174-8. doi: 10.1002/bdra.20512. Birth Defects Res A Clin Mol Teratol. 2009. PMID: 19086019

9

A common variant on chromosome 11q13 is associated with atopic dermatitis.

Esparza-Gordillo J, Weidinger S, Fölster-Holst R, Bauerfeind A, Ruschendorf F, Patone G, Rohde K, Marenholz I, Schulz F, Kerscher T, Hubner N, Wahn U, Schreiber S, Franke A, Vogler R, Heath S, Baurecht H, Novak N, Rodriguez E, Illig T, Lee-Kirsch MA, Ciechanowicz A, Kurek M, Piskackova T, Macek M, Lee YA, Ruether A. Esparza-Gordillo J, et al. Among authors: hubner n. Nat Genet. 2009 May;41(5):596-601. doi: 10.1038/ng.347. Epub 2009 Apr 6. Nat Genet. 2009. PMID: 19349984

10

Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation.

Huck K, Feyen O, Niehues T, Rüschendorf F, Hübner N, Laws HJ, Telieps T, Knapp S, Wacker HH, Meindl A, Jumaa H, Borkhardt A. Huck K, et al. Among authors: hubner n. J Clin Invest. 2009 May;119(5):1350-8. doi: 10.1172/jci37901. J Clin Invest. 2009. PMID: 19425169 Free PMC article.

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