Wienker TF - Search Results

1

Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma.

Niemann S, Becker-Follmann J, Nürnberg G, Rüschendorf F, Sieweke N, Hügens-Penzel M, Traupe H, Wienker TF, Reis A, Müller U. Niemann S, et al. Among authors: wienker tf. Am J Med Genet. 2001 Jan 1;98(1):32-6. Am J Med Genet. 2001. PMID: 11426453

2

Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13.

Lee YA, Rüschendorf F, Windemuth C, Schmitt-Egenolf M, Stadelmann A, Nürnberg G, Ständer M, Wienker TF, Reis A, Traupe H. Lee YA, et al. Among authors: wienker tf. Am J Hum Genet. 2000 Oct;67(4):1020-4. doi: 10.1086/303075. Epub 2000 Sep 13. Am J Hum Genet. 2000. PMID: 10986047 Free PMC article.

3

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.

Saar K, Chrzanowska KH, Stumm M, Jung M, Nürnberg G, Wienker TF, Seemanová E, Wegner RD, Reis A, Sperling K. Saar K, et al. Among authors: wienker tf. Am J Hum Genet. 1997 Mar;60(3):605-10. Am J Hum Genet. 1997. PMID: 9042920 Free PMC article.

4

The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.

Vollmer M, Jung M, Rüschendorf F, Ruf R, Wienker T, Reis A, Krapf R, Hildebrandt F. Vollmer M, et al. Am J Hum Genet. 1998 Dec;63(6):1724-31. doi: 10.1086/302162. Am J Hum Genet. 1998. PMID: 9837825 Free PMC article.

5

Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.

Jung M, Poepping I, Perrot A, Ellmer AE, Wienker TF, Dietz R, Reis A, Osterziel KJ. Jung M, et al. Among authors: wienker tf. Am J Hum Genet. 1999 Oct;65(4):1068-77. doi: 10.1086/302580. Am J Hum Genet. 1999. PMID: 10486326 Free PMC article.

6

Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

Bosse K, Betz RC, Lee YA, Wienker TF, Reis A, Kleen H, Propping P, Cichon S, Nöthen MM. Bosse K, et al. Among authors: wienker tf. Am J Hum Genet. 2000 Aug;67(2):492-7. doi: 10.1086/303028. Epub 2000 Jun 30. Am J Hum Genet. 2000. PMID: 10877983 Free PMC article.

7

Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.

Stöber G, Saar K, Rüschendorf F, Meyer J, Nürnberg G, Jatzke S, Franzek E, Reis A, Lesch KP, Wienker TF, Beckmann H. Stöber G, et al. Among authors: wienker tf. Am J Hum Genet. 2000 Nov;67(5):1201-7. doi: 10.1016/S0002-9297(07)62950-4. Epub 2000 Sep 19. Am J Hum Genet. 2000. PMID: 11001582 Free PMC article.

8

Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus.

Meyer J, Ortega G, Schraut K, Nürnberg G, Rüschendorf F, Saar K, Mössner R, Wienker TF, Reis A, Stöber G, Lesch KP. Meyer J, et al. Among authors: wienker tf. Mol Psychiatry. 2002;7(2):220-3. doi: 10.1038/sj.mp.4000970. Mol Psychiatry. 2002. PMID: 11840317

9

Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping.

Laass MW, Hennies HC, Preis S, Stevens HP, Jung M, Leigh IM, Wienker TF, Reis A. Laass MW, et al. Among authors: wienker tf. Hum Genet. 1997 Dec;101(3):376-82. doi: 10.1007/s004390050645. Hum Genet. 1997. PMID: 9439671

10

A major susceptibility locus for atopic dermatitis maps to chromosome 3q21.

Lee YA, Wahn U, Kehrt R, Tarani L, Businco L, Gustafsson D, Andersson F, Oranje AP, Wolkertstorfer A, v Berg A, Hoffmann U, Küster W, Wienker T, Rüschendorf F, Reis A. Lee YA, et al. Nat Genet. 2000 Dec;26(4):470-3. doi: 10.1038/82625. Nat Genet. 2000. PMID: 11101848

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