Wienker TF - Search Results

1

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.

2

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.

3

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.

4

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.

5

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.

6

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

7

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

8

Localisation of a Fanconi anaemia gene to chromosome 9p.

Saar K, Schindler D, Wegner RD, Reis A, Wienker TF, Hoehn H, Joenje H, Sperling K, Digweed M. Saar K, et al. Among authors: wienker tf. Eur J Hum Genet. 1998 Sep-Oct;6(5):501-8. doi: 10.1038/sj.ejhg.5200241. Eur J Hum Genet. 1998. PMID: 9801875

9

Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster.

Weber A, Wienker TF, Jung M, Easton D, Dean HJ, Heinrichs C, Reis A, Clark AJ. Weber A, et al. Among authors: wienker tf. Hum Mol Genet. 1996 Dec;5(12):2061-6. doi: 10.1093/hmg/5.12.2061. Hum Mol Genet. 1996. PMID: 8968764

10

Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers.

Starfield M, Hennies HC, Jung M, Jenkins T, Wienker T, Hull P, Spurdle A, Küster W, Ramsay M, Reis A. Starfield M, et al. Am J Hum Genet. 1997 Aug;61(2):370-8. doi: 10.1086/514848. Am J Hum Genet. 1997. PMID: 9311742 Free PMC article.

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