Wienker TF - Search Results

1

Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 gene.

Omran H, Sasmaz G, Häffner K, Volz A, Olbrich H, Melkaoui R, Otto E, Wienker TF, Korinthenberg R, Brandis M, Antignac C, Hildebrandt F. Omran H, et al. Among authors: wienker tf. J Am Soc Nephrol. 2002 Jan;13(1):75-79. doi: 10.1681/ASN.V13175. J Am Soc Nephrol. 2002. PMID: 11752023

2

Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p.

Ruf RG, Fuchshuber A, Karle SM, Lemainque A, Huck K, Wienker T, Otto E, Hildebrandt F. Ruf RG, et al. J Am Soc Nephrol. 2003 Jul;14(7):1897-900. doi: 10.1097/01.asn.0000070070.03811.02. J Am Soc Nephrol. 2003. PMID: 12819251

3

Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene.

Omran H, Häffner K, Völkel A, Kuehr J, Ketelsen UP, Ross UH, Konietzko N, Wienker T, Brandis M, Hildebrandt F. Omran H, et al. Am J Respir Cell Mol Biol. 2000 Nov;23(5):696-702. doi: 10.1165/ajrcmb.23.5.4257. Am J Respir Cell Mol Biol. 2000. PMID: 11062149

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

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.

Sander T, Bockenkamp B, Hildmann T, Blasczyk R, Kretz R, Wienker TF, Volz A, Schmitz B, Beck-Mannagetta G, Riess O, Epplen JT, Janz D, Ziegler A. Sander T, et al. Among authors: wienker tf. Neurology. 1997 Sep;49(3):842-7. doi: 10.1212/wnl.49.3.842. Neurology. 1997. PMID: 9305351

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

A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.

Betz RC, Lee YA, Bygum A, Brandrup F, Bernal AI, Toribio J, Alvarez JI, Kukuk GM, Ibsen HH, Rasmussen HB, Wienker TF, Reis A, Propping P, Kruse R, Cichon S, Nöthen MM. Betz RC, et al. Among authors: wienker tf. Am J Hum Genet. 2000 Jun;66(6):1979-83. doi: 10.1086/302934. Epub 2000 May 2. Am J Hum Genet. 2000. PMID: 10793007 Free PMC article.

8

Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome.

Kloos DU, Jakubiczka S, Wienker T, Wolff G, Wieacker P. Kloos DU, et al. Hum Genet. 1997 Sep;100(3-4):426-30. doi: 10.1007/s004390050528. Hum Genet. 1997. PMID: 9272167

9

Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization.

Strauch K, Fimmers R, Kurz T, Deichmann KA, Wienker TF, Baur MP. Strauch K, et al. Among authors: wienker tf. Am J Hum Genet. 2000 Jun;66(6):1945-57. doi: 10.1086/302911. Epub 2000 May 4. Am J Hum Genet. 2000. PMID: 10796874 Free PMC article.

10

Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease).

Wolff G, Mayerová A, Wienker TF, Atalianis P, Ioannou P, Warburg M. Wolff G, et al. Among authors: wienker tf. J Med Genet. 1992 Nov;29(11):816-9. doi: 10.1136/jmg.29.11.816. J Med Genet. 1992. PMID: 1453434 Free PMC article.

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