Reis A - Search Results

1

A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany.

Hoffmann K, Planitz C, Rüschendorf F, Müller-Myhsok B, Stassen HH, Lucke B, Mattheisen M, Stumvoll M, Bochmann R, Zschornack M, Wienker TF, Nürnberg P, Reis A, Luft FC, Lindner TH. Hoffmann K, et al. Among authors: reis a. J Hypertens. 2009 May;27(5):983-90. doi: 10.1097/HJH.0b013e328328123d. J Hypertens. 2009. PMID: 19373111

2

Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene cluster.

Hennies HC, Küster W, Mischke D, Reis A. Hennies HC, et al. Among authors: reis a. Hum Mol Genet. 1995 Jun;4(6):1015-20. doi: 10.1093/hmg/4.6.1015. Hum Mol Genet. 1995. PMID: 7544663

3

Trinucleotide repeat polymorphism at the PKLR locus.

Lenzner C, Jacobasch G, Reis A, Thiele B, Nürnberg P. Lenzner C, et al. Among authors: reis a. Hum Mol Genet. 1994 Mar;3(3):523. doi: 10.1093/hmg/3.3.523-a. Hum Mol Genet. 1994. PMID: 8012373 No abstract available.

4

Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemia.

Lenzner C, Nürnberg P, Thiele BJ, Reis A, Brabec V, Sakalova A, Jacobasch G. Lenzner C, et al. Among authors: reis a. Blood. 1994 May 15;83(10):2817-22. Blood. 1994. PMID: 8180378 Free article.

5

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: reis a. Hum Mol Genet. 1996 Dec;5(12):2061-6. doi: 10.1093/hmg/5.12.2061. Hum Mol Genet. 1996. PMID: 8968764

6

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: reis a. Am J Hum Genet. 1997 Mar;60(3):605-10. Am J Hum Genet. 1997. PMID: 9042920 Free PMC article.

7

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. Among authors: reis a. Am J Hum Genet. 1997 Aug;61(2):370-8. doi: 10.1086/514848. Am J Hum Genet. 1997. PMID: 9311742 Free PMC article.

8

The gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor gene.

Nürnberg P, Tinschert S, Mrug M, Hampe J, Müller CR, Fuhrmann E, Braun HS, Reis A. Nürnberg P, et al. Among authors: reis a. Am J Hum Genet. 1997 Oct;61(4):918-23. doi: 10.1086/514880. Am J Hum Genet. 1997. PMID: 9382103 Free PMC article.

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: reis a. Hum Genet. 1997 Dec;101(3):376-82. doi: 10.1007/s004390050645. Hum Genet. 1997. PMID: 9439671

10

Gene localization for an autosomal dominant familial periodic fever to 12p13.

Mulley J, Saar K, Hewitt G, Rüschendorf F, Phillips H, Colley A, Sillence D, Reis A, Wilson M. Mulley J, et al. Among authors: reis a. Am J Hum Genet. 1998 Apr;62(4):884-9. doi: 10.1086/301793. Am J Hum Genet. 1998. PMID: 9529351 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3,434 results

Search Page

Filters