Lindner TH - Search Results

1

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly).

Hoffmann K, Dreger CK, Olins AL, Olins DE, Shultz LD, Lucke B, Karl H, Kaps R, Müller D, Vayá A, Aznar J, Ware RE, Sotelo Cruz N, Lindner TH, Herrmann H, Reis A, Sperling K. Hoffmann K, et al. Among authors: lindner th. Nat Genet. 2002 Aug;31(4):410-4. doi: 10.1038/ng925. Epub 2002 Jul 15. Nat Genet. 2002. PMID: 12118250

2

Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects.

Arélin M, Schulze B, Müller-Myhsok B, Horn D, Diers A, Uhlenberg B, Nürnberg P, Nürnberg G, Becker C, Mundlos S, Lindner TH, Sperling K, Hoffmann K. Arélin M, et al. Among authors: lindner th. Eur J Hum Genet. 2013 Apr;21(4):367-72. doi: 10.1038/ejhg.2012.198. Epub 2012 Oct 3. Eur J Hum Genet. 2013. PMID: 23032112 Free PMC article.

3

easyLINKAGE-Plus--automated linkage analyses using large-scale SNP data.

Hoffmann K, Lindner TH. Hoffmann K, et al. Among authors: lindner th. Bioinformatics. 2005 Sep 1;21(17):3565-7. doi: 10.1093/bioinformatics/bti571. Epub 2005 Jul 12. Bioinformatics. 2005. PMID: 16014370

4

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: lindner th. J Hypertens. 2009 May;27(5):983-90. doi: 10.1097/HJH.0b013e328328123d. J Hypertens. 2009. PMID: 19373111

5

HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing.

Seifert W, Beninde J, Hoffmann K, Lindner TH, Bassir C, Aksu F, Hübner C, Verbeek NE, Mundlos S, Horn D. Seifert W, et al. Among authors: lindner th. Eur J Hum Genet. 2009 Dec;17(12):1570-6. doi: 10.1038/ejhg.2009.104. Epub 2009 Jul 1. Eur J Hum Genet. 2009. PMID: 19568269 Free PMC article.

6

easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses.

Lindner TH, Hoffmann K. Lindner TH, et al. Bioinformatics. 2005 Feb 1;21(3):405-7. doi: 10.1093/bioinformatics/bti009. Epub 2004 Sep 3. Bioinformatics. 2005. PMID: 15347576

7

AssociationDB: web-based exploration of genomic association.

Seelow D, Hoffmann K, Lindner TH. Seelow D, et al. Among authors: lindner th. Bioinformatics. 2007 Oct 1;23(19):2643-4. doi: 10.1093/bioinformatics/btm376. Epub 2007 Jul 27. Bioinformatics. 2007. PMID: 17660207

8

Faulty initiation of proteoglycan synthesis causes cardiac and joint defects.

Baasanjav S, Al-Gazali L, Hashiguchi T, Mizumoto S, Fischer B, Horn D, Seelow D, Ali BR, Aziz SA, Langer R, Saleh AA, Becker C, Nürnberg G, Cantagrel V, Gleeson JG, Gomez D, Michel JB, Stricker S, Lindner TH, Nürnberg P, Sugahara K, Mundlos S, Hoffmann K. Baasanjav S, et al. Among authors: lindner th. Am J Hum Genet. 2011 Jul 15;89(1):15-27. doi: 10.1016/j.ajhg.2011.05.021. Am J Hum Genet. 2011. PMID: 21763480 Free PMC article.

9

Hidden population substructures in an apparently homogeneous population bias association studies.

Berger M, Stassen HH, Köhler K, Krane V, Mönks D, Wanner C, Hoffmann K, Hoffmann MM, Zimmer M, Bickeböller H, Lindner TH. Berger M, et al. Among authors: lindner th. Eur J Hum Genet. 2006 Feb;14(2):236-44. doi: 10.1038/sj.ejhg.5201546. Eur J Hum Genet. 2006. PMID: 16333311

10

A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.

Hoffmann K, Mattheisen M, Dahm S, Nürnberg P, Roe C, Johnson J, Cox NJ, Wichmann HE, Wienker TF, Schulze J, Schwarz PE, Lindner TH. Hoffmann K, et al. Among authors: lindner th. Diabetologia. 2007 Jul;50(7):1418-22. doi: 10.1007/s00125-007-0658-4. Epub 2007 Apr 27. Diabetologia. 2007. PMID: 17464498

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