Illig T - Search Results

1

Association of the interleukin-1 receptor antagonist gene with asthma.

Gohlke H, Illig T, Bahnweg M, Klopp N, André E, Altmüller J, Herbon N, Werner M, Knapp M, Pescollderungg L, Boner A, Malerba G, Pignatti PF, Wjst M. Gohlke H, et al. Among authors: illig t. Am J Respir Crit Care Med. 2004 Jun 1;169(11):1217-23. doi: 10.1164/rccm.200302-281OC. Epub 2004 Mar 12. Am J Respir Crit Care Med. 2004. PMID: 15020290 Clinical Trial.

2

STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study.

Duetsch G, Illig T, Loesgen S, Rohde K, Klopp N, Herbon N, Gohlke H, Altmueller J, Wjst M. Duetsch G, et al. Among authors: illig t. Hum Mol Genet. 2002 Mar 15;11(6):613-21. doi: 10.1093/hmg/11.6.613. Hum Mol Genet. 2002. PMID: 11912176

3

Asthma and IL-4 receptor alpha gene variants.

Wjst M, Kruse S, Illig T, Deichmann K. Wjst M, et al. Among authors: illig t. Eur J Immunogenet. 2002 Jun;29(3):263-8. doi: 10.1046/j.1365-2370.2002.00300.x. Eur J Immunogenet. 2002. PMID: 12047364

4

Genetics of asthma and related phenotypes.

Illig T, Wjst M. Illig T, et al. Paediatr Respir Rev. 2002 Mar;3(1):47-51. doi: 10.1053/prrv.2002.0185. Paediatr Respir Rev. 2002. PMID: 12065182 Review.

5

Large-scale determination of SNP allele frequencies in DNA pools using MALDI-TOF mass spectrometry.

Werner M, Sych M, Herbon N, Illig T, König IR, Wjst M. Werner M, et al. Among authors: illig t. Hum Mutat. 2002 Jul;20(1):57-64. doi: 10.1002/humu.10094. Hum Mutat. 2002. PMID: 12112658

6

Further support for the association of CCR5 allelic variants with asthma susceptibility.

McGinnis R, Child F, Clayton S, Davies S, Lenney W, Illig T, Wjst M, Spurr N, Debouck C, Hajeer AH, Ollier WE, Strange R, Fryer AA. McGinnis R, et al. Among authors: illig t. Eur J Immunogenet. 2002 Dec;29(6):525-8. doi: 10.1046/j.1365-2370.2002.00357.x. Eur J Immunogenet. 2002. PMID: 12437612

7

Further genetic heterogeneity for autosomal dominant human sutural cataracts.

Klopp N, Héon E, Billingsley G, Illig T, Wjst M, Rudolph G, Graw J. Klopp N, et al. Among authors: illig t. Ophthalmic Res. 2003 Mar-Apr;35(2):71-7. doi: 10.1159/000069134. Ophthalmic Res. 2003. PMID: 12646746 Free article.

8

High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases.

Herbon N, Werner M, Braig C, Gohlke H, Dütsch G, Illig T, Altmüller J, Hampe J, Lantermann A, Schreiber S, Bonifacio E, Ziegler A, Schwab S, Wildenauer D, van den Boom D, Braun A, Knapp M, Reitmeir P, Wjst M. Herbon N, et al. Among authors: illig t. Genomics. 2003 May;81(5):510-8. doi: 10.1016/s0888-7543(02)00035-6. Genomics. 2003. PMID: 12706109

9

Melanocortin-4 receptor gene variant I103 is negatively associated with obesity.

Geller F, Reichwald K, Dempfle A, Illig T, Vollmert C, Herpertz S, Siffert W, Platzer M, Hess C, Gudermann T, Biebermann H, Wichmann HE, Schäfer H, Hinney A, Hebebrand J. Geller F, et al. Among authors: illig t. Am J Hum Genet. 2004 Mar;74(3):572-81. doi: 10.1086/382490. Epub 2004 Feb 17. Am J Hum Genet. 2004. PMID: 14973783 Free PMC article.

10

Prion protein codon 129 polymorphism and risk of Alzheimer disease.

Riemenschneider M, Klopp N, Xiang W, Wagenpfeil S, Vollmert C, Müller U, Förstl H, Illig T, Kretzschmar H, Kurz A. Riemenschneider M, et al. Among authors: illig t. Neurology. 2004 Jul 27;63(2):364-6. doi: 10.1212/01.wnl.0000130198.72589.69. Neurology. 2004. PMID: 15277640

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