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698 results

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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.
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
Linkage disequilibrium patterns and tagSNP transferability among European populations.
Mueller JC, Lõhmussaar E, Mägi R, Remm M, Bettecken T, Lichtner P, Biskup S, Illig T, Pfeufer A, Luedemann J, Schreiber S, Pramstaller P, Pichler I, Romeo G, Gaddi A, Testa A, Wichmann HE, Metspalu A, Meitinger T. Mueller JC, et al. Among authors: illig t. Am J Hum Genet. 2005 Mar;76(3):387-98. doi: 10.1086/427925. Epub 2005 Jan 6. Am J Hum Genet. 2005. PMID: 15637659 Free PMC article.
Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study.
Pfeufer A, Jalilzadeh S, Perz S, Mueller JC, Hinterseer M, Illig T, Akyol M, Huth C, Schöpfer-Wendels A, Kuch B, Steinbeck G, Holle R, Näbauer M, Wichmann HE, Meitinger T, Kääb S. Pfeufer A, et al. Among authors: illig t. Circ Res. 2005 Apr 1;96(6):693-701. doi: 10.1161/01.RES.0000161077.53751.e6. Epub 2005 Mar 3. Circ Res. 2005. PMID: 15746444
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group.
Kamm C, Healy DG, Quinn NP, Wüllner U, Moller JC, Schols L, Geser F, Burk K, Børglum AD, Pellecchia MT, Tolosa E, del Sorbo F, Nilsson C, Bandmann O, Sharma M, Mayer P, Gasteiger M, Haworth A, Ozawa T, Lees AJ, Short J, Giunti P, Holinski-Feder E, Illig T, Wichmann HE, Wenning GK, Wood NW, Gasser T; European Multiple System Atrophy Study Group. Kamm C, et al. Among authors: illig t. Brain. 2005 Aug;128(Pt 8):1855-60. doi: 10.1093/brain/awh535. Epub 2005 Jun 9. Brain. 2005. PMID: 15947063
Association of NOD1 polymorphisms with atopic eczema and related phenotypes.
Weidinger S, Klopp N, Rummler L, Wagenpfeil S, Novak N, Baurecht HJ, Groer W, Darsow U, Heinrich J, Gauger A, Schafer T, Jakob T, Behrendt H, Wichmann HE, Ring J, Illig T. Weidinger S, et al. Among authors: illig t. J Allergy Clin Immunol. 2005 Jul;116(1):177-84. doi: 10.1016/j.jaci.2005.02.034. J Allergy Clin Immunol. 2005. PMID: 15990792
Association of CARD15 polymorphisms with atopy-related traits in a population-based cohort of Caucasian adults.
Weidinger S, Klopp N, Rümmler L, Wagenpfeil S, Baurecht HJ, Gauger A, Darsow U, Jakob T, Novak N, Schäfer T, Heinrich J, Behrendt H, Wichmann HE, Ring J, Illig T; KORA study group. Weidinger S, et al. Among authors: illig t. Clin Exp Allergy. 2005 Jul;35(7):866-72. doi: 10.1111/j.1365-2222.2005.02269.x. Clin Exp Allergy. 2005. PMID: 16008671
698 results