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924 results

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Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia.
Kamm C, Asmus F, Mueller J, Mayer P, Sharma M, Muller UJ, Beckert S, Ehling R, Illig T, Wichmann HE, Poewe W, Mueller JC, Gasser T. Kamm C, et al. Among authors: wichmann he. Neurology. 2006 Nov 28;67(10):1857-9. doi: 10.1212/01.wnl.0000244423.63406.17. Neurology. 2006. PMID: 17130424
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures.
Schlachter K, Gruber-Sedlmayr U, Stogmann E, Lausecker M, Hotzy C, Balzar J, Schuh E, Baumgartner C, Mueller JC, Illig T, Wichmann HE, Lichtner P, Meitinger T, Strom TM, Zimprich A, Zimprich F. Schlachter K, et al. Among authors: wichmann he. Neurology. 2009 Mar 17;72(11):974-8. doi: 10.1212/01.wnl.0000344401.02915.00. Neurology. 2009. PMID: 19289736
Association study of mast cell chymase polymorphisms with atopy.
Weidinger S, Rümmler L, Klopp N, Wagenpfeil S, Baurecht HJ, Fischer G, Holle R, Gauger A, Schäfer T, Jakob T, Ollert M, Behrendt H, Wichmann HE, Ring J, Illig T. Weidinger S, et al. Among authors: wichmann he. Allergy. 2005 Oct;60(10):1256-61. doi: 10.1111/j.1398-9995.2005.00879.x. Allergy. 2005. PMID: 16134991
Genetic variants in the USF1 gene are associated with low-density lipoprotein cholesterol levels and incident type 2 diabetes mellitus in women: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.
Holzapfel C, Baumert J, Grallert H, Müller AM, Thorand B, Khuseyinova N, Herder C, Meisinger C, Hauner H, Wichmann HE, Koenig W, Illig T, Klopp N. Holzapfel C, et al. Among authors: wichmann he. Eur J Endocrinol. 2008 Oct;159(4):407-16. doi: 10.1530/EJE-08-0356. Epub 2008 Jul 1. Eur J Endocrinol. 2008. PMID: 18593823
First investigation of two obesity-related loci (TMEM18, FTO) concerning their association with educational level as well as income: the MONICA/KORA study.
Holzapfel C, Grallert H, Baumert J, Thorand B, Döring A, Wichmann HE, Hauner H, Illig T, Mielck A. Holzapfel C, et al. Among authors: wichmann he. J Epidemiol Community Health. 2011 Feb;65(2):174-6. doi: 10.1136/jech.2009.106492. Epub 2010 Jul 13. J Epidemiol Community Health. 2011. PMID: 20628085 Free PMC article.
Genetic variants in the leukemia-associated Rho guanine nucleotide exchange factor (ARHGEF12) gene are not associated with T2DM and related parameters in Caucasians (KORA study).
Holzapfel C, Klopp N, Grallert H, Huth C, Gieger C, Meisinger C, Strassburger K, Giani G, Wichmann HE, Laumen H, Hauner H, Herder C, Rathmann W, Illig T. Holzapfel C, et al. Among authors: wichmann he. Eur J Endocrinol. 2007 Sep;157(3):R1-5. doi: 10.1530/EJE-07-0297. Eur J Endocrinol. 2007. PMID: 17766704
Replication of restless legs syndrome loci in three European populations.
Kemlink D, Polo O, Frauscher B, Gschliesser V, Högl B, Poewe W, Vodicka P, Vavrova J, Sonka K, Nevsimalova S, Schormair B, Lichtner P, Silander K, Peltonen L, Gieger C, Wichmann HE, Zimprich A, Roeske D, Müller-Myhsok B, Meitinger T, Winkelmann J. Kemlink D, et al. Among authors: wichmann he. J Med Genet. 2009 May;46(5):315-8. doi: 10.1136/jmg.2008.062992. Epub 2009 Mar 10. J Med Genet. 2009. PMID: 19279021 Free PMC article.
924 results