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9 Records found.
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1.
Zhao, H.* et al.: Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. Cephalalgia 36, 648-657 (2016)
2.
Nyholt, D.R.* et al.: Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies. Cephalalgia 35, 489-499 (2015)
3.
Anttila, V.* et al.: Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nat. Genet. 45, 912-917 (2013)
4.
Ludwig, K.U.* et al.: A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. Transl. Psychiatry 3:e229 (2013)
5.
Rietschel, M.* et al.: Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Mol. Psychiatry 17, 906-917 (2012)
6.
Cichon, S.* et al.: Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am. J. Hum. Genet. 88, 372-381 (2011)
7.
Anttila, V.* et al.: Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nat. Genet. 42, 869-873 (2010)
8.
di Angelantonio, E.* et al.: Major lipids, apolipoproteins, and risk of vascular disease. JAMA 302, 1993-2000 (2009)
9.
Erqou, S.* et al.: Lipoprotein(a) concentration and the risk of coronary heart disease, stroke, and nonvascular mortality. JAMA 302, 412-423 (2009)