PuSH - Publication Server of Helmholtz Zentrum München

8 Records found.
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1.
Moore, C.* et al.: Resequencing study confirms host defense and cell senescence gene variants contribute to the risk of idiopathic pulmonary fibrosis. Am. J. Respir. Crit. Care Med., accepted (2019)
2.
Ostaszewski, M.* et al.: Community-driven roadmap for integrated disease maps. Brief. Bioinform. 20, 659-670 (2019)
3.
Said, E.* et al.: Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1. Am. J. Med. Genet. A 173, 3098-3103 (2017)
4.
McCarthy, S.* et al.: A reference panel of 64,976 haplotypes for genotype imputation. Nat. Genet. 48, 1279-1283 (2016)
5.
Lange, L.A.* et al.: Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am. J. Hum. Genet. 94, 233-245 (2014)
6.
Stitziel, N.O.* et al.: Inactivating mutations in NPC1L1 and protection from coronary heart disease. N. Engl. J. Med. 371, 2072-2082 (2014)
7.
Teslovich, T.M.* et al.: Biological, clinical and population relevance of 95 loci for blood lipids. Nature 466, 707-713 (2010)
8.
Zhu, X.* et al.: Localization of a Small Genomic Region Associated with Elevated ACE. Am. J. Hum. Genet. 67, 1144-1153 (2000)