PuSH - Publication Server of Helmholtz Zentrum München

23 Records found.
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1.
Kueffner, R.* et al.: Stratification of amyotrophic lateral sclerosis patients: A crowdsourcing approach. Sci. Rep. 9:690 (2019)
2.
Böhm, J.* et al.: Understanding the molecular basis of salt sequestration in epidermal bladder cells of Chenopodium quinoa. Curr. Biol. 28, 3075-3085.e7 (2018)
3.
Felix, J.F.* et al.: Cohort profile: Pregnancy and childhood epigenetics (PACE) consortium. Int. J. Epidemiol. 47, 22-23u (2018)
4.
Gu, F.* et al.: Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia. Int. J. Cancer 141, 1794-1802 (2017)
5.
Lu, X.* et al.: Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease. Nat. Genet. 49, 1722–1730 (2017)
6.
Webb, T.R.* et al.: Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease. J. Am. Coll. Cardiol. 69, 823-836 (2017)
7.
Zou, C.* et al.: A high-quality genome assembly of quinoa provides insights into the molecular basis of salt bladder-based salinity tolerance and the exceptional nutritional value. Cell Res. 27, 1327-1340 (2017)
8.
Ma, C.* et al.: NAFLD causes selective CD4+ T lymphocyte loss and promotes hepatocarcinogenesis. Nature 531, 253-257 (2016)
9.
McCarthy, S.* et al.: A reference panel of 64,976 haplotypes for genotype imputation. Nat. Genet. 48, 1279-1283 (2016)
10.
Nestor, C.E.* et al.: 5-hydroxymethylcytosine remodeling precedes lineage specification during differentiation of human CD4+ T cells. Cell Rep. 16, 559-570 (2016)
11.
Stitziel, N.O.* et al.: Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease. N. Engl. J. Med. 374, 1134-1144 (2016)
12.
Stitziel, N.O.* et al.: Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease (vol 374, pg 1134, 2016). N. Engl. J. Med. 374, 1898-1898 (2016)
13.
Surendran, P.* et al.: Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat. Genet. 48, 1151-1161 (2016)
14.
Ganesh, S.K.* et al.: Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. Am. J. Hum. Genet. 95, 49-65 (2014)
15.
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)
16.
Ellinghaus, D.* et al.: Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies. Gastroenterology 145, 339-347 (2013)
17.
Horikoshi, M.* et al.: New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nat. Genet. 45, 76-82 (2013)
18.
Lanktree, M.B.* et al.: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height. Am. J. Hum. Genet. 88, 6-18 (2011)
19.
Nalls, M.A.* et al.: Failure to validate association between 12p13 variants and ischemic stroke. N. Engl. J. Med. 362, 1547-1550 (2010)
20.
Itoh, T.* et al.: Curated genome annotation of Oryza sativa ssp. japonica and comparative genome analysis with Arabidopsis thaliana. Genome Res. 17, 175-183 (2007)