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121.
Deloukas, P.* et al.: Large-scale association analysis identifies new risk loci for coronary artery disease. Nat. Genet. 45, 25-35 (2013)
122.
den Hoed, M.* et al.: Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat. Genet. 45, 621-631 (2013)
123.
Do, R.* et al.: Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat. Genet. 45, 1345-1352 (2013)
124.
Ellinghaus, D.* et al.: High-density genotyping study identifies four new susceptibility loci for atopic dermatitis. Nat. Genet. 45, 808-812 (2013)
125.
Garcia-Closas, M.* et al.: Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nat. Genet. 45, 392-398 (2013)
126.
Hoff, S.* et al.: ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3. Nat. Genet. 45, 951-956 (2013)
127.
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)
128.
International Multiple Sclerosis Genetics Consortium (Illig, T. ; Lichtner, P.) et al.: Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat. Genet. 45, 1353-1360 (2013)
129.
Kornblum, C.* et al.: Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease. Nat. Genet. 45, 214-219 (2013)
130.
Köttgen, A.* et al.: Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat. Genet. 45, 145-154 (2013)
131.
Liu, J.Z.* et al.: Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nat. Genet. 45, 670-675 (2013)
132.
Michailidou, K.* et al.: Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat. Genet. 45, 353-361 (2013)
133.
Verhoeven, V.J.M.* et al.: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat. Genet. 45, 314-318 (2013)
134.
Westra, H.J.* et al.: Systematic identification of trans eQTLs as putative drivers of known disease associations. Nat. Genet. 45, 1238-1243 (2013)
135.
Bonnefond, A.* et al.: Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. Nat. Genet. 44, 297-301 (2012)
136.
Bradfield, J.P.* et al.: A genome-wide association meta-analysis identifies new childhood obesity loci. Nat. Genet. 44, 526-531 (2012)
137.
Cho, Y.S.* et al.: Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nat. Genet. 44, 67-72 (2012)
138.
Ellinor, P.T.* et al.: Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat. Genet. 44, 670-675 (2012)
139.
Freilinger, T.* et al.: Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nat. Genet. 44, 777-782 (2012)
140.
Ghoussaini, M.* et al.: Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nat. Genet. 44, 312-319 (2012)