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101.
Duering, M.* et al.: Co-aggregate formation of CADASIL-mutant NOTCH3: A single-particle analysis. Hum. Mol. Genet. 20, 3256-3265 (2011)
102.
Fox, E.R.* et al.: Association of genetic variation with systolic and diastolic blood pressure among African Americans: The Candidate Gene Association Resource study. Hum. Mol. Genet. 20, 2273-2284 (2011)
103.
Kaplan, R.C.* et al.: A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. Hum. Mol. Genet. 20, 1241-1251 (2011)
104.
Oexle, K.* et al.: Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. Hum. Mol. Genet. 20, 1042-1047 (2011)
105.
Sanson, M.* et al.: Chromosome 7p11.2 (EGFR) variation influences glioma risk. Hum. Mol. Genet. 20, 2897-2904 (2011)
106.
Barbalic, M.* et al.: Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. Hum. Mol. Genet. 19, 1863-1872 (2010)
107.
Burbulla, L.F.* et al.: Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: Functional impact of disease-related variants on mitochondrial homeostasis. Hum. Mol. Genet. 19, 4437-4452 (2010)
108.
Eijgelsheim, M.* et al.: Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum. Mol. Genet. 19, 3885-3894 (2010)
109.
Kettunen, J.* et al.: European lactase persistence genotype shows evidence of association with increase in body mass index. Hum. Mol. Genet. 19, 1129-1136 (2010)
110.
Perry, J.R.B.* et al.: Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes. Hum. Mol. Genet. 19, 535-544 (2010)
111.
Qi, L.* et al.: Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. Hum. Mol. Genet. 19, 2706-2715 (2010)
112.
Chio, A.* et al.: A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Hum. Mol. Genet. 18, 1524-1532 (2009)
113.
Deplazes, J.* et al.: Rac1 and Rho contribute to the migratory and invasive phenotype associated with somatic E-cadherin mutation. Hum. Mol. Genet. 18, 3632-3644 (2009)
114.
Johansson, A.* et al.: Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. Hum. Mol. Genet. 18, 373-380 (2009)
115.
Kollerits, B.* et al.: Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein b-containing lipoproteins. Hum. Mol. Genet. 18, 4669-4676 (2009)
116.
Org, E.* et al.: Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. Hum. Mol. Genet. 18, 2288-2296 (2009)
117.
Schneider, M.R.* ; Wolf, E.* ; Braun, J.* ; Kolb, H.-J. & Adler, H.: Canine embryo-derived stem cells and models for human diseases. Hum. Mol. Genet. 17, R42-R47 (2008)
118.
Baessler, A.* et al.: Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease. Hum. Mol. Genet. 16, 887-899 (2007)
119.
Koch, W.* et al.: Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in Europeans. Hum. Mol. Genet. 16, 1821-1827 (2007)
120.
Perveen, R.* ; Favor, J. ; Jamieson, R.V.* ; Ray, D.W.* & Black, G.C.*: A heterozygous c-Maf transactivation domain mutation causes congenital cataract and enhances target gene activation. Hum. Mol. Genet. 16, 1030-1038 (2007)
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