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21.
Laaksonen, J.* et al.: Discovery of mitochondrial DNA variants associated with genome-wide blood cell gene expression: A population-based mtDNA sequencing study. Hum. Mol. Genet. 28, 1381-1391 (2019)
22.
Sharapov, S.Z.* et al.: Defining the genetic control of human blood plasma N-glycome using genome-wide association study. Hum. Mol. Genet. 28, 2062-2077 (2019)
23.
Sung, Y.J.* et al.: A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Hum. Mol. Genet. 28, 2615-2633 (2019)
24.
Brockmann, S.J.* et al.: CHCHD10 mutations p. R15L and p. G66V cause motoneuron disease by haploinsufficiency. Hum. Mol. Genet. 27, 706-715 (2018)
25.
Haworth, S.* et al.: Consortium-based genome-wide meta-analysis for childhood dental caries traits. Hum. Mol. Genet. 27, 3113-3127 (2018)
26.
Tönjes, A.* et al.: Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin. Hum. Mol. Genet. 27, 546-558 (2018)
27.
Vogel, H.* et al.: A collective diabetes cross in combination with a computational framework to dissect the genetics of human obesity and Type 2 diabetes. Hum. Mol. Genet. 27, 3099-3112 (2018)
28.
Zaghlool, S.B.* et al.: Deep molecular phenotypes link complex disorders and physiological insult to CpG methylation. Hum. Mol. Genet. 27, 1106-1121 (2018)
29.
Cooper, H.M.* et al.: ATPase-deficient mitochondrial inner membrane protein ATAD3a disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia. Hum. Mol. Genet. 26, 1432-1443 (2017)
30.
Dand, N.* et al.: Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling. Hum. Mol. Genet. 26, 4301-4313 (2017)
31.
van den Berg, M.* et al.: Discovery of novel heart rate-associated loci using the Exome Chip. Hum. Mol. Genet. 26, 2346-2363 (2017)
32.
Bustamante, M.* et al.: A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. Hum. Mol. Genet. 25, 4127-4142 (2016)
33.
Cornelis, M.C.* et al.: Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior. Hum. Mol. Genet. 25, 5472-5482 (2016)
34.
de Vries, P.S.* et al.: A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Hum. Mol. Genet. 25, 358-370 (2016)
35.
Felix, J.F.* et al.: Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Hum. Mol. Genet. 25, 389-403 (2016)
36.
Huan, T.* et al.: A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking. Hum. Mol. Genet. 25, 4611-4623 (2016)
37.
Kanoni, S.* et al.: Analysis with the exome array identifies multiple new independent variants in lipid loci. Hum. Mol. Genet. 25, 4094-4106 (2016)
38.
Kortvely, E.* ; Hauck, S.M. ; Behler, J. ; Ho, N.* & Ueffing, M.*: The unconventional secretion of ARMS2. Hum. Mol. Genet. 25, 3143-3151 (2016)
39.
Lamina, C.* et al.: A genome-wide association meta-analysis on apolipoprotein A-IV concentrations. Hum. Mol. Genet. 25, 3635-3646 (2016)
40.
Lessard, S.* et al.: Testing the role of predicted gene knockouts in human anthropometric trait variation. Hum. Mol. Genet. 25, 2082-2092 (2016)
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