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61.
Keller, M.F.* et al.: Trans-ethnic meta-analysis of white blood cell phenotypes. Hum. Mol. Genet. 23, 6944-6960 (2014)
62.
Kuo, D.S.* et al.: Allelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutations. Hum. Mol. Genet. 23, 1709-1722 (2014)
63.
Liu, C.-T.* et al.: Multi-ethnic fine-mapping of 14 central adiposity loci. Hum. Mol. Genet. 23, 4738-4744 (2014)
64.
Nalls, M.A.* et al.: Genetic comorbidities in Parkinson's disease. Hum. Mol. Genet. 23, 831-841 (2014)
65.
Perry, J.R.* et al.: DNA mismatch repair gene MSH6 implicated in determining age at natural menopause. Hum. Mol. Genet. 23, 2490-2497 (2014)
66.
Petersen, A.-K. et al.: Epigenetics meets metabolomics: An epigenome-wide association study with blood serum metabolic traits. Hum. Mol. Genet. 23, 534-545 (2014)
67.
Rafii, A.* ; Touboul, C.* ; Al Thani, H.* ; Suhre, K. & Malek, J.A.*: Where cancer genomics should go next: A clinician's perspective. Hum. Mol. Genet. 23, R69-R75 (2014)
68.
Reinthaler, E.M.* et al.: 16p11.2 600 kb duplications confer risk for typical and atypical Rolandic epilepsy. Hum. Mol. Genet. 23, 6069-6080 (2014)
69.
Ried, J.S. et al.: Novel genetic associations with serum level metabolites identified by phenotype set enrichment analyses. Hum. Mol. Genet. 23, 5847-5857 (2014)
70.
Yan, X. et al.: Peroxidasin is essential for eye development in the mouse. Hum. Mol. Genet. 23, 5597-5614 (2014)
71.
Yoneyama, S.* et al.: Gene-centric meta-analyses for central adiposity traits in up to 57412 individuals of European descent confirm known loci and reveal several novel associations. Hum. Mol. Genet. 23, 2498-2510 (2014)
72.
Cousminer, D.L.* et al.: Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Hum. Mol. Genet. 22, 2735-2747 (2013)
73.
Enciso-Mora, V.* et al.: Deciphering the 8q24.21 association for glioma. Hum. Mol. Genet. 22, 2293-2302 (2013)
74.
Ganesh, S.K.* et al.: Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum. Mol. Genet. 22, 1663-1678 (2013)
75.
Gispert, S.* et al.: Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA, and inflammatory factors. Hum. Mol. Genet. 22, 4871-4887 (2013)
76.
Graff, M.* et al.: Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. Hum. Mol. Genet. 22, 3597-3607 (2013)
77.
Guo, Y.* et al.: Gene-centric meta-analyses of 108912 individuals confirm known body mass index loci and reveal three novel signals. Hum. Mol. Genet. 22, 184-201 (2013)
78.
Holmans, P.* et al.: A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. Hum. Mol. Genet. 22, 1039-1049 (2013)
79.
Kemter, E.* et al.: Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in mice. Hum. Mol. Genet. 22, 4148-4163 (2013)
80.
Melka, M.G.* et al.: FTO, obesity and the adolescent brain. Hum. Mol. Genet. 22, 1050-1058 (2013)
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