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41.
Lubbe, S.J.* et al.: Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: Evidence for oligogenic inheritance. Hum. Mol. Genet. 25, 5483-5489 (2016)
42.
Simpkin, A.J.* et al.: Prenatal and early life influences on epigenetic age in children: A study of mother-offspring pairs from two cohort studies. Hum. Mol. Genet. 25, 191-201 (2016)
43.
Trifunovic, D.* et al.: HDAC inhibition in the cpfl1 mouse protects degenerating cone photoreceptors in vivo. Hum. Mol. Genet. 25, 4462-4472 (2016)
44.
Yang, J.* et al.: Catenin delta-1 (CTNND1) phosphorylation controls the mesenchymal to epithelial transition in astrocytic tumors. Hum. Mol. Genet. 25, 4201-4210 (2016)
45.
Zhang, Y.* ; Xu, H.* & Frishman, D.: Genomic determinants of somatic copy number alterations across human cancers. Hum. Mol. Genet. 25, 1019-1030 (2016)
46.
Beleggia, F.* et al.: CRIM1 haploinsufficiency causes defects in eye development in human and mouse. Hum. Mol. Genet. 24, 2267-2273 (2015)
47.
Gharib, S.A.* et al.: Integrative pathway genomics of lung function and airflow obstruction. Hum. Mol. Genet. 24, 6836-6848 (2015)
48.
Kastenmüller, G. ; Raffler, J. ; Gieger, C. & Suhre, K.: Genetics of human metabolism: An update. Hum. Mol. Genet. 24, R93-R101 (2015)
49.
Kun-Rodrigues, C.* et al.: A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease. Hum. Mol. Genet. 24, 6711-6720 (2015)
50.
Lee, S.* et al.: Overexpression of the mitochondrial methyltransferase TFB1M in the mouse does not impact mitoribosomal methylation status of hearing. Hum. Mol. Genet. 24, 7286-7294 (2015)
51.
Nead, K.T.* et al.: Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: A systematic review and meta-analysis with evidence from up to 331 175 individuals. Hum. Mol. Genet. 24, 3582-3594 (2015)
52.
Qian, D.C.* et al.: Identification of shared and unique susceptibility pathways among cancers of the lung, breast, and prostate from genome-wide association studies and tissue-specific protein interactions. Hum. Mol. Genet. 24, 7406-7420 (2015)
53.
Rahmioglu, N.* et al.: Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci. Hum. Mol. Genet. 24, 1185-1199 (2015)
54.
Schiff, M.* et al.: Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency. Hum. Mol. Genet. 24, 3238-3247 (2015)
55.
Shin, J.T.* et al.: Layered genetic control of DNA methylation and gene expression: A locus of multiple sclerosis in healthy individuals. Hum. Mol. Genet. 24, 5733-5745 (2015)
56.
Tischner, C.* et al.: MTO1 mediates tissue-specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention. Hum. Mol. Genet. 24, 2247-2266 (2015)
57.
van der Valk, R.J.* et al.: A novel common variant in DCST2 is associated with length in early life and height in adulthood. Hum. Mol. Genet. 24, 1155-1168 (2015)
58.
Zhang, C.* et al.: Genetic determinants of telomere length and risk of common cancers: A Mendelian randomization study. Hum. Mol. Genet. 24, 5356-5366 (2015)
59.
Becirovic, E.* et al.: Peripherin-2 couples rhodopsin to the CNG channel in outer segments of rod photoreceptors. Hum. Mol. Genet. 23, 5989-5997 (2014)
60.
Hara, K.* et al.: Genome-wide association study identifies three novel loci for type 2 diabetes. Hum. Mol. Genet. 23, 239-246 (2014)
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