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1.
Brandt, V.P.* ; Holland, H.* ; Blüher, M. & Klöting, N.: High-resolution genomic profiling and locus-specific FISH in subcutaneous and visceral adipose tissue of obese patients. Front. Genet. 14:1323052 (2023)
2.
de Las Fuentes, L.* et al.: Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci. Front. Genet. 14:1235337 (2023)
3.
Rajcsanyi, L.S.* et al.: Genetic variants in genes involved in creatine biosynthesis in patients with severe obesity or anorexia nervosa. Front. Genet. 14:1128133 (2023)
4.
Hu, Y. et al.: Network embedding across multiple tissues and data modalities elucidates the context of host factors important for COVID-19 infection. Front. Genet. 13:909714 (2022)
5.
Huang, C.H.* ; Han, W. ; Wu, Y.Z.* & Shen, G.L.*: Identification of aberrantly methylated differentially expressed genes and pro-tumorigenic role of KIF2C in melanoma. Front. Genet. 13:817656 (2022)
6.
Ban, R. et al.: Biallelic COA7-variants leading to developmental regression with progressive spasticity and brain atrophy in a Chinese patient. Front. Genet. 12:685035 (2021)
7.
Molitor, L. ; Bacher, S. ; Burczyk, S.* & Niessing, D.: The molecular function of PURA andi Its implications in neurological diseases. Front. Genet. 12:638217 (2021)
8.
Ostner, J. ; Carcy, S. & Müller, C.L.: tascCODA: Bayesian tree-aggregated analysis of compositional amplicon and single-cell data Front. Genet. 12:766405 (2021)
9.
Pol-Fuster, J.* et al.: Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16q23.3, affecting the CNTN6 and CDH13 genes. Front. Genet. 12:622886 (2021)
10.
Xu, M. et al.: Identification of a novel variant in MT-CO3 causing MELAS. Front. Genet. 12:638749 (2021)
11.
Gusic, M. & Prokisch, H.: ncRNAs: New players in mitochondrial health and disease? Front. Genet. 11:95 (2020)
12.
Gusic, M. & Prokisch, H.: Corrigendum: ncRNAs: New players in mitochondrial health and disease?(Frontiers in Genetics, (2020), 11, (95), 10.3389/fgene.2020.00095). Front. Genet. 11:288 (2020)
13.
Ummethum, H. & Hamperl, S.: Proximity labeling techniques to study chromatin. Front. Genet. 11:450 (2020)
14.
Contreras, R. ; Schriever, S.C. & Pfluger, P.T.: Physiological and epigenetic features of yoyo dieting and weight control. Front. Genet. 10:1015 (2019)
15.
Hawe, J. ; Theis, F.J. & Heinig, M.: Inferring interaction networks from multi-omics data. Front. Genet. 10:535 (2019)
16.
Shahryari, A. et al.: Development and clinical translation of approved gene therapy products for genetic disorders. Front. Genet. 10:868 (2019)
17.
Wang, Y.* et al.: Prognostic and predictive value of three DNA methylation signatures in lung adenocarcinoma. Front. Genet. 10:349 (2019)
18.
Westphal, D.S. ; Andres, S.* ; Makowski, C.* ; Meitinger, T. & Hoefele, J.*: MAP2 - A candidate gene for epilepsy, developmental delay and behavioral abnormalities in a patient with microdeletion 2q34. Front. Genet. 9:99 (2018)
19.
Ahting, U.* et al.: Clinical, biochemical, and genetic spectrum of seven new patients with NFU1 deficiency. Front. Genet. 6:123 (2015)
20.
Venco, P.* et al.: Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+. Front. Genet. 6:185 (2015)
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