PuSH - Publication Server of Helmholtz Zentrum München

8 Records found.
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1.
Feichtinger, R.G.* et al.: Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy. Genet. Med., accepted (2019)
2.
Kishore, A.* et al.: Understanding the role of genetic variability in LRRK2 in Indian population. Mov. Disord. 34, 496-505 (2019)
3.
Fritzen, D.* et al.: De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. Hum. Genet. 137, 401-411 (2018)
4.
Penkert, J.* et al.: Breast cancer patients suggestive of Li-Fraumeni syndrome: Mutational spectrum, candidate genes, and unexplained heredity. Breast Cancer Res. 20:87 (2018)
5.
Synofzik, M.* et al.: SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: A large scale multi-centre study. Brain 139, 1378-1393 (2016)
6.
Sturm, M. ; Hackenberg, M.* ; Langenberger, D.* & Frishman, D.: TargetSpy: A supervised machine learning approach for microRNA target prediction. BMC Bioinformatics 11:292 (2010)
7.
Sturm, M.: Prediction and analysis of microRNAs and their targets in eukaryotic genomes. München, Technische Universität, Fakultät Wissenschaftszentrum Weihenstephan, Diss., 2010, 119 S.
8.
Hackenberg, M.* ; Sturm, M. ; Langenberger, D.* ; Falcón-Pérez, J.M.* & Aransay, A.M.*: miRanalyzer: A microRNA detection and analysis tool for next-generation sequencing experiments. Nucleic Acids Res. 37, (Suppl.1), W68-W76 (2009)