Fröhlich H - Search Results

1

Genetic and epigenetic insights into uveal melanoma.

Sharma A, Stei MM, Fröhlich H, Holz FG, Loeffler KU, Herwig-Carl MC. Sharma A, et al. Among authors: frohlich h. Clin Genet. 2018 May;93(5):952-961. doi: 10.1111/cge.13136. Epub 2018 Jan 24. Clin Genet. 2018. PMID: 28902406 Review.

2

Inter-locus as well as intra-locus heterogeneity in LINE-1 promoter methylation in common human cancers suggests selective demethylation pressure at specific CpGs.

Nüsgen N, Goering W, Dauksa A, Biswas A, Jamil MA, Dimitriou I, Sharma A, Singer H, Fimmers R, Fröhlich H, Oldenburg J, Gulbinas A, Schulz WA, El-Maarri O. Nüsgen N, et al. Among authors: frohlich h. Clin Epigenetics. 2015 Mar 1;7(1):17. doi: 10.1186/s13148-015-0051-y. eCollection 2015. Clin Epigenetics. 2015. PMID: 25798207 Free PMC article.

3

DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations.

Sharma A, Jamil MA, Nuesgen N, Schreiner F, Priebe L, Hoffmann P, Herns S, Nöthen MM, Fröhlich H, Oldenburg J, Woelfle J, El-Maarri O. Sharma A, et al. Among authors: frohlich h. Clin Epigenetics. 2015 Jul 28;7(1):76. doi: 10.1186/s13148-015-0112-2. eCollection 2015. Clin Epigenetics. 2015. PMID: 26221191 Free PMC article.

4

Skewed X-chromosome inactivation and XIST locus methylation levels do not contribute to the lower prevalence of Parkinson's disease in females.

Sharma A, Kaut O, Pavlova A, Fröhlich H, Ahmad A, Schmitt I, El-Maarri O, Oldenburg J, Wüllner U. Sharma A, et al. Among authors: frohlich h. Neurobiol Aging. 2017 Sep;57:248.e1-248.e5. doi: 10.1016/j.neurobiolaging.2017.05.021. Epub 2017 Jun 6. Neurobiol Aging. 2017. PMID: 28663000

5

Corrigendum.

Sharma A, Stei MM, Fröhlich H, Holz FG, Loeffler KU, Herwig-Carl MC. Sharma A, et al. Among authors: frohlich h. Clin Genet. 2018 Oct;94(3-4):398. doi: 10.1111/cge.13407. Clin Genet. 2018. PMID: 30199087 No abstract available.

6

Towards a Central Role of ISL1 in the Bladder Exstrophy⁻Epispadias Complex (BEEC): Computational Characterization of Genetic Variants and Structural Modelling.

Sharma A, Dakal TC, Ludwig M, Fröhlich H, Mathur R, Reutter H. Sharma A, et al. Among authors: frohlich h. Genes (Basel). 2018 Dec 5;9(12):609. doi: 10.3390/genes9120609. Genes (Basel). 2018. PMID: 30563179 Free PMC article.

7

Classic bladder exstrophy and adenocarcinoma of the bladder: Methylome analysis provide no evidence for underlying disease-mechanisms of this association.

Sharma A, Fröhlich H, Zhang R, Ebert AK, Rösch W, Reis H, Kristiansen G, Ellinger J, Reutter H. Sharma A, et al. Among authors: frohlich h. Cancer Genet. 2019 Jun;235-236:18-20. doi: 10.1016/j.cancergen.2019.05.004. Epub 2019 May 31. Cancer Genet. 2019. PMID: 31296310

8

Using Multi-Scale Genetic, Neuroimaging and Clinical Data for Predicting Alzheimer's Disease and Reconstruction of Relevant Biological Mechanisms.

Khanna S, Domingo-Fernández D, Iyappan A, Emon MA, Hofmann-Apitius M, Fröhlich H. Khanna S, et al. Among authors: frohlich h. Sci Rep. 2018 Jul 24;8(1):11173. doi: 10.1038/s41598-018-29433-3. Sci Rep. 2018. PMID: 30042519 Free PMC article.

9

Comprehensive Profiling of Blood Coagulation and Fibrinolysis Marker Reveals Elevated Plasmin-Antiplasmin Complexes in Parkinson's Disease.

Sharma A, Müller J, Schuetze K, Rolfes V, Bissinger R, Rosero N, Ahmad A, Franklin BS, Zur B, Fröhlich H, Lang F, Oldenburg J, Pötzsch B, Wüllner U. Sharma A, et al. Among authors: frohlich h. Biology (Basel). 2021 Jul 28;10(8):716. doi: 10.3390/biology10080716. Biology (Basel). 2021. PMID: 34439949 Free PMC article.

10

Network based consensus gene signatures for biomarker discovery in breast cancer.

Fröhlich H. Fröhlich H. PLoS One. 2011;6(10):e25364. doi: 10.1371/journal.pone.0025364. Epub 2011 Oct 25. PLoS One. 2011. PMID: 22046239 Free PMC article.

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