Ehrhart F - Search Results

1

Overlap of vitamin A and vitamin D target genes with CAKUT-related processes.

Ozisik O, Ehrhart F, Evelo CT, Mantovani A, Baudot A. Ozisik O, et al. Among authors: ehrhart f. F1000Res. 2021 May 18;10:395. doi: 10.12688/f1000research.51018.2. eCollection 2021. F1000Res. 2021. PMID: 35528959 Free PMC article.

2

New insights in Rett syndrome using pathway analysis for transcriptomics data.

Ehrhart F, Coort SL, Cirillo E, Smeets E, Evelo CT, Curfs L. Ehrhart F, et al. Wien Med Wochenschr. 2016 Sep;166(11-12):346-52. doi: 10.1007/s10354-016-0488-4. Epub 2016 Aug 12. Wien Med Wochenschr. 2016. PMID: 27517371 Free PMC article.

3

Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes.

Ehrhart F, Coort SL, Cirillo E, Smeets E, Evelo CT, Curfs LM. Ehrhart F, et al. Orphanet J Rare Dis. 2016 Nov 25;11(1):158. doi: 10.1186/s13023-016-0545-5. Orphanet J Rare Dis. 2016. PMID: 27884167 Free PMC article. Review.

4

WikiPathways: a multifaceted pathway database bridging metabolomics to other omics research.

Slenter DN, Kutmon M, Hanspers K, Riutta A, Windsor J, Nunes N, Mélius J, Cirillo E, Coort SL, Digles D, Ehrhart F, Giesbertz P, Kalafati M, Martens M, Miller R, Nishida K, Rieswijk L, Waagmeester A, Eijssen LMT, Evelo CT, Pico AR, Willighagen EL. Slenter DN, et al. Among authors: ehrhart f. Nucleic Acids Res. 2018 Jan 4;46(D1):D661-D667. doi: 10.1093/nar/gkx1064. Nucleic Acids Res. 2018. PMID: 29136241 Free PMC article.

5

A Data Fusion Pipeline for Generating and Enriching Adverse Outcome Pathway Descriptions.

Nymark P, Rieswijk L, Ehrhart F, Jeliazkova N, Tsiliki G, Sarimveis H, Evelo CT, Hongisto V, Kohonen P, Willighagen E, Grafström RC. Nymark P, et al. Among authors: ehrhart f. Toxicol Sci. 2018 Mar 1;162(1):264-275. doi: 10.1093/toxsci/kfx252. Toxicol Sci. 2018. PMID: 29149350

6

Prader-Willi syndrome and Angelman syndrome: Visualisation of the molecular pathways for two chromosomal disorders.

Ehrhart F, Janssen KJM, Coort SL, Evelo CT, Curfs LMG. Ehrhart F, et al. World J Biol Psychiatry. 2019 Nov;20(9):670-682. doi: 10.1080/15622975.2018.1439594. Epub 2018 Mar 1. World J Biol Psychiatry. 2019. PMID: 29425059 Review.

7

MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases.

Townend GS, Ehrhart F, van Kranen HJ, Wilkinson M, Jacobsen A, Roos M, Willighagen EL, van Enckevort D, Evelo CT, Curfs LMG. Townend GS, et al. Among authors: ehrhart f. Hum Mutat. 2018 Jul;39(7):914-924. doi: 10.1002/humu.23542. Epub 2018 May 21. Hum Mutat. 2018. PMID: 29704307 Free PMC article.

8

Review and gap analysis: molecular pathways leading to fetal alcohol spectrum disorders.

Ehrhart F, Roozen S, Verbeek J, Koek G, Kok G, van Kranen H, Evelo CT, Curfs LMG. Ehrhart F, et al. Mol Psychiatry. 2019 Jan;24(1):10-17. doi: 10.1038/s41380-018-0095-4. Epub 2018 Jun 11. Mol Psychiatry. 2019. PMID: 29892052 Free PMC article. Review.

9

Integration among databases and data sets to support productive nanotechnology: Challenges and recommendations.

Karcher S, Willighagen EL, Rumble J, Ehrhart F, Evelo CT, Fritts M, Gaheen S, Harper SL, Hoover MD, Jeliazkova N, Lewinski N, Marchese Robinson RL, Mills KC, Mustad AP, Thomas DG, Tsiliki G, Ogilvie Hendren C. Karcher S, et al. Among authors: ehrhart f. NanoImpact. 2018 Jan;9:85-101. doi: 10.1016/j.impact.2017.11.002. NanoImpact. 2018. PMID: 30246165 Free PMC article.

10

Beyond Pathway Analysis: Identification of Active Subnetworks in Rett Syndrome.

Miller RA, Ehrhart F, Eijssen LMT, Slenter DN, Curfs LMG, Evelo CT, Willighagen EL, Kutmon M. Miller RA, et al. Among authors: ehrhart f. Front Genet. 2019 Feb 21;10:59. doi: 10.3389/fgene.2019.00059. eCollection 2019. Front Genet. 2019. PMID: 30847002 Free PMC article.

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