User:Fehrhart

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(Pathways of Interest)
Current revision (10:28, 26 March 2019) (view source)
(About Me)
 
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== Pathways of Interest ==
== Pathways of Interest ==
* MECP2 and Associated Rett Syndrome http://www.wikipathways.org/index.php/Pathway:WP3584
* MECP2 and Associated Rett Syndrome http://www.wikipathways.org/index.php/Pathway:WP3584
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* Ciliary landscape https://www.wikipathways.org/index.php/Pathway:WP4352
* Cytosine methylation http://www.wikipathways.org/index.php/Pathway:WP3585
* Cytosine methylation http://www.wikipathways.org/index.php/Pathway:WP3585
* Valproic acid pathway http://www.wikipathways.org/index.php/Pathway:WP3871
* Valproic acid pathway http://www.wikipathways.org/index.php/Pathway:WP3871
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== Portals ==
== Portals ==
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* Disease
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* Rare diseases [https://www.wikipathways.org/index.php/Portal:RareDisease]
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* Nanomaterials
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* Disease [https://www.wikipathways.org/index.php/Portal:Disease]
== Links ==
== Links ==
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== About Me ==
== About Me ==
* ''Real name'': Friederike Ehrhart
* ''Real name'': Friederike Ehrhart
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* ''Work'': Bioinformatics
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* ''Work'': Department of Bioinformatics and GKC-Rett Expertise Centre
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* ''Location'': Maastricht University
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* ''Location'': Maastricht University and Maastricht University Medical Centre
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* ''Professional Interests'': Rare diseases, especially Rett Syndrome, tissue engineering, nanoparticle and drug pathways
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* ''Professional Interests'': Rare diseases, especially neurological rare diseases, Rett Syndrome, Neuroscience, omics data analysis, linked data, tissue engineering, drug development
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* ''Contact'': ...
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I hereby elect to apply CC0 to all my contributions to WikiPathways.

Current revision

iD This user has the ORCID identifier:
0000-0002-7770-620X

Contents

My WikiPathways

Pathways of Interest

Portals

  • Rare diseases [1]
  • Disease [2]

Links

  • ...

About Me

  • Real name: Friederike Ehrhart
  • Work: Department of Bioinformatics and GKC-Rett Expertise Centre
  • Location: Maastricht University and Maastricht University Medical Centre
  • Professional Interests: Rare diseases, especially neurological rare diseases, Rett Syndrome, Neuroscience, omics data analysis, linked data, tissue engineering, drug development

I hereby elect to apply CC0 to all my contributions to WikiPathways.

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