Mert Karakaya

Years Active: 2018-2021
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Natalie Keller, Cem Paketci, Janine Altmueller, Nico Fuhrmann, Gilbert Wunderlich, Bertold Schrank, Olcay Unver, Sanem Yilmaz, Reza Boostani, Ehsan Ghayoor Karimiani, Susanne Motameny, Holger Thiele, Peter Nürnberg, Reza Maroofian, Uluc Yis, Brunhilde Wirth, Mert Karakaya
Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease. Human mutation 42 (4) (2021)
Mert Karakaya, Markus Storbeck, Eike A Strathmann, Andrea Delle Vedove, Irmgard Hölker, Janine Altmueller, Leyla Naghiyeva, Lea Schmitz-Steinkrüger, Katharina Vezyroglou, Susanne Motameny, Salem Alawbathani, Holger Thiele, Ayse Ipek Polat, Derya Okur, Reza Boostani, Ehsan Ghayoor Karimiani, Gilbert Wunderlich, Didem Ardicli, Haluk Topaloglu, Janbernd Kirschner, Bertold Schrank, Reza Maroofian, Olafur Magnusson, Uluc Yis, Peter Nürnberg, Raoul Heller, Brunhilde Wirth
Targeted sequencing with expanded gene profile enables high diagnostic yield in non-5q-spinal muscular atrophies. Human mutation 39 (9) (2018)

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