Cordula Knopp

3PUBLICATIONS
72CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Central nervous systemDevelopmental genetics (incl. sex determination)
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Publications (3)

|Dec 12, 2024
Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot Study.

Luise Kessler, Jeremias Krause, Florian Kraft

|Oct 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC.

Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan

|Aug 20, 2021
Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability.

Natja Haag, Ene-Choo Tan, Matthias Begemann

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Frequent Collaborators

3 joint publications

Miriam Elbracht

3 joint publications

Florian Kraft

2 joint publications

Ingo Kurth

2 joint publications

Miriam Elbracht