Hannah Klinkhammer

18PUBLICATIONS
225CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsGene mappingLarge and complex data theoryEpigenetics (incl. genome methylation and epigenomics)
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Publications (18)

|Jul 08, 2026
An introduction to polygenic scores - methodological basics and recent advances.

|Jul 03, 2026
Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome.

|May 18, 2026
Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

|Apr 08, 2026
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Rocio Rius, Alexander J M Blakes, Yuyang Chen

|Apr 01, 2026
Detecting gene-environment interactions to guide personalized intervention: Boosting distributional regression for polygenic scores.

Qiong Wu, Hannah Klinkhammer, Kiran Kunwar

|Feb 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Benita Menden, Rana D Incebacak Eltemur, German Demidov

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Frequent Collaborators

9 joint publications

Peter M Krawitz

7 joint publications

Tzung-Chien Hsieh

6 joint publications

Tobias Haack

6 joint publications

Shahida Moosa