Kerstin Kutsche

35PUBLICATIONS
114CO-AUTHORS
Neurology and neuromuscular diseasesMolecular evolutionEpigenetics (incl. genome methylation and epigenomics)Nutritional epidemiologyCancer diagnosis
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (35)

|Jul 14, 2026
Heart Transplant for Noncompaction Cardiomyopathy in NONO-Related Syndromic Intellectual Disability.

|Mar 09, 2026
Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial Dysplasia.

Dorothea Stojanovic, Dorota Garczarczyk-Asim, Julia Vodopiutz

|Jul 29, 2025
Homozygous DHCR7 p.Val330Met Variant Associated with Mild Non-Syndromic Intellectual Disability and Elevated Serum 7-Dehydrocholesterol Levels in Two Siblings.

Lukas Hackl, Edda Haberlandt, Thomas Müller

|Mar 26, 2025
Congenital enteropathy caused by ezrin deficiency.

Georg F Vogel, Katharina M C Klee, Arzu Meltem Demir

|Feb 01, 2025
Pathogenic Deep Intronic PCSK1 Variant Causes Proprotein Convertase 1/3 Deficiency in a Family.

Leah M Huber, Aslı Subaşıoğlu, Dorota Garczarczyk-Asim

|Dec 02, 2024
Missense variants in the TRPM7 α-kinase domain are associated with recurrent pediatric acute liver failure.

Lea D Schlieben, Melanie T Achleitner, Billy Bourke

Pageof 6

Frequent Collaborators

7 joint publications

Georg-Friedrich Vogel

7 joint publications

Thomas Müller

5 joint publications

Julia Vodopiutz

3 joint publications

Lukas A Huber