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Kerstin Kutsche

34PUBLICATIONS

112CO-AUTHORS

Molecular evolutionEpigenetics (incl. genome methylation and epigenomics)Nutritional epidemiologyCancer diagnosisInfant and child health

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Publications (34)

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|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

|Nov 27, 2024

The Recurrent E-Cadherin (CDH1) Mutation c.760G>A Causes Orofacial Clefts but Does Not Predispose to Hereditary Cancer.

Lea Gossner, Dietmar Rieder, Thomas Müller

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Frequent Collaborators

7 joint publications

Georg-Friedrich Vogel

7 joint publications

Thomas Müller

5 joint publications

Julia Vodopiutz

3 joint publications

Lukas A Huber

2 joint publications

Pauline E Schneeberger

1 joint publications

René G Feichtinger

1 joint publications

Robert Hegarty

1 joint publications

Valentina Stanley

1 joint publications

Johannes A Mayr

1 joint publications

Vorasuk Shotelersuk

Frequent Collaborators

7 joint publications

Georg-Friedrich Vogel

7 joint publications

Thomas Müller

5 joint publications

Julia Vodopiutz

3 joint publications

Lukas A Huber

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