Karin Writzl

6PUBLICATIONS
33CO-AUTHORS
Neurology and neuromuscular diseasesApplied immunology (incl. antibody engineering, xenotransplantation and t-cell therapies)Cardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (6)

|Sep 27, 2025
Novel ATP7A Splice-Site Variant Causing Distal Motor Neuropathy and Occipital Horn Syndrome: Two Siblings and Literature Review.

Karin Writzl, Maruša Škrjanec Pušenjak, Matevž Jus

|Feb 28, 2025
TTN:c.12478del in proximal I-band of titin represents a common molecular cause of dilated cardiomyopathy in Slovenian patients.

Nina Vodnjov, Andraž Cerar, Aleš Maver

|Aug 19, 2024
Clinical Outcome of Hypertrophic Cardiomyopathy in Probands with the Founder Variant c.913_914del in MYBPC3: A Slovenian Cohort Study.

Nina Vodnjov, Aleš Maver, Nataša Teran

|Jan 31, 2024
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.

Sissy Bassani, Jacqueline Chrast, Giovanna Ambrosini

|Dec 05, 2023
A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study.

Nina Vodnjov, Janez Toplišek, Aleš Maver

|Jan 03, 2018
Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss.

Tina Likar, Mensuda Hasanhodžić, Nataša Teran

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Frequent Collaborators

3 joint publications

Borut Peterlin

2 joint publications

Nina Vodnjov

2 joint publications

Ales Maver

1 joint publications

Olivera Miljanović