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Mario Cuk

4PUBLICATIONS

8CO-AUTHORS

Developmental genetics (incl. sex determination)Neurology and neuromuscular diseasesGene mapping

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Publications (4)

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|Feb 26, 2025

Novel <i>TBR1</i> c.1303C>T Variant Led to Diagnosis of Intellectual Developmental Disorder with Autism and Speech Delay: Application of Comprehensive Family-Based Whole-Genome Analysis.

Mario Ćuk, Busra Unal, Matea Bagarić

|Oct 26, 2024

Novel Variant in <i>ANO5</i> Muscular Dystrophy: Identification by Whole Genome Sequencing and Quad Analysis.

Mario Ćuk, Busra Unal, Luka Lovrenčić

|Sep 28, 2024

Novel <i>RAI1</i>:c.2736delC Variant in Smith-Magenis Syndrome: Identification by Whole Genome Sequencing and Joint Analysis.

Mario Cuk, Busra Unal, Nives Jandric

|Jul 27, 2024

Diagnosis of Two Unrelated Syndromes of Prader-Willi and Calpainopathy: Insight from Trio Whole Genome Analysis and Isodisomy Mapping.

Mario Cuk, Busra Unal, Andjela Bevanda

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Frequent Collaborators

4 joint publications

Arezou A Ghazani

3 joint publications

Busra Unal

2 joint publications

Connor P Hayes

2 joint publications

Goran Krakar

1 joint publications

Andjela Bevanda

1 joint publications

Luka Lovrenčić

1 joint publications

Matea Bagarić

1 joint publications

Goran Skular

Frequent Collaborators

4 joint publications

Arezou A Ghazani

3 joint publications

Busra Unal

2 joint publications

Connor P Hayes

2 joint publications

Goran Krakar

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