Magda K Kadlubowska

A monoallelic variant in EYA1 is associated with Branchio‐Otic syndrome in a Malian family

S. Leal, K. Esoh, G. Landouré, 2022, Molecular genetics & genomic medicine.

Methods to Improve Molecular Diagnosis in Genomic Cold Cases in Pediatric Neurology

I. Schrauwen, Magda K Kadlubowska, 2022, Genes.

Rare-variant association analysis reveals known and new age-related hearing loss genes

Gao T. Wang, S. Leal, A. Dewan, 2023, European Journal of Human Genetics.

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

S. Leal, K. Esoh, O. Quaye, 2022, Communications Biology.