Whole-exome sequencing in pediatric patients with glomerulonephritis
WES helped us detect hereditary diseases that have a clinical presentation like GN, including Alport syndrome and possible aHUS. Finding susceptibility genes in GN helped us understand disease pathophysiology.
Authors
- Vladislav Vukomanović (ORCID: https://orcid.org/0000-0002-5244-1436)
- Aleksandra Paripović (ORCID: https://orcid.org/0009-0008-1788-489X)
- Marina Perić (ORCID: https://orcid.org/0000-0002-9817-816X)
- Jovana Putnik (ORCID: https://orcid.org/0000-0002-2085-4834)
- Nataša Stajić (ORCID: https://orcid.org/0000-0001-9384-1973)
- Milena Janković (ORCID: https://orcid.org/0000-0002-3939-9739)
- Filip Milanović (ORCID: https://orcid.org/0000-0002-4530-998X)
- Ivana V. Novaković (ORCID: https://orcid.org/0000-0003-0202-0673)
- Marija Branković (ORCID: https://orcid.org/0000-0001-5208-147X)
- Dejan Nikolić (ORCID: https://orcid.org/0000-0002-7367-8723)
Institutions
- University of Belgrade (RS)
- Centar za Promociju Nauke (RS)
- Institute of Public Health of Serbia (RS)
- University Children's Hospital, Belgrade (RS)
- University of Belgrade – Faculty of Medicine
Publication Details
- Journal
- Frontiers in Genetics
- Published
- 2025-09-12
- DOI
- https://doi.org/10.3389/fgene.2025.1611340
- Primary Topic
- Renal Diseases and Glomerulopathies
- Type
- article
- Field-Weighted Citation Impact
- 0.00