Author

Danijela Krgović

Observed names: D Krgović, D. Krgović, Danijela Krgovic

Institutions: University of Maribor, University Clinical Centre Maribor

Observed institutions: University of Maribor, University Clinical Centre Maribor

ORCID: 0000-0002-0428-793X

Observed ORCID: 0000-0002-0428-793X

OpenAlex ID: A5083672799

Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar

2018 · Erin R. Riggs, Tristan Nelson, et al. · Human Mutation · 36

Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders

2018 · Danijela Krgovic, Nadja Kokalj Vokac, et al. · Scientific Reports · 19

Deletion of the last exon of SHANK3 gene produces the full Phelan–McDermid phenotype: A case report

2013 · Marta Macedoni-Lukšič, Danijela Krgović, et al. · Gene · 18

Simpson–Golabi–Behmel syndrome: a prenatal diagnosis in a foetus with GPC3 and GPC4 gene microduplications

2016 · F Mujezinović, D Krgović, et al. · Clinical Genetics · 16

Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report

2011 · Danijela Krgovic, Natasa Marcun Varda, et al. · Molecular Cytogenetics · 13

Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions

2011 · Sarah Vergult, Danijela Krgovic, et al. · European Journal of Human Genetics · 13

Specific behavioural phenotype and secondary cognitive decline as a result of an 8.6 Mb deletion of 2q32.2q33.1

2016 · Hojka Gregoric Kumperscak, Danijela Krgovic, et al. · Journal of International Medical Research · 11

Impaired Neurodevelopmental Genes in Slovenian Autistic Children Elucidate the Comorbidity of Autism With Other Developmental Disorders

2022 · Danijela Krgovic, Mario Gorenjak, et al. · Frontiers in Molecular Neuroscience · 10

De novo KMT2D heterozygous frameshift deletion in a newborn with a congenital heart anomaly

2020 · Š Stangler Herodež, N Marčun Varda, et al. · Balkan Journal of Medical Genetics · 10

A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5

2014 · Danijela Krgovic, Ana Blatnik, et al. · BMC Medical Genetics · 10

CNVs and Chromosomal Aneuploidy in Patients With Early-Onset Schizophrenia and Bipolar Disorder: Genotype-Phenotype Associations

2021 · Hojka Gregoric Kumperscak, Danijela Krgovic, et al. · Frontiers in Psychiatry · 8

Identification of potentially pathogenic variants for autism spectrum disorders using gene-burden analysis

2023 · Nika Rihar, Danijela Krgovic, et al. · PLoS ONE · 4

Identification of genomic copy number variations associated with specific clinical features of head and neck cancer

2018 · Boris Zagradišnik, Danijela Krgović, et al. · Molecular Cytogenetics · 3

Case Report: Wide spectrum of SALL1 variants—a rare cause of pediatric chronic kidney disease

2025 · Martina Filipič, Špela Stangler Herodež, et al. · Frontiers in Pediatrics · 2

How does LAMB2 contribute to kidney disease? Insights from a pediatric case

2025 · I. Trutin, L. Oletić, et al. · BMC Nephrology · 2

The Role of Next-Generation Sequencing in the Management of Patients with Suspected Non-Ischemic Cardiomyopathy after Syncope or Termination of Sudden Arrhythmic Death

2024 · Damijan Vokač, Špela Stangler Herodež, et al. · Genes · 2

Role of Copy Number Variations in ADHD

2020 · Danijela Krgović · IntechOpen eBooks · 2

Resolving Diagnostic Uncertainty in Neurodevelopmental Disorders Using Exome Sequencing Supported by Literature-Based Multi-Omics Evidence

2026 · Danijela Krgovic, Peter Gradisnik, et al. · Biomolecules · 1

Editorial: Multiomics approaches for understanding autism spectrum disorder

2025 · Jernej Kovac, Branko Aleksic, et al. · Frontiers in Neuroscience · 1

A 15-year experience highlighting the spectrum of Alport kidney disease in the pediatric population and novel genetic variants in COL4A3–5

2025 · Nastja Andrejašič, Anja Blejc Novak, et al. · Pediatric Nephrology · 1

The Role of Next-Generation Sequencing in the Management of Asymptomatic, Young Slovenian Athletes for Distinction Between Athlete’s Heart and Cardiomyopathy

2026 · Špela Stangler Herodež, Eva Čokolič, et al. · Biomedicines

Homozygous Missense Variant in the Otof Gene: a Case Report of a Boy With Hearing Loss

2026 · Andreja Bajič, Alenka Erjavec Škerget, et al. · Slovenska pediatrija revija pediatrov Slovenije in specialistov šolske ter visokošolske medicine Slovenije

Homozigotna Drugačnopomenska Različica V Genu Otof: Prikaz Kliničnega Primera Dečka Z Gluhostjo

2026 · Andreja Bajič, Alenka Erjavec Škerget, et al. · Slovenska pediatrija revija pediatrov Slovenije in specialistov šolske ter visokošolske medicine Slovenije

Analiza klinično pomembnih strukturnih genomskih variabilnosti pri slovenskih otrocih z nepojasnjenim razvojnim ali duševnim zaostankom, s prirojenimi nepravilnostmi in z motnjami avtističnega spektra

2015 · Danijela Krgović · University of Maribor digital library (University of Maribor)

Nasal speech in patients with 12q15 microdeletions

2011 · Sarah Vergult, Danijela Krgovic, et al. · European Journal of Human Genetics

Works count: 25

Citation count: 183

H-index: 10

I10-index: 10