Nina Maric

Banja Luka, SRP 78000, Bosnia and Herzegovina

Last Updated: 09/26/2026

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Found 8 publications

Neuromuscular Disorders in Children Through the Lens of Next-Generation Sequencing: A Study of Diagnostic Yield.

Neuromuscular Disorders in Children Through the Lens of Next-Generation Sequencing: A Study of Diagnostic Yield.

Journal: International journal of molecular sciences

Published: March 23, 2026

Current Status of Newborn Screening in Southeastern and Central Europe.

Current Status of Newborn Screening in Southeastern and Central Europe.

Journal: International journal of neonatal screening

Published: December 30, 2025

The Artificial Intelligence-Assisted Diagnosis of Skeletal Dysplasias in Pediatric Patients: A Comparative Benchmark Study of Large Language Models and a Clinical Expert Group.

The Artificial Intelligence-Assisted Diagnosis of Skeletal Dysplasias in Pediatric Patients: A Comparative Benchmark Study of Large Language Models and a Clinical Expert Group.

Journal: Genes

Published: June 13, 2025

Noonan Syndrome: Relation of Genotype to Cardiovascular Phenotype-A Multi-Center Retrospective Study.

Noonan Syndrome: Relation of Genotype to Cardiovascular Phenotype-A Multi-Center Retrospective Study.

Journal: Genes

Published: September 25, 2024

Role of MMP-2, MMP-9, TIMP-1, and TIMP-2 in children with ventricular septal defect.

Role of MMP-2, MMP-9, TIMP-1, and TIMP-2 in children with ventricular septal defect.

Journal: Biomolecules & biomedicine

Published: August 19, 2024

Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?

Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?

Journal: Genes

Published: May 02, 2024

UGT1A1 (TA)n Promoter Genotype: Diagnostic and Population Pharmacogenetic Marker in Serbia.

UGT1A1 (TA)n Promoter Genotype: Diagnostic and Population Pharmacogenetic Marker in Serbia.

Journal: Balkan journal of medical genetics : BJMG

Published: November 15, 2018

Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants.

Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants.

Journal: PloS one

Published: April 13, 2018

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Last Updated: 09/26/2026