Get started
Author

Sanja Cirković

Observed names: S. Cirkovic, Sanja Cirkovic, Sanja Ćirković, Ćirković Sanja
ORCID: 0000-0001-6238-5936
Observed ORCID: 0000-0001-6238-5936
OpenAlex ID: A5030646580
Complex small supernumerary marker chromosomes – an update
2013 · Thomas Liehr, Sanja Cirkovic, et al. · Molecular Cytogenetics · 42
PDF
Successful Treatment of Hodgkin Lymphoma in Nijmegen Breakage Syndrome
2008 · Ankica Jovanovic, Predrag Minic, et al. · Journal of Pediatric Hematology/Oncology · 13
Lower Incidence of Deletions in the Survival of Motor Neuron Gene and the Neuronal Apoptosis Inhibitory Protein Gene in Children with Spinal Muscular Atrophy from Serbia
2011 · Marijana Miskovic, Tanja Lalic, et al. · The Tohoku Journal of Experimental Medicine · 9
PDF
Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia
2013 · Marijana Miskovic, Tanja Lalic, et al. · International Journal of Gynecology & Obstetrics · 8
Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature
2017 · Cinthia Aguilera, Marina Viñas-Jornet, et al. · BMC Medical Genetics · 7
PDF
Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability—An Exception or a Necessity?
2024 · Nikola Ilic, Nina Maric, et al. · Genes · 5
Prevalence of FA-D2 Rare Complementation Group of Fanconi Anemia in Serbia
2013 · Vujić Dragana, Petrović Sandra, et al. · The Indian Journal of Pediatrics · 3
Cytogenetic diepoxybutane sensitivity in Serbian children with Fanconi anemia
2006 · Sanja Cirkovic, Marija Guc-Scekic, et al. · Archives of Biological Sciences · 3
PDF
Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism
2021 · Milica Pešić, Nataša Dragašević Mišković, et al. · Neurological Research · 2
Neuroblastoma Occurring in Nijmegen Breakage Syndrome
2024 · Marina Djurisic, Adrijan Sarajlija, et al. · Journal of Pediatric Hematology/Oncology · 1
Age-dependent dissociation between sleep-disordered breathing severity and ventilatory impairment in children with Prader–Willi syndrome
2026 · Mihail Basa, Jelena Visekruna, et al. · Frontiers in Pediatrics
PDF
From Suspected Congenital Cytomegalovirus Infection to Malan Syndrome: Delayed Genetic Diagnosis Due to Diagnostic Anchoring
2026 · Gordana Kovacevic, Sanja Cirkovic, et al. · Diseases
Incidence of genetic causes of idiopathic male infertility in Serbia: Ten years’ experience of single centre
2019 · Bojana Dobric, Danijela Radivojevic, et al. · Genetika
PDF
Comet assay and cytogenetic findings in differential diagnosis of Fanconi anemia
2019 · Karolina Sunjog, Sanja Cirkovic, et al. · Genetika
PDF
P001 Two decades of experience in prenatal diagnosis and carrier screening of cystic fibrosis in Serbia
2018 · D. Radivojevic, P. Minic, et al. · Journal of Cystic Fibrosis
PDF
Chromosomal instability in patients with Fanconi anemia from Serbia
2014 · Sanja Cirkovic, Marija Guc-Scekic, et al. · Vojnosanitetski pregled
PDF
Cell cycle analysis in patients with Fanconi anemia from Serbia
2013 · Sanja Cirkovic, Tatjana Srdic-Rajic, et al. · Genetika
PDF
Genome sensitivity in patients with chromosomal instability disorders
2012 · Sanja Cirkovic
PDF
Works count: 19
Citation count: 93
H-index: 5
I10-index: 2
Year
Topic
Type