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Activities

Employment (3)

Medical University Sofia: Sofia, Sofia, BG

2013 to present | Ophthalmogenetics (Molecular Medicine Center)
Employment
Source: Self-asserted source
Kunka Kamenarova

Andalusian Molecular Biology and Regenerative Medicine Centre: Seville, ES

2008 to 2013 | Postdoctoral fellow in Ophthalmogenetics (Genetics of Inherited Retinal Degenerations)
Employment
Source: Self-asserted source
Kunka Kamenarova

Medical University Sofia: Sofia, Sofia, BG

2007 to 2008 | Postdoctoral fellow in Ophthalmogenetics (Molecular Medicine Center)
Employment
Source: Self-asserted source
Kunka Kamenarova

Education and qualifications (3)

Agrobioinstitute: Sofia, BG

2003 to 2007 | PhD/Genetics
Education
Source: Self-asserted source
Kunka Kamenarova

University of Chemical Technology and Metallurgy: Sofia, BG

2000 to 2003 | Environmental Protection Inspector
Education
Source: Self-asserted source
Kunka Kamenarova

University of Chemical Technology and Metallurgy: Sofia, BG

1997 to 2002 | MSc/Engineer - Biotechnologist
Education
Source: Self-asserted source
Kunka Kamenarova

Works (13)

Panel‐based next‐generation sequencing identifies novel mutations in Bulgarian patients with inherited retinal dystrophies

Molecular Genetics & Genomic Medicine
2022-08 | Journal article
Part of ISSN: 2324-9269
Part of ISSN: 2324-9269
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova
grade
Preferred source (of 2)‎

A rare case of <i>RGR/CDHR1</i> haplotype identified in Bulgarian patient with cone-rod dystrophy

Ophthalmic Genetics
2021-11-02 | Journal article
Part of ISSN: 1381-6810
Part of ISSN: 1744-5094
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

Scn1a mutation spectrum in a cohort of bulgarian patients with gefs+ phenotype

The Turkish Journal of Pediatrics
2020 | Journal article
Part of ISSN: 0041-4301
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability

Gene
2018-08 | Journal article
Part of ISSN: 0378-1119
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova
grade
Preferred source (of 2)‎

Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene

Stem Cell Research
2018-04 | Journal article
Part of ISSN: 1873-5061
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome

Seizure
2018-01 | Journal article
Part of ISSN: 1059-1311
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

A familial case of severe infantile nephronophthisis explained by oligogenic inheritance

European Journal of Medical Genetics
2017-06 | Journal article
Part of ISSN: 1769-7212
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova
grade
Preferred source (of 2)‎

Identification of a novel de novo mutation of CREBBP in a patient with Rubinstein-Taybi syndrome by targeted next-generation sequencing: a case report

Human Pathology
2016-01 | Journal article
Part of ISSN: 0046-8177
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population

Investigative Opthalmology &amp; Visual Science
2015-12-30 | Journal article
Part of ISSN: 1552-5783
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

Human iPSC derived disease model of MERTK-associated retinitis pigmentosa

Scientific Reports
2015-10 | Journal article
Part of ISSN: 2045-2322
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

Novel<i>GUCA1A</i>Mutations Suggesting Possible Mechanisms of Pathogenesis in Cone, Cone-Rod, and Macular Dystrophy Patients

BioMed Research International
2013 | Journal article
Part of ISSN: 2314-6133
Part of ISSN: 2314-6141
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q

European Journal of Human Genetics
2013-03 | Journal article
Part of ISSN: 1018-4813
Part of ISSN: 1476-5438
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies

Clinical Genetics
2008-06-05 | Journal article
Part of ISSN: 0009-9163
Contributors: Kunka Kamenarova
Source: Self-asserted source
Kunka Kamenarova

Peer review (1 review for 1 publication/grant)

Review activity for PloS one. (1)