RNDr. Vladimíra Vallová, Ph.D.
Assistant professor, Section of Genetics and Molecular Biology
Office: bldg. C13/322
Kamenice 753/5
625 00 Brno
Phone: | +420 549 49 5446 |
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E‑mail: |
social and academic networks: |
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Total number of publications: 117
2019
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The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
BMC MEDICAL GENOMICS, year: 2019, volume: 12, edition: 1, DOI
2016
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Detection of oncogenic mutations in cervical carcinoma using method "High Resolution Melting" (HRM).
Neoplasma, year: 2016, volume: 63, edition: 5, DOI
2015
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A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms
MOLECULAR CYTOGENETICS, year: 2015, volume: 8, edition: 57, DOI
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Molecular cytogenetic analyses of hTERC (3q26) and MYC (8q24) genes amplifications in correlation with oncogenic human papillomavirus infection in Czech patients with cervical intraepithelial neoplasia and cervical carcinomas
Neoplasma, year: 2015, volume: 62, edition: 1, DOI
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První zkušenosti s preimplantačním genetickým screeningem chromozomových abnormalit pomocí komparativní genomové hybridizace na oligonukleotidových DNA mikročipech
Časopis lékařů českých, year: 2015, volume: 154, edition: 3
2014
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Genome-Wide Screening of Cytogenetic Abnormalities in Multiple Myeloma Patients Using Array-CGH Technique: A Czech Multicenter Experience
BioMed Research International, year: 2014, volume: Neuveden, edition: MAY, DOI
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Genome-wide screening of DNA copy number alterations in cervical carcinoma patients with CGH+SNP microarrays and HPV-FISH
International Journal of Clinical and Experimental Pathology, year: 2014, volume: 7, edition: 8
2013
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Cytogenetické vyšetření lymfocytů periferní krve po stimulaci IL 2 a CpG oligonukleotidem DSP30 u pacientů s chronickou lymfocytární leukemiíridization and conventional cytogenetics after stimulation with CpG oligonucleotides and interleukin-2: A prospective analysis.
Klinická onkologie, year: 2013, volume: 26, edition: 4
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Molekulární cytogenetika v diagnostice genetických abnormalit u karcinomu děložního hrdla
Praktická gynekologie, year: 2013, volume: 17, edition: 1
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První zkušenosti s metodou aCGH u 19 jedinců s monoklonální gamapatií nejasného významu
Year: 2013, type: Conference abstract