Concepedia

Author

Vladimíra Vallová

Masaryk University

Also Known As

V. VALLOVA, V. Vallova, Vallova, Vladimira, Vladimira Vallova, Vladimíra Vallová

40

Publications

222

Citations

9

H-Index

10

Concepts

All Affiliations

Masaryk UniversityUniversity Hospital BrnoNewcastle UniversityCharles University
VV

About

Vladimíra Vallová is an author at Masaryk University specializing in genomics, genetics, and cancer research.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Health Sciences

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Medicine

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Pathology

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Genetics

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Genomics

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Vladimíra Vallová

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8

Publications

202

Citations

8

H-Index

YearCitations

A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms

Eva Hladílková, Tuva Barøy, Madeleine Fannemel,

Molecular Cytogenetics

2015

66

The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay

Markéta Wayhelová, Jan Smetana, Vladimíra Vallová,

BMC Medical Genomics

2019

32

Genome-Wide Screening of Cytogenetic Abnormalities in Multiple Myeloma Patients Using Array-CGH Technique: A Czech Multicenter Experience

Jan Smetana, Jan Fröhlich, Romana Zaoralová,

BioMed Research International

2014

25

Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype

Jan Smetana, Vladimíra Vallová, Markéta Wayhelová,

Frontiers in Genetics

2021

19

Novel de novo pathogenic variant in the GNAI1 gene as a cause of severe disorders of intellectual development

Markéta Wayhelová, Vladimíra Vallová, Petr Brož,

Journal of Human Genetics

2021

18

A unique case of Bloom syndrome with a combination of genetic hits: A lesson from trio‑based exome sequencing: A case report

Markéta Wayhelová, Vladimíra Vallová, Petr Brož,

Molecular Medicine Reports

2023

16

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

Petr Kuglík, Kateřina Kašíková, Jan Smetana,

Neoplasma

2015

14

Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders

Markéta Wayhelová, Vladimíra Vallová, Petr Brož,

Orphanet Journal of Rare Diseases

2024

12

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