Markéta Wayhelová

Genomewide profiling of copy‐number alteration in monoclonal gammopathy of undetermined significance

Aneta Mikulášová, Jan Smetana, Markéta Wayhelová et al. · European Journal Of Haematology · 2016 · 35 citations

Life Sciences, Genetics, Molecular Genetics +17

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 et al. · BMC Medical Genomics · 2019 · 33 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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 et al. · Frontiers in Genetics · 2021 · 20 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Markéta Wayhelová, Vladimíra Vallová, Petr Brož et al. · Journal of Human Genetics · 2021 · 19 citations

Life Sciences, Genetics, Molecular Genetics +17

Novel de novo frameshift variant in the ASXL3 gene in a child with microcephaly and global developmental delay

Markéta Wayhelová, Jan Oppelt, Jan Smetana et al. · Molecular Medicine Reports · 2019 · 17 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17