An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks
2017 · BMC Systems Biology · 307 citations
https://doi.org/10.1186/s12918-017-0420-6
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Jana Vandrovcová
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Jana Vandrovcová is an academic researcher from National Hospital for Neurology and Neurosurgery. The author has contributed to research in topics: Parkinson's Disease Mechanisms and Treatments & Genetic Neurodegenerative Diseases & Genomics and Rare Diseases. The author has an h-index of 45, co-authored 142 publications.
ORCID: 0000-0001-9508-0477Papers by this author
worksAMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
2019 · Nature Communications · 242 citations
https://doi.org/10.1038/s41467-019-10910-w
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing
2017 · Genome biology · 121 citations
https://doi.org/10.1186/s13059-017-1147-9
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , which Encode Subcomponents C1r and C1s of Complement
2016 · The American Journal of Human Genetics · 116 citations
https://doi.org/10.1016/j.ajhg.2016.08.019
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
2021 · European Journal of Human Genetics · 101 citations
https://doi.org/10.1038/s41431-021-00859-0
<i>PDXK</i> mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation
2019 · Annals of Neurology · 72 citations
https://doi.org/10.1002/ana.25524
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