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Daria Grafodatskaya

The Centre for Applied Genomics

15

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1889

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EHMT1 pathogenic variants and 9q34.3 microdeletions share altered DNA methylation patterns in patients with Kleefstra syndrome

2020
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Citations (3)
Genome-wide DNA methylation analysis of Chinese patients with systemic lupus erythematosus identified hypomethylation in genes related to the type i interferon pathway

2017 PLOS ONE
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A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two families.

2014 Human Mutation
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Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray

2013 Epigenetics
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Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C

2013 BMC Medical Genomics
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Cross-Reactive DNA Microarray Probes Lead to False Discovery of Autosomal Sex-Associated DNA Methylation

2012 American Journal of Human Genetics
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Citations (26)
Assessment of methylation level prediction accuracy in methyl-DNA immunoprecipitation and sodium bisulfite based microarray platforms.

2011 Epigenetics
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WNT2 promoter methylation in human placenta is associated with low birthweight percentile in the neonate

2011 Epigenetics
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Sequence overlap between autosomal and sex-linked probes on the Illumina HumanMethylation27 microarray

2011 Genomics
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Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation

2011 Human Molecular Genetics
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Citations (222)