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Daria Grafodatskaya

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Journal of the American Academy of Child and Adolescent Psychiatry|July 21, 2010
Autism spectrum disorders and epigeneticsDaria Grafodatskaya, Brian Chung, Peter Szatmari, et al.
Journal of Pediatric Genetics|February 10, 2017
An Update on Molecular Diagnostic Testing of Human Imprinting DisordersDaria Grafodatskaya, Sanaa Choufani, Raveen Basran, et al.
Genomics|January 8, 2011
Sequence overlap between autosomal and sex-linked probes on the Illumina HumanMethylation27 microarrayYi-an Chen, Sanaa Choufani, Jose Carlos Ferreira, et al.
Genes|November 11, 2022
Evaluation of DNA Methylation Array for Glioma Tumor Profiling and Description of a Novel Epi-Signature to Distinguish IDH1/IDH2 Mutant and Wild-Type TumorsLaila C Schenkel, Joseph Mathew, Hal Hirte, et al.
Human Molecular Genetics|March 5, 2011
Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivationAaron Y L Cheung, Lindsay M Horvath, Daria Grafodatskaya, et al.
Epigenetics|February 24, 2011
Assessment of methylation level prediction accuracy in methyl-DNA immunoprecipitation and sodium bisulfite based microarray platformsRageen Rajendram, Jose Carlos Ferreira, Daria Grafodatskaya, et al.
Epigenetics|April 9, 2011
WNT2 promoter methylation in human placenta is associated with low birthweight percentile in the neonateJose C Ferreira, Sanaa Choufani, Daria Grafodatskaya, et al.
Epigenetics|January 15, 2013
Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarrayYi-an Chen, Mathieu Lemire, Sanaa Choufani, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|August 25, 2007
Search for the sex-determining switch in monotremes: mapping WT1, SF1, LHX1, LHX2, FGF9, WNT4, RSPO1 and GATA4 in platypusDaria Grafodatskaya, Willem Rens, Mary C Wallis, et al.
European Journal of Medical Genetics|June 22, 2011
Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum DisorderBrian H Y Chung, Irene Drmic, Christian R Marshall, et al.
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Showing results (1-10 of 23) with videos related to

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Journal of the American Academy of Child and Adolescent Psychiatry|July 21, 2010
Autism spectrum disorders and epigeneticsDaria Grafodatskaya, Brian Chung, Peter Szatmari, et al.
Journal of Pediatric Genetics|February 10, 2017
An Update on Molecular Diagnostic Testing of Human Imprinting DisordersDaria Grafodatskaya, Sanaa Choufani, Raveen Basran, et al.
Genomics|January 8, 2011
Sequence overlap between autosomal and sex-linked probes on the Illumina HumanMethylation27 microarrayYi-an Chen, Sanaa Choufani, Jose Carlos Ferreira, et al.
Genes|November 11, 2022
Evaluation of DNA Methylation Array for Glioma Tumor Profiling and Description of a Novel Epi-Signature to Distinguish IDH1/IDH2 Mutant and Wild-Type TumorsLaila C Schenkel, Joseph Mathew, Hal Hirte, et al.
Human Molecular Genetics|March 5, 2011
Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivationAaron Y L Cheung, Lindsay M Horvath, Daria Grafodatskaya, et al.
Epigenetics|February 24, 2011
Assessment of methylation level prediction accuracy in methyl-DNA immunoprecipitation and sodium bisulfite based microarray platformsRageen Rajendram, Jose Carlos Ferreira, Daria Grafodatskaya, et al.
Epigenetics|April 9, 2011
WNT2 promoter methylation in human placenta is associated with low birthweight percentile in the neonateJose C Ferreira, Sanaa Choufani, Daria Grafodatskaya, et al.
Epigenetics|January 15, 2013
Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarrayYi-an Chen, Mathieu Lemire, Sanaa Choufani, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|August 25, 2007
Search for the sex-determining switch in monotremes: mapping WT1, SF1, LHX1, LHX2, FGF9, WNT4, RSPO1 and GATA4 in platypusDaria Grafodatskaya, Willem Rens, Mary C Wallis, et al.
European Journal of Medical Genetics|June 22, 2011
Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum DisorderBrian H Y Chung, Irene Drmic, Christian R Marshall, et al.
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