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Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array

Epigenetics & chromatin, 2013-03, Vol.6 (1), p.4-4, Article 4

2013

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Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation

Human molecular genetics, 2015-03, Vol.24 (6), p.1528-1539

2015

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Profiling placental DNA methylation associated with maternal SSRI treatment during pregnancy

Scientific reports, 2022-12, Vol.12 (1), p.22576-14, Article 22576

2022

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Accurate ethnicity prediction from placental DNA methylation data

Epigenetics & chromatin, 2019-08, Vol.12 (1), p.51-14, Article 51

2019

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Human placental piwi-interacting RNA transcriptome is characterized by expression from the DLK1-DIO3 imprinted region

Scientific reports, 2021-07, Vol.11 (1), p.14981-14981, Article 14981

2021

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Different measures of "genome-wide" DNA methylation exhibit unique properties in placental and somatic tissues

Epigenetics, 2012-06, Vol.7 (6), p.652-663

2012

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DNA methylation profiling of acute chorioamnionitis-associated placentas and fetal membranes: insights into epigenetic variation in spontaneous preterm births

Epigenetics & chromatin, 2018-10, Vol.11 (1), p.63-63, Article 63

2018

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Profiling the small non-coding RNA transcriptome of the human placenta

Scientific data, 2021-07, Vol.8 (1), p.1-8, Article 166

2021

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Illuminating potential technical artifacts of DNA-methylation array probes

American journal of human genetics, 2012-10, Vol.91 (4), p.760-762

2012

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No evidence for association of MTHFR 677C>T and 1298A>C variants with placental DNA methylation

Clinical epigenetics, 2018-03, Vol.10 (1), p.34-34, Article 34

2018

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Response to: "Response to Different measures of 'genome-wide' DNA methylation exhibit unique properties in placental and somatic tissues

Epigenetics, 2012-08, Vol.7 (8), p.965-965

2012

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The human placental methylome

Cold Spring Harbor perspectives in medicine, 2015-05, Vol.5 (5), p.a023044-a023044

2015

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Improved reporting of DNA methylation data derived from studies of the human placenta

Epigenetics, 2014-03, Vol.9 (3), p.333-337

2014

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Profiling placental and fetal DNA methylation in human neural tube defects

Epigenetics & chromatin, 2016-02, Vol.9 (6), p.6-6, Article 6

2016

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P597: All for One Clinical Genomics Network: Linking Canadian diagnostic laboratories to share genome-wide sequencing data to support rare disease diagnosis

Genetics in Medicine Open, 2024, Vol.2, p.101503, Article 101503

2024

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Transcriptomic profiling of sncRNA in placenta by RNAseq

Placenta (Eastbourne), 2016-09, Vol.45, p.64-64

2016

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Nucleated red blood cells impact DNA methylation and expression analyses of cord blood hematopoietic cells

Clinical epigenetics, 2015-09, Vol.7 (1), p.95-95, Article 95

2015

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P642: Development and deployment of clinical genome sequencing using a cloud-based platform

Genetics in Medicine Open, 2024, Vol.2, p.101548, Article 101548

2024

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Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario

CMAJ open, 2022-04, Vol.10 (2), p.E460-E465

2022

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Variant ATRX Syndrome with Dysfunction of ATRX and MAGT1 Genes

Human mutation, 2014-01, Vol.35 (1), p.58-62

2014

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Placental MTHFR 677C>T genotypes in pregnancy pathologies

Placenta (Eastbourne), 2016-09, Vol.45, p.112-112

2016

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Using DNA methylation signatures in placental tissue and cells to gain insight into chorioamnionitis

Placenta (Eastbourne), 2016-09, Vol.45, p.113-113

2016

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No evidence for association of MTHFR 677CT and 1298AC variants with placental DNA methylation

Clinical epigenetics, 2018-03, Vol.10 (1)

2018

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Patterns of cis regulatory variation in diverse human populations

PLoS genetics, 2012-04, Vol.8 (4), p.e1002639-e1002639

2012

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Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array

Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation

Profiling placental DNA methylation associated with maternal SSRI treatment during pregnancy

Accurate ethnicity prediction from placental DNA methylation data

Human placental piwi-interacting RNA transcriptome is characterized by expression from the DLK1-DIO3 imprinted region

Different measures of "genome-wide" DNA methylation exhibit unique properties in placental and somatic tissues

DNA methylation profiling of acute chorioamnionitis-associated placentas and fetal membranes: insights into epigenetic variation in spontaneous preterm births

Profiling the small non-coding RNA transcriptome of the human placenta

Illuminating potential technical artifacts of DNA-methylation array probes

No evidence for association of MTHFR 677C>T and 1298A>C variants with placental DNA methylation

Response to: "Response to Different measures of 'genome-wide' DNA methylation exhibit unique properties in placental and somatic tissues

The human placental methylome

Genomics4RD: An integrated platform to share Canadian deep‐phenotype and multiomic data for international rare disease gene discovery

Improved reporting of DNA methylation data derived from studies of the human placenta

Profiling placental and fetal DNA methylation in human neural tube defects

P597: All for One Clinical Genomics Network: Linking Canadian diagnostic laboratories to share genome-wide sequencing data to support rare disease diagnosis

Transcriptomic profiling of sncRNA in placenta by RNAseq

Nucleated red blood cells impact DNA methylation and expression analyses of cord blood hematopoietic cells

P642: Development and deployment of clinical genome sequencing using a cloud-based platform

Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario

Variant ATRX Syndrome with Dysfunction of ATRX and MAGT1 Genes

Placental MTHFR 677C>T genotypes in pregnancy pathologies

Using DNA methylation signatures in placental tissue and cells to gain insight into chorioamnionitis

No evidence for association of MTHFR 677CT and 1298AC variants with placental DNA methylation

Patterns of cis regulatory variation in diverse human populations

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