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The importance of imprinting in the human placenta

PLoS genetics, 2010-07, Vol.6 (7), p.e1001015-e1001015

2010

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Maternal activating KIRs protect against human reproductive failure mediated by fetal HLA-C2

The Journal of clinical investigation, 2010-11, Vol.120 (11), p.4102-4110

2010

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Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

Journal of investigative dermatology, 2013-09, Vol.133 (9), p.2229-2236

2013

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Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects

Scientific reports, 2017-05, Vol.7 (1), p.2441-8, Article 2441

2017

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SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20

Human molecular genetics, 2018-06, Vol.27 (11), p.1927-1940

2018

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Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo

Nucleic acids research, 2022-07, Vol.50 (12), p.6735-6752

2022

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The role and interaction of imprinted genes in human fetal growth

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2015-03, Vol.370 (1663), p.20140074

2015

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Imprinted Chromatin around DIRAS3 Regulates Alternative Splicing of GNG12-AS1, a Long Noncoding RNA

American journal of human genetics, 2013-08, Vol.93 (2), p.224-235

2013

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Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome

Nature genetics, 2014-01, Vol.46 (1), p.70-76

2014

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The role of imprinted genes in humans

Molecular aspects of medicine, 2013-07, Vol.34 (4), p.826-840

2013

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Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome

Frontiers in endocrinology (Lausanne), 2022-08, Vol.13, p.953707

2022

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Paternally expressed, imprinted insulin-like growth factor-2 in chorionic villi correlates significantly with birth weight

PloS one, 2014-01, Vol.9 (1), p.e85454-e85454

2014

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Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression

Human molecular genetics, 2009-08, Vol.18 (16), p.3066-3074

2009

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Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortion

Reproductive biomedicine online, 2015-11, Vol.31 (5), p.681-688

2015

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Fat dads must not be blamed for their children's health problems

BMC medicine, 2013-02, Vol.11 (1), p.30-30, Article 30

2013

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The emerging role of epigenetic mechanisms in the etiology of neural tube defects

Epigenetics, 2011-07, Vol.6 (7), p.875-883

2011

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Maternal Inheritance of a Promoter Variant in the Imprinted PHLDA2 Gene Significantly Increases Birth Weight

American journal of human genetics, 2012-04, Vol.90 (4), p.715-719

2012

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A screen for retrotransposed imprinted genes reveals an association between X chromosome homology and maternal germ-line methylation

PLoS genetics, 2007-02, Vol.3 (2), p.e20-e20

2007

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Enrichment of Clinically Relevant Organisms in Spontaneous Preterm-Delivered Placentas and Reagent Contamination across All Clinical Groups in a Large Pregnancy Cohort in the United Kingdom

Applied and environmental microbiology, 2018-07, Vol.84 (14), p.e00483-18

2018

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Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop

Nucleic acids research, 2013-02, Vol.41 (4), p.2171-2179

2013

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Analysis of CDKN1C in fetal growth restriction and pregnancy loss [version 1; peer review: 2 approved]

F1000 research, 2019, Vol.8, p.90

2019

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Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages [version 1; peer review: 2 approved]

F1000 research, 2019, Vol.8, p.273-273

2019

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The importance of imprinting in the human placenta

Maternal activating KIRs protect against human reproductive failure mediated by fetal HLA-C2

Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects

SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20

Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo

The role and interaction of imprinted genes in human fetal growth

Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate

Imprinted Chromatin around DIRAS3 Regulates Alternative Splicing of GNG12-AS1, a Long Noncoding RNA

Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome

The role of imprinted genes in humans

Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome

Paternally expressed, imprinted insulin-like growth factor-2 in chorionic villi correlates significantly with birth weight

Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression

Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortion

Fat dads must not be blamed for their children's health problems

The emerging role of epigenetic mechanisms in the etiology of neural tube defects

Maternal Inheritance of a Promoter Variant in the Imprinted PHLDA2 Gene Significantly Increases Birth Weight

A screen for retrotransposed imprinted genes reveals an association between X chromosome homology and maternal germ-line methylation

Enrichment of Clinically Relevant Organisms in Spontaneous Preterm-Delivered Placentas and Reagent Contamination across All Clinical Groups in a Large Pregnancy Cohort in the United Kingdom

Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop

Diagnosis and management of Silver-Russell syndrome: first international consensus statement

Analysis of CDKN1C in fetal growth restriction and pregnancy loss [version 1; peer review: 2 approved]

Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages [version 1; peer review: 2 approved]

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