Lista de obras - Wendy P Robinson - Dominio Público Uruguay

A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder

artículo científico publicado en 2017

A skewed view of X chromosome inactivation

artículo científico publicado en 2008

ADAM12-directed ectodomain shedding of E-cadherin potentiates trophoblast fusion.

artículo científico publicado en 2015

Accurate ethnicity prediction from placental DNA methylation data

artículo científico publicado en 2019

Adjusting for Batch Effects in DNA Methylation Microarray Data, a Lesson Learned.

artículo científico publicado en 2018

Altered levels of placental miR-338-3p and miR-518b are associated with acute chorioamnionitis and IL6 genotype

artículo científico publicado en 2019

An empirically driven data reduction method on the human 450K methylation array to remove tissue specific non-variable CpGs

artículo científico publicado en 2017

An integrated transcriptional, epigenetic, and clinical analysis of preeclamptic placentas

scholarly article by Katherine Leavey et al published September 2015 in Placenta

Are we ready for DNA methylation-based prenatal testing?

artículo científico publicado en 2011

Association of a placental Interleukin-6 genetic variant (rs1800796) with DNA methylation, gene expression and risk of acute chorioamnionitis

artículo científico publicado en 2019

Cell-Free Placental DNA in Maternal Plasma in Relation to Placental Health and Function

artículo científico publicado en 2016

Cell-specific characterization of the placental methylome

artículo científico publicado en 2021

Characterizing the hypomethylated DNA methylation profile of nucleated red blood cells from cord blood

artículo científico publicado en 2016

Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers

artículo científico publicado en 2017

Chromosomal Genetic Disease: Numerical Aberrations

Clues to IDDM pathogenesis from genetic and serological traits in multiply affected families

article

Considerations when processing and interpreting genomics data of the placenta

scientific article published on 07 January 2019

Cord blood hematopoietic cells from preterm infants display altered DNA methylation patterns

artículo científico publicado en 2017

Cytogenetic investigation of fetuses and infants conceived through intracytoplasmic sperm injection

scientific article published on 01 December 2001

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

scholarly article by Chaini Konwar published in October 2018

Developmental transcription factor NFIB is a putative target of oncofetal miRNAs and is associated with tumour aggressiveness in lung adenocarcinoma

artículo científico publicado en 2016

Differences in DNA methylation of white blood cell types at birth and in adulthood reflect postnatal immune maturation and influence accuracy of cell type prediction

Early onset pre-eclampsia is associated with altered DNA methylation of cortisol-signalling and steroidogenic genes in the placenta

artículo científico publicado en 2013

Epigenetic regulation of placental gene expression in transcriptional subtypes of preeclampsia.

artículo científico publicado en 2018

Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication

article

Genomic imbalances in the placenta are associated with poor fetal growth

artículo científico publicado en 2021

Global analysis of DNA methylation changes during progression of oral cancer

artículo científico publicado en 2013

Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes

artículo científico publicado en 2009

Hypoxia alters the epigenetic profile in cultured human placental trophoblasts

artículo científico publicado en 2013

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

artículo científico publicado en 2014

Low oxygen enhances trophoblast column growth by potentiating differentiation of the extravillous lineage and promoting LOX activity

scientific article published on 23 January 2020

Mining DNA methylation alterations towards a classification of placental pathologies.

artículo científico publicado en 2018

Molecular Detection of Uniparental Disomy

scientific article published on 01 January 2002

Multipoint genetic mapping with uniparental disomy data

artículo científico publicado en 2000

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

artículo científico publicado en 2018

Number of Children and Telomere Length in Women: A Prospective, Longitudinal Evaluation

artículo científico publicado en 2016

Pervasive polymorphic imprinted methylation in the human placenta

artículo científico publicado en 2016

Phenotype of maternal UPD(14)

artículo científico publicado en 1996

Placental biomarkers for assessing fetal health

artículo científico publicado en 2017

Placental telomere length decline with gestational age differs by sex and TERT, DNMT1, and DNMT3A DNA methylation

artículo científico publicado en 2016

Prenatally detected trisomy 4 and 6 mosaicism?cytogenetic results and clinical phenotype

artículo científico publicado en 2003

Profiling placental and fetal DNA methylation in human neural tube defects

artículo científico publicado en 2016

Quantification of cell-free DNA in normal and complicated pregnancies: overcoming biological and technical issues

artículo científico publicado en 2014

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

artículo científico publicado en 2012

The significance of the placental genome and methylome in fetal and maternal health

artículo científico publicado en 2019

Transient and placenta-specific imprinting in human development

article

Utility of DNA methylation to assess placental health

artículo científico publicado en 2017

Whole exome sequencing of families with 1q21.1 microdeletion or microduplication

artículo científico publicado en 2017

Lista de obras de Wendy P Robinson

A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder

A skewed view of X chromosome inactivation

ADAM12-directed ectodomain shedding of E-cadherin potentiates trophoblast fusion.

Accurate ethnicity prediction from placental DNA methylation data

Adjusting for Batch Effects in DNA Methylation Microarray Data, a Lesson Learned.

Altered levels of placental miR-338-3p and miR-518b are associated with acute chorioamnionitis and IL6 genotype

An empirically driven data reduction method on the human 450K methylation array to remove tissue specific non-variable CpGs

An integrated transcriptional, epigenetic, and clinical analysis of preeclamptic placentas

Are we ready for DNA methylation-based prenatal testing?

Association of a placental Interleukin-6 genetic variant (rs1800796) with DNA methylation, gene expression and risk of acute chorioamnionitis

Cell-Free Placental DNA in Maternal Plasma in Relation to Placental Health and Function

Cell-specific characterization of the placental methylome

Characterizing the hypomethylated DNA methylation profile of nucleated red blood cells from cord blood

Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers

Chromosomal Genetic Disease: Numerical Aberrations

Clues to IDDM pathogenesis from genetic and serological traits in multiply affected families

Considerations when processing and interpreting genomics data of the placenta

Cord blood hematopoietic cells from preterm infants display altered DNA methylation patterns

Cytogenetic investigation of fetuses and infants conceived through intracytoplasmic sperm injection

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

Developmental transcription factor NFIB is a putative target of oncofetal miRNAs and is associated with tumour aggressiveness in lung adenocarcinoma

Differences in DNA methylation of white blood cell types at birth and in adulthood reflect postnatal immune maturation and influence accuracy of cell type prediction

Early onset pre-eclampsia is associated with altered DNA methylation of cortisol-signalling and steroidogenic genes in the placenta

Epigenetic regulation of placental gene expression in transcriptional subtypes of preeclampsia.

Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication

Genomic imbalances in the placenta are associated with poor fetal growth

Global analysis of DNA methylation changes during progression of oral cancer

Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes

Hypoxia alters the epigenetic profile in cultured human placental trophoblasts

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

Low oxygen enhances trophoblast column growth by potentiating differentiation of the extravillous lineage and promoting LOX activity

Mining DNA methylation alterations towards a classification of placental pathologies.

Molecular Detection of Uniparental Disomy

Multipoint genetic mapping with uniparental disomy data

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

Number of Children and Telomere Length in Women: A Prospective, Longitudinal Evaluation

Pervasive polymorphic imprinted methylation in the human placenta

Phenotype of maternal UPD(14)

Placental biomarkers for assessing fetal health

Placental telomere length decline with gestational age differs by sex and TERT, DNMT1, and DNMT3A DNA methylation

Prenatally detected trisomy 4 and 6 mosaicism?cytogenetic results and clinical phenotype

Profiling placental and fetal DNA methylation in human neural tube defects

Quantification of cell-free DNA in normal and complicated pregnancies: overcoming biological and technical issues

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

The significance of the placental genome and methylome in fetal and maternal health

Transient and placenta-specific imprinting in human development

Utility of DNA methylation to assess placental health

Whole exome sequencing of families with 1q21.1 microdeletion or microduplication

X-Chromosome inactivation (XCI) patterns in placental tissues of a paternally derived bal t(X;20) case