Lista de obras - Deborah E McFadden - Dominio Público Uruguay

A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma

artículo científico publicado en 1998

Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia.

artículo científico publicado en 2005

Anterolateral diaphragmatic hernia with body wall defect understood in relation to the abaxial domain

scientific article published on 03 April 2014

Assessing the role of placental trisomy in preeclampsia and intrauterine growth restriction

article

Carnitine palmitoyltransferase I and sudden unexpected infant death in British Columbia First Nations

artículo científico

Chorioamnionitis in the pathogenesis of brain injury in preterm infants

artículo científico publicado en 2013

Chromosome abnormalities in human beings.

artículo científico publicado en 1997

Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation

artículo científico publicado en 2011

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences

artículo científico publicado en 1996

Congenital gliosarcoma: detailed clinicopathologic documentation of a rare neoplasm

artículo científico publicado en 2009

DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia

artículo científico publicado en 2010

De novo mutation of theDHCR7 gene in a fetus with severe Smith–Lemli–Opitz (or RSH) syndrome

article

Developmental origin of chorionic villus cultures from spontaneous abortion and chorionic villus sampling

artículo científico publicado en 2011

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

artículo científico publicado en 2012

Dispermy--origin of diandric triploidy: Brief Communication

artículo científico publicado en 2002

Early inflammation in the absence of overt infection in preterm neonates exposed to intensive care

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Effect of chorioamnionitis on brain development and injury in premature newborns

artículo científico publicado en 2009

Extensive epigenetic reprogramming in human somatic tissues between fetus and adult

artículo científico publicado en 2011

Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies

artículo científico publicado en 2011

Immunolocalization of estrogen receptor alpha and beta in human fetal prostate

artículo científico publicado en 2005

Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage ⬇️

artículo científico publicado el 20 de marzo de 2013

Maternal serum screening in triploidy

artículo científico publicado en 2002

Origin and outcome of pregnancies affected by androgenetic/biparental chimerism.

artículo científico publicado en 2006

Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism

artículo científico publicado en 2002

Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsia

artículo científico publicado en 2014

Parental and meiotic origin of triploidy in the embryonic and fetal periods

artículo científico publicado en 2000

Pervasive polymorphic imprinted methylation in the human placenta

artículo científico publicado en 2016

Phenotype of triploid embryos.

artículo científico publicado en 2005

Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5

artículo científico publicado en 2007

Placental pathology of triploidy

artículo científico publicado en 1996

Placental weight in pregnancies with trisomy confined to the placenta

artículo científico publicado en 2009

Pleural relapse during hematopoietic remission in childhood acute lymphoblastic leukemia.

artículo científico publicado en 1997

Prenatal and postnatal inflammation in relation to cortisol levels in preterm infants at 18 months corrected age.

artículo científico publicado en 2013

Profiling placental and fetal DNA methylation in human neural tube defects

artículo científico publicado en 2016

Protein kinase profiling in miscarriage: implications for the pathogenesis of trisomic pregnancy

artículo científico publicado en 2012

Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants

artículo científico publicado en 2014

Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13)

artículo científico publicado en 2001

Renal tubular dysgenesis with calvarial hypoplasia: report of two additional cases and review ⬇️

artículo científico publicado el 1 de octubre de 1997

Renal–hepatic–pancreatic dysplasia: An autosomal recessive condition that is not linked to thePKHD1 gene on chromosome 6p21.1-p12

article

The Origin of Abnormalities in Recurrent Aneuploidy/Polyploidy ⬇️

artículo científico publicado el 23 de octubre de 2001

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders

article

Widespread DNA hypomethylation at gene enhancer regions in placentas associated with early-onset pre-eclampsia

artículo científico publicado en 2013

Lista de obras de Deborah E McFadden

A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma

Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia.

Anterolateral diaphragmatic hernia with body wall defect understood in relation to the abaxial domain

Assessing the role of placental trisomy in preeclampsia and intrauterine growth restriction

Carnitine palmitoyltransferase I and sudden unexpected infant death in British Columbia First Nations

Chorioamnionitis in the pathogenesis of brain injury in preterm infants

Chromosome abnormalities in human beings.

Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences

Congenital gliosarcoma: detailed clinicopathologic documentation of a rare neoplasm

DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia

De novo mutation of theDHCR7 gene in a fetus with severe Smith–Lemli–Opitz (or RSH) syndrome

Developmental origin of chorionic villus cultures from spontaneous abortion and chorionic villus sampling

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

Dispermy--origin of diandric triploidy: Brief Communication

Early inflammation in the absence of overt infection in preterm neonates exposed to intensive care

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

Effect of chorioamnionitis on brain development and injury in premature newborns

Extensive epigenetic reprogramming in human somatic tissues between fetus and adult

Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies

Immunolocalization of estrogen receptor alpha and beta in human fetal prostate

Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage ⬇️

Maternal serum screening in triploidy

Origin and outcome of pregnancies affected by androgenetic/biparental chimerism.

Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism

Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsia

Parental and meiotic origin of triploidy in the embryonic and fetal periods

Pervasive polymorphic imprinted methylation in the human placenta

Phenotype of triploid embryos.

Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5

Placental pathology of triploidy

Placental weight in pregnancies with trisomy confined to the placenta

Pleural relapse during hematopoietic remission in childhood acute lymphoblastic leukemia.

Prenatal and postnatal inflammation in relation to cortisol levels in preterm infants at 18 months corrected age.

Profiling placental and fetal DNA methylation in human neural tube defects

Protein kinase profiling in miscarriage: implications for the pathogenesis of trisomic pregnancy

Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants

Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13)

Renal tubular dysgenesis with calvarial hypoplasia: report of two additional cases and review ⬇️

Renal–hepatic–pancreatic dysplasia: An autosomal recessive condition that is not linked to thePKHD1 gene on chromosome 6p21.1-p12

The Origin of Abnormalities in Recurrent Aneuploidy/Polyploidy ⬇️

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders

Widespread DNA hypomethylation at gene enhancer regions in placentas associated with early-onset pre-eclampsia