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Links from GEO DataSets

Items: 20

1.

Epigenome analysis of cord blood DNA from infants born into the SWS study

(Submitter supplied) Genome wide DNA methylation profiling of umbilical cord blood DNA samples. The Illumina Infinium MethylationEPIC array was used to obtain DNA methylation profiles across approximately 850,000 CpGs. Samples included 470 cord blood samples from infants born to women in the Southampton Women's Survery (SWS) cohort, to examine the association between DNA methylation in the infant and aspects of health and disease in early and life and childhood.
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL21145
470 Samples
Download data: IDAT
Series
Accession:
GSE154915
ID:
200154915
2.

Epigenome analysis of cord blood DNA from infants born into the UPBEAT study

(Submitter supplied) Genome-wide DNA methylation profiling of umbilical cord blood buffy coat DNA samples. The Illumina Infinium MethylationEPIC array was used to obtain DNA methylation profiles across approximately 850,000 CpGs. Samples included 557 cord blood samples born to obese women in the UPBEAT trial, with and without gestational diabetes mellitus (GDM), to determine the association between maternal GDM and hyperglycaemia during pregnancy on the methylation in the infant.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL21145
557 Samples
Download data: IDAT, TXT
Series
Accession:
GSE141065
ID:
200141065
3.

A cord blood multi-omic analysis of birthweight reveals new underlying mechanisms related to cholesterol metabolism [gene expression]

(Submitter supplied) Birthweight reflects in utero exposures and later health evolution. Despite existing studies employing high-dimensional molecular measurements, the understanding of underlying mechanisms of birthweight remains limited. To investigate the systems biology of birthweight, we cross-sectionally integrated the methylome, the transcriptome, the metabolome and a set of inflammatory proteins measured in cord blood samples, collected from four birth-cohorts (n=489). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17077
194 Samples
Download data: TXT
Series
Accession:
GSE151373
ID:
200151373
4.

A cord blood multi-omic analysis of birthweight reveals new underlying mechanisms related to cholesterol metabolism

(Submitter supplied) Birthweight reflects in utero exposures and later health evolution. Despite existing studies employing high-dimensional molecular measurements, the understanding of underlying mechanisms of birthweight remains limited. To investigate the systems biology of birthweight, we cross-sectionally integrated the methylome, the transcriptome, the metabolome and a set of inflammatory proteins measured in cord blood samples, collected from four birth-cohorts (n=489). more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
492 Samples
Download data: IDAT, TXT
Series
Accession:
GSE151042
ID:
200151042
5.

Early-Onset Preeclampsia Placentas and Controls

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array; Expression profiling by array
Platforms:
GPL13534 GPL10558
56 Samples
Download data
Series
Accession:
GSE44712
ID:
200044712
6.

Gene expression in Early-Onset Preeclampsia Placentas and Controls

(Submitter supplied) We investigated the DNA methylation and gene expression of 20 chorionic villi samples from early onset preeclampsia placentas to 20 gestational age matched controls. From this we were able to see a widespread disregulation in DNA methylation across a subset of genes in the genome. This may help to elucidate the underlying biological problems that lead to early onset preeclampsia. We noted that there were DNA methylation changes in many genes of importance as well as in different genomic elements such as enhancers.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
16 Samples
Download data: TXT
Series
Accession:
GSE44711
ID:
200044711
7.

DNA methylation in Early Onset Preeclamptic placentas

(Submitter supplied) We investigated the DNA methylation and gene expression of 20 chorionic villi samples from early onset preeclampsia placentas to 20 gestational age matched controls. From this we were able to see a widespread disregulation in DNA methylation across a subset of genes in the genome. This may help to elucidate the underlying biological problems that lead to early onset preeclampsia. We noted that there were DNA methylation changes in many genes of importance as well as in different genomic elements such as enhancers.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
40 Samples
Download data: TXT
Series
Accession:
GSE44667
ID:
200044667
8.

DNA methylation of insulin signalling pathways in human primary muscle stem cells is associated with HOMA2-IR in older adults

(Submitter supplied) Context: While ageing is associated with increased insulin resistance (IR), the molecular mechanisms underlying increased IR in muscle, the primary organ for glucose clearance, have yet to be elucidated in older individuals. As epigenetic processes are suggested to contribute to development of ageing-associated diseases, in human primary muscle stem cells (myoblasts) from community dwelling older individuals we investigated whether differential DNA methylation was associated with IR. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL21145
119 Samples
Download data: IDAT, TXT
Series
Accession:
GSE221540
ID:
200221540
9.

Amnion as a surrogate tissue reporter of the effects of maternal preeclampsia on the fetus

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL16791
91 Samples
Download data: TXT
Series
Accession:
GSE79783
ID:
200079783
10.

Amnion as a surrogate tissue reporter of the effects of maternal preeclampsia on the fetus [RNA-Seq]

(Submitter supplied) Background: Preeclampsia, traditionally characterized by high blood pressure and proteinuria, is a common pregnancy complication, which affects 2-8% of all pregnancies. Although children born to women with preeclampsia have a higher risk of hypertension in later life, the mechanism of this increased risk is unknown. DNA methylation is an epigenetic modification that has been studied as a mediator of cellular memory of adverse exposures in utero. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
29 Samples
Download data: TXT
11.

Amnion as a surrogate tissue reporter of the effects of maternal preeclampsia on the fetus [Help-tagging]

(Submitter supplied) Background: Preeclampsia, traditionally characterized by high blood pressure and proteinuria, is a common pregnancy complication, which affects 2-8% of all pregnancies. Although children born to women with preeclampsia have a higher risk of hypertension in later life, the mechanism of this increased risk is unknown. DNA methylation is an epigenetic modification that has been studied as a mediator of cellular memory of adverse exposures in utero. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL16791
62 Samples
Download data: TXT
Series
Accession:
GSE79781
ID:
200079781
12.

Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes

(Submitter supplied) Autism spectrum disorder (ASD) is a neurodevelopmental disorder with complex heritability and higher prevalence in males. The neonatal epigenome has the potential to reflect past interactions between genetic and environmental factors during early development and influence future health outcomes. We performed whole-genome bisulfite sequencing of 152 umbilical cord blood samples from the MARBLES and EARLI high-familial risk prospective cohorts to identify an epigenomic signature of ASD at birth. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platforms:
GPL20795 GPL20301
130 Samples
Download data: TXT
Series
Accession:
GSE140730
ID:
200140730
13.

Epigenome analysis of muscle tissue samples from male participants of the Hertfordshire Sarcopenia Study (HSS) and Hertfordshire Sarcopenia Study extension (HSSe)

(Submitter supplied) Genome wide DNA methylation profiling of muscle tissue genomic DNA. The Illumina Infinium MethylationEPIC array was used to obtain DNA methylation profiles across approximately 850,000 CpGs. Samples were male, taken from both the Hertfordshire Sarcopenia Study (HSS, n=34) and the Hertfordshire Sarcoepnia Study exension (HSSe, n=44), to determine DNA methylation associations with measures of muscle mass and function. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL21145
78 Samples
Download data: IDAT
Series
Accession:
GSE154980
ID:
200154980
14.

A randomised controlled trial of folic acid intervention in pregnancy highlights a putative methylation-regulated control element at ZFP57

(Submitter supplied) Background: Maternal blood folate concentrations during pregnancy have been previously linked with DNA methylation patterns, but this has been done predominantly through observational studies. We showed recently in an epigenetic analysis of the first randomized controlled trial (RCT) of folic acid supplementation specifically in the second and third trimesters (the EpiFASSTT trial) that methylation at some imprinted genes was altered in cord blood samples in response to treatment. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL23976
86 Samples
Download data: TXT
Series
Accession:
GSE176325
ID:
200176325
15.

Early- and late-onset preeclampsia and the tissue-specific epigenome of the placenta and newborn

(Submitter supplied) Introduction. Preeclampsia (PE) carries increased risks of cardiovascular- and metabolic diseases in mothers and offspring during the life course. While the severe early-onset PE (EOPE) phenotype originates from impaired placentation in early pregnancy, late-onset PE (LOPE) is in particular associated with pre-existing maternal cardiovascular- and metabolic risk factors. We hypothesize that PE is associated with altered epigenetic programming of placental and fetal tissues and that these epigenetic changes might elucidate the increased cardiovascular- and metabolic disease susceptibility in PE offspring. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
245 Samples
Download data: TXT
Series
Accession:
GSE103253
ID:
200103253
16.

Epigenome analysis of CHAMACOS cord blood

(Submitter supplied) Genome wide DNA methylation profiling of CHAMACOS cord blood. The Illumina Infinium 450k Human DNA methylation Beadchip was used to obtain DNA methylation profiles across approximately 450,000 CpGs. Methylation was assessed in 380 cord blood samples of members of the CHAMACOS cohort.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
380 Samples
Download data: CSV
Series
Accession:
GSE97628
ID:
200097628
17.

Genome-wide placental gene methylations in gestational diabetes mellitus, fetal growth and metabolic health biomarkers in cord blood

(Submitter supplied) Gestational diabetes mellitus (GDM) “program” an elevated risk of metabolic syndrome in the offspring. Epigenetic alterations are a suspected mechanism. GDM has been associated with placental DNA methylation changes in some epigenome-wide association studies. It remains unclear which genes or pathways are affected, and whether any placental differential gene methylations are correlated to fetal growth or circulating metabolic health biomarkers. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL23976
60 Samples
Download data: TXT
Series
Accession:
GSE200659
ID:
200200659
18.

Transcriptional analysis of placenta samples exposed to maternal smoking during pregnancy

(Submitter supplied) RNAseq analysis of placental gene expression in samples obtained from 59 smokers (enrolled in the VCSIP RCT: NCT03203603) and 20 never-smokers for reference.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
79 Samples
Download data: CSV
Series
Accession:
GSE253158
ID:
200253158
19.

Cytosine methylation profiling in small and large for gestational age newborns

(Submitter supplied) In 1990, David Barker proposed that prenatal nutrition is directly linked to adult cardiovascular disease. Since then, the relationship between adult cardiovascular risk, metabolic syndrome and birth weight has been widely documented. Here we used the TruSeq Methyl Capture EPIC platform to compare the methylation patterns in cord blood from large for gestational age (LGA), small for gestational age (SGA) and adequate for gestational age/Control (AGA/Ctl) newborns. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL18573
36 Samples
Download data: TXT
Series
Accession:
GSE238155
ID:
200238155
20.

Genome wide effects of maternal undernutrition

(Submitter supplied) DNA methylation profiles of the livers of 1 day old rats from mothers fed with three different diets during gestation. The first animal group was fed with a normal diet (c=control); second group received much less protein than normal and slighlty more carbs (p=low protein, or programmed); third group diet was same as low protein but with extra folic acid (f=low protein+folate). All diets were matched for energy.
Organism:
Rattus norvegicus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL10287
3 Samples
Download data: BED, WIG
Series
Accession:
GSE50935
ID:
200050935
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