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GenomicsSearch for Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (GoKinD study participants and parents), NIDDK
Genetics of Kidneys in Diabetes (GoKinD) study is an initiative aimed at identifying susceptibility genes for diabetic nephropathy in type 1 diabetes. A large number of individuals with type 1 diabetes were screened to identify two subsets, one with clear-cut kidney disease and another with normal r...
phs000088.v1.p1 | EGA
GenomicsSearch for Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (GoKinD study participants), GAIN

Genetics of Kidneys in Diabetes (GoKinD) study is an initiative aimed at identifying susceptibility genes for diabetic nephropathy in type 1 diabetes. A large number of individuals with type 1 diabetes were screened to identify two subsets, one with clear-cut kidney disease and another with norma...

phs000018.v1.p1 | EGA
TranscriptomicsSomatic copy-number mosaicism in human skin revealed by induced pluripotent stem cells
Reprogramming human somatic cells into induced pluripotent stem cells (iPSC) has been suspected of causing de novo copy number variations (CNVs). To explore this issue, we performed a whole-genome and transcriptome analysis of 20 human iPSC lines derived from primary skin fibroblasts of 7 individual...
ORGANISM(S): Homo sapiens 
2012-10-19 | E-GEOD-41563 | biostudies-arrayexpress
TranscriptomicsModeling Human Cortical Development in vitro using induced Pluripotent Stem Cells
Human iPSCs grown in suspension in the presence of rostral neuralizing factors generated three-dimensional structures containing polarized radial glia, intermediate progenitors and a spectrum of layer-specific cortical neurons reminiscent of their organization in vivo. The hiPSC-derived multilayered...
ORGANISM(S): Homo sapiens 
2012-10-19 | E-GEOD-41565 | biostudies-arrayexpress
TranscriptomicsSomatic copy-number mosaicism in human skin revealed by induced pluripotent stem cells (sequencing)
Reprogramming human somatic cells into induced pluripotent stem cells (iPSC) has been suspected of causing de novo copy number variations (CNVs). To explore this issue, we performed a whole-genome and transcriptome analysis of 20 human iPSC lines derived from primary skin fibroblasts of 7 individual...
ORGANISM(S): Homo sapiens 
2012-10-31 | E-GEOD-41716 | biostudies-arrayexpress
UnknownLifetime ovulatory years and risk of epithelial ovarian cancer: a multinational pooled analysis.
Not available
S-EPMC10165492 | biostudies-literature
Unknownp53 and ovarian carcinoma survival: an Ovarian Tumor Tissue Analysis consortium study.
Not available
S-EPMC10073933 | biostudies-literature
UnknownClinical and pathological associations of PTEN expression in ovarian cancer: a multicentre study from the Ovarian Tumour Tissue Analysis Consortium.
Not available
S-EPMC7463007 | biostudies-literature
UnknownInherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration.
Not available
S-EPMC5340123 | biostudies-literature
UnknownGenome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.
Not available
S-EPMC4063682 | biostudies-literature
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