Nilüfer Rahmioğlu

ORCID: 0000-0002-5169-8571 · 91 papers in corpus
article 2018
review 2017
Biochimica et biophysica acta. Molecular basis of disease ·doi:10.1016/j.bbadis.2017.06.018

In order to uncover miRNA changes in endometriosis pathogenesis, both endometriotic lesions and endometrial biopsies, as well as stromal and epithelial cells isolated from these tissues have been investigated and a large number of dysregula…

2017
Scientific reports ·doi:10.1038/s41598-017-03682-0

The inner uterine lining (endometrium) is a unique tissue going through remarkable changes each menstrual cycle. Endometrium has its characteristic DNA methylation profile, although not much is known about the endometrial methylome changes …

article 2017

Study Question Do genome-wide association study (GWAS) data for endometriosis provide insight into novel biological pathways associated with its pathogenesis? Summary Answer GWAS analysis uncovered multiple pathways that are statistically e…

article 2017
Human Reproduction ·doi:10.1093/humrep/dex024

Study question: Do genome-wide association study (GWAS) data for endometriosis provide insight into novel biological pathways associated with its pathogenesis? Summary answer: GWAS analysis uncovered multiple pathways that are statistically…

book-chapter 2017
·doi:10.1007/978-3-319-59856-7_11
article 2017

Around 50% of endometriosis risk is due to genetic factors. Ten genome-wide significant loci have been associated with endometriosis, but most are located in intergenic regions of the genome. To understand how transcriptomic profiles are pe…

meta-analysis 2017
Nature communications ·doi:10.1038/ncomms15539

Endometriosis is a heritable hormone-dependent gynecological disorder, associated with severe pelvic pain and reduced fertility; however, its molecular mechanisms remain largely unknown. Here we perform a meta-analysis of 11 genome-wide ass…

article 2017

Endometriosis affects 5-10% of premenopausal women causing pelvic pain and impaired fertility. Diagnosis can only be established surgically, thus, less invasive means of diagnosis are urgently needed. Endometriosis has been suggested to ind…

other 2017
Molecular medicine reports ·doi:10.3892/mmr.2017.7398

Endometriosis is a benign gynecologic disorder, affecting up to 10% of women, characterized by the presence of functional endometrial tissue at ectopic positions generally within the peritoneum. It is a heritable condition influenced by mul…

other 2017
Epigenetics ·doi:10.1080/15592294.2017.1367475

Genome-wide association studies in the fields of reproductive medicine and endocrinology are yielding robust genetic variants associated with disease. Integrated genomic, transcriptomic, and epigenomic molecular profiling studies are common…

dataset 2016
·doi:10.6084/m9.figshare.c.3641012_d5

Differentially methylated regions between women with endometriosis and healthy women. The methylation data of all patients was compared to controls. Menstrual cycle day has not been taken into account. (XLSX 15 kb)

dataset 2016
·doi:10.6084/m9.figshare.c.3641012_d7

Differentially methylated regions between different menstrual cycle phases. The methylation data of each menstrual cycle phase was compared to other phases. (XLSX 2676 kb)

dataset 2016
·doi:10.6084/m9.figshare.c.3641012_d1

Functional annotation clustering of hypo- and hypermethylated genes in endometrial tissue using g:profiler bioinformatics tool. The complete lists of DMRs between different menstrual cycle phases was used to create the lists of Gene Ontolog…

dataset 2016
·doi:10.6084/m9.figshare.c.3641012_d2

Pathway analysis of hypo- and hypermethylated genes in endometrial tissue using g:profiler bioinformatics tool. The complete lists of DMRs between different menstrual cycle phases was used to create the list of Kyoto Encyclopedia of Genes a…

dataset 2016
·doi:10.6084/m9.figshare.c.3641012_d3

Menstrual cycle phase specific genes. The list of late-secretory and menstrual phase specific hyper- and hypomethylated genes. (XLSX 28 kb)

dataset 2016
·doi:10.6084/m9.figshare.c.3641012_d8

PCR primers used in the methylation validation analysis. PCR primers for the bisulfite-treated DNA were designed using MethPrimer[42]. (XLSX 9 kb)

review 2016
Seminars in reproductive medicine ·doi:10.1055/s-0036-1585408

Endometriosis is a heritable, complex chronic inflammatory disease, for which much of the causal pathogenic mechanism remains unknown. Genome-wide association studies (GWAS) to date have identified 12 single nucleotide polymorphisms at 10 i…

2016
Nature ·doi:10.1038/nature19806

Birth weight (BW) has been shown to be influenced by both fetal and maternal factors and in observational studies is reproducibly associated with future risk of adult metabolic diseases including type 2 diabetes (T2D) and cardiovascular dis…

article 2016
article 2016
article 2016
Clinical epigenetics ·doi:10.1186/s13148-015-0168-z

BACKGROUND: Alterations in endometrial DNA methylation profile have been proposed as one potential mechanism initiating the development of endometriosis. However, the normal endometrial methylome is influenced by the cyclic hormonal changes…

article 2015
Molecular human reproduction ·doi:10.1093/molehr/gav021

Endometriosis is primarily characterized by the presence of tissue resembling endometrium outside the uterine cavity and is usually diagnosed by laparoscopy. The most commonly used classification of disease, the revised American Fertility S…

article 2015

Free to read Endometriosis is primarily characterized by the presence of tissue resembling endometrium outside the uterine cavity and is usually diagnosed by laparoscopy. The most commonly used classification of disease, the revised America…

review 2015
Women's health (London, England) ·doi:10.2217/whe.15.41

Endometriosis is a heritable complex disorder that is influenced by multiple genetic and environmental factors. Identification of these genetic factors will aid a better understanding of the underlying biology of the disease. In this articl…