Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Methylation analysis of idiopathic recurrent spontaneous miscarriage cases reveals aberrant imprinting at H19 ICR in normozoospermic individuals.

Fertility and sterility - 1 Nov 2012

Ankolkar Mandar, Patil Anushree, Warke Himangi, Salvi Vinita, Kedia Mokashi Neelam, Pathak Shilpa, Balasinor N H

Abstract excerpt

OBJECTIVE: To study H19 ICR methylation levels in association with sperm parameters routinely analyzed in idiopathic recurrent spontaneous miscarriage cases. DESIGN: Case-control study. SETTING: Academic research setting. PATIENT(S): Male partners of couples with a history of idiopathic recurrent spontaneous miscarriage (RSM group) and male partners of couples with proven fertility (control group)....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abortion, Habitual
Share to Cell Shape

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromatin Assembly and Disassembly

Share to Insulin-Like Growth Factor II

Share to Semen Analysis

Share to Sperm Count

Share to Sperm Motility

Share to Spermatozoa

Source

Identifiers

PMID: 22959455
DOI: 10.1016/j.fertnstert.2012.07.1143

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Methylation analysis of idiopathic recurrent spontaneous miscarriage cases reveals aberrant imprinting at H19 ICR in normozoospermic individuals.PMID 22959455Read ↗

Idiopathic male infertility is strongly associated with aberrant DNA methylation of imprinted loci in sperm: a case-control studySemantic proximity Read ↗

Higher sperm H3K4me3 levels are associated with idiopathic recurrent pregnancy lossSemantic proximity Read ↗

Comprehensive DNA methylation profiling of sperm in male partners of couples with unexplained recurrent pregnancy lossSemantic proximity Read ↗

Whole genome bisulfite sequencing of sperm reveals differentially methylated regions in male partners of idiopathic recurrent pregnancy loss casesSemantic proximity Read ↗

The sperm epigenome does not display recurrent epimutations in patients with severely impaired spermatogenesisSemantic proximity Read ↗

DNA methylation defects in spermatozoa of male partners from couples experiencing recurrent pregnancy lossSemantic proximity Read ↗

Analysis of H19 methylation in control and abnormal human embryos, sperm and oocytes.Semantic proximity Read ↗

Idiopathic male infertility is strongly associated with aberrant promoter methylation of methylenetetrahydrofolate reductase (MTHFR).Semantic proximity Read ↗

Impairment of sperm DNA methylation in male infertility: a meta-analytic study.Semantic proximity Read ↗

Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniquesSemantic proximity Read ↗

Sperm DNA methylation ofH19imprinted gene and male infertilitySemantic proximity Read ↗

Bringing epigenetics into the diagnostics of the andrology laboratory: challenges and perspectivesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.