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

PLoV: a comprehensive database of genetic variants leading to pregnancy loss.

Database : the journal of biological databases and curation - 18 Jan 2025

Maksiutenko Evgeniia M, Bezdvornykh Igor V, Barbitoff Yury A, Nasykhova Yulia A, Glotov Andrey S

Abstract excerpt

Pregnancy loss is an important reproductive health problem that affects many couples. Genetic factors play an important role in both spontaneous miscarriage and recurrent pregnancy loss, and the effect of genomic variants is recognized as one of the major causes of pregnancy loss in euploid foetuses. In this work, we extend our previous analysis of the genetic landscape of pregnancy loss and develop a Pregnancy...

Read the complete abstract on PubMed

Topics

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

Share to Abortion, Spontaneous
Share to Databases, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Genome, Human

Share to Pregnancy

Source

Open in PubMed Open full text

Identifiers

PMID: 40625169
DOI: 10.1093/database/baaf037
PMCID: PMC12462621

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PLoV: a comprehensive database of genetic variants leading to pregnancy loss.PMID 40625169Read ↗

The genomic basis of sporadic and recurrent pregnancy loss: a comprehensive in-depth analysis of 24,900 miscarriagesSemantic proximity Read ↗

Genetic Variants in Recurrent Euploid Pregnancy LossSemantic proximity Read ↗

Whole-exome sequencing analysis on products of conception: A cohort study to evaluate clinical utility and genetic etiology for pregnancy lossSemantic proximity Read ↗

Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot studySemantic proximity Read ↗

Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot studySemantic proximity Read ↗

Genetic causes of sporadic and recurrent miscarriage.Semantic proximity Read ↗

Genetics of recurrent pregnancy loss: a reviewSemantic proximity Read ↗

The Human Intolerome: a curated database to prioritize genomic variants in stillbirth, pregnancy loss, and neonatal deathSemantic proximity Read ↗

Sequence diversity lost in early pregnancy.Semantic proximity Read ↗

Identification of genetic alterations in couples and their products of conceptions from recurrent pregnancy loss in North Indian populationSemantic proximity Read ↗

Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches.Semantic proximity Read ↗

Genetics of Recurrent Miscarriage and Pregnancy Loss in Women’s Reproductive HealthSemantic proximity Read ↗

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