Inherited genetic risk in stillbirth: A shared genomic segments analysis of high-risk pedigrees.

doi:10.1016/j.xhgg.2025.100546

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

Back to search

Article

Inherited genetic risk in stillbirth: A shared genomic segments analysis of high-risk pedigrees.

HGG advances - 15 Jan 2026

Workalemahu Tsegaselassie, Madsen Michael J, Lopez Sarah, Page Jessica M, Blue Nathan R, Avery Cecile, Sargent Rob, Yu Zhe, Guinto Emily, Branch D Ware, Leisher Susannah, Jorde Lynn B, Quinlan Aaron, Coon Hilary, Varner Michael W, Roberts Claire T, Neklason Deborah W, Camp Nicola J, Silver Robert M

Abstract excerpt

Stillbirth is a devastating adverse pregnancy outcome affecting 2 million pregnancies worldwide. Although an etiology may be found in some stillbirths, one-third remain unexplained. Stillbirth clusters in families and few underlying inherited genes associated with stillbirth are known. Well-characterized family-based studies may aid in identifying genetic contributors to unexplained stillbirth. Using the Utah...

Topics

Humans
Stillbirth
Pedigree
Female
Pregnancy
Genetic Predisposition to Disease
Male
Genome-Wide Association Study
Genomics
Haplotypes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Adult

Whole Genome Sequencing

Source

Open in PubMed Open full text

Identifiers

PMID: 41229114
DOI: 10.1016/j.xhgg.2025.100546
PMCID: PMC12686895

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.