NIH-funded research Career grant

Understanding genetic and physical traits linked to stillbirth and fetal anomalies to improve prenatal care

Official title: Dissecting the Genetic and Phenotypic Architecture of Stillbirth and Fetal Structural Anomalies to Improve Prenatal Diagnosis

Funded at Boston Children's Hospital · NIH-11352326 · Data updated 2026-11-12

A clinician-scientist at Boston Children’s Hospital is leading a five-year plan to map how genes and visible fetal features relate to stillbirth and fetal structural problems, with the goal of better prenatal diagnosis.

More Stillbirth research and trials

Quick facts

Grant typeCareer grant
Study typeNIH-funded research
Funding institutionBoston Children's Hospital
NIH-funded
Lab location1 site (Boston, United States)
Project startJuly 1, 2026
Project endJune 30, 2031
Funding year2026
Award (this year)$167,400
NIH project number1K08HD121809-01
Project IDNIH-11352326 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates are expectant patients or families facing high-risk pregnancies with fetal structural concerns or prior stillbirth risk factors, whose data could be contributed to large datasets.

Less likely to help

Some pregnancies may not show clear genetic or phenotypic links, so they may not directly benefit from the findings.

What this research studies

This program will combine large sets of genomic and phenotypic data from pregnancies to find genetic variants and patterns that explain stillbirth and fetal anomalies. It will harmonize data across sources, apply advanced statistics, and develop phenotype-driven methods to prioritize variants. The effort is designed to train the investigator to become an independent physician-scientist and leader in perinatal precision diagnosis. The work aims to move from data to clearer, more actionable prenatal findings that could guide care.

Why it matters

Potential benefit: If successful, it could lead to more accurate prenatal diagnoses and personalized guidance for pregnancies affected by stillbirth or fetal anomalies.

How similar studies have gone: Previous studies show that integrating genomic and phenotypic data improves diagnostic precision in perinatal medicine, but large-scale, harmonized analyses are still developing.

Where this research is happening

  • Boston Children's Hospital
    Boston, United States
    Active

Researchers

  • Principal investigator: Duyzend, Michael H — Boston Children's Hospital
  • Study coordinator: Duyzend, Michael H

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.