Evidence map›Paper›PMID 40912664›Full record

ArticleNeuroImage2025

Conditional deep generative normative modeling for structural and developmental anomaly detection in the fetal brain.

Sungmin You, Andrea Gondova, Carlos Simon Amador Izaguirre, Guillermo Tafoya Milo, Seungyoon Jeong, Han-Jui Lee, Tomo Tarui, Caitlin K Rollins, Hyuk Jin Yun, P Ellen Grant and 1 more

Abstract read
In one paragraph

Article in NeuroImage, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Sungmin YouFetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Division of Newborn Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Andrea GondovaFetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Division of Newborn Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Carlos Simon Amador IzaguirreFetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Guillermo Tafoya MiloFetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Seungyoon JeongFetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Division of Newborn Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Han-Jui LeeDepartment of Radiology, Taipei Veterans General Hospital, Taipei 112, Taiwan; School of Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Tomo TaruiMother Infant Research Institute, Tufts Medical Center, Boston, MA 02111, USA; Pediatric Neurology, Hasbro Children's Hospital, Providence, RI 02905, USA.
Caitlin K RollinsDepartment of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Hyuk Jin YunFetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Division of Newborn Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA.
P Ellen GrantFetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Division of Newborn Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA; Department of Radiology, Harvard Medical School, Boston, MA 02115, USA.
Kiho ImFetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Division of Newborn Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA. Electronic address: kiho.im@childrens.harvard.edu.

Funding

Novel MRI Assessment of Placental Structure and Function Throughout PregnancyR01HD100009 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI ADALSTEINSSON, ELFAR, GRANT, PATRICIA ELLEN · 2019 to 2023
$3.6M
Genetic and Hemodynamic Effects on Prenatal Cortical Development in Congenital Heart DiseaseR01NS114087 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI IM, KIHO · 2020 to 2024
$2.8M
Fetal MRI: robust self-driving brain acquisition and body movement quantificationR01EB032708 · NIBIB · BOSTON CHILDREN'S HOSPITAL · PI ADALSTEINSSON, ELFAR, GRANT, PATRICIA ELLEN · 2022 to 2025
$2.8M
Measuring cortical plate and subplate thickness in the human fetal brain from magnetic resonance imagesR01EB031170 · NIBIB · BOSTON CHILDREN'S HOSPITAL · PI IM, KIHO · 2021 to 2025
$2.5M
Fetal Brain MRI as a Predictor of Late Neurodevelopmental Outcome in Congenital Heart DiseaseR01NS121334 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Caitlin Rollins · 2022 to 2026
$2.2M
NIBIB NIH HHS R01 EB031170NIBIB NIH HHS R01 EB032708NICHD NIH HHS R01 HD100009NINDS NIH HHS R01 NS114087NINDS NIH HHS R01 NS121334
6 · The paper itself

Abstract

Fetal brain development is a complex and dynamic process, and its disruption can lead to significant neurological disorders. Early detection of brain aberrations during pregnancy is critical for optimizing postnatal medical intervention. We propose a deep generative anomaly detection framework, conditional cyclic variational autoencoding generative adversarial network (CCVAEGAN), that can identify structural brain anomalies using fetal brain magnetic resonance imaging. CCVAEGAN leverages covariate conditioning on gestational age and cyclic consistency training to generate high-fidelity normative fetal brain images to enhance anomaly detection across various neurodevelopmental stages and diagnoses. Using MRI data from typically developing and clinically abnormal fetuses across multiple sites, CCVAEGAN achieves superior image generation quality and anomaly detection accuracy than other comparable models, consistently producing anatomically precise images with lower reconstruction errors and higher structural similarities. Anomaly detection experiments yielded near-perfect AUROC values (>0.99) across various anomaly score metrics, and visual assessments confirmed the model's ability to localize and characterize structural abnormalities. Additionally, external validation on separated-site cohorts demonstrated the generalizability of the CCVAEGAN framework, showing robust detection performance despite data variations. These findings demonstrate CCVAEGAN's potential as a powerful tool for automated, objective anomaly screening, that could significantly enhance the efficiency of clinical workflows for early diagnosis of fetal brain anomalies. Furthermore, this approach has the potential universality to apply to other medical imaging not limited to specific organs or imaging modalities in the future.

Indexed as

BrainDeep LearningFetusMagnetic Resonance ImagingNeuroimagingPrenatal DiagnosisFemaleGestational AgeHumansPregnancyAnomaly detectionDeep generative modelFetal MRINormative modeling

Identifiers

PMID40912664
PMCPMC12535477

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.