Evidence map›Paper›PMID 41018045›Full record

ArticleProceedings. IEEE International Symposium on Biomedical Imaging2024

CONUNETR: A CONDITIONAL TRANSFORMER NETWORK FOR 3D MICRO-CT EMBRYONIC CARTILAGE SEGMENTATION.

Nishchal Sapkota, Yejia Zhang, Susan M Motch Perrine, Yuhan Hsi, Sirui Li, Meng Wu, Greg Holmes, Abdul R Abdulai, Ethylin W Jabs, Joan T Richtsmeier and 1 more

Abstract read
In one paragraph

Article in Proceedings. IEEE International Symposium on Biomedical Imaging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Nishchal SapkotaDepartment of Computer Science and Engineering, University of Notre Dame, IN 46556.
Yejia ZhangDepartment of Computer Science and Engineering, University of Notre Dame, IN 46556.
Susan M Motch PerrineDepartment of Anthropology, The Pennsylvania State University, PA 16801.
Yuhan HsiDepartment of Anthropology, The Pennsylvania State University, PA 16801.
Sirui LiDepartment of Computer Science and Engineering, University of Notre Dame, IN 46556.
Meng WuDepartment of Clinical Genomics, Mayo Clinic, Rochester, MN 55905.
Greg HolmesDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, NY 10029.
Abdul R AbdulaiDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, NY 10029.
Ethylin W JabsDepartment of Clinical Genomics, Mayo Clinic, Rochester, MN 55905.
Joan T RichtsmeierDepartment of Anthropology, The Pennsylvania State University, PA 16801.
Danny Z ChenDepartment of Computer Science and Engineering, University of Notre Dame, IN 46556.

Funding

Cartilage and bone of the lower jaw in development and diseaseR01DE031439 · NIDCR · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI Ethylin Wang Jabs, Kazuhiko Kawasaki · 2022 to 2026
$3.8M
Genetic, Tissue, and Anatomical Interactions in Mandibulofacial DysmorphogenesisR01DE029832 · NIDCR · MAYO CLINIC ROCHESTER · PI JABS, ETHYLIN WANG, KAWASAKI, KAZUHIKO · 2021 to 2024
$2.9M
The chondrocranium in craniofacial development and diseaseR01DE027677 · NIDCR · PENNSYLVANIA STATE UNIVERSITY, THE · PI RICHTSMEIER, JOAN THERESE · 2018 to 2022
$2.6M
NIDCR NIH HHS R01 DE027677NIDCR NIH HHS R01 DE029832NIDCR NIH HHS R01 DE031439
6 · The paper itself

Abstract

Studying the morphological development of cartilaginous and osseous structures is critical to the early detection of life-threatening skeletal dysmorphology. Embryonic cartilage undergoes rapid structural changes within hours, introducing biological variations and morphological shifts that limit the generalization of deep learning-based segmentation models that infer across multiple embryonic age groups. Obtaining individual models for each age group is expensive and less effective, while direct transfer (predicting an age unseen during training) suffers a potential performance drop due to morphological shifts. We propose a novel Transformer-based segmentation model with improved biological priors that better distills morphologically diverse information through conditional mechanisms. This enables a single model to accurately predict cartilage across multiple age groups. Experiments on the mice cartilage dataset show the superiority of our new model compared to other competitive segmentation models. Additional studies on a separate mice cartilage dataset with a distinct mutation show that our model generalizes well and effectively captures age-based cartilage morphology patterns. Code is available in GitHub.

Indexed as

Cartilage SegmentationConditional ModelCranial DysmorphologyTransformers

Identifiers

PMID41018045
PMCPMC12476089

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.