Evidence map›Paper›PMID 40100426›Full record

ReviewMammalian genome : official journal of the International Mammalian Genome Society2025

The power of mouse models in the diagnostic odyssey of patients with rare congenital anomalies.

Stephen R F Twigg, Nicholas D E Greene, Deborah J Henderson, Pleasantine Mill, Karen J Liu

Abstract readReview
In one paragraph

Review in Mammalian genome : official journal of the International Mammalian Genome Society, 2025. 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. Review
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

5 authors.

Stephen R F TwiggMRC National Mouse Genetics Network, Congenital Anomalies Cluster, Mary Lyon Centre at MRC Harwell, UK. stephen.twigg@imm.ox.ac.uk.ORCID 0000-0001-5024-049X
Nicholas D E GreeneMRC National Mouse Genetics Network, Congenital Anomalies Cluster, Mary Lyon Centre at MRC Harwell, UK. n.greene@ich.ucl.ac.uk.ORCID 0000-0002-4170-5248
Deborah J HendersonMRC National Mouse Genetics Network, Congenital Anomalies Cluster, Mary Lyon Centre at MRC Harwell, UK. deborah.henderson@newcastle.ac.uk.ORCID 0000-0002-2705-5998
Pleasantine MillMRC National Mouse Genetics Network, Congenital Anomalies Cluster, Mary Lyon Centre at MRC Harwell, UK. pleasantine.mill@ed.ac.uk.ORCID 0000-0001-5218-134X
Karen J LiuMRC National Mouse Genetics Network, Congenital Anomalies Cluster, Mary Lyon Centre at MRC Harwell, UK. karen.liu@kcl.ac.uk.ORCID 0000-0002-2483-2165

Funding

Medical Research Council MC_PC_21044
6 · The paper itself

Abstract

Congenital anomalies are structural or functional abnormalities present at birth, which can be caused by genetic or environmental influences. The availability of genome sequencing has significantly increased our understanding of congenital anomalies, but linking variant identification to functional relevance and definitive diagnosis remains challenging. Many genes have unknown or poorly understood functions, and with a lack of clear genotype-to-phenotype correlations, it can be difficult to move from variant discovery to diagnosis. Thus, for most congenital anomalies, there still exists a "diagnostic odyssey" which presents a significant burden to patients, families and society. Animal models are essential in the gene discovery process because they allow researchers to validate candidate gene function and disease progression within intact organisms. However, use of advanced model systems continues to be limited due to the complexity of efficiently generating clinically relevant animals. Here we focus on the use of precisely engineered mice in variant-to-function studies for resolving molecular diagnoses and creating powerful preclinical models for congenital anomalies, covering advances in genomics, genome editing and phenotyping approaches as well as the necessity for future initiatives aligning animal modelling to deep patient multimodal datasets.

Indexed as

Congenital AbnormalitiesDisease Models, AnimalRare DiseasesAnimalsGene EditingGenetic Association StudiesGenomicsHumansMicePhenotypeCongenital anomaliesDiagnostic odysseyGenotype-to-phenotype correlationMolecular diagnosisMouse modelsVariant of uncertain significance

Identifiers

PMID40100426
PMCPMC12130163

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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.