Evidence map›Paper›PMID 42489670›Full record

ArticlePrenatal diagnosis2026

Identification of a Novel De Novo HECW2 Gene Pathogenic Variant in a Fetus With Cardiac Abnormalities.

Kristina Nimchenko, Bettina Bessieres, Gihad E Chalouhi, Antonia Pop, Vanina Castaigne, Bertrand Stos, Marie-Paule Beaujard, Diane Roy, Daniela Laux, Tania Attie-Bitach

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Prenatal diagnosis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Kristina NimchenkoService de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.ORCID https://orcid.org/0000-0002-0268-2493
Bettina BessieresService de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
Gihad E ChalouhiService d'Obstétrique-Maternité, Chirurgie, Médecine et Imageries fœtales, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
Antonia PopService Maternité-Obstétrique, CHIC. Centre hospitalier intercommunal de Créteil, Créteil, France.
Vanina CastaigneService Maternité-Obstétrique, CHIC. Centre hospitalier intercommunal de Créteil, Créteil, France.
Bertrand StosCardiologie médicale pédiatrique, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
Marie-Paule BeaujardService de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
Diane RoyLaboratoire de Biologie Médicale multisites SeqOIA, Paris, France.
Daniela LauxCardiologie médicale pédiatrique, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
Tania Attie-BitachService de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.ORCID https://orcid.org/0000-0002-1155-3626

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

cardiac anomaliesfetal hydropsHECW2long QT syndromeprenatal diagnosis

Identifiers

PMID42489670
PMCPMC13571798

What OpenQuestion holds

Textmetadata
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.