Reclassifying

Christopher Connolly, Rachel Fisher, Chen Yang, Susan Schelley, Bryce A Mendelsohn, Chung Lee, Ayesha Ahmad

Abstract read

In one paragraph

Article in International journal of neonatal screening, 2025. 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

7 authors.

Christopher ConnollyDepartment of Pediatrics, Division of Pediatric Genetics, University of Michigan, 1500 E Medical Center Drive, Ann Arbor, MI 48109, USA.

Rachel FisherDepartment of Pediatrics, Division of Pediatric Genetics, University of Michigan, 1500 E Medical Center Drive, Ann Arbor, MI 48109, USA.ORCID 0009-0007-7606-1597

Chen YangDepartment of Pediatrics, Division of Pediatric Genetics, University of Michigan, 1500 E Medical Center Drive, Ann Arbor, MI 48109, USA.ORCID 0000-0002-9385-5774

Susan SchelleyDepartment of Pediatrics, Division of Medical Genetics, Stanford Medicine Children's Health, 453 Quarry Road, Palo Alto, CA 94304, USA.

Bryce A MendelsohnDepartment of Medical Genetics, Kaiser Permanente, Northern California, 3505 Broadway, Oakland, CA 94611, USA.ORCID 0000-0001-8174-5116

Chung LeeDepartment of Pediatrics, Division of Medical Genetics, Stanford Medicine Children's Health, 453 Quarry Road, Palo Alto, CA 94304, USA.

Ayesha AhmadDepartment of Pediatrics, Division of Pediatric Genetics, University of Michigan, 1500 E Medical Center Drive, Ann Arbor, MI 48109, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate variant classification is crucial for newborn screening (NBS) to prevent missed diagnoses or unnecessary interventions. The

Indexed as

Hurler syndromelysosomal storage disordersMPS Imucopolysaccharidosisnewborn screeningpseudodeficiency allelestype I

Identifiers

PMID41283362

DOI10.3390/ijns11040100

PMCPMC12641733

What OpenQuestion holds

Textmetadata

LicenceCC BY

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.