Evidence map›Paper›PMID 39763973›Full record

ArticlebioRxiv : the preprint server for biology2024

Mutation in

Brandon L Meyerink, Krishna S Karia, Mitchell J Rechtzigel, Prithvi R Patthi, Ariana C Edwards, Jessica M Howard, Elizabeth R Aaseng, Jill M Weimer, Louis-Jan Pilaz

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

5 · Who and what money

Authors and funding

9 authors.

Brandon L MeyerinkPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.ORCID 0000-0002-4058-1685
Krishna S KariaPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Mitchell J RechtzigelPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.ORCID 0000-0002-5298-7391
Prithvi R PatthiPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.ORCID 0009-0005-2324-7211
Ariana C EdwardsPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.ORCID 0009-0005-0156-1795
Jessica M HowardPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Elizabeth R AasengPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Jill M WeimerPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.ORCID 0000-0003-2504-4942
Louis-Jan PilazPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.ORCID 0000-0002-9035-1327

Funding

Yeast 2 HybridP20GM103620 · NIGMS · SANFORD RESEARCH/USD · PI ROUX, KYLE J · 2013 to 2023
$24.2M
The Impact of PD-1 Inhibition on Immune-Response to ChemoradiotherapyP20GM103548 · NIGMS · SANFORD RESEARCH/USD · PI EGLAND, KRISTI A · 2012 to 2020
$20.8M
The Pediatric Biomedical Research ProgramR25HD097633 · NICHD · SANFORD RESEARCH/USD · PI LEE, LANCE, WEIMER, JILL M · 2019 to 2023
$527k
NICHD NIH HHS R25 HD097633NIGMS NIH HHS P20 GM103548NIGMS NIH HHS P20 GM103620
6 · The paper itself

Abstract

Beta-propeller Protein Associated Neurodegeneration (BPAN) is a devastating neurodevelopmental and neurodegenerative disease linked to variants in

Indexed as

AutophagyAxon degenerationBPANNeurodevelopmentWDR45

Identifiers

PMID39763973
PMCPMC11702570

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.