Evidence map›Paper›PMID 35732497›Full record

ArticleCold Spring Harbor molecular case studies2022

Expanding the phenotype of

Subit Barua, Sara Berger, Elaine M Pereira, Vaidehi Jobanputra

Open access · diamondAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Cold Spring Harbor molecular case studies, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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

4 authors at 3 institutions in 1 country.

Subit BaruaDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York 10032, USA.
Sara BergerDivision of Clinical Genetics, Department of Pediatrics, Columbia University, Vagelos College of Physicians and Surgeons, New York, New York 10032, USA.
Elaine M Pereira *Division of Clinical Genetics, Department of Pediatrics, Columbia University Vagelos College of Physicians and Surgeons and NewYork-Presbyterian Morgan Stanley Children's Hospital, New York, New York 10032, USA.
Vaidehi Jobanputra *Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York 10032, USA.
Columbia University Irving Medical Center · USColumbia University · USMorgan Stanley Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vacuolar ATPases (V-ATPases) are large multisubunit proton pumps conserved among all eukaryotic cells that are involved in diverse functions including acidification of membrane-bound intracellular compartments. The

Indexed as

Congenital Disorders of GlycosylationHydrocephalusHypospadiasLiver DiseasesPectus CarinatumVacuolar Proton-Translocating ATPasesHumansMalePhenotypeATP6AP1 protein, humanVacuolar Proton-Translocating ATPasescongenital septal defectfetal cystic hygromajaundice

Identifiers

PMID35732497
PMCPMC9235842
OpenAlexW4283258395

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.