Evidence map›Paper›PMID 34716203›Full record

ArticleCold Spring Harbor molecular case studies2022

Autosomal recessive

Robert Kleyner, Mohammad Arif, Elaine Marchi, Naomi Horowitz, Andrea Haworth, Brian King, Maureen Gavin, Karen Amble, Milen Velinov, Gholson J Lyon

Open access · diamondAbstract readCase Reports
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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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

10 authors at 5 institutions in 2 countries.

Robert KleynerDepartment of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314, USA.
Mohammad ArifDepartment of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314, USA.
Elaine MarchiDepartment of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314, USA.
Naomi HorowitzDepartment of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314, USA.
Andrea HaworthCongenica Limited, BioData Innovation Centre, Wellcome Genome Campus, Cambridge, CB10 1DR, United Kingdom.
Brian KingCongenica Limited, BioData Innovation Centre, Wellcome Genome Campus, Cambridge, CB10 1DR, United Kingdom.
Maureen GavinGeorge A. Jervis Clinic, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314, USA.
Karen AmbleGeorge A. Jervis Clinic, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314, USA.
Milen VelinovDepartment of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314, USA.
Gholson J LyonDepartment of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314, USA.ORCID 0000-0002-5869-0716
New York State Office for People With Developmental Disabilities · USWellcome Trust · GBRutgers, The State University of New Jersey · USState University of New York · USThe Graduate Center, CUNY · US

Funding

Amino-terminal acetylation of proteins in mammalian biology and diseaseR35GM133408 · NIGMS · INSTITUTE FOR BASIC RES IN DEV DISABIL · PI LYON, GHOLSON · 2019 to 2023
$2.4M
NIGMS NIH HHS R35 GM133408
6 · The paper itself

Abstract

An

Indexed as

Cation Transport ProteinsIntellectual DisabilityCell Cycle ProteinsConsanguinityFamilyFemaleHumansInheritance PatternsParentsPedigreeSyndromeTranscription FactorsCation Transport ProteinsCell Cycle ProteinsSLC30A9 protein, humanTranscription Factorsintellectual disabilitymild

Identifiers

PMID34716203
PMCPMC8958918
OpenAlexW3211167042

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.