Evidence map›Paper›PMID 38647370›Full record

ArticleAmerican journal of medical genetics. Part A2024

Phenotypic consequences of GBA1 pathological variant R463C (p.R502C).

Emory Ryan, Samantha Nishimura, Grisel Lopez, Nahid Tayebi, Ellen Sidransky

Open access · hybridAbstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 43% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

5 authors at 1 institution in 1 country.

Emory RyanNational Human Genome Research Institute, National Institutes of Health, Bethesda, USA.
Samantha NishimuraNational Human Genome Research Institute, National Institutes of Health, Bethesda, USA.ORCID 0009-0000-2920-5315
Grisel LopezNational Human Genome Research Institute, National Institutes of Health, Bethesda, USA.
Nahid TayebiNational Human Genome Research Institute, National Institutes of Health, Bethesda, USA.
Ellen SidranskyNational Human Genome Research Institute, National Institutes of Health, Bethesda, USA.
National Institutes of Health · US

Funding

Genetic and clinical studies of Gaucher disease and other lysosomal disordersZIAHG200336 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI SIDRANSKY, ELLEN · 2009 to 2025
$45.2M
Intramural NIH HHS Z99 HG999999Intramural Research ProgramsNational Human Genome Research Institute and National Institutes of HealthNational Institutes of Health Intramural Program
6 · The paper itself

Abstract

Gaucher disease (GD) is an autosomal recessively inherited lysosomal storage disorder caused by biallelic pathological variants in the GBA1 gene. Patients present along a broad clinical spectrum, and phenotypes are often difficult to predict based on genotype alone. The variant R463C (p.Arg502Cys) exemplifies this challenge. To better characterize its different clinical presentations, we examined the records of 25 current and historical patients evaluated at the National Institutes of Health. Nine patients were classified as GD1, 14 were classified as GD3, and two had an ambiguous diagnosis between GD1 and GD3. In addition, we reviewed the published literature in PubMed and Web of Science through December 2023, identifying 62 cases with an R463C variant from 18 countries. Within the NIH cohort, the most common second variants were N370S (p.N409S) and L444P (p.L483P). R463C/L444P was encountered in patients with GD1 and GD3 in both the NIH cohort and worldwide. In the literature, R463C/R463C was also reported in both GD1 and GD3, although sparse phenotypic information was shared. Often the phenotype reflected what might be predicted for the second mutant allele. This diversity of phenotypes emphasizes the need for longitudinal follow-up to assess symptom development and neurological involvement.

Indexed as

Gaucher DiseaseGlucosylceramidasePhenotypeAdolescentAdultAllelesChildChild, PreschoolFemaleGenotypeHumansInfantMaleMutationYoung AdultGBA protein, humanGlucosylceramidaseGaucher diseaseGBA1lysosomal storage disorderR463C

Identifiers

PMID38647370
PMCPMC11315629
OpenAlexW4395011386

What OpenQuestion holds

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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.