Evidence map›Paper›PMID 38501057›Full record

ReviewFrontiers in genetics2024

Genetic interrogation for sequence and copy number variants in systemic lupus erythematosus.

Nicholas Kim-Wah Yeo, Che Kang Lim, Katherine Nay Yaung, Nicholas Kim Huat Khoo, Thaschawee Arkachaisri, Salvatore Albani, Joo Guan Yeo

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in genetics, 2024. 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
2.4field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
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 at 2 institutions in 1 country.

Nicholas Kim-Wah Yeo *Translational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Che Kang Lim *Duke-NUS Medical School, Singapore, Singapore.
Katherine Nay YaungTranslational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Nicholas Kim Huat KhooTranslational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Thaschawee Arkachaisri *Translational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Salvatore Albani *Translational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Joo Guan Yeo *Translational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
SingHealth Duke-NUS Academic Medical Centre · SGSingapore General Hospital · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early-onset systemic lupus erythematosus presents with a more severe disease and is associated with a greater genetic burden, especially in patients from Black, Asian or Hispanic ancestries. Next-generation sequencing techniques, notably whole exome sequencing, have been extensively used in genomic interrogation studies to identify causal disease variants that are increasingly implicated in the development of autoimmunity. This Review discusses the known casual variants of polygenic and monogenic systemic lupus erythematosus and its implications under certain genetic disparities while suggesting an age-based sequencing strategy to aid in clinical diagnostics and patient management for improved patient care.

Indexed as

copy number variationgenomicsmonogenicnext-generation sequencingsystemic lupus erythematosuswhole exome sequencing

Identifiers

PMID38501057
PMCPMC10944961
OpenAlexW4392401867

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.