Evidence map›Paper›PMID 35707784›Full record

ArticleGlobal medical genetics2022

Genotype-Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature.

Xiaolei Xie, Hongyan Chai, Autumn DiAdamo, Brittany Grommisch, Jiadi Wen, Hui Zhang, Peining Li

Open access · diamondAbstract read
In one paragraph

Article in Global medical genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  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 1 institution in 2 countries.

Xiaolei XieDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States.
Hongyan ChaiDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States.
Autumn DiAdamoDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States.
Brittany GrommischDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States.
Jiadi WenDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States.
Hui ZhangDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States.
Peining LiDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States.
Yale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

array comparative hybridizationdeletions of 6q26-q27genotype–phenotype correlationshaploinsufficient gene

Identifiers

PMID35707784
PMCPMC9192176
OpenAlexW4226083075

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.