Evidence map›Paper›PMID 34113375›Full record

ArticleFrontiers in genetics2021

Whole-Exome Sequencing Reveals a Rare Variant of

Mohd Fareed, Varun Sharma, Inderpal Singh, Sayeed Ur Rehman, Gurdarshan Singh, Mohammad Afzal

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

Article in Frontiers in genetics, 2021. 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
0.9field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Association of R1939W and P1987R variants ofPakistan journal of medical sciences
    Article
  6. 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

6 authors at 3 institutions in 1 country.

Mohd FareedPK-PD Formulation and Toxicology Division, CSIR Indian Institute of Integrative Medicine, Jammu, India.
Varun SharmaAncient DNA Laboratory, Birbal Sahni Institute of Palaeosciences, Lucknow, Uttar Pradesh, India.
Inderpal SinghBioinfoRes, Jammu, India.
Sayeed Ur RehmanDepartment of Biochemistry, School of Chemical and Life Sciences, Jamia Hamdard, New Delhi, India.
Gurdarshan SinghPK-PD Formulation and Toxicology Division, CSIR Indian Institute of Integrative Medicine, Jammu, India.
Mohammad AfzalHuman Genetics and Toxicology Laboratory, Section of Genetics, Department of Zoology, Aligarh Muslim University, Aligarh, India.
Academy of Scientific and Innovative Research · INAligarh Muslim University · INJamia Hamdard · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-syndromic hearing loss (NSHL) is one of the most frequent auditory deficits in humans characterized by high clinical and genetic heterogeneity. Very few studies have reported the relationship between

Indexed as

autosomal recessive (AR) diseasescousin marriagesdeaf mutesgenetic counselinghearing disordershearing impairmentIndian populationJammu and Kashmir (J and K)

Identifiers

PMID34113375
PMCPMC8185570
OpenAlexW3151272695

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.