Evidence map›Paper›PMID 35330423›Full record

ArticleJournal of personalized medicine2022

Middle Eastern Genetic Variation Improves Clinical Annotation of the Human Genome.

Sathishkumar Ramaswamy, Ruchi Jain, Maha El Naofal, Nour Halabi, Sawsan Yaslam, Alan Taylor, Ahmad Abou Tayoun

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Reclassification ofBiomolecules & biomedicine · 2026
    Article
  5. FivePharmacogenomics and personalized medicine · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. 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.

Sathishkumar RamaswamyAl Jalila Genomics Center, Al Jalila Children's Hospital, Dubai, United Arab Emirates.
Ruchi JainAl Jalila Genomics Center, Al Jalila Children's Hospital, Dubai, United Arab Emirates.
Maha El NaofalAl Jalila Genomics Center, Al Jalila Children's Hospital, Dubai, United Arab Emirates.
Nour HalabiAl Jalila Genomics Center, Al Jalila Children's Hospital, Dubai, United Arab Emirates.
Sawsan YaslamAl Jalila Genomics Center, Al Jalila Children's Hospital, Dubai, United Arab Emirates.
Alan TaylorAl Jalila Genomics Center, Al Jalila Children's Hospital, Dubai, United Arab Emirates.
Ahmad Abou TayounAl Jalila Genomics Center, Al Jalila Children's Hospital, Dubai, United Arab Emirates.ORCID 0000-0002-9134-1673

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic variation in populations of Middle Eastern origin remains highly underrepresented in most comprehensive genomic databases. This underrepresentation hampers the functional annotation of the human genome and challenges accurate clinical variant interpretation. To highlight the importance of capturing genetic variation in the Middle East, we aggregated whole exome and genome sequencing data from 2116 individuals in the Middle East and established the Middle East Variation (MEV) database. Of the high-impact coding (missense and loss of function) variants in this database, 53% were absent from the most comprehensive Genome Aggregation Database (gnomAD), thus representing a unique Middle Eastern variation dataset which might directly impact clinical variant interpretation. We highlight 39 variants with minor allele frequency >1% in the MEV database that were previously reported as rare disease variants in ClinVar and the Human Gene Mutation Database (HGMD). Furthermore, the MEV database consisted of 281 putative homozygous loss of function (LoF) variants, or complete knockouts, of which 31.7% (89/281) were absent from gnomAD. This set represents either complete knockouts of 83 unique genes in reportedly healthy individuals, with implications regarding disease penetrance and expressivity, or might affect dispensable exons, thus refining the clinical annotation of those regions. Intriguingly, 24 of those genes have several clinically significant variants reported in ClinVar and/or HGMD. Our study shows that genetic variation in the Middle East improves functional annotation and clinical interpretation of the genome and emphasizes the need for expanding sequencing studies in the Middle East and other underrepresented populations.

Indexed as

common variantsknockoutsMiddle East Variantswhole exome sequencingwhole genome sequencing

Identifiers

PMID35330423
PMCPMC8956070

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.