Evidence map›Paper›PMID 35065882›Full record

ReviewTrends in parasitology2022

Revisiting the malaria hypothesis: accounting for polygenicity and pleiotropy.

Emily R Ebel, Lawrence H Uricchio, Dmitri A Petrov, Elizabeth S Egan

Open access · greenAbstract readReview
In one paragraph

Review in Trends in parasitology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Local genetic adaptation to habitat in wild chimpanzees.bioRxiv : the preprint server for biology · 2024
    Article
  5. Tropical medicine and infectious disease · 2023
    Review
  6. Article
  7. Article
  8. 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

4 authors at 3 institutions in 1 country.

Emily R EbelDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: ebel@stanford.edu.
Lawrence H UricchioDepartment of Biology, Tufts University, Medford, MA 02155, USA.
Dmitri A PetrovDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Elizabeth S EganDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: eegan@stanford.edu.
Stanford University · USStanford Medicine · USTufts University · US

Funding

Genomics of rapid adaptation in the lab and in the wildR35GM118165 · NIGMS · STANFORD UNIVERSITY · PI Dmitri Petrov · 2016 to 2026
$8.3M
Identifying critical erythrocyte host factors for Plasmodium falciparum malariaDP2HL137186 · NHLBI · STANFORD UNIVERSITY · PI EGAN, ELIZABETH S. · 2016 to 2016
$2.4M
NHLBI NIH HHS DP2 HL137186
6 · The paper itself

Abstract

The malaria hypothesis predicts local, balancing selection of deleterious alleles that confer strong protection from malaria. Three protective variants, recently discovered in red cell genes, are indeed more common in African than European populations. Still, up to 89% of the heritability of severe malaria is attributed to many genome-wide loci with individually small effects. Recent analyses of hundreds of genome-wide association studies (GWAS) in humans suggest that most functional, polygenic variation is pleiotropic for multiple traits. Interestingly, GWAS alleles and red cell traits associated with small reductions in malaria risk are not enriched in African populations. We propose that other selective and neutral forces, in addition to malaria prevalence, explain the global distribution of most genetic variation impacting malaria risk.

Indexed as

Genome-Wide Association StudyMalariaErythrocytesHumansMultifactorial InheritancePhenotypePolymorphism, Single Nucleotideevolutionmalariapleiotropypolygenicred blood cells

Identifiers

PMID35065882
PMCPMC8916997
OpenAlexW4206341758

What OpenQuestion holds

Textmetadata
LicenceTDM
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.