Evidence map›Paper›PMID 32988995›Full record

ReviewDevelopment (Cambridge, England)2020

Using

Nichole Link, Hugo J Bellen

Abstract readReview
In one paragraph

Review in Development (Cambridge, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–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

33 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Why just fly?Fly · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. EFFICIENT RIBOSOMAL RNA DEPLETION FROMWellcome open research · 2025
    Article
  9. A novelFly · 2024
    Article
  10. Insects · 2024
    Review
  11. Modelling phenotypes, variants and pathomechanisms of syndromic diseases in different systems.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2024
    Article
  12. The fruit flyFrontiers in pharmacology · 2024
    Article
  13. Animal Models of Human Disease.International journal of molecular sciences · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Delineating Purinergic Signaling inInternational journal of molecular sciences · 2022
    Review
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

2 authors.

Nichole LinkHoward Hughes Medical Institute, BCM, Houston, TX, 77030, USA.ORCID 0000-0002-4825-9615
Hugo J BellenHoward Hughes Medical Institute, BCM, Houston, TX, 77030, USA hbellen@bcm.edu.ORCID 0000-0001-5992-5989

Funding

Transposon induced disruption of most Drosophila genesR01GM067858 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J · 2003 to 2020
$15.7M
Baylor-Johns Hopkins Center for Mendelian GeneticsUM1HG006542 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI VALLE, DAVID · 2016 to 2020
$14.5M
Zebrafish CoreU54NS093793 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J · 2015 to 2022
$7.5M
Expansion and characterization of the Drosophila Toolkit to study SARS-CoV-2R24OD022005 · OD · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J · 2016 to 2023
$7.4M
Functional analysis of ANKLE2 in microcephaly using a genetic model systemF32NS092270 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI LINK, NICHOLE L · 2015 to 2017
$136k
Howard Hughes Medical InstituteNHGRI NIH HHS UM1 HG006542NIGMS NIH HHS R01 GM067858NIH HHS R24 OD022005NINDS NIH HHS F32 NS092270NINDS NIH HHS U54 NS093793
6 · The paper itself

Abstract

Next-generation sequencing has greatly accelerated the discovery of rare human genetic diseases. Nearly 45% of patients have variants associated with known diseases but the unsolved cases remain a conundrum. Moreover, causative mutations can be difficult to pinpoint because variants frequently map to genes with no previous disease associations and, often, only one or a few patients with variants in the same gene are identified. Model organisms, such as

Indexed as

AnimalsDisease Models, AnimalDrosophila melanogasterGenetic TechniquesHuman GeneticsHumansMicrocephalyRare DiseasesAnkle2Asymmetric divisionDrosophilaMicrocephalyModel of human disease

Identifiers

PMID32988995
PMCPMC7541339

What OpenQuestion holds

Textmetadata
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.