Evidence map›Paper›PMID 30801013›Full record

ArticleScience advances2019

Transcriptional profiling at the

Walid Abi Habib, Frédéric Brioude, Salah Azzi, Sylvie Rossignol, Agnès Linglart, Marie-Laure Sobrier, Éloïse Giabicani, Virginie Steunou, Madeleine D Harbison, Yves Le Bouc and 1 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Journal of the Endocrine Society · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Approach to the Patient With Suspected Silver-Russell Syndrome.The Journal of clinical endocrinology and metabolism · 2024
    Review
  12. Article
  13. Imprinted Long Non-Coding RNAs in Mammalian Development and Disease.International journal of molecular sciences · 2023
    Review
  14. Article
  15. Imprinting disorders.Nature reviews. Disease primers · 2023
    Review
  16. Article
  17. Article
  18. Cells · 2022
    Review
  19. Article
  20. 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

11 authors at 3 institutions in 2 countries.

Walid Abi HabibSorbonne Université, INSERM, UMRS 938, Centre de Recherche Saint-Antoine, Paris, France.ORCID 0000-0001-7017-7854
Frédéric BrioudeSorbonne Université, INSERM, UMRS 938, Centre de Recherche Saint-Antoine, Paris, France.ORCID 0000-0001-8122-760X
Salah AzziSorbonne Université, INSERM, UMRS 938, Centre de Recherche Saint-Antoine, Paris, France.
Sylvie RossignolService de Génétique Médicale, Centre de Référence pour les Anomalies du Développement (FECLAD), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Agnès LinglartEndocrinology and Diabetology for Children and Reference Center for Rare Disorders of Calcium and Phosphate Metabolism, Bicêtre Paris Sud, AP-HP, Le Kremlin-Bicêtre, France.
Marie-Laure SobrierSorbonne Université, INSERM, UMRS 938, Centre de Recherche Saint-Antoine, Paris, France.
Éloïse GiabicaniSorbonne Université, INSERM, UMRS 938, Centre de Recherche Saint-Antoine, Paris, France.ORCID 0000-0001-5360-8616
Virginie SteunouSorbonne Université, INSERM, UMRS 938, Centre de Recherche Saint-Antoine, Paris, France.
Madeleine D HarbisonDepartment of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0002-7623-8475
Yves Le BoucSorbonne Université, INSERM, UMRS 938, Centre de Recherche Saint-Antoine, Paris, France.
Irène NetchineSorbonne Université, INSERM, UMRS 938, Centre de Recherche Saint-Antoine, Paris, France.
Inserm · FRHôpitaux Universitaires de Strasbourg · FRIcahn School of Medicine at Mount Sinai · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Imprinting disorders (IDs) often affect growth in humans, leading to diseases with overlapping features, regardless of the genomic region affected. IDs related to hypomethylation of the human 14q32.2 region and its

Indexed as

Calcium-Binding ProteinsChromosomes, Human, Pair 11Chromosomes, Human, Pair 14DNA MethylationEpigenesis, GeneticGenomic ImprintingMembrane ProteinsSilver-Russell SyndromeFemaleHumansMaleCalcium-Binding ProteinsDLK1 protein, humanMembrane Proteins

Identifiers

PMID30801013
PMCPMC6382400
OpenAlexW2916260425

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.