Evidence map›Paper›PMID 32273475›Full record

ArticleHaematologica2021

Identification of biallelic germline variants of SRP68 in a sporadic case with severe congenital neutropenia.

Barbara Schmaltz-Panneau, Anne Pagnier, Séverine Clauin, Julien Buratti, Caroline Marty, Odile Fenneteau, Klaus Dieterich, Blandine Beaupain, Jean Donadieu, Isabelle Plo and 1 more

Abstract read
In one paragraph

Article in Haematologica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Human SRP Subunits Coordinate Protein Targeting and mRNA Quality Control.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Targeting of Proteins for Translocation at the Endoplasmic Reticulum.International journal of molecular sciences · 2022
    Review
  7. Article
  8. Review
  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

11 authors.

Barbara Schmaltz-PanneauINSERM U1287, Gustave Roussy, Villejuif, France; Paris Saclay University, U1287, Villejuif, France.
Anne PagnierDepartment of Pediatric Hematology and Oncology, CHU Grenoble Alpes, Grenoble, France.
Séverine ClauinDepartment of Genetics, Pitié-Salpêtrière Hospital, APHP, Paris, France.
Julien BurattiDepartment of Genetics, Pitié-Salpêtrière Hospital, APHP, Paris, France.
Caroline MartyINSERM U1287, Gustave Roussy, Villejuif, France; Paris Saclay University, U1287, Villejuif, France.
Odile FenneteauLaboratory of Hematology, Robert Debré Hospital - Université de Paris, France.
Klaus DieterichDepartment of Medical Genetics, Univ. Grenoble Alpes, INSERM U1216, CHU Grenoble Alpes, Grenoble.
Blandine BeaupainFrench Registry of Chronic Neutropenia, Trousseau Hospital, Paris, France.
Jean DonadieuDepartment of Pediatric Hematology and Oncology, Trousseau Hospital, AP-HP, Paris, France.
Isabelle PloINSERM U1287, Gustave Roussy, Villejuif, France; Paris Saclay University, U1287, Villejuif, France.
Christine Bellanné-ChantelotDept of Genetics, Pitié-Salpêtrière Hospital, Sorbonne University, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

NeutropeniaCongenital Bone Marrow Failure SyndromesGerm CellsGerm-Line MutationHumansSignal Recognition ParticleSignal Recognition ParticleSRP68 protein, human

Identifiers

PMID32273475
PMCPMC8018125

What OpenQuestion holds

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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.