Evidence map›Paper›PMID 30185935›Full record

ArticleLeukemia2019

Characterization of an X-chromosome-linked telomere biology disorder in females with DKC1 mutation.

Elina A M Hirvonen, Saara Peuhkuri, Anna Norberg, Sofie Degerman, Katariina Hannula-Jouppi, Hannamari Välimaa, Outi Kilpivaara, Ulla Wartiovaara-Kautto

Abstract read
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In one paragraph

Article in Leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. 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

8 authors.

Elina A M HirvonenGenome-Scale Biology/Research Programs Unit, and Department of Medical and Clinical Genetics/Medicum, University of Helsinki, Helsinki, Finland.
Saara PeuhkuriGenome-Scale Biology/Research Programs Unit, and Department of Medical and Clinical Genetics/Medicum, University of Helsinki, Helsinki, Finland.
Anna NorbergDepartment of Medical Biosciences, Medical and Clinical Genetics, Umeå University, Umeå, Sweden.
Sofie DegermanDepartment of Medical Biosciences, Medical and Clinical Genetics, Umeå University, Umeå, Sweden.ORCID http://orcid.org/0000-0002-2783-0712
Katariina Hannula-JouppiDepartment of Dermatology and Allergology, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland.
Hannamari VälimaaDepartment of Virology, University of Helsinki and Department of Oral and Maxillofacial Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Outi KilpivaaraGenome-Scale Biology/Research Programs Unit, and Department of Medical and Clinical Genetics/Medicum, University of Helsinki, Helsinki, Finland. outi.kilpivaara@helsinki.fi.
Ulla Wartiovaara-KauttoDepartment of Hematology, Helsinki University Hospital Comprehensive Cancer Center and University of Helsinki, Helsinki, Finland. ulla.wartiovaara-kautto@hus.fi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosomes, Human, XMutationTelomere HomeostasisAdultCell Cycle ProteinsFemaleGenetic Diseases, X-LinkedHumansMiddle AgedNuclear ProteinsPedigreePhenotypePrognosisTelomereCell Cycle ProteinsDKC1 protein, humanNuclear Proteins

Identifiers

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.