Evidence map›Paper›PMID 22328589›Full record

ArticleThorax2012

Cutting edge genetic studies in primary ciliary dyskinesia.

Michael R Knowles, Margaret W Leigh, Maimoona A Zariwala

3 registry-linked trialsAbstract readLetterComment
PubMed Publisher
In one paragraph

Article in Thorax, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT00323167 completednot on this map

Rare Genetic Disorders of the Airways: Cross-sectional Comparison of Clinical Features, and Development of Novel Screening and Genetic Tests

TypeobservationalSponsorUniversity of North Carolina, Chapel HillRan2006 to 2012Enrolled367ConditionsKartagener Syndrome, Cystic Fibrosis, Pseudohypoaldosteronism, Primary Ciliary Dyskinesia
NCT00450918 completednot on this map

Longitudinal Study of Primary Ciliary Dyskinesia: Participants 5-18 Years of Age

TypeobservationalSponsorUniversity of North Carolina, Chapel HillRan2006 to 2019Enrolled150ConditionsPrimary Ciliary Dyskinesia
NCT00722878 completednot on this map

Early Onset and Progression of Primary Ciliary Dyskinesia Lung Disease Prior to 10 Years of Age

TypeobservationalSponsorUniversity of North Carolina, Chapel HillRan2008 to 2019Enrolled48ConditionsKartagener Syndrome
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Michael R Knowles
Margaret W Leigh
Maimoona A Zariwala

Funding

GENETIC DISORDERS OF MUCOCILIARY CLEARANCE: RARE DISEASES: PCD, CF, &PHA U54RR019480 · NCRR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KNOWLES, MICHAEL R · 2004 to 2008
$6.0M
NCRR NIH HHS U54 RR019480
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationAxonemal DyneinsCiliaCiliary Motility DisordersFemaleHumansMaleAxonemal DyneinsDNAH11 protein, human

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.