Evidence map›Paper›PMID 29388943›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2018

Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests.

Alison Dalton Archibald, Melanie Jane Smith, Trent Burgess, Katrina Louise Scarff, Justine Elliott, Clare Elizabeth Hunt, Caitlin Barns-Jenkins, Chelsea Holt, Karina Sandoval, Vanessa Siva Kumar and 12 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Alison Dalton ArchibaldVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Melanie Jane SmithVictorian Clinical Genetics Services, Parkville, Victoria, Australia. melanie.smith@vcgs.org.au.
Trent BurgessVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Katrina Louise ScarffVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Justine ElliottVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Clare Elizabeth HuntVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Caitlin Barns-JenkinsVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Chelsea HoltVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Karina SandovalVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Vanessa Siva KumarVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Lisa WardVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Emily Caroline AllenMurdoch Childrens Research Institute, Parkville, Victoria, Australia.
Sarah Valerie CollisMurdoch Childrens Research Institute, Parkville, Victoria, Australia.
Shannon CowieVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
David FrancisVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Martin B DelatyckiVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Eppie Mildred YiuMurdoch Childrens Research Institute, Parkville, Victoria, Australia.
R John MassieMurdoch Childrens Research Institute, Parkville, Victoria, Australia.
Mark Domenic PertileVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Desirée du SartVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
Damien BrunoVictorian Clinical Genetics Services, Parkville, Victoria, Australia.
David J AmorVictorian Clinical Genetics Services, Parkville, Victoria, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zoe McDonald, BSc, was omitted from the list of article coauthors. Her name should have been included as the seventh author, following Clare Elizabeth Hunt. Her affiliation is Victorian Clinical Genetics Services, Parkville, Victoria, Australia. The authors regret the error.

Identifiers

PMID29388943

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.