Evidence map›Paper›PMID 29178644›Full record

ArticleMolecular genetics & genomic medicine2017

Medical genetics and genomic medicine in the United States. Part 2: Reproductive genetics, newborn screening, genetic counseling, training, and registries.

Debra S Regier, Carlos R Ferreira, Suzanne Hart, Donald W Hadley, Maximilian Muenke

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular genetics & genomic medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. The Future of DTC Genomics and the Law.The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2020
    Article
  5. Review
  6. Looking back and looking forward.Molecular genetics & genomic medicine · 2018
    Article
  7. 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

5 authors.

Debra S RegierRare Disease Institute, Children's National Health System, Washington, DC, USA.ORCID 0000-0001-7525-0088
Carlos R FerreiraRare Disease Institute, Children's National Health System, Washington, DC, USA.
Suzanne HartNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Donald W HadleyNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Maximilian MuenkeNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

Funding

Rare Diseases Clinical Research Scholar’s ProgramR25HD078229 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI REGIER, DEBRA S, SUMMAR, MARSHALL L · 2015 to 2020
$528k
NICHD NIH HHS R25 HD078229
6 · The paper itself

Abstract

Review of genetics in the United States with emphasis on the prenatal, metabolic, genetic counseling, and training aspects of the field.

Indexed as

Genetic CounselingNeonatal ScreeningGenetics, MedicalGenomicsHumansInfant, NewbornMetabolism, Inborn ErrorsPrenatal DiagnosisRegistriesUnited States

Identifiers

PMID29178644
PMCPMC5702569

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.