Evidence map›Paper›PMID 31225937›Full record

ArticleAmerican journal of medical genetics. Part A2019

Birth seasonality studies in a large Prader-Willi syndrome cohort.

Merlin G Butler, Virginia Kimonis, Elisabeth Dykens, June Anne Gold, Roy Tamura, Jennifer L Miller, Daniel J Driscoll

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in American journal of medical genetics. Part A, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 31% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Birth seasonality studies in a large Prader-Willi syndrome cohort.American journal of medical genetics. Part A · 2019
    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

7 authors at 6 institutions in 1 country.

Merlin G ButlerDepartment of Psychiatry, Behavioral Sciences and Pediatrics, University of Kansas Medical Center, Kansas City, Kansas.ORCID 0000-0002-2911-0524
Virginia KimonisDepartment of Pediatrics, University of California, Irvine, California.ORCID 0000-0003-1567-4449
Elisabeth DykensVanderbilt Kennedy Center for Research on Human Development, Vanderbilt University, Nashville, Tennessee.
June Anne GoldDepartment of Pediatrics, Loma Linda University Medical School, Loma Linda, California.
Roy TamuraHealth Informatics Institute, University of South Florida College of Medicine, Tampa, Florida.
Jennifer L MillerDepartment of Pediatrics, University of Florida College of Medicine, Gainesville, Florida.
Daniel J DriscollDepartment of Pediatrics, University of Florida College of Medicine, Gainesville, Florida.
University of Florida · USLoma Linda University Medical Center · USUniversity of California, Irvine · USUniversity of Kansas Medical Center · USUniversity of South Florida · USVanderbilt University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prader-Willi syndrome (PWS) is generally due to sporadic paternal deletions of the chromosome 15q11-q13 region followed by maternal disomy 15. Advanced maternal age is more commonly seen in those with maternal disomy 15. Environmental factors (e.g., drug use, occupational chemical exposure, infectious agents, and irradiation) could account for chromosome changes. Previous evidence of differences in male and female gametogenesis could suggest an environmental role in the causation of the paternal 15q11-q13 deletion seen in PWS. Certain occupations such as hydrocarbon-exposing occupations (e.g., landscaping, farming, and painting) and viral exposure (e.g., human coronavirus 229E causing upper respiratory infections in adults with an incorporation site in the human genome at chromosome 15q11) can be seasonal in nature and contribute to chromosome damage. To assess, we reviewed birth seasonality data in a large cohort of individuals with PWS recruited nationally (N = 355) but no significant differences were seen by month between those with the 15q11-q13 deletion compared with maternal disomy 15 when analyzing quarterly seasonal patterns. Although early evidence supported birth seasonality differences in PWS, a larger number of individuals in our recent study using advanced genetic testing methods did not find this observation.

Indexed as

Chromosome DeletionChromosomes, Human, Pair 15SeasonsAdolescentAdultChildChild, PreschoolCohort StudiesFemaleGametogenesisGenetic TestingHumansInfantMaleOccupational ExposureOccupationsbirth seasonalityenvironmental factorsPrader-Willi syndrome (PWS)PWS genetic subtypes

Identifiers

PMID31225937
PMCPMC7159461
OpenAlexW2950710269

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.