Evidence map›Paper›PMID 35223824›Full record

ArticleFrontiers in cell and developmental biology2022

Genome-wide Interaction Study Implicates

Jenna C Carlson, John R Shaffer, Fred Deleyiannis, Jacqueline T Hecht, George L Wehby, Kaare Christensen, Eleanor Feingold, Seth M Weinberg, Mary L Marazita, Elizabeth J Leslie

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. MicroRNAs and Gene Regulatory Networks Related to Cleft Lip and Palate.International journal of molecular sciences · 2023
    Review
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

10 authors at 6 institutions in 2 countries.

Jenna C CarlsonDepartment of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, United States.
John R ShafferDepartment of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, United States.
Fred DeleyiannisUCHealth Medical Group, Colorado Springs, United States.
Jacqueline T HechtDepartment of Pediatrics, University of Texas Health Science Center at Houston, Houston, United States.
George L WehbyDepartment of Health Management and Policy, College of Public Health, University of Iowa, Iowa City, United States.
Kaare ChristensenDepartment of Epidemiology, Institute of Public Health, University of Southern Denmark, Odense, Denmark.
Eleanor FeingoldDepartment of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, United States.
Seth M WeinbergDepartment of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, United States.
Mary L MarazitaDepartment of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, United States.
Elizabeth J LeslieDepartment of Human Genetics, Emory University School of Medicine, Atlanta, United States.
University of Pittsburgh · USUniversity of Southern Denmark · DKEmory University · USThe University of Texas Health Science Center at Houston · USUniversity of Colorado Health · USUniversity of Iowa · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect, affecting approximately 1 in 700 births. NSCL/P has complex etiology including several known genes and environmental factors; however, known genetic risk variants only account for a small fraction of the heritability of NSCL/P. It is commonly suggested that gene-by-environment (G×E) interactions may help explain some of the "missing" heritability of NSCL/P. We conducted a genome-wide G×E interaction study in cases and controls of European ancestry with three common maternal exposures during pregnancy: alcohol, smoking, and vitamin use using a two-stage design. After selecting 127 loci with suggestive 2df tests for gene and G x E effects, 40 loci showed significant G x E effects after correcting for multiple tests. Notable interactions included SNPs of 6q22 near VGLL2 with alcohol and 6p22.3 near PRL with smoking. These interactions could provide new insights into the etiology of CL/P and new opportunities to modify risk through behavioral changes.

Indexed as

case- controlgene-environement interactionsGWASmaternal exposuresorofacial cleft

Identifiers

PMID35223824
PMCPMC8866867
OpenAlexW4225873341

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.