Evidence map›Paper›PMID 31247704›Full record

ArticlePsychiatry investigation2019

Investigation of Maternal Effects, Maternal-Fetal Interactions, and Parent-of-Origin Effects (Imprinting) for Candidate Genes Positioned on Chromosome 18q21, in Probands with Schizophrenia and their First-Degree Relatives.

Kang Yoon Lee, Byung Dae Lee, Je Min Park, Young Min Lee, Eunsoo Moon, Hee Jeong Jeong, Soo Yeon Kim, Hwagyu Suh, Young In Chung, Seung Chul Kim

Open access · diamondAbstract read
In one paragraph

Article in Psychiatry investigation, 2019. 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, top 92% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Kang Yoon LeeDepartment of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.
Byung Dae LeeDepartment of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.
Je Min ParkDepartment of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.
Young Min LeeDepartment of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.
Eunsoo MoonDepartment of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.
Hee Jeong JeongDepartment of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.
Soo Yeon KimDepartment of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.
Hwagyu SuhDepartment of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.
Young In ChungDepartment of Psychiatry, Pusan National University College of Medicine, Busan, Republic of Korea.
Seung Chul KimDepartment of Obstetrics and Gynecology, Pusan National University Hospital, Busan, Republic of Korea.
Pusan National University Hospital · KRPusan National University · KR

Funding

Pusan National University Hospital 2016A006
6 · The paper itself

Abstract

objectiveA popular design for the investigation of such effects, including effects of parent-of-origin (imprinting), maternal genotype, and maternal-fetal genotype interactions, is to collect deoxyribonucleic acid (DNA) from affected offspring and their mothers and to compare with an appropriate control sample. We investigate the effects of estimation of maternal, imprinting and interaction effects using multimodal modeling using parents and their offspring with schizophrenia in Korean population.

methodsWe have recruited 27 probands (with schizophrenia) with their parents and siblings whenever possible. We analyzed 20 SNPs of 7 neuronal genes in chromosome 18. We used EMIM analysis program for the estimation of maternal, imprinting and interaction effects using multimodal modeling.

resultsOf analyzed 20 single nucleotide polymorphisms (SNPs), significant SNP (rs 2276186) was suggested in EMIM analysis for child genetics effects (p=0.0225438044) and child genetic effects allowing for maternal genetic effects (p=0.0209453210) with very stringent multiple comparison Bonferroni correction.

conclusionOur results are the pilot study for epigenetic study in mental disorder and help to understanding and use of EMIM statistical genetics analysis program with many limitations including small pedigree numbers.

Indexed as

Case/parent trioEpigeneticLog-linear modelSchizophrenia

Identifiers

PMID31247704
PMCPMC6603700
OpenAlexW2955212697

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LicenceCC BY-NC
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Registered trials

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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.