Evidence map›Paper›PMID 40285827›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2026

Secondary analysis of GenRED data (Genetics of Recurrent Early-Onset major Depression) using MERLIN.

Mutaz Amin, Claudia Gragnoli

Abstract read
In one paragraph

Article in European archives of psychiatry and clinical neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

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

2 authors.

Mutaz AminDepartment of Biochemistry and Molecular Biology, Faculty of Medicine, Al-Neelain University, Khartoum, 11121, Sudan.
Claudia GragnoliDivision of Endocrinology, Department of Medicine, Creighton University School of Medicine, Omaha, NE, 68124, USA. claudia.gragnoli@gmail.com.

Funding

Eunice Kennedy Shriver National Institute of Child Health and Human Development 5R01HD086911Nebraska Department of Health and Human Services Funds received under Nebraska Laws 2021, LB 380, Section 109
6 · The paper itself

Abstract

The familial relevance of depression is a critical aspect, with evidence suggesting a substantial hereditary component. Investigating the inheritance patterns within families can provide valuable insights into the genetic underpinnings of depression. To gain a new perspective on the genetics underpinning of depression, we conducted a novel analysis of the Genetics of Recurrent Early-onset Depression (GenRED) dataset including 683 U.S. Caucasian families, each with one proband with recurrent early-onset major depression and at least one sibling with depression. Using the MERLIN tool, we identified 37 genomic markers with nominal significance linkage to early-onset recurrent depression. The findings differ from prior analyses of GenRED using a different analytical tool. Our findings highlight the variability and potential discrepancies that can arise from using different analytical tools on the same dataset. Given the chance of microsatellites undergoing duplication, mutations, and amplification errors, our two-point analysis can be more robust compared to the previous multipoint analysis. Also, one limitation is genetic admixture; studies with more homogenous ethnic groups are warranted.

Indexed as

Genetic Predisposition to DiseaseMajor Depressive DisorderNeurofibromin 2AdolescentAdultAge of OnsetFemaleHumansMaleRecurrenceYoung AdultNeurofibromin 2DepressionEarly-onsetFamiliesGenetic linkageMicrosatellitesRecurrent

Identifiers

PMID40285827
PMCPMC12953334

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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.