Olga Bulenko

Dr. Olga Bulenko


Research Focus & Metrics

Academic Career Length

1Year (2026-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
10 November 2026 in Preprints.org
Verified
Preprint
Open access
PDF file
OBOlga Bulenko
Olga Bulenko
MNMaria Nazarova
Maria Nazarova
KKKarina Karis
Karina Karis
CKCarolin Kuuskmae
Carolin Kuuskmae
RMRaiko Marrandi
Raiko Marrandi
MPMari-Anne Philips
Mari-Anne Philips
Genetic association studies have implicated neural adhesion-related genes in suicidal behaviour and related psychiatric phenotypes, whereas postmortem brain transcriptomic studies have yielded heterogeneous findings with limited support after multiple-testing correction. We synthesized genetic evidence and examined IgLON expression in bilateral anterior midcingulate cortex (aMCC) samples from 14 suicide and 10 non-suicide donors. RT-qPCR measured eight transcripts from five IgLON genes, including alternative promoter-derived transcripts of LSAMP, NTM and OPCML. We additionally reanalysed published dorsolateral prefrontal cortex (DLPFC) expression data and examined public transcriptomic datasets. The genetic synthesis identified several adhesion-related candidate genes, while exploratory DLPFC reanalysis suggested potentially informative promoter-specific differences in LSAMP expression. In the aMCC, NEGR1 expression was lower in the right hemisphere of suicide donors (suicide/non-suicide ratio = 0.54; FDR-adjusted q = 0.027), but not significantly different in the left. Directional NEGR1 asymmetry also differed between groups (q = 0.026), although this result was sensitive to covariate adjustment and the scope of multiple-testing correction. Blood ethanol adjustment minimally changed effect estimates. No other aMCC transcript or public transcriptomic comparison showed FDR-significant differences. Our findings support anatomically focused, bilateral and transcript-specific investigation of neural adhesion genes in larger, independent cohorts.