Erdem Gönültaş

Mr. Erdem Gönültaş

orcid

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

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30 October 2026 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
TKTuğçe Keles
Tuğçe Keles
MBMehmet Baygin
Mehmet Baygin
İTİrem Taşcı
İrem Taşcı
EGErdem Gönültaş
Erdem Gönültaş
TAHA MÜEZZİNOĞLUTAHA MÜEZZİNOĞLU
TAHA MÜEZZİNOĞLU
Türker TuncerTürker Tuncer
Türker Tuncer
Background/Objectives: EEG-based mental performance classification requires participant-separated validation and traceable feature identities. Methods: BioTWavePat-XFE constructs five single-rhythm and 15 signed cross-rhythm channel-rank transition layers, uses four cumulative-weighted selectors and tkNN/IMV classification, and decodes retained identities with Directed Lobish. We compared Protocol A (whole-dataset feature and pooled-test outcome selection), Protocol B (training-fold outcome selection with Protocol A features), and Protocol C (all data-dependent steps restricted to outer training data). STEW and MAT used participant-wise LOSO. TMPD included all 55 participants in 54 identifier groups; two same-class participants sharing an identifier were withheld together. Results: Protocol A segment accuracies were 83.08% (STEW), 93.14% (TMPD), and 91.15% (MAT). Protocol C accuracies were 80.46%, 82.50%, and 74.65%, with balanced accuracies of 80.46%, 75.17%, and 64.15%, respectively. These are the primary estimates without the identified selection leakage under the stated participant-separated validation design. Conclusions: Whole-dataset selection inflated the original estimates, particularly for TMPD and MAT. MAT Protocol C performance was close to majority prediction. Directed Lobish exposes selected feature identities without establishing physiological connectivity, causality or biomarker validity.