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deep
205 studies tagged deep, dated 2006-12-06 to 2026-10-30. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Tau-CTFP: A connectome-informed continuous-time first-passage model for forecasting the onset of regional tau PET abnormality 2026-10-30
- A Wasserstein Weisfeiler-Lehman Kernel Framework for Multimodal Brain Connectome Analysis 2026-10-29
- Current gaps in downstream applications of fMRI foundation models: lessons learned from BrainLM & BrainHarmonix on Prevent-AD 2026-10-26
Studies
205 studies carry this tag.
Date range
2006 to 2026
Top journals
- Research Square 22
- medRxiv 22
- NeuroImage 14
- bioRxiv 14
- Preprints.org 7
87 journals in all.
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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Tau PET burden is associated with subsequent cognitive decline in Alzheimer's disease, motivating forecasts for monitoring and studies of spatially targeted therapies.
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Under nested cross-validation, the WWL kernel achieves a balanced accuracy of $0.651\pm0.028$, significantly outperforming both a raw-feature SVM and a histogram-based WL-kernel baseline.
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Foundation models have driven major advancements in the language and vision domains, as seen in the popularity of Artificial Intelligence (AI) tools, and a growing number of studies are bringing the approach to human brain imaging.
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Alzheimer’s disease (AD) is a prevalent neurodegenerative disorder, and early diagnosis is essential for timely intervention.
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Accurate differential diagnosis between Alzheimer’s disease (AD) and frontotemporal dementia (FTD) is of critical importance for the early screening of neurodegenerative diseases.
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A bstract In this study, we build EEG based graph model that uses frequency-resolved connectivity features, with Coherence, phase locking value (PLV) and phase lag index (PLI) in five frequency bands as multi-dimensional edge features.
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Although advances have been made in dementia symptom management, early detection during stages when interventions are most effective remains a significant challenge.
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Quantitative analysis of dendritic spine morphology is central to understanding synaptic function and its disruption in neurological disease, yet reliable measurement depends on accurate segmentation of spines from fluorescence microscopy images — a task still limited by faint or discontinuous spine necks and by tools that require extensive manual correction.
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Alzheimer’s disease (AD) target evidence is distributed across biological, chemical, structural, regulatory, and trial-registry sources, complicating reproducible target evaluation and modeling.
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Longitudinal clinical cohorts contain heterogeneous progression patterns that are obscured by coarse diagnostic labels.
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Alzheimer’s Disease (AD) changes how the brain’s electrical activity behaves, and these changes can, in principle, be picked up directly from a resting-state EEG recording without any invasive testing.
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To distinguish these cases, we trained three types of supervised 3D transformers (ViT3D, MINiT, NIT) and, as a non-collapsing alternative, a frozen self-supervised encoder (DINO), to classify people with dementia or mild cognitive impairment (MCI) versus cognitively normal (CN) individuals from 3D brain MRI, using data from the Alzheimer’s Disease Neuroimaging Initiative (ADNI).
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Magnetic resonance imaging (MRI) of the brain routinely combines complementary contrasts—including T1-weighted (T1w), T2-weighted (T2w) and FLAIR sequences—to capture anatomy and pathology.
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Alzheimer disease (AD) is a disorder of the nervous system that mostly impacts the brain cells and causes the slow destruction of the brain.
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Resting-state EEG is a scalable modality for neurophysiological screening, but conventional spectral descriptors capture only part of the signal organization altered in neurodegenerative disease.
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Electroencephalography (EEG) records cortical activity with high temporal resolution without radiation and at low cost, which makes it a practical signal for automated screening of neurological disorders.
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A continuous amyloid staging score complements global amyloid burden for early AD staging and cognitive risk stratification.
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A bstract Deep learning models for electroencephalography (EEG) pathology detection achieve competitive accuracy but offer limited interpretability.
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Unlike traditional eager decision trees (eagerDT), which lacked sufficient training data for 17%-33% of patient profiles, lazyDT-MCCPath successfully modeled all profiles and achieved a 0.17 improvement in AUROC (0.66 vs. 0.83). lazyDT-MCCPath effectively translates pre-existing MCC profiles into personalized dementia risk probabilities for emerging conditions, which may help clinicians prioritize MCCs to monitor more closely.
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Symptom chronology emerged as a robust diagnostic discriminator, underscoring the clinical value of temporal disease trajectories.
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Machine learning (ML) methods have shown promise in modeling clinical trajectories associated with neurodegenerative disorders such as Alzheimer’s disease (AD).
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The ViTamyloid classifier achieved strong feature-separation metrics, yielding area under the receiver operating characteristic curve (AUROC) and precision-recall curve (AUPRC) values of 0.994/0.958 for CCP, 0.989/0.945 for CGP, 0.992/0.977 for CAA Type 1, and 0.997/0.978 for CAA Type 2.
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Parkinson’s disease (PD) exhibits considerable variability in symptom onset, severity, and clinical trajectories, making prediction of individual disease progression a complex challenge.
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Neuroimaging studies that pool data across clinical sites often suffer from site effects — variability in imaging measures that arises from technical heterogeneity across sites as opposed to true biological signal.
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By comparing these unsupervised representations to a depression-labelled source corpus, one cluster demonstrated mathematical proximity (measured via cosine similarity in a shared latent space) to the source depression centroid.
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The neurodegenerative processes underlying Alzheimer’s disease and related dementias (ADRD) begin years before clinical diagnosis, motivating scalable approaches for earlier identification.
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Open-source deep learning models promise scalable quantification of MRI-visible perivascular spaces (PVS), an emerging marker of glymphatic dysfunction in Alzheimer’s disease (AD).
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The global burden of dementia is heavily concentrated in low- and middle-income countries (LMICs), yet biological diagnosis of Alzheimer’s Disease (AD) relies on positron emission tomography (PET) and cerebrospinal fluid (CSF) analysis that are operationally inaccessible in these regions.
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Precision psychiatry aims to identify biomarkers and develop prediction models to improve diagnosis, prognosis, and treatment selection.
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Artificial-intelligence (AI) systems for Alzheimer’s disease (AD) increasingly use neuroimaging or spontaneous speech, but reported performance is difficult to interpret across studies because cohorts, endpoints, languages, preprocessing, and validation protocols differ.
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16/100
The Alzheimer’s Disease Neuroimaging Initiative (ADNI) is widely used to train machine learning models for Alzheimer’s disease, yet whether it provides consistent ground truth for predictive modeling has not been systematically tested.
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Subcortical brain alterations are a key feature of dementia disease progression.
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Digital medication-management tools for Alzheimer's disease (AD) typically record only whether a dose was taken, leaving the temporal and behavioral structure of adherence largely unused as a predictive signal.
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Deep learning classifiers trained on structural magnetic resonance imaging (MRI) are increasingly proposed for early detection of Alzheimer’s disease (AD) and mild cognitive impairment (MCI), yet the pipelines that produce these models depend on shared datasets, pre-trained weights, and federated updates that an adversary can poison.
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Alzheimer’s disease (AD) is a neurodegenerative disorder that is characterized by structural changes of the hippocampus, thus hippocampal morphology becomes an important biomarker for early diagnosis.
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Aging is the greatest risk factor for Alzheimer's disease (AD), yet how and when AD-related pathological progression diverges from aging remains poorly understood.
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Fairness in clinical machine-learning (ML) remains a critical challenge, particularly in neurodegenerative disease where demographic factors may confound disease-related patterns.
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Early detection of Alzheimer’s disease (AD) from spontaneous speech remains a clinically significant challenge.
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Reported dementia-classification performance depends on how the label is defined, which clinical information the model sees, and whether participants are separated between training and test data.
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Alzheimer's disease classification by means of Magnetic Resonance Imaging demands strong models that are able to generalise to different stages of dementia.
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Sensitive human data underpin discoveries across medicine, biology and the social sciences, yet privacy regulation often prevents sharing them with collaborators or artificial intelligence (AI) systems.
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Alzheimer's Disease (AD) detection from spoken language has advanced considerably with the rise of large pre-trained speech and language models, including wav2vec 2.0, BERT, generative LLMs, and emerging audio-LLMs.
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After more than three decades of intensive research, Alzheimer disease care remains largely palliative, and the field has drawn sustained criticism, both for that reason and for pursuing some directions of inquiry over others.
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Using two large-scale longitudinal datasets covering more than 75,000 patients or stays and 7.8 million clinical observations—spanning emergency vasopressor titration in sepsis (MIMIC- IV; 6,243 ICU admissions drawn from 73,141 encounters) and serial cognitive assessment in Alzheimer’s disease (ADNI; 2,262 longitudinal participants)—we train a 13-family computa- tional model zoo and perform a novel experiment: auditing whether clinician and AI treatment decisions jointly or individually match the subsequent patient trajectory, and testing whether cooperation between the two actors resolves their disagreements.
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Explainability methods applied to deep learning models for Alzheimer’s disease neuroimaging produce attribution maps that vary substantially across methods and architectures, yet no validated quantitative framework exists for determining which method most faithfully localises attribution signal within established AD neuroimaging biomarker anatomy at the individual subject level.
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Alzheimer’s disease (AD) pathology develops years in advance prior to its clinical presentation.
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The MoE-derived DNN-IR index demonstrated robust and stable performance in predicting atherosclerosis, incident CVD, cardiovascular mortality, and all-cause mortality in the general population.
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Accurate long-term forecasting of cognitive trajectories across the Alzheimer’s disease continuum is essential for early intervention, personalized prognosis, patient stratification, and clinical trial enrichment.
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Alzheimer’s disease (AD) detection from structural magnetic resonance imaging (MRI) using deep learning depends on large, labelled datasets.
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Dementia affects more than 55 million people worldwide, and its progressive decline is difficult to track using infrequent in-person assessments, which can miss subtle changes between visits and add to clinician burden.
From across this tag
9 of the 205 studies in this tag, picked by a fixed rule (a hash of each study's address), not by score or date; each page of this list shows a different 9. The same 9 appear here every time.
- Image-driven population analysis through mixture modeling
- Predicting cognitive decline with deep learning of brain metabolism and amyloid imaging
- PLASMA-CYCLEGAN: PLASMA BIOMARKER-GUIDED MRI TO PET CROSS-MODALITY TRANSLATION USING CONDITIONAL CYCLEGAN
- Deep learning-based brain age prediction in normal aging and dementia
- Deep learning-based amyloid PET harmonization to predict cognitive decline in non-demented elderly
- Classification and Visualization of Alzheimer’s Disease using Volumetric Convolutional Neural Network and Transfer Learning
- Machine learning-based estimation of the mild cognitive impairment stage using multimodal physical and behavioral measures
- Transformer-based deep neural network language models for Alzheimer's disease risk assessment from targeted speech
- Deep Learning Analysis of Retinal Structures and Risk Factors of Alzheimer's Disease