Evidence map›Paper›PMID 26886973›Full record

ArticleIEEE transactions on medical imaging2016

Probabilistic Modeling of Imaging, Genetics and Diagnosis.

Nematollah K Batmanghelich, Adrian Dalca, Gerald Quon, Mert Sabuncu, Polina Golland

Abstract read
In one paragraph

Article in IEEE transactions on medical imaging, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Multi-modal intermediate integrative methods in neuropsychiatric disorders: A review.Computational and structural biotechnology journal · 2022
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Brain Imaging Genomics: Integrated Analysis and Machine Learning.Proceedings of the IEEE. Institute of Electrical and Electronics Engineers · 2020
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  16. Article
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

5 authors.

Nematollah K Batmanghelich
Adrian Dalca
Gerald Quon
Mert Sabuncu
Polina Golland

Funding

Washington University ConsoritumU54EB005149 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI MACLEOD, ROB · 2004 to 2013
$39.3M
WHITE MATTER ARCHITECTURE FROM DT-MRIP41RR013218 · NCRR · BRIGHAM AND WOMEN'S HOSPITAL · PI KIKINIS, RON · 1998 to 2011
$30.6M
Training and DisseminationP41EB015902 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI KIKINIS, RON, WESTIN, CARL-FREDRIK · 2012 to 2022
$20.9M
Rodent Behavior CoreU54HD079125 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ABBEDUTO, LEONARD J. · 2013 to 2019
$8.5M
Multivariate Pattern Analysis Methods for Neuroimaging Genetics StudiesK25EB013649 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI SABUNCU, MERT RORY · 2011 to 2015
$877k
A Structural Brain MRI Dementia Forecast ToolR41AG052246 · NIA · CORTICOMETRICS, LLC · PI SABUNCU, MERT RORY, SCHMANSKY, NICHOLAS JOHN · 2015 to 2015
$225k
NCRR NIH HHS P41 RR013218NIA NIH HHS R41 AG052246NIBIB NIH HHS K25 EB013649NIBIB NIH HHS P41 EB015902NIBIB NIH HHS U54 EB005149
6 · The paper itself

Abstract

We propose a unified Bayesian framework for detecting genetic variants associated with disease by exploiting image-based features as an intermediate phenotype. The use of imaging data for examining genetic associations promises new directions of analysis, but currently the most widely used methods make sub-optimal use of the richness that these data types can offer. Currently, image features are most commonly selected based on their relevance to the disease phenotype. Then, in a separate step, a set of genetic variants is identified to explain the selected features. In contrast, our method performs these tasks simultaneously in order to jointly exploit information in both data types. The analysis yields probabilistic measures of clinical relevance for both imaging and genetic markers. We derive an efficient approximate inference algorithm that handles the high dimensionality of image and genetic data. We evaluate the algorithm on synthetic data and demonstrate that it outperforms traditional models. We also illustrate our method on Alzheimer's Disease Neuroimaging Initiative data.

Indexed as

Models, StatisticalAlgorithmsAlzheimer DiseaseBayes TheoremHumansNeuroimagingPhenotype

Identifiers

PMID26886973
PMCPMC5364030

What OpenQuestion holds

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Registered trials

None linked

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.