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Record W3013660197 · doi:10.1038/s41588-020-0594-5

Minimal phenotyping yields genome-wide association signals of low specificity for major depression

2020· article· en· W3013660197 on OpenAlexaff
Na Cai, Joana Revez, Mark J. Adams, Till F. M. Andlauer, Gerome Breen, Enda M. Byrne, Toni‐Kim Clarke, Andreas J. Forstner, Hans J. Grabe, Steven P. Hamilton, Douglas F. Levinson, Cathryn M. Lewis, Glyn Lewis, Nicholas G. Martin, Yuri Milaneschi, Ole Mors, Bertram Müller‐Myhsok, Brenda W.J.H. Penninx, Roy H. Perlis, Giorgio Pistis, James B. Potash, Martin Preisig, Jianxin Shi, Jordan W. Smoller, Fabien Streit, Henning Tiemeier, Rudolf Uher, Sandra Van der Auwera, Alexander Viktorin, Myrna M. Weissman, Kenneth S. Kendler, Jonathan Flint

Bibliographic record

VenueNature Genetics · 2020
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetic Associations and Epidemiology
Canadian institutionsDalhousie University
FundersCilagNational Institute of Mental HealthNeuraxpharmChinese Society of Clinical OncologyUniversity of OxfordEuropean Bioinformatics InstituteKing's College LondonNational Institute for Health and Care ResearchFresenius Medical Care North AmericaSchweizerischer Nationalfonds zur Förderung der Wissenschaftlichen ForschungWellcome TrustNIHR Maudsley Biomedical Research CentreGlaxoSmithKlineJohn Templeton FoundationLundbeckfondenNational Science Foundation
KeywordsBiologyGenome-wide association studyGeneticsComputational biologyGenomeGenetic associationAssociation (psychology)Evolutionary biologyGeneSingle-nucleotide polymorphismGenotype

Abstract

fetched live from OpenAlex

Minimal phenotyping refers to the reliance on the use of a small number of self-reported items for disease case identification, increasingly used in genome-wide association studies (GWAS). Here we report differences in genetic architecture between depression defined by minimal phenotyping and strictly defined major depressive disorder (MDD): the former has a lower genotype-derived heritability that cannot be explained by inclusion of milder cases and a higher proportion of the genome contributing to this shared genetic liability with other conditions than for strictly defined MDD. GWAS based on minimal phenotyping definitions preferentially identifies loci that are not specific to MDD, and, although it generates highly predictive polygenic risk scores, the predictive power can be explained entirely by large sample sizes rather than by specificity for MDD. Our results show that reliance on results from minimal phenotyping may bias views of the genetic architecture of MDD and impede the ability to identify pathways specific to MDD. Genetic analyses of depression based on minimal phenotyping identify nonspecific genetic risk factors shared between major depressive disorder (MDD) and other psychiatric conditions, suggesting that this approach may have limited ability to identify pathways specific to MDD.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.002
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.098
Threshold uncertainty score0.672

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0010.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.013
GPT teacher head0.262
Teacher spread0.249 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations375
Published2020
Admission routes1
Has abstractyes

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