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Record W4391771437 · doi:10.1101/2024.02.12.24302716

Fine-mapping genomic loci refines bipolar disorder risk genes

2024· preprint· en· W4391771437 on OpenAlexafffund
Maria Koromina, Ashvin Ravi, Georgia Panagiotaropoulou, Brian M. Schilder, Jack Humphrey, Alice Braun, Tim Bidgeli, Chris Chatzinakos, Brandon J. Coombes, Jaeyoung Kim, Xiaoxi Liu, Chikashi Terao, Kevin S. O’ Connell, Mark J. Adams, Rolf Adolfsson, Martin Alda, Lars Alfredsson, Till F. M. Andlauer, Ole A. Andreassen, Anastasia Antoniou, Bernhard T. Baune, Susanne Bengesser, Joanna M. Biernacka, Michael Boehnke, Rosa Bosch, Murray J. Cairns, Vaughan J. Carr, Miguel Casas, Stanley V. Catts, Sven Cichon, Aiden Corvin, Nicholas Craddock, Konstantinos Dafnas, Nina Dalkner, Udo Dannlowski, Franziska Degenhardt, Arianna Di Florio, Dimitris Dikeos, Frederike T. Fellendorf, Panagiotis Ferentinos, Andreas J. Forstner, Liz Forty, Mark A. Frye, Janice M. Fullerton, Micha Gawlik, Ian R. Gizer, Katherine Gordon‐Smith, Melissa J. Green, Maria Grigoroiu‐Serbânescu, José Guzmán‐Parra, Tim Hahn, Frans Henskens, Jan Hillert, Assen Jablensky, Lisa Jones, Ian Jones, Lina Jönsson, John R. Kelsoe, Tilo Kircher, George Kirov, Sarah Kittel‐Schneider, Manolis Kogevinas, Mikael Landén, Marion Leboyer, Melanie Lenger, Jolanta Lissowska, Christine Löchner, Carmel M. Loughland, Donald J. MacIntyre, Nicholas G. Martin, Eirini Maratou, Carol A. Mathews, Fermín Mayoral, Susan L. McElroy, Nathaniel W. McGregor, Andrew M. McIntosh, Andrew McQuillin, Patricia T. Michie, Philip B. Mitchell, Paraskevi Moutsatsou, Bryan Mowry, Bertram Müller-Myhsok, R Myers, Igor Nenadić, Caroline M. Nievergelt, Markus M. Nöthen, John I. Nürnberger, Michael O‘Donovan, Claire O’Donovan, Roel A. Ophoff, Michael J. Owen, Christos Pantelis, Carlos N. Pato, Michele T. Pato, George P. Patrinos, Joanna Pawlak, Roy H. Perlis, Evgenia Porichi, Daniëlle Posthuma, Josep Antoni Ramos‐Quiroga, Andreas Reif, Eva Z. Reininghaus, Marta Ribasés, Marcella Rietschel, Ulrich Schall, Peter R. Schofield, Thomas G. Schulze, Laura J. Scott, Rodney J. Scott, Alessandro Serretti, Cynthia Shannon Weickert, Jordan W. Smoller, María Soler Artigas, Dan J. Stein, Fabian Streit, Claudio Toma, Paul A. Tooney, Marquis P. Vawter, Eduard Vieta, John B. Vincent, Irwin D. Waldman, Thomas W. Weickert, Stephanie H. Witt, Nakao Iwata, Beata Świątkowska, Hong‐Hee Won, Howard J. Edenberg, Stephan Ripke, Towfique Raj, Jonathan R. I. Coleman, Niamh Mullins

Bibliographic record

VenuemedRxiv · 2024
Typepreprint
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetic Syndromes and Imprinting
Canadian institutionsUniversity of British ColumbiaCentre for Addiction and Mental HealthDalhousie University
FundersNational Health and Medical Research CouncilCanadian Institutes of Health ResearchNIHR Maudsley Biomedical Research CentreStanley Center for Psychiatric Research, Broad InstituteNational Institutes of HealthVetenskapsrådetNational Institute of Mental HealthStockholms Läns LandstingInstituto de Salud Carlos IIIUniversitat de BarcelonaNational Research FoundationMedical Research CouncilUniversità di BolognaDepartment of Health and Social CareNational Research Foundation of KoreaKing's College LondonDepartament d'Innovació, Universitats i Empresa, Generalitat de CatalunyaVictoria General Hospital FoundationGeneralitat de CatalunyaEuropean Regional Development FundBundesministerium für Bildung und ForschungNational Institute for Health and Care ResearchKarl-Franzens-Universität GrazJapan Agency for Medical Research and DevelopmentDeutsche ForschungsgemeinschaftJapan Society for the Promotion of ScienceMedizinische Universität GrazAmt der Steiermärkischen LandesregierungGlaxoSmithKlineCentres de Recerca de CatalunyaMichael Smith Health Research BCMaudsley CharityWellcome TrustMinisterio de Ciencia e InnovaciónEuropean CommissionUniversity of California, IrvineBroad InstituteMinisterio de Economía y CompetitividadUniversity of PittsburghCentro de Investigación Biomédica en Red de Salud MentalNational Alliance for Research on Schizophrenia and DepressionU.S. Department of Health and Human Services
KeywordsBiologyGeneticsSingle-nucleotide polymorphismComputational biologyExome sequencingGeneEpigenomicsGenomeGenome-wide association studyPhenotypeDNA methylation

Abstract

fetched live from OpenAlex

Abstract Bipolar disorder (BD) is a heritable mental illness with complex etiology. While the largest published genome-wide association study identified 64 BD risk loci, the causal SNPs and genes within these loci remain unknown. We applied a suite of statistical and functional fine-mapping methods to these loci, and prioritized 17 likely causal SNPs for BD. We mapped these SNPs to genes, and investigated their likely functional consequences by integrating variant annotations, brain cell-type epigenomic annotations, brain quantitative trait loci, and results from rare variant exome sequencing in BD. Convergent lines of evidence supported the roles of genes involved in neurotransmission and neurodevelopment including SCN2A, TRANK1, DCLK3, INSYN2B, SYNE1, THSD7A, CACNA1B, TUBBP5, PLCB3, PRDX5, KCNK4, CRTC3, AP001453 . 3, TRPT1, FKBP2, DNAJC4, RASGRP1, FURIN, FES, DPH1, GSDMB, MED24 and THRA in BD. These represent promising candidates for functional experiments to understand biological mechanisms and therapeutic potential. Additionally, we demonstrated that fine-mapping effect sizes can improve performance of BD polygenic risk scores across diverse populations, and present a high-throughput fine-mapping pipeline ( https://github.com/mkoromina/SAFFARI ).

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)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.834
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
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 science0.0010.003
Research integrity0.0010.001
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 head0.241
Teacher spread0.228 · 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.

Study designNot applicable
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

Citations6
Published2024
Admission routes2
Has abstractyes

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