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Record W2790965658 · doi:10.1016/j.cell.2018.09.049

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

2018· article· en· W2790965658 on OpenAlexfundno aff
Mitja Mitrovič, Nikolaos A. Patsopoulos, Ashley Beecham, Theresa Dankowski, An Goris, Bénédicte Dubois, Marie D’hooghe, Robin Lemmens, Philip Van Damme, Helle Bach Søndergaard, Finn Sellebjerg, Per Soelberg Sorensen, Henrik Ullum, Lise Wegner Thørner, Thomas Werge, Janna Saarela, Isabelle Cournu‐Rebeix, Vincent Damotte, Bertrand Fontaine, Léna Guillot‐Noël, Mark Lathrop, Sandra Vukusik, Pierre‐Antoine Gourraud, Till F. M. Andlauer, Viola Pongratz, Dorothea Buck, Christiane Gasperi, Antonios Bayas, Christoph Heesen, Tania Kümpfel, Ralf A. Linker, Friedemann Paul, Martin Stangel, Björn Tackenberg, Florian Then Bergh, Clemens Warnke, Heinz Wiendl, Brigitte Wildemann, Uwe K. Zettl, Ulf Ziemann, Hayrettin Tumani, Ralf Gold, Verena Grummel, Bernhard Hemmer, Benjamin Knier, Christina M. Lill, Felix Luessi, Efthimios Dardiotis, Cristina Agliardi, Nadia Barizzone, Elisabetta Mascia, Luisa Bernardinelli, Giancarlo Comi, Daniele Cusi, Federica Esposito, Laura Ferrè, Cristoforo Comi, Daniela Galimberti, Maurizio Leone, Melissa Sorosina, Julia Mescheriakova, Rogier Hintzen, Cornelia M. van Duijn, Charlotte E. Teunissen, Steffan D. Bos, Kjell‐Morten Myhr, Elisabeth Gulowsen Celius, Benedicte A. Lie, Anne Spurkland, Manuel Comabella, Xavier Montalbán, Lars Alfredsson, Pernilla Stridh, Jan Hillert, Maja Jagodic, Fredrik Piehl, Ilijas Jelčić, Roland Martinꝉ, Mireia Sospedra, Maria Ban, Clive Hawkins, Pirro G. Hysi, Seema Kalra, Fredrik Karpe, Jyoti Khadake, Geneviève Lachance, Matthew Neville, Adam Santaniello, Stacy J. Caillier, Peter A. Calabresi, Bruce Cree, Anne H. Cross, Mary F. Davis, Jonathan L. Haines, Paul I. W. de Bakker, Silvia Delgado, Marieme Dembele, Keith R. Edwards, Kathryn C. Fitzgerald, Håkon Håkonarson, Ioanna Konidari, Ellen Lathi, Clara P. Manrique, Margaret A. Pericak‐Vance, Laura Piccio, Cathy Schaefer, Cristin McCabe, Howard L. Weiner, Jacqueline I. Goldstein, Tomas Olsson, Georgios M. Hadjigeorgiou, Bruce Taylor, Lotti Tajouri, Jac Charlesworth, David R. Booth, Hanne F. Harbo, Adrian J. Ivinson, Stephen L. Hauser, Alastair Compston, Graeme J. Stewart, Frauke Zipp, Lisa F. Barcellos, Sergio E. Baranzini, Filippo Martinelli Boneschi, Sandra D’Alfonso, Andreas Ziegler, Annette Oturai, Jacob L. McCauley, Stephen Sawcer, Jorge R. Oksenberg, Philip L. De Jager, Ingrid Kockum, David A. Hafler, Chris Cotsapas

Bibliographic record

VenueCell · 2018
Typearticle
Languageen
FieldMedicine
TopicViral Infections and Immunology Research
Canadian institutionsnot available
FundersUCB PharmaNational Institute of Neurological Disorders and StrokeSanofi GenzymeEMD SeronoMedDay PharmaceuticalsGrifolsNeuroförbundetForskningsrådet om Hälsa, Arbetsliv och VälfärdKnut och Alice Wallenbergs StiftelseFonds Wetenschappelijk OnderzoekDeutsche ForschungsgemeinschaftKing's College LondonFondazione CariploMultiple Sclerosis SocietyNational Institutes of HealthMylanNational Institute for Health and Care ResearchCSL BehringNHS Blood and TransplantGenentechNorges ForskningsrådAlberta Foundation for the ArtsBristol-Myers SquibbNational Health and Medical Research CouncilAstraZenecaNIHR Oxford Biomedical Research CentreBiogenUniversity of MiamiWellcome TrustAlexion PharmaceuticalsBayer HealthCareMedicinska ForskningsrådetHjärnfondenEuropean CommissionBundesministerium für Bildung und FrauenCompass TherapeuticsSanofiMedical Research CouncilVerily Life SciencesTeva Pharmaceutical IndustriesCelgene
KeywordsBiologyHeritabilityLinkage disequilibriumGeneticsEpistasisMissing heritability problemGenome-wide association studyGeneGenetic variationGenetic associationComputational biologyEvolutionary biologyHaplotypeSingle-nucleotide polymorphismGenotype

Abstract

fetched live from OpenAlex

Multiple sclerosis is a complex neurological disease, with ∼20% of risk heritability attributable to common genetic variants, including >230 identified by genome-wide association studies. Multiple strands of evidence suggest that much of the remaining heritability is also due to additive effects of common variants rather than epistasis between these variants or mutations exclusive to individual families. Here, we show in 68,379 cases and controls that up to 5% of this heritability is explained by low-frequency variation in gene coding sequence. We identify four novel genes driving MS risk independently of common-variant signals, highlighting key pathogenic roles for regulatory T cell homeostasis and regulation, IFNγ biology, and NFκB signaling. As low-frequency variants do not show substantial linkage disequilibrium with other variants, and as coding variants are more interpretable and experimentally tractable than non-coding variation, our discoveries constitute a rich resource for dissecting the pathobiology of MS.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation 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 score0.002
Threshold uncertainty score0.007

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.001
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0020.000

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 head0.031
GPT teacher head0.272
Teacher spread0.241 · 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 source (direct Gemma or distilled Codex), 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

Citations171
Published2018
Admission routes1
Has abstractyes

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