Author

Jesse Tyler Valliere

Broad Institute

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 5 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 6 Organism:human· 6 Approach:statistical model· 6 Assay:GWAS summary statistics· 4 Assay:whole-genome sequencing· 2 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Hanna Maria OllilaiD· 6 shared Erik AbneriD· 4 shared Nasa Sinnott-ArmstrongiD· 4 shared FinnGen· 3 shared Lea UrpaiD· 3 shared Lovemore KunorozvaiD· 3 shared Richa Saxena· 3 shared Richa SaxenaiD· 3 shared

Activity by Year

2025-2026 · peak 4/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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6 shared papersGenetic & Genomic Medicine

Hanna Maria OllilaORCID

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Author profile →

6 papers

Recent·Most cited

The genetic architecture of fibromyalgia across 2.5 million individuals

Isabel Kerrebijn, Gyða Björnsdóttir, Keon Arbabi, Lea Urpa, Hele Haapaniemi, Guðmar Þorleifsson, Lilja Stefánsdóttir, Stephan G. Frangakis, Jesse Tyler Valliere, Lovemore Kunorozva, Erik Abner, Caleb Ji, Markus Kangur, Bitten Aagaard, Henning Bliddal, , Michael Wainberg

This study identifies 26 risk loci for fibromyalgia through a genome-wide association analysis of 2.5 million individuals, revealing genetic links to neural functions and chronic pain disorders.

Nature Medicine · Jul 28, 2026Peer-reviewedGenetic & Genomic Medicine

Rare Coding Variants Reveal Distinct Genetic Architectures Across Multidimensional Sleep Phenotypes

Yingzhe Zhang, Wenhan Lu, Lovemore Kunorozva, Samuel E. Jones, Matthew Maher, Jesse Tyler Valliere, Andrew R. Wood, Michael N. Weedon, Justin D. Tubbs, Konrad J. Karczewski, Tian Ge, Henning W. Tiemeier, Jacqueline M. Lane, Richa Saxena, Hanna Maria Ollila, Chia‐Yen Chen

The paper identifies 260 genes associated with sleep phenotypes using rare coding variants from large-scale sequencing data, revealing distinct genetic architectures and biological mechanisms across different sleep measurements.

medRxiv · Jun 18, 2026 · PreprintGenetic & Genomic Medicine

Genetic variants affect diurnal glucose levels throughout the day

FinnGen, Estonian Biobank Research Team, VA Million Veteran Program, Nasa Sinnott-Armstrong, Satu J. Strausz, Lea Urpa, Erik Abner, Josephine P. Johnson, Jesse Tyler Valliere, Teele Palumaa, Priit Palta, Hassan S. Dashti, Kyong‐Mi Chang, Marijana Vujković, Mark J. Daly, , Hanna Maria Ollila

The paper identifies genetic variants associated with diurnal glucose levels and their role in type 2 diabetes risk.

Nature Communications · May 22, 2026Peer-reviewedGenetics

Meta-analysis of Cannabis Use Identifies Shared Genetic Loci with Sleep and Circadian Rhythms

Jesse Tyler Valliere, Satu J. Strausz, Cynthia Ines Mantho Tchio, Oona Shigeno Risse-Adams, Nasa Sinnott-Armstrong, Hanna Maria Ollila, Richa Saxena

This study identifies 39 genetic loci shared between cannabis use and sleep traits through a meta-analysis of 152,807 cases and 220,272 controls.

medRxiv · Apr 16, 2026 · PreprintGenetic & Genomic Medicine

From Normal Variation in Sleep to Clinical Sleep Disorders: Genetic Insights from Over One Million Individuals

Lovemore Kunorozva, Jesse Tyler Valliere, Chia‐Yen Chen, Matthew Maher, Cynthia Ines Mantho Tchio, Angus C. Burns, Yingzhe Zhang, Satu J. Strausz, FinnGen, John Weyl Winkelman, Daniel J. Gottlieb, Tian Ge, Andrew R. Wood, Michael N. Weedon, Samuel E. Jones, , Jacqueline M. Lane

This study identifies genetic associations for multiple sleep disorders and medications in over 1.6 million individuals, revealing shared and unique genetic factors across sleep traits.

medRxiv · Nov 21, 2025 · PreprintGenetic & Genomic Medicine

Initial findings from the DecodeME genome-wide association study of myalgic encephalomyelitis/chronic fatigue syndrome

Genetics Delivery Team, Thibaud Boutin, Andrew D. Bretherick, Joshua J Dibble, Esther Oluwada Ewaoluwagbemiga, Emma Northwood, Gemma L. Samms, Véronique Vitart, Project and Cohort Delivery Team, Øyvind Almelid, Tom Baker, Malgorzata Clyde, Anne Connolly, Diana Garcia, Shona M. Kerr, , Chris Paul Ponting

This study conducts a genome-wide association study (GWAS) of ME/CFS, identifying eight genetic loci associated with the disease, suggesting involvement of immune and neurological processes.

medRxiv · Aug 6, 2025 · PreprintGenetic & Genomic Medicine