Author

Anne Marja Remes

University of Eastern Finland

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· 2 Neuroscience· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 5 Approach:statistical model· 5 Research Focus:GWAS / association mapping· 3 Assay:GWAS summary statistics· 3 Research Focus:differential expression· 2 Research Focus:fine-mapping· 1 Assay:imaging· 1

Frequent Co-Authors

Adam E. Ziemann· 3 shared Anders MälarstigiD· 3 shared Anne Lehtonen· 3 shared Anne PitkärantaiD· 3 shared Arto MannermaaiD· 3 shared Dawn M. WaterworthiD· 3 shared Edmond TengiD· 3 shared FinnGeniD· 3 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Adam E. Ziemann

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5 papers

Recent·Most cited

Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty

Jonathan K. L. Mak, Chenxi Qin, Moritz Krüger, Anna Kuukka, FinnGen, Aarno V. Palotie, Mark J. Daly, Bridget Riley-Gillis, Howard J. Jacob, Dirk S. Paul, Slavé Petrovski, Heiko Runz, Sally John, George Okafo, Robert M. Plenge, , Ekaterina A. Khramtsova

This study identifies 1,242 novel genetic variants and 31 novel genes associated with frailty through genome-wide association and proteomics integration.

Nature Aging · Aug 5, 2025Peer-reviewedGenetic & Genomic Medicine

Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations

Ville Salo, Juhani H. Määttä, Eeva Sliz, FinnGen, Aarno V. Palotie, Mark J. Daly, Bridget Riley-Gills, Howard J. Jacob, Dirk S. Paul, Slavé Petrovski, Heiko Runz, Sally John, George Okafo, Nathan Lawless, Heli Salminen‐Mankonen, , Jukka T. Koskela

This study conducts a genome-wide meta-analysis across three biobanks to identify new genetic loci associated with lumbar disc herniation, expanding the known genetic landscape.

Nature Communications · Nov 7, 2024Peer-reviewedGenetic & Genomic Medicine

Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia

Aurélie Bussy, Jake P. Levy, Tristin Best, Raihaan Patel, Lani Cupo, Tim Van Langenhove, Jørgen Erik Nielsen, Yolande A.L. Pijnenburg, Maria Landqvist Waldö, Anne Marja Remes, Matthias Leopold Schroeter, Isabel J. Santana, Florence Pasquier, Markus Otto, Adrian Danek, , GENetic Frontotemporal dementia Initiative (GENFI)

This study investigates the association between cerebellar and subcortical atrophy and neuropsychiatric symptoms in genetic frontotemporal dementia, finding significant differences across genetic mutations.

Human Brain Mapping · Mar 9, 2023Peer-reviewedNeuroscience

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

Sanni Ruotsalainen, Juulia Partanen, Anna Cichońska, Jake Lin, Christian Benner, Ida L. Surakka, FinnGen, Aarno Palotie, Mark J. Daly, Pharmaceutical companies, Howard J. Jacob, Athena Matakidou, Heiko Runz, Sally John, Robert M. Plenge, , Kari Linden

The paper introduces a multivariate GWAS framework that identifies functional variants and disease associations by transforming multivariate results into univariate phenotypes for follow-up analysis.

European Journal of Human Genetics · Oct 27, 2020Peer-reviewedGenetics

Altered BOLD signal variation in Alzheimer’s disease and frontotemporal dementia

Timo Tuovinen, Janne Kananen, Riikka Rytty, Virpi Moilanen, Ahmed Abou Elseoud, Anne Marja Remes, Vesa J. Kiviniemi, ADNI

This study uses CVBOLD to detect altered physiological pulsations in Alzheimer’s disease and frontotemporal dementia, finding disease-specific patterns in brain regions.

bioRxiv · Oct 29, 2018 · PreprintNeuroscience