Author

Joni A. Turunen

University of HelsinkiORCID 0000-0002-9569-9146Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

Aarno V. PalotieiD· 2 shared Mark J. DalyiD· 2 shared Aki Samuli HavulinnaiD· 1 shared Bryan R. GormaniD· 1 shared Camiel J. F. BooniD· 1 shared Cari L. NealoniD· 1 shared Christopher W. HalladayiD· 1 shared Elizabeth J. RossiniD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aarno V. PalotieORCID

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Author profile →

2 papers

Recent·Most cited

Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucoma

Joel T Rämö, Bryan R. Gorman, Lu-Chen C Weng, Sean Joseph Jurgens, Panisa Singhanetr, Marisa Gobuty Tieger, Elon H. C. van Dijk, Christopher W. Halladay, Xin Wang, Joost Brinks, Seung Hoan Choi, Yuyang Luo, FinnGen, Program VA Million Veteran, Saiju Pyarajan, Cari L. Nealon, , Elizabeth J. Rossin

The paper identifies a rare variant in VE-PTP associated with CSC, varicose veins, and glaucoma using genome-wide data from multiple cohorts.

medRxiv · May 8, 2024 · PreprintGenetic & Genomic Medicine

Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma

Yosuke Tanigawa, Michael Wainberg, Juha M Karjalainen, Tuomo Kiiskinen, Guhan Ram Venkataraman, Susanna M. Lemmelä, Joni A. Turunen, Robert Graham, Aki Samuli Havulinna, Markus Perola, Aarno V. Palotie, FinnGen, Mark J. Daly, Manuel A. Rivas

The paper identifies rare protein-altering variants in ANGPTL7 that lower intraocular pressure and reduce glaucoma risk by analyzing genotyping data from UK Biobank and FinnGen.

PLoS Genetics · May 5, 2020Peer-reviewedGenetics