Author

Anders J. Kämpe

University of HelsinkiORCID 0000-0002-1829-3855Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Aarno V. PalotieiD· 2 shared Annamari Tuulio‐HenrikssoniD· 2 shared Benjamin M. NealeiD· 2 shared Erkki Tapio IsometsäiD· 2 shared Jaana SuvisaariiD· 2 shared Jouko K LönnqvistiD· 2 shared Kaisla Lahdensuo· 2 shared Lea UrpaiD· 2 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aarno V. PalotieORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 1, 2026

Ultra-rare coding variants in schizophrenia risk genes are associated with longitudinal phenotypic differences across psychotic disorders

Anders J. Kämpe, Julia Sealock, Evan Jeffrey Giangrande…·Olli P. H. Pietiläinen

This study identifies ultra-rare damaging variants in schizophrenia risk genes and shows they are associated with earlier hospitalizations, greater childhood adversity, and poorer neuropsychological outcomes across psychotic disorders.

DOI 10.64898/2026.10.30.26366332

humanwhole-exome sequencing

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GenomicsCell Reports MedicinePeer-reviewedMay 1, 2024

Genetic variants for head size share genes and pathways with cancer

Maria J. Knol, Raymond A. Poot, Tavia E. Evans…·Saud Alhusaini

This study identifies 67 genetic loci associated with head size, finding strong overlaps with cancer pathways and genes, suggesting shared genetic mechanisms between head growth and cancer risk.

10 citations

humanGWAS summary statistics

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Genetic & Genomic MedicineNature GeneticsPeer-reviewedMay 25, 2023

The impact of rare protein coding genetic variation on adult cognitive function

Chia‐Yen Chen, Ruoyu Tian, Tian Ge…·Heiko Runz

This study identifies eight genes associated with adult cognitive function through rare coding variants and shows how KDM5B dosage affects cognitive traits in mice and humans.

71 citationstop 1%

humanwhole-exome sequencing

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