Katri Pylkäs

19PUBLICATIONS
194CO-AUTHORS
Cell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)Microelectromechanical systems (MEMS)Cancer geneticsGene mapping
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Publications (19)

|May 14, 2026
Optical Genome Mapping Reveals Frequent Cryptic Structural Aberrations in Normal Karyotype Acute Myeloid Leukemia.

|Nov 13, 2025
Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women.

Peh Joo Ho, Christine Kim Yan Loo, Ryan Jak Yang Lim

|Sep 21, 2024
Optical Genome Mapping Identifies a Second Xq27.1 Rearrangement Associated With Charcot-Marie-Tooth Neuropathy CMTX3.

Elisa Rahikkala, Jonna Komulainen-Ebrahim, Jussi-Pekka Tolonen

|Apr 10, 2024
PALB2-mutated human mammary cells display a broad spectrum of morphological and functional abnormalities induced by increased TGFβ signaling.

Hanna Tuppurainen, Niina Laurila, Marjut Nätynki

|Aug 14, 2023
Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility.

Timo A Kumpula, Sandra Vorimo, Taneli T Mattila

|Aug 13, 2023
Infantile onset encephalomyopathy, retinopathy, optic atrophy, and mitochondrial DNA depletion associated with a novel pathogenic DHX16 variant.

Milla-Riikka Hautakangas, Paula Widgren, Paavo Korpelainen

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Frequent Collaborators

4 joint publications

Anna Jakubowska

4 joint publications

Gad Rennert

4 joint publications

Irene L Andrulis

4 joint publications

Thilo Dörk