Optical Genome Mapping as an Alternative to FISH-Based Cytogenetic Assessment in Chronic Lymphocytic Leukemia

por Valkama, Andriana, Vorimo, Sandra, Kumpula, Timo A., Räsänen, Hannele, Savolainen, Eeva-Riitta, Pylkäs, Katri, Mantere, Tuomo
Publicado 2023

Evaluating the role of CHEK2 p.(Asp438Tyr) allele in inherited breast cancer predisposition

por Kumpula, Timo A., Koivuluoma, Susanna, Soikkonen, Leila, Vorimo, Sandra, Moilanen, Jukka, Winqvist, Robert, Mantere, Tuomo, Kuismin, Outi, Pylkäs, Katri
Publicado 2023

Truncating TINF2 p.Tyr312Ter variant and inherited breast cancer susceptibility

por Koivuluoma, Susanna, Vorimo, Sandra, Mattila, Tiina M., Tervasmäki, Anna, Kumpula, Timo, Kuismin, Outi, Winqvist, Robert, Moilanen, Jukka, Mantere, Tuomo, Pylkäs, Katri
Publicado 2022

Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility

por Kumpula, Timo A., Vorimo, Sandra, Mattila, Taneli T., O’Gorman, Luke, Astuti, Galuh, Tervasmäki, Anna, Koivuluoma, Susanna, Mattila, Tiina M., Grip, Mervi, Winqvist, Robert, Kuismin, Outi, Moilanen, Jukka, Hoischen, Alexander, Gilissen, Christian, Mantere, Tuomo, Pylkäs, Katri
Publicado 2023