Minna Kankuri‐Tammilehto

Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland

Irma Järvelä, Tuomo Määttä, Anushree Acharya et al. · Human Genetics · 2021 · 55 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Copy Number Variation Analysis in Familial BRCA1/2-Negative Finnish Breast and Ovarian Cancer

Kirsi M. Kuusisto, Oyediran Akinrinade, Mauno Vihinen et al. · PLoS ONE · 2013 · 30 citations · Full text

Medicine, Genetics, Oncology +17

Prognostic evaluation of COX-2 expression in renal cell carcinoma.

Minna Kankuri‐Tammilehto, Karl‐Ove Söderström, Tarja‐Terttu Pelliniemi et al. · PubMed · 2010 · 25 citations

Medicine, Oncology, Pathology +16

Whole-exome sequencing of Finnish hereditary breast cancer families

Kirsi Määttä, Tommi Rantapero, Anna Lindström et al. · European Journal of Human Genetics · 2016 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13