Two novel mutations in the DNAH11 gene in primary ciliary dyskinesia (CILD7) with considerable variety in the clinical and beating cilia phenotype

por Schultz, Rüdiger, Elenius, Varpu, Lukkarinen, Heikki, Saarela, Tanja
Publicado 2020

Role of an automated screening tool for familial hypercholesterolemia in patients with premature coronary artery disease

por Jokiniitty, Antti, Eskola, Markku, Saarela, Tanja, Huhtala, Heini, Metso, Saara
Publicado 2022

Associations of polygenic risk scores for preeclampsia and blood pressure with hypertensive disorders of pregnancy

por Nurkkala, Jouko, Kauko, Anni, FinnGen, Laivuori, Hannele, Saarela, Tanja, Tyrmi, Jaakko S., Vaura, Felix, Cheng, Susan, Bello, Natalie A., Aittokallio, Jenni, Niiranen, Teemu
Publicado 2023

Increased Risk of Preeclampsia in Women With a Genetic Predisposition to Elevated Blood Pressure

por Kivioja, Anna, Toivonen, Elli, Tyrmi, Jaakko, Ruotsalainen, Sanni, Ripatti, Samuli, Huhtala, Heini, Jääskeläinen, Tiina, Heinonen, Seppo, Kajantie, Eero, Kere, Juha, Kivinen, Katja, Pouta, Anneli, Saarela, Tanja, Laivuori, Hannele
Publicado 2022