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Head & Face Medicine|October 23, 2023
Psychiatric disorders and interventions in patients sustaining facial fractures from interpersonal violenceAnnamari Arpalahti, Aleksi Haapanen, Kirsi Auro, et al.
JAMA Network Open|June 27, 2024
Attention-Deficit/Hyperactivity Disorder Diagnoses in Finland During the COVID-19 PandemicKirsi Auro, Ida Holopainen, Markus Perola, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|December 18, 2022
Psychiatric morbidity is common in orthognathic surgery patients-a retrospective studySakari Kettunen, Olli-Pekka Lappalainen, Tuula Palotie, et al.
Human Genetics|July 21, 2007
Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohortsMervi Alanne, Kati Kristiansson, Kirsi Auro, et al.
Plos Genetics|August 7, 2007
Combined effects of thrombosis pathway gene variants predict cardiovascular eventsKirsi Auro, Mervi Alanne, Kati Kristiansson, et al.
Bone|January 16, 2007
The A1330V polymorphism of the low-density lipoprotein receptor-related protein 5 gene (LRP5) associates with low peak bone mass in young healthy menAnne Saarinen, Ville-Valtteri Välimäki, Matti J Välimäki, et al.
Research Square|April 22, 2024
Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsiaA Lokki, Michael Triebwasser, Emma Daly, et al.
Plos Genetics|May 16, 2006
Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studiesKati Komulainen, Mervi Alanne, Kirsi Auro, et al.
Genes and Immunity|December 17, 2024
Understanding rare genetic variants within the terminal pathway of complement system in preeclampsiaA Inkeri Lokki, Michael Triebwasser, Emma Daly, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|May 8, 2023
Identification of complement factor H variants that predispose to pre-eclampsia: A genetic and functional studyA Inkeri Lokki, Zhen Ren, Michael Triebwasser, et al.
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