| Sleep alterations following exposure to stress predict fear-associated memory impairments in a rodent model of PTSD WM Vanderheyden, SA George, L Urpa, M Kehoe, I Liberzon, GR Poe Experimental brain research 233, 2335-2346, 2015 | 82 | 2015 |
| Focused multidimensional scaling: interactive visualization for exploration of high-dimensional data LM Urpa, S Anders BMC bioinformatics 20, 1-8, 2019 | 22 | 2019 |
| Stress-free automatic sleep deprivation using air puffs BA Gross, WM Vanderheyden, LM Urpa, DE Davis, CJ Fitzpatrick, ... Journal of neuroscience methods 251, 83-91, 2015 | 19 | 2015 |
| The impact of rare protein coding genetic variation on adult cognitive function CY Chen, R Tian, T Ge, M Lam, G Sanchez-Andrade, T Singh, L Urpa, ... Nature Genetics 55 (6), 927-938, 2023 | 16 | 2023 |
| The bradykinin system in stress and anxiety in humans and mice A Rouhiainen, N Kulesskaya, M Mennesson, Z Misiewicz, T Sipilä, ... Scientific reports 9 (1), 19437, 2019 | 14 | 2019 |
| Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants EC Saarentaus, AS Havulinna, N Mars, A Ahola-Olli, TTJ Kiiskinen, ... Molecular Psychiatry 26 (9), 4884-4895, 2021 | 8 | 2021 |
| A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development E Rahikkala, L Urpa, B Ghimire, H Topa, MI Kurki, M Koskela, M Airavaara, ... European Journal of Human Genetics 30 (5), 619-627, 2022 | 7 | 2022 |
| Increase in rem sleep following trauma exposure W Vanderheyden, L Urpa, G Poe Sleep Medicine 14, e293, 2013 | 3 | 2013 |
| Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability L Urpa, MI Kurki, E Rahikkala, E Hämäläinen, V Salomaa, J Suvisaari, ... European Journal of Human Genetics, 1-8, 2024 | 1 | 2024 |
| Functional Characterization of Six SLCO1B1 (OATP1B1) Variants Observed in Finnish Individuals with a Psychotic Disorder K Hakkinen, W Kiander, H Kidron, M Lahteenvuo, L Urpa, J Lintunen, ... Molecular Pharmaceutics 20 (3), 1500-1508, 2023 | 1 | 2023 |
| Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders A Kämpe, J Suvisaari, M Lähteenvuo, T Singh, A Ahola-Olli, L Urpa, ... Molecular Psychiatry, 1-9, 2024 | | 2024 |
| Genetic Architecture of Intellectual Disability in Northern Finland L Urpa Helsingin yliopisto, 2024 | | 2024 |
| W88. PHENOTYPIC AND GENETIC CHARACTERIZATION OF INDIVIDUALS WITH SCHIZOPHRENIA AND HIGH PSYCHIATRIC HOSPITALIZATION BURDEN A Kämpe, J Suvisaari, M Lähteenvuo, E Vartiainen, T Singh, A Ahola-Olli, ... European Neuropsychopharmacology 75, S151-S152, 2023 | | 2023 |
| A novel SMG9 variant enriched in the Finnish population causes intellectual disability E Rahikkala, L Urpa, B Ghimire, H Topa, MI Kurki, M Koskela, M Airavaara, ... EUROPEAN JOURNAL OF HUMAN GENETICS 31, 172-172, 2023 | | 2023 |
| Enrichment of Rare, Damaging Variants in Schizophrenia-related Genes in Intellectual Disability Patients with Psychotic Disorders L Urpa, M Kurki, T Singh, E Hamalainen, E Rahikkala, J Moilanen, ... European Neuropsychopharmacology 63, E45-E45, 2022 | | 2022 |
| Human well-being and capabilities: Thematic Module B E Oinas, H Katsui, M Jauhola, NHP Korpelainen, P Kuusela, TJ Lammi, ... | | 2021 |
| CNV Association with Neurodevelopmental Phenotypes in Finnish Population Cohort E Saarentaus, M Kurki, L Urpa, AS Havulinna, M Perola, V Salomaa, ... | | 2019 |
| Focused Multidimensional Scaling: An Interactive, User-Friendly Tool for Visualization of Distance Matrices L Urpa, S Anders HUMAN HEREDITY 81 (4), 233-233, 2016 | | 2016 |
| Mouse strain-specific differences in transposable element expression following psychosocial stress LM Urpa Helsingfors universitet, 2016 | | 2016 |
