| The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions N Rahmioglu, S Mortlock, M Ghiasi, PL Møller, L Stefansdottir, ... Nature genetics 55 (3), 423-436, 2023 | 71 | 2023 |
| Large-scale genome-wide association meta-analysis of endometriosis reveals 13 novel loci and genetically-associated comorbidity with other pain conditions R Nilufer, B Karina, C Paraskevi, D Rebecca, G Genevieve, G Ayush, ... BioRxiv, 406967, 2018 | 50 | 2018 |
| Intrauterine growth restriction and placental gene expression in severe preeclampsia, comparing early-onset and late-onset forms J Nevalainen, S Skarp, ER Savolainen, M Ryynänen, J Järvenpää Journal of Perinatal Medicine 45 (7), 869-877, 2017 | 42 | 2017 |
| The interplay of matrix metalloproteinase-8, transforming growth factor-β1 and vascular endothelial growth factor-C cooperatively contributes to the aggressiveness of oral … P Åström, K Juurikka, ES Hadler-Olsen, G Svineng, NK Cervigne, ... British journal of cancer 117 (7), 1007-1016, 2017 | 40 | 2017 |
| Rare copy number variants in array-based comparative genomic hybridization in early-onset skeletal fragility A Costantini, S Skarp, A Kämpe, RE Mäkitie, M Pettersson, M Männikkö, ... Frontiers in Endocrinology 9, 380, 2018 | 26 | 2018 |
| TUFT1, a novel candidate gene for metatarsophalangeal osteoarthritis, plays a role in chondrogenesis on a calcium-related pathway E Sliz, M Taipale, M Welling, S Skarp, V Alaraudanjoki, J Ignatius, ... PloS one 12 (4), e0175474, 2017 | 26 | 2017 |
| Extracellular matrix proteins produced by stromal cells in idiopathic pulmonary fibrosis and lung adenocarcinoma M Kreus, S Lehtonen, S Skarp, R Kaarteenaho PLoS One 16 (4), e0250109, 2021 | 22 | 2021 |
| NRF1 and NRF2 mRNA and protein expression decrease early during melanoma carcinogenesis: an insight into survival and microRNAs M Hämäläinen, HR Teppo, S Skarp, KM Haapasaari, K Porvari, ... Oxidative medicine and cellular longevity 2019, 2019 | 21 | 2019 |
| Whole‐exome sequencing suggests multiallelic inheritance for childhood‐onset Ménière's disease S Skarp, L Kanervo, J Kotimäki, M Sorri, M Männikkö, E Hietikko Annals of Human Genetics 83 (6), 389-396, 2019 | 19 | 2019 |
| Breast cancer carcinoma-associated fibroblasts differ from breast fibroblasts in immunological and extracellular matrix regulating pathways I Pasanen, S Lehtonen, R Sormunen, S Skarp, E Lehtilahti, M Pietilä, ... Experimental Cell Research 344 (1), 53-66, 2016 | 19 | 2016 |
| Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes M Freidin, M Kraatari, S Skarp, J Määttä, J Kettunen, J Niinimäki, ... Journal of Medical Genetics 56 (7), 420-426, 2019 | 16 | 2019 |
| New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière’s Disease S Skarp, J Korvala, J Kotimäki, M Sorri, M Männikkö, E Hietikko Genes 13 (6), 998, 2022 | 13 | 2022 |
| MiR-185-5p regulates the development of myocardial fibrosis R Lin, L Rahtu-Korpela, Z Szabo, A Kemppi, S Skarp, AM Kiviniemi, ... Journal of Molecular and Cellular Cardiology 165, 130-140, 2022 | 11 | 2022 |
| A whole exome study identifies novel candidate genes for vertebral bone marrow signal changes (Modic changes) M Kraatari, S Skarp, J Niinimäki, J Karppinen, M Männikkö Spine 42 (16), 1201-1206, 2017 | 10 | 2017 |
| Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis M Taipale, E Jakkula, OP Kämäräinen, P Gao, S Skarp, S Barral, ... Osteoarthritis and Cartilage 24 (4), 655-663, 2016 | 10 | 2016 |
| Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis S Skarp, OP Kämäräinen, GH Wei, E Jakkula, I Kiviranta, H Kröger, ... PLoS One 13 (8), e0203313, 2018 | 8 | 2018 |
| Exome Sequencing Reveals a Phenotype Modifying Variant in ZNF528 in Primary Osteoporosis With a COL1A2 Deletion S Skarp, JH Xia, Q Zhang, M Löija, A Costantini, LW Ruddock, O Mäkitie, ... Journal of Bone and Mineral Research 35 (12), 2381-2392, 2020 | 6 | 2020 |
| NRF3 decreases during melanoma carcinogenesis and is an independent prognostic marker in melanoma A Immonen, KM Haapasaari, S Skarp, P Karihtala, HR Teppo Oxidative medicine and cellular longevity 2022, 2022 | 5 | 2022 |
| A single genetic locus associated with pediatric fractures: A genome-wide association study on 3,230 patients R Parviainen, S Skarp, L Korhonen, W Serlo, M Männikkö, JJ Sinikumpu Experimental and Therapeutic Medicine 20 (2), 1716-1724, 2020 | 5 | 2020 |
| Rare copy number variants in array-based comparative genomic hybridization in early-onset skeletal fragility front. Endocrinol (Lausanne) 9: 380 A Costantini, S Skarp, A Kämpe, RE Mäkitie, M Pettersson, M Männikkö, ... | 5 | 2018 |
