1. A Family With A20 Haploinsufficiency Presenting With Novel Clinical Manifestations and Challenges for Treatment. Issue 8 (December 2021) Authors: Hautala, Timo; Vähäsalo, Paula; Kuismin, Outi; Keskitalo, Salla; Rajamäki, Kristiina; Väänänen, Antti; Simojoki, Marja; Säily, Marjaana; Pelkonen, Ilpo; Tokola, Heikki; Mäkinen, Markus; Kaarteenaho, Riitta; Jartti, Airi; Hautala, Nina; Kantola, Saara; Jackson, Päivi; Glumoff, Virpi; Saarela, Jann... Journal: Journal of clinical rheumatology Issue: Volume 27:Issue 8(2021) Page Start: e583 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Family With A20 Haploinsufficiency Presenting With Novel Clinical Manifestations and Challenges for Treatment. Issue 8 (December 2021) Authors: Hautala, Timo; Vähäsalo, Paula; Kuismin, Outi; Keskitalo, Salla; Rajamäki, Kristiina; Väänänen, Antti; Simojoki, Marja; Säily, Marjaana; Pelkonen, Ilpo; Tokola, Heikki; Mäkinen, Markus; Kaarteenaho, Riitta; Jartti, Airi; Hautala, Nina; Kantola, Saara; Jackson, Päivi; Glumoff, Virpi; Saarela, Jann... Journal: Journal of clinical rheumatology Issue: Volume 27:Issue 8(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association study of MMP8 gene in osteoarthritis. (2nd January 2016) Authors: Näkki, Annu; Rodriguez-Fontenla, Cristina; Gonzalez, Antonio; Harilainen, Arsi; Leino-Arjas, Päivi; Heliövaara, Markku; Eriksson, Johan G.; Tallroth, Kaj; Videman, Tapio; Kaprio, Jaakko; Saarela, Janna; Kujala, Urho M. Journal: Connective tissue research Issue: Volume 57:Number 1(2016) Page Start: 44 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetics of multiple sclerosis: lessons from polygenicity. Issue 9 (September 2022) Authors: Goris, An; Vandebergh, Marijne; McCauley, Jacob L; Saarela, Janna; Cotsapas, Chris Journal: Lancet neurology Issue: Volume 21:Issue 9(2022) Page Start: 830 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Haploinsufficiency of A20 impairs protein–protein interactome and leads into caspase-8-dependent enhancement of NLRP3 inflammasome activation. Issue 2 (17th October 2018) Authors: Rajamäki, Kristiina; Keskitalo, Salla; Seppänen, Mikko; Kuismin, Outi; Vähäsalo, Paula; Trotta, Luca; Väänänen, Antti; Glumoff, Virpi; Keskitalo, Paula; Kaarteenaho, Riitta; Jartti, Airi; Hautala, Nina; Jackson, Päivi; Nordström, Dan C; Saarela, Janna; Hautala, Timo; Eklund, Kari K; Varjosalo, Ma... Journal: RMD open Issue: Volume 4:Issue 2(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation. (December 2020) Authors: Hautala, Timo; Chen, Jie; Tervonen, Laura; Partanen, Terhi; Winqvist, Satu; Lehtonen, Johanna; Saarela, Janna; Kraatari, Minna; Kuismin, Outi; Vuorinen, Tytti; Glumoff, Virpi; Åström, Pirjo; Huuskonen, Usko; Lorenzo, Lazaro; Casanova, Jean-Laurent; Zhang, Shen-Ying; Seppänen, Mikko R.J. Journal: Neurology Issue: Volume 6:Number 6(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22. Issue 2 (10th November 2010) Authors: Evangelou, Evangelos; Valdes, Ana M; Kerkhof, Hanneke J M; Styrkarsdottir, Unnur; Zhu, YanYan; Meulenbelt, Ingrid; Lories, Rik J; Karassa, Fotini B; Tylzanowski, Przemko; Bos, Steffan D; Akune, Toru; Arden, Nigel K; Carr, Andrew; Chapman, Kay; Cupples, L Adrienne; Dai, Jin; Deloukas, Panos; Doher... Journal: Annals of the rheumatic diseases Issue: Volume 70:Issue 2(2011) Page Start: 349 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Pharmacogenomics of Hypertension: A Genome‐Wide, Placebo‐Controlled Cross‐Over Study, Using Four Classes of Antihypertensive Drugs. Issue 1 (12th May 2015) Authors: Hiltunen, Timo P.; Donner, Kati M.; Sarin, Antti‐Pekka; Saarela, Janna; Ripatti, Samuli; Chapman, Arlene B.; Gums, John G.; Gong, Yan; Cooper‐DeHoff, Rhonda M.; Frau, Francesca; Glorioso, Valeria; Zaninello, Roberta; Salvi, Erika; Glorioso, Nicola; Boerwinkle, Eric; Turner, Stephen T.; Johnson, J... Journal: Journal of the American Heart Association Issue: Volume 4:Issue 1(2015:Feb.) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Recessive MYH3 variants cause "Contractures, pterygia, and variable skeletal fusions syndrome 1B" mimicking Escobar variant multiple pterygium syndrome. Issue 11 (9th September 2020) Authors: Hakonen, Anna H.; Lehtonen, Johanna; Kivirikko, Sirpa; Keski‐Filppula, Riikka; Moilanen, Jukka; Kivisaari, Reetta; Almusa, Henrikki; Jakkula, Eveliina; Saarela, Janna; Avela, Kristiina; Aittomäki, Kristiina Journal: American journal of medical genetics Issue: Volume 182:Issue 11(2020) Page Start: 2605 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. SLC18A3 variants lead to fetal akinesia deformation sequence early in pregnancy. Issue 7 (6th May 2019) Authors: Hakonen, Anna H.; Polvi, Anne; Saloranta, Carola; Paetau, Anders; Heikkilä, Päivi; Almusa, Henrikki; Ellonen, Pekka; Jakkula, Eveliina; Saarela, Janna; Aittomäki, Kristiina Journal: American journal of medical genetics Issue: Volume 179:Issue 7(2019) Page Start: 1362 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗