| A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception E Einarsdottir, A Carlsson, J Minde, G Toolanen, O Svensson, G Solders, ... Human molecular genetics 13 (8), 799-805, 2004 | 361 | 2004 |
| Localization of a susceptibility gene for common forms of stroke to 5q12 S Gretarsdottir, S Sveinbjörnsdottir, HH Jonsson, F Jakobsson, ... The American Journal of Human Genetics 70 (3), 593-603, 2002 | 294 | 2002 |
| Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes M Kaustio, E Haapaniemi, H Göös, T Hautala, G Park, J Syrjänen, ... Journal of Allergy and Clinical Immunology 140 (3), 782-796, 2017 | 125 | 2017 |
| IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease E Einarsdottir, LLE Koskinen, E Dukes, K Kainu, S Suomela, ... BMC medical genetics 10 (1), 8, 2009 | 111 | 2009 |
| Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish population AS Parmar, N Alakulppi, P Paavola‐Sakki, K Kurppa, L Halme, M Färkkilä, ... HLA 80 (6), 488-493, 2012 | 107 | 2012 |
| Association of IL23R, TNFRSF1A, and HLA‐DRB1* 0103 allele variants with inflammatory bowel disease phenotypes in the Finnish population M Lappalainen, L Halme, U Turunen, P Saavalainen, E Einarsdottir, ... Inflammatory bowel diseases 14 (8), 1118-1124, 2008 | 103 | 2008 |
| Single-cell transcriptome analysis of endometrial tissue K Krjutškov, S Katayama, M Saare, M Vera-Rodriguez, D Lubenets, ... Human Reproduction 31 (4), 844-853, 2016 | 101 | 2016 |
| Influence of female hormonal factors, in relation to autoantibodies and genetic markers, on the development of rheumatoid arthritis in northern Sweden: a case-control study E Berglin, H Kokkonen, E Einarsdottir, Å Ågren, S Rantapää Dahlqvist Scandinavian journal of rheumatology 39 (6), 454-460, 2010 | 90 | 2010 |
| The CTLA4 region as a general autoimmunity factor: an extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto … E Einarsdottir, I Söderström, A Löfgren-Burström, S Haraldsson, ... European journal of human genetics 11 (1), 81-84, 2003 | 87 | 2003 |
| Genetics and pathogenesis of idiopathic scoliosis A Grauers, E Einarsdottir, P Gerdhem Scoliosis and Spinal Disorders 11 (1), 45, 2016 | 86 | 2016 |
| Tyrosine kinase 2 and interferon regulatory factor 5 polymorphisms are associated with discoid and subacute cutaneous lupus erythematosus TM Järvinen, A Hellquist, S Koskenmies, E Einarsdottir, LLE Koskinen, ... Experimental dermatology 19 (2), 123-131, 2010 | 83 | 2010 |
| MANF protects human pancreatic beta cells against stress-induced cell death E Hakonen, V Chandra, CL Fogarty, NYL Yu, J Ustinov, S Katayama, ... Diabetologia 61 (10), 2202-2214, 2018 | 77 | 2018 |
| Estrogen receptor β, a regulator of androgen receptor signaling in the mouse ventral prostate W Wu, L Maneix, J Insunza, I Nalvarte, P Antonson, J Kere, NYL Yu, ... Proceedings of the National Academy of Sciences 114 (19), E3816-E3822, 2017 | 68 | 2017 |
| Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis A Grauers, J Wang, E Einarsdottir, A Simony, A Danielsson, K Åkesson, ... The Spine Journal 15 (10), 2239-2246, 2015 | 68 | 2015 |
| Unexpectedly high prevalence of common variable immunodeficiency in Finland JS Selenius, T Martelius, S Pikkarainen, S Siitonen, E Mattila, ... Frontiers in immunology, 1190, 2017 | 64 | 2017 |
| The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency K Haimila, E Einarsdottir, A De Kauwe, LLE Koskinen, ... Genes and immunity 10 (2), 151-161, 2009 | 61 | 2009 |
| Polymorphisms of the ITGAM gene confer higher risk of discoid cutaneous than of systemic lupus erythematosus TM Järvinen, A Hellquist, S Koskenmies, E Einarsdottir, J Panelius, ... PLoS One 5 (12), e14212, 2010 | 55 | 2010 |
| Novel TMEM173 mutation and the role of disease modifying alleles S Keskitalo, E Haapaniemi, E Einarsdottir, K Rajamäki, H Heikkilä, ... Frontiers in Immunology 10, 2770, 2019 | 53 | 2019 |
| Comprehensive mapping of the effects of azacitidine on DNA methylation, repressive/permissive histone marks and gene expression in primary cells from patients with MDS and MDS … M Tobiasson, H Abdulkadir, A Lennartsson, S Katayama, F Marabita, ... Oncotarget, 2017 | 53 | 2017 |
| Melatonin pathway genes are associated with progressive subtypes and disability status in multiple sclerosis among Finnish patients R Natarajan, E Einarsdottir, A Riutta, S Hagman, M Raunio, N Mononen, ... Journal of Neuroimmunology 250 (1), 106-110, 2012 | 51 | 2012 |
Ádány RózaUniversity of DebrecenVerified email at med.unideb.hu
