Riitta Sallinen

Confirmation of the Type 2 Myotonic Dystrophy (CCTG) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect

Linda L. Bachinski, Bjarne Udd, G. Meola et al. · The American Journal of Human Genetics · 2003 · 140 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Individual and stable autoantibody repertoires in healthy individuals

Maja Neiman, Cecilia Hellström, David Just et al. · Autoimmunity · 2019 · 74 citations · Full text

Life Sciences, Immunology, Molecular Biology +15

New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)

Riitta Sallinen, Anna Vihola, Linda L. Bachinski et al. · Neuromuscular Disorders · 2004 · 45 citations

Life Sciences, Genetics, Molecular Genetics +9

Elevated MBL Concentrations Are Not an Indication of Association Between the <i>MBL2</i> Gene and Type 1 Diabetes or Diabetic Nephropathy

Mari Kaunisto, Lisa Sjölind, Riitta Sallinen et al. · Diabetes · 2009 · 38 citations · Full text

Medicine, Genetics, Molecular Genetics +13

Multiomics and digital monitoring during lifestyle changes reveal independent dimensions of human biology and health

Francesco Marabita, T. E. JAMES, Anu Karhu et al. · Cell Systems · 2021 · 37 citations

Life Sciences, Health Informatics, Health Sciences +14