Agata Skórka

Lymphoid tyrosine phosphatase (<i>PTPN22</i>/LYP) variant and Graves’ disease in a Polish population: association and gene dose‐dependent correlation with age of onset

Agata Skórka, Tomasz Bednarczuk, Ewa Bar‐Andziak et al. · Clinical Endocrinology · 2005 · 127 citations

M34T and V37I mutations in <i>GJB2</i> associated hearing impairment: Evidence for pathogenicity and reduced penetrance

Agnieszka Pollak, Agata Skórka, Małgorzata Mueller‐Malesińska et al. · American Journal of Medical Genetics Part A · 2007 · 104 citations

Molecular background of polyendocrinopathy–candidiasis–ectodermal dystrophy syndrome in a Polish population: novel <i>AIRE</i> mutations and an estimate of disease prevalence

Bartosz Stolarski, Ewa Pronicka, L Korniszewski et al. · Clinical Genetics · 2006 · 77 citations

Genetics, Immunodeficiencies, Genetic Epidemiology +19

The risk factors of ketoacidosis in children with newly diagnosed type 1 diabetes mellitus

Agnieszka Szypowska, Agata Skórka · Pediatric Diabetes · 2010 · 75 citations

Association of CD40 Gene Polymorphism (C-1T) with Susceptibility and Phenotype of Graves' Disease

Alina Kuryłowicz, Dorota Kula, Agata Skórka et al. · Thyroid · 2005 · 64 citations