Tuija Löppönen

GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann et al. · The American Journal of Human Genetics · 2005 · 551 citations · Full text

Genetic Disorder, Genetics, Audiology +9

Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis

Sylvain Hanein, Isabelle Perrault, S. Gerber et al. · Human Mutation · 2004 · 348 citations

Prediction of insulin-dependent diabetes mellitus in siblings of children with diabetes. A population-based study. The Childhood Diabetes in Finland Study Group.

Petri Kulmala, K. Savola, Jacob Petersen et al. · Journal of Clinical Investigation · 1998 · 288 citations · Full text

Genetic Epidemiology, Diagnosis, Unselected Population +19

Growth and Biochemical Markers of Growth in Children With Snoring and Obstructive Sleep Apnea

Peter Nieminen, Tuija Löppönen, Uolevi Tolonen et al. · PEDIATRICS · 2002 · 269 citations

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children

Johanna Uusimaa, Jukka S. Moilanen, Leena Vainionpää et al. · Annals of Neurology · 2007 · 107 citations