Marja‐Leena Väisänen

Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles

Sarah L. Nolin, W. Ted Brown, Anne Glicksman et al. · The American Journal of Human Genetics · 2003 · 418 citations · Full text

Allelic Variant, Genetic Disorder, Genetics +6

The effect of withdrawal of food iron fortification in Sweden as studied with phlebotomy in subjects with genetic hemochromatosis

K. Sigvard Olsson, Marja‐Leena Väisänen, Jan Konar et al. · European Journal of Clinical Nutrition · 1997 · 53 citations

Anemia, Nutrition, Nutritional Requirement +8

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.

Graeme Suthers, John C. Mulley, Marie‐Antoinette Voelckel et al. · PubMed · 1991 · 44 citations

Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented

Eve Õiglane‐Shlik, Tiina Talvik, Riina Žordania et al. · American Journal of Medical Genetics Part A · 2006 · 37 citations

Connexin 26 mutations and nonsyndromic hearing impairment in Northern Finland

Tuija Löppönen, Marja‐Leena Väisänen, Mirja Luotonen et al. · The Laryngoscope · 2003 · 33 citations