Marita Lipsanen‐Nyman

The mutation spectrum in RECQL4 diseases

H. Annika Siitonen, Jenni Sotkasiira, Martine Biervliet et al. · European Journal of Human Genetics · 2008 · 233 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism

Kristiina Avela, Marita Lipsanen‐Nyman, Niina Idänheimo et al. · Nature Genetics · 2000 · 189 citations

Life Sciences, Genetics, Molecular Genetics +7

Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia

Lars Feuk, Aino Kalervo, Marita Lipsanen‐Nyman et al. · The American Journal of Human Genetics · 2006 · 185 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes

Markku Lehto, C. Wipemo, S A Ivarsson et al. · Diabetologia · 1999 · 137 citations · Full text

Medicine, Genetics, Molecular Genetics +15

A Narrow Segment of Maternal Uniparental Disomy of Chromosome 7q31-qter in Silver-Russell Syndrome Delimits a Candidate Gene Region

Katariina Hannula‐Jouppi, Marita Lipsanen‐Nyman, Tero Kontiokari et al. · The American Journal of Human Genetics · 2001 · 127 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13