Marja Hietala
mahehi@utu.fi +358 50 520 1822 Kiinamyllynkatu 10 Turku |
Publications
- Primary mediastinal large B-cell lymphoma segregating in a family: exome sequencing identifies MLL as a candidate predisposition gene (2013)
- Blood
(A1 Refereed original research article in a scientific journal) - Exploring the transcriptomic variation caused by the Finnish founder mutation of lysinuric protein intolerance (LPI) (2012)
- Molecular Genetics and Metabolism
(A1 Refereed original research article in a scientific journal) - High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results (2012)
- BMC Medical Genetics
(A1 Refereed original research article in a scientific journal) - Lastentaudit ja periytyminen (2010) Lastentaudit Penttinen M, Hietala M
(D2 Article in a professional compilation book) - Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations (2010)
- European Journal of Paediatric Neurology
(A1 Refereed original research article in a scientific journal) - No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome (2010)
- Familial Cancer
(A1 Refereed original research article in a scientific journal)



