Tarja Mononen

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Claire Redin, Harrison Brand, Ryan L. Collins et al. · Nature Genetics · 2016 · 354 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis et al. · Nature Genetics · 2005 · 264 citations

Life Sciences, Genetics, Neuroscience +12

Chromosome 2q terminal deletion: Report of 6 new patients and review of phenotype‐breakpoint correlations in 66 individuals

Kari Casas, Tarja Mononen, Claudia N. Mikail et al. · American Journal of Medical Genetics Part A · 2004 · 95 citations

Life Sciences, Genetics, Molecular Genetics +12

More severe epilepsy and cognitive impairment in the offspring of a mother with mosaicism for the ring 20 chromosome

Eila Herrgård, Tarja Mononen, Esa Mervaala et al. · Epilepsy Research · 2006 · 94 citations

Life Sciences, Genetics, Molecular Genetics +16

Risk of obstetric cholestasis in sisters of index patients

M‐L Eloranta, Seppo Heinonen, Tarja Mononen et al. · Clinical Genetics · 2001 · 74 citations

Medicine, Genetics, Obstetrics +12