Eija H. Seppälä

Germline Alterations of the RNASEL Gene, a Candidate HPC1 Gene at 1q25, in Patients and Families with Prostate Cancer

Annika Rökman, Tarja Ikonen, Eija H. Seppälä et al. · The American Journal of Human Genetics · 2002 · 239 citations · Full text

Medicine, Genetics, Molecular Genetics +15

CHEK2 variants associate with hereditary prostate cancer

Eija H. Seppälä, Tarja Ikonen, Nina Mononen et al. · British Journal of Cancer · 2003 · 145 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex

Maria Wilbe, Päivi Jokinen, Katarina Truvé et al. · Nature Genetics · 2010 · 139 citations

Life Sciences, Genetics, Molecular Genetics +14

A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers

Fabiana Farias, Rong Zeng, Gary S. Johnson et al. · Neurobiology of Disease · 2011 · 128 citations · Full text

Life Sciences, Molecular Genetics, Pathobiology +6

LGI2 Truncation Causes a Remitting Focal Epilepsy in Dogs

Eija H. Seppälä, Tarja S. Jokinen, Masaki Fukata et al. · PLoS Genetics · 2011 · 109 citations · Full text

Medicine, Genetics, Neurology +17