Auli Sirén

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

Michael Steffens, Costin Leu, Ann‐Kathrin Ruppert et al. · Human Molecular Genetics · 2012 · 149 citations · Full text

X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes

Anju K. Philips, Auli Sirén, Kristiina Avela et al. · Orphanet Journal of Rare Diseases · 2014 · 81 citations · Full text

Linkage and association analysis of CACNG3 in childhood absence epilepsy

Kate V. Everett, Barry A. Chioza, Jean Aicardi et al. · European Journal of Human Genetics · 2007 · 73 citations · Full text

Association Analysis, Molecular Neuroscience, Pediatrics +5

Beneficial effects of antiepileptic medication on absence seizures and cognitive functioning in children

Auli Sirén, Anneli Kylliäinen, M. Tenhunen et al. · Epilepsy & Behavior · 2007 · 51 citations

Neuropsychological Functioning, Neuropsychology, Cognitive Functioning +7

Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland

Irma Järvelä, Tuomo Määttä, Anushree Acharya et al. · Human Genetics · 2021 · 51 citations · Full text