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Dazzo, Emanuela; Fanciulli, Manuela; Serioli, Elena et al. (2015) Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy. Am J Hum Genet 96:992-1000
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Helbig, Ingo; Hodge, Susan E; Ottman, Ruth (2013) Familial cosegregation of rare genetic variants with disease in complex disorders. Eur J Hum Genet 21:444-50
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Van Gompel, Jamie J; Ottman, Ruth; Worrell, Gregory A et al. (2012) Use of anterior temporal lobectomy for epilepsy in a community-based population. Arch Neurol 69:1476-81
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Ho, Yuan-Yuan; Ionita-Laza, Iuliana; Ottman, Ruth (2012) Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF. Neurology 78:563-8
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Ionita-Laza, Iuliana; Ottman, Ruth (2011) Study designs for identification of rare disease variants in complex diseases: the utility of family-based designs. Genetics 189:1061-8
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Shostak, Sara; Zarhin, Dana; Ottman, Ruth (2011) What's at stake? Genetic information from the perspective of people with epilepsy and their family members. Soc Sci Med 73:645-54
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Madsen, Ann M; Ottman, Ruth; Hodge, Susan E (2011) Causal models for investigating complex genetic disease: II. what causal models can tell us about penetrance for additive, heterogeneity, and multiplicative two-locus models. Hum Hered 72:63-72
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Madsen, Ann M; Hodge, Susan E; Ottman, Ruth (2011) Causal models for investigating complex disease: I. A primer. Hum Hered 72:54-62
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Ottman, Ruth; Hirose, Shinichi; Jain, Satish et al. (2010) Genetic testing in the epilepsies--report of the ILAE Genetics Commission. Epilepsia 51:655-70
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Heiman, Gary A; Kamberakis, Kay; Gill, Richard et al. (2010) Evaluation of depression risk in LGI1 mutation carriers. Epilepsia 51:1685-90
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Showing the most recent 10 out of 23 publications
