Kars, Meltem Ece

Genome-wide prediction of pathogenic gain- and loss-of-function variants from ensemble learning of a diverse feature set

Stein, D., Sevim Bayrak, Ç., Wu, Y., Kars, M. E., Stenson, P. D., Cooper, D. N., Schlessinger, A., & Itan, Y. (2022) · Genome Medicine

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 53

Genome-wide prediction of pathogenic gain- and loss-of-function variants from ensemble learning of a diverse feature set

Stein, D., Kars, M. E., Wu, Y., Bayrak, Ç. S., Stenson, P. D., Cooper, D. N., Schlessinger, A., & Itan, Y. (2023) · Genome Medicine

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 53

Human CRY1 variants associate with attention deficit/hyperactivity disorder

Onat, O. E., Kars, M. E., Gül, Ş., Bilguvar, K., Wu, Y., Özhan, A., Aydın, C., Başak, A. N., Trusso, M. A., Goracci, A., et al. (2020) · Journal of Clinical Investigation

Circadian rhythm and melatoninAttention Deficit Hyperactivity Disorder

Cited by 47