Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene

Por Deng, Zemin, Morse, Jane H., Slager, Susan L., Cuervo, Nieves, Moore, Keith J., Venetos, George, Kalachikov, Sergey, Cayanis, Eftihia, Fischer, Stuart G., Barst, Robyn J., Hodge, Susan E., Knowles, James A.
Publicado em 2000

Malic Enzyme 2 May Underlie Susceptibility to Adolescent-Onset Idiopathic Generalized Epilepsy

Por Greenberg, David A., Cayanis, Eftihia, Strug, Lisa, Marathe, Sudhir, Durner, Martina, Pal, Deb K., Alvin, Gabriele B., Klotz, Irene, Dicker, Elisa, Shinnar, Shlomo, Bromfield, Edward B., Resor, Stanley, Cohen, Jeffrey, Moshe, Solomon L., Harden, Cynthia, Kang, Harriet
Publicado em 2005

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

Por Kalachikov, Sergey, Evgrafov, Oleg, Ross, Barbara, Winawer, Melodie, Barker-Cummings, Christie, Boneschi, Filippo Martinelli, Choi, Chang, Morozov, Pavel, Das, Kamna, Teplitskaya, Elita, Yu, Andrew, Cayanis, Eftihia, Penchaszadeh, Graciela, Kottmann, Andreas H., Pedley, Timothy A., Hauser, W. Allen, Ottman, Ruth, Gilliam, T. Conrad
Publicado em 2002