Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT.
Acta Neuropathologica Communications
Jungwirth, Gerhard G; Warta, Rolf R; Beynon, Christopher C; Sahm, Felix F; von Deimling, Andreas A; Unterberg, Andreas A; Herold-Mende, Christel C; Jungk, Christine C
Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach.
Plos One
Hennings, Johannes M JM; Kohli, Martin A MA; Czamara, Darina D; Giese, Maria M; Eckert, Anne A; Wolf, Christiane C; Heck, Angela A; Domschke, Katharina K; Arolt, Volker V; Baune, Bernhard T BT; Horstmann, Sonja S; Brückl, Tanja T; Klengel, Torsten T; Menke, Andreas A; Müller-Myhsok, Bertram B; Ising, Marcus M; Uhr, Manfred M; Lucae, Susanne S
Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.
American Journal Of Medical Genetics. Part A
Shi, Min M; Murray, Jeffrey C JC; Marazita, Mary L ML; Munger, Ronald G RG; Ruczinski, Ingo I; Hetmanski, Jacqueline B JB; Wu, Tao T; Murray, Tanda T; Redett, Richard J RJ; Wilcox, Allen J AJ; Lie, Rolv T RT; Jabs, Ethylin Wang EW; Wu-Chou, Yah Huei YH; Chen, Philip K PK; Wang, Hong H; Ye, Xiaoqian X; Yeow, Vincent V; Chong, Samuel S SS; Shi, Bing B; Christensen, Kaare K; Scott, Alan F AF; Patel, Poorav P; Cheah, Felicia F; Beaty, Terri H TH