Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defects.
Osteoporosis International : A Journal Established As Result Of Cooperation Between The European Foundation For Osteoporosis And The National Osteoporosis Foundation Of The Usa
Yang, Lin L; Liu, Bo B; Dong, Xinran X; Wu, Jing J; Sun, Chengjun C; Xi, Li L; Cheng, Ruoqian R; Wu, Bingbing B; Wang, Huijun H; Tong, Shiyuan S; Wang, Dahui D; Luo, Feihong F
Genetic polymorphisms in ADRB2 and ADRB1 are associated with differential survival in heart failure patients taking β-blockers.
The Pharmacogenomics Journal
Guerra, Leonardo A LA; Lteif, Christelle C; Arwood, Meghan J MJ; McDonough, Caitrin W CW; Dumeny, Leanne L; Desai, Ankit A AA; Cavallari, Larisa H LH; Duarte, Julio D JD
Brain volumetric deficits in MAPT mutation carriers: a multisite study.
Annals Of Clinical And Translational Neurology
Chu, Stephanie A SA; Flagan, Taru M TM; Staffaroni, Adam M AM; Jiskoot, Lize C LC; Deng, Jersey J; Spina, Salvatore S; Zhang, Liwen L; Sturm, Virginia E VE; Yokoyama, Jennifer S JS; Seeley, William W WW; Papma, Janne M JM; Geschwind, Dan H DH; Rosen, Howard J HJ; Boeve, Bradley F BF; Boxer, Adam L AL; Heuer, Hilary W HW; Forsberg, Leah K LK; Brushaber, Danielle E DE; Grossman, Murray M; Coppola, Giovanni G; Dickerson, Bradford C BC; Bordelon, Yvette M YM; Faber, Kelley K; Feldman, Howard H HH; Fields, Julie A JA; Fong, Jamie C JC; Foroud, Tatiana T; Gavrilova, Ralitza H RH; Ghoshal, Nupur N; Graff-Radford, Neill R NR; Hsiung, Ging-Yuek Robin GR; Huey, Edward D ED; Irwin, David J DJ; Kantarci, Kejal K; Kaufer, Daniel I DI; Karydas, Anna M AM; Knopman, David S DS; Kornak, John J; Kramer, Joel H JH; Kukull, Walter A WA; Lapid, Maria I MI; Litvan, Irene I; Mackenzie, Ian R A IRA; Mendez, Mario F MF; Miller, Bruce L BL; Onyike, Chiadi U CU; Pantelyat, Alexander Y AY; Rademakers, Rosa R; Marisa Ramos, Eliana E; Roberson, Erik D ED; Carmela Tartaglia, Maria M; Tatton, Nadine A NA; Toga, Arthur W AW; Vetor, Ashley A; Weintraub, Sandra S; Wong, Bonnie B; Wszolek, Zbigniew K ZK; , ; Van Swieten, John C JC; Lee, Suzee E SE
Seidlitz, Therese T; Merker, Sebastian R SR; Rothe, Alexander A; Zakrzewski, Falk F; von Neubeck, Cläre C; Grützmann, Konrad K; Sommer, Ulrich U; Schweitzer, Christine C; Schölch, Sebastian S; Uhlemann, Heike H; Gaebler, Anne-Marlene AM; Werner, Kristin K; Krause, Mechthild M; Baretton, Gustavo B GB; Welsch, Thilo T; Koo, Bon-Kyoung BK; Aust, Daniela E DE; Klink, Barbara B; Weitz, Jürgen J; Stange, Daniel E DE
Recurrent inactivating RASA2 mutations in melanoma.
Nature Genetics
Arafeh, Rand R; Qutob, Nouar N; Emmanuel, Rafi R; Keren-Paz, Alona A; Madore, Jason J; Elkahloun, Abdel A; Wilmott, James S JS; Gartner, Jared J JJ; Di Pizio, Antonella A; Winograd-Katz, Sabina S; Sindiri, Sivasish S; Rotkopf, Ron R; Dutton-Regester, Ken K; Johansson, Peter P; Pritchard, Antonia L AL; Waddell, Nicola N; Hill, Victoria K VK; Lin, Jimmy C JC; Hevroni, Yael Y; Rosenberg, Steven A SA; Khan, Javed J; Ben-Dor, Shifra S; Niv, Masha Y MY; Ulitsky, Igor I; Mann, Graham J GJ; Scolyer, Richard A RA; Hayward, Nicholas K NK; Samuels, Yardena Y
Whole genome analyses of a well-differentiated liposarcoma reveals novel SYT1 and DDR2 rearrangements.
Plos One
Egan, Jan B JB; Barrett, Michael T MT; Champion, Mia D MD; Middha, Sumit S; Lenkiewicz, Elizabeth E; Evers, Lisa L; Francis, Princy P; Schmidt, Jessica J; Shi, Chang-Xin CX; Van Wier, Scott S; Badar, Sandra S; Ahmann, Gregory G; Kortuem, K Martin KM; Boczek, Nicole J NJ; Fonseca, Rafael R; Craig, David W DW; Carpten, John D JD; Borad, Mitesh J MJ; Stewart, A Keith AK
No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease.
Bmc Medical Genetics
Sánchez-Juan, Pascual P; Bishop, Matthew T MT; Green, Alison A; Giannattasio, Claudia C; Arias-Vasquez, Alejandro A; Poleggi, Anna A; Knight, Richard S G RS; van Duijn, Cornelia M CM