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Issue Date
Title
Author(s)
2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Zhang, M.
;
Ferrari, R.
;
Tartaglia, M.C.
;
Keith, J.
;
Surace, E.I.
;
Wolf, U.
;
Sato, C.
;
Grinberg, M.
;
Liang, Y.
;
Xi, Z.
;
Dupont, K.
;
McGoldrick, P.
;
Weichert, A.
;
McKeever, P.M.
;
Schneider, R.
;
McCorkindale, M.D.
;
Manzoni, C.
;
Rademakers, R.
;
Graff-Radford, N.R.
;
Dickson, D.W.
;
et al.
2018
A four-gene lincRNA expression signature predicts risk in multiple cohorts of acute myeloid leukemia patients
Beck, D.
;
Thoms, J.
;
Palu, C.
;
Herold, T.
;
Shah, A.
;
Olivier, J.
;
Boelen, L.
;
Huang, Y.
;
Chacon, D.
;
Brown, A.
;
Babic, M.
;
Hahn, C.
;
Perugini, M.
;
Zhou, X.
;
Huntly, B.
;
Schwarzer, A.
;
Klusmann, J.-H.
;
Berdel, W.
;
Wörmann, B.
;
Büchner, T.
;
et al.
2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease
Stitziel, N.O.
;
Won, H.H.
;
Morrison, A.C.
;
Peloso, G.M.
;
Do, R.
;
Lange, L.A.
;
Fontanillas, P.
;
Gupta, N.
;
Duga, S.
;
Goel, A.
;
Farrall, M.
;
Saleheen, D.
;
Ferrario, P.
;
König, I.
;
Asselta, R.
;
Merlini, P.A.
;
Marziliano, N.
;
Notarangelo, M.F.
;
Schick, U.
;
Auer, P.
;
et al.
2014
Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing
Buchanan, D.
;
Tan, Y.
;
Walsh, M.
;
Clendenning, M.
;
Metcalf, A.
;
Ferguson, K.
;
Arnold, S.
;
Thompson, B.
;
Lose, F.
;
Parsons, M.
;
Walters, R.
;
Pearson, S.
;
Cummings, M.
;
Oehler, M.
;
Blomfield, P.
;
Quinn, M.
;
Kirk, J.
;
Stewart, C.
;
Obermair, A.
;
Young, J.
;
et al.
2017
Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study
Zewinger, S.
;
Kleber, M.E.
;
Tragante, V.
;
McCubrey, R.O.
;
Schmidt, A.F.
;
Direk, K.
;
Laufs, U.
;
Werner, C.
;
Koenig, W.
;
Rothenbacher, D.
;
Mons, U.
;
Breitling, L.P.
;
Brenner, H.
;
Jennings, R.T.
;
Petrakis, I.
;
Triem, S.
;
Klug, M.
;
Filips, A.
;
Blankenberg, S.
;
Waldeyer, C.
;
et al.
2012
Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22
Cicek, M.
;
Cunningham, J.
;
Fridley, B.
;
Serie, D.
;
Bamlet, W.
;
Diergaarde, B.
;
Haile, R.
;
Le Marchand, L.
;
Krontiris, T.
;
Younghusband, H.
;
Gallinger, S.
;
Newcomb, P.
;
Hopper, J.
;
Jenkins, M.
;
Casey, G.
;
Schumacher, F.
;
Chen, Z.
;
DeRycke, M.
;
Templeton, A.
;
Winship, I.
;
et al.
;
Lo, A.
2013
A phase 2 trial of ponatinib in Philadelphia chromosome-positive leukemias
Cortes, J.E.
;
Kim, D.W.
;
Pinilla-Ibarz, J.
;
Le Coutre, P.
;
Paquette, R.
;
Chuah, C.
;
Nicolini, F.E.
;
Apperley, J.F.
;
Khoury, H.J.
;
Talpaz, M.
;
DiPersio, J.
;
DeAngelo, D.J.
;
Abruzzese, E.
;
Rea, D.
;
Baccarani, M.
;
Müller, M.C.
;
Gambacorti-Passerini, C.
;
Wong, S.
;
Lustgarten, S.
;
Rivera, V.M.
;
et al.
2019
Chromosomal abnormalities and prognosis in NPM1-mutated acute myeloid leukemia: a pooled analysis of individual patient data from nine international cohorts
Angenendt, L.
;
Röllig, C.
;
Montesinos, P.
;
Martínez-Cuadrón, D.
;
Barragan, E.
;
García, R.
;
Botella, C.
;
Martínez, P.
;
Ravandi, F.
;
Kadia, T.
;
Kantarjian, H.M.
;
Cortes, J.
;
Juliusson, G.
;
Lazarevic, V.
;
Höglund, M.
;
Lehmann, S.
;
Recher, C.
;
Pigneux, A.
;
Bertoli, S.
;
Dumas, P.Y.
;
et al.
2019
Myocilin gene Gln368Ter variant penetrance and association with glaucoma in population-based and registry-based studies
Han, X.
;
Souzeau, E.
;
Ong, J.S.
;
An, J.
;
Siggs, O.M.
;
Burdon, K.P.
;
Best, S.
;
Goldberg, I.
;
Healey, P.R.
;
Graham, S.L.
;
Ruddle, J.B.
;
Mills, R.A.
;
Landers, J.
;
Galanopoulos, A.
;
White, A.J.R.
;
Casson, R.
;
Mackey, D.A.
;
Hewitt, A.W.
;
Gharahkhani, P.
;
Craig, J.E.
;
et al.
2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Jansen, I.E.
;
Ye, H.
;
Heetveld, S.
;
Lechler, M.C.
;
Michels, H.
;
Seinstra, R.I.
;
Lubbe, S.J.
;
Drouet, V.
;
Lesage, S.
;
Majounie, E.
;
Gibbs, J.R.
;
Nalls, M.A.
;
Ryten, M.
;
Botia, J.A.
;
Vandrovcova, J.
;
Simon-Sanchez, J.
;
Castillo-Lizardo, M.
;
Rizzu, P.
;
Blauwendraat, C.
;
Chouhan, A.K.
;
et al.
Discover
Author
5
Vos, T.
4
Buchanan, D.
4
Choi, D.
4
Clendenning, M.
4
Czyz, C.
4
Dailey, R.
4
Dolman, P.
4
Foster, J.
4
Grossniklaus, H.
4
Harrington, C.
.
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32
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29
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28
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20
Treatment Outcome
17
Genetic Predisposition to Disease
17
Polymorphism, Single Nucleotide
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