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Issue Date
Title
Author(s)
2015
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis
Ramos-Brossier, M.
;
Montani, C.
;
Lebrun, N.
;
Gritti, L.
;
Martin, C.
;
Seminatore-Nole, C.
;
Toussaint, A.
;
Moreno, S.
;
Poirier, K.
;
Dorseuil, O.
;
Chelly, J.
;
Hackett, A.
;
Gecz, J.
;
Bieth, E.
;
Faudet, A.
;
Heron, D.
;
Kooy, R.
;
Loeys, B.
;
Humeau, Y.
;
Sala, C.
;
et al.
2014
Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function
Tang, W.
;
Kowgier, M.
;
Loth, D.
;
Soler Artigas, M.
;
Joubert, B.
;
Hodge, E.
;
Gharib, S.
;
Smith, A.
;
Ruczinski, I.
;
Gudnason, V.
;
Mathias, R.
;
Harris, T.
;
Hansel, N.
;
Launer, L.
;
Barnes, K.
;
Hansen, J.
;
Albrecht, E.
;
Aldrich, M.
;
Allerhand, M.
;
Barr, R.
;
et al.
;
Chen, L.
2012
A genome-wide association search for type 2 diabetes genes in African Americans
Palmer, N.
;
McDonough, C.
;
Hicks, P.
;
Roh, B.
;
Wing, M.
;
Sandy An, S.
;
Hester, J.
;
Cooke, J.
;
Bostrom, M.
;
Rudock, M.
;
Talbert, M.
;
Lewis, J.
;
DIAGRAM Consortium,
;
MAGIC Consortium,
;
Ferrara, A.
;
Lu, L.
;
Ziegler, J.
;
Sale, M.
;
Divers, J.
;
Shriner, D.
;
et al.
;
Kronenberg, F.
2016
A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples
Cohen, O.
;
Weickert, T.
;
Hess, J.
;
Paish, L.
;
McCoy, S.
;
Rothmond, D.
;
Galletly, C.
;
Liu, D.
;
Weinberg, D.
;
Huang, X.
;
Xu, Q.
;
Shen, Y.
;
Zhang, D.
;
Yue, W.
;
Yan, J.
;
Wang, L.
;
Lu, T.
;
He, L.
;
Shi, Y.
;
Xu, M.
;
et al.
2018
A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetes
Van Zuydam, N.R.
;
Ahlqvist, E.
;
Sandholm, N.
;
Deshmukh, H.
;
William Rayner, N.
;
Abdalla, M.
;
Ladenvall, C.
;
Ziemek, D.
;
Fauman, E.
;
Robertson, N.R.
;
McKeigue, P.M.
;
Valo, E.
;
Forsblom, C.
;
Harjutsalo, V.
;
Perna, A.
;
Rurali, E.
;
Loredana Marcovecchio, M.
;
Igo, R.P.
;
Salem, R.M.
;
Perico, N.
;
et al.
2014
LgG4 immunostaining and its implications in orbital inflammatory disease
Wong, A.
;
Planck, S.
;
Choi, D.
;
Harrington, C.
;
Troxell, M.
;
Houghton, D.
;
Stauffer, P.
;
Wilson, D.
;
Grossniklaus, H.
;
Dailey, R.
;
Ng, J.
;
Steele, E.
;
Harris, G.
;
Czyz, C.
;
Foster, J.
;
White, V.
;
Dolman, P.
;
Kazim, M.
;
Patel, P.
;
Edward, D.
;
et al.
;
Wallace, G.
2015
Efficacy of thiopurines and adalimumab in preventing Crohn's disease recurrence in high-risk patients - a POCER study analysis
De Cruz, P.
;
Kamm, M.A.
;
Hamilton, A.L.
;
Ritchie, K.J.
;
Krejany, E.O.
;
Gorelik, A.
;
Liew, D.
;
Prideaux, L.
;
Lawrance, I.C.
;
Andrews, J.M.
;
Bampton, P.A.
;
Jakobovits, S.
;
Florin, T.H.
;
Gibson, P.R.
;
Debinski, H.
;
Gearry, R.B.
;
Macrae, F.A.
;
Leong, R.W.
;
Kronborg, I.
;
Radford-Smith, G.
;
et al.
2015
Randomized phase II study of carboplatin and paclitaxel with either linifanib or placebo for advanced nonsquamous non–small-cell lung cancer
Ramalingam, S.S.
;
Shtivelband, M.
;
Soo, R.A.
;
Barrios, C.H.
;
Makhson, A.
;
Segalla, J.G.
;
Pittman, K.B.
;
Kolman, P.
;
Pereira, J.R.
;
Srkalovic, G.
;
Belani, C.P.
;
Axelrod, R.
;
Owonikoko, T.K.
;
Qin, Q.
;
Qian, J.
;
McKeegan, E.M.
;
Devanarayan, V.
;
McKee, M.D.
;
Ricker, J.L.
;
Carlson, D.M.
;
et al.
2016
HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study
Friez, M.
;
Brooks, S.
;
Stevenson, R.
;
Field, M.
;
Basehore, M.
;
Adès, L.
;
Sebold, C.
;
Mcgee, S.
;
Saxon, S.
;
Skinner, C.
;
Craig, M.
;
Murray, L.
;
Simensen, R.
;
Yap, Y.
;
Shaw, M.
;
Gardner, A.
;
Corbett, M.
;
Kumar, R.
;
Bosshard, M.
;
Van Loon, B.
;
et al.
2015
Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene
Ishibashi, M.
;
Manning, E.
;
Shoubridge, C.
;
Krecsmarik, M.
;
Hawkins, T.
;
Giacomotto, J.
;
Zhao, T.
;
Mueller, T.
;
Bader, P.
;
Cheung, S.
;
Stankiewicz, P.
;
Bain, N.
;
Hackett, A.
;
Reddy, C.
;
Mechaly, A.
;
Peers, B.
;
Wilson, S.
;
Lenhard, B.
;
Bally-Cuif, L.
;
Gecz, J.
;
et al.
Discover
Author
6
Gecz, J.
5
Vos, T.
4
Choi, D.
4
Czyz, C.
4
Dailey, R.
4
Dolman, P.
4
Foster, J.
4
Grossniklaus, H.
4
Hackett, A.
4
Harrington, C.
.
next >
Subject
101
Female
80
Middle Aged
51
Aged
40
Adolescent
33
Young Adult
26
Child
22
Aged, 80 and over
21
Mutation
19
Child, Preschool
17
Polymorphism, Single Nucleotide
.
next >
Date issued
9
2020 - 2021
89
2010 - 2019
9
2000 - 2009
1
1997 - 1999