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Issue Date
Title
Author(s)
2013
PIK3CA and PTEN gene and exon mutation-specific clinicopathologic and molecular associations in colorectal cancer
Day, F.
;
Jorissen, R.
;
Lipton, L.
;
Mouradov, D.
;
Sakthianandeswaren, A.
;
Christie, M.
;
Li, S.
;
Tsui, C.
;
Tie, J.
;
Desai, J.
;
Xu, Z.
;
Molloy, P.
;
Whitehall, V.
;
Leggett, B.
;
Jones, I.
;
McLaughlin, S.
;
Ward, R.
;
Hawkins, N.
;
Ruszkiewicz, A.
;
Moore, J.
;
et al.
2015
Crohn's disease management after intestinal resection: a randomised trial
De Cruz, P.
;
Kamm, M.
;
Hamilton, A.
;
Ritchie, K.
;
Krejany, E.
;
Gorelik, A.
;
Liew, D.
;
Prideaux, L.
;
Lawrance, I.
;
Andrews, J.
;
Bampton, P.
;
Gibson, P.
;
Sparrow, M.
;
Leong, R.
;
Florin, T.
;
Gearry, R.
;
Radford-Smith, G.
;
Macrae, F.
;
Debinski, H.
;
Selby, W.
;
et al.
2013
Phase III randomized, placebo-controlled study of cetuximab plus brivanib alaninate versus cetuximab plus placebo in patients with metastatic, chemotherapy-refractory, wild-type K-RAS colorectal carcinoma: The NCIC clinical trials group and AGITG co.
Siu, L.
;
Shapiro, J.
;
Jonker, D.
;
Karapetis, C.
;
Zalcberg, J.
;
Simes, J.
;
Couture, F.
;
Moore, M.
;
Price, T.
;
Siddiqui, J.
;
Nott, L.
;
Charpentier, D.
;
Liauw, W.
;
Sawyer, M.
;
Jefford, M.
;
Magoski, N.
;
Haydon, A.
;
Walters, I.
;
Ringash, J.
;
Tu, D.
;
et al.
2012
Glucokinase links Kruppel-like factor 6 to the regulation of hepatic insulin sensitivity in nonalcoholic fatty liver disease
Bechmann, L.
;
Gastaldelli, A.
;
Vetter, D.
;
Patman, G.
;
Pascoe, L.
;
Hannivoort, R.
;
Lee, U.
;
Fiel, I.
;
Munoz, U.
;
Ciociaro, D.
;
Lee, Y.
;
Buzzigoli, E.
;
Miele, L.
;
Hui, K.
;
Bugianesi, E.
;
Burt, A.
;
Day, C.
;
Mari, A.
;
Agius, L.
;
Walker, M.
;
et al.
2013
Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features
Bonnefond, A.
;
Raimondo, A.
;
Stutzmann, F.
;
Ghoussaini, M.
;
Ramachandrappa, S.
;
Bersten, D.
;
Durand, E.
;
Vatin, V.
;
Balkau, B.
;
Lantieri, O.
;
Raverdy, V.
;
Pattou, F.
;
Van Hul, W.
;
Van Gaal, L.
;
Peet, D.
;
Weill, J.
;
Miller, J.
;
Horber, F.
;
Goldstone, A.
;
Driscoll, D.
;
et al.
2016
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
van Bon, B.W.M.
;
Coe, B.P.
;
Bernier, R.
;
Green, C.
;
Gerdts, J.
;
Witherspoon, K.
;
Kleefstra, T.
;
Willemsen, M.H.
;
Kumar, R.
;
Bosco, P.
;
Fichera, M.
;
Li, D.
;
Amaral, D.
;
Cristofoli, F.
;
Peeters, H.
;
Haan, E.
;
Romano, C.
;
Mefford, H.C.
;
Scheffer, I.
;
Gecz, J.
;
et al.
2012
Pemetrexed versus pemetrexed and carboplatin as second-line chemotherapy in advanced non-small-cell lung cancer: Results of the GOIRC 02-2006 randomized phase II study and pooled analysis with the NVALT7 trial
Ardizzoni, A.
;
Tiseo, M.
;
Boni, L.
;
Vincent, A.
;
Passalacqua, R.
;
Buti, S.
;
Amoroso, D.
;
Camerini, A.
;
Labianca, R.
;
Genestreti, G.
;
Boni, C.
;
Ciuffreda, L.
;
Di Costanzo, F.
;
De Marinis, F.
;
Crino, L.
;
Santo, A.
;
Pazzola, A.
;
Barbieri, F.
;
Zilembo, N.
;
Colantonio, I.
;
et al.
2011
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Yokoyama, S.
;
Woods, S.
;
Boyle, G.
;
Aoude, L.
;
MacGregor, S.
;
Zismann, V.
;
Gartside, M.
;
Cust, A.
;
Haq, R.
;
Harland, M.
;
Taylor, J.
;
Duffy, D.
;
Holohan, K.
;
Dutton-Regester, K.
;
Palmer, J.
;
Bonazzi, V.
;
Stark, M.
;
Symmons, J.
;
Law, M.
;
Schmidt, C.
;
et al.
2014
Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma
Aoude, L.
;
Pritchard, A.
;
Robles-Espinoza, C.
;
Wadt, K.
;
Harland, M.
;
Choi, J.
;
Gartside, M.
;
Quesada, V.
;
Johansson, P.
;
Palmer, J.
;
Ramsay, A.
;
Zhang, X.
;
Jones, K.
;
Symmons, J.
;
Holland, E.
;
Schmid, H.
;
Bonazzi, V.
;
Woods, S.
;
Dutton-Regester, K.
;
Stark, M.
;
et al.
2011
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
Strawbridge, R.
;
Dupuis, J.
;
Prokopenko, I.
;
Barker, A.
;
Ahlqvist, E.
;
Rybin, D.
;
Petrie, J.
;
Travers, M.
;
Bouatia-Naji, N.
;
Dimas, A.
;
Nica, A.
;
Wheeler, E.
;
Chen, H.
;
Voight, B.
;
Taneera, J.
;
Kanoni, S.
;
Peden, J.
;
Turrini, F.
;
Gustafsson, S.
;
Zabena, C.
;
et al.
Discover
Author
5
Vos, T.
4
Choi, D.
4
Czyz, C.
4
Dailey, R.
4
Dolman, P.
4
Foster, J.
4
Gecz, J.
4
Grossniklaus, H.
4
Harrington, C.
4
Harris, G.
.
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Subject
64
Humans
48
Middle Aged
36
Aged
22
Young Adult
19
Adolescent
16
Aged, 80 and over
13
Treatment Outcome
12
Child
12
Mutation
12
Polymorphism, Single Nucleotide
.
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Date issued
3
2017
7
2016
21
2015
5
2014
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2013
10
2012
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2011
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2010