-
2
-
-
15444350658
-
Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors
-
Bahuau M, Vidaud D, Jenkins RB, et al. Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors. Cancer Res 1998;58:2298-2303.
-
(1998)
Cancer Res
, vol.58
, pp. 2298-2303
-
-
Bahuau, M.1
Vidaud, D.2
Jenkins, R.B.3
-
3
-
-
68149180890
-
Genome-wide association study identifies five susceptibility loci for glioma
-
Shete S, Hosking FJ, Robertson LB, et al. Genome-wide association study identifies five susceptibility loci for glioma. Nat Genet 2009;41:899-904.
-
(2009)
Nat Genet
, vol.41
, pp. 899-904
-
-
Shete, S.1
Hosking, F.J.2
Robertson, L.B.3
-
4
-
-
68149180891
-
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility
-
Wrensch M, Jenkins RB, Chang JS, et al. Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. Nat Genet 2009;41:905-908.
-
(2009)
Nat Genet
, vol.41
, pp. 905-908
-
-
Wrensch, M.1
Jenkins, R.B.2
Chang, J.S.3
-
5
-
-
72149129508
-
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
-
Landi MT, Chatterjee N, Yu K, et al. A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. Am J Hum Genet 2009;85:679-691.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 679-691
-
-
Landi, M.T.1
Chatterjee, N.2
Yu, K.3
-
6
-
-
69349102630
-
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22. 2.
-
Song H, Ramus SJ, Tyrer J, et al. A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Nat Genet 2009;41:996-1000.
-
(2009)
Nat Genet
, vol.41
, pp. 996-1000
-
-
Song, H.1
Ramus, S.J.2
Tyrer, J.3
-
7
-
-
77953431645
-
Germline and somatic JAK2 mutations and susceptibility to chronic myeloproliferative neoplasms
-
Goldin LR, Bjorkholm M, Kristinsson SY, et al. Germline and somatic JAK2 mutations and susceptibility to chronic myeloproliferative neoplasms. Genome Med 2009;1:55.
-
(2009)
Genome Med
, vol.1
, pp. 55
-
-
Goldin, L.R.1
Bjorkholm, M.2
Kristinsson, S.Y.3
-
8
-
-
0033951824
-
Alterations of chromosome arms 1p and 19q as predictors of survival in oligodendrogliomas, astrocytomas, and mixed oligoastrocytomas
-
Smith JS, Perry A, Borell TJ, et al. Alterations of chromosome arms 1p and 19q as predictors of survival in oligodendrogliomas, astrocytomas, and mixed oligoastrocytomas. J Clin Oncol 2000; 18:636-645.
-
(2000)
J Clin Oncol
, vol.18
, pp. 636-645
-
-
Smith, J.S.1
Perry, A.2
Borell, T.J.3
-
10
-
-
33846301441
-
Nonsynonymous coding single-nucleotide polymorphisms spanning the genome in relation to glioblastoma survival and age at diagnosis
-
Wrensch M, McMillan A, Wiencke J, et al. Nonsynonymous coding single-nucleotide polymorphisms spanning the genome in relation to glioblastoma survival and age at diagnosis. Clin Cancer Res 2007;13:197-205.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 197-205
-
-
Wrensch, M.1
McMillan, A.2
Wiencke, J.3
-
11
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007;81:559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
-
12
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
Pritchard JK, Stephens M, Donnelly P. Inference of population structure using multilocus genotype data. Genetics 2000;155: 945-959.
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
13
-
-
73649088347
-
Mutant metabolic enzymes are at the origin of gliomas
-
Yan H, Bigner DD, Velculescu V, et al. Mutant metabolic enzymes are at the origin of gliomas. Cancer Res 2009;69: 9157-9159.
-
(2009)
Cancer Res
, vol.69
, pp. 9157-9159
-
-
Yan, H.1
Bigner, D.D.2
Velculescu, V.3
-
14
-
-
65349150503
-
IDH1 mutations are early events in the development of astrocytomas and oligodendrogliomas
-
Watanabe T, Nobusawa S, Kleihues P, et al. IDH1 mutations are early events in the development of astrocytomas and oligodendrogliomas. Am J Pathol 2009;174:1149-1153.
-
(2009)
Am J Pathol
, vol.174
, pp. 1149-1153
-
-
Watanabe, T.1
Nobusawa, S.2
Kleihues, P.3
-
15
-
-
77952108366
-
Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma
-
Noushmehr H, Weisenberger DJ, Diefes K, et al. Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma. Cancer Cell 2010;17:510-522
-
(2010)
Cancer Cell
, vol.17
, pp. 510-522
-
-
Noushmehr, H.1
Weisenberger, D.J.2
Diefes, K.3
-
16
-
-
55049112064
-
Sequence variant on 8q24 confers susceptibility to urinary bladder cancer
-
Kiemeney LA, Thorlacius S, Sulem P, et al. Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. Nat Genet 2008;40:1307-1312.
-
(2008)
Nat Genet
, vol.40
, pp. 1307-1312
-
-
Kiemeney, L.A.1
Thorlacius, S.2
Sulem, P.3
-
17
-
-
0036074561
-
Clinical significance of alterations of chromosome 8 detected by fluorescence in situ hybridization analysis in pathologic organ-confined prostate cancer
-
Tsuchiya N, Slezak JM, Lieber MM, et al. Clinical significance of alterations of chromosome 8 detected by fluorescence in situ hybridization analysis in pathologic organ-confined prostate cancer. Genes Chromosomes Cancer 2002;34:363-371.
-
(2002)
Genes Chromosomes Cancer
, vol.34
, pp. 363-371
-
-
Tsuchiya, N.1
Slezak, J.M.2
Lieber, M.M.3
-
18
-
-
53549122238
-
RTEL1 maintains genomic stability by suppressing homologous recombination
-
Barber LJ, Youds JL, Ward JD, et al. RTEL1 maintains genomic stability by suppressing homologous recombination. Cell 2008; 135:261-271.
-
(2008)
Cell
, vol.135
, pp. 261-271
-
-
Barber, L.J.1
Youds, J.L.2
Ward, J.D.3
-
19
-
-
67649635974
-
Mammalian telomeres resemble fragile sites and require TRF1 for efficient replication
-
Sfeir A, Kosiyatrakul ST, Hockemeyer D, et al. Mammalian telomeres resemble fragile sites and require TRF1 for efficient replication. Cell 2009;138:90-103.
-
(2009)
Cell
, vol.138
, pp. 90-103
-
-
Sfeir, A.1
Kosiyatrakul, S.T.2
Hockemeyer, D.3
-
20
-
-
0035844234
-
Stathmin family proteins display specific molecular and tubulin binding properties
-
Charbaut E, Curmi PA, Ozon S, et al. Stathmin family proteins display specific molecular and tubulin binding properties. J Biol Chem 2001;276:16146-16154.
-
(2001)
J Biol Chem
, vol.276
, pp. 16146-16154
-
-
Charbaut, E.1
Curmi, P.A.2
Ozon, S.3
-
21
-
-
0031745284
-
SCLIP: a novel SCG10-like protein of the stathmin family expressed in the nervous system
-
Ozon S, Byk T, Sobel A. SCLIP: a novel SCG10-like protein of the stathmin family expressed in the nervous system. J Neurochem 1998;70:2386-2396.
-
(1998)
J Neurochem
, vol.70
, pp. 2386-2396
-
-
Ozon, S.1
Byk, T.2
Sobel, A.3
-
22
-
-
65549110895
-
Coordinated expression of stathmin family members by far upstream sequence elementbinding protein-1 increases motility in nonesmall cell lung cancer
-
Singer S, Malz M, Herpel E, et al. Coordinated expression of stathmin family members by far upstream sequence elementbinding protein-1 increases motility in nonesmall cell lung cancer. Cancer Res 2009;69:2234-2243.
-
(2009)
Cancer Res
, vol.69
, pp. 2234-2243
-
-
Singer, S.1
Malz, M.2
Herpel, E.3
-
23
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
International HapMap Consortium
-
International HapMap Consortium. A second generation human haplotype map of over 3.1 million SNPs. Nature 2007;449: 851-861
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
|