-
1
-
-
33644545382
-
Infection, immune responses and the aetiology of childhood leukaemia
-
Greaves M. Infection, immune responses and the aetiology of childhood leukaemia. Nat Rev Cancer 2006;6:193-203.
-
(2006)
Nat Rev Cancer
, vol.6
, pp. 193-203
-
-
Greaves, M.1
-
2
-
-
84877969387
-
Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations
-
Xu H, Yang W, Perez-Andreu V, Devidas M, Fan Y, Cheng C, et al. Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. J Natl Cancer Inst 2013;105:733-42.
-
(2013)
J Natl Cancer Inst
, vol.105
, pp. 733-742
-
-
Xu, H.1
Yang, W.2
Perez-Andreu, V.3
Devidas, M.4
Fan, Y.5
Cheng, C.6
-
3
-
-
84891671233
-
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype
-
Migliorini G, Fiege B, Hosking FJ, Ma Y, Kumar R, Sherborne AL, et al. Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. Blood 2013;122:3298-307.
-
(2013)
Blood
, vol.122
, pp. 3298-3307
-
-
Migliorini, G.1
Fiege, B.2
Hosking, F.J.3
Ma, Y.4
Kumar, R.5
Sherborne, A.L.6
-
4
-
-
84888311432
-
Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse
-
Perez-Andreu V, Roberts KG, Harvey RC, Yang W, Cheng C, Pei D, et al. Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse. Nat Genet 2013;45:1494-8.
-
(2013)
Nat Genet
, vol.45
, pp. 1494-1498
-
-
Perez-Andreu, V.1
Roberts, K.G.2
Harvey, R.C.3
Yang, W.4
Cheng, C.5
Pei, D.6
-
5
-
-
77952884769
-
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk
-
Sherborne AL, Hosking FJ, Prasad RB, Kumar R, Koehler R, Vijayakrishnan J, et al. Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk. Nat Genet 2010;42:492-4.
-
(2010)
Nat Genet
, vol.42
, pp. 492-494
-
-
Sherborne, A.L.1
Hosking, F.J.2
Prasad, R.B.3
Kumar, R.4
Koehler, R.5
Vijayakrishnan, J.6
-
6
-
-
80054996042
-
Genome-wide association study identifies three new melanoma susceptibility loci
-
Barrett JH, Iles MM, Harland M, Taylor JC, Aitken JF, Andresen PA, et al. Genome-wide association study identifies three new melanoma susceptibility loci. Nat Genet 2011;43:1108-13.
-
(2011)
Nat Genet
, vol.43
, pp. 1108-1113
-
-
Barrett, J.H.1
Iles, M.M.2
Harland, M.3
Taylor, J.C.4
Aitken, J.F.5
Andresen, P.A.6
-
7
-
-
68149180891
-
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility
-
Wrensch M, Jenkins RB, Chang JS, Yeh RF, Xiao Y, Decker PA, et al. Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. Nat Genet 2009;41:905-8.
-
(2009)
Nat Genet
, vol.41
, pp. 905-908
-
-
Wrensch, M.1
Jenkins, R.B.2
Chang, J.S.3
Yeh, R.F.4
Xiao, Y.5
Decker, P.A.6
-
8
-
-
77954143076
-
A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci
-
Bei JX, Li Y, Jia WH, Feng BJ, Zhou G, Chen LZ, et al. A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. Nat Genet 2010;42:599-603.
-
(2010)
Nat Genet
, vol.42
, pp. 599-603
-
-
Bei, J.X.1
Li, Y.2
Jia, W.H.3
Feng, B.J.4
Zhou, G.5
Chen, L.Z.6
-
9
-
-
84868156549
-
Influence of common genetic variation on lung cancer risk: Meta-analysis of 14 900 cases and 29 485 controls
-
Timofeeva MN, Hung RJ, Rafnar T, Christiani DC, Field JK, Bickeböller H, et al. Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. Hum Mol Genet 2012;21:4980-95.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 4980-4995
-
-
Timofeeva, M.N.1
Hung, R.J.2
Rafnar, T.3
Christiani, D.C.4
Field, J.K.5
Bickeböller, H.6
-
10
-
-
84879593764
-
Genes commonly deleted in childhood B-cell precursor acute lymphoblastic leukemia: Association with cytogenetics and clinical features
-
Schwab CJ, Chilton L, Morrison H, Jones L, Al-Shehhi H, Erhorn A, et al. Genes commonly deleted in childhood B-cell precursor acute lymphoblastic leukemia: association with cytogenetics and clinical features. Haematologica 2013;98:1081-8.
-
(2013)
Haematologica
, vol.98
, pp. 1081-1088
-
-
Schwab, C.J.1
Chilton, L.2
Morrison, H.3
Jones, L.4
Al-Shehhi, H.5
Erhorn, A.6
-
11
-
-
84890432336
-
Associations between genome-wide Native American ancestry, known risk alleles and B-cell ALL risk in Hispanic children
-
Walsh KM, Chokkalingam AP, Hsu LI, Metayer C, de Smith AJ, Jacobs DI, et al. Associations between genome-wide Native American ancestry, known risk alleles and B-cell ALL risk in Hispanic children. Leukemia 2013; 27:2416-9.
-
(2013)
Leukemia
, vol.27
, pp. 2416-2419
-
-
Walsh, K.M.1
Chokkalingam, A.P.2
Hsu, L.I.3
Metayer, C.4
De Smith, A.J.5
Jacobs, D.I.6
-
12
-
-
84869854208
-
Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia
-
Yang JJ, Cheng C, Devidas M, Cao X, Campana D, Yang W, et al. Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia. Blood 2012;120:4197-204.
-
(2012)
Blood
, vol.120
, pp. 4197-4204
-
-
Yang, J.J.1
Cheng, C.2
Devidas, M.3
Cao, X.4
Campana, D.5
Yang, W.6
-
13
-
-
79952188025
-
Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia
-
Yang JJ, Cheng C, Devidas M, Cao X, Fan Y, Campana D, et al. Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia. Nat Genet 2011;43:237-41.
-
(2011)
Nat Genet
, vol.43
, pp. 237-241
-
-
Yang, J.J.1
Cheng, C.2
Devidas, M.3
Cao, X.4
Fan, Y.5
Campana, D.6
-
14
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007;447:661-78.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
15
-
-
81855199793
-
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma
-
Amos CI, Wang LE, Lee JE, Gershenwald JE, Chen WV, Fang S, et al. Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Hum Mol Genet 2011;20:5012-23.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 5012-5023
-
-
Amos, C.I.1
Wang, L.E.2
Lee, J.E.3
Gershenwald, J.E.4
Chen, W.V.5
Fang, S.6
-
16
-
-
84904101984
-
Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk
-
Walsh KM, Codd V, Smirnov IV, Rice T, Decker PA, Hansen HM, et al. Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. Nat Genet 2014;46:731-5.
-
(2014)
Nat Genet
, vol.46
, pp. 731-735
-
-
Walsh, K.M.1
Codd, V.2
Smirnov, I.V.3
Rice, T.4
Decker, P.A.5
Hansen, H.M.6
-
17
-
-
84866932650
-
A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation
-
Jenkins RB, Xiao Y, Sicotte H, Decker PA, Kollmeyer TM, Hansen HM, et al. A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation. Nat Genet 2012;44:1122-5.
-
(2012)
Nat Genet
, vol.44
, pp. 1122-1125
-
-
Jenkins, R.B.1
Xiao, Y.2
Sicotte, H.3
Decker, P.A.4
Kollmeyer, T.M.5
Hansen, H.M.6
-
18
-
-
77649188501
-
A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33
-
Petersen GM, Amundadottir L, Fuchs CS, Kraft P, Stolzenberg-Solomon RZ, Jacobs KB, et al. A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. Nat Genet 2010;42:224-8.
-
(2010)
Nat Genet
, vol.42
, pp. 224-228
-
-
Petersen, G.M.1
Amundadottir, L.2
Fuchs, C.S.3
Kraft, P.4
Stolzenberg-Solomon, R.Z.5
Jacobs, K.B.6
-
19
-
-
69349097813
-
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
-
Amundadottir L, Kraft P, Stolzenberg-Solomon RZ, Fuchs CS, Petersen GM, Arslan AA, et al. Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nat Genet 2009;41:986-90.
-
(2009)
Nat Genet
, vol.41
, pp. 986-990
-
-
Amundadottir, L.1
Kraft, P.2
Stolzenberg-Solomon, R.Z.3
Fuchs, C.S.4
Petersen, G.M.5
Arslan, A.A.6
-
20
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie BN, Donnelly P, Marchini J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 2009;5:e1000529.
-
(2009)
PLoS Genet
, vol.5
, pp. e1000529
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
21
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
1000 Genomes Project Consortium, Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, et al. A map of human genome variation from population-scale sequencing. Nature 2010;467:1061-73.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Abecasis, G.R.1
Altshuler, D.2
Auton, A.3
Brooks, L.D.4
Durbin, R.M.5
Gibbs, R.A.6
-
22
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
Marchini J, Howie B. Genotype imputation for genome-wide association studies. Nat Rev Genet 2010;11:499-511.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 499-511
-
-
Marchini, J.1
Howie, B.2
-
23
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D. Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006;38:904-9.
-
(2006)
Nat Genet
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
Reich, D.6
-
24
-
-
84864865859
-
Matching on race and ethnicity in case-control studies as a means of control for population stratification
-
Chokkalingam AP, Aldrich MC, Bartley K, Hsu LI, Metayer C, Barcellos LF, et al. Matching on race and ethnicity in case-control studies as a means of control for population stratification. Epidemiology (Sunnyvale) 2011;1:101.
-
(2011)
Epidemiology (Sunnyvale)
, vol.1
, pp. 101
-
-
Chokkalingam, A.P.1
Aldrich, M.C.2
Bartley, K.3
Hsu, L.I.4
Metayer, C.5
Barcellos, L.F.6
-
25
-
-
77951751034
-
Metaanalysis and imputation refines the association of 15q25 with smoking quantity
-
Liu JZ, Tozzi F, Waterworth DM, Pillai SG, Muglia P, Middleton L, et al. Metaanalysis and imputation refines the association of 15q25 with smoking quantity. Nat Genet 2010;42:436-40.
-
(2010)
Nat Genet
, vol.42
, pp. 436-440
-
-
Liu, J.Z.1
Tozzi, F.2
Waterworth, D.M.3
Pillai, S.G.4
Muglia, P.5
Middleton, L.6
-
26
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007;81:559-75.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
-
27
-
-
39749181521
-
Worldwide human relationships inferred from genome-wide patterns of variation
-
Li JZ, Absher DM, Tang H, Southwick AM, Casto AM, Ramachandran S, et al. Worldwide human relationships inferred from genome-wide patterns of variation. Science 2008;319:1100-4.
-
(2008)
Science
, vol.319
, pp. 1100-1104
-
-
Li, J.Z.1
Absher, D.M.2
Tang, H.3
Southwick, A.M.4
Casto, A.M.5
Ramachandran, S.6
-
28
-
-
0041817568
-
Inference of population structure using multilocus genotype data: Linked loci and correlated allele frequencies
-
Falush D, Stephens M, Pritchard JK. Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. Genetics 2003;164:1567-87.
-
(2003)
Genetics
, vol.164
, pp. 1567-1587
-
-
Falush, D.1
Stephens, M.2
Pritchard, J.K.3
-
29
-
-
84902801372
-
Genomic ancestry and somatic alterations correlatewith age at diagnosis in Hispanic childrenwith B-cell acute lymphoblastic leukemia
-
Walsh KM, de Smith AJ, Welch TC, Smirnov I, Cunningham MJ, Ma X, et al. Genomic ancestry and somatic alterations correlatewith age at diagnosis in Hispanic childrenwith B-cell acute lymphoblastic leukemia. Am J Hematol 2014;89:721-5.
-
(2014)
Am J Hematol
, vol.89
, pp. 721-725
-
-
Walsh, K.M.1
De Smith, A.J.2
Welch, T.C.3
Smirnov, I.4
Cunningham, M.J.5
Ma, X.6
-
30
-
-
81255175501
-
High-throughput droplet digital PCR system for absolute quantitation of DNA copy number
-
Hindson BJ, Ness KD, Masquelier DA, Belgrader P, Heredia NJ, Makarewicz AJ, et al. High-throughput droplet digital PCR system for absolute quantitation of DNA copy number. Anal Chem 2011;83:8604-10.
-
(2011)
Anal Chem
, vol.83
, pp. 8604-8610
-
-
Hindson, B.J.1
Ness, K.D.2
Masquelier, D.A.3
Belgrader, P.4
Heredia, N.J.5
Makarewicz, A.J.6
-
31
-
-
84891707511
-
GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL
-
Walsh KM, de Smith AJ, Chokkalingam AP, Metayer C, Roberts W, Barcellos LF, et al. GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL. Blood 2013;122:3385-7.
-
(2013)
Blood
, vol.122
, pp. 3385-3387
-
-
Walsh, K.M.1
De Smith, A.J.2
Chokkalingam, A.P.3
Metayer, C.4
Roberts, W.5
Barcellos, L.F.6
-
32
-
-
84865712382
-
Annotation of functional variation in personal genomes using Regulome DB
-
Boyle AP, Hong EL, Hariharan M, Cheng Y, Schaub MA, Kasowski M, et al. Annotation of functional variation in personal genomes using Regulome DB. Genome Res 2012;22:1790-7.
-
(2012)
Genome Res
, vol.22
, pp. 1790-1797
-
-
Boyle, A.P.1
Hong, E.L.2
Hariharan, M.3
Cheng, Y.4
Schaub, M.A.5
Kasowski, M.6
-
33
-
-
84858779229
-
HaploReg: A resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants
-
Ward LD, Kellis M. HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants. Nucleic Acids Res 2012;40 Database issue:D930-4.
-
(2012)
Nucleic Acids Res
, vol.40
, pp. D930-D934
-
-
Ward, L.D.1
Kellis, M.2
-
34
-
-
84878682420
-
The genotype-tissue expression (GTEx) project
-
The Genotype-Tissue Expression (GTEx) project. Nat Genet 2013;45: 580-5.
-
(2013)
Nat Genet
, vol.45
, pp. 580-585
-
-
-
35
-
-
15444350658
-
Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors
-
Bahuau M, Vidaud D, Jenkins RB, Biéche I, Kimmel DW, Assouline B, et al. Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors. Cancer Res 1998;58: 2298-303.
-
(1998)
Cancer Res
, vol.58
, pp. 2298-2303
-
-
Bahuau, M.1
Vidaud, D.2
Jenkins, R.B.3
Biéche, I.4
Kimmel, D.W.5
Assouline, B.6
-
36
-
-
0029129816
-
Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations
-
Goldstein AM, Fraser MC, Struewing JP, Hussussian CJ, Ranade K, Zametkin DP, et al. Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations. N Engl J Med 1995;333:970-4.
-
(1995)
N Engl J Med
, vol.333
, pp. 970-974
-
-
Goldstein, A.M.1
Fraser, M.C.2
Struewing, J.P.3
Hussussian, C.J.4
Ranade, K.5
Zametkin, D.P.6
-
37
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
Kumar P, Henikoff S, Ng PC. Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat Protoc 2009;4:1073-81.
-
(2009)
Nat Protoc
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
Henikoff, S.2
Ng, P.C.3
-
38
-
-
77955151784
-
MutationTaster evaluates disease-causing potential of sequence alterations
-
Schwarz JM, Rodelsperger C, Schuelke M, Seelow D. MutationTaster evaluates disease-causing potential of sequence alterations. Nat Methods 2010;7:575-6.
-
(2010)
Nat Methods
, vol.7
, pp. 575-576
-
-
Schwarz, J.M.1
Rodelsperger, C.2
Schuelke, M.3
Seelow, D.4
-
39
-
-
0028971677
-
P16 proteins from melanoma-prone families are deficient in binding to Cdk4
-
Reymond A, Brent R. p16 proteins from melanoma-prone families are deficient in binding to Cdk4. Oncogene 1995;11:1173-8.
-
(1995)
Oncogene
, vol.11
, pp. 1173-1178
-
-
Reymond, A.1
Brent, R.2
-
41
-
-
84876067164
-
TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal
-
Killela PJ, Reitman ZJ, Jiao Y, Bettegowda C, Agrawal N, Diaz LA Jr, et al. TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal. Proc Natl Acad Sci U S A 2013;110:6021-6.
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. 6021-6026
-
-
Killela, P.J.1
Reitman, Z.J.2
Jiao, Y.3
Bettegowda, C.4
Agrawal, N.5
Diaz, L.A.6
-
42
-
-
84921288028
-
Cancer etiology. Variation in cancer risk among tissues can be explained by the number of stem cell divisions
-
Tomasetti C, Vogelstein B. Cancer etiology. Variation in cancer risk among tissues can be explained by the number of stem cell divisions. Science 2015;347:78-81.
-
(2015)
Science
, vol.347
, pp. 78-81
-
-
Tomasetti, C.1
Vogelstein, B.2
-
43
-
-
79957611419
-
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1
-
Burdon KP, Macgregor S, Hewitt AW, Sharma S, Chidlow G, Mills RA, et al. Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nat Genet 2011;43:574-8.
-
(2011)
Nat Genet
, vol.43
, pp. 574-578
-
-
Burdon, K.P.1
Macgregor, S.2
Hewitt, A.W.3
Sharma, S.4
Chidlow, G.5
Mills, R.A.6
-
44
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, Jonasdottir A, et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 2007;316:1491-3.
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
Blondal, T.5
Jonasdottir, A.6
-
45
-
-
77951768060
-
Genome-wide association study of intracranial aneurysm identifies three new risk loci
-
Yasuno K, Bilguvar K, Bijlenga P, Low SK, Krischek B, Auburger G, et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet 2010;42:420-5.
-
(2010)
Nat Genet
, vol.42
, pp. 420-425
-
-
Yasuno, K.1
Bilguvar, K.2
Bijlenga, P.3
Low, S.K.4
Krischek, B.5
Auburger, G.6
-
46
-
-
84881049493
-
Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype
-
Walsh KM, de Smith AJ, Chokkalingam AP, Metayer C, Dahl GV, Hsu LI, et al. Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype. Blood 2013;121:4808-9.
-
(2013)
Blood
, vol.121
, pp. 4808-4809
-
-
Walsh, K.M.1
De Smith, A.J.2
Chokkalingam, A.P.3
Metayer, C.4
Dahl, G.V.5
Hsu, L.I.6
-
47
-
-
84895803000
-
RAGmediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia
-
Papaemmanuil E, Rapado I, Li Y, Potter NE, Wedge DC, Tubio J, et al. RAGmediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia. Nat Genet 2014;46:116-25.
-
(2014)
Nat Genet
, vol.46
, pp. 116-125
-
-
Papaemmanuil, E.1
Rapado, I.2
Li, Y.3
Potter, N.E.4
Wedge, D.C.5
Tubio, J.6
-
48
-
-
84872401601
-
Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies
-
Walsh KM, Anderson E, Hansen HM, Decker PA, Kosel ML, Kollmeyer T, et al. Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies. Genet Epidemiol 2013;37:222-8.
-
(2013)
Genet Epidemiol
, vol.37
, pp. 222-228
-
-
Walsh, K.M.1
Anderson, E.2
Hansen, H.M.3
Decker, P.A.4
Kosel, M.L.5
Kollmeyer, T.6
-
49
-
-
84898851921
-
Rare variants in TP53 and susceptibility to neuroblastoma
-
Diskin SJ, Capasso M, Diamond M, Oldridge DA, Conkrite K, Bosse KR, et al. Rare variants in TP53 and susceptibility to neuroblastoma. J Natl Cancer Inst 2014;106:dju047.
-
(2014)
J Natl Cancer Inst
, vol.106
, pp. dju047
-
-
Diskin, S.J.1
Capasso, M.2
Diamond, M.3
Oldridge, D.A.4
Conkrite, K.5
Bosse, K.R.6
-
50
-
-
80055009292
-
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility
-
Stacey SN, Sulem P, Jonasdottir A, Masson G, Gudmundsson J, Gudbjartsson DF, et al. A germline variant in the TP53 polyadenylation signal confers cancer susceptibility. Nat Genet 2011;43:1098-103.
-
(2011)
Nat Genet
, vol.43
, pp. 1098-1103
-
-
Stacey, S.N.1
Sulem, P.2
Jonasdottir, A.3
Masson, G.4
Gudmundsson, J.5
Gudbjartsson, D.F.6
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