-
1
-
-
84867145464
-
Molecular genetics of B-precursor acute lymphoblastic leukemia
-
Mullighan, C. G. Molecular genetics of B-precursor acute lymphoblastic leukemia. J. Clin. Invest. 122, 3407-3415 (2012).
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 3407-3415
-
-
Mullighan, C.G.1
-
2
-
-
81555205127
-
Developmental origins and impact of BCR-ABL1 fusion and IKZF1 deletions in monozygotic twins with Ph+ acute lymphoblastic leukemia
-
Cazzaniga, G. et al. Developmental origins and impact of BCR-ABL1 fusion and IKZF1 deletions in monozygotic twins with Ph+ acute lymphoblastic leukemia. Blood 118, 5559-5564 (2011).
-
(2011)
Blood
, vol.118
, pp. 5559-5564
-
-
Cazzaniga, G.1
-
3
-
-
79960991127
-
Modeling the evolution of ETV6-RUNX1-induced B-cell precursor acute lymphoblastic leukemia in mice
-
van der Weyden, L. et al. Modeling the evolution of ETV6-RUNX1-induced B-cell precursor acute lymphoblastic leukemia in mice. Blood 118, 1041-1051 (2011).
-
(2011)
Blood
, vol.118
, pp. 1041-1051
-
-
Van Der Weyden, L.1
-
4
-
-
84867401980
-
Common genetic variation contributes significantly to the risk of childhood B-cell precursor acute lymphoblastic leukemia
-
Enciso-Mora, V. et al. Common genetic variation contributes significantly to the risk of childhood B-cell precursor acute lymphoblastic leukemia. Leukemia 26, 2212-2215 (2012).
-
(2012)
Leukemia
, vol.26
, pp. 2212-2215
-
-
Enciso-Mora, V.1
-
5
-
-
69349091330
-
Germline genomic variants associated with childhood acute lymphoblastic leukemia
-
Trevino, L. R. et al. Germline genomic variants associated with childhood acute lymphoblastic leukemia. Nat. Genet. 41, 1001-1005 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1001-1005
-
-
Trevino, L.R.1
-
6
-
-
69349101565
-
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia
-
Papaemmanuil, E. et al. Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. Nat. Genet. 41, 1006-1010 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1006-1010
-
-
Papaemmanuil, E.1
-
7
-
-
84877969387
-
Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations
-
Xu, H. et al. Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. J. Natl Cancer Inst. 105, 733-742 (2013).
-
(2013)
J. Natl Cancer Inst.
, vol.105
, pp. 733-742
-
-
Xu, H.1
-
8
-
-
77952884769
-
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk
-
Sherborne, A. L. et al. Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk. Nat. Genet. 42, 492-494 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 492-494
-
-
Sherborne, A.L.1
-
9
-
-
84860709956
-
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia
-
Ellinghaus, E. et al. Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. Leukemia 26, 902-909 (2012).
-
(2012)
Leukemia
, vol.26
, pp. 902-909
-
-
Ellinghaus, E.1
-
10
-
-
84891671233
-
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype
-
Migliorini, G. et al. Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. Blood 122, 3298-3307 (2013).
-
(2013)
Blood
, vol.122
, pp. 3298-3307
-
-
Migliorini, G.1
-
11
-
-
84888311432
-
Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse
-
Perez-Andreu, V. et al. Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse. Nat. Genet. 45, 1494-1498 (2013).
-
(2013)
Nat. Genet.
, vol.45
, pp. 1494-1498
-
-
Perez-Andreu, V.1
-
12
-
-
84871208154
-
Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE)
-
Orsi, L. et al. Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE). Leukemia 26, 2561-2564 (2012).
-
(2012)
Leukemia
, vol.26
, pp. 2561-2564
-
-
Orsi, L.1
-
13
-
-
77958570394
-
Childhood acute leukemia, early common infections, and allergy: The ESCALE study
-
Rudant, J. et al. Childhood acute leukemia, early common infections, and allergy: the ESCALE study. Am. J. Epidemiol. 172, 1015-1027 (2010).
-
(2010)
Am. J. Epidemiol.
, vol.172
, pp. 1015-1027
-
-
Rudant, J.1
-
14
-
-
47049093795
-
Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia and its relationship to other prognostic factors: A Children's Oncology Group study
-
Borowitz, M. J. et al. Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia and its relationship to other prognostic factors: a Children's Oncology Group study. Blood 111, 5477-5485 (2008).
-
(2008)
Blood
, vol.111
, pp. 5477-5485
-
-
Borowitz, M.J.1
-
15
-
-
84907996741
-
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures
-
Evans, T. J. et al. Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures. PLoS ONE 9, e110255 (2014).
-
(2014)
PLoS ONE
, vol.9
-
-
Evans, T.J.1
-
16
-
-
34147161800
-
Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)
-
Akasaka, T. et al. Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL). Blood 109, 3451-3461 (2007).
-
(2007)
Blood
, vol.109
, pp. 3451-3461
-
-
Akasaka, T.1
-
17
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
McVean, G. A. et al. An integrated map of genetic variation from 1,092 human genomes. Nature 491, 56-65 (2012).
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
McVean, G.A.1
-
18
-
-
84881049493
-
Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype
-
Walsh, K. M. et al. Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype. Blood 121, 4808-4809 (2013).
-
(2013)
Blood
, vol.121
, pp. 4808-4809
-
-
Walsh, K.M.1
-
19
-
-
34248547495
-
Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: Identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF
-
Pasmant, E. et al. Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF. Cancer Res. 67, 3963-3969 (2007).
-
(2007)
Cancer Res.
, vol.67
, pp. 3963-3969
-
-
Pasmant, E.1
-
20
-
-
77951439152
-
Trait-associated SNPs are more likely to be eQTLs: Annotation to enhance discovery from GWAS
-
Nicolae, D. L. et al. Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS. PLoS Genet. 6, e1000888 (2010).
-
(2010)
PLoS Genet.
, vol.6
-
-
Nicolae, D.L.1
-
21
-
-
84873086126
-
Chromatin marks identify critical cell types for fine mapping complex trait variants
-
Trynka, G. et al. Chromatin marks identify critical cell types for fine mapping complex trait variants. Nat. Genet. 45, 124-130 (2013).
-
(2013)
Nat. Genet.
, vol.45
, pp. 124-130
-
-
Trynka, G.1
-
22
-
-
84878682420
-
The Genotype-Tissue Expression (GTEx) project
-
Lonsdale, J. et al. The Genotype-Tissue Expression (GTEx) project. Nat. Genet. 45, 580-585 (2013).
-
(2013)
Nat. Genet.
, vol.45
, pp. 580-585
-
-
Lonsdale, J.1
-
23
-
-
84891685308
-
Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals
-
Battle, A. et al. Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals. Genome Res. 24, 14-24 (2014).
-
(2014)
Genome Res.
, vol.24
, pp. 14-24
-
-
Battle, A.1
-
24
-
-
84858779229
-
HaploReg: A resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants
-
Ward, L. D. & Kellis, M. HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants. Nucleic Acids Res. 40, D930-D934 (2012).
-
(2012)
Nucleic Acids Res.
, vol.40
, pp. D930-D934
-
-
Ward, L.D.1
Kellis, M.2
-
25
-
-
84865712382
-
Annotation of functional variation in personal genomes using RegulomeDB
-
Boyle, A. P. et al. Annotation of functional variation in personal genomes using RegulomeDB. Genome Res. 22, 1790-1797 (2012).
-
(2012)
Genome Res.
, vol.22
, pp. 1790-1797
-
-
Boyle, A.P.1
-
26
-
-
84865790047
-
An integrated encyclopedia of DNA elements in the human genome
-
Dunham, I. et al. An integrated encyclopedia of DNA elements in the human genome. Nature 489, 57-74 (2012).
-
(2012)
Nature
, vol.489
, pp. 57-74
-
-
Dunham, I.1
-
27
-
-
84876529535
-
Factorbook.org: A Wiki-based database for transcription factor-binding data generated by the ENCODE consortium
-
Wang, J. et al. Factorbook.org: a Wiki-based database for transcription factor-binding data generated by the ENCODE consortium. Nucleic Acids Res. 41, D171-D176 (2013).
-
(2013)
Nucleic Acids Res.
, vol.41
, pp. D171-D176
-
-
Wang, J.1
-
28
-
-
33644876958
-
TRANSFAC and its module TRANSCompel: Transcriptional gene regulation in eukaryotes
-
Matys, V. et al. TRANSFAC and its module TRANSCompel: transcriptional gene regulation in eukaryotes. Nucleic Acids Res. 34, D108-D110 (2006).
-
(2006)
Nucleic Acids Res.
, vol.34
, pp. D108-D110
-
-
Matys, V.1
-
29
-
-
84885645853
-
Transcriptome and genome sequencing uncovers functional variation in humans
-
Lappalainen, T. et al. Transcriptome and genome sequencing uncovers functional variation in humans. Nature 501, 506-511 (2013).
-
(2013)
Nature
, vol.501
, pp. 506-511
-
-
Lappalainen, T.1
-
30
-
-
84860596557
-
Patterns of cis regulatory variation in diverse human populations
-
Stranger, B. E. et al. Patterns of cis regulatory variation in diverse human populations. PLoS Genet. 8, e1002639 (2012).
-
(2012)
PLoS Genet.
, vol.8
-
-
Stranger, B.E.1
-
31
-
-
84868120556
-
Variants affecting exon skipping contribute to complex traits
-
Lee, Y. et al. Variants affecting exon skipping contribute to complex traits. PLoS Genet. 8, e1002998 (2012).
-
(2012)
PLoS Genet.
, vol.8
-
-
Lee, Y.1
-
32
-
-
0029587551
-
Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest
-
Quelle, D. E., Zindy, F., Ashmun, R. A. & Sherr, C. J. Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest. Cell 83, 993-1000 (1995).
-
(1995)
Cell
, vol.83
, pp. 993-1000
-
-
Quelle, D.E.1
Zindy, F.2
Ashmun, R.A.3
Sherr, C.J.4
-
33
-
-
35548998832
-
Human p16gamma, a novel transcriptional variant of p16(INK4A), coexpresses with p16(INK4A) in cancer cells and inhibits cell-cycle progression
-
Lin, Y. C. et al. Human p16gamma, a novel transcriptional variant of p16(INK4A), coexpresses with p16(INK4A) in cancer cells and inhibits cell-cycle progression. Oncogene 26, 7017-7027 (2007).
-
(2007)
Oncogene
, vol.26
, pp. 7017-7027
-
-
Lin, Y.C.1
-
34
-
-
0032169516
-
The alternative product from the human CDKN2A locus, p14(ARF), participates in a regulatory feedback loop with p53 and MDM2
-
Stott, F. J. et al. The alternative product from the human CDKN2A locus, p14(ARF), participates in a regulatory feedback loop with p53 and MDM2. EMBO J. 17, 5001-5014 (1998).
-
(1998)
EMBO J
, vol.17
, pp. 5001-5014
-
-
Stott, F.J.1
-
35
-
-
0029655282
-
Translational efficiency is regulated by the length of the 3′ untranslated region
-
Tanguay, R. L. & Gallie, D. R. Translational efficiency is regulated by the length of the 3′ untranslated region. Mol. Cell. Biol. 16, 146-156 (1996).
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 146-156
-
-
Tanguay, R.L.1
Gallie, D.R.2
-
36
-
-
0028967263
-
Deletions and rearrangement of CDKN2 in lymphoid malignancy
-
Stranks, G. et al. Deletions and rearrangement of CDKN2 in lymphoid malignancy. Blood 85, 893-901 (1995).
-
(1995)
Blood
, vol.85
, pp. 893-901
-
-
Stranks, G.1
-
37
-
-
44849129491
-
Failure of CDKN2A/B (INK4A/B-ARF)-mediated tumor suppression and resistance to targeted therapy in acute lymphoblastic leukemia induced by BCR-ABL
-
Mullighan, C. G., Williams, R. T., Downing, J. R. & Sherr, C. J. Failure of CDKN2A/B (INK4A/B-ARF)-mediated tumor suppression and resistance to targeted therapy in acute lymphoblastic leukemia induced by BCR-ABL. Genes Dev. 22, 1411-1415 (2008).
-
(2008)
Genes Dev.
, vol.22
, pp. 1411-1415
-
-
Mullighan, C.G.1
Williams, R.T.2
Downing, J.R.3
Sherr, C.J.4
-
38
-
-
34147224008
-
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
-
Mullighan, C. G. et al. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature 446, 758-764 (2007).
-
(2007)
Nature
, vol.446
, pp. 758-764
-
-
Mullighan, C.G.1
-
39
-
-
84885354288
-
Aberrant alternative splicing is another hallmark of cancer
-
Ladomery, M. Aberrant alternative splicing is another hallmark of cancer. Int. J. Cell Biol. 2013, 463786 (2013).
-
(2013)
Int. J. Cell Biol.
, vol.2013
-
-
Ladomery, M.1
-
40
-
-
84887460995
-
Misregulation of pre-mRNA alternative splicing in cancer
-
Zhang, J. & Manley, J. L. Misregulation of pre-mRNA alternative splicing in cancer. Cancer Discov. 3, 1228-1237 (2013).
-
(2013)
Cancer Discov
, vol.3
, pp. 1228-1237
-
-
Zhang, J.1
Manley, J.L.2
-
41
-
-
0142072167
-
Germline splicing mutations of CDKN2A predispose to melanoma
-
Loo, J. C. et al. Germline splicing mutations of CDKN2A predispose to melanoma. Oncogene 22, 6387-6394 (2003).
-
(2003)
Oncogene
, vol.22
, pp. 6387-6394
-
-
Loo, J.C.1
-
42
-
-
0035510173
-
A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees
-
Harland, M., Mistry, S., Bishop, D. T. & Bishop, J. A. A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees. Hum. Mol. Genet. 10, 2679-2686 (2001).
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2679-2686
-
-
Harland, M.1
Mistry, S.2
Bishop, D.T.3
Bishop, J.A.4
-
43
-
-
58149466825
-
Delayed intensification (DI) enhances event-free survival (EFS) of children with B-precursor acute lymphoblastic leukemia (ALL) who received intensification therapy with six courses of intravenous methotrexate (MTX): POG 9904/9905: A Children's Oncology Group Study (COG)
-
Winick, N. et al. Delayed intensification (DI) enhances event-free survival (EFS) of children with B-precursor acute lymphoblastic leukemia (ALL) who received intensification therapy with six courses of intravenous methotrexate (MTX): POG 9904/9905: A Children's Oncology Group Study (COG). ASH Annu. Meet. Abs. 110, 583 (2007).
-
(2007)
ASH Annu. Meet. Abs
, vol.110
, pp. 583
-
-
Winick, N.1
-
44
-
-
34548340684
-
New models of collaboration in genome-wide association studies: The Genetic Association Information Network
-
Manolio, T. A. et al. New models of collaboration in genome-wide association studies: the Genetic Association Information Network. Nat. Genet. 39, 1045-1051 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 1045-1051
-
-
Manolio, T.A.1
-
45
-
-
52949085789
-
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
-
Korn, J. M. et al. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat. Genet. 40, 1253-1260 (2008).
-
(2008)
Nat. Genet.
, vol.40
, pp. 1253-1260
-
-
Korn, J.M.1
-
46
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
Ehret, G. B. et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 478, 103-109 (2011).
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
Ehret, G.B.1
-
47
-
-
84876310972
-
The Childhood Leukemia International Consortium
-
Metayer, C. et al. The Childhood Leukemia International Consortium. Cancer Epidemiol. 37, 336-347 (2013).
-
(2013)
Cancer Epidemiol.
, vol.37
, pp. 336-347
-
-
Metayer, C.1
-
48
-
-
33344470090
-
PopGen: Population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships
-
Krawczak, M. et al. PopGen: Population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships. Community Genet. 9, 55-61 (2006).
-
(2006)
Community Genet.
, vol.9
, pp. 55-61
-
-
Krawczak, M.1
-
49
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell, S. et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559-575 (2007).
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 559-575
-
-
Purcell, S.1
-
50
-
-
84875404794
-
The UCSC Genome Browser database: Extensions and updates 2013
-
Meyer, L. R. et al. The UCSC Genome Browser database: Extensions and updates 2013. Nucleic Acids Res. 41, D64-D69 (2013).
-
(2013)
Nucleic Acids Res.
, vol.41
, pp. D64-D69
-
-
Meyer, L.R.1
-
51
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price, A. L. et al. Principal components analysis corrects for stratification in genome-wide association studies. Nat. Genet. 38, 904-909 (2006).
-
(2006)
Nat. Genet.
, vol.38
, pp. 904-909
-
-
Price, A.L.1
-
52
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie, B. N., Donnelly, P. & Marchini, J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet. 5, e1000529 (2009).
-
(2009)
PLoS Genet.
, vol.5
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
53
-
-
84856478855
-
A linear complexity phasing method for thousands of genomes
-
Delaneau, O., Marchini, J. & Zagury, J. F. A linear complexity phasing method for thousands of genomes. Nat. Methods 9, 179-181 (2012).
-
(2012)
Nat. Methods
, vol.9
, pp. 179-181
-
-
Delaneau, O.1
Marchini, J.2
Zagury, J.F.3
-
54
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini, J., Howie, B., Myers, S., McVean, G. & Donnelly, P. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat. Genet. 39, 906-913 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
55
-
-
77955894071
-
METAL: Fast and efficient meta-analysis of genomewide association scans
-
Willer, C. J., Li, Y. & Abecasis, G. R. METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 26, 2190-2191 (2010).
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
56
-
-
0041876133
-
Measuring inconsistency in meta-analyses
-
Higgins, J. P., Thompson, S. G., Deeks, J. J. & Altman, D. G. Measuring inconsistency in meta-analyses. BMJ 327, 557-560 (2003).
-
(2003)
BMJ
, vol.327
, pp. 557-560
-
-
Higgins, J.P.1
Thompson, S.G.2
Deeks, J.J.3
Altman, D.G.4
-
57
-
-
0032714352
-
Genomic control for association studies
-
Devlin, B. & Roeder, K. Genomic control for association studies. Biometrics 55, 997-1004 (1999).
-
(1999)
Biometrics
, vol.55
, pp. 997-1004
-
-
Devlin, B.1
Roeder, K.2
-
58
-
-
77956586071
-
LocusZoom: Regional visualization of genome-wide association scan results
-
Pruim, R. J. et al. LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics 26, 2336-2337 (2010).
-
(2010)
Bioinformatics
, vol.26
, pp. 2336-2337
-
-
Pruim, R.J.1
-
59
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett, J. C., Fry, B., Maller, J. & Daly, M. J. Haploview: Analysis and visualization of LD and haplotype maps. Bioinformatics 21, 263-265 (2005).
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
60
-
-
0036840537
-
Multi-ethnic study of atherosclerosis: Objectives and design
-
Bild, D. E. et al. Multi-ethnic study of atherosclerosis: Objectives and design. Am. J. Epidemiol. 156, 871-881 (2002).
-
(2002)
Am. J. Epidemiol.
, vol.156
, pp. 871-881
-
-
Bild, D.E.1
-
61
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
Pritchard, J. K., Stephens, M. & Donnelly, P. Inference of population structure using multilocus genotype data. Genetics 155, 945-959 (2000).
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
62
-
-
79952188025
-
Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia
-
Yang, J. J. et al. Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia. Nat. Genet. 43, 237-241 (2011).
-
(2011)
Nat. Genet.
, vol.43
, pp. 237-241
-
-
Yang, J.J.1
-
63
-
-
34250882721
-
A genomewide admixture mapping panel for Hispanic/Latino populations
-
Mao, X. et al. A genomewide admixture mapping panel for Hispanic/Latino populations. Am. J. Hum. Genet. 80, 1171-1178 (2007).
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 1171-1178
-
-
Mao, X.1
-
64
-
-
77956637896
-
Genetics and beyond - The transcriptome of human monocytes and disease susceptibility
-
Zeller, T. et al. Genetics and beyond - the transcriptome of human monocytes and disease susceptibility. PLoS ONE 5, e10693 (2010).
-
(2010)
PLoS ONE
, vol.5
-
-
Zeller, T.1
-
65
-
-
77957940722
-
The NIH Roadmap Epigenomics Mapping Consortium
-
Bernstein, B. E. et al. The NIH Roadmap Epigenomics Mapping Consortium. Nat. Biotechnol. 28, 1045-1048 (2010).
-
(2010)
Nat. Biotechnol
, vol.28
, pp. 1045-1048
-
-
Bernstein, B.E.1
-
66
-
-
77956331627
-
Integrating common and rare genetic variation in diverse human populations
-
International HapMap Consortium et al. Integrating common and rare genetic variation in diverse human populations. Nature 467, 52-58 (2010).
-
(2010)
Nature
, vol.467
, pp. 52-58
-
-
International HapMap Consortium1
-
67
-
-
0347125328
-
JASPAR: An open-access database for eukaryotic transcription factor binding profiles
-
Sandelin, A., Alkema, W., Engstrom, P., Wasserman, W. W. & Lenhard, B. JASPAR: An open-access database for eukaryotic transcription factor binding profiles. Nucleic Acids Res. 32, D91-D94 (2004).
-
(2004)
Nucleic Acids Res.
, vol.32
, pp. D91-D94
-
-
Sandelin, A.1
Alkema, W.2
Engstrom, P.3
Wasserman, W.W.4
Lenhard, B.5
-
68
-
-
77952123055
-
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation
-
Trapnell, C. et al. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nat. Biotechnol. 28, 511-515 (2010).
-
(2010)
Nat. Biotechnol
, vol.28
, pp. 511-515
-
-
Trapnell, C.1
-
69
-
-
84907095419
-
R: A Language and Environment for Statistical Computing
-
R Development Core Team. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing. ISBN 3-900051-07-0. (2008).
-
(2008)
R Foundation for Statistical Computing
-
-
-
70
-
-
33748486517
-
AceView: A comprehensive cDNA-supported gene and transcripts annotation
-
Thierry-Mieg, D. & Thierry-Mieg, J. AceView: A comprehensive cDNA-supported gene and transcripts annotation. Genome Biol. 7 Suppl 1, S12+1-14 (2006).
-
(2006)
Genome Biol.
, vol.7
-
-
Thierry-Mieg, D.1
Thierry-Mieg, J.2
|