-
1
-
-
2942584865
-
Chronic lymphocytic leukemia: Revelations from the B-cell receptor
-
Stevenson, F.K. & Caligaris-Cappio, F. Chronic lymphocytic leukemia: revelations from the B-cell receptor. Blood 103, 4389-4395 (2004).
-
(2004)
Blood
, vol.103
, pp. 4389-4395
-
-
Stevenson, F.K.1
Caligaris-Cappio, F.2
-
2
-
-
66049151296
-
Elevated risk of chronic lymphocytic leukemia and other indolent non-Hodgkin's lymphomas among relatives of patients with chronic lymphocytic leukemia
-
Goldin, L.R., Bjorkholm, M., Kristinsson, S.Y., Turesson, I. & Landgren, O. Elevated risk of chronic lymphocytic leukemia and other indolent non-Hodgkin's lymphomas among relatives of patients with chronic lymphocytic leukemia. Haematologica 94, 647-653 (2009).
-
(2009)
Haematologica
, vol.94
, pp. 647-653
-
-
Goldin, L.R.1
Bjorkholm, M.2
Kristinsson, S.Y.3
Turesson, I.4
Landgren, O.5
-
3
-
-
52949139429
-
A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia
-
Di Bernardo, M.C. et al. A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. Nat. Genet. 40, 1204-1210 (2008).
-
(2008)
Nat. Genet
, vol.40
, pp. 1204-1210
-
-
Di Bernardo, M.C.1
-
4
-
-
75749138023
-
Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk
-
Crowther-Swanepoel, D. et al. Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk. Nat. Genet. 42, 132-136 (2010).
-
(2010)
Nat. Genet
, vol.42
, pp. 132-136
-
-
Crowther-Swanepoel, D.1
-
5
-
-
84864471868
-
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia
-
Slager, S.L. et al. Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. Blood 120, 843-846 (2012).
-
(2012)
Blood
, vol.120
, pp. 843-846
-
-
Slager, S.L.1
-
6
-
-
84881023533
-
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
-
Berndt, S.I. et al. Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. Nat. Genet. 45, 868-876 (2013).
-
(2013)
Nat. Genet
, vol.45
, pp. 868-876
-
-
Berndt, S.I.1
-
7
-
-
78650747491
-
Discovery and characterization of chromatin states for systematic annotation of the human genome
-
Ernst, J. & Kellis, M. Discovery and characterization of chromatin states for systematic annotation of the human genome. Nat. Biotechnol. 28, 817-825 (2010).
-
(2010)
Nat. Biotechnol
, vol.28
, pp. 817-825
-
-
Ernst, J.1
Kellis, M.2
-
8
-
-
78049353079
-
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
-
Houlston, R.S. et al. Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. Nat. Genet. 42, 973-977 (2010).
-
(2010)
Nat. Genet
, vol.42
, pp. 973-977
-
-
Houlston, R.S.1
-
9
-
-
84885022887
-
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
-
Chubb, D. et al. Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Nat. Genet. 45, 1221-1225 (2013).
-
(2013)
Nat. Genet
, vol.45
, pp. 1221-1225
-
-
Chubb, D.1
-
10
-
-
84855194845
-
TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres
-
Jones, A.M. et al. TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres. Gut 61, 248-254 (2012).
-
(2012)
Gut
, vol.61
, pp. 248-254
-
-
Jones, A.M.1
-
11
-
-
84874967142
-
Identification of seven loci affecting mean telomere length and their association with disease
-
Codd, V. et al. Identification of seven loci affecting mean telomere length and their association with disease. Nat. Genet. 45, 422-427 (2013).
-
(2013)
Nat. Genet
, vol.45
, pp. 422-427
-
-
Codd, V.1
-
12
-
-
84862626662
-
Negative feedback regulation of antigen receptors through calmodulin inhibition of E2A
-
Verma-Gaur, J., Hauser, J. & Grundstrom, T. Negative feedback regulation of antigen receptors through calmodulin inhibition of E2A. J. Immunol. 188, 6175-6183 (2012).
-
(2012)
J. Immunol
, vol.188
, pp. 6175-6183
-
-
Verma-Gaur, J.1
Hauser, J.2
Grundstrom, T.3
-
13
-
-
84878551940
-
POT1 mutations cause telomere dysfunction in chronic lymphocytic leukemia
-
Ramsay, A.J. et al. POT1 mutations cause telomere dysfunction in chronic lymphocytic leukemia. Nat. Genet. 45, 526-530 (2013).
-
(2013)
Nat. Genet
, vol.45
, pp. 526-530
-
-
Ramsay, A.J.1
-
14
-
-
77649188501
-
A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33
-
Petersen, G.M. et al. A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. Nat. Genet. 42, 224-228 (2010).
-
(2010)
Nat. Genet
, vol.42
, pp. 224-228
-
-
Petersen, G.M.1
-
15
-
-
80054996042
-
Genome-wide association study identifies three new melanoma susceptibility loci
-
Barrett, J.H. et al. Genome-wide association study identifies three new melanoma susceptibility loci. Nat. Genet. 43, 1108-1113 (2011).
-
(2011)
Nat. Genet
, vol.43
, pp. 1108-1113
-
-
Barrett, J.H.1
-
16
-
-
68149170036
-
New common variants affecting susceptibility to basal cell carcinoma
-
Stacey, S.N. et al. New common variants affecting susceptibility to basal cell carcinoma. Nat. Genet. 41, 909-914 (2009).
-
(2009)
Nat. Genet
, vol.41
, pp. 909-914
-
-
Stacey, S.N.1
-
17
-
-
56749163357
-
Common 5p15.33 and 6p21.33 variants influence lung cancer risk
-
Wang, Y. et al. Common 5p15.33 and 6p21.33 variants influence lung cancer risk. Nat. Genet. 40, 1407-1409 (2008).
-
(2008)
Nat. Genet
, vol.40
, pp. 1407-1409
-
-
Wang, Y.1
-
18
-
-
84947899485
-
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
-
Rothman, N. et al. A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. Nat. Genet. 42, 978-984 (2010).
-
(2010)
Nat. Genet
, vol.42
, pp. 978-984
-
-
Rothman, N.1
-
19
-
-
84875717832
-
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
-
Bojesen, S.E. et al. Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer. Nat. Genet. 45, 371-384 (2013).
-
(2013)
Nat. Genet
, vol.45
, pp. 371-384
-
-
Bojesen, S.E.1
-
20
-
-
82255183150
-
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
-
Haiman, C.A. et al. A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer. Nat. Genet. 43, 1210-1214 (2011).
-
(2011)
Nat. Genet
, vol.43
, pp. 1210-1214
-
-
Haiman, C.A.1
-
21
-
-
84881244262
-
Investigation of six testicular germ cell tumor susceptibility genes suggests a parent-of-origin effect in SPRY4
-
Karlsson, R. et al. Investigation of six testicular germ cell tumor susceptibility genes suggests a parent-of-origin effect in SPRY4. Hum. Mol. Genet. 22, 3373-3380 (2013).
-
(2013)
Hum. Mol. Genet
, vol.22
, pp. 3373-3380
-
-
Karlsson, R.1
-
22
-
-
0033567907
-
Unmutated Ig V(H genes are associated with a more aggressive form of chronic lymphocytic leukemia
-
Hamblin, T.J., Davis, Z., Gardiner, A., Oscier, D.G. & Stevenson, F.K. Unmutated Ig V(H) genes are associated with a more aggressive form of chronic lymphocytic leukemia. Blood 94, 1848-1854 (1999).
-
(1999)
Blood
, vol.94
, pp. 1848-1854
-
-
Hamblin, T.J.1
Davis, Z.2
Gardiner, A.3
Oscier, D.G.4
Stevenson, F.K.5
-
23
-
-
84866871814
-
Mapping cis-and trans-regulatory effects across multiple tissues in twins
-
Grundberg, E. et al. Mapping cis-and trans-regulatory effects across multiple tissues in twins. Nat. Genet. 44, 1084-1089 (2012).
-
(2012)
Nat. Genet
, vol.44
, pp. 1084-1089
-
-
Grundberg, E.1
-
24
-
-
84874548735
-
Common genetic variation contributes significantly to the risk of developing chronic lymphocytic leukemia
-
Di Bernardo, M.C., Broderick, P., Catovsky, D. & Houlston, R.S. Common genetic variation contributes significantly to the risk of developing chronic lymphocytic leukemia. Haematologica 98, e23-e24 (2013).
-
(2013)
Haematologica
, vol.98
-
-
Di Bernardo, M.C.1
Broderick, P.2
Catovsky, D.3
Houlston, R.S.4
-
26
-
-
34447530283
-
Assessment of fludarabine plus cyclophosphamide for patients with chronic lymphocytic leukaemia (the LRF CLL4 Trial): A randomised controlled trial
-
Catovsky, D. et al. Assessment of fludarabine plus cyclophosphamide for patients with chronic lymphocytic leukaemia (the LRF CLL4 Trial): a randomised controlled trial. Lancet 370, 230-239 (2007).
-
(2007)
Lancet
, vol.370
, pp. 230-239
-
-
Catovsky, D.1
-
27
-
-
32144461525
-
Cohort profile: 1958 British birth cohort (National Child Development Study)
-
Power, C. & Elliott, J. Cohort profile: 1958 British birth cohort (National Child Development Study). Int. J. Epidemiol. 35, 34-41 (2006).
-
(2006)
Int. J. Epidemiol
, vol.35
, pp. 34-41
-
-
Power, C.1
Elliott, J.2
-
28
-
-
35648977025
-
National study of colorectal cancer genetics
-
Penegar, S. et al. National study of colorectal cancer genetics. Br. J. Cancer 97, 1305-1309 (2007).
-
(2007)
Br. J. Cancer
, vol.97
, pp. 1305-1309
-
-
Penegar, S.1
-
29
-
-
52049111037
-
Identification of low penetrance alleles for lung cancer: The GEnetic Lung CAncer Predisposition Study (GELCAPS)
-
Eisen, T., Matakidou, A. & Houlston, R. Identification of low penetrance alleles for lung cancer: the GEnetic Lung CAncer Predisposition Study (GELCAPS). BMC Cancer 8, 244 (2008).
-
(2008)
BMC Cancer
, vol.8
, pp. 244
-
-
Eisen, T.1
Matakidou, A.2
Houlston, R.3
-
30
-
-
13744258994
-
Ultraviolet radiation exposure and risk of malignant lymphomas
-
Smedby, K.E. et al. Ultraviolet radiation exposure and risk of malignant lymphomas. J. Natl. Cancer Inst. 97, 199-209 (2005).
-
(2005)
J. Natl. Cancer Inst
, vol.97
, pp. 199-209
-
-
Smedby, K.E.1
-
31
-
-
9144265458
-
Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: Report of the BIOMED-2 Concerted Action BMH4-CT98-3936
-
van Dongen, J.J. et al. Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT98-3936. Leukemia 17, 2257-2317 (2003).
-
(2003)
Leukemia
, vol.17
, pp. 2257-2317
-
-
Van Dongen, J.J.1
-
32
-
-
33846528976
-
Improved reliability of lymphoma diagnostics via PCR-based clonality testing: Report of the BIOMED-2 Concerted Action BHM4-CT98-3936
-
van Krieken, J.H. et al. Improved reliability of lymphoma diagnostics via PCR-based clonality testing: report of the BIOMED-2 Concerted Action BHM4-CT98-3936. Leukemia 21, 201-206 (2007).
-
(2007)
Leukemia
, vol.21
, pp. 201-206
-
-
Van Krieken, J.H.1
-
33
-
-
2342419515
-
Telomere measurement by quantitative PCR
-
Cawthon, R.M. Telomere measurement by quantitative PCR. Nucleic Acids Res. 30, e47 (2002).
-
(2002)
Nucleic Acids Res
, vol.30
-
-
Cawthon, R.M.1
-
34
-
-
34248177465
-
HTERT (-1327)T/C polymorphism is not associated with age-related telomere attrition in peripheral blood
-
Nordfjäll, K., Osterman, P., Melander, O., Nilsson, P. & Roos, G. hTERT (-1327)T/C polymorphism is not associated with age-related telomere attrition in peripheral blood. Biochem. Biophys. Res. Commun. 358, 215-218 (2007).
-
(2007)
Biochem. Biophys. Res. Commun
, vol.358
, pp. 215-218
-
-
Nordfjäll, K.1
Osterman, P.2
Melander, O.3
Nilsson, P.4
Roos, G.5
-
35
-
-
84880817281
-
Short telomere length is associated with NOTCH1/SF3B1/TP53 aberrations and poor outcome in newly diagnosed chronic lymphocytic leukemia patients
-
Mansouri, L. et al. Short telomere length is associated with NOTCH1/SF3B1/TP53 aberrations and poor outcome in newly diagnosed chronic lymphocytic leukemia patients. Am. J. Hematol. 88, 647-651 (2013).
-
(2013)
Am. J. Hematol
, vol.88
, pp. 647-651
-
-
Mansouri, L.1
-
36
-
-
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
-
37
-
-
27644546712
-
Population structure, differential bias and genomic control in a large-scale, case-control association study
-
Clayton, D.G. et al. Population structure, differential bias and genomic control in a large-scale, case-control association study. Nat. Genet. 37, 1243-1246 (2005).
-
(2005)
Nat. Genet
, vol.37
, pp. 1243-1246
-
-
Clayton, D.G.1
-
39
-
-
0037098199
-
Quantifying heterogeneity in a meta-analysis
-
Higgins, J.P. & Thompson, S.G. Quantifying heterogeneity in a meta-analysis. Stat. Med. 21, 1539-1558 (2002).
-
(2002)
Stat. Med
, vol.21
, pp. 1539-1558
-
-
Higgins, J.P.1
Thompson, S.G.2
-
40
-
-
26844482093
-
A fine-scale map of recombination rates and hotspots across the human genome
-
Myers, S., Bottolo, L., Freeman, C., McVean, G. & Donnelly, P. A fine-scale map of recombination rates and hotspots across the human genome. Science 310, 321-324 (2005).
-
(2005)
Science
, vol.310
, pp. 321-324
-
-
Myers, S.1
Bottolo, L.2
Freeman, C.3
McVean, G.4
Donnelly, P.5
-
41
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel, S.B. et al. The structure of haplotype blocks in the human genome. Science 296, 2225-2229 (2002).
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
-
42
-
-
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
-
-
Ward, L.D.1
Kellis, M.2
-
43
-
-
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
-
44
-
-
22244452677
-
Distribution and intensity of constraint in mammalian genomic sequence
-
Cooper, G.M. et al. Distribution and intensity of constraint in mammalian genomic sequence. Genome Res. 15, 901-913 (2005).
-
(2005)
Genome Res
, vol.15
, pp. 901-913
-
-
Cooper, G.M.1
-
45
-
-
77957232748
-
Genevar: A database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies
-
Yang, T.P. et al. Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies. Bioinformatics 26, 2474-2476 (2010).
-
(2010)
Bioinformatics
, vol.26
, pp. 2474-2476
-
-
Yang, T.P.1
|