Year |
Citation |
Score |
2019 |
Vijayakrishnan J, Qian M, Studd JB, Yang W, Kinnersley B, Law PJ, Broderick P, Raetz EA, Allan J, Pui CH, Vora A, Evans WE, Moorman A, Yeoh A, Yang W, et al. Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk. Nature Communications. 10: 5348. PMID 31767839 DOI: 10.1038/s41467-019-13069-6 |
0.315 |
|
2018 |
Vijayakrishnan J, Studd J, Broderick P, Kinnersley B, Holroyd A, Law PJ, Kumar R, Allan JM, Harrison CJ, Moorman AV, Vora A, Roman E, Rachakonda S, Kinsey SE, Sheridan E, et al. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. Nature Communications. 9: 1340. PMID 29632299 DOI: 10.1038/s41467-018-03178-z |
0.302 |
|
2017 |
Law PJ, Berndt SI, Speedy HE, Camp NJ, Sava GP, Skibola CF, Holroyd A, Joseph V, Sunter NJ, Nieters A, Bea S, Monnereau A, Martin-Garcia D, Goldin LR, Clot G, ... ... Allan JM, et al. Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia. Nature Communications. 8: 14175. PMID 28165464 DOI: 10.1038/Ncomms14175 |
0.311 |
|
2015 |
Vijayakrishnan J, Henrion M, Moorman AV, Fiege B, Kumar R, Inacio da Silva Filho M, Holroyd A, Koehler R, Thomsen H, Irving JA, Allan JM, Lightfoot T, Roman E, Kinsey SE, Sheridan E, et al. The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A. Scientific Reports. 5: 15065. PMID 26463672 DOI: 10.1038/srep15065 |
0.304 |
|
2014 |
Speedy HE, Di Bernardo MC, Sava GP, Dyer MJ, Holroyd A, Wang Y, Sunter NJ, Mansouri L, Juliusson G, Smedby KE, Roos G, Jayne S, Majid A, Dearden C, Hall AG, ... ... Allan JM, et al. A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. Nature Genetics. 46: 56-60. PMID 24292274 DOI: 10.1038/ng.2843 |
0.315 |
|
2013 |
Migliorini G, Fiege B, Hosking FJ, Ma Y, Kumar R, Sherborne AL, da Silva Filho MI, Vijayakrishnan J, Koehler R, Thomsen H, Irving JA, Allan JM, Lightfoot T, Roman E, Kinsey SE, et al. Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. Blood. 122: 3298-307. PMID 23996088 DOI: 10.1182/blood-2013-03-491316 |
0.324 |
|
2013 |
Chubb D, Weinhold N, Broderick P, Chen B, Johnson DC, Försti A, Vijayakrishnan J, Migliorini G, Dobbins SE, Holroyd A, Hose D, Walker BA, Davies FE, Gregory WA, Jackson GH, ... ... Allan JM, et al. Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Nature Genetics. 45: 1221-5. PMID 23955597 DOI: 10.1038/ng.2733 |
0.386 |
|
2009 |
Papaemmanuil E, Hosking FJ, Vijayakrishnan J, Price A, Olver B, Sheridan E, Kinsey SE, Lightfoot T, Roman E, Irving JA, Allan JM, Tomlinson IP, Taylor M, Greaves M, Houlston RS. Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. Nature Genetics. 41: 1006-10. PMID 19684604 DOI: 10.1038/ng.430 |
0.315 |
|
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