Richard Houlston - Selected Publications#

From Google Scholar: Citations 59,436; h-index 119; i10-index 591; Selected Recent Publications (from 746)

1. Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features. Robbe P, Ridout KE, Vavoulis DV, Dréau H, Kinnersley B, Denny N, Chubb D, ......Devereux S, Pettitt AR, Hillmen P, Caulfield MJ, Houlston RS, Martín-Subero JI, Schuh A. Nat Genet. 2022;54(11):1675-1689. doi: 10.1038/s41588-022-01211-y.

2. Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Ajore R, Niroula A, Pertesi M, Cafaro C, Thodberg M, Went M, Bao EL, Duran-Lozano L, Lopez de Lapuente Portilla A, ...., Jonsdottir I, Munshi N, Rafnar T, Waage A, Weinhold N, Thorsteinsdottir U, Sankaran VG, Stefansson K, Houlston R, Nilsson B. Nat Commun. 2022;13(1):151. doi: 10.1038/s41467-021-27666-x.

3. Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk. Vijayakrishnan J, Qian M, Studd JB, Yang W, Kinnersley B, Law PJ, Broderick P, ...., Schrappe M, Relling MV, Stanulla M, Loh ML, Houlston RS, Yang JJ. Nat Commun. 2019;10(1):5348. doi: 10.1038/s41467-019-13069-6.

4. Modifiable pathways for colorectal cancer: a mendelian randomisation analysis. Cornish AJ, Law PJ, Timofeeva M, Palin K, Farrington SM, Palles C, Jenkins MA, Casey G, Brenner H, Chang-Claude J, Hoffmeister M, Kirac I, Maughan T, Brezina S, Gsur A, Cheadle JP, Aaltonen LA, Tomlinson I, Dunlop MG, Houlston RS. Lancet Gastroenterol Hepatol. 2020;5(1):55-62. doi: 10.1016/S2468-1253(19)30294-8.

5. Promoter capture Hi-C-based identification of recurrent noncoding mutations in colorectal cancer. Orlando G, Law PJ, Cornish AJ, Dobbins SE, Chubb D, Broderick P, Litchfield K, Hariri F, Pastinen T, Osborne CS, Taipale J, Houlston RS. Nat Genet. 2018;50(10):1375-1380. doi: 10.1038/s41588-018-0211-z.

6. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. Went M, Sud A, Försti A, Halvarsson BM, Weinhold N, Kimber S, van Duin M, Thorleifsson G, Holroyd A, Johnson DC, Li N, Orlando G, Law PJ, Ali M, Chen B, Mitchell JS, Gudbjartsson DF, Kuiper R, Stephens OW, Bertsch U, Broderick P, Campo C, Bandapalli OR, .....Hansson M, Goldschmidt H, Kaiser M, Sonneveld P, Stefansson K, Morgan GJ, Hemminki K, Nilsson B, Houlston RS; PRACTICAL consortium. Nat Commun. 2018;9(1):3707. doi: 10.1038/s41467-018-04989-w.

7. Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma. Sud A, Thomsen H, Orlando G, Försti A, Law PJ, Broderick P, Cooke R, Hariri F, Pastinen T, Easton DF, Pharoah PDP, Dunning AM, Peto J, Canzian F, Eeles R, Kote-Jarai Z, Muir K, Pashayan N, Campa D; PRACTICAL Consortium, Hoffmann P, Nöthen MM, Jöckel KH, von Strandmann EP, Swerdlow AJ, Engert A, Orr N, Hemminki K, Houlston RS. Blood. 2018;132(19):2040-2052. doi: 10.1182/blood-2018-06-855296.

8. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia.Vijayakrishnan J, Studd J, Broderick P, Kinnersley B, Holroyd A, Law PJ, Kumar R, Allan JM, Harrison CJ, Moorman AV, Vora A, ....., Greaves M, Zimmerman M, Bartram CR, Schrappe M, Stanulla M, Hemminki K, Houlston RS. Nat Commun. 2018;9(1):1340. doi: 10.1038/s41467-018-03178-z.

9. Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Melin BS, Barnholtz-Sloan JS, Wrensch MR, Johansen C, Il'yasova D, Kinnersley B, Ostrom QT, .... Bernstein JL, Davis F, Lachance D, Lau C, Merrell RT, Shildkraut J, Ali-Osman F, Sadetzki S, Scheurer M, Shete S, Lai RK, Claus EB, Olson SH, Jenkins RB, Houlston RS, Bondy ML. Nat Genet. 2017;49(5):789-794. doi: 10.1038/ng.3823.

10. Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2. Studd JB, Vijayakrishnan J, Yang M, Migliorini G, Paulsson K, Houlston RS. Nat Commun. 2017;8:14616. doi: 10.1038/ncomms14616.