Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancerEvaluation of NTHL1, NEIL1, NEIL2, MPG, TDG, UNG and SMUG1 genes in familial colorectal cancer predispositionSequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndromeGenome-wide association study of glioma and meta-analysisMutations in PTF1A cause pancreatic and cerebellar agenesisA cancer-associated aurora A mutant is mislocalized and misregulated due to loss of interaction with TPX2Risk of breast and prostate cancer is not associated with increased homozygosity in outbred populationsGermline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomasDICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumorsDeciphering the impact of common genetic variation on lung cancer risk: a genome-wide association studyCommon 5p15.33 and 6p21.33 variants influence lung cancer riskThe colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expressionIs the E133K allele of VG5Q associated with Klippel-Trenaunay and other overgrowth syndromes?Unregulated smooth-muscle myosin in human intestinal neoplasiaA genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinomaGenetic variants of UGT1A6 influence risk of colorectal adenoma recurrenceLow-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutationsPolymorphisms in PTGS1, PTGS2 and IL-10 do not influence colorectal adenoma recurrence in the context of a randomized aspirin intervention trialComprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancerGermline mutations in shelterin complex genes are associated with familial gliomaLoci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemiaA systematic review and meta-analysis of the relationship between chromosome 18q genotype, DCC status and colorectal cancer prognosisMultiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arraysSystematic review of microsatellite instability and colorectal cancer prognosisRelationship between ARLTS1 polymorphisms and risk of chronic lymphocytic leukemiaThe Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International ConsortiumPleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortiaInherited variation in immune genes and pathways and glioblastoma riskAssociation of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer--a finding from Texas lung cancer genome-wide association studyTargeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene ConsortiumMosaic PPM1D mutations are associated with predisposition to breast and ovarian cancerCross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic AssociationsDeciphering associations for lung cancer risk through imputation and analysis of 12,316 cases and 16,831 controlsNovel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer RiskThe 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2AGermline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancerCross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal CancerGenetic advances in glioma: susceptibility genes and networksTelomere structure and maintenance gene variants and risk of five cancer types
P50
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P50
description
Professor of Molecular and Population Genetics, Institute of Cancer Research
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Richard Houlston
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Richard Houlston
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Richard Houlston
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Richard Houlston
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Houlston RS
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Richard S Houlston
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Richard S. Houlston
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Richard Somerset Houlston
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Richard Houlston
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Richard Houlston
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Richard Houlston
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Richard Houlston
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Richard Houlston
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Richard Houlston
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Richard Houlston
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Richard Houlston
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Richard Houlston
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Richard Houlston
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P101
P106
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richard-houlston-13397
P21
P31
P496
0000-0002-5268-0242
P569
1956-07-10T00:00:00Z