Works matching AU Houlston, Richard S
Results: 155
Evaluation of germline BMP4 mutation as a cause of colorectal cancer.
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- Human Mutation, 2011, v. 32, n. 1, p. E1928, doi. 10.1002/humu.21376
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- Publication type:
- Article
Increasing evidence that germline mutations in CHEK2 do not cause Li-Fraumeni syndrome.
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- Human Mutation, 2002, v. 20, n. 6, p. 460, doi. 10.1002/humu.10136
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- Publication type:
- Article
A robust method for detecting CHK2/RAD53 mutations in genomic DNA.
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- Human Mutation, 2002, v. 19, n. 2, p. 173, doi. 10.1002/humu.10031
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- Publication type:
- Article
Diffuse gliomas classified by 1p/19q co-deletion, <italic>TERT</italic> promoter and IDH mutation status are associated with specific genetic risk loci.
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- Acta Neuropathologica, 2018, v. 135, n. 5, p. 743, doi. 10.1007/s00401-018-1825-z
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- Article
Putative cis-regulatory drivers in colorectal cancer.
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- Nature, 2014, v. 512, n. 7512, p. 87, doi. 10.1038/nature13602
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- Article
Associations between genetic variants in mRNA splicing-related genes and risk of lung cancer: a pathway-based analysis from published GWASs.
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- Scientific Reports, 2017, p. 44634, doi. 10.1038/srep44634
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- Publication type:
- Article
Frequency of pathogenic germline variants in cancer susceptibility genes in 1336 renal cell carcinoma cases.
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- Human Molecular Genetics, 2022, v. 31, n. 17, p. 3001, doi. 10.1093/hmg/ddac089
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- Article
Elongin C (ELOC/TCEB1)-associated von Hippel–Lindau disease.
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- Human Molecular Genetics, 2022, v. 31, n. 16, p. 2728, doi. 10.1093/hmg/ddac066
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- Article
Genetic variation in ST6GAL1 is a determinant of capecitabine and oxaliplatin induced hand‐foot syndrome.
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- International Journal of Cancer, 2022, v. 151, n. 6, p. 957, doi. 10.1002/ijc.34046
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- Article
Alcohol consumption, DNA methylation and colorectal cancer risk: Results from pooled cohort studies and Mendelian randomization analysis.
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- International Journal of Cancer, 2022, v. 151, n. 1, p. 83, doi. 10.1002/ijc.33945
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- Article
Bidirectional Mendelian randomisation analysis of the relationship between circulating vitamin D concentration and colorectal cancer risk.
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- International Journal of Cancer, 2022, v. 150, n. 2, p. 303, doi. 10.1002/ijc.33779
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- Article
Genome‐wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer.
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- International Journal of Cancer, 2021, v. 149, n. 9, p. 1713, doi. 10.1002/ijc.33739
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- Article
Prediction of colorectal cancer risk based on profiling with common genetic variants.
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- International Journal of Cancer, 2020, v. 147, n. 12, p. 3431, doi. 10.1002/ijc.33191
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- Publication type:
- Article
Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia.
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- International Journal of Cancer, 2017, v. 141, n. 9, p. 1794, doi. 10.1002/ijc.30883
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- Article
The Challenges of Genome Analysis in the Health Care Setting.
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- Genes, 2014, v. 5, n. 3, p. 576, doi. 10.3390/genes5030576
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- Publication type:
- Article
Architecture of Inherited Susceptibility to Colorectal Cancer: A Voyage of Discovery.
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- Genes, 2014, v. 5, n. 2, p. 270, doi. 10.3390/genes5020270
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- Publication type:
- Article
Meta-Analyses of Splicing and Expression Quantitative Trait Loci Identified Susceptibility Genes of Glioma.
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- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.609657
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- Publication type:
- Article
Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays.
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- Nucleic Acids Research, 2004, v. 32, n. 20, p. e164, doi. 10.1093/nar/gnh163
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- Article
Polygenic susceptibility to testicular cancer: implications for personalised health care.
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- 2016
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- Publication type:
- journal article
Polygenic susceptibility to testicular cancer: implications for personalised health care.
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- 2015
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- Publication type:
- journal article
Glioma-related seizures in relation to histopathological subtypes: a report from the glioma international case-control study.
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- Journal of Neurology, 2018, v. 265, n. 6, p. 1432, doi. 10.1007/s00415-018-8857-0
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- Publication type:
- Article
Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study.
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- Journal of Neuro-Oncology, 2019, v. 145, n. 2, p. 287, doi. 10.1007/s11060-019-03294-w
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- Article
Candidate gene association studies and risk of Hodgkin lymphoma: a systematic review and meta-analysis.
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- 2017
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- Publication type:
- journal article
Reference bias in the Illumina Isaac aligner.
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- Bioinformatics, 2020, v. 36, n. 17, p. 4671, doi. 10.1093/bioinformatics/btaa514
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- Publication type:
- Article
Relationship between genetically determined telomere length and glioma risk.
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- Neuro-Oncology, 2022, v. 24, n. 2, p. 171, doi. 10.1093/neuonc/noab208
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- Publication type:
- Article
Partitioned glioma heritability shows subtype-specific enrichment in immune cells.
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- Neuro-Oncology, 2021, v. 23, n. 8, p. 1304, doi. 10.1093/neuonc/noab072
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- Article
Lack of association between modifiable exposures and glioma risk: a Mendelian randomization analysis.
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- Neuro-Oncology, 2020, v. 22, n. 2, p. 207, doi. 10.1093/neuonc/noz209
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- Publication type:
- Article
Sex-specific gene and pathway modeling of inherited glioma risk.
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- Neuro-Oncology, 2019, v. 21, n. 1, p. 71, doi. 10.1093/neuonc/noy135
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- Publication type:
- Article
Genetic variation in the DNA repair genes is predictive of outcome in lung cancer.
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- Human Molecular Genetics, 2007, v. 16, n. 19, p. 2333, doi. 10.1093/hmg/ddm190
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- Article
MTHFR C677T has differential influence on risk of MSI and MSS colorectal cancer.
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- Human Molecular Genetics, 2007, v. 16, n. 9, p. 1072, doi. 10.1093/hmg/ddm055
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- Publication type:
- Article
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3592, doi. 10.1093/hmg/ddl435
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- Publication type:
- Article
Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives.
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- Human Molecular Genetics, 2006, v. 15, n. 21, p. 3263, doi. 10.1093/hmg/ddl401
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- Publication type:
- Article
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2903, doi. 10.1093/hmg/ddl231
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- Article
Genome-wide association studies for detecting cancer susceptibility.
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- British Medical Bulletin, 2011, v. 97, n. 1, p. 27, doi. 10.1093/bmb/ldq038
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- Publication type:
- Article
The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium.
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- American Journal of Epidemiology, 2016, v. 183, n. 2, p. 85, doi. 10.1093/aje/kwv235
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- Publication type:
- Article
Comprehensive Evaluation of the Impact of 14 Genetic Variants on Colorectal Cancer Phenotype and Risk.
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- 2012
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- Publication type:
- Journal Article
Comprehensive Evaluation of the Impact of 14 Genetic Variants on Colorectal Cancer Phenotype and Risk.
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- American Journal of Epidemiology, 2012, v. 175, n. 1, p. 1, doi. 10.1093/aje/kwr285
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- Publication type:
- Article
Interaction Between 5 Genetic Variants and Allergy in Glioma Risk.
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- American Journal of Epidemiology, 2010, v. 171, n. 11, p. 1165, doi. 10.1093/aje/kwq075
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- Article
Germline variation in RASAL2 may predict survival in patients with RAS‐activated colorectal cancer.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 6, p. 332, doi. 10.1002/gcc.23133
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- Article
Investigation of the effects of DNA repair gene polymorphisms on the risk of colorectal cancer.
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- Mutagenesis, 2012, v. 27, n. 2, p. 219, doi. 10.1093/mutage/ger070
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- Article
COGENT (COlorectal cancer GENeTics) revisited.
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- Mutagenesis, 2012, v. 27, n. 2, p. 143
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- Publication type:
- Article
SNPLINK: multipoint linkage analysis of densely distributed SNP data incorporating automated linkage disequilibrium removal.
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- Bioinformatics, 2005, v. 21, n. 13, p. 3060
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- Article
Exploiting gene dependency to inform drug development for multiple myeloma.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-16940-7
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- Publication type:
- Article
RISK OF CANCER IN RELATIVES OF PATIENTS WITH CUTANEOUS MELANOMA.
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- 1993
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- Publication type:
- Report
Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2.
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- Nature Communications, 2017, v. 8, n. 3, p. 14616, doi. 10.1038/ncomms14616
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- Publication type:
- Article
The non-coding variant rs1800734 enhances DCLK3 expression through long-range interaction and promotes colorectal cancer progression.
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- Nature Communications, 2017, v. 8, n. 2, p. 14418, doi. 10.1038/ncomms14418
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- Publication type:
- Article
Rare disruptive mutations in ciliary function genes contribute to testicular cancer susceptibility.
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- Nature Communications, 2016, v. 7, n. 12, p. 13840, doi. 10.1038/ncomms13840
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- Publication type:
- Article
Multiple myeloma risk variant at 7p15.3 creates an IRF4-binding site and interferes with CDCA7L expression.
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- Nature Communications, 2016, v. 7, n. 11, p. 13656, doi. 10.1038/ncomms13656
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- Publication type:
- Article
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.
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- Nature Communications, 2016, v. 7, n. 6, p. 11883, doi. 10.1038/ncomms11883
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- Publication type:
- Article
Identification of four new susceptibility loci for testicular germ cell tumour.
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- Nature Communications, 2015, v. 6, n. 10, p. 8690, doi. 10.1038/ncomms9690
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- Publication type:
- Article