Daniel D Buchanan


Ontology type: schema:Person     


Person Info

NAME

Daniel D

SURNAME

Buchanan

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-01-22 Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene in FAMILIAL CANCER
  • 2019-01 Discovery of common and rare genetic risk variants for colorectal cancer in NATURE GENETICS
  • 2018-12 DUSP5 is methylated in CIMP-high colorectal cancer but is not a major regulator of intestinal cell proliferation and tumorigenesis in SCIENTIFIC REPORTS
  • 2018-10 Correction: Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 in GENETICS IN MEDICINE
  • 2018-10 DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome in MODERN PATHOLOGY
  • 2018-08 Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 in GENETICS IN MEDICINE
  • 2018-06 Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2018-04 Novel associations between blood DNA methylation and body mass index in middle-aged and older adults in INTERNATIONAL JOURNAL OF OBESITY
  • 2018-01 RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers in FAMILIAL CANCER
  • 2018-01 Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas in FAMILIAL CANCER
  • 2016-12 Promoter methylation of ITF2, but not APC, is associated with microsatellite instability in two populations of colorectal cancer patients in BMC CANCER
  • 2016-12 GWASeq: targeted re-sequencing follow up to GWAS in BMC GENOMICS
  • 2016-08 Cholecystectomy and the risk of colorectal cancer by tumor mismatch repair deficiency status in INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
  • 2016-07 Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2016-04 Determining the familial risk distribution of colorectal cancer: a data mining approach in FAMILIAL CANCER
  • 2015-12 Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene in FAMILIAL CANCER
  • 2015-12 Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 in SCIENTIFIC REPORTS
  • 2015-12 Childhood cancers in families with and without Lynch syndrome in FAMILIAL CANCER
  • 2015-09 A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer in SCIENTIFIC REPORTS
  • 2014-12 High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry in FAMILIAL CANCER
  • 2014-07 Characterisation of Familial Colorectal Cancer Type X, Lynch syndrome, and non-familial colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2014-03 The Association of Telomere Length with Colorectal Cancer Differs by the Age of Cancer Onset in CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY
  • 2013-12 Expression of MUC2, MUC5AC, MUC5B, and MUC6 mucins in colorectal cancers and their association with the CpG island methylator phenotype in MODERN PATHOLOGY
  • 2013-09 Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything? in FAMILIAL CANCER
  • 2013-07 Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins in MODERN PATHOLOGY
  • 2013-06 Colorectal carcinomas with KRAS mutation are associated with distinctive morphological and molecular features in MODERN PATHOLOGY
  • 2013-06 Risk of Metachronous Colon Cancer Following Surgery for Rectal Cancer in Mismatch Repair Gene Mutation Carriers in ANNALS OF SURGICAL ONCOLOGY
  • 2013-04 KRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markers in BRITISH JOURNAL OF CANCER
  • 2012-12 A study of cancer risks in relatives of patients with serrated polyposis in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-12 Serrated polyposis syndrome and colonoscopic surveillance: who is it safe to follow? in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-12 Estimation of probabilities in favour of pathogenicity for missense substitutions for use in clinical evaluation of mismatch repair gene variants in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-12 Colorectal tumour BRAF V600E and MLH1 promoter methylation status in the assessment of mismatch repair gene sequence variants of unknown clinical significance in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-12 Substantial unexplained variation in cancer risks for MLH1 and MSH2 mutation carriers in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-12 The relationship between the BRAF p.V600E mutation and a family history of CRC in the early-onset CRC cases from the Australasian Colon Cancer Family Study in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-05 Cancer Risks for Relatives of Patients With Serrated Polyposis in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2012-05 Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry in MODERN PATHOLOGY
  • 2011-12 Colorectal cancer in hyperplastic polyposis syndrome: In search of the polyp of origin in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2011-12 Risks of cancers for carriers of monoallelic MUTYH mutation with a family history of colorectal cancer in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2011-12 Hyperplastic Polyposis and the smoking paradox in females in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2011-06 Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome) in FAMILIAL CANCER
  • 2011-06 Mutation deep within an intron of MSH2 causes Lynch syndrome in FAMILIAL CANCER
  • 2011-06 Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patients in BRITISH JOURNAL OF CANCER
  • 2011-06 Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes in BRITISH JOURNAL OF CANCER
  • 2010-12 Erratum to: Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study in INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
  • 2010-12 Linkage to chromosome 2q32.2-q35 in families with serrated neoplasia in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2010-06 Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study in INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
  • 2009-12 Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis in FAMILIAL CANCER
  • 2007-12 Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants? in BREAST CANCER RESEARCH
  • 2007-02 Stability of BAT26 in Lynch syndrome colorectal tumours in EUROPEAN JOURNAL OF HUMAN GENETICS
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