Published in QJM on May 01, 2003
Survival in refractory coeliac disease and enteropathy-associated T-cell lymphoma: retrospective evaluation of single-centre experience. Gut (2007) 1.92
Hematologic manifestations of celiac disease. Blood (2006) 1.87
Epidemiology of cancer of the small intestine. World J Gastrointest Oncol (2011) 1.75
Increased risk for non-Hodgkin lymphoma in individuals with celiac disease and a potential familial association. Gastroenterology (2008) 1.36
Small bowel malignancy in coeliac disease. Gut (2004) 1.18
The immune recognition of gluten in coeliac disease. Clin Exp Immunol (2005) 1.10
Duodenal carcinoma at the ligament of Treitz. A molecular and clinical perspective. BMC Gastroenterol (2010) 1.09
Prevalence of celiac disease in adult patients with refractory functional dyspepsia: value of routine duodenal biopsy. World J Gastroenterol (2008) 1.07
Delayed diagnosis of coeliac disease increases cancer risk. BMC Gastroenterol (2007) 1.07
Prevalence and demographic characteristics of celiac disease among blood donors in Ribeirão Preto, State of São Paulo, Brazil. Dig Dis Sci (2006) 0.89
Geographic trends and risk of gastrointestinal cancer among patients with celiac disease in Europe and Asian-Pacific region. Gastroenterol Hepatol Bed Bench (2013) 0.88
Management of Enteropathy-Associated T-Cell Lymphoma: An Algorithmic Approach. Case Rep Oncol (2009) 0.86
Small bowel adenocarcinoma complicating coeliac disease: a report of three cases and the literature review. Case Rep Oncol Med (2012) 0.84
Duodenal Signet Ring Cell Carcinoma in a Celiac Patient. Case Rep Gastroenterol (2009) 0.84
A blinded pilot comparison of capsule endoscopy and small bowel histology in unresponsive celiac disease. Dig Dis Sci (2008) 0.83
Multiphoton tomographic imaging: a potential optical biopsy tool for detecting gastrointestinal inflammation and neoplasia. Cancer Prev Res (Phila) (2012) 0.83
Anti-calreticulin immunoglobulin A (IgA) antibodies in refractory coeliac disease. Clin Exp Immunol (2008) 0.82
Adult celiac disease and its malignant complications. Gut Liver (2009) 0.82
Malignancy in adult celiac disease. World J Gastroenterol (2009) 0.81
Obscure gastrointestinal bleeding and video capsule retention due to enteropathy-associated T-cell lymphoma. Gastroenterol Hepatol (N Y) (2013) 0.80
An unusual case of obscure gastrointestinal bleeding in a patient with coeliac disease. Case Rep Gastrointest Med (2011) 0.77
Duodenal adenocarcinoma might be the cause of intractable nausea and vomiting in patient with coeliac disease. Gastroenterol Hepatol Bed Bench (2012) 0.76
Small bowel carcinoma and coeliac disease. Gut (2004) 0.76
Small Bowel Adenocarcinoma as the Cause of Gastrointestinal Bleeding in Celiac Disease: A Rare Malignancy in a Common Disease. Case Rep Oncol Med (2015) 0.75
Intestinal invagination secondary to intestinal adenocarcinoma in coeliac disease. BMJ Case Rep (2015) 0.75
Small intestinal mucosa expression of putative chaperone fls485. BMC Gastroenterol (2010) 0.75
Aggressive Burkitt-like lymphoma of colon in a patient with prior celiac disease. Yale J Biol Med (2006) 0.75
Computed Tomographic presentation of obstructive jejunal adenocarcinoma associated with celiac disease and incomplete intestinal malrotation. Int J Surg Case Rep (2015) 0.75
Small Bowel Adenocarcinoma in a Patient with Coeliac Disease: Case Report and Review of the Literature. Case Rep Gastroenterol (2010) 0.75
Recurrent small bowel obstruction in a 60-year-old celiac patient: a rare entity of a common disease. Ann Gastroenterol (2014) 0.75
Primary small intestinal lymphoma presenting as a groin abscess. Saudi J Gastroenterol (2009) 0.75
Systematic review of microsatellite instability and colorectal cancer prognosis. J Clin Oncol (2005) 8.15
Mutations in the SMAD4/DPC4 gene in juvenile polyposis. Science (1998) 7.08
A systematic review and meta-analysis of familial colorectal cancer risk. Am J Gastroenterol (2001) 4.61
Seroprevalence, correlates, and characteristics of undetected coeliac disease in England. Gut (2003) 3.30
Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling. Gut (2009) 2.50
Identification of the cystic fibrosis gene. BMJ (1990) 2.34
Interobserver agreement in grading of colorectal cancers-findings from a nationwide web-based survey of histopathologists. Histopathology (2008) 2.32
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A systematic review and meta-analysis of familial prostate cancer risk. BJU Int (2003) 2.01
Systematic review of the relationship between family history and lung cancer risk. Br J Cancer (2005) 1.99
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes. Am J Hum Genet (2001) 1.81
Coeliac disease: a biopsy is not always necessary for diagnosis. Aliment Pharmacol Ther (2008) 1.67
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COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. Br J Cancer (2009) 1.62
Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer. Am J Hum Genet (1997) 1.42
Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43. Am J Hum Genet (2001) 1.42
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. J Med Genet (2006) 1.39
Analysis of genetic and phenotypic heterogeneity in juvenile polyposis. Gut (2000) 1.34
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome. Br J Cancer (2003) 1.33
Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21. Circulation (1998) 1.31
Fracture experience of patients with coeliac disease: a population based survey. Gut (2003) 1.30
Genetics and the common cancers. Eur J Cancer (2001) 1.27
TP53 polymorphisms and lung cancer risk: a systematic review and meta-analysis. Mutagenesis (2003) 1.24
Replication study of SNP associations for colorectal cancer in Hong Kong Chinese. Br J Cancer (2010) 1.24
Risk of malignancy in diagnosed coeliac disease: a 24-year prospective, population-based, cohort study. Aliment Pharmacol Ther (2004) 1.24
Contribution of the MHC region to the familial risk of coeliac disease. J Med Genet (1999) 1.20
Magnetic endoscope imaging: a new technique for localizing colonic lesions. Endoscopy (2002) 1.20
Small bowel malignancy in coeliac disease. Gut (2004) 1.18
Explaining variation in familial adenomatous polyposis: relationship between genotype and phenotype and evidence for modifier genes. Gut (2002) 1.17
Patient perceptions of the burden of coeliac disease and its treatment in the UK. Aliment Pharmacol Ther (2009) 1.16
Familial chronic lymphocytic leukaemia: a survey and review of published studies. Br J Haematol (2000) 1.11
Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas. Br J Cancer (2002) 1.08
Lobular carcinoma in situ of the breast is not caused by constitutional mutations in the E-cadherin gene. Br J Cancer (2000) 1.07
CASP8 variants D302H and -652 6N ins/del do not influence the risk of colorectal cancer in the United Kingdom population. Br J Cancer (2008) 1.06
Microarray comparative genomic hybridisation analysis of intraocular uveal melanomas identifies distinctive imbalances associated with loss of chromosome 3. Br J Cancer (2005) 1.06
The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype. Am J Hum Genet (2001) 1.06
Immunohistochemistry for MSH2 and MHL1: a method for identifying mismatch repair deficient colorectal cancer. J Clin Pathol (2001) 1.05
The TERT variant rs2736100 is associated with colorectal cancer risk. Br J Cancer (2012) 1.05
Genetic predisposition to gastric cancer. QJM (1999) 1.03
Search for inherited susceptibility to radiation-associated meningioma by genomewide SNP linkage disequilibrium mapping. Br J Cancer (2011) 1.03
Chromosomal imbalances in familial chronic lymphocytic leukaemia: a comparative genomic hybridisation analysis. Leukemia (2002) 1.02
Cigarette smoking and adult coeliac disease. Scand J Gastroenterol (2002) 1.01
Further evidence that germline CEBPA mutations cause dominant inheritance of acute myeloid leukaemia. Leukemia (2005) 1.01
Risk of cancer death in first-degree relatives of patients with hereditary non-polyposis cancer syndrome (Lynch type II): a study of 130 kindreds in the United Kingdom. Br J Surg (1990) 1.00
IgA antibodies to human tissue transglutaminase: audit of routine practice confirms high diagnostic accuracy. Scand J Gastroenterol (2004) 0.99
A retrospective observational study of the relationship between family history and survival from colorectal cancer. Br J Cancer (2013) 0.97
A two-phase case-control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22. Br J Cancer (2011) 0.97
CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours. Br J Cancer (2002) 0.97
Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222. Br J Cancer (2013) 0.96
Common genetic variation contributes significantly to the risk of childhood B-cell precursor acute lymphoblastic leukemia. Leukemia (2012) 0.94
STK11 status and intussusception risk in Peutz-Jeghers syndrome. J Med Genet (2006) 0.93
Fluorescent BAT-25 and BAT-26 analysis of T cell prolymphocytic leukaemia. Leukemia (1999) 0.93
Case-control, kin-cohort and meta-analyses provide no support for STK15 F31I as a low penetrance colorectal cancer allele. Br J Cancer (2006) 0.93
Comprehensive analysis of SMAD4 mutations and protein expression in juvenile polyposis: evidence for a distinct genetic pathway and polyp morphology in SMAD4 mutation carriers. Am J Pathol (2001) 0.92
Anticipation in familial chronic lymphocytic leukaemia. Leukemia (1998) 0.91
N-acetyl transferase-2 and bladder cancer risk: a meta-analysis. Environ Mol Mutagen (2000) 0.91
Glutathione S-transferase mu1 (GSTM1) status and bladder cancer risk: a meta-analysis. Mutagenesis (2000) 0.90
Transverse limb deficiency, facial clefting and hypoxic renal damage: an association with treatment of maternal hypertension? Clin Dysmorphol (1995) 0.90
TGFBR1 variants TGFBR1(*)6A and Int7G24A are not associated with an increased familial colorectal cancer risk. Br J Cancer (2009) 0.90
Comprehensive analysis of common mitochondrial DNA variants and colorectal cancer risk. Br J Cancer (2008) 0.89
Linkage analysis for ATM in familial B cell chronic lymphocytic leukaemia. Leukemia (1999) 0.89
Folate and colorectal cancer prevention. Br J Cancer (2008) 0.89
HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease. Br J Cancer (2002) 0.89
Neurological complications of coeliac disease. Postgrad Med J (2002) 0.89
Effects of medications on post-endoscopic retrograde cholangiopancreatography pancreatitis. Pancreatology (2010) 0.88
The neurology of enteric disease. J Neurol Neurosurg Psychiatry (2006) 0.88
A comprehensive analysis of MNG1, TCO1, fPTC, PTEN, TSHR, and TRKA in familial nonmedullary thyroid cancer: confirmation of linkage to TCO1. J Clin Endocrinol Metab (2001) 0.88
Further observations on the relationship between the FGFR4 Gly388Arg polymorphism and lung cancer prognosis. Br J Cancer (2007) 0.88
CDX2 mutations do not account for juvenile polyposis or Peutz-Jeghers syndrome and occur infrequently in sporadic colorectal cancers. Br J Cancer (2001) 0.88
Genome screening of coeliac disease. J Med Genet (2002) 0.87
The 14q22.2 colorectal cancer variant rs4444235 shows cis-acting regulation of BMP4. Oncogene (2011) 0.87
Prediction of genetic risks from segregation analyses of morbid risks. Hum Hered (1994) 0.87
Low frequency of germline E-cadherin mutations in familial and nonfamilial gastric cancer. Br J Cancer (1999) 0.86
Variant IRF4/MUM1 associates with CD38 status and treatment-free survival in chronic lymphocytic leukaemia. Leukemia (2010) 0.86
CLL family 'Pedigree 14' revisited: 1947-2004. Leukemia (2005) 0.86
Is the E133K allele of VG5Q associated with Klippel-Trenaunay and other overgrowth syndromes? J Med Genet (2006) 0.85
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3. Gut (2008) 0.85
Apparent Mendelian inheritance of breast and colorectal cancer: chance, genetic heterogeneity or a new gene? Fam Cancer (2001) 0.85
Disparity between apolipoprotein E phenotypes and genotypes (as determined by polymerase chain reaction and oligonucleotide probes) in patients with non-insulin-dependent diabetes mellitus. Clin Chim Acta (1991) 0.85
Microsatellite instability indicative of defects in the major mismatch repair genes is rare in patients with B-cell chronic lymphocytic leukemia: Evaluation with disease stage and family history. Leuk Lymphoma (2007) 0.83
Catabolic rate of low density lipoprotein is influenced by variation in the apolipoprotein B gene. J Clin Invest (1988) 0.83
Genetic susceptibility to gluten sensitive enteropathy in Irish setter dogs is not linked to the major histocompatibility complex. Tissue Antigens (1998) 0.82
Two hits revisited again. J Med Genet (2001) 0.82
Germline mutations in Dok1 do not predispose to chronic lymphocytic leukemia. Leuk Res (2005) 0.82
Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instability. Cancer Genet Cytogenet (2003) 0.82
Optimising methods for determining RER status in colorectal cancers. Cancer Lett (2000) 0.82
Prognostic significance of folate metabolism polymorphisms for lung cancer. Br J Cancer (2007) 0.81
Increased sex concordance of sibling pairs with chronic lymphocytic leukemia. Leukemia (2004) 0.81
IgA-antitissue transglutaminase: validation of a commercial assay for diagnosing coeliac disease. Clin Lab (2002) 0.81
Risk of developing chronic lymphocytic leukemia is influenced by HLA-A class I variation. Leukemia (2012) 0.80
Linkage analysis for major histocompatibility complex-related genetic susceptibility in familial chronic lymphocytic leukemia. Blood (2000) 0.80
Thymidylate synthase polymorphisms, folate and B-vitamin intake, and risk of colorectal adenoma. Br J Cancer (2007) 0.80
Localisation of the gene for glycogen storage disease type 1c by homozygosity mapping to 11q. J Med Genet (1998) 0.80
Monoclonal B-cell lymphocytosis (MBL) in CLL families: substantial increase in relative risk for young adults. Leukemia (2006) 0.80
Distinct genetic and epigenetic changes in medullary breast cancer. Int J Surg Pathol (2003) 0.80
Autoantibodies to human tissue transglutaminase: superior predictors of coeliac disease. Scand J Gastroenterol (2002) 0.80
Analysis of Li-Fraumeni syndrome and Li-Fraumeni-like families for germline mutations in Bcl10. Cancer Lett (1999) 0.79
Contribution of germline MLH1 and MSH2 mutations to lobular carcinoma in situ of the breast. Cancer Lett (2001) 0.79
Inherited pericentric inversion (X)(p11.4q11.2) associated with delayed puberty and obesity in two brothers. Cytogenet Genome Res (2005) 0.78
Relative power of linkage and transmission disequilibrium test strategies to detect non-HLA linked coeliac disease susceptibility genes. Gut (1999) 0.78