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Peutz–Jeghers syndrome: a systematic review and recommendations for management

Gut, 2010-07, Vol.59 (7), p.975-986

2010

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Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations

Human molecular genetics, 2005-08, Vol.14 (15), p.2231-2239

2005

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Expression and DNA methylation of TNF, IFNG and FOXP3 in colorectal cancer and their prognostic significance

British journal of cancer, 2014-10, Vol.111 (8), p.1581-1589

2014

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Fanconi anaemia

Journal of medical genetics, 2003-01, Vol.40 (1), p.1-10

2003

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TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres

Gut, 2012-02, Vol.61 (2), p.248-254

2012

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Refining the Amsterdam Criteria and Bethesda Guidelines: Testing Algorithms for the Prediction of Mismatch Repair Mutation Status in the Familial Cancer Clinic

Journal of clinical oncology, 2004-12, Vol.22 (24), p.4934-4943

2004

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The risk of subsequent primary cancers after colorectal cancer in southeast England

Gut, 2002-05, Vol.50 (5), p.647-652

2002

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Deletion and reduced expression of the fanconi anemia FANCA gene in sporadic acute myeloid leukemia

Leukemia, 2004-03, Vol.18 (3), p.420-425

2004

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Incidence of multiple primary cancers in a cohort of women diagnosed with breast cancer in southeast England

British journal of cancer, 2001-02, Vol.84 (3), p.435-440

2001

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Second primary cancers after cervical intraepithelial neoplasia III and invasive cervical cancer in Southeast England

Gynecologic oncology, 2003-07, Vol.90 (1), p.131-136

2003

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An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome

American journal of human genetics, 2003-05, Vol.72 (5), p.1261-1267

2003

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Analysis of Chromosomal Instability in Human Colorectal Adenomas with Two Mutational Hits at APC

Proceedings of the National Academy of Sciences - PNAS, 2002-12, Vol.99 (26), p.16910-16915

2002

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Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome

British journal of cancer, 2003-07, Vol.89 (2), p.308-313

2003

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Polyclonal Origin of Colonic Adenomas in an XO/XY Patient with FAP

Science (American Association for the Advancement of Science), 1996-05, Vol.272 (5265), p.1187-1190

1996

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Analysis of genetic and phenotypic heterogeneity in juvenile polyposis

Gut, 2000-05, Vol.46 (5), p.656-660

2000

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Analysis of candidate modifier loci for the severity of colonic familial adenomatous polyposis, with evidence for the importance of the N-acetyl transferases

Gut, 2004-02, Vol.53 (2), p.271-276

2004

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Germline PTEN mutations in Cowden syndrome-like families

Journal of medical genetics, 1998-11, Vol.35 (11), p.881-885

1998

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Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome

Journal of medical genetics, 2006-04, Vol.43 (4), p.e15-e15

2006

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Explaining variation in familial adenomatous polyposis: relationship between genotype and phenotype and evidence for modifier genes

Gut, 2002-09, Vol.51 (3), p.420-423

2002

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Clinical and molecular features of the hereditary mixed polyposis syndrome

Gastroenterology (New York, N.Y. 1943), 1997-02, Vol.112 (2), p.327-334

1997

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A study of genomic instability in early preneoplastic colonic lesions

Oncogene, 2013-11, Vol.32 (46), p.5333-5337

2013

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Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC families

Journal of medical genetics, 2005-10, Vol.42 (10), p.756-762

2005

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Apoptosis, ageing and cancer susceptibility

British journal of cancer, 2003-02, Vol.88 (4), p.487-490

2003

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Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors

Nature medicine, 2003-05, Vol.9 (5), p.568-574

2003

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A survey of phenotypic features in juvenile polyposis

Journal of medical genetics, 1998-06, Vol.35 (6), p.476-481

1998

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Peutz–Jeghers syndrome: a systematic review and recommendations for management

Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations

Expression and DNA methylation of TNF, IFNG and FOXP3 in colorectal cancer and their prognostic significance

Fanconi anaemia

TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres

Refining the Amsterdam Criteria and Bethesda Guidelines: Testing Algorithms for the Prediction of Mismatch Repair Mutation Status in the Familial Cancer Clinic

The risk of subsequent primary cancers after colorectal cancer in southeast England

Deletion and reduced expression of the fanconi anemia FANCA gene in sporadic acute myeloid leukemia

Incidence of multiple primary cancers in a cohort of women diagnosed with breast cancer in southeast England

Second primary cancers after cervical intraepithelial neoplasia III and invasive cervical cancer in Southeast England

An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome

Analysis of Chromosomal Instability in Human Colorectal Adenomas with Two Mutational Hits at APC

Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome

Polyclonal Origin of Colonic Adenomas in an XO/XY Patient with FAP

Analysis of genetic and phenotypic heterogeneity in juvenile polyposis

Analysis of candidate modifier loci for the severity of colonic familial adenomatous polyposis, with evidence for the importance of the N-acetyl transferases

Germline PTEN mutations in Cowden syndrome-like families

Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome

Explaining variation in familial adenomatous polyposis: relationship between genotype and phenotype and evidence for modifier genes

Clinical and molecular features of the hereditary mixed polyposis syndrome

A study of genomic instability in early preneoplastic colonic lesions

Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC families

Apoptosis, ageing and cancer susceptibility

Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors

A survey of phenotypic features in juvenile polyposis

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