Literature DB >> 11602375

Genetics and the common cancers.

J Peto1, R S Houlston.   

Abstract

Rare highly penetrant genes cannot account for much of the familial risk for most common cancers, and there is increasing evidence that a high proportion of cancers arise in a susceptible minority who carry low-penetrance genes or gene combinations. The evidence for the existence of such genes and the prospects for identifying them are reviewed.

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Year:  2001        PMID: 11602375     DOI: 10.1016/s0959-8049(01)00255-6

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  24 in total

1.  The future of association studies of common cancers.

Authors:  Richard S Houlston; Julian Peto
Journal:  Hum Genet       Date:  2003-02-06       Impact factor: 4.132

2.  Mechanisms of the formation of radiation-induced chromosomal aberrations.

Authors:  Peter E Bryant; Andrew C Riches; Samantha Y A Terry
Journal:  Mutat Res       Date:  2010-03-27       Impact factor: 2.433

3.  Family history of cancer and head and neck cancer survival.

Authors:  Kayla R Getz; Laura S Rozek; Lisa A Peterson; Emily L Bellile; Jeremy M G Taylor; Gregory T Wolf; Alison M Mondul
Journal:  Laryngoscope       Date:  2017-03-07       Impact factor: 3.325

4.  Family history and risk of renal cell carcinoma: results from a case-control study and systematic meta-analysis.

Authors:  Jessica Clague; Jie Lin; Adrian Cassidy; Surena Matin; Nizar M Tannir; Pheroze Tamboli; Christopher G Wood; Xifeng Wu
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2009-02-24       Impact factor: 4.254

Review 5.  Epidemiological and genetic factors underlying melanoma development in Italy.

Authors:  Giuseppe Palmieri; Maria Colombino; Milena Casula; Mario Budroni; Antonella Manca; Maria Cristina Sini; Amelia Lissia; Ignazio Stanganelli; Paolo A Ascierto; Antonio Cossu
Journal:  Melanoma Manag       Date:  2015-05-18

6.  Ordinal Logic Regression: A classifier for discovering combinations of binary markers for ordinal outcomes.

Authors:  Bethany J Wolf; Elizabeth H Slate; Elizabeth G Hill
Journal:  Comput Stat Data Anal       Date:  2015-02-01       Impact factor: 1.681

7.  Two functional coding single nucleotide polymorphisms in STK15 (Aurora-A) coordinately increase esophageal cancer risk.

Authors:  Makoto T Kimura; Takahiro Mori; Jeffrey Conroy; Norma J Nowak; Susumu Satomi; Katsuyuki Tamai; Hiroki Nagase
Journal:  Cancer Res       Date:  2005-05-01       Impact factor: 12.701

8.  PLCE1 rs2274223 A>G polymorphism and cancer risk: a meta-analysis.

Authors:  Meenakshi Umar; Rohit Upadhyay; Balraj Mittal
Journal:  Tumour Biol       Date:  2013-12

9.  Family history of cancer: pooled analysis in the International Head and Neck Cancer Epidemiology Consortium.

Authors:  Eva Negri; Paolo Boffetta; Julien Berthiller; Xavier Castellsague; Maria Paula Curado; Luigino Dal Maso; Alexander W Daudt; Eleonora Fabianova; Leticia Fernandez; Victor Wünsch-Filho; Silvia Franceschi; Richard B Hayes; Rolando Herrero; Sergio Koifman; Philip Lazarus; Juan J Lence; Fabio Levi; Dana Mates; Elena Matos; Ana Menezes; Joshua Muscat; Jose Eluf-Neto; Andrew F Olshan; Peter Rudnai; Oxana Shangina; Erich M Sturgis; Neonilia Szeszenia-Dabrowska; Renato Talamini; Qingyi Wei; Deborah M Winn; David Zaridze; Jolanta Lissowska; Zuo-Feng Zhang; Gilles Ferro; Paul Brennan; Carlo La Vecchia; Mia Hashibe
Journal:  Int J Cancer       Date:  2009-01-15       Impact factor: 7.396

10.  Null association between histology of first and second primary malignancies in men with bilateral testicular germ cell tumors.

Authors:  Jennifer Phay Johnson Thomas; Carol Davis-Dao; Juan Pablo Lewinger; Kimberly D Siegmund; Ann S Hamilton; Siamak Daneshmand; Eila C Skinner; Duncan C Thomas; Victoria K Cortessis
Journal:  Am J Epidemiol       Date:  2013-08-08       Impact factor: 4.897

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