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1

1959-, Eeles Rosalind A., ed. Genetic predisposition to cancer. 2nd ed. London: Arnold, 2004.

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2

1959-, Eeles Rosalind A., ed. Genetic predisposition to cancer. London: Chapman & Hall Medical, 1996.

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3

Côté, Gilbert B. Cancer cytogenetics lookup. Ontario, Canada: Canell, 1999.

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4

Hoda, Anton-Guirgis, and Lynch Henry T, eds. Biomarkers, genetics, and cancer. New York: Van Nostrand Reinhold, 1985.

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5

Garte, Seymour. Genetic Susceptibility to Cancer. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4989-5.

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6

Eeles, Rosalind A., Bruce A. J. Ponder, Douglas F. Easton, and Alan Horwich, eds. Genetic Predisposition to Cancer. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-4501-3.

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7

T, Lynch Henry, and Hirayama Takeshi 1923-, eds. Genetic epidemiology of cancer. Boca Raton, Fla: CRC Press, 1989.

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8

1959-, Eeles Rosalind A., ed. Genetic predisposition to cancer. London: Chapman & Hall Medical, 1996.

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9

1938-, Lindahl T., and Imperial Cancer Research Fund (Great Britain)., eds. Genetic instability in cancer. Plainview, NY: Cold Spring Harbor Laboratory Press, 1996.

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10

W, Weber, Mulvihill John J. 1943-, and Narod Steven A, eds. Familial cancer management. Boca Raton: CRC Press, 1996.

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11

O, Tollefsbol Trygve, ed. Cancer epigenetics. Boca Raton: CRC Press/Taylor & Francis Group, 2009.

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12

K, Cowell John, ed. Molecular genetics of cancer. 2nd ed. Oxford: Bios, 2001.

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13

L, Shaw Gail, ed. Cancer genetics for the clinician. New York: Kluwer Academic/Plenum, 1999.

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14

Antonio, Giordano. Cancer epigenetics: Biomolecular therapeutics in human cancer. Hoboken, N.J: Wiley-Blackwell, 2011.

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15

International Research Conference on Familial Cancer (2nd 1995 Basel, Switzerland). Hereditary cancer: Second International Research Conference on Familial Cancer, Basel, September 11-15, 1995. Edited by Müller Hj, Scott R. J, and Weber W. Basel: Karger, 1996.

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16

Chung, Daniel C., and Daniel A. Haber. Principles of clinical cancer genetics: A handbook from the Massachusetts General Hospital. Edited by Massachusetts General Hospital. New York: Springer, 2010.

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17

Gould, Randi L. Cancer and genetics: Answering your patients' questions. Huntington, NY: PRR, 1997.

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18

M, Lynch Patrick, and Lynch Henry T, eds. Colon cancer genetics. New York: Van Nostrand Reinhold Co., 1985.

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19

Sameer, Aga Syed, Mujeeb Zafar Banday, and Saniya Nissar, eds. Genetic Polymorphism and cancer susceptibility. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6699-2.

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20

Campaign, Cancer Research, ed. Genetic testing for cancer risk. London: Cancer Research Campaign, 1994.

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21

K, Hunt Kelly, Vorburger Stephan A, and Swisher Stephen G, eds. Gene therapy for cancer. Totowa, N.J: Humana Press, 2007.

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22

T, Lynch Henry, and Tăutu Petre, eds. Recent progress in the genetic epidemiology of cancer. Berlin: Springer-Verlag, 1991.

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23

Macadam, Ian. Race against cancer: A genetic approach to control of cancer. Edinburgh: I. Macadam, 1996.

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24

Pasche, Boris. Cancer Genetics. Springer, 2011.

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25

Pasche, Boris. Cancer Genetics. Springer, 2012.

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26

Cancer genetics. New York: Springer, 2010.

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27

Ponder, Bruce, Charis Eng, Douglas Easton, Rosalind Eeles, and Ros Eng. Genetic Predisposition to Cancer. Taylor & Francis Group, 2004.

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28

Cancer Principles and Practice of Oncology: Handbook of Clinical Cancer Genetics. LWW, 2013.

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29

Isaacs, Claudine, and Timothy R. Rebbeck. Hereditary Breast Cancer. Taylor & Francis Group, 2007.

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30

Isaacs, Claudine, and Timothy R. Rebbeck. Hereditary Breast Cancer. Taylor & Francis Group, 2007.

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31

Isaacs, Claudine, and Timothy R. Rebbeck. Hereditary Breast Cancer. Taylor & Francis Group, 2019.

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32

(Editor), Claudine Isaacs, and Timothy R. Rebbeck (Editor), eds. Hereditary Breast Cancer. Informa Healthcare, 2007.

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33

Bunz, Fred. Principles of Cancer Genetics. Springer, 2008.

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34

Bunz, Fred. Principles of Cancer Genetics. Springer, 2010.

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35

Bunz, Fred. Principles of Cancer Genetics. Springer, 2016.

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36

Bunz, Fred. Principles of Cancer Genetics. Springer Netherlands, 2018.

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37

Bunz, Fred. Principles of Cancer Genetics. Springer London, Limited, 2016.

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38

Bunz, Fred. Principles of Cancer Genetics. Springer International Publishing AG, 2022.

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39

Genetic susceptibility to cancer. Boston: Kluwer Academic, 1998.

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40

B. A. J. Ponder (Editor), Webster K. Cavenee (Editor), and E. Solomon (Editor), eds. Genetics and Cancer: A Second Look (Cancer Surveys, Vol 25). Cold Spring Harbor Laboratory Press, 1996.

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41

Penney, Kathryn L., Kyriaki Michailidou, Deanna Alexis Carere, Chenan Zhang, Brandon Pierce, Sara Lindström, and Peter Kraft. Genetic Epidemiology of Cancer. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0005.

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Chapter 5 reviews epidemiologic studies conducted to identify germline (inherited) susceptibility loci. These studies can involve associations observed within high-risk family pedigrees or in large studies of unrelated individuals. The chapter reviews the methods used to estimate the aggregate contribution of inherited genetic susceptibility and to identify specific genetic loci associated with risk. Although there is considerable variability across cancers, most cancers exhibit familial clustering, driven in part by a small number of known rare variants with large relative risks and a larger number of common variants with modest relative risks. The chapter discusses the implications of these findings for clinical care, public health, and tumor biology. It closes with a discussion of open questions, most notably the puzzle of “missing heritability”: the fact that—despite tremendous advances—multiple lines of evidence suggest that most specific risk variants, both rare and common, have yet to be discovered.
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42

Genetic Recombination in Cancer. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-126-39881-6.x5000-3.

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43

Haiman, Christopher, and David J. Hunter. Genetic Epidemiology of Cancer. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190676827.003.0004.

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This chapter explores the genetic epidemiology of cancer: the identification and quantification of inherited genetic factors, and their potential interaction with the environment, in the etiology of cancer in human populations. It also describes the techniques used to identify genetic variants that contribute to cancer susceptibility. It describes the older research methods for identifying the chromosomal localization of high-risk predisposing genes, such as linkage analysis within pedigrees and allele-sharing methods, as it is important to understand the foundations of the field. It also reviews the epidemiologic study designs that can be helpful in identifying low-risk alleles in candidate gene and genome-wide association studies, as well as gene–environment interactions. Finally, it describes some of the genotyping and sequencing platforms commonly employed for high-throughput genome analysis, and the concept of Mendelian randomization and how it may be useful in the study of biomarkers and environmental causes of cancer.
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44

Genetic Susceptibility to Cancer. Springer, 2011.

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45

Horwich, Alan. Genetic Predisposition to Cancer. A Hodder Arnold Publication, 1996.

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46

Koenig, Barbara A., and Henry T. Greely. Genetic Testing for Cancer. University of Cambridge ESOL Examinations, 2004.

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47

Koenig, Barbara A., and Henry T. Greely. Genetic Testing for Cancer. University of Cambridge ESOL Examinations, 2004.

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48

Garte, Seymour. Genetic Susceptibility to Cancer. Springer London, Limited, 2012.

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49

Sherbet, Gajanan V. Genetic Recombination in Cancer. Elsevier Science & Technology Books, 2003.

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50

Eeles, Rosalind A. Genetic Predisposition to Cancer. Springer London, Limited, 2013.

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