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Books on the topic 'Genetic risk factors'

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Author: Grafiati

Published: 4 June 2021

Last updated: 15 June 2024

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1

Uri, Goldbourt, De Faire Ulf, and Berg Kåre, eds. Genetic factors in coronary heart disease. Dordrecht: Kluwer Academic, 1994.

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2

Petrakis, Peter L. Alcoholism, and inherited disease. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute on Alcohol Abuse and Alcoholism, 1985.

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3

Kåre, Berg, ed. Genetic approaches of coronary heart disease and hypertension. Berlin: Springer-Verlag, 1991.

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4

Offit, Kenneth. Clinical cancer genetics: Risk counseling and management. New York: Wiley-Liss, 1998.

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5

Introduction to risk calculation in genetic counselling. Oxford: Oxford University Press, 1991.

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6

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

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7

A, Levin Morris, and Strauss Harlee S, eds. Risk assessment in genetic engineering. New York: McGraw-Hill, 1991.

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8

J, Alberts Mark, ed. Genetics of cerebrovascular disease. Armonk, NY: Futura Pub. Co., 1999.

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9

Ovarian cancer: The signs, symptoms, treatments, and genetic risk factors. [United States]: Fort Press, 2010.

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10

Introduction to risk calculation in genetic counseling. 2nd ed. Oxford [England]: Oxford University Press, 1999.

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11

Introduction to risk calculation in genetic counseling. 3rd ed. Oxford: Oxford University Press, 2007.

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12

H, Benum Sara, ed. Genetic nutritioneering. Los Angeles: Keats Pub., 1998.

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13

Symposium on Phenotypic Variation in Populations: Relevance to Risk Assessment (1986 Brookhaven National Laboratory). Phenotypic variation in populations: Relevance to risk assessment. New York: Plenum Press, 1988.

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14

To test or not to test: A guide to genetic screening and risk. New Brunswick, N.J: Rutgers University Press, 2008.

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15

Teichler-Zallen, Doris. To test or not to test: A guide to genetic screening and risk. New Brunswick, N.J: Thorndike Press, 2009.

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16

1960-, Foulkes William D., and Hodgson S. V, eds. Inherited susceptibility to cancer: Clinical, predictive, and ethical perspectives. Cambridge: Cambridge University Press, 1998.

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17

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

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18

Hiroshi, Hiai, and Hino Okio, eds. Animal models of cancer predisposition syndromes. Basel: Karger, 1999.

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19

Batsheva, Bonné-Tamir, and Adam Avinoam, eds. Genetic diversity among Jews: Diseases and markers at the DNA level. New York: Oxford University Press, 1992.

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20

1961-, Rodríguez Santiago, ed. Genetic endocrinology of the metabolic syndrome. Hauppauge NY: Nova Science Publishers, 2009.

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21

1966-, Gordon Ora Karp, ed. Positive results: Making the best decisions when you're at high risk for breast or ovarian cancer. Amherst, N.Y: Prometheus Books, 2010.

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22

The calculation of genetic risks: Worked examples in DNA diagnostics. Baltimore: Johns Hopkins University Press, 1994.

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23

The calculation of genetic risks: Worked examples in DNA diagnostics. 2nd ed. Baltimore: Johns Hopkins University Press, 1997.

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24

Rebecca, Sutphen, and Steligo Kathy, eds. Confronting hereditary breast and ovarian cancer: Identify your risk, understand your options, change your destiny. Baltimore: Johns Hopkins University Press, 2012.

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25

Mukesh, Verma, Dunn Barbara K, Umar Asad, and National Cancer Institute (U.S.). Division of Cancer Prevention., eds. Epigenetics in cancer prevention: Early detection and risk assessment. New York: New York Academy of Sciences, 2003.

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26

V, Hodgson S., ed. A practical guide to human cancer genetics. 3rd ed. Cambridge: Cambridge University Press, 2007.

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27

Hodgson, S. V. A practical guide to human cancer genetics. Cambridge [England]: Cambridge University Press, 1993.

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28

Macular degeneration: Causes, diagnosis and treatment. New York: Nova Science Publishers, 2011.

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29

Ueland, Per Magne, and Rima Rozen. MTHFR polymorphisms and disease. Georgetown, Tex: Landes Bioscience, 2005.

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30

Magne, Ueland Per, and Rozen Rima, eds. MTHFR polymorphisms and disease. Georgetown, Tex: Landes Bioscience/ Eurekah.com, 2005.

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31

Robert, Cloninger C., and Begleiter Henri, eds. Genetics and biology of alcoholism. Plainview, N.Y: Cold Spring Harbor Laboratory Press, 1990.

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32

Risky genes: Genetics, breast cancer, and Jewish identity. Abingdon, Oxon: Routledge, 2013.

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33

Transhumanist dreams and dystopian nightmares: The promise and peril of genetic engineering. Baltimore: Johns Hopkins University Press, 2012.

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34

A, Bray George, and Ryan Donna H, eds. Nutrition, genetics, and heart disease. Baton Rouge: Louisiana State University Press, 1996.

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35

1952-, Andrews Lori B., ed. Assessing genetic risks: Implications for health and social policy. Washington, D.C: National Academy Press, 1994.

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36

From the feet up. 2nd ed. North Sydney, N.S.W: Harlequin Mira, 2014.

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37

Busby, Chris C. Radiation and cancer in Wales: The biological consequencesof low-level radiation. Machynlleth, Powys: Green Audit (Wales) Ltd., 1994.

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38

Choy, Wai Nang. Genetic Toxicology and Cancer Risk Assessment. Taylor & Francis Group, 2001.

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39

Choy, Wai Nang. Genetic Toxicology and Cancer Risk Assessment. Taylor & Francis Group, 2001.

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40

Choy, Wai Nang. Genetic Toxicology and Cancer Risk Assessment. Taylor & Francis Group, 2001.

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41

Choy, Wai Nang. Genetic Toxicology and Cancer Risk Assessment. Taylor & Francis Group, 2001.

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42

Choy, Wai Nang. Genetic Toxicology and Cancer Risk Assessment. Taylor & Francis Group, 2001.

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43

Holdt, Lesca M., and Daniel Teupser. Genetic background of atherosclerosis and its risk factors. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656653.003.0002.

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This chapter is concerned with how atherosclerosis risk is modulated by a complex interplay between genetic and environmental risk factors. The contribution of genetics to the variability of atherosclerosis risk is estimated as 50%. Recent genome-wide association studies have led to the identification of over 50 gene variants which modulate atherogenesis. Risk factors for atherosclerosis are also partly genetically determined and some of the variants which play a role in atherogenesis overlap with those modulating its risk factors. However, the current relevance of these findings for clinical practice is limited, mainly due to the small effect sizes of identified risk variants with insufficient discriminatory power, and a large portion of the genetic contribution to atherosclerosis is still unknown. The major promise therefore lies in understanding the pathophysiology of newly identified genes with the perspective of novel therapeutic approaches.

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44

Putaala, Jukka, and Nicolas Martinez-Majander. Risk factors. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198722366.003.0002.

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Risk factors in young-onset stroke include both traditional and unconventional as well as both chronic and temporal ones. In young patients, unconventional risk factors such as oral contraceptive use, antiphospholipid antibodies, genetic thrombophilia, acute infections, illicit drug use, and migraine may play a greater role than in elderly patients. However, recent large studies have challenged this traditional view suggesting that young adult stroke would occur mostly due to such unconventional risk factors. These studies have shown a high prevalence of in particular modifiable behavioural risk factors, including physical inactivity, high-risk alcohol consumption, and smoking. Since consequences of a young-onset stroke are greater regarding quality-adjusted life and economic impact, detection and treatment of especially modifiable risk factors are of paramount importance. This chapter reviews the burden of both traditional and less well-documented risk factors in young ischaemic stroke patients and discusses their strength of evidence and mechanisms of association.

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45

Choy, Wai Nang. Genetic Toxicology and Cancer Risk Assessment. Informa Healthcare, 2001.

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46

Choy, Wai Nang. Genetic Toxicology and Cancer Risk Assessment. Taylor & Francis Group, 2001.

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47

1946-, Choy Wai Nang, ed. Genetic toxicology and cancer risk assessment. New York: Marcel Dekker, 2001.

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48

Gaff, Clara, Louise Keogh, and Elizabeth Lobb. Communicating genetic risk. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198736134.003.0034.

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The discovery of cancer predisposing genetic mutations has heightened community awareness of the link between family history, genetic constitution, and personal risk. The component of an individual’s cancer risk that is due to their genetic make-up can be described as their ‘genetic risk’. Knowledge of genetic risk can assist both individuals with cancer and unaffected individuals to make decisions about healthcare and inform relatives who may share that genetic risk. Accordingly, patients seek advice about their risk and its implications and management from general practitioners (primary healthcare physician) or cancer specialists. In this chapter, we discuss the interlinked processes of risk assessment, risk perception, and risk communication in the context of genetic risk of cancer. While this is only one component of an individual’s risk of cancer—other factors including lifestyle, medical history, and environmental exposures—the principles of risk communication are applicable to each of these individual risk factors.

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49

Bianchi, Filippo, and Salvatore De Rossi. Aneuploidy: Etiology, Disorders, and Risk Factors. Nova Science Publishers, Incorporated, 2012.

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50

CLARK, ROSS D. Medical, Genetic & Behavioral Risk Factors of the Sporting Breeds. Xlibris, 2017.

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