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Books on the topic 'Genetic risk of disease'

Author: Grafiati

Published: 11 March 2023

Last updated: 31 July 2025

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1

National Institute on Alcohol Abuse and Alcoholism (U.S.) and Editorial Experts Inc, eds. Alcoholism, an inherited disease. U.S. Department 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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2

Petrakis, Peter L. Alcoholism, and inherited disease. 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. Springer-Verlag, 1991.

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4

Gormley, Myra Vanderpool. Family diseases: Are you at risk? Genealogical Pub. Co., 1989.

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5

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

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6

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

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7

Wexler, Alice. Mapping fate: A memoir of family, risk, and genetic research. University of California Press, 1995.

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8

Dimond, Rebecca, and Jamie Lewis. Analysing Semi-Structured Interviews: Understanding Family Experience of Rare Disease and Genetic Risk. SAGE Publications, Ltd., 2015. http://dx.doi.org/10.4135/9781473947467.

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9

United States. Congress. Office of Technology Assessment., ed. Genetic monitoring and screening in the workplace. Congress of the U.S., Office of Technology Assessment, 1990.

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10

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

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11

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

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12

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

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13

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

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14

National Cancer Institute (U.S.) and National Action Plan on Breast Cancer (Organization : U.S.), eds. Genetic testing for breast cancer risk: It's your choice. National Cancer Institute, 1999.

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15

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

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16

International, Conference on Carcinogenesis and Risk Assessment (8th 1994 Austin Tex ). Genetics and cancer susceptibility: Implications for risk assessment : proceedings of the Eighth International Conference on Carcinogenesis and Risk Assessment, held in Austin, Texas, November 30-December 3, 1994. Wiley-Liss, 1996.

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17

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

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18

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

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19

Uehara Memorial Foundation Symposium on Common Disease (1999 Tokyo). Common disease: Genetic and pathogenetic aspects of multifactorial diseases, proceedings of the Uehara Memorial Foundation Symposium on Common Disease, Tokyo on June 30-July 2, 1999. Edited by Imura Hiroo, Kasuga Masato, and Nakao Kazuwa 1948-. Elsevier Science B.V., 1999.

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20

Great Britain. Genetics and Insurance Committee. Decision of the Genetics and Insurance Committee (GAIC) concerning the application for approval to use genetic test results for life insurance risk assessment in Huntington's disease. Department of Health, 2000.

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21

National Research Council (U.S.). Committee on Genetically Modified Pest-Protected Plants., ed. Genetically modified pest-protected plants: Science and regulation. National Academy Press, 2000.

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22

National Cancer Institute (U.S.). Clinical Genetics Branch. Inherited bone marrow failure syndromes: Studying families with rare blood disorders and risk of cancer. U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Cancer Institute, Division of Cancer Epidemiology and Genetics, Clinical Genetics Branch, 2002.

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23

National Council on Radiation Protection and Measurements. Potential impact of individual genetic susceptibility and previous radiation exposure on radiation risk for astronauts. National Council on Radiation Protection and Measurements, 2011.

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24

Frohlich, Edward D. Take heart: Cut your inherited risks of heart disease. Crown Publishers, 1990.

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25

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

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26

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

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27

1947-, Lusis Aldons J., Rotter Jerome I, and Sparkes Robert S. 1930-, eds. Molecular genetics of coronary artery disease: Candidate genes and processes in atherosclerosis. Karger, 1992.

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28

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

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29

Seshadri, Sudha, and Stéphanie Debette, eds. Risk Factors for Cerebrovascular Disease and Stroke. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199895847.001.0001.

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Risk Factors for Cerebrovascular Disease and Stroke describes environmental and genetic determinants for cerebrovascular disease and stroke from the perspective of an international group of neurologists, epidemiologists, and geneticists who are at the forefront of research and education on these issues. Unlike other books in the field, which solely deal with physiology, diagnosis, and management of stroke, this essential book discusses prevention factors as well as the causes. This unique book takes a comprehensive approach to risk prediction while integrating epidemiological, genetic, and sta

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30

Ueland, Per Magne. MTHFR Polymorphisms and Disease. Taylor & Francis Group, 2005.

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31

Mapping Fate: A Memoir of Family, Risk, and Genetic Research. University of California Press, 1996.

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32

Mapping fate: A memoir of family, risk, and genetic research. Times Books, 1995.

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33

Banerjee, Amitava, and Kaleab Asrress. Risk factors for cardiovascular disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0086.

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The most prevalent cardiovascular diseases (CVDs) are atherosclerotic, affecting all arterial territories. Epidemiologic studies such as the Framingham and INTERHEART studies have firmly established the commonest or ‘traditional’ risk factors for CVD; namely, smoking, hypertension, diabetes mellitus, hypercholesterolaemia, and a family history of CVD. The ‘risk-factors approach’ to CVD looks at these factors, individually and in combination, in the causation of disease. The complex causation pathways involve interplay of individual factors, whether genetic or environmental. More recently, ther

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34

(Editor), Fiona Lalloo, Bronwyn Kerr (Editor), Jan M. Friedman (Editor), and D. Gareth Evans (Editor), eds. Risk Assessment and Management in Cancer Genetics. Oxford University Press, USA, 2005.

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35

MTHFR polymorphisms and disease. Landes Bioscience/ Eurekah.com, 2005.

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36

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

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37

Genetic susceptibility to cancer. Kluwer Academic, 1998.

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38

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

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39

(Editor), William D. Foulkes, and Shirley V. Hodgson (Editor), eds. Inherited Susceptibility to Cancer: Clinical, Predictive and Ethical Perspectives (Cambridge Cancer Series). Cambridge University Press, 1998.

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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

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

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44

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

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45

Walsh, Richard A. “Are My Children at Risk, Doctor?”. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190607555.003.0007.

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Few patients with Parkinson’s disease will be found to have a monogenic cause of their disease, even among those with early onset symptoms. The identification of a genetic etiology will in general have no implications on management but can be helpful in offering a prediction on prognosis, predicting response to treatment, and allowing genetic counseling to take place. Insights into the molecular mechanisms provided by a greater understanding of the genetics of Parkinson’s disease may offer the best hope for identifying future disease-modifying therapies. Next-generation sequencing techniques o

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46

Stroke genetics. Oxford University Press, 2003.

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47

Elliott, Perry, Pier D. Lambiase, and Dhavendra Kumar, eds. Inherited Cardiac Disease. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198829126.001.0001.

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Every year, thousands of people die or suffer chronic disability as the result of inherited diseases of the cardiovascular system. In many cases, diagnosis of inherited disease is delayed or missed owing to a lack of awareness, and an even greater number of relatives are exposed to unnecessary risk. This new edition of Inherited Cardiac Disease provides a comprehensive summary of the aetiology, presentation, and management of genetic disorders of the cardiovascular system. Fully updated to reflect the advances in molecular genetic technologies and the publication of national guidelines for the

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48

Ingles, Jodie, Charlotte Burns, and Laura Yeates. Genetic counselling. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0145.

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Cardiac genetic counselling is an emerging but important subspecialty. The qualifications of cardiac genetic counsellors depend on the country of practice, but at a minimum they are Master’s-level trained health professionals with expertise in genetics, and are integral members of the multidisciplinary inherited cardiovascular disease clinic. Though the framework is diverse in different countries, key roles include investigation and confirmation of family history details, discussion of inheritance risks and facilitation of cardiac genetic testing, communication with at-risk relatives, and incr

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49

(Editor), Batsheva Bonne-Tamir, and Avinoam Adam (Editor), eds. New Perspectives on Genetic Markers and Diseases among Jewish People. Oxford University Press, USA, 1992.

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50

Turney, Ben, and John Reynard. Epidemiology of stone disease. Edited by John Reynard. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0012.

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In developed countries, the lifetime prevalence of kidney stones is around 10% and most commonly affects people in the working age-group. The incidence is increasing internationally. After passage of a first stone, the risk of recurrence is high. Direct and indirect costs involved in treating stones are considerable. Intrinsic risk factors include age, gender, genetics, and metabolic syndromes. The incidence of stone disease peaks between the ages of 20 and 60 years. While historically the male to female ratio was around 3:1, the gender gap is closing. The reasons for increased incidence are d

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