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Books on the topic 'Genetic disorders; Disease genes'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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1

Nicholas, Hastie, ed. Genes and common diseases. Cambridge: Cambridge University Press, 2007.

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2

Case studies in genes and disease: A primer for clinicians. Philadelphia: American College of Physicians, 2004.

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3

Wiwanitkit, Viroj. Genes and nutrition. Hauppauge, NY: Nova Science, 2009.

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4

Cornish, Kim. Attention, genes, and developmental disorders. Oxford: Oxford University Press, 2010.

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5

Genes, chromosomes, and disease: From simple traits, to complex traits, to personalized medicine. Upper Saddle River, New Jersey: FT Press Science, 2011.

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6

McKusick, Victor A. Mendelian inheritance in man: A catalog of human genes and genetic disorders. Baltimore: John Hopkins University Press, 1994.

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7

McKusick, Victor A. Mendelian inheritance in man: A catalog of human genes and genetic disorders. Baltimore: Johns Hopkins University Press, 1994.

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8

Mendelian inheritance in man: A catalog of human genes and genetic disorders. Baltimore: Johns Hopkins University Press, 1994.

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9

McKusick, Victor A. Mendelian inheritance in man: A catalog of human genes and genetic disorders. Baltimore: Johns Hopkins University Press, 1998.

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10

International Symposium on Human Origins and Genetics (2005 National Centre for Biological Sciences). Genes, evolution, and complex disease: An International Symposium on Human Origins and Genetics, February 17-19, 2005, National Centre for Biological Sciences, Bangalore, India. Bangalore: National Centre for Biological Sciences, Tata Institute of Fundamental Research, 2005.

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11

Miami Bio/Technology Winter Symposium (1994). Advances in gene technology: Molecular biology and human disease : proceedings of the 1994 Miami Bio/Technology Winter Symposium. Oxford: IRL Press at Oxford University Press, 1994.

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12

Bellenir, Karen. Genetic disorders sourcebook: Basic consumer health information about hereditary diseases and disorders, including facts about the human genome, genetic inheritance patterns, disorders associated with specific genes ... 3rd ed. Detroit, Mich: Omnigraphics, 2004.

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13

Joseph, Jay. The missing gene: Psychiatry, heredity, and the fruitless search for genes. New York: Algora Pub., 2005.

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14

1939-, Read Andrew P., ed. Molecular basis of inherited disease. 2nd ed. Oxford: IRL Press at Oxford University Press, 1992.

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15

Davies, K. E. Molecular basis of inherited disease. Oxford: IRL Press, 1988.

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16

1935-, Ahmad Fazal, ed. Advances in gene technology: The molecular biology of human genetic disease : proceedings of the 1991 Miami/Bio Technology Winter Symposium. Oxford: IRL Press, 1991.

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17

The Apoe gene diet: A breakthrough in lowering cholesterol, weight, and the risk of cardiovascular and Alzheimer's disease through knowledge of your body's genes. Santa Rosa, CA: Elite Books, 2007.

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18

Am I my genes?: Confronting fate and family secrets in the age of genetic testing. Oxford: Oxford University Press, 2012.

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19

Verma, Ram S. Genetics of human neoplasia. Greenwich, Conn: JAI Press, 1995.

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20

I, Hashimoto, ed. Molecular medicine: Novel findings of gene diagnosis, regulation of gene expression, and gene therapy : proceedings of the Second Meeting of Hirosaki International Forum of Medical Science, Hirosaki, Japan, 7 July 1998. Amsterdam: Elsevier, 1999.

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21

S, Rajadhyaksha Medha, ed. New biology and genetic diseases. New Delhi: Oxford University Press, 1999.

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22

1950-, Waldholz Michael, ed. Genome: The story of the most astonishing scientific adventure of our time--the attempt to map all the genes in the human body. New York, N.Y: Simon and Schuster, 1990.

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23

Bishop, Jerry E. Genome: The story of the most astonishing scientific adventure of our time--the attempt to map all the genes in the human body. New York, N.Y: Simon and Schuster, 1990.

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24

Bishop, Jerry E. Genome: The story of the most astonishing scientific adventure of our time, the attempt to map all the genes in the human body. New York: Open Road Integrated Media, 2014.

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25

McDonald, Pamela. Apo e gene diet. Livermore, CA: WingSpan Press, 2006.

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26

S, Downes C., ed. Genes in medicine: Molecular biology and human genetic disorders. London: Chapman & Hall, 1995.

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27

Choosing children: Genes, disability, and design. Oxford: Clarendon Press, 2006.

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28

John, Justin C. St. Mitochondrial DNA, mitochondria, disease, and stem cells. New York: Humana Press, 2013.

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29

Ivar-Harry, Pawlowitzki, Edwards J. H, and Thompson E. A. 1949-, eds. Genetic mapping of disease genes. San Diego: Academic Press, 1997.

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30

Genes and Common Diseases: Genetics in Modern Medicine. Cambridge University Press, 2007.

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31

1958-, Barnes Marcia A., ed. Genes, brain, and development: The neurocognition of genetic disorders. Cambridge: Cambridge University Press, 2010.

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32

Loos, Friedemann. Transcriptional Gene Regulation in Health and Disease. Elsevier Science & Technology Books, 2018.

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33

1931-, McHugh Paul R., and McKusick Victor A. 1921-, eds. Genes, brain, and behavior. New York: Raven Press, 1991.

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34

Is It In Your Genes: How Genes Influence Common Disorders and Diseases That Affect You and Your Family. Cold Spring Harbor Laboratory Press, 2004.

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35

A, McKusick Victor. Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders. Johns Hopkins Univ Pr, 1997.

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36

Genes, Brain and Development. Cambridge University Press, 2008.

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37

Is It in Your Genes?: The Influence of Genes on Common Disorders and Diseases That Affect You and Your Family. Cold Spring Harbor Laboratory Press, 2004.

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38

Your Genetic Destiny : Know Your Genes, Secure Your Health, Save Your Life. Perseus Pub., 2001.

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39

Khatri, Sunil P., and Pey-Chang Kent Kent Lin. Logic Synthesis for Genetic Diseases: Modeling Disease Behavior Using Boolean Networks. Springer, 2016.

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40

Khatri, Sunil P., and Pey-Chang Kent Lin. Logic Synthesis for Genetic Diseases: Modeling Disease Behavior Using Boolean Networks. Springer, 2013.

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41

Khatri, Sunil P., and Pey-Chang Kent Lin. Logic Synthesis for Genetic Diseases: Modeling Disease Behavior Using Boolean Networks. Springer, 2013.

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42

Poretti, Andrea, and Michael V. Johnston. Genetic Disorders and Stroke. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0110.

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A variety of monogenic and polygenic genetic disorders have been linked to stroke, making it important for the clinician to keep up with the new discoveries and the potential to provide new gene-based therapies. Hematologic disorders such as sickle cell disease and thrombophilia due to mutations in prothrombin, factor V Leiden, and homocysteine metabolism are fairly well known, but mutations in mitochondrial metabolism and matrix metalloproteinases are less recognized. In addition, results of genome-wide association studies (GWAS) in stroke populations are revealing mutations that could predispose to stroke in specific ethnic populations. These studies are also revealing some crossover in mutations between stroke and familial hemiplegic migraine as well as mutations in growth factors such as brain derived neurotrophic factor (BDNF) that appear to influence the recovery from stroke by altering cortical plasticity.

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43

Graves, Tracey. Neurogenetic disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0223.

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There are many genetic diseases which affect the nervous system. Although some of these are extremely rare, several are quite common and, as a group, they comprise a significant proportion of neurological disease. Almost all clinical neurological syndromes can have a genetic cause. Not all of these have been genetically elucidated, but some have been extensively characterized in terms of clinical phenotype, molecular genetics, and cellular pathophysiology. Given the improvement in laboratory techniques and subsequent reduction in the cost of direct DNA sequencing, there is likely to be a rapid expansion over the next decade in the identification of causative genes and hence the availability of genetic tests. Thus, all clinicians should have a basic understanding about genetic disease; inheritance patterns; availability of genetic tests; genetic counselling; and ethics. Particular subspeciality areas where neurogenetic disease is common include neuromuscular disease and movement disorders.

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44

Genetic disorders sourcebook: Basic consumer health information about hereditary diseases and disorders, including facts about the human genome, genetic inheritance patterns, disorders associated with specific genes ... 3rd ed. Detroit, MI: Omnigraphics, 2005.

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45

Cazeneuve, Cécile, and Alexandra Durr. Genetic and Molecular Studies. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199929146.003.0006.

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Huntington’s disease (HD) is a rare inherited neurologic disorder due to a single mutational mechanism in a large gene (HTT). The mutation is an abnormal CAG repeat expansion, which is translated to a polyglutamine stretch in the huntingtin protein. The growing field of repeat expansion disorders benefits greatly from the lessons learned from the role of the CAG repeat expansion in HD and its resulting phenotype–genotype correlations. The molecular diagnosis can be difficult, and there are some pitfalls for accurate sizing of the CAG repeat, especially in juvenile HD and for intermediate alleles. Correlation between CAG length and age of onset accounts for up to 72% of the variance in different populations, but the search for genes modifying age of onset or progression of HD is still ongoing.

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46

(Editor), Jürgen Fuchs, Maurizio Podda (Editor), and Lester Packer (Editor), eds. Redox-Genome Interactions in Health and Disease (Oxidative Stress and Disease). CRC, 2003.

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47

Joseph, Jay. The Missing Gene: Psychiatry, Heredity, And the Fruitless Search for Genes. Algora Pub, 2006.

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48

G, Thoene Jess, ed. Small molecule therapy for genetic disease. Cambridge: Cambridge University Press, 2010.

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49

Joseph, Jay. The Missing Gene: Psychiatry, Heredity, and the Fruitless Search for Genes (Hc). Algora Publishing, 2006.

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50

Fuchs, Jürgen, 1957 June 28-, Podda Maurizio 1965-, and Packer Lester, eds. Redox-genome interactions in health and disease. New York: M. Dekker, 2004.

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