Literature DB >> 11315420

Can it be a "sin" to understand disease? On "genes" and "eugenics" and an "unconnected connection".

E M Neumann-Held1.   

Abstract

Particularly, but not exclusively, in Germany, concerns are uttered as to the consequences of modern biotechnological advances and their range of applications in the field of human genetics. Whereas the proponents of this research are mainly focussing on the possible knowledge that could be gained by understanding the causes of developmental processes and of disease on the molecular level, the critics fear the beginnings of a new eugenics movement. Without claiming a logical relationship between genetic sciences and eugenics movements, it is nevertheless suggested in this article that a connection between both can become established when the distinction between scientifically validated statements on one hand and guiding hypotheses and assumptions on the other hand is blurred, as is observed particularly when scientists report their results to the public. This claim is demonstrated in comparisons between the current state of scientific knowledge on the role of genes in development and causation of diseases, and the way this is presented to the public. It is required that a debate on biotechnology should include reflections on the validity of claims made by scientists.

Entities:  

Keywords:  Genetics and Reproduction

Mesh:

Year:  2001        PMID: 11315420     DOI: 10.1023/a:1009974111171

Source DB:  PubMed          Journal:  Med Health Care Philos        ISSN: 1386-7423


  12 in total

1.  Frankenstein in the land of Dichter and Denker.

Authors:  M D Laubichler
Journal:  Science       Date:  1999-12-03       Impact factor: 47.728

2.  A post-genomic challenge: learning to read patterns of protein synthesis.

Authors:  A Abbott
Journal:  Nature       Date:  1999-12-16       Impact factor: 49.962

Review 3.  A new model for the origins of chronic disease.

Authors:  D J Barker
Journal:  Med Health Care Philos       Date:  2001

Review 4.  On the difficulty of defining disease: a Darwinian perspective.

Authors:  R M Nesse
Journal:  Med Health Care Philos       Date:  2001

5.  The evolution of information storage and heredity.

Authors:  E Jablonka; E Szathmáry
Journal:  Trends Ecol Evol       Date:  1995-05       Impact factor: 17.712

Review 6.  Identical mutations and phenotypic variation.

Authors:  U Wolf
Journal:  Hum Genet       Date:  1997-09       Impact factor: 4.132

Review 7.  Monogenic traits are not simple: lessons from phenylketonuria.

Authors:  C R Scriver; P J Waters
Journal:  Trends Genet       Date:  1999-07       Impact factor: 11.639

Review 8.  The genetic contribution to the phenotype.

Authors:  U Wolf
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132

9.  The dream of the human genome: doubts about the Human Genome Project.

Authors:  Richard Lewontin
Journal:  New York Rev Books       Date:  1992-05-28

10.  A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.

Authors:  P Heutink; A G van der Mey; L A Sandkuijl; A P van Gils; A Bardoel; G J Breedveld; M van Vliet; G J van Ommen; C J Cornelisse; B A Oostra
Journal:  Hum Mol Genet       Date:  1992-04       Impact factor: 6.150

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  1 in total

1.  What is a genetic cause? The example of Alzheimer's Disease.

Authors:  Wim Dekkers; Marcel Olde Rikkert
Journal:  Med Health Care Philos       Date:  2006
  1 in total

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