Diane B. Paul – författare

Originally published in 2001, this is the second of two volumes published by Cambridge University Press in honour of Richard Lewontin. This second volume of essays honours the philosophical, historical and political dimensions of his work. It is fitting that the volume covers such a wide range of perspectives on modern biology, given the range of Lewontin's own contributions. He is not just a very successful practitioner of evolutionary genetics, but a rigorous critic of the practices of genetics and evolutionary biology and an articulate analyst of the social, political and economic contexts and consequences of genetic and evolutionary research. The volume begins with an essay by Lewontin on Natural History and Formalism in Evolutionary Genetics, and includes contributions by former students, post-docs, colleagues and collaborators, which cover issues ranging from the history and conceptual foundations of evolutionary biology and genetics, to the implications of human genetic diversity.

Explores the political forces underlying shifts in thinking about the respective influence of heredity and environment in shaping human behavior, and the feasibility and morality of eugenics.The essays collected in The Politics of Heredity explore the political factors underlying shifts in thinking about the role of nature and nurture in shaping human behavior, and about the desirability and feasibility of controlling human reproduction. They ask why many assumptions that were simply taken for granted as late as the 1950s and '60s came to be considered fundamentally mistaken in the 1970s and '80s. They also suggest that some apparent shifts in thinking were not as deep as they may seem, and that changes in rhetoric may obscure the stability of core underlying beliefs.

In a lifetime of practice, most physicians will never encounter a single case of PKU. Yet every physician in the industrialized world learns about the disease in medical school and, since the early 1960s, the newborn heel stick test for PKU has been mandatory in many countries. Diane B. Paul and Jeffrey P. Brosco's beautifully written book explains this paradox. PKU (phenylketonuria) is a genetic disorder that causes severe cognitive impairment if it is not detected and treated with a strict and difficult diet. Programs to detect PKU and start treatment early are deservedly considered a public health success story. Some have traded on this success to urge expanded newborn screening, defend basic research in genetics, and confront proponents of genetic determinism. In this context, treatment for PKU is typically represented as a simple matter of adhering to a low-phenylalanine diet. In reality, the challenges of living with PKU are daunting. In this first general history of PKU, a historian and a pediatrician explore how a rare genetic disease became the object of an unprecedented system for routine testing.The PKU Paradox is informed by interviews with scientists, clinicians, policymakers, and individuals who live with the disease. The questions it raises touch on ongoing controversies about newborn screening and what happens to blood samples collected at birth.

In the late nineteenth and the early twentieth century, it was widely assumed that society ought to foster the breeding of those who possessed favorable traits and discourage the breeding of those who did not. Controlled human breeding, or "eugenics" as it was called, was a movement with broad support that lasted into the 1930s. In this concise historical account, the author answers the questions of why eugenics, the search for means to propagate only "good genes," was so attractive earlier in the twentieth century, why it then fell into disrepute, and whether it has returned today in the new guise of genetic counseling.

This volume explores the history of eugenics in four Dominions of the British Empire: New Zealand, Australia, Canada, and South Africa.