Project acronym AIDSRIGHTS
Project "Rights, Responsibilities, and the HIV/AIDS Pandemic: Global Impact on Moral and Political Subjectivity"
Researcher (PI) Jarrett Zigon
Host Institution (HI) UNIVERSITEIT VAN AMSTERDAM
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary "This project will undertake a transnational, multi-sited ethnographic study of moral and political subjectivity in HIV/AIDS prevention and treatment programs from the perspective of socio-cultural anthropology. The main research question is: what kinds of politico-moral persons are constituted in institutional contexts that combine human rights and personal responsibility approaches to health, and how these kinds of subjectivities relate to local, national, and global forms of the politico-moral represented in health policies? In particular, this research will be carried out in Indonesia (Jakarta and Bali), South Africa (Western Cape), USA (New York City), and various locations throughout Eastern Europe in HIV/AIDS programs and institutions that increasingly combine human rights and personal responsibility approaches to treatment and prevention. This project is the first anthropological research on health governance done on a global scale. Until now most anthropological studies have focused on one health program in one location without simultaneously studying similar processes in comparable contexts in other parts of the world. In contrast, this project will take a global perspective on the relationship between health issues, morality, and governance by doing transnational multi-sited research. This project will significantly contribute to the current anthropological focus on bio-citizenship and push it in new directions, resulting in a new anthropological theory of global bio-political governance and global politico-moral subjectivities. This theory will describe and explain recent transnational processes of shaping particular kinds of politico-moral subjectivities through health initiatives. By doing research in comparable world areas this project will significantly contribute to the development of a theory of politico-moral governance with global reach."
Summary
"This project will undertake a transnational, multi-sited ethnographic study of moral and political subjectivity in HIV/AIDS prevention and treatment programs from the perspective of socio-cultural anthropology. The main research question is: what kinds of politico-moral persons are constituted in institutional contexts that combine human rights and personal responsibility approaches to health, and how these kinds of subjectivities relate to local, national, and global forms of the politico-moral represented in health policies? In particular, this research will be carried out in Indonesia (Jakarta and Bali), South Africa (Western Cape), USA (New York City), and various locations throughout Eastern Europe in HIV/AIDS programs and institutions that increasingly combine human rights and personal responsibility approaches to treatment and prevention. This project is the first anthropological research on health governance done on a global scale. Until now most anthropological studies have focused on one health program in one location without simultaneously studying similar processes in comparable contexts in other parts of the world. In contrast, this project will take a global perspective on the relationship between health issues, morality, and governance by doing transnational multi-sited research. This project will significantly contribute to the current anthropological focus on bio-citizenship and push it in new directions, resulting in a new anthropological theory of global bio-political governance and global politico-moral subjectivities. This theory will describe and explain recent transnational processes of shaping particular kinds of politico-moral subjectivities through health initiatives. By doing research in comparable world areas this project will significantly contribute to the development of a theory of politico-moral governance with global reach."
Max ERC Funding
1 499 370 €
Duration
Start date: 2012-05-01, End date: 2017-04-30
Project acronym AISMA
Project An anthropological investigation of muscular politics in South Asia
Researcher (PI) Lucia Michelutti
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary Over the past decade, the media, international organisations, as well as policy-making bodies have voiced increasing concern about a growing overlap between the criminal and political spheres in South Asia. Many 'criminal politicians' are accused not simply of embezzlement, but of burglary, kidnapping and murder, so that the observed political landscape emerges not only as a 'corrupt', but also a highly violent sphere. This project is a collaborative and cross-national ethnographic study of the criminalisation of politics in India, Pakistan and Bangladesh. Bringing together local-level investigation, surveys and historical analysis, the project will produce comprehensive political ethnographies in sixteen sites across the subcontinent, providing empirical material and theoretical directives for further charting of the virtually unexplored terrain of extra-legal muscular politics in the region. Central to the proposed programme of research are the following interrelated objectives: 1) To further develop the method of collaborative political ethnography by designing, collecting and producing case studies which will allow us to write thematically across sites; 2) To generate policy relevant research in the fields of security, conflict, democracy and development; 3) To produce capability by forging an international network of scholars on issues related to democratisation, violence, crime and support the work and careers of the project's 4 Post-docs. The study capitalises on previous research and skills of the PI in the cross-cultural study of democracy and muscular politics in the global South. All members of the research team have expertise in ethnographic research in the difficult spheres of criminal politics, informal economies, and political violence and are hence well and sometimes uniquely equipped to pursue this challenging research thematic.
Summary
Over the past decade, the media, international organisations, as well as policy-making bodies have voiced increasing concern about a growing overlap between the criminal and political spheres in South Asia. Many 'criminal politicians' are accused not simply of embezzlement, but of burglary, kidnapping and murder, so that the observed political landscape emerges not only as a 'corrupt', but also a highly violent sphere. This project is a collaborative and cross-national ethnographic study of the criminalisation of politics in India, Pakistan and Bangladesh. Bringing together local-level investigation, surveys and historical analysis, the project will produce comprehensive political ethnographies in sixteen sites across the subcontinent, providing empirical material and theoretical directives for further charting of the virtually unexplored terrain of extra-legal muscular politics in the region. Central to the proposed programme of research are the following interrelated objectives: 1) To further develop the method of collaborative political ethnography by designing, collecting and producing case studies which will allow us to write thematically across sites; 2) To generate policy relevant research in the fields of security, conflict, democracy and development; 3) To produce capability by forging an international network of scholars on issues related to democratisation, violence, crime and support the work and careers of the project's 4 Post-docs. The study capitalises on previous research and skills of the PI in the cross-cultural study of democracy and muscular politics in the global South. All members of the research team have expertise in ethnographic research in the difficult spheres of criminal politics, informal economies, and political violence and are hence well and sometimes uniquely equipped to pursue this challenging research thematic.
Max ERC Funding
1 200 000 €
Duration
Start date: 2012-03-01, End date: 2016-02-29
Project acronym ASCENT
Project Advanced materials and devices for hybrid spin coherent technologies
Researcher (PI) John Julian Larrarte Morton
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), PE3, ERC-2011-StG_20101014
Summary The property of spin has been harnessed in an array of revolutionary technologies, from nuclear spins in magnetic resonance imaging to spintronics in magnetic recording media. Nature at its deepest level is quantum mechanical and spins are capable of demonstrating superposition and entanglement, yet such coherent properties have not yet been fully exploited. The exquisite control over materials fabrication and spin control techniques has reached a maturity where spintronics can go beyond purely classical effects and begin to fully exploit these quantum properties. Potential applications range from quantum information processors, including the transmission of quantum information via itinerant electron spins, single microwave photon storage within spin ensembles, and a new generation of sensors exploiting entanglement to yield fundamentally enhanced precision.
The aim of ASCENT is to develop materials and devices in which electron and nuclear spins exhibit long-lived coherent quantum behaviour and interactions which can be harnessed for technological purposes. Specifically, ASCENT will exploit in range of condensed matter systems from molecular materials to silicon-based structures, the possibility of transiently generating and removing electron spins in the vicinity of nuclear spins. The project represents a new and promising direction for the development of coherent interactions between spins in materials, and one which builds upon foundations I have established in my earlier work, often supported by preliminary investigations. Strong interactions with theory throughout this project will provide insights to refine and improve the experiments. In addition to direct applications in quantum technologies, the insights and methodology gained will be fed back into the wider field of spin resonance, including dynamic nuclear polarisation, structural biology and medical imaging.
Summary
The property of spin has been harnessed in an array of revolutionary technologies, from nuclear spins in magnetic resonance imaging to spintronics in magnetic recording media. Nature at its deepest level is quantum mechanical and spins are capable of demonstrating superposition and entanglement, yet such coherent properties have not yet been fully exploited. The exquisite control over materials fabrication and spin control techniques has reached a maturity where spintronics can go beyond purely classical effects and begin to fully exploit these quantum properties. Potential applications range from quantum information processors, including the transmission of quantum information via itinerant electron spins, single microwave photon storage within spin ensembles, and a new generation of sensors exploiting entanglement to yield fundamentally enhanced precision.
The aim of ASCENT is to develop materials and devices in which electron and nuclear spins exhibit long-lived coherent quantum behaviour and interactions which can be harnessed for technological purposes. Specifically, ASCENT will exploit in range of condensed matter systems from molecular materials to silicon-based structures, the possibility of transiently generating and removing electron spins in the vicinity of nuclear spins. The project represents a new and promising direction for the development of coherent interactions between spins in materials, and one which builds upon foundations I have established in my earlier work, often supported by preliminary investigations. Strong interactions with theory throughout this project will provide insights to refine and improve the experiments. In addition to direct applications in quantum technologies, the insights and methodology gained will be fed back into the wider field of spin resonance, including dynamic nuclear polarisation, structural biology and medical imaging.
Max ERC Funding
1 875 550 €
Duration
Start date: 2011-12-01, End date: 2017-06-30
Project acronym Bionetworking
Project Bionetworking in Asia – A social science approach to international collaboration, informal exchanges, and responsible innovation in the life sciences
Researcher (PI) Margaret Elizabeth Sleeboom-Faulkner
Host Institution (HI) THE UNIVERSITY OF SUSSEX
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary Bio-medical innovation makes a substantial contribution to Western societies and economies. But leading research organisations in the West are increasingly reliant on clinical research conducted beyond the West. Such initiatives are challenged by uncertainties about research quality and therapeutic practices in Asian countries. These only partly justified uncertainties are augmented by unfamiliar conditions. This study examines how to create responsible innovation in the life sciences by looking for ways to overcome existing obstacles to safe, just and ethical international science collaborations.
Building on observations of scientists, managers and patients and supported by Asian language expertise, biology background, and experience with science and technology policy-making, we examine the roles of regional differences and inequalities in the networks used for patient recruitment and international research agreements. Profit-motivated networks in the life sciences also occur underground and at an informal, unregulated level, which we call bionetworking. Bionetworking is a social entrepreneurial activity involving biomedical research, healthcare and patient networks that are maintained by taking advantage of regionally differences in levels of science and technology, healthcare, education and regulatory regimes.
Using novel social-science methods, the project studies two main themes. Theme 1 examines patient recruitment networks for experimental stem cell therapies and cooperation between research and health institutions involving exchanges of patients against other resources. Theme 2 maps and analyses exchanges of biomaterials of human derivation, and forms of ‘ownership’ rights, benefits and burdens associated with their donation, possession, maintenance, and application. Integral analysis of the project nodes incorporates an analysis of public health policy and patient preference in relation to Responsible innovation, Good governance and Global assemblages.
Summary
Bio-medical innovation makes a substantial contribution to Western societies and economies. But leading research organisations in the West are increasingly reliant on clinical research conducted beyond the West. Such initiatives are challenged by uncertainties about research quality and therapeutic practices in Asian countries. These only partly justified uncertainties are augmented by unfamiliar conditions. This study examines how to create responsible innovation in the life sciences by looking for ways to overcome existing obstacles to safe, just and ethical international science collaborations.
Building on observations of scientists, managers and patients and supported by Asian language expertise, biology background, and experience with science and technology policy-making, we examine the roles of regional differences and inequalities in the networks used for patient recruitment and international research agreements. Profit-motivated networks in the life sciences also occur underground and at an informal, unregulated level, which we call bionetworking. Bionetworking is a social entrepreneurial activity involving biomedical research, healthcare and patient networks that are maintained by taking advantage of regionally differences in levels of science and technology, healthcare, education and regulatory regimes.
Using novel social-science methods, the project studies two main themes. Theme 1 examines patient recruitment networks for experimental stem cell therapies and cooperation between research and health institutions involving exchanges of patients against other resources. Theme 2 maps and analyses exchanges of biomaterials of human derivation, and forms of ‘ownership’ rights, benefits and burdens associated with their donation, possession, maintenance, and application. Integral analysis of the project nodes incorporates an analysis of public health policy and patient preference in relation to Responsible innovation, Good governance and Global assemblages.
Max ERC Funding
1 497 711 €
Duration
Start date: 2012-02-01, End date: 2017-01-31
Project acronym CARBONNEMS
Project NanoElectroMechanical Systems based on Carbon Nanotube and Graphene
Researcher (PI) Adrian Bachtold
Host Institution (HI) FUNDACIO INSTITUT DE CIENCIES FOTONIQUES
Call Details Starting Grant (StG), PE3, ERC-2011-StG_20101014
Summary Carbon nanotubes and graphene form a class of nanoscale objects with exceptional electrical, mechanical and structural properties. I propose to exploit these unique properties to fabricate and study various nanoelectromechanical systems (NEMS) based on graphene and nanotubes. Specifically, I will address two directions with major scientific interests:
1- I propose to study electromechanical resonators based on an individual nanotube or on a single layer of graphene. My group has a leading position in this recent research field and the idea is to take advantage of our expertise for two sets of experiments, one on inertial mass sensing and one on the exploration of quantum motion. These two topics are generating at present an intense activity in the NEMS community. Experiments are usually carried out using microfabricated silicon resonators but the ultra low mass of nanotubes and graphene has here an enormous asset. It drastically improves the sensitivity of mass sensing and it dramatically enhances the amplitude of the motion in the quantum regime.
2- My team will fabricate and exploit nanomotors based on nanotube and graphene. Only few man-made nanomotors have been demonstrated so far. Reasons are multiple. For instance, the fabrication of nanomotors is technically challenging. In addition, friction forces are often so strong that they hinder motion. Because of their unique properties, nanotubes and graphene represent a material of choice for the development of new nanomotors. We will construct nanomotors with different layouts and address how electrical, thermal or chemical energy can be transformed into mechanical energy in order to drive motion at the nanoscale.
Summary
Carbon nanotubes and graphene form a class of nanoscale objects with exceptional electrical, mechanical and structural properties. I propose to exploit these unique properties to fabricate and study various nanoelectromechanical systems (NEMS) based on graphene and nanotubes. Specifically, I will address two directions with major scientific interests:
1- I propose to study electromechanical resonators based on an individual nanotube or on a single layer of graphene. My group has a leading position in this recent research field and the idea is to take advantage of our expertise for two sets of experiments, one on inertial mass sensing and one on the exploration of quantum motion. These two topics are generating at present an intense activity in the NEMS community. Experiments are usually carried out using microfabricated silicon resonators but the ultra low mass of nanotubes and graphene has here an enormous asset. It drastically improves the sensitivity of mass sensing and it dramatically enhances the amplitude of the motion in the quantum regime.
2- My team will fabricate and exploit nanomotors based on nanotube and graphene. Only few man-made nanomotors have been demonstrated so far. Reasons are multiple. For instance, the fabrication of nanomotors is technically challenging. In addition, friction forces are often so strong that they hinder motion. Because of their unique properties, nanotubes and graphene represent a material of choice for the development of new nanomotors. We will construct nanomotors with different layouts and address how electrical, thermal or chemical energy can be transformed into mechanical energy in order to drive motion at the nanoscale.
Max ERC Funding
1 996 789 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym CIRCUMVENT
Project Closing in on Runx3 and CXCL4 to open novel avenues for therapeutic intervention in systemic sclerosis
Researcher (PI) Timothy Radstake
Host Institution (HI) UNIVERSITAIR MEDISCH CENTRUM UTRECHT
Call Details Starting Grant (StG), LS6, ERC-2011-StG_20101109
Summary Systemic sclerosis (SSc) is an autoimmune disease that culminates in excessive extra-cellular matrix deposition (fibrosis) in skin and internal organs. SSc is a severe disease in which fibrotic events lead to organ failure such as renal failure, deterioration of lung function and development of pulmonary arterial hypertension (PAH). Together, these disease hallmarks culminate in profound disability and premature death.
Over the past three years several crucial observations by my group changed the landscape of our thinking about the ethiopathogenesis of this disease. First, plasmacytoid dendritic (pDCs) cells were found to be extremely frequent in the circulation of SSc patients (1000-fold) compared with healthy individuals. In addition, we observed that pDCs from SSc patients are largely dedicated to synthesize CXCL4 that was proven to be directly implicated in fibroblast biology and endothelial cell activation, two events recapitulating SSc. Finally, research aimed to decipher the underlying cause of this increased pDCs frequency led to the observation that Runx3, a transcription factor that controls the differentiation of DC subsets, was almost not expressed in pDC of SSc patients. Together, these observations led me to pose the “SSc immune postulate” in which the pathogenesis of SSc is explained by a multi-step process in which Runx3 and CXCL4 play a central role.
The project CIRCUMVENT is designed to provide proof of concept for the role of CXCL4 and RUNX3 in SSc. For this aim we will exploit a unique set of patient material (cell subsets, protein and DNA bank), various recently developed in vitro techniques (siRNA for pDCs, viral over expression of CXCL4/RUNX3) and apply three recently optimised experimental models (CXCL4 subcutaneous pump model, DC specific RUNX3 KO and the SCID/NOD/rag2 KO mice).
The project CIRCUMVENT aims to proof the direct role for Runx3 and CXCL4 that could provide the final step towards the development of novel therapeutic targets
Summary
Systemic sclerosis (SSc) is an autoimmune disease that culminates in excessive extra-cellular matrix deposition (fibrosis) in skin and internal organs. SSc is a severe disease in which fibrotic events lead to organ failure such as renal failure, deterioration of lung function and development of pulmonary arterial hypertension (PAH). Together, these disease hallmarks culminate in profound disability and premature death.
Over the past three years several crucial observations by my group changed the landscape of our thinking about the ethiopathogenesis of this disease. First, plasmacytoid dendritic (pDCs) cells were found to be extremely frequent in the circulation of SSc patients (1000-fold) compared with healthy individuals. In addition, we observed that pDCs from SSc patients are largely dedicated to synthesize CXCL4 that was proven to be directly implicated in fibroblast biology and endothelial cell activation, two events recapitulating SSc. Finally, research aimed to decipher the underlying cause of this increased pDCs frequency led to the observation that Runx3, a transcription factor that controls the differentiation of DC subsets, was almost not expressed in pDC of SSc patients. Together, these observations led me to pose the “SSc immune postulate” in which the pathogenesis of SSc is explained by a multi-step process in which Runx3 and CXCL4 play a central role.
The project CIRCUMVENT is designed to provide proof of concept for the role of CXCL4 and RUNX3 in SSc. For this aim we will exploit a unique set of patient material (cell subsets, protein and DNA bank), various recently developed in vitro techniques (siRNA for pDCs, viral over expression of CXCL4/RUNX3) and apply three recently optimised experimental models (CXCL4 subcutaneous pump model, DC specific RUNX3 KO and the SCID/NOD/rag2 KO mice).
The project CIRCUMVENT aims to proof the direct role for Runx3 and CXCL4 that could provide the final step towards the development of novel therapeutic targets
Max ERC Funding
1 500 000 €
Duration
Start date: 2012-08-01, End date: 2017-07-31
Project acronym COMPNET
Project Dynamics and Self-organisation in Complex Cytoskeletal Networks
Researcher (PI) Andreas Bausch
Host Institution (HI) TECHNISCHE UNIVERSITAET MUENCHEN
Call Details Starting Grant (StG), PE3, ERC-2011-StG_20101014
Summary The requirements on the eukaryotic cytoskeleton are not only of high complexity, but include demands that are actually contradictory in the first place: While the dynamic character of cytoskeletal structures is essential for the motility of cells, their ability for morphological reorganisations and cell division, the structural integrity of cells relies on the stability of cytoskeletal structures. From a biophysical point of view, this dynamic structure formation and stabilization stems from a self-organisation process that is tightly controlled by the simultaneous and competing function of a plethora of actin binding proteins (ABPs). To understand the self-organisation phenomena observed in the cytoskeleton it is therefore indispensable to first shed light on the functional role of ABPs and their underlying molecular mechanisms. Hereby development of reliable reconstituted model systems as has been proven by the great progress achieved in our understanding of individual crosslinking proteins that turn the cytoskeleton into a viscoelastic physical gel. The advantage of such reconstituted systems is that the biological complexity is decreased to an accessible level that the physical principles can be explored and identified.
It is the aim of the present proposal to successively increase the complexity in a well defined manner to further progress in understanding the functional units of a cell. On the way to a sound physical understanding of cellular self organizing principles, the planned major step comprises the incorporation of active processes like the active (de-)polymerisation of filaments and motor mediated active reorganisation and contraction. We plan to develop new tools and approaches to address how the different kinds of ABPs are interacting with each other and how the structure, dynamics and function of the cytoskeleton is locally governed by the competition and interplay between them.
Summary
The requirements on the eukaryotic cytoskeleton are not only of high complexity, but include demands that are actually contradictory in the first place: While the dynamic character of cytoskeletal structures is essential for the motility of cells, their ability for morphological reorganisations and cell division, the structural integrity of cells relies on the stability of cytoskeletal structures. From a biophysical point of view, this dynamic structure formation and stabilization stems from a self-organisation process that is tightly controlled by the simultaneous and competing function of a plethora of actin binding proteins (ABPs). To understand the self-organisation phenomena observed in the cytoskeleton it is therefore indispensable to first shed light on the functional role of ABPs and their underlying molecular mechanisms. Hereby development of reliable reconstituted model systems as has been proven by the great progress achieved in our understanding of individual crosslinking proteins that turn the cytoskeleton into a viscoelastic physical gel. The advantage of such reconstituted systems is that the biological complexity is decreased to an accessible level that the physical principles can be explored and identified.
It is the aim of the present proposal to successively increase the complexity in a well defined manner to further progress in understanding the functional units of a cell. On the way to a sound physical understanding of cellular self organizing principles, the planned major step comprises the incorporation of active processes like the active (de-)polymerisation of filaments and motor mediated active reorganisation and contraction. We plan to develop new tools and approaches to address how the different kinds of ABPs are interacting with each other and how the structure, dynamics and function of the cytoskeleton is locally governed by the competition and interplay between them.
Max ERC Funding
1 495 196 €
Duration
Start date: 2011-10-01, End date: 2012-03-31
Project acronym CONSTEURGLOBGOV
Project The Role and Future of National Constitutions in European and Global Governance
Researcher (PI) Anneli Albi
Host Institution (HI) UNIVERSITY OF KENT
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary At a time when the discourse on constitutionalism has come to focus on the constitutionalisation processes at the European and global level, this project will turn the spotlight on national constitutions. It embarks on an analysis and rethinking of the role and future of national constitutions in the context where decision-making has increasingly shifted to transnational level. The project will have three objectives. The first objective is concerned with the role of constitutions internally within the state: the project assesses how credible the content of constitutions remains given the realities of European integration. To this end, it will undertake a comprehensive, comparative and issue-based analysis of EU-related amendments in national constitutions. The second objective concerns the role of constitutions externally with regard to European integration. While national constitutions have increasingly been regarded as a manifestation of sovereignty, and therefore representing values that are often viewed as parochial, the project will turn the focus on other values contained in the constitutions, such as protection of rights and the rule of law. It will explore constitutional courts’ judgements articulating the rights and values that mandate upholding at supranational level, and assess the responsiveness of the European Court of Justice with regard to such concerns. The third objective applies experiences from the EU context to the new research area of global governance. The project aims to assess whether the constitutional provisions on international treaties suffice to reflect the sheer extent to which decision-making has shifted to international institutions and global regulatory networks. It will also explore how constitutions could respond to the problems increasingly highlighted in the context of global governance in relation to legitimacy, democratic control, accountability and the rule of law.
Summary
At a time when the discourse on constitutionalism has come to focus on the constitutionalisation processes at the European and global level, this project will turn the spotlight on national constitutions. It embarks on an analysis and rethinking of the role and future of national constitutions in the context where decision-making has increasingly shifted to transnational level. The project will have three objectives. The first objective is concerned with the role of constitutions internally within the state: the project assesses how credible the content of constitutions remains given the realities of European integration. To this end, it will undertake a comprehensive, comparative and issue-based analysis of EU-related amendments in national constitutions. The second objective concerns the role of constitutions externally with regard to European integration. While national constitutions have increasingly been regarded as a manifestation of sovereignty, and therefore representing values that are often viewed as parochial, the project will turn the focus on other values contained in the constitutions, such as protection of rights and the rule of law. It will explore constitutional courts’ judgements articulating the rights and values that mandate upholding at supranational level, and assess the responsiveness of the European Court of Justice with regard to such concerns. The third objective applies experiences from the EU context to the new research area of global governance. The project aims to assess whether the constitutional provisions on international treaties suffice to reflect the sheer extent to which decision-making has shifted to international institutions and global regulatory networks. It will also explore how constitutions could respond to the problems increasingly highlighted in the context of global governance in relation to legitimacy, democratic control, accountability and the rule of law.
Max ERC Funding
1 230 958 €
Duration
Start date: 2012-01-01, End date: 2018-12-31
Project acronym DENOVO
Project Detection and interpretation of de novo mutations and structural genomic variations in mental retardation
Researcher (PI) Joris Andre Veltman
Host Institution (HI) STICHTING KATHOLIEKE UNIVERSITEIT
Call Details Starting Grant (StG), LS2, ERC-2011-StG_20101109
Summary Mental retardation, like most common neurodevelopmental and psychiatric diseases, shows a strong genetic component, but these underlying genetic causes remain largely unknown. For a long time it was hypothesized that these kind of common diseases are mainly caused by common inherited genetic variants with reduced penetrance. In contrast to this common variant-common disease hypothesis, I here hypothesize that a large proportion of this so-called “missing heritability” for conditions such as mental retardation, schizophrenia, and autism lies in de novo genetic variation that is rapidly eliminated from the population because individuals with such diseases have severely compromised fecundity.
My previous work using microarrays has already demonstrated de novo genomic copy number variations in mental retardation and in schizophrenia. However, microarrays do not allow us to capture the most common form of de novo mutations, those occurring at the nucleotide level. Technological innovations now for the first time allow us to comprehensively study the entire genome of an individual for genomic variations at all levels. In this project I will explore the de novo mutation hypothesis in whole exome and whole genome sequence data from patients with mental retardation. I will optimize and apply whole genome sequencing strategies using patient-parent trios, both in rare mental retardation syndromes as well as common forms of mental retardation. Guidelines for pathogenicity will be established by computational studies aimed at unraveling genotype-phenotype correlations in these family-based genome sequence type datasets.
This project will contribute significantly to resolving the genetic causes of reproductively lethal disorders such as mental retardation, provide critical knowledge on the frequency and consequences of de novo mutations in our genome and help to establish medical genome sequencing as a routine diagnostic approach.
Summary
Mental retardation, like most common neurodevelopmental and psychiatric diseases, shows a strong genetic component, but these underlying genetic causes remain largely unknown. For a long time it was hypothesized that these kind of common diseases are mainly caused by common inherited genetic variants with reduced penetrance. In contrast to this common variant-common disease hypothesis, I here hypothesize that a large proportion of this so-called “missing heritability” for conditions such as mental retardation, schizophrenia, and autism lies in de novo genetic variation that is rapidly eliminated from the population because individuals with such diseases have severely compromised fecundity.
My previous work using microarrays has already demonstrated de novo genomic copy number variations in mental retardation and in schizophrenia. However, microarrays do not allow us to capture the most common form of de novo mutations, those occurring at the nucleotide level. Technological innovations now for the first time allow us to comprehensively study the entire genome of an individual for genomic variations at all levels. In this project I will explore the de novo mutation hypothesis in whole exome and whole genome sequence data from patients with mental retardation. I will optimize and apply whole genome sequencing strategies using patient-parent trios, both in rare mental retardation syndromes as well as common forms of mental retardation. Guidelines for pathogenicity will be established by computational studies aimed at unraveling genotype-phenotype correlations in these family-based genome sequence type datasets.
This project will contribute significantly to resolving the genetic causes of reproductively lethal disorders such as mental retardation, provide critical knowledge on the frequency and consequences of de novo mutations in our genome and help to establish medical genome sequencing as a routine diagnostic approach.
Max ERC Funding
1 499 154 €
Duration
Start date: 2012-02-01, End date: 2017-01-31
Project acronym DIASPORACONTEST
Project Diasporas and Contested Sovereignty: Transnational Diaspora Mobilization in Europe and Its Impact on Political Proceses in the Balkans, the Caucasus, and the Middle East
Researcher (PI) Maria Velinova Koinova
Host Institution (HI) THE UNIVERSITY OF WARWICK
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary This groundbreaking multi-methods political science study investigates the transnational mobilization of conflict-generated diasporas in Europe and its impact on polities experiencing contested sovereignty in the Balkans, the Caucasus, and the Middle East. Four researchers study how diasporas mobilize when a specific aspect of sovereignty is contested in the original homeland: The PI focuses on the emergence of new states (Kosovo, Nagorno-Karabakh, Palestine). The Post-doc focuses on a secessionist movement (Kurdish separatism in Turkey and Iraqi Kurdistan). The two Ph.D. students focus on challenges to sovereignty stemming from international military intervention (Iraq) and long-term international governance of a weak state (Bosnia-Herzegovina). Since the scholarly field of diasporas and conflicts still lacks theoretical rigor, this study brings a much needed systematization and innovates in several ways. First, it uses a sequential qualitative and quantitative analysis and multi-sited research techniques that have not been utilized so far. Second, the team seeks to develop a typological theory to incorporate in a single framework: 1) diasporic identities, 2) conditions providing political opportunity structures for transnational mobilization, 3) causal mechanisms concatenating in mobilization processes, and 4) transnational diaspora networks, penetrating various local and global institutions. The study further focuses on five levels of analysis: 1) the attitudes of individuals, 2) characteristics of specific groups, 3) five nation-states with different migrant incorporation regimes (France, Germany, the Netherlands, Sweden, and the UK), 4) supranational EU and global institutions penetrated by diaspora networks, 5) and patterns of mobilization specific to a certain region. The project also conducts a cross-country representative survey across 25 country-groups, creating a much needed quantitative dataset, sensitive both to transnationalism and specific context.
Summary
This groundbreaking multi-methods political science study investigates the transnational mobilization of conflict-generated diasporas in Europe and its impact on polities experiencing contested sovereignty in the Balkans, the Caucasus, and the Middle East. Four researchers study how diasporas mobilize when a specific aspect of sovereignty is contested in the original homeland: The PI focuses on the emergence of new states (Kosovo, Nagorno-Karabakh, Palestine). The Post-doc focuses on a secessionist movement (Kurdish separatism in Turkey and Iraqi Kurdistan). The two Ph.D. students focus on challenges to sovereignty stemming from international military intervention (Iraq) and long-term international governance of a weak state (Bosnia-Herzegovina). Since the scholarly field of diasporas and conflicts still lacks theoretical rigor, this study brings a much needed systematization and innovates in several ways. First, it uses a sequential qualitative and quantitative analysis and multi-sited research techniques that have not been utilized so far. Second, the team seeks to develop a typological theory to incorporate in a single framework: 1) diasporic identities, 2) conditions providing political opportunity structures for transnational mobilization, 3) causal mechanisms concatenating in mobilization processes, and 4) transnational diaspora networks, penetrating various local and global institutions. The study further focuses on five levels of analysis: 1) the attitudes of individuals, 2) characteristics of specific groups, 3) five nation-states with different migrant incorporation regimes (France, Germany, the Netherlands, Sweden, and the UK), 4) supranational EU and global institutions penetrated by diaspora networks, 5) and patterns of mobilization specific to a certain region. The project also conducts a cross-country representative survey across 25 country-groups, creating a much needed quantitative dataset, sensitive both to transnationalism and specific context.
Max ERC Funding
1 498 771 €
Duration
Start date: 2012-02-01, End date: 2017-09-30