medical genetics
26 projects
HEIndividual fellowship2026–2028France
SKM-REFORMAT · SKeletal Muscle - REgulation of FORce and Maturation through Tubulin isotypes
H2020Individual fellowship2020–2022Italy
INNERVATE · Investigating the functional impact of neurodegeneration-causing rare variants in the teleost model zebrafish
H2020Individual fellowship2020–2022Austria
JS_SCZ · Investigating impact of schizophrenia-associated non-coding variants on enhancer activity using brain organoids
H2020Doctoral network2019–2024Switzerland
CANCERPREV · Innovative strategies for cancer prevention with focus on sex hormone signaling and chronic inflammation
7 partners · 6 countries
H2020Individual fellowship2019–2021France
SingCelCD · Single Cell approaches for the study of oncogenic processes during coeliac disease.
H2020Doctoral network2019–2023Belgium
V.A. Cure · A multidisciplinary approach towards sustainable improvement in rare diseases care uniting Europe's top class vascular research to find new treatment strategies for vascular anomalies
17 partners · 5 countries
H2020COFUND2019–2024Denmark
iMED · International Doctoral Programme in Molecular Mechanisms of Disease
H2020Individual fellowship2017–2020Germany
IMAGENE · Characterizing Function Genetic Variants Linking Immunity and Psychiatric Disorders
2 partners · 2 countries
H2020Staff exchange2017–2022Portugal
LysoMod · Genetic and Small Molecule Modifiers of Lysosomal Function
14 partners · 9 countries
H2020Individual fellowship2016–2018United Kingdom
MITOBIOPATH · DISCOVERING NEW DISEASE PATHWAYS AFFECTING mtDNA METABOLISM
2 partners
H2020Individual fellowship2016–2018United Kingdom
HairGen · Genetics of human hair form diversity
H2020Individual fellowship2016–2018United Kingdom
RADIOGENFF · RADIOGENOMICS: Finding Genetic Functional Variants Through Fine Mapping
H2020Individual fellowship2015–2017Netherlands
MOvE-ECG · Moving from genome wide association to elucidating causal mechanisms of electrocardiographic traits
2 partners · 2 countries
H2020Individual fellowship2015–2018United Kingdom
SOX10mutants · Investigating genotype-phenotype correlations in SOX10 neurocristopathies
H2020Individual fellowship2015–2017France
GATTACA · Genetics of Alternative Transcript Abundance upon immune Cellular Activation
H2020Doctoral network2015–2018Netherlands
MiND · Mastering skills in the training Network for attention deficit hyperactivity and autism spectrum Disorders
22 partners · 9 countries
FP7Individual fellowship2013–2015Austria
SAXCESS · Structure-function analysis of the human plasma glycoprotein afamin, a potential drug target in the treatment of metabolic syndrome.""
FP7Staff exchange2012–2016United Kingdom
TRIP · Translational Research into Psychiatric disorders: genetics, genomics and neurobiology of psychosis and autism
2 partners · 2 countries
FP7Individual fellowship2008–2010Switzerland
WGIMPRINT · A Whole-Genome Screen for Novel Imprinted Loci
FP7Individual fellowship2008–2010Sweden
GENTRECAD · GENOME-WIDE CHARACTERIZATION OF TRANSCRIPTIONAL REGULATORY ELEMENTS, PATHWAYS AND ASSOCIATED GENETIC VARIATIONS INVOLVED IN THE PATHOGENESIS OF CORONARY ARTERY DISEASE
FP6Individual fellowship2007–2009United Kingdom
TRKB AND OB-R · Functional characterization of TrkB and Ob-R mutations identified in severely obese children
FP6Individual fellowship2005–2007United Kingdom
COMPSNPS · A new approach for genic SNP discovery in polyploid bread wheat
FP6Excellence award2004–2008Austria
NOVEL BREAST CANCER · Novel genetic approaches to study breast cancer
FP6Individual fellowship2004–2007Belgium
ARRAYCGH-MC · Marie Curie Conferences and Training Courses on arrayCGH and Molecular Cytogenetics
5 partners · 4 countries