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SynGenes SIGNED

Defining the genetics of grapheme-colour synaesthesia

Total Cost €

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EC-Contrib. €

0

Partnership

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 SynGenes project word cloud

Explore the words cloud of the SynGenes project. It provides you a very rough idea of what is the project "SynGenes" about.

interrogation    date    technologies    population    training    variants    competitiveness    community    heterogeneous    opening    discovered    newly    candidates    supports    complementary    wp2    sense    career    rare    scientific    measured    hyperconnectivity    triggers    skills    perform    plans    wp4    neural    diverse    familial    researcher    clustering    genes    ascertained    professional    genome    wp3    multigenerational    phenomenon    sequencing    unrelated    public    underlying    outreach    contributions    colour    heritable    remove    individuals    neurodevelopmental    wp1    deepen    1000    theory    genetic    genotyping    synaesthetes    silico    add    sensory    informatics    neurobiology    milestones    automatically    synaesthesia    reliably    barrier    fellowship    avenues    platform    associate    aetiology    stimulation    contribution    neurogenetics    advancing       stones    hindrance    utilizing    landscape    genetics    strategy    toward    quality    grapheme    parallel    stepping    indicates    suite    skillset    perception    significantly    prevailing    variation    integrative    independent    families    letters    stakeholders    poorly    unmask   

Project "SynGenes" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: Munich
postcode: 80539
website: www.mpg.de

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Project website http://www.mpi.nl/synaesthesia
 Total cost 171˙460 €
 EC max contribution 171˙460 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2016
 Duration (year-month-day) from 2016-06-01   to  2018-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (Munich) coordinator 171˙460.00

Map

 Project objective

Synaesthesia is a common neurodevelopmental phenomenon (2-5% of the population) where stimulation of one sense automatically triggers an experience of another. Familial clustering indicates that synaesthesia is highly heritable. However, this genetic contribution is poorly understood and likely heterogeneous, a major hindrance to our understanding of the neurobiology. My objective is to remove this barrier through the most comprehensive interrogation of synaesthesia genetics to date, utilizing state-of-the-art technologies and integrative approaches. This study will focus on individuals who associate letters and numbers with colour (grapheme-colour synaesthesia), as this type of synaesthesia is common and the most reliably measured. I will apply two complementary approaches in parallel. Whole genome sequencing in two newly ascertained multigenerational synaesthesia families will determine the role of rare genetic variants (Work Package 1, WP1), while genome-wide genotyping of 1000 unrelated synaesthetes will unmask contributions from common variation (WP2). Using existing candidates and novel genes discovered in this work, I will perform multi-level in silico analyses to test if genetic information supports the prevailing theory of neural hyperconnectivity as an underlying aetiology (WP3). WP1-3 will help to define the genetic landscape of synaesthesia, while opening novel research avenues into the neurobiology of sensory perception. This fellowship will provide a diverse set of stepping-stones toward my professional goal of becoming an independent researcher in the rapidly advancing field of neurogenetics. The research and training plans will deepen my current skillset and add a suite of complementary informatics skills that will significantly enhance the quality and competitiveness of my scientific career. The multi-platform dissemination and public outreach strategy involves both the scientific community and main stakeholders at the major milestones (WP4).

 Publications

year authors and title journal last update
List of publications.
2018 Amanda K. Tilot, Katerina S. Kucera, Arianna Vino, Julian E. Asher, Simon Baron-Cohen, Simon E. Fisher
Rare variants in axonogenesis genes connect three families with sound–color synesthesia
published pages: 3168-3173, ISSN: 0027-8424, DOI: 10.1073/pnas.1715492115
Proceedings of the National Academy of Sciences 115/12 2019-06-14

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