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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.

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

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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