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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.

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

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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