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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.

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

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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