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  Absolute pitch exhibits phenotypic and genetic overlap with synesthesia

Gregersen, P. K., Kowalsky, E., Lee, A., Baron-Cohen, S., Fisher, S. E., Asher, J. E., et al. (2013). Absolute pitch exhibits phenotypic and genetic overlap with synesthesia. Human Molecular Genetics, 22, 2097-2104. doi:10.1093/hmg/ddt059.

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 Creators:
Gregersen, Peter K.1, Author
Kowalsky, Elena1, Author
Lee, Annette1, Author
Baron-Cohen, Simon2, Author
Fisher, Simon E.3, 4, Author           
Asher, Julian E.2, Author
Ballard, David1, Author
Freudenberg, Jan1, Author
Li, Wentian1, Author
Affiliations:
1Robert S. Boas Center for Genomics and Human Genetics, The Feinstein Institute for Medical Research, North Shore-LIJ, Manhasset, NY. 11030 , ou_persistent22              
2Autism Research Centre, Psychiatry Department, Cambridge University, Cambridge CB2 8AH , ou_persistent22              
3Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, ou_792549              
4Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, ou_persistent22              

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 Abstract: Absolute pitch and synesthesia are two uncommon cognitive traits that reflect increased neuronal connectivity and have been anecdotally reported to occur together in a same individual. Here we systematically evaluate the occurrence of syesthesia in a population of 768 subjects with documented absolute pitch. Out of these 768 subjects, 151(20.1%) reported synesthesia, most commonly with color. These self-reports of synesthesia were validated in a subset of 21 study subjects using an established methodology. We further carried out combined linkage analysis of 53 multiplex families with absolute pitch and 36 multiplex families with synesthesia. We observed a peak NPL LOD=4.68 on chromosome 6q, as well as evidence of linkage on chromosome 2 using a dominant model. These data establish the close phenotypic and genetic relationship between absolute pitch and synesthesia. The chromosome 6 linkage region contains 73 genes; several leading candidate genes involved in neurodevelopment were investigated by exon resequencing. However, further studies will be required to definitively establish the identity of the causative gene(s) in the region.

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Language(s): eng - English
 Dates: 20132013
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1093/hmg/ddt059
 Degree: -

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Title: Human Molecular Genetics
Source Genre: Journal
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Publ. Info: Oxford, England : OUP
Pages: - Volume / Issue: 22 Sequence Number: - Start / End Page: 2097 - 2104 Identifier: ISSN: 0964-6906
CoNE: https://pure.mpg.de/cone/journals/resource/954925581153