(Q30427847)

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Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music

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scholarly article

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Europe PubMed Central

PMC publication ID

15 August 2017

Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Harri Lähdesmäki

8

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4

object named as

Gemma Buck

0 references

Chakravarthi Kanduri

object named as

Chakravarthi Kanduri

2

0 references

object named as

Jaana Oikkonen

3

0 references

object named as

Irma Järvelä

9

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author name string

Liisa Ukkola-Vuoti

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Christine Blancher

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Pirre Raijas

6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Kai Karma

7

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

language of work or name

0 references

publication date

27 February 2013

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

e56356

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

copyright license

Creative Commons Attribution 4.0 International

27 February 2013

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April 2022 Public Data File from Crossref

copyright status

0 references

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1 reference

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1 reference

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1 reference

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Association of the arginine vasopressin receptor 1A (AVPR1A) haplotypes with listening to music

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New copy number variations in schizophrenia.

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Functional impact of global rare copy number variation in autism spectrum disorders

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Variation in transcription factor binding among humans

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Functional specializations for music processing in the human newborn brain.

1 reference

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Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

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Global variation in copy number in the human genome

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Human copy number variation and complex genetic disease.

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Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype

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Protocadherin-alpha family is required for serotonergic projections to appropriately innervate target brain areas.

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Music, maestro, please!

1 reference

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Polygenic inheritance of breast cancer: Implications for design of association studies

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https://pubmed.ncbi.nlm.nih.gov/23460800

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based on heuristic

inferred from PubMed ID database lookup

The protocadherin-alpha family is involved in axonal coalescence of olfactory sensory neurons into glomeruli of the olfactory bulb in mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/23460800

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Perception of music by infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/23460800

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0056356

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

2013PLoSO...856356U

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

0 references

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