Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies. (Q30620584)

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English	Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies.	scientific article

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23631511%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23631511%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

genome-wide association study

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2

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29 February 2020

John A.L. Armour

3

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29 February 2020

author name string

I C McManus

1

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29 February 2020

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30 April 2013

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29 February 2020

Annals of the New York Academy of Sciences

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29 February 2020

1288

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29 February 2020

48-58

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29 February 2020

The protocadherin 11X/Y (PCDH11X/Y) gene pair as determinant of cerebral asymmetry in modern Homo sapiens

1 reference

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What is complex about complex disorders?

1 reference

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14 July 2018

Schizophrenia as variation in the sapiens-specific epigenetic instruction to the embryo

1 reference

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Genome-wide association studies establish that human intelligence is highly heritable and polygenic

1 reference

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Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.

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Estimating missing heritability for disease from genome-wide association studies

1 reference

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PCSK6 is associated with handedness in individuals with dyslexia

1 reference

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Hundreds of variants clustered in genomic loci and biological pathways affect human height

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Web-based, participant-driven studies yield novel genetic associations for common traits

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The genetics of human adaptation: hard sweeps, soft sweeps, and polygenic adaptation

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The neuroscience of human intelligence differences

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Evolution in health and medicine Sackler colloquium: Genetic architecture of a complex trait and its implications for fitness and genome-wide association studies

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Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome

1 reference

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Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip

1 reference

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14 July 2018

Genetic influences on handedness: data from 25,732 Australian and Dutch twin families

1 reference

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Sex differences in left-handedness: a meta-analysis of 144 studies

1 reference

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When cilia go bad: cilia defects and ciliopathies

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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

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Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

14 July 2018

Confirmatory evidence for linkage of relative hand skill to 2p12-q11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

14 July 2018

Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

14 July 2018

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

14 July 2018

A genomewide linkage screen for relative hand skill in sibling pairs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

14 July 2018

Handedness and hemispheric language dominance in healthy humans

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

14 July 2018

https://api.crossref.org/works/10.1111%2FNYAS.12102

21 January 2018

Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

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A locus for primary ciliary dyskinesia maps to chromosome 19q

1 reference

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Language lateralization in healthy right-handers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

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Genetic models for handedness, brain lateralization, schizophrenia, and manic-depression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

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Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosome

1 reference

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A model for the genetics of handedness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4298034

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Handedness, language dominance and aphasia: a genetic model.

1 reference

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Random determination of a developmental process: reversal of normal visceral asymmetry in the mouse

1 reference

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14 July 2018

Primary ciliary dyskinesia: diagnosis and standards of care

1 reference

https://api.crossref.org/works/10.1111%2FNYAS.12102

21 January 2018

Cilia propel the embryo in the right direction.

1 reference

https://api.crossref.org/works/10.1111%2FNYAS.12102

21 January 2018

Handedness and situs inversus in primary ciliary dyskinesia.

1 reference

https://api.crossref.org/works/10.1111%2FNYAS.12102

21 January 2018

Heritability and linkage analysis of hand, foot, and eye preference in Mexican Americans

1 reference

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Precisely wrong? The problems with the Jones and Martin genetic model of sex differences in handedness and language lateralisation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23631511

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Left-handedness in twins: genes or environment?

1 reference

https://pubmed.ncbi.nlm.nih.gov/23631511

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/NYAS.12102

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23631511%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

PMC publication ID

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Europe PubMed Central

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29 February 2020

PubMed publication ID

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Europe PubMed Central

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29 February 2020

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