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Recent Advances in Handedness Genetics

Symmetry (Basel), 2021-10, Vol.13 (10), p.1792

Paracchini, Silvia

2021

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KIAA0319 influences cilia length, cell migration and mechanical cell-substrate interaction

Scientific reports, 2022-01, Vol.12 (1), p.722-722, Article 722

2022

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Four meta-analyses across 164 studies on atypical footedness prevalence and its relation to handedness

Scientific reports, 2020-09, Vol.10 (1), p.14501-14501, Article 14501

2020

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Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrix

Scientific reports, 2022-07, Vol.12 (1), p.12086-12086, Article 12086

2022

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Different laterality indexes are poorly correlated with one another but consistently show the tendency of males and females to be more left- and right-lateralized, respectively

Royal Society open science, 2020-04, Vol.7 (4), p.191700-191700

2020

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Handedness in twins: meta-analyses

BMC Psychology, 2022-01, Vol.10 (1), p.11-11, Article 11

2022

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Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion

Case reports in genetics, 2021-06, Vol.2021, p.1-5

2021

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Cytogenomic Abnormalities in 19 Cases of Salivary Gland Tumors of Parotid Gland Origin

Case reports in genetics, 2020-12, Vol.2020, p.8897541-6

2020

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An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination

Case reports in genetics, 2020-08, Vol.2020, p.1-8

2020

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Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review

Case reports in genetics, 2020-08, Vol.2020, p.1-5

2020

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Prevalence and heritability of handedness in a Hong Kong Chinese twin and singleton sample

BMC Psychology, 2020-04, Vol.8 (1), p.37-37, Article 37

2020

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Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome

Case reports in genetics, 2020-01, Vol.2019, p.7250838-10

2020

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Human Handedness: A Meta-Analysis

Psychological bulletin, 2020-06, Vol.146 (6), p.481-524

2020

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A Start Codon Variant in NOG Underlies Symphalangism and Ossicular Chain Malformations Affecting Both the Incus and the Stapes

Case reports in genetics, 2019-08, Vol.2019, p.2836263-5

2019

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Chromosomal Abnormalities in Syndromic Orofacial Clefts: Report of Three Children

Case reports in genetics, 2018, Vol.2018, p.1928918-5

2018

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Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene

Case reports in genetics, 2018, Vol.2018, p.9468049-5

2018

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Neoplasia in Cri du Chat Syndrome from Italian and German Databases

Case reports in genetics, 2017-01, Vol.2017, p.5181624-3

2017

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An Interstitial Deletion at 7q33-36.1 in a Patient with Intellectual Disability, Significant Language Delay, and Severe Microcephaly

Case reports in genetics, 2016-01, Vol.2016, p.6046351-5

2016

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Deletion of 7q33-q35 in a Patient with Intellectual Disability and Dysmorphic Features: Further Characterization of 7q Interstitial Deletion Syndrome

Case reports in genetics, 2015-01, Vol.2015, p.131852-5

2015

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SA13FUNCTIONAL CHARACTERIZATION OF ATP2C2, A RISK FACTOR FOR LANGUAGE DISORDERS

European neuropsychopharmacology, 2019, Vol.29, p.S1194-S1195

2019

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SA14THE KIAA0319 DYSLEXIA SUSCEPTIBILITY GENE PRESENTS A HIGHLY SPECIFIC EXPRESSION PATTERN DURING ZEBRAFISH DEVELOPMENT AND PLAYS A ROLE IN CYTOSKELETON DYNAMICS

European neuropsychopharmacology, 2019, Vol.29, p.S1195-S1195

2019

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GENOME-WIDE ASSOCIATION STUDY META-ANALYSIS OF SOCIAL ANXIETY DISORDER

European neuropsychopharmacology, 2022-10, Vol.63, p.e243

2022

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Hand preference and Mathematical Learning Difficulties: New data from Greece, the United Kingdom, and Germany and two meta-analyses of the literature

Laterality (Hove), 2021-09, Vol.26 (5), p.485-538

2021

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The Genetics of Dyslexia

The Science of Reading, 2022, p.491-514

2022

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Recent Advances in Handedness Genetics

KIAA0319 influences cilia length, cell migration and mechanical cell-substrate interaction

Four meta-analyses across 164 studies on atypical footedness prevalence and its relation to handedness

Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrix

Different laterality indexes are poorly correlated with one another but consistently show the tendency of males and females to be more left- and right-lateralized, respectively

Handedness in twins: meta-analyses

Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion

Cytogenomic Abnormalities in 19 Cases of Salivary Gland Tumors of Parotid Gland Origin

An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination

Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review

Prevalence and heritability of handedness in a Hong Kong Chinese twin and singleton sample

Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome

Human Handedness: A Meta-Analysis

A Start Codon Variant in NOG Underlies Symphalangism and Ossicular Chain Malformations Affecting Both the Incus and the Stapes

Chromosomal Abnormalities in Syndromic Orofacial Clefts: Report of Three Children

Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene

Neoplasia in Cri du Chat Syndrome from Italian and German Databases

An Interstitial Deletion at 7q33-36.1 in a Patient with Intellectual Disability, Significant Language Delay, and Severe Microcephaly

Deletion of 7q33-q35 in a Patient with Intellectual Disability and Dysmorphic Features: Further Characterization of 7q Interstitial Deletion Syndrome

SA13FUNCTIONAL CHARACTERIZATION OF ATP2C2, A RISK FACTOR FOR LANGUAGE DISORDERS

SA14THE KIAA0319 DYSLEXIA SUSCEPTIBILITY GENE PRESENTS A HIGHLY SPECIFIC EXPRESSION PATTERN DURING ZEBRAFISH DEVELOPMENT AND PLAYS A ROLE IN CYTOSKELETON DYNAMICS

GENOME-WIDE ASSOCIATION STUDY META-ANALYSIS OF SOCIAL ANXIETY DISORDER

Hand preference and Mathematical Learning Difficulties: New data from Greece, the United Kingdom, and Germany and two meta-analyses of the literature

Language and reading impairments are associated with increased prevalence of non‐right‐handedness

The Genetics of Dyslexia

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