Angela Martinelli

University Of St Andrews
Saint Andrews, SCT KY169TF, United Kingdom

Last Updated: 09/26/2026

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Found 8 publications

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Journal: Recenti progressi in medicina

Published: August 02, 2023

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: August 23, 2022

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

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

Journal: Scientific reports

Published: April 05, 2021

A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.

A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.

Journal: Human molecular genetics

Published: January 16, 2021

The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration.

The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration.

Journal: The Journal of comparative neurology

Published: September 10, 2018

O015. Evaluation of the genetic polymorphism of the α3 (CHRNA3) and α5 (CHRNA5) nicotinic receptor subunits, in patients with cluster headache.

O015. Evaluation of the genetic polymorphism of the α3 (CHRNA3) and α5 (CHRNA5) nicotinic receptor subunits, in patients with cluster headache.

Journal: The journal of headache and pain

Published: January 30, 2017

A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.

A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.

Journal: The journal of headache and pain

Published: November 01, 2016

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.

Journal: PloS one

Published: March 03, 2015

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Last Updated: 09/26/2026