Angela Martinelli

University of St Andrews — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

16h-index839citations49works0.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(7), Smoking Behavior and Cessation(5), Disaster Response and Management(4), Congenital heart defects research(4), Reading and Literacy Development(3)

Publications48 total

Insieme “CONpatibilMENTE” – Riflessione sui Tempi di handover per rendere “visibile l’invisibile”
Recenti Progressi in Medicina·2023Open Access
Integrating extracellular vesicle and circulating cell‐free DNA analysis using a single plasma aliquot improves the detection of HER2 positivity in breast cancer patients
Journal of Extracellular Biology·2023· 12 citedOpen Access
Integrating extracellular vesicle and circulating cell-free DNA analysis on a single plasma aliquot from breast cancer patients improves the detection of HER2 positivity
2023Open Access
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia
Nature Genetics·2023Open Access
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities
Translational Psychiatry·2022· 14 citedOpen Access
Discovery of 42 genome-wide significant loci associated with dyslexia
Nature Genetics·2022· 134 citedOpen Access
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
Proceedings of the National Academy of Sciences·2022· 126 citedOpen Access
A Community Study of SARS-CoV-2 Detection by RT-PCR in Saliva: A Reliable and Effective Method
Viruses·2022· 11 citedOpen Access
KIAA0319 influences cilia length, cell migration and mechanical cell–substrate interaction
Scientific Reports·2022· 12 citedOpen Access
Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
2021· 14 citedOpen Access
Detection of SARS-CoV-2 in the community by nucleic acid amplification testing of saliva
2021Open Access
A rare missense variant in the <i>ATP2C2</i> gene is associated with language impairment and related measures
Human Molecular Genetics·2021· 16 citedOpen Access
A rare missense variant in the <i>ATP2C2</i> gene is associated with language impairment and related measures
2021· 1 citedOpen Access
A study of health locus of control, self-efficacy, health promotion behaviors, and environmental factors related to the self-report of the avoidance of environmental tobacco smoke in young adults
2020
KIAA0319 influences cilia length, cell migration and mechanical cell-substrate interaction
2019Open Access
The dyslexia susceptibility <i>KIAA0319</i> gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration
The Journal of Comparative Neurology·2019· 19 citedOpen Access
SA13FUNCTIONAL CHARACTERIZATION OF ATP2C2, A RISK FACTOR FOR LANGUAGE DISORDERS
European Neuropsychopharmacology·2019
SA14THE KIAA0319 DYSLEXIA SUSCEPTIBILITY GENE PRESENTS A HIGHLY SPECIFIC EXPRESSION PATTERN DURING ZEBRAFISH DEVELOPMENT AND PLAYS A ROLE IN CYTOSKELETON DYNAMICS
European Neuropsychopharmacology·2019
The dyslexia susceptibility KIAA0319 gene shows a highly specific expression pattern during zebrafish development supporting a role beyond neuronal migration
2018· 1 citedOpen Access
The DCDC2 deletion is not a risk factor for dyslexia
Translational Psychiatry·2017· 24 citedOpen Access
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Frequent Co-authors

Silvia Paracchini(13), Marianna E. Hayiou‐Thomas(9), Dianne F. Newbury(8), John Stein(6), Joel B. Talcott(6), Rebeca Diaz(6), Else Eising(5), Scott D. Gordon(5), Filippo Abbondanza(5), Andrea G. Allegrini(5), Till F. M. Andlauer(5), Cathy L. Barr(5), Manon Bernard(5), Kirsten Blokland(5), Dorret I. Boomsma(5), Thomas Bourgeron(5), Daniel Brandeis(5), Manuel Carreiras(5), Fabiola Ceroni(5), Philip S. Dale(5)