Concepedia

Cecilia Lai

CL

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Publications

15

Citations

5.7K

H-Index

15

Active since

1999

Affiliations

Centre for Human Genetics(Current)

University of Oxford

Queen Mary University of London

University College London

John Radcliffe Hospital

Cecilia Lai is an author at Centre for Human Genetics specializing in medicine, genetics, and molecular genetics.

ORCID

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Publications per year

1999–2017

15

Publications

15

A forkhead-domain gene is mutated in a severe speech and language disorder

Cecilia Lai, Simon E. Fisher, Jane A. Hurst et al. · Nature · 2001 · 2.1K citations · Full text

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Molecular evolution of FOXP2, a gene involved in speech and language

Wolfgang Enard, Molly Przeworski, Simon E. Fisher et al. · Nature · 2002 · 1.6K citations · Full text

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Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

Kay MacDermot, Elena Bonora, Nuala Sykes et al. · The American Journal of Human Genetics · 2005 · 414 citations · Full text

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FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder

Cecilia Lai · Brain · 2003 · 389 citations · Full text

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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration

Silvia Paracchini, Ankur Thomas, Sandra C. de Castro et al. · Human Molecular Genetics · 2006 · 274 citations · Full text

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