Cecilia Lai
Värnamo Sjukhus(SE)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genetic factors in colorectal cancer, Inflammatory Bowel Disease, Language Development and Disorders, Congenital heart defects research
Most-Cited Works
- → A forkhead-domain gene is mutated in a severe speech and language disorder(2001)2,064 cited
- → Molecular evolution of FOXP2, a gene involved in speech and language(2002)1,595 cited
- → Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits(2005)415 cited
- → FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder(2003)392 cited
- → The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration(2006)274 cited
- → Analysis of colorectal cancers in British Bangladeshi identifies early onset, frequent mucinous histotype and a high prevalence of RBFOX1 deletion(2013)232 cited
- → FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment(2002)216 cited
- → The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language Disorder(2000)206 cited
- → DECIPHERING THE GENETIC BASIS OF SPEECH AND LANGUAGE DISORDERS(2003)170 cited
- → Serotonin transporter (5-HTT) and ?-aminobutyric acid receptor subunit ?3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families(1999)160 cited