Angela J. Marlow
Centre for Human Genetics(GB)University of Oxford(GB)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, Reading and Literacy Development, Genomic variations and chromosomal abnormalities, Rheumatoid Arthritis Research and Therapies
Most-Cited Works
- → A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium(1998)540 cited
- → A Genomewide Scan for Loci Involved in Attention-Deficit/Hyperactivity Disorder(2002)293 cited
- → Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia(2001)270 cited
- → A Quantitative-Trait Locus on Chromosome 6p Influences Different Aspects of Developmental Dyslexia(1999)267 cited
- → A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States(2004)240 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
- → Use of Multivariate Linkage Analysis for Dissection of a Complex Cognitive Trait(2003)128 cited
- → A Genomewide Linkage Screen for Relative Hand Skill in Sibling Pairs(2002)126 cited
- → Familial and Genetic Effects on Motor Coordination, Laterality, and Reading-Related Cognition(2003)61 cited
- → Linkage of cytokine genes to rheumatoid arthritis. Evidence of genetic heterogeneity(1998)55 cited