I. L. Macphie

发表

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.

C. Francks, A. Monaco, L. Cardon, 2004, American journal of human genetics.

Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18

A. Morris, A. Monaco, B. Pennington, 2010, PloS one.

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia

Lon R. Cardon, Richard K. Olson, John C. DeFries, 2002, Nature Genetics.

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18

A. Morris, A. Monaco, B. Pennington, 2010, PLoS ONE.

The genetic basis of dyslexia

C. Francks, A. Monaco, I. L. Macphie, 2002, The Lancet Neurology.

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.

C. Francks, V. Kustanovich, S. Nelson, 2002, American journal of human genetics.

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11.

C. Francks, S. Nelson, R. Cantor, 2003, American journal of human genetics.

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.

C. Francks, S. Nelson, A. Monaco, 2002, American journal of human genetics.

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

C. Francks, S. Fisher, S. Paracchini, 2004, Journal of Medical Genetics.

Familial and genetic effects on motor coordination, laterality, and reading-related cognition.

Simon E Fisher, C. Francks, A. Monaco, 2003, The American journal of psychiatry.

Use of multivariate linkage analysis for dissection of a complex cognitive trait.

Simon E Fisher, Stacey S Cherny, Lon R Cardon, 2003, American journal of human genetics.

A genomewide linkage screen for relative hand skill in sibling pairs.

C. Francks, A. Monaco, S. Fisher, 2002, American journal of human genetics.

Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects

C. Francks, A. Monaco, J. McGough, 2004, Molecular Psychiatry.